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Vertigo by Dr. Sayeed Ahmad

Vertigo, sensation of spinning around or of seeing nearby objects revolve. Vertigo tends to be accompanied by nausea, vomiting, headache, or sweating. Read More

DRUG PROVING by Dr. Mujeeburahman Thekkethodika

The drugs have been used since antiquity for curing of the disease but without any proper basis. At that time for the application of drugs, ‘Doctrine of Signature’ were followed founded on the belief that each member of the plant kingdom carried with in itself the likeness of some organ or the part of the economy, as a sign that this particular plant was applicable to disturbances of the organ. That was probably most consisted method among all the ancient systems of applying drugs.

Paracelsus (1493-1541) gained considerable insight in to the action of drugs, and Halle, the Swedish physician, was a fore runner of Hahnemann in his experiments to discover the nature of certain medicines. These attempts were not coordinated, and made little impression up on the medical world. Needless to say, Hahnemann was the first to adduce scientific proof of the truth of Homoeopathy. He and his colleagues tested the effect of some 90 odd drugs up on themselves and others. This genuine process of ascertaining the pure and peculiar effects of medicine is known as ‘DRUG PROVING’. Besides Hahnemann, great and immortal Albrecht von Haller (1708-1777) saw the necessity of this.

Definition of Drug-Proving

Drug proving is the process of acquiring knowledge of instruments intended for the cure of the natural diseases ($105)

It is the systematic and orderly way of investigating the pathogenetic power of a medicine on a healthy person. By ‘drug proving’ we mean the positive effects of drug up on living organism, i.e., to know the pathogenetic effects of the drug. Drug provings are experiments with drug substances on healthy human beings to note the disease- producing powers known as ‘curative powers’ of the particular drugs.

Evolution of the Concept of Drug Proving

According to Hahnemann, it was Albrecht von Haller, who besides himself saw the necessity of this genuine mode of testing medicines for their pure and peculiar effects in deranging the health of man, in order to learn what morbid state each medicine is capable of curing [footnote to aphorism 108].

Haller said – “Indeed, a medicine must first of all be assayed in a healthy body, without any foreign admixture. When the odor and taste have been examined, a small dose must be taken and attention must be paid to every change that occurs, to the pulse, the temperature, respiration and excretions. Then having examined the symptoms encountered in the healthy person, one may proceed to trials in the body of a sick person.”

Not one single physician, during the previous two thousand five hundred years before Hahnemann who saw the importance of such an exercise and was the first to open up this path that demanded perseverance, with a perfect conviction of truth.

Hahnemann had studied different languages and his eight translations from English, French and Italian into German included works of considerable significance. Dr. Cullen was an authority on Materia Medica. In Cullen’s Materia Medica was established the first milestone on the road of development of the new method of treatment. When Hahnemann commenced upon this translation, he did not have any particular medical theories, but only a growing disgust for the medical fallacies of the day.

The first edition of Cullen’s work appeared in 1773, the second followed in two volumes: in the year 1789, under the title “Treatise of the Materia Medica”. Hahnemann used these for his translation. In the second volume Cullen devoted twenty pages to Cinchona bark (Cortex Peruvianus).

Regarding the question of medicinal effect of Peruvian bark, Cullen defended the old opinion of the efficacy of this remedy through its “tonic effect on the stomach”.

Cullen remarked – “I have endeavored to explain, in my first outlines of practical medical science, that the bark in this instance acts through its tonic effect on the stomach, and I have found nothing in any writings which could make me doubt the truth of my statements.”

Hahnemann became indignant over the affected, theoretical explanations of the antipyretic power of cinchona bark that Cullen was asserting. Hahnemann attacked this opinion vigorously in his notes – “By combining the strongest bitters and the strongest astringents we can obtain a compound which, in small doses, possesses much more of both these properties than the bark, and yet in all eternity no fever specific can be made from such a compound. The author should have accounted for this. This undiscovered principle of the effect of the bark is probably not easy to find.”

The researches of Cullen induced Hahnemann to make experiments upon himself with this remedy. Hahnemann therefore resolved to ascertain, by the natural method of experience, wherein lay the power of cinchona bark to allay intermittent fever.

“Let us consider the following: Substances which produce some kind of fever (very strong coffee, pepper, arnica, ignatia bean, arsenic) counteract these types of intermittent fever. I took for several days, as an experiment, four drachms of good Cinchona twice daily. ‘My feet and finger tips, etc at first became cold; I became languid and drowsy; then my heart began to palpitate, my pulse became hard and quick; an intolerable anxiety and trembling (but without a rigor), prostration in all the limbs, then pulsation in the head, redness of the cheeks, thirst; briefly, all the symptoms usually associated with intermittent fever appeared in succession, yet without the actual rigor.

To sum up: all those symptoms which to me are typical of intermittent fever, as the stupefaction of the senses, a kind of rigidity of all joints, but above all the numb, disagreeable sensation which seems to have its seat in the periosteum over all the bones of the body – all made their appearance. This paroxysm lasted from two to three hours every time, and recurred when I repeated the dose, not otherwise. I discontinued the medicine and I was once more in good health’.”

Hahnemann remarked, in opposition to Cullen – “If the author had detected that the bark had the power of producing artificial, antagonistic fever . . . certainly he would not have held so firmly to his mode of explanation. Peruvian bark, which is used as a remedy for intermittent fever, acts because it can produce symptoms similar to those of intermittent fever in healthy people.”

The “Cinchona experiment” brought out not only the exact physiological effects of the bark; it had shown him that those effects were apparently the same as the symptoms of the disease for which it was used (ague).

Does the bark produce the same symptoms as it removes?
Does it alike produce and cure ague?
Is the “Specific” curing power of drugs founded on such a principle?
Do they all uniformly excite a counterfeit disease to that which they remedy?
Drug after drug, specific after specific was tested by Hahnemann on himself and on his family and friends, all with one result – each remedy of recognized specific power excited a spurious disease resembling that for which it was considered specific.

He verified his discoveries and observations by exploring volumes of recorded experiments on Materia Medica and history of poisonings.

Hahnemann here sensed a law that taught him to recognize, that, in the effect that a substance has on the healthy organism is to be found its curative power for similar disease symptoms, because he could not doubt that here prevailed more than a simple coincidence.

Hahnemann had, thus, recorded the effects of a drug administered to a healthy person. This led Hahnemann to a six-year study of different drugs on himself and others. The results were published in his work Fragmenta de Viribus Medicamentorum Positivis sive in sano corpore humano observatis in 1805. The first part contained twenty-seven drugs; symptoms cited in it were those of the provings and of the observations from the work of others and at the end of each remedy, he gave the effects recorded by previous observers in cases of poisoning. It was the first collection ever made of provings of medicines upon the healthy body.

But many more symptoms than that diagnostic of any one disease resulted from almost every medicine. These uncommon, peculiar, non-diagnostic symptoms produced after the employment of a drug to a healthy prover was confirmed over series of experiments.

This is how Hahnemann traveled from the realm of “specifics” into the realm of “individualization” which formed the actual reason and basis of homoeopathic drug provings – determination of the more striking, singular, uncommon and peculiar (characteristic) signs and symptoms rather than the common, diagnostic (specific) symptoms of diseases.

In 1806, he published his essay, Medicine of Experience, in which he mentioned that, for ascertaining the pure and positive effect of the drug it is necessary to give a single dose to a normal healthy person. Gradually Hahnemann started collected disciples around him.

Hahnemann then published his provings in Materia Medica Pura in six parts from 1811 to 1821.

Hahnemann’s Provings and His Prover’s Union

The provers whom Hahnemann selected and who appeared worthy to him (he was very strict in his selection) he invited into his family and so attached them to himself in a personal and friendly way. Franz Hartmann was a member of the Provers’ Union along with Stapf, Gross, Hornburg, Franz, Wislicenus, Teuthorn, Herrmann, Rückert and Langhammer.

The initial provings were carried out with simple substances and tinctures. For at that time Hahnemann had scarcely thought, if at all, of the original causes of chronic diseases and of the infinite dilution of medicines and their effect in the highest dilutions on the healthy body.

Provings were carried out according to an exact system and from detailed instructions. Sometimes those engaged in the provings had to provide for themselves the medicinal substances, particularly the herbal ones. By this means they learned to recognize herbaria by habitat, period of bloom, etc. They learned to dry them methodically or to obtain a tincture from the fresh plant. The observations of the results, which every individual had to make on himself at definite times, were entered up in carefully prescribed manner. After that, the comparative relationships of the medicinal effects observed by the individual provers were taken, and the power of a medicine was only established after comparison of different participants.

Dr. Franz Hartmann, a member of Hahnemann’s Provers’ Union gave a detailed account of Hahnemann’s provings:

During a proving, Hahnemann absolutely forbade coffee, tea, wine, brandy and all other heating drinks, as well as spices, such as pepper, ginger, also strongly salted foods and acids. He cautioned against close and continued application to study, or reading novels, as well as against many games that exercised not merely the imagination, but which required continued thought, such as cards, chess or billiards, by which observation was disturbed and rendered untrustworthy. Hahnemann did not recommend idleness, but advised moderate labor only, agreeable conversation, with walking in the open air, temperance in eating and drinking and early rising. For a bed he recommended a mattress with light covering.

The medicines that were to be proved were supplied by Hahnemann himself. The vegetable drugs were in the form of essence or tincture, the others in the first or second trituration. Hahnemann never concealed from his provers the names of the drugs that were proved and it was his wish that they should, in the future prepare all the remedies whose effects they had tried.

Hahnemann, for the most part, had previously proved the drugs upon himself and his family, and was sufficiently acquainted with their strength and properties to prescribe for each prover according to his individuality, the number of drops or grains with which he might commence, without experiencing any injurious effects.

The dose to be taken was mixed with a great quantity of water and was taken early in the morning, fasting, and nothing was taken for an hour. If no effect was experienced in three or four hours, a few more drops were to be taken; the dose might even be doubled and the reckoning of time was to be from the last dose. If, upon the third repetition, no change was remarked, Hahnemann concluded that the organism was not susceptible to this agent and did not require the prover to make any further experiments with it, but after several days gave him another drug to prove.

In order to note down every symptom that presented itself, he required each one to carry a tablet and lead pencil with him, which had this advantage that they could describe with precision the sensation they had experienced at that time. This precision might be lost if these sensations were noted down at some subsequent period. Every symptom that presented itself must be given in its connection. After every symptom, they had to specify in brackets, the time of its occurrence, which time was reckoned from the last dose. It was only when one or two days had passed without the occurrence of any symptoms that Hahnemann supposed the action of the drug to be exhausted. He then allowed the system a time to rest before another proving was undertaken. Hahnemann always reviewed the symptoms once with the provers to be sure that they had used just the right expressions and signs and had said neither too much nor too little.

At first it often happened that there were errors, but these became fewer with every proving and finally there were none at all. Proving is an art and it is not easy as it appears. It requires a particular type of attention to grasp properly the symptoms that could only be felt faintly and these are often just the most important, the really characteristic ones and of much greater significance than those which set in more violently. The former set is as a rule only after small, delicate doses, while the latter owe their onset to the stronger doses.
The provers had to be as healthy as possible and keen to explore the high truths that one is expecting to find, with a strong sense of conscientious honesty, without expecting the slightest worldly advantage, not even the honor of being publicly mentioned as a prover.

Hahnemann had condemned a physician, Fickel, who invented all the printed symptoms in his so-called proving of Osmium, which he had never seen, just for the sake of snapping up a bookseller’s fee.

Hahnemann recounts -

Each one of them was interrogated daily or every two or three days on the symptoms experienced by them, partly in order to enquire if any one of them had previously experienced similar sensations (that this might be put in brackets when printing as not altogether due to the medicine), partly that the exact character of his sensations and observations might be compared with the words written down, and perhaps afterwards be able to choose with his consent more definite expressions. All the important secondary considerations of any value were mentioned at the same time together with the symptoms under which they occurred.

As regards my own experiments and those of my disciples every possible care was taken to insure their purity. They were performed on people as healthy as possible and under regulated external conditions as nearly as possible alike. But if during the experiment some extraordinary circumstance from without happened that might be supposed to be capable of altering the result – e.g. a shock, vexation, a fright, an external injury of sufficient severity, dissipation or overindulgence in something or other, or any other circumstance of importance – from that time no symptom that occurred in the experiment was registered. They were all rejected to remove any suspicion of impurity about it. If some little circumstance happened during the experiment, which could hardly be expected to interfere with the effects of the medicinal action, the symptoms subsequently noticed were enclosed within brackets as not certainly pure.

With respect to the duration of action ascribed to each medicinal substance, which I endeavored to determine by repeated experiment, I should state that it was only learned from the experiments on the healthiest possible persons.

Proving Guidelines as per Organon of Medicine – Sixth Edition

For the selection of a suitable homoeopathic remedy for the natural diseases, the whole pathogenetic powers of medicines must be known. All the morbid symptoms and alterations in the health that each medicine is capable of producing in a healthy individual must first be observed before administering the similimum. [aphorism 106]

As Hahnemann’s observations on the action of drugs were confirmed by earlier writers who noted the toxicological effects of many drugs used in large doses (though they had no idea of their therapeutic indications), he concludes that the pathogenetic effects or pharmacological actions are produced according to fixed, eternal laws of nature and by virtue of these they produce certain reliable disease symptoms each according to its own peculiar character. [aphorism 111]

Object of Proving

Every plant species differs in its external form, mode of life and growth, in its taste and smell from every other species and genus of plant; so also every mineral and salt differs from all others in its external and internal physical and chemical properties.

Each of the medicinal substances that are derived from these sources also differs and diverges among themselves in their pathogenetic and therapeutic effects.

They produce alterations in the health of human beings in a peculiar and different, unique and determinate manner. Hence is essential for determining their peculiar therapeutics so as not to confound one with another.

As the selection of the similimum is based on the homoeopathic philosophy of Totality and Individualization, it is the peculiar technique of drug proving that provides the true, complete ‘portrait of the drug’ that can be compared with the portrait of the disease. Anyone understanding this basic principle will never resort to ‘surrogates’ or substitutes in prescription. [aphorism 119]

Hence medicines, on which depend man’s life and death, disease and health, must be thoroughly and most carefully distinguished from one another and tested by careful, pure experiments on the healthy body for the purpose of ascertaining their powers and real effects, in order to obtain an accurate knowledge of them. It is only then, can a correct selection of them can be made for the permanent restoration of the health of the body and of the mind. [aphorism 120]

Selection of Prover

 

(A) Animal proving

(a) Disadvantages;

Proving on lower animals should not be done due to following defects;

1.      Subjective and mental symptoms cannot be studied as they cannot express themselves by speaking.

2.      Modalities and finer sensations are lacking to make a symptom complete.

3.      The effect of same drug on animals and on humans is different.

4.       Proper individualization of knowledge of drugs is never possible on animal provings.

5.      The question of susceptibility and idiosyncrasy is difficult to judge from animal provings.

(b) Advantages

1. The drug may be proved in any quantity, but not possible in human proving due to toxicological effects of drugs.

2. The drug may be proved for any length of time, but not possible in human proving due to fear of poisoning.

3. We may go to ultimate pathology and dare to lose the prover.

4. Proving with unknown substance may give a first hand information with regards to action on living organism.

5. To assay the physiological action of drugs.

(B) Human proving

 

Proving in Sick and Healthy Individuals

Medicines, even though singly and alone, must not be administered to sick persons because little or nothing precise is seen of their true effects, as those peculiar alterations of the health to be expected from the medicine are mixed up with the symptoms of the disease and can seldom be distinctly observed. [aphorism 107] There is no other sure, possible and natural way in which the peculiar effects of medicines on the health of individuals can be accurately ascertained than to administer the medicines in moderate doses to healthy individuals. [aphorism 108]

(a) Proving on sick persons ($107)

Should not be done because;

1. The true effects of medicine can seldom be distinctly observed as the symptoms of natural disease and the peculiar alterations of medicines are mixed up, even though they are administered singly and alone.

2. In disease state the person may be hypersensitive or hyposensitive and so the intensity of the symptoms may be increased or decreased accordingly.

3. If accidentally the symptoms of the medicines are similar to his disease, he will be cured or partially relieved. Neither the symptoms of the disease nor of the drug shall be visible externally.

4. If the drug used is of opposite nature to his disease, it shall bring temporary relief.

5. If the drug is dissimilar to the disease, either there will be no effect or will form a complex disease.

(b) Proving on healthy human being ($108)

The best possible way of ascertaining the pure and peculiar effects of medicine is to make a proving by administering several medicines experimentally, on healthy human beings, in moderate doses.

Advantages;

Except the negligible amount of disadvantages, human proving serves all our purposes. They are;

1.      Subjective and mental with their modalities and concomitants may only be recorded in human proving.

2.       From such proving we get pure and accurate pathogenetic effects of medicine which help to cure the natural disease on the basis of symptom similarity.

3.      Administration of medicine in healthy human being gives response properly according to full capability of vital force.

4.      Peculiar and characteristics of the drug-the rare unusual symptoms that distinguish it from all others is only possible during human proving especially from this susceptible one.

Qualities of Human Prover

1. Ideal prover;

The qualities of an ideal prover are;

a) Healthy;

The prover must posses sound health, free from disease, and individual     can determine the effects of medicines very distinctly.

b).Intelligent

c).Delicate, irritable and sensitive ;( $121)

d).Lover of truth, temperate in all respects of delicate feelings, who can direct the       minutest attention to his sensations ($137). He must avoid all over exertions of mind and body, disturbing passion and distractions.

2. Best prover;($141)

The healthy unprejudiced and sensitive physician himself is the best   prover.

3. Idiosyncratic prover;

The idiosyncratic person is a best possible prover of the substance to which he is idiosyncratic.

 

 

 

Choice of Prover.

 

The medicine must be tested on both sexes-males and females, in different ages,    and many individuals with various constitutions.

1. Both males and females ;( $127); Drug proving must be done in both sexes, because of the following causes;

a.      in order to reveal the alterations of health they produce in the sexual sphere.($127)

b.      Males and females are different in anatomical, physiological and psychological sphere. So to treat the disease of both sexes, we must know the pathogenetic power of medicine in sexual sphere.

c.       More over there are certain diseases which are specific for male and some for females. So for treatment of specific diseases, we must know the effects of drugs through drug proving , on both sexes.

2. Different ages; Drug should be proved in persons of different ages because                                                 of the following reasons;

a.      Physical appearance, anatomical development and functions vary according to the age. We have to treat the patients of different age groups. So we must be certain of the curative powers of medicine in different age groups.

b.      There are diseases which are more common in certain age groups, e.g., measles, whooping cough, rheumatic fever, are common in children, where as, enlarged prostate, cataract are common in aged individuals.

c.      Susceptibilities and physical irritability varies with age.

3. Many individuals ($136); Drug proving must be done on many individuals. All the symptoms peculiar to a medicine do not appear in one person , nor all at once, nor in the same experiment, but some occur in one person chiefly at one time, others again during a second or third trial($134). So in order to get the whole pathogenetic power of a medicine, proving should be done on many different individuals, varying in their corporeal and mental constitutions ($136)
Action of Drugs in Relation to their Doses

Hahnemann observed the following facts regarding the action of drugs in relation to their specificity and the varying doses in which they are to be administered to healthy human beings.

1. Administration of drugs in excessively large doses leads to production of certain symptoms during the initial stage that are followed later by symptoms that were of an exactly opposite nature to those that first appeared. The first set of symptoms constitutes the primary action of remedies and the following set of symptoms is the reaction of the vital force of the organism and constitutes its secondary action. [aphorism 112]

2. Administration of drugs in moderate doses seldom or hardly ever produces the least trace of secondary actions. Only their primary action is observed.[aphorism 112]

3. Administration of drugs in small doses does never produce secondary action. [aphorism 112]

4. In the homoeopathic curative operation, the living organism reacts from these only so much as is requisite to raise the health again to the normal healthy state. [aphorism 112]

5. An exception is in case of narcotic medicines. Even with moderate doses the narcotic medicines have been observed to produce secondary action in the form of increased sensibility and greater irritability. In their primary action these narcotic medicines take away sometimes the sensibility and sensation, sometimes the irritability of the healthy organism. [aphorism 113]

6. With the exception of narcotic substances, the primary actions of the medicines are to be noted. [aphorism 114]

7. Among the symptoms of the primary action of drugs administered in moderate doses, there occur in the case of some medicines not a few which are partially or under certain conditions, directly opposite to other symptoms that have previously or subsequently appeared – which represent the alternating state of the various paroxysms of the primary action and are termed alternating action. [aphorism 115]

8. Referring to the symptoms produced by a medicine, it has been noted that (a) some symptoms are produced more frequently, i.e. in many individuals; (b) others more rarely or in few persons; (c) some only in very few healthy bodies. [aphorism 116]

Symptoms are the manifestations of the actions of the drug on the vital force and the reaction of the vital force to the same drug. So they are, in all cases, the product of their actions and reactions. The variability in the manifestation of symptoms depends on the inherent power of the influencing substance and the capability of the vital force that animates the organism to be influenced by it.

In case of some symptoms appearing only in very healthy bodies, the condition is called idiosyncrasy. Though the state of idiosyncrasy implies a peculiar constitution, but this must also be ascribed to the influencing drug in which must lie the power of making the same impression on all human bodies, yet in such manner that but a small number or healthy constitution have a tendency to allow themselves to be brought into such an obvious morbid condition by them. [aphorism 117]

9. As each man differs from another man in their individual aspects, so each drug differs from another in their pharmacological properties and each of these substances produces alterations in the health of human beings in a peculiar, different, yet determinate manner, so as to preclude the possibility of confounding one with another. [aphorism 118] Ascertainment of Doses of Medicines   for Proving

1. Strong medicines are liable even in small doses to produce changes in the health even in robust persons. [aphorism 121]

2. Those of milder power must be given in more considerable quantities. [aphorism 121]

3. In order to observe the action of the very weakest medicines, the subjects of experiment should be healthy persons who are delicate, irritable and sensitive. [aphorism 121]

 

Method of Preparation of Drugs for Proving

The purity, genuineness and energy of the medicines must be thoroughly assured, and for this purpose [aphorism 122] -

1. Each of the medicine must be taken in a perfectly simple, unadulterated form. [aphorism 123]

2. The indigenous plants in the form of freshly expressed juice must be mixed with a little alcohol to prevent its spoiling. [aphorism 123]

3. Exotic vegetable substances must be prepared in the form of powder or tincture prepared with alcohol when they are in the fresh state and afterwards mixed with a certain proportion of water. [aphorism 123]

4. Salts and gums should be dissolved in water just before being taken. [aphorism 123]

5. If the plant can only be procured in its dry state, an infusion of it may be made by cutting the herb into small pieces and pouring boiling water on it, so as to extract its medicinal parts.

Immediately after its preparation, it must be swallowed while still warm as all expressed vegetable juices and all aqueous infusions of herbs without the addition of the spirit pass rapidly into fermentation and decomposition whereby all their medicinal properties are lost. [aphorism 123] Precautionary Measures to be taken during Proving

1.Regarding the medicine to be proved

Every medicinal substance must be employed quite alone and perfectly pure without the admixture of any foreign substance and without taking anything else of a medicinal nature the same day, or yet on the subsequent days, or during all the time, the effects of the medicine are to be observed. [aphorism 124] 2. Regarding the prover

(a) During the whole period of the experiment the diet of the prover must be strictly regulated – it should be as much possible destitute of spices, of roots and all salads and herb soups. The diet should be of a purely nutritious and simple character, consisting of green vegetables. Young green peas, green French beans, boiled potatoes and in all cases carrots are allowable, as the least medicinal vegetables. [aphorism 125]

(b) The drinks are to be those usually partaken of, as little stimulating as possible. The prover must either be not in the habit of taking pure wine, brandy, coffee or tea or he must have totally abstained for a considerable time previously from the use of these beverages, some of which are stimulating, others medicinal. [aphorism 125]

(c) The prover must be pre-eminently trustworthy and conscientious. [aphorism 126]

(d) During the whole period of proving he must avoid all overexertion of mind and body, all sorts of dissipation and disturbing passions. [aphorism 126]

(e) He should have no urgent business to distract his attention. [aphorism 126]

(f) He must be self-observing and not be disturbed whilst so engaged. [aphorism 126]

(g) He must possess a sufficient amount of intelligence to be able to express and describe his sensation in accurate terms. [aphorism 126]

(h) The medicines must be tested on both males and females in order to ascertain especially the changes in the sexual sphere. [aphorism 127]

Determination of Dosage and its Difficulties – Mode of Administration

Drug proving is not so simple and easy  matter for the following reasons -

Medicinal substances, in their crude state, do not exhibit nearly the full amount of the powers that lie hidden in them, which they do when they are taken in high dilutions. In this manner, one can investigate the medicinal powers even of substances that are deemed weak. [aphorism 128] Medicine should be given to the prover, on an empty stomach, daily from four to six very small globules of the thirtieth potency, moistened with a little water or dissolved in more or less water and thoroughly mixed and this is continued for several days. [aphorism 128] If the effects of this dose are but slight, a few more globules may be taken daily, until they become more distinct and stronger and the alterations of the health more conspicuous. [aphorism 129] All persons are not affected by a medicine in an equally great degree. On the contrary, there is a vast variety in this respect. An apparently weak individual may be scarcely affected by moderate doses of a medicine known to be of a powerful character, whilst he is strongly enough acted on by others of a much weaker kind. [aphorism 129] On the other hand, there are very robust persons who experience very considerable morbid symptoms from an apparently mild medicine and only slighter symptoms from stronger drugs. [aphorism 129] As this cannot be known beforehand, it is advisable to commence in every instance with a small dose of the drug and, where suitable and requisite, to increase the dose more and more from day to day. [aphorism 129] If at the very commencement, the first dose administered is sufficiently strong, it is advantageous in a way that the experimenter learns the order of succession of the symptoms and can note down accurately the period at which each occurs, which is very useful in leading to a knowledge of the genius of the medicine, for then the order of the primary actions and alternating actions is observed in the most unambiguous manner. [aphorism 130] A very moderate dose even often suffices for the experiment, provided only the prover is sufficiently delicate and sensitive and is very attentive to his sensations. [aphorism 130] The duration of a drug can only be ascertained by a comparison of several experiments. [aphorism 130]

Rules for an Exhaustive Proving of Drug

The drug must be proved, both in dilutions and in massive doses.
If the same medicine is given to the same person to test for several successive days in ever-increasing doses, the various morbid states that the medicine is capable of producing in a general manner is learnt, but not their order of succession; and the second dose often removes curatively, some of the symptoms caused by the previous dose, or develops in its stead an opposite state. Such symptoms should be enclosed in brackets, to mark their ambiguity, until subsequent purer experiments show whether they are the reaction of the organism and secondary action or an alternating action of the medicine. [aphorism 131] But when the object is only to ascertain the symptoms, especially of a weak medicinal substance and not the sequential order of symptoms, or the duration of action of the drug, then it is to be administered for several successive days, increasing the dose every day. In this manner, the action of an unknown medicine, even of the mildest nature, will be revealed, especially if tested on sensitive persons. [aphorism 132] On experiencing any particular sensation, the exact nature of symptoms needs to be determined, as for example – to observe whether, by moving the affected part, by walking in the room or open air, by standing, sitting or lying the symptom is increased, diminished or removed and whether it returns on again assuming the position in which it was first observed – whether it is altered by eating or drinking, or by another condition, or by speaking, coughing, sneezing or any other action of the body and at the same time to note at what time of the day or night it usually occurs in the most marked manner. In short, what is peculiar to and characteristic of each symptom will become apparent. [aphorism 133] All the symptoms peculiar to a medicine do not appear in one person, nor all at once, nor in the same experiment, but some occur in one person chiefly at one time, others again during a subsequent trial. In another person, some other symptoms may appear; moreover they may not recur at the same hour. [aphorism 134] The greatest care should be exercised in verifying symptoms by repeated experiments, in order that “imaginary” symptoms as well as chemical and mechanical symptoms may be excluded.

When a Medicine can be considered to have been thoroughly Proved

A medicine is regarded to have been completely proved when

Numerous observations are made on suitable persons of both sexes and of various constitutions. [aphorism 135] Subsequent experiments can notice little of novel character from its action. [aphorism 135] During reproving only the same symptoms are noticed as had been already observed by others. [aphorism 135] The symptoms are recorded complete with regard to their sensations, localities, modalities and concomitant factors so that a complete individual picture of the drug disease has been ascertained.
Although a medicine on being proved on healthy subjects cannot develop in one person all the alterations of health it is capable of causing, but can only do this when given to many different individuals, varying in their corporeal and mental constitution, yet the tendency to excite all these symptoms in every human being exists in it. [aphorism 136]

 

Relative Merits of Employing Large and Moderate Doses of Medicine in Proving

(A) Disadvantage of Employing Large Doses of Medicine Proving

If excessively large doses are used, there occur at the same time not only a number of secondary effects among the symptoms, but the primary effects also come on in such hurried confusion and with such impetuosity that nothing can be accurately observed. [aphorism 137]

(B) Advantages of Employing Moderate Doses of Medicine Proving

The more moderate the doses of the medicines – so much the more distinctly are the primary effects developed, and only these occur without any admixture of secondary effects. [aphorism 137]

Other sources besides Drug – Proving to know the curative properties of drugs.

Drug proving is the only reliable source to know the curative properties of drugs, but however, we can acquire knowledge about the drugs to some extend through ;

1. Histories of poisonings, narcotics or any toxic substances (toxicology)

2. Emperical sources;

3. Chemistry.

4. Biochemistry.

1. Poisonings;

The symptoms collected from the cases of poisoning have been of immense value. They have great curative properties. They are occupied in materia medica as ‘clinical symptoms’. They give information about the sphere of action, chemical action and common symptoms of a drug. Even poisonous substances when used in minute quantity produce finer symptoms. The knowledge of a toxic effect of a substance helps in the identification of power of power of a drug but not in obtaining complete knowledge of curative properties of it. Many dreadful poisons like Lachesis, Crotalus and other snake poisons, Arsenic,Stramonium,Croton tig etc. are found to be very useful Homoeopathic medicine when they are given on their toxicological symptoms in minimum doses.

2. Emperical;

Empirical knowledge gave only superficial view and did not help in acquiring the complete and rational knowledge about the curative power of drugs.

3. Chemistry;

From the chemistry we got the general information about the authenticity, standardization and active principle of drugs. Chemical action of a drug is different from its dynamic action. Chemical action produces only the common symptoms of the medicine. But it does not give knowledge about dynamic properties of a drug.

4. Biochemistry;

It gives information about the biochemical actions of drugs, which deals with the sphere of actions of drugs on one or two systems or organ. As a result this knowledge is suitable only for palliative treatment. In Homoeopathy, only few drugs have been included because of their biochemical action.

Recording of Proving

All the sufferings, accidents and changes of the health of the prover during the action of a medicine are solely derived from the medicine that is being proved and must be regarded and registered as belonging peculiarly to this medicine, as symptoms of this medicine, even though the experimenter had observed, a considerable time previously, the spontaneous occurrence of similar phenomena in himself.

The reappearance of these during the trial of the medicine only show that this individual is by virtue of his peculiar constitution, particularly disposed to have such symptoms excited in him. In this case they are the effect of the medicine; the symptoms do not arise spontaneously while the medicine that has been taken is exercising an influence over the health of the whole system, but are produced by the medicine. [aphorism 138]

The Day – Book

The prover would do well to give first a description of himself-age, sex, temperament, former ailments or diseases, habits and the influence which changes in the weather have to him. Next, a full description of the substance or drug proved, how and where it was obtained and how it was prepared. Next mention the dose and the time of the day. This self-examination should be as carefully conducted as the examination of a sick person. A daily journal should be kept, in which nothing is omitted; some symptoms, or groups of symptoms, may often reappear, they should be very distinctly related again, as these frequently recurring disturbances, however long they may continue, often denote the most characteristic symptoms of the substance or drug prove. And, as in the examination of the sick, so in proving, the experimenter should describe very minutely under what circumstances certain symptoms appear. Also state whether food, changes in the weather, exercise or rest in certain position, cause new, or aggravate, or ameliorate old symptoms.

(A) Symptoms to be recorded during proving;-

(1) Except narcotics; Symptoms produced by primary action of all medicines are recorded, except narcotics ($114)

(2) Narcotic substances; In case of narcotic substances symptoms of secondary action are to be recorded. ($113)

(3) Alternating actions; which are produced by some medicines are also to be noted. ($115)

(4) Modalities ;( $133); In order to determine the exact character of symptoms the modalities are recorded which mean slight intensification or decrease of symptoms in relation to time, position, weather etc, by various factors.

(5) Any alterations from normal health; should be recorded.

(6) Proving on sick persons ($142, F.N-2) Symptoms which, during the course of disease, might have been observed or never before, consequently new ones, belonging to the medicines.

(B) Noting down of Symptoms;

1. The physician may take other persons on whom the drug is administered.

(a) The prover must note down distinctly the sensations, sufferings, accidents and changes of health, he experiences at the time of their occurrence, mentioning the time after the ingestion of the drug when each symptom arose and if it lasts long, the period of its duration, and to keep a day book for the purpose. [aphorism 139])

(b The physician looks over the report in the presence of the prover immediately after the experiment is concluded; or

(c) If the experiment is continued for a long period of time he inspects the day book of the prover daily while everything is still fresh in his memory and questioning him about the exact nature of every one of those circumstances, write down the more precise details and makes each symptom precisely complete with regard to its sensation, localities, modalities and other concomitant factors. [aphorism 139]

(d) If the prover is illiterate and cannot note down his alterations in health, he must inform the physician every day of what has occurred to him, and how it took place. What is noted down as authentic information must be chiefly the voluntary narration of the person who makes the experiment, nothing conjectural and not derived from answers to leading questions, to ensure authenticity. [aphorism 140]

2. The physician may prove the medicine on himself. The best provings are those that the healthy, unprejudiced and sensitive physician institutes on himself [aphorism 141]

Advantages -

(a) He knows with the greatest certainty the things he has experienced in his own person.

(b) The great truth that the medicinal virtue of all drugs lies in the changes of health he has himself undergone from the medicines he has proved becomes for him an incontrovertible fact.

(c) By such self-observation the physician will be brought to understand his own sensations, his mode of thinking and his disposition and he will also get trained to be a good observer.

(d) The uncertainty about the exact changes in the health of others produced by a drug ceases entirely when a physician proves the drug on himself. The experiments on himself give him a reliable knowledge of the true value and significance of the medicinal agents.

(e) He who makes the trials on himself knows for certain what he has felt and each trial is a new inducement for him to investigate the powers of other medicines.

(f) He thus becomes more and more practiced in the art of observing, by continuing to observe himself.

(g) Experience shows that the organism of the prover becomes, by the frequent attacks on his health, all the more expert in repelling all external influences inimical to his system and all artificial and natural morbific noxious agents and becomes more hardened to resist everything of an injurious character by means of these moderate experiments on his own person with medicines. His body resistance against all sorts of infections is increased, health becomes more unalterable and he becomes more robust.

Symptoms that, during the whole course of the disease, might have been observed only a long time previously or never before, consequently new ones, belong to the medicine. [Foot note to aphorism 142]

Proving of medicines to unknown persons at a distance, who are paid for their work is uncertain in its results and loses all its value, as the proving demands the greatest moral certainty and trustworthiness that is doubtful in such a case. [Foot note to aphorism 143]

Building up of the Materia Medica

If tests with a considerable number of simple medicines have thus been carried out on healthy individuals, and a careful and faithful recording of all the disease elements and symptoms that they are capable of developing is done, then only a true Materia Medica can be built up.

This will be then a collection of real, pure, reliable modes of action of simple medicinal substances, a volume, wherein is recorded a considerable array of the peculiar changes of the health and symptoms ascertained to belong to each of the powerful medicines, as they were revealed to the attention of the observer, in which the likeliness of the (homoeopathic) disease elements of many natural diseases to be hereafter cured by them are present, which, in a word, contain artificial morbid states, that furnish for the similar natural morbid states the only true, homoeopathic, that is to say, specific, therapeutic instruments for effecting their certain and permanent cure. [aphorism 143]

From such a Materia Medica,. Everything that is conjectural, all that is mere assertion or imaginary should be strictly excluded.

Everything should be the pure language of nature carefully and honestly interrogated. [aphorism 144]

Of a truth it is only by a very considerable store of medicines accurately known in respect of these their pure modes of action in altering the health of man that we can be placed in a position of discover a homoeopathic remedy, a suitable artificial (curative) morbific analogue for each of the infinitely numerous morbid sates in nature, for every malady in the world.

Few disease remain for, which a tolerably suitable homoeopathic remedy may not be met with among those now proved as to their pure action, which without much disturbance, restores health in a gentle, sure and permanent manner infinitely more surely and safely than can be effected by all the general and special therapeutics of the old allopathic medical art with its unknown composite remedies, which do but alter and aggravate but cannot cure chronic diseases, and rather retard than promote recovery from acute diseases and frequently endanger life. [aphorism 145]

We thus build a complete Materia Medica.

Hahnemann called it Materia Medica Pura, because it consisted of the collective statements of the positive and perceptible reactions of the healthy human body recorded in the words of persons acted upon by drugs and admits no misinterpretations with changing medical terminology, altered biological concepts and newer scientific developments.

It is to borne in mind that the daybooks are not the Materia Medica. Not until the masses of symptoms have been analyzed, sifted, classified.

Methodology for Drug Proving

a.      Drug proving will be started with 1st quota and the prover will be asked to take 4-6 globules of the coded drug (quota) dry on tongue or dissolved in a little quantity of distilled water, four times a day daily for fourteen days. (Total of  56 doses).

b.      Drug administration will be suspended as soon as any change is felt by the prover after taking the drug or any sign(s)/Symptom(s) develop during the trial. Prover will note down these sign(s)/symptom(s) in the Prover’s Day Book Proforma  in sequence of their appearance, number of doses after which the symptom(s) appeared, time of onset and duration of the symptom(s), as well as the details of location, sensation, modalities and concomitants, if any. If no symptom is observed, the prover will note this fact as ‘No Symptom’ with date and time of intake of the respective dose of the drug daily.

c.      In the prover where sign(s)/Symptom(s) develop, the drug administration shall remain suspended till the sign(s)/symptom(s) totally disappear and this will be followed by a further rest period (no drug) of 7 days.

d.      The administration of the drug (remaining doses) will be started again in the same dose schedule as above (a) and in case of appearance of new sign(s)/Symptom(s) or re-appearance of the earlier sign(s)/symptom(s) the same procedure as stated above (b & c) will be followed till the quota is completed.

e.      Before commencing the administration of the next quota of the drug, the prover would be put on a rest period for 14 days and same procedure as mentioned above (item No. a, b, c & d) will be adopted for administering and suspending the administration of the subsequent quota.

f.      The provers will be called by the Proving Master or Proving Associate every day or as the need be for the purpose of interrogation whereupon details of each sign and symptom noted by the prover, viz. location, sensation, modality, concomitants, extension and duration will be recorded in ‘Symptoms Elaboration Proforma for any change(s) in the physical/mental/generalities of the provers by the Proving Master/Proving Associate’. Care should also be taken to record the intensity of symptom(s).

g.      Pathological tests will be performed to facilitate observation of any correlation between the subjective and objective changes. During the course of proving, the prover may also be referred for specific laboratory investigations to rule out any cause other than the drug pathogenesis. The expert opinion of the Honorary Consultant(s) may also be taken, if needed.

h.  Provers will be advised to maintain a spontaneous diary notation to note down any changes observed during the trial by them, to prevent errors due to memory lapses. Same changes should be reflected in Prover’s Day Book on the same day.

i.  After completion of all the quotas, the provers will undergo the prescribed ‘Terminal Medical Examination’ (TME).

The Effect of Provings.

The purpose of proving is primarily to find the pictures of new remedies, or to deepen the understanding of old ones. There are, however, many important side effects. New remedies have helped many patients, who might never have been so deeply cured if remedies like Chocolate, Hydrogen and Scorpion had not been understood.
Several provers found that the proving had a substantial effect that seemed to help other remedies to work much better. Provings are not always pleasant; some of the symptoms experienced can be painful or uncomfortable. It is important that provers have the support of the proving structure and of an experienced homoeopath. Sometimes the prover will become stuck in some part of the proving state and he will need another remedy, an antidote, to bring him out of it. However, almost all provers come out of the experienced unchanged, or more often, healthier, stronger and wiser.
Provings are also a powerful pedagogic tool. They help
students to learn and understand the process, through which the remedies they use came to be understood. They also help students to better understand what symptoms are and what they feel like. We all become so used to our own selves and our own symptoms that we do not see them clearly in ourselves or in our patients; a proving forces homoeopaths to look very closely at symptoms and so to understand what exactly a symptom is and what it means.

Research on Drug Proving

 

1. Proving of new drugs;

Proving of antibiotics, steroids and other modern drugs should be done over healthy human beings, in potentised form, to get many valuable data. These drugs may be effective in curing many obstinate and complicated chronic diseases. When well selected medicine fail to produce any favorable effect, in continued fever, chloromycetine (i.e. chloramphenicol ) cured the patient. In vertigo potentised streptomycin are very useful. Equally good results are obtained from Aspirin in acute migrainous headaches. So, we should get the full proving picture of these Isode groups of drugs, if we get full picture of these drugs (i.e. steroids, antibiotics) we can easily combat the iatrogenic diseases coming from allopathic system.

2. Proving and reproving of nosodes and sarcodes

The nosodes and sarcodes which are not proved at all or partially proved and are empirically used require thorough reproving or new proving. The nosodes and sarcodes have great role in curing chronic complicated and incurable diseases. Even in acute diseases, complete cure is unnecessarily delayed unless a dose of the indicated nosode administered. The drugs like Thyroidinum, Insilin, Carcinosin, Lyssin, Scirrhinum, X-ray and bowel nosodes require proper proving and re proving.

3. Proving on lower animals.

Homoeopathic drug proving is not continued up to the stage of organic changes on healthy human being. Because, it may be hazardous on the life of a prover to continue proving till the end of organic changes. But to get a complete picture of a drug pathogenesis , we should know the various structural changes in different organs. So, there is no other alternative than to prove the medicines on lower animals. Only well proved and fully proved drugs should be used for proving on lower animals to find out the organic changes (organic pathology), where the picture of dynamic pathology is known to us.

. The Relevance of Proving Today
During his life Hahnemann proved at least a hundred different remedies and built the basis of the Materia Medica, that is used today. During the hundred and fifty years since, some two and a half thousand remedies have been added, some through rigorous provings, others through noting the effects of accidental poisonings. Some homoeopaths feel that there are now more medicines than we need and that new provings are a waste of time; others feel that there are still many important medicines to be discovered and that old remedies need to be reproved both to clarify their symptoms and to bring them into focus in the light of the changes in society over two hundred years.
An example of this is; Sepia is the brown pigment that results from drying cuttlefish ink. It was proved by Hahnemann after he observed that one of his patients, a painter, was in the habit of licking his paintbrush whenever he was using a sepia paint. The proving brought out a clear picture of the remedy and it became one of the most important homoeopathic remedies. The picture of Sepia that emerged through the Nineteenth and the first half of this Century was of the worn out housewife. Kent, the great American homoeopath working at the turn of the century, describes her as “A woman who is not built well as a woman.” She becomes the housewife and mother because that is the only role open to her, she is “dragged down” by domestic toil and she resents it. During the last thirty years the role of women in western society has changed dramatically. The woman with a Sepia susceptibility would no longer be forced to stay at home; she can go out into the world and get a job, a high flying one if she wants. The situation is now reversed; the Sepia woman is out working in a man’s world and she is “dragged down” by the fact she is a woman and the pressures that this puts on her. These can be the pressures of having children and running a household, or they can be the physical pressures of being a woman, pressures such as menstruation and menopause. Sepia is such a large and well-known remedy that it is not too difficult to recognize it on some of its more idiosyncratic features and so this modified picture has developed over recent years. However, there must be many other remedies that have a modern picture that is different from that which they revealed when they were proved more than a century ago and, because the details of their pictures are less well known, only new provings will fully reveal the pictures that are relevant today.

The Problems in Contemporary Provings.

Hahnemann was, among his many skills, what we would call today a research scientist and the provings that he conducted were of a very high standard. Sadly not all those that followed him were as scrupulous and many very poor provings were conducted over the years. Over the last twenty years there has been enormous growth in professional homoeopathy all over the world. Provings have now become much more common and the way in which they are conducted is much more rigorous than it was just a few years ago.
Provings should be conducted on healthy individuals; however, very few people would claim to be a hundred per cent healthy and this is one of the many areas where compromises have to be made. No proving is perfect, but if it is well conducted the imperfections are above board and can be taken into account when it is interpreted. Most of the provings done today are done by student homoeopaths, just as they were in Hahnemann’s time. As most students are women, at least ninety per cent, and some classes contain no men at all, there is a gender imbalance in the results. This is the reverse of the situation in conventional medicine. In medical research, whether it is on drugs or of an epidemiological nature, the use of women subjects is thought to introduce too many variables, childbearing, hormonal changes, etc., and, unless it is on a gender specific disease such as breast cancer, research is conducted exclusively on men. Thus although heart disease kills many more women than breast cancer does, there has been almost no research at all on heart disease in women.

Dr. MUJEEBURAHMAN THEKKETHODIKA

MIASMATIC ANALYSIS OF REMEDIES (Part-10)

MIASMATIC ANALYSIS OF REMEDIES

DR.C.J VAGHESE DHMS Dip.NIH

No.

0

Name of Remedy

Thuja

Pso

1

Syp

2

Syc

4

Tub

3

Can

2

Tot

12

1. Thymol 0 1 0 0 0 1
2. Thyroidin 1 2 1 0 0 4
3. Trifloium Prat 1 0 0 0 1 2
4. Triosteum Perf 1 0 0 0 0 1
5. Tuberculin M 0 0 0 1 0 1
6. Tuberculin Sp 0 0 0 1 0 1
7. Tuberculin Av 0 0 0 1 0 1
8. Tuberculin D 0 0 0 1 0 1
9. Tuberculin Koch 0 0 0 2 0 2
10. Tuberculin Res 1 0 0 1 0 2
11. Tuberculinum 0 0 0 2 0 2
12. Ulmus Camp 0 1 0 0 0 1
13. Uran Nit 0 0 1 0 0 1
14. Urea 0 0 0 1 0 1
15. Vaccininum 0 1 0 0 0 1
16. Venus Mercena 1 0 1 0 0 2
17. Veratrum Alb 1 0 0 0 0 1
18. Vibrinum Opul 0 0 1 0 0 1
19. Viola Odor 0 0 0 0 1 1
20. Viola Trich 0 1 0 0 0 1
21. Viscum Alb 1 0 0 0 1 2
22. X  Ray 0 0 0 1 2 3
23. Xantoxylum 0 1 0 0 0 1
24. Zincum Met 1 0 0 0 1 2
25. Zingiber 0 0 1 0 0 1
26.

MIASMATIC ANALYSIS OF REMEDIES (Part-9)

MIASMATIC ANALYSIS OF REMEDIES

DR.C.J VAGHESE DHMS Dip.NIH

No.

0

Name of Remedy

Sambucus

Pso

1

Syp

0

Syc

0

Tub

0

Can

0

Tot

1

1. Sangunaria 0 2 0 0 2 4
2. Sanicula 0 0 1 0 0 1
3. Sarasaparilla 0 2 2 0 0 4
4. Sarcolact Acid 0 0 0 0 1 1
5. Sarothamnus Sco 1 0 0 0 0 1
6. Sarracenna Pur 1 0 0 0 0 1
7. Sarasaparilla Off 1 0 0 0 0 1
8. Sec Cor 1 1 2 0 1 5
9. Sedum Repens 0 0 0 0 1 1
10. Seirrhinum 0 0 0 0 2 2
11. Selenium 1 1 2 0 0 4
12. Simper Vivum 0 0 0 0 2 2
13. Senecio Aur 0 0 1 0 0 1
14. Senega 1 0 1 0 0 2
15. Sepia 0 2 3 1 1 7
16. Sigesbeck 0 0 0 0 1 1
17. Sil 2 3 2 2 3
18. Silphinum Lac 0 0 0 0 1 1
19. Spigelia 1 0 1 0 0 2
20. Spongia T 1 1 0 1 0 3
21. Squilla M 1 0 0 0 1 2
22. Stann Met 1 0 0 0 0 1
23. Staph 1 2 3 1 0 7
24. Sticta P 0 1 0 0 0 1
25. Stillingia Sil V 0 3 1 0 0 4
26. Stramon 1 0 1 0 0 2
27. Strnt Carb 1 0 0 0 0 1
28. Strychnos Gaul 0 1 0 0 2 3
29. Sul Ac 1 0 0 0 1 2
30. Sulph Iod 0 2 0 0 0 2
31. Sulph 3 2 2 1 2 10
32. Symph 0 0 0 0 1 1
33. Tabacum 0 0 1 0 0 1
34. Tarax 1 0 0 0 1 2
35. Taxus Bucc 0 0 0 0 1 1
36. Tellurium 1 0 1 0 0 2
37. Teribinthina 0 1 1 0 2 4
38. Teucrium 1 0 0 0 0 1
39. Thalamus 0 1 0 0 0 1
40. Thalaspi B P 1 0 0 0 0 1
41. Thioproperaz 1 1 0 0 0 2
42. Thiosin 0 0 0 1 0 1

MIASMATIC ANALYSIS OF REMEDIES (Part-8)

MIASMATIC ANALYSIS OF REMEDIES

DR.C.J VAGHESE DHMS Dip.NIH

No.

0

Name of Remedy

Palladium

Pso

0

Syp

0

Syc

1

Tub

0

Can

0

Tot

1

1. Paloonda 1 0 0 0 0 1
2. Paraphenylend 1 0 0 0 0 1
3. Parreira brava 0 0 1 0 0 1
4. Pediculus Capitis 1 0 0 0 0 1
5. Penicillinum 0 1 0 0 0 1
6. Perhexilinum 0 1 0 0 0 1
7. Persea Americana 1 0 0 0 0 1
8. Petr 2 1 0 0 0 3
9. Petrocelinum 0 1 1 0 0 2
10. Phenobarbitalum 1 0 0 0 0 1
11. Phos Acid 1 2 1 0 1 5
12. Phos 0 2 1 1 3 7
13. Phytolacca 0 3 2 2 3 10
14. Picric Acid 0 0 1 0 1 2
15. Pilocarpinum 0 1 0 0 0 1
16. Piper Nigrum 0 0 1 0 0 1
17. Pituitary 0 1 0 0 0 1
18. Platina 1 0 1 0 0 2
19. Platinum Mur 0 1 0 0 0 1
20. Plumbum Acet 1 0 0 0 0 1
21. Plumbum Met 1 0 1 0 0 2
22. Podophyllum 1 0 0 0 0 1
23. Proteus Bac (Bach) 1 0 0 0 0 1
24. Prunus spinosa 0 0 1 0 0 1
25. Psor 3 1 1 2 1 8
26. Pueumococcin 1 0 1 0 0 2
27. Puls 1 0 1 0 0 2
28. Radium Brom 0 0 0 0 1 1
29. Ran Bulb 1 0 0 1 1 3
30. Ratanhia 0 0 1 0 0 1
31. Rauwolfia Serp 1 0 1 0 0 2
32. Reserpinum 1 1 0 0 0 2
33. Rheum 1 0 0 0 0 1
34. Rhododendron 1 1 0 0 0 2
35. Rhus Tox 1 0 1 1 0 3
36. Ribonucl Ac 1 0 0 0 0 1
37. Rumex  Acetosa 0 0 0 0 1 1
38. Rumex Crisp 1 0 0 0 0 1
39. Ruta G 1 0 0 0 0 1
40. Sabadilla 1 2 1 0 0 4
41. Sabina 1 0 1 1 0 3
42. Saccharum Lac 0 0 1 0 0 1

MIASMATIC ANALYSIS OF REMEDIES (Part-7)

MIASMATIC ANALYSIS OF REMEDIES

DR.C.J VAGHESE DHMS Dip.NIH

No.

0

Name of Remedy

Malandrinum

Pso

0

Syp

1

Syc

0

Tub

3

Can

1

Tot

5

1. Mandragora Off 1 0 0 0 0 1
2. Manganum Acet 1 0 2 0 0 3
3. Mattiola  Gracea 0 0 0 0 1 1
4. Med 0 0 3 0 1 4
5. Merc Aur 0 1 0 0 0 1
6. Merc Cor 1 3 2 0 0 6
7. Merc I  R 0 3 1 0 0 4
8. Merc Dul 0 2 1 0 0 3
9. Merc I  F 0 3 0 0 2 5
10. Merc Sul 0 0 2 0 0 2
11. Merc 2 4 1 0 2 9
12. Methyl Coe 0 0 0 0 1 1
13. Mez 1 2 2 0 0 5
14. Millifolium 1 1 1 0 2 5
15. Mimosa Pud 1 0 0 0 0 1
16. Morphinum &salt 1 0 0 0 0 1
17. Mophium 0 0 0 0 2 2
18. Moschus 1 0 1 0 0 2
19. Mur.Ac 1 0 0 0 0 1
20. Murex Purp 1 0 1 0 0 2
21. Nat C 2 0 1 0 0 3
22. Nat Mur 2 0 2 0 1 5
23. Nat Phos 0 0 2 0 0 2
24. Nat Sul 0 1 3 0 0 4
25. Nectrianium 0 0 0 0 1 1
26. Nepenthes Dist 0 1 0 0 0 1
27. Niccolum Met 1 0 0 0 0 1
28. Nit Acid 2 3 3 2 3 13
29. Nux Vom 1 1 1 0 0 3
30. Ocimum Sanct 1 0 0 0 0 1
31. Okoubaka Aub 1 0 0 0 0 1
32. Oleum Ani 0 0 0 0 2 2
33. Oleum Jac 2 0 1 1 0 4
34. Oleum Sant 0 1 0 0 0 1
35. Onopordon Acan 1 0 0 0 0 1
36. Opium 1 0 0 0 2 3
37. Origanam Vulg 0 0 1 0 0 1
38. Origanam 1 0 0 0 0 1
39. Ornithogalam 0 0 0 0 1 1
40. Osmium Met 0 1 0 0 0 1
41. Oxygenum 0 0 0 0 1 1
42. Pair Quadrifolia 1 0 0 0 0 1

MIASMATIC ANALYSIS OF REMEDIES (Part-6)

MIASMATIC ANALYSIS OF REMEDIES

DR.C.J VAGHESE DHMS Dip.NIH

No.

0

Name of Remedy

Hyoscyamus Nig

Pso

1

Syp

0

Syc

0

Tub

0

Can

0

Tot

1

1. Hypothalamus 1 1 0 0 0 2
2. Iberis 1 1 0 0 0 2
3. Ignatia 1 0 0 0 0 1
4. Influenzinum 0 0 1 0 0 1
5. Iodum 1 2 2 0 2 7
6. Ipecac 1 0 0 0 0 1
7. Iridium Met 0 0 0 1 0 1
8. Iris Vers 0 2 0 0 0 2
9. Jacaranda Car 0 1 0 0 0 1
10. Jacaranda Gual 0 2 0 0 0 2
11. Juglans Rad 0 1 0 0 0 1
12. Kali Cy 0 0 0 0 2 2
13. Kali Ars 1 2 0 1 0 4
14. Kali Bich 1 2 1 2 2 8
15. Kali Brom 0 1 0 0 0 1
16. Kali Carb 2 1 1 1 0 5
17. Kali Chlor 0 2 0 2 1 5
18. Kali Iod 1 3 1 2 2 9
19. Kali Mur 0 2 1 1 0 4
20. Kali Nit 1 0 1 0 0 2
21. Kali Phos 1 0 0 0 2 3
22. Kali Sul 0 3 3 1 2 9
23. Kalmia 0 2 1 0 0 3
24. Kreosot 1 2 1 2 2 8
25. Kreosolum 1 0 1 0 1 3
26. Lac Can 1 2 1 0 0 4
27. Lac D 1 1 0 0 0 2
28. Lachesis 1 2 2 1 2 8
29. Lapis Alb 0 0 0 0 2 2
30. Laurocerrasus 1 3 0 0 0 4
31. Ledum Pal 1 2 0 0 0 3
32. Levomepromaz 1 0 0 0 0 1
33. Lilium Tig 1 0 1 0 0 2
34. Lithium Carb 0 1 1 0 0 2
35. Lobelia Erinus 0 0 0 0 0 1
36. Lobelia Inflata 1 0 0 0 0 1
37. Lyc 2 2 2 0 3 9
38. Mag Pol Austr 1 0 0 1 0 2
39. Mag Carb 2 0 1 0 0 3
40. Mag Mur 2 0 0 0 0 2
41. Mag Sul 1 0 0 0 0 1
42. Magnetics Pol Ar 1 0 0 0 0 1

MIASMATIC ANALYSIS OF REMEDIES (Part-5)

MIASMATIC ANALYSIS OF REMEDIES

DR.C.J VAGHESE DHMS Dip.NIH

No

0

Name of Remedy

Euphorbia Lath

Pso

1

Syph

0

Syc

0

Tub

0

Can

0

Tot

1

1. Euphorbia Pil 0 0 1 0 0 1
2. Euphorbium Off 1 0 0 0 0 1
3. Euphrsia 1 1 1 0 1 4
4. Fagopyrum 0 0 1 0 0 1
5. Ferr  Pic 0 0 0 1 1 2
6. Ferr Ars 1 0 0 0 0 1
7. Ferr Iod 0 1 0 0 1 2
8. Ferr Met 1 1 1 0 0 3
9. Ferr Magnet 1 0 0 0 0 1
10. Ferr Phos 1 0 0 0 0 1
11. Fl Ac 1 2 2 0 0 5
12. Flavus 1 0 1 0 0 2
13. Formica Acid 0 0 0 1 1 2
14. Formica Rufa 0 0 0 1 0 1
15. Franccisc Uni 0 1 0 0 0 1
16. Fuligo Ligni 0 0 0 0 1 1
17. Galium Ap 0 0 0 0 2 2
18. Galphimia Gluca 1 0 0 0 0 1
19. Gambogia 0 0 1 0 0 1
20. Gels 0 0 1 0 0 1
21. Gentiana Lutea 0 0 0 0 1 1
22. Gnaph 0 0 1 0 0 1
23. Graph 1 2 0 1 2 6
24. Gaujcum  Off 1 1 1 0 1 4
25. Guare Trichlor 0 0 0 1 0 1
26. Guatteria Gua 1 0 0 0 0 1
27. Gurana 0 0 0 1 0 1
28. Haloperidolum 1 0 0 0 0 1
29. Hamamilis 1 2 0 0 2 5
30. Harpago Proc 1 0 0 0 0 1
31. Hecla Lava 0 1 0 0 0 1
32. Helliborus Nig 1 0 0 0 0 1
33. Helonias 1 0 1 0 0 2
34. Hepar Sul 2 2 1 1 1 7
35. Hippozaenium 0 2 0 1 2 5
36. Hippuric Acid 1 1 0 0 0 2
37. Hirudo Medicinal 1 1 0 0 0 2
38. Histaminum 1 0 0 0 0 1
39. Hydrastinum Mur 0 0 0 0 1 1
40. Hydrastis 1 1 1 2 2 7
41. Hydrocotyl As 0 1 0 2 0 3
42. Hydrocyan Ac 1 0 0 0 0 1

MIASMATIC ANALYSIS OF REMEDIES (Part-4)

MIASMATIC ANALYSIS OF REMEDIES

DR.C.J VAGHESE DHMS Dip.NIH

No.

0

Name of Remedy

Cobalt Nit

Pso

0

Syp

1

Syc

1

Tub

0

Can

0

Tot

2

1. Coc C 1 0 1 0 0 2
2. Coca 1 0 0 0 0 1
3. Cochleria 0 0 1 0 0 1
4. Coffea Crud 1 0 0 0 0 1
5. Colch 1 2 1 0 0 4
6. Coloc 1 0 1 0 0 2
7. Conium Mac 1 2 1 0 3 7
8. Convolvulus St 0 1 0 0 0 1
9. Copavia 0 1 1 0 0 2
10. Cor Rub 0 1 0 0 0 1
11. Cortiso 1 0 0 0 0 1
12. Coridalis For 0 1 0 0 1 2
13. Croc 1 0 1 0 0 2
14. Crot H 0 1 1 0 1 3
15. Crot T 0 0 1 0 0 1
16. Cubeba Off 0 0 1 0 0 1
17. Cundurango 0 1 0 1 2 4
18. Cupr S 0 1 0 0 0 1
19. Cupr Acet 0 0 1 0 1 2
20. Cupr 2 1 0 0 1 4
21. Curare 0 0 0 0 1 1
22. Cyclamen 1 0 1 0 0 2
23. Cynara Scol 1 0 1 0 0 2
24. Daphine Ind 1 0 0 0 0 1
25. Desox Rib Nuc Ac 1 0 0 0 0 1
26. Digitalis 1 0 1 0 0 2
27. Doryphora Dec 0 0 1 0 0 1
28. Drosera 1 0 2 0 0 3
29. Dulc 1 0 0 0 1 2
30. Echinacea 0 1 0 0 0 1
31. Elaps Cor 0 0 0 0 1 1
32. Eosinum 0 0 0 0 1 1
33. Epiga Rep 0 0 1 0 0 1
34. Epiphegus 0 0 0 0 1 1
35. Erechthites Hie 0 0 0 0 0 0
36. Erigeron 0 0 1 0 0 1
37. Eringium Aqua 0 1 1 0 0 2
38. Erythrinus 0 1 0 0 0 1
39. Eucalyptus 0 1 0 0 1 2
40. Eupatorium Pur 0 0 1 0 0 1
41. Euphorbia cypr 1 0 0 0 0 1
42. Euphorbia He 0 0 0 0 1 1

MIASMATIC ANALYSIS OF REMEDIES (Part-3)

MIASMATIC ANALYSIS OF REMEDIES

DR.C.J VAGHESE DHMS Dip.NIH

No.

0

Name of Remedy

Caladium

Pso

0

Syp

0

Syc

1

Tub

0

Can

0

Tot

1

1. Calc Ars 0 0 0 1 0 1
2. Calc Iod 0 0 0 0 2 2
3. Calc Ox 0 0 0 0 1 1
4. Calc P 2 0 0 1 0 3
5. Calc Acet 1 0 0 0 0 1
6. Calc Flour 1 2 0 0 0 3
7. Calc Sil 0 0 0 1 0 1
8. Calc Sul 1 2 0 1 2 6
9. Calc 2 0 2 1 2 7
10. Calendula 0 0 0 0 2 2
11. Calotropis 0 1 0 1 0 2
12. Caltha Pul 0 0 0 0 1 1
13. Camphor 1 0 0 0 0 1
14. Can Ind 0 0 1 0 0 1
15. Can Sat 0 0 1 0 0 1
16. Canth 1 0 1 0 0 2
17. Caps 1 0 1 0 0 2
18. Carbo Ani 2 2 1 0 3 8
19. Carbo Veg 2 1 1 2 2 8
20. Carbolic Acid 0 0 1 2 2 5
21. Carbonium Sul 0 0 1 2 2 5
22. Carcinocin 0 0 0 0 1 1
23. Castoreum 0 0 1 0 0 1
24. Caulophyllum 0 0 1 0 0 1
25. Caust 1 2 2 1 1 7
26. Cedron 0 0 1 0 0 1
27. Cham 1 0 1 0 0 2
28. Chel 1 0 0 0 1 2
29. Chimaphila 0 2 1 0 0 3
30. China 1 0 1 0 0 2
31. Chinin Ars 0 1 0 0 0 1
32. Cholinum 0 0 0 0 1 1
33. Chromium Ox 0 1 0 1 0 2
34. Cicuta 1 0 1 1 2 5
35. Cimic 0 0 1 0 0 1
36. Cina 1 0 0 0 0 1
37. Cinnabaris 1 2 1 0 0 4
38. Cinnamon 0 0 0 0 1 1
39. Cistus Can 0 0 0 2 2 4
40. Citric Acid 0 0 0 0 2 2
41. Citrus Limonum 0 0 0 0 1 1
42. Clematis 1 1 1 0 1 4

MIASMATIC ANALYSIS OF REMEDIES (Part-2)

MIASMATIC ANALYSIS OF REMEDIES

DR.C.J VAGHESE DHMS Dip.NIH

No          Medicine                                         Psora   Syph    Syc Tub Can Tot

1. Arg Iod 0 1 0 0 0 1
2. Arg Met 1 1 0 0 1 3
3. Arnica 1 1 1 0 0 3
4. Ars Iod 2 3 0 2 2 9
5. Ars Alb 1 2 2 3 3 11
6. Ars Bro 0 0 0 0 1 1
7. Ars Met 1 1 0 0 0 2
8. Ars Sul Fl 1 2 0 1 0 4
9. Asaf 1 2 1 0 0 4
10. Asar 1 1 1 0 0 3
11. Asclapis Tub 0 2 0 0 0 2
12. Asimina Triloba 0 0 1 0 0 1
13. Asparagus Off 0 0 1 0 0 1
14. Asteria Rub 0 0 2 0 2 4
15. Astra E 1 1 0 0 0 2
16. Aur Mur 1 3 2 1 2 9
17. Aur Ars 0 1 0 2 1 4
18. Aur Fulminans 0 0 0 1 0 1
19. Aur Iod 0 1 0 1 1 3
20. Aur Mur Nat 0 3 1 0 1 5
21. Aur Sul 0 1 0 0 1 2
22. Aur 1 3 1 0 2 8
23. Bacilinum Bur 0 0 0 1 0 1
24. Bacilinum 1 0 0 0 0 1
25. Badiaga 0 1 0 0 0 1
26. Baptisia 0 0 0 0 2 2
27. Bar C 2 0 2 2 1 7
28. Bar Iod 0 0 0 0 1 1
29. Bell 1 1 0 1 1 4
30. Benz Ac 0 1 2 0 0 3
31. Berb Aq 1 1 1 0 0 3
32. Berb 1 1 1 0 0 3
33. Beryllium Met 1 0 0 0 0 1
34. Bismuthum 1 0 0 0 1 2
35. Bor Acid 1 0 0 0 0 1
36. Borax 1 0 1 0 0 2
37. Bovista 1 0 1 0 0 2
38. Brom 0 0 0 0 3 3
39. Bryonia 1 0 1 0 2 4
40. Bufo Ran 1 0 1 0 1 3
41. Bunias Orient 1 1 0 0 0 2
42. Cadm Met 0 1 0 0 0 1
43. Cadm S 0 0 0 0 2 2

MIASMATIC ANALYSIS OF REMEDIES (Part-1)

MIASMATIC

ANALYSIS OF REMEDIES

DR:C.J.VARGHESE.DHMS,Dip.NIH

NO

NAME OF REMEDY

PSO

SYP

SYO

TUB

CAN

TOT

1. Abrus Prec 0 0 0 1 0 1
2. Acetic Acid 0 0 0 0 1 1
3. Acon 1 0 0 0 0 1
4. Adulmia Fl 1 0 1 0 0 2
5. Aese 1 0 1 0 0 2
6. Aethiops Ant 0 1 0 0 0 1
7. Agar 2 0 2 1 0 5
8. Agnus Cast 0 1 1 0 0 2
9. Ailanthus 0 1 0 0 0 1
10. Alcoholus 1 0 0 0 0 1
11. Alloxanum 0 1 0 0 0 1
12. Alnus Rubra 1 1 0 0 0 2
13. Alum Sil 0 0 0 1 0 1
14. Alumina 0 0 1 1 1 3
15. Alumn 1 0 1 1 1 4
16. Ambr 1 0 0 0 2 3
17. Ammon Carb 1 1 1 0 0 3
18. Ammon Mur 1 0 1 0 0 2
19. Amyglad 1 0 0 0 0 1
20. Anac 1 0 1 0 0 2
21. Anagallis Arv 0 1 0 0 0 1
22. Anatherum Mur 0 2 2 0 1 5
23. Angusta Ver 1 2 1 0 0 4
24. Anhalon Lev 1 0 0 0 0 1
25. Anilinum 0 0 0 0 1 1
26. Ant Cru 2 1 1 1 0 5
27. Ant  Tart 1 2 1 0 0 4
28. Anthracokali 0 0 2 0 0 2
29. Ant Mur 0 0 0 0 2 2
30. Apis 1 2 2 1 2 8
31. Apocynum 0 0 0 0 1 1
32. Aran 1 0 1 0 0 2
33. Arg Nit 1 0 3 1 1 6

DR:C.J.VARGHESE.DHMS,Dip.NIH

QUESTION BANK OF ANATOMY

QUESTION BANK OF ANATOMY

  1. Name the dural folds & describe the tentorium cerebelli
  2. Enumerate the dural venous sinuses & describe cavernous sinus
  3. Describe the anatomy of scalp. Write about its applied anatomy.
  4. Describe the intrinsic muscles of larynx
  5. Describe the movements of vocal chords & enumerate muscles producing them
  6. Name muscles of pharynx & describe the constrictors of pharynx
  7. Describe the extra ocular muscles of eyeball
  8. Describe the middle ear cavity.
  9. Describe the movements of temporo-mandibular joint & muscles of mastication.
  10. Describe the temporo-mandibular joint
  11. Describe anatomy of tongue. Add a note on its development.
  12. Describe anatomy of thyroid gland. Add a note on its development.
  13. Give the relations, blood supply, & development of the thyroid gland.
  14. Describe the anatomy of parotid gland
  15. Describe relations, nerve supply, histology, & applied anatomy of parotid gland
  16. Describe the submandibular salivary gland
  17. Describe relations, blood supply, histology, & nerve supply of submandibular salivary gland. Add a note on its applied anatomy.
  18. Describe the hypophysis cereberi. Add a note on its development.
  19. Describe the nerve supply of face.
  20. Describe the external carotid artery.
  21. Describe anatomy of palatine tonsil.
  22. Describe in details muscles of mastication,

Short Notes

  1. Posterior triangle
  2. Carotid triangle
  3. Digastric triangle
  4. External muscles of eye
  5. External carotid artery
  6. Movements of larynx
  7. Lachrymal apparatus
  8. Waldeyers ring
  9. Cavernous sinus
  10. Pharyngotympanic tube
  11. Lateral wall of nose
  12. Chordae tympanii nerve
  13. Recurrent laryngeal nerve (both sides)
  14. Boundaries of middle ear
  15. Relations, blood supply, & clinical anatomy of palatine tonsil
  16. Mylohoid muscle & its relations
  17. Sternocleidomastoid & its relations
  18. Tympanic membrane
  19. Hyoglossus
  20. Oblique muscles of eye
  21. Common carotid artery
  22. Internal jugular vein
  23. Interior of larynx
  24. Tonsil
  25. Vocal chords
  26. Submandibular salivary gland
  27. Medial wall of middle ear
  28. Maxillary air sinus
  29. Soft palate

Neuroanatomy

Full Questions

  1. Describe the internal capsule & its blood supply.
  2. Describe the lateral ventricle
  3. Describe the third ventricle
  4. Describe anatomy of the cerebellum
  5. Describe the corpus callosum
  6. Describe the third cranial nerve
  7. Describe the seventh cranial nerve. Write effects of its lesion at various levels
  8. Describe the seventh cranial nerve with a note on its clinical anatomy
  9. Describe the extra cranial part of facial nerve & its applied anatomy
  10. Describe the ninth cranial nerve
  11. Describe the twelveth cranial nerve
  12. Describe course, connections, nuclei, branches, & clinical anatomy of XII nerve
  13. Describe the auditory pathway. Write effects of its lesion at various levels
  14. Describe the auditory pathway
  15. Describe the visual pathway.

Short Notes

  1. Spino-thalamic tract
  2. Cortical spinal tract
  3. Inferior cerebellar peduncle
  4. Visual pathway & applied anatomy.
  5. Third ventricle
  6. Lateral ventricle
  7. Basal nuclei
  8. Midbrain section at superior colliculus
  9. Parietal lobe
  10. Post central gyrus
  11. Internal capsule
  12. Cerebellar peduncles
  13. Auditory pathway
  14. Floor of fourth ventricle
  15. Circle of Willis
  16. Thalamus
  17. Pones
  18. Mid brain section at inferior colliculus
  19. Frontal lobe
  20. Spino cerebellar pathway

Draw & label

  1. Cross section of medulla at level of fourth ventricle
  2. Draw & label medial surface of cerebrum
  3. Describe blood supply of superolateral surface of cerebrum
  4. Blood supply of cerebral cortex with its clinical anatomy
  5. Transverse section of spinal cord at mid-thoracic level
  6. Connections of thalamus
  7. Corpus callosum

Chest

Full Questions

  1. Describe the left ventricle & add a note on its blood supply
  2. Describe the right atrium. Write about its development.
  3. Describe the right lung.
  4. Describe the mediastinal surface of right lung. Give its bronchopulmonary segments.
  5. Describe the superior mediastinum. Write in details about any one of its contents
  6. Enumerate all structures of superior mediastinum. Describe arch of aorta
  7. Describe the arch of aorta & give its development
  8. Describe the thoracic part of oesophagus. Add a note on its development
  9. Describe the thoraco-abdominal diaphragm & give its development
  10. Describe a typical intercostal space. Add a note on mechanism of respiration
  11. Describe movements of the thoracic cage during respiration

Abdomen-Pelvis

Full Questions

  1. Describe the inguinal canal
  2. Describe the right kidney
  3. Describe the left kidney
  4. Describe the kidney
  5. Describe the urinary bladder
  6. Describe the suprarenal glands. Give their development
  7. Describe the stomach
  8. Describe the anatomy of pancreas
  9. Describe the anatomy of spleen
  10. Describe the duodenum & give its histology & development
  11. Describe the caecum & appendix and give their applied anatomy
  12. Describe the extra hepatic biliary apparatus
  13. Describe the anatomy of prostate
  14. Describe the anatomy of rectum & anal canal
  15. Describe the anal canal
  16. Describe the anatomy of uterus. Add a note on its supports
  17. Describe the anatomy of uterus.
  18. Describe the supports of uterus.
  19. Describe the perineal pouches

Short Notes

  1. Rectus sheath
  2. Gall bladder
  3. Male urethra
  4. Prostrate
  5. Rectum
  6. Left ureter
  7. Head of pancreas
  8. Broad ligament
  9. Urinary bladder
  10. Right Suprarenal gland
  11. Posterior relations of both kidneys
  12. Internal iliac artery
  13. Inferior vena cava
  14. Porto-systemic anastomosis & its clinical importance
  15. Inguinal canal
  16. Ischio rectal fossa
  17. Vas deferens
  18. Fallopian tube
  19. Anal canal
  20. Psoas major muscle
  21. Ovary
  22. Supports of uterus
  23. Appendix
  24. Suprarenal gland
  25. Spleen
  26. Superior mesenteric artery
  27. Portal vein

Superior Extremity

Full Questions

  1. Describe axilla.
  2. Describe the axillary artery
  3. Describe the mammary gland
  4. Describe in detail anatomy of female mammary gland. Add note on its lymphatic drainage
  5. Describe the radial nerve
  6. Describe the ulnar nerve in hand
  7. Describe the ulnar nerve. What are the effects of its lesion at wrist joint.
  8. Describe the medium nerve
  9. Describe the wrist joint
  10. Describe the elbow joint
  11. Describe the movements of thumb
  12. Describe the shoulder joint
  13. Describe the movements of the shoulder joint
  14. Name muscles which move the shoulder joint & describe deltoid in detail
  15. Describe pronation & supination of forearm

Short Notes

  1. Radial nerve in arm
  2. Movements of shoulder joint
  3. Axillary artery
  4. Give attachments, nerve supply, & actions of- Trapezius, Latissimus dorsi, Brachialis, Supinator
  5. Ulnar nerve in hand
  6. Elbow joint
  7. Axillary lymph nodes

Genetics

Short Notes

  1. Kleinefelter’s syndrome
  2. Turner’s syndrome
  3. Chromosome
  4. Y-Chromosome
  5. Chromosomal anomalies
  6. Meiosis
  7. Barr body
  8. Non disjunction
  9. Transcription
  10. Autosomal recessive inheritance
  11. X-linked recessive inheritance
  12. Hemophilia
  13. Genetics of ABO blood groups system
  14. Rh. Inheritance
  15. Prenatal diagnosis
  16. Ultrasonography
  17. Dermatoglyphics
  18. Genotype
  19. Mosaicism
  20. Down’s syndrome
  21. Ribosome
  22. Trisomy
  23. X-Chromosome
  24. Structural chromosomal anomalies
  25. Gene
  26. R.N.A.
  27. Mitosis
  28. Sex chromatin
  29. Mutation
  30. Lyon’s hypothesis
  31. Inheritance of color blindness
  32. Autosomal dominant inheritance
  33. X-linked inheritance
  34. Genetics of Rh blood group system
  35. Inheritance of ABO blood groups
  36. Multifactorial inheritance
  37. ABO blood groups
  38. Amniocentesis
  39. Karyotyping
  40. Genetic counseling
  1. Codon

Short Notes on Microscopic Structure of

  1. Tonsil.
  2. Lymph node
  3. White fibro cartilage
  4. Costal cartilage
  5. Hyaline cartilage
  6. Skeletal muscle
  7. Tendon
  8. Large size artery
  9. Transverse section Aorta
  10. Pancreas
  11. Loose connective tissue
  12. Scalp
  13. Oesophagus
  14. Large intestine
  15. Duodenum
  16. Trachea
  17. Super renal gland
  18. Thyroid
  19. Testis
  20. Vas deferens
  21. Eyelid
  22. Cornea
  23. Lens
  24. Myelinated nerve fiber
  25. Cerebellum
  26. Autonomic & Spinal ganglion
  27. Spleen
  28. Thymus
  29. Elastic cartilage
  30. Articular cartilage
  31. Compact bone
  32. Cardiac muscle
  33. Tendon
  34. Medium size artery
  35. Mixed salivary gland
  36. Skin
  37. Thick skin
  38. Lip
  39. Stomach
  40. Stomach-fundus
  41. Ileum
  42. Lung
  43. Pituitary gland
  44. Urinary bladder
  45. Prostate
  46. Ovary
  47. Retina
  48. Neuron
  49. Organ of Corti
  50. Cerebrum
  51. Autonomic ganglion

Embryology

Short Notes

  1. Oogenesis
  2. Fertilization
  3. Zygote
  4. Primitive streak
  5. Neural tube
  6. Chorionic villi
  7. Amnion
  8. Placenta
  9. Derivatives of three germ layers
  10. Mesonephric duct
  11. Kidney
  12. First pharyngeal arch
  13. Second pharyngeal arch
  14. Tooth
  15. Diaphragm
  16. Ductus arteriosus
  17. Inter-atrial septum
  18. Subclavian artery
  19. Stomach
  20. Liver
  21. Midgut & its rotation
  22. Palate
  23. Thyroid
  24. Testis
  25. Superior vena cava
  26. Face
  27. Spermatogenesis
  28. Implantation
  29. Yolk sac
  30. Notochord
  31. Neural crest
  32. Chorion
  33. Amniotic sac
  34. Functions of placenta
  35. Allantois
  36. Para mesonephric duct
  37. Urinary bladder
  38. Fate of first pharyngeal arch
  39. Fate of second pharyngeal arch
  40. Tongue
  41. Sinous venosus
  42. Inter-ventricular septum
  43. Right atrium
  44. Arch of aorta
  45. Meckel’s diverticulum
  46. Duodenum
  47. Large Intestine
  48. Spleen
  49. Supra renal
  50. Pituitary gland
  51. Middle ear
  52. Spinal cord
  53. Retina

Inferior Extremity

Full Questions

  1. Describe the knee joint
  2. Describe the movements of knee joint
  3. Describe the anatomy of hip joint
  4. Describe the movements of the hip joint. Name the muscles producing the movements
  5. Describe in details inversion & eversion of foot
  6. Describe the sciatic nerve
  7. Describe the femoral triangle
  8. Describe the anatomy of femoral sheath. Add a note of femoral hernia
  9. Describe the femoral artery
  10. Describe the popliteal fossa
  11. Describe venous drainage of lower limb. Add a note on varicose veins.
  12. Describe the great saphenous vein. Give its applied anatomy
  13. Describe two abductors & two flexors of hip joint
  14. Describe the gluteus maximus muscle. Describe the arches of the foot

Short Notes

  1. Gluteus maximus with its relations
  2. Plantar flexors
  3. Inversion & eversion of foot
  4. Intra Articular structures of knee joint
  5. Femoral nerve
  6. Abductors of hip joint
  7. Gluteus medius
  8. Ligaments of the knee joint
  9. Arches of the foot
  10. Longitudinal arches of foot
  11. Femoral artery

w

QUESTION BANK OF ANATOMY

  1. Name the dural folds & describe the tentorium cerebelli
  2. Enumerate the dural venous sinuses & describe cavernous sinus
  3. Describe the anatomy of scalp. Write about its applied anatomy.
  4. Describe the intrinsic muscles of larynx
  5. Describe the movements of vocal chords & enumerate muscles producing them
  6. Name muscles of pharynx & describe the constrictors of pharynx
  7. Describe the extra ocular muscles of eyeball
  8. Describe the middle ear cavity.
  9. Describe the movements of temporo-mandibular joint & muscles of mastication.
  10. Describe the temporo-mandibular joint
  11. Describe anatomy of tongue. Add a note on its development.
  12. Describe anatomy of thyroid gland. Add a note on its development.
  13. Give the relations, blood supply, & development of the thyroid gland.
  14. Describe the anatomy of parotid gland
  15. Describe relations, nerve supply, histology, & applied anatomy of parotid gland
  16. Describe the submandibular salivary gland
  17. Describe relations, blood supply, histology, & nerve supply of submandibular salivary gland. Add a note on its applied anatomy.
  18. Describe the hypophysis cereberi. Add a note on its development.
  19. Describe the nerve supply of face.
  20. Describe the external carotid artery.
  21. Describe anatomy of palatine tonsil.
  22. Describe in details muscles of mastication,

Short Notes

  1. Posterior triangle
  2. Carotid triangle
  3. Digastric triangle
  4. External muscles of eye
  5. External carotid artery
  6. Movements of larynx
  7. Lachrymal apparatus
  8. Waldeyers ring
  9. Cavernous sinus
  10. Pharyngotympanic tube
  11. Lateral wall of nose
  12. Chordae tympanii nerve
  13. Recurrent laryngeal nerve (both sides)
  14. Boundaries of middle ear
  15. Relations, blood supply, & clinical anatomy of palatine tonsil
  16. Mylohoid muscle & its relations
  17. Sternocleidomastoid & its relations
  18. Tympanic membrane
  19. Hyoglossus
  20. Oblique muscles of eye
  21. Common carotid artery
  22. Internal jugular vein
  23. Interior of larynx
  24. Tonsil
  25. Vocal chords
  26. Submandibular salivary gland
  27. Medial wall of middle ear
  28. Maxillary air sinus
  29. Soft palate

Neuroanatomy

Full Questions

  1. Describe the internal capsule & its blood supply.
  2. Describe the lateral ventricle
  3. Describe the third ventricle
  4. Describe anatomy of the cerebellum
  5. Describe the corpus callosum
  6. Describe the third cranial nerve
  7. Describe the seventh cranial nerve. Write effects of its lesion at various levels
  8. Describe the seventh cranial nerve with a note on its clinical anatomy
  9. Describe the extra cranial part of facial nerve & its applied anatomy
  10. Describe the ninth cranial nerve
  11. Describe the twelveth cranial nerve
  12. Describe course, connections, nuclei, branches, & clinical anatomy of XII nerve
  13. Describe the auditory pathway. Write effects of its lesion at various levels
  14. Describe the auditory pathway
  15. Describe the visual pathway.

Short Notes

  1. Spino-thalamic tract
  2. Cortical spinal tract
  3. Inferior cerebellar peduncle
  4. Visual pathway & applied anatomy.
  5. Third ventricle
  6. Lateral ventricle
  7. Basal nuclei
  8. Midbrain section at superior colliculus
  9. Parietal lobe
  10. Post central gyrus
  11. Internal capsule
  12. Cerebellar peduncles
  13. Auditory pathway
  14. Floor of fourth ventricle
  15. Circle of Willis
  16. Thalamus
  17. Pones
  18. Mid brain section at inferior colliculus
  19. Frontal lobe
  20. Spino cerebellar pathway

Draw & label

  1. Cross section of medulla at level of fourth ventricle
  2. Draw & label medial surface of cerebrum
  3. Describe blood supply of superolateral surface of cerebrum
  4. Blood supply of cerebral cortex with its clinical anatomy
  5. Transverse section of spinal cord at mid-thoracic level
  6. Connections of thalamus
  7. Corpus callosum

Chest

Full Questions

  1. Describe the left ventricle & add a note on its blood supply
  2. Describe the right atrium. Write about its development.
  3. Describe the right lung.
  4. Describe the mediastinal surface of right lung. Give its bronchopulmonary segments.
  5. Describe the superior mediastinum. Write in details about any one of its contents
  6. Enumerate all structures of superior mediastinum. Describe arch of aorta
  7. Describe the arch of aorta & give its development
  8. Describe the thoracic part of oesophagus. Add a note on its development
  9. Describe the thoraco-abdominal diaphragm & give its development
  10. Describe a typical intercostal space. Add a note on mechanism of respiration
  11. Describe movements of the thoracic cage during respiration

Abdomen-Pelvis

Full Questions

  1. Describe the inguinal canal
  2. Describe the right kidney
  3. Describe the left kidney
  4. Describe the kidney
  5. Describe the urinary bladder
  6. Describe the suprarenal glands. Give their development
  7. Describe the stomach
  8. Describe the anatomy of pancreas
  9. Describe the anatomy of spleen
  10. Describe the duodenum & give its histology & development
  11. Describe the caecum & appendix and give their applied anatomy
  12. Describe the extra hepatic biliary apparatus
  13. Describe the anatomy of prostate
  14. Describe the anatomy of rectum & anal canal
  15. Describe the anal canal
  16. Describe the anatomy of uterus. Add a note on its supports
  17. Describe the anatomy of uterus.
  18. Describe the supports of uterus.
  19. Describe the perineal pouches

Short Notes

  1. Rectus sheath
  2. Gall bladder
  3. Male urethra
  4. Prostrate
  5. Rectum
  6. Left ureter
  7. Head of pancreas
  8. Broad ligament
  9. Urinary bladder
  10. Right Suprarenal gland
  11. Posterior relations of both kidneys
  12. Internal iliac artery
  13. Inferior vena cava
  14. Porto-systemic anastomosis & its clinical importance
  15. Inguinal canal
  16. Ischio rectal fossa
  17. Vas deferens
  18. Fallopian tube
  19. Anal canal
  20. Psoas major muscle
  21. Ovary
  22. Supports of uterus
  23. Appendix
  24. Suprarenal gland
  25. Spleen
  26. Superior mesenteric artery
  27. Portal vein

Superior Extremity

Full Questions

  1. Describe axilla.
  2. Describe the axillary artery
  3. Describe the mammary gland
  4. Describe in detail anatomy of female mammary gland. Add note on its lymphatic drainage
  5. Describe the radial nerve
  6. Describe the ulnar nerve in hand
  7. Describe the ulnar nerve. What are the effects of its lesion at wrist joint.
  8. Describe the medium nerve
  9. Describe the wrist joint
  10. Describe the elbow joint
  11. Describe the movements of thumb
  12. Describe the shoulder joint
  13. Describe the movements of the shoulder joint
  14. Name muscles which move the shoulder joint & describe deltoid in detail
  15. Describe pronation & supination of forearm

Short Notes

  1. Radial nerve in arm
  2. Movements of shoulder joint
  3. Axillary artery
  4. Give attachments, nerve supply, & actions of- Trapezius, Latissimus dorsi, Brachialis, Supinator
  5. Ulnar nerve in hand
  6. Elbow joint
  7. Axillary lymph nodes

Genetics

Short Notes

  1. Kleinefelter’s syndrome
  2. Turner’s syndrome
  3. Chromosome
  4. Y-Chromosome
  5. Chromosomal anomalies
  6. Meiosis
  7. Barr body
  8. Non disjunction
  9. Transcription
  10. Autosomal recessive inheritance
  11. X-linked recessive inheritance
  12. Hemophilia
  13. Genetics of ABO blood groups system
  14. Rh. Inheritance
  15. Prenatal diagnosis
  16. Ultrasonography
  17. Dermatoglyphics
  18. Genotype
  19. Mosaicism
  20. Down’s syndrome
  21. Ribosome
  22. Trisomy
  23. X-Chromosome
  24. Structural chromosomal anomalies
  25. Gene
  26. R.N.A.
  27. Mitosis
  28. Sex chromatin
  29. Mutation
  30. Lyon’s hypothesis
  31. Inheritance of color blindness
  32. Autosomal dominant inheritance
  33. X-linked inheritance
  34. Genetics of Rh blood group system
  35. Inheritance of ABO blood groups
  36. Multifactorial inheritance
  37. ABO blood groups
  38. Amniocentesis
  39. Karyotyping
  40. Genetic counseling
  1. Codon

Short Notes on Microscopic Structure of

  1. Tonsil.
  2. Lymph node
  3. White fibro cartilage
  4. Costal cartilage
  5. Hyaline cartilage
  6. Skeletal muscle
  7. Tendon
  8. Large size artery
  9. Transverse section Aorta
  10. Pancreas
  11. Loose connective tissue
  12. Scalp
  13. Oesophagus
  14. Large intestine
  15. Duodenum
  16. Trachea
  17. Super renal gland
  18. Thyroid
  19. Testis
  20. Vas deferens
  21. Eyelid
  22. Cornea
  23. Lens
  24. Myelinated nerve fiber
  25. Cerebellum
  26. Autonomic & Spinal ganglion
  27. Spleen
  28. Thymus
  29. Elastic cartilage
  30. Articular cartilage
  31. Compact bone
  32. Cardiac muscle
  33. Tendon
  34. Medium size artery
  35. Mixed salivary gland
  36. Skin
  37. Thick skin
  38. Lip
  39. Stomach
  40. Stomach-fundus
  41. Ileum
  42. Lung
  43. Pituitary gland
  44. Urinary bladder
  45. Prostate
  46. Ovary
  47. Retina
  48. Neuron
  49. Organ of Corti
  50. Cerebrum
  51. Autonomic ganglion

Embryology

Short Notes

  1. Oogenesis
  2. Fertilization
  3. Zygote
  4. Primitive streak
  5. Neural tube
  6. Chorionic villi
  7. Amnion
  8. Placenta
  9. Derivatives of three germ layers
  10. Mesonephric duct
  11. Kidney
  12. First pharyngeal arch
  13. Second pharyngeal arch
  14. Tooth
  15. Diaphragm
  16. Ductus arteriosus
  17. Inter-atrial septum
  18. Subclavian artery
  19. Stomach
  20. Liver
  21. Midgut & its rotation
  22. Palate
  23. Thyroid
  24. Testis
  25. Superior vena cava
  26. Face
  27. Spermatogenesis
  28. Implantation
  29. Yolk sac
  30. Notochord
  31. Neural crest
  32. Chorion
  33. Amniotic sac
  34. Functions of placenta
  35. Allantois
  36. Para mesonephric duct
  37. Urinary bladder
  38. Fate of first pharyngeal arch
  39. Fate of second pharyngeal arch
  40. Tongue
  41. Sinous venosus
  42. Inter-ventricular septum
  43. Right atrium
  44. Arch of aorta
  45. Meckel’s diverticulum
  46. Duodenum
  47. Large Intestine
  48. Spleen
  49. Supra renal
  50. Pituitary gland
  51. Middle ear
  52. Spinal cord
  53. Retina

Inferior Extremity

Full Questions

  1. Describe the knee joint
  2. Describe the movements of knee joint
  3. Describe the anatomy of hip joint
  4. Describe the movements of the hip joint. Name the muscles producing the movements
  5. Describe in details inversion & eversion of foot
  6. Describe the sciatic nerve
  7. Describe the femoral triangle
  8. Describe the anatomy of femoral sheath. Add a note of femoral hernia
  9. Describe the femoral artery
  10. Describe the popliteal fossa
  11. Describe venous drainage of lower limb. Add a note on varicose veins.
  12. Describe the great saphenous vein. Give its applied anatomy
  13. Describe two abductors & two flexors of hip joint
  14. Describe the gluteus maximus muscle. Describe the arches of the foot

Short Notes

  1. Gluteus maximus with its relations
  2. Plantar flexors
  3. Inversion & eversion of foot
  4. Intra Articular structures of knee joint
  5. Femoral nerve
  6. Abductors of hip joint
  7. Gluteus medius
  8. Ligaments of the knee joint
  9. Arches of the foot
  10. Longitudinal arches of foot
  11. Femoral artery

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Question Bank of Forensic Medicine

QUESTION BANK OF FORENSIC MEDICINE

Full Questions

  1. Define and explain the term `Death’. How will you assess the time since death.
  2. Define and explain the term `Infanticide’. How will you establish the proof of live-birth by examining the dead body of a new born?
  3. Define `drowning.’ Describe the positive findings in a case of death due to drowning in sea.
  4. Describe the contractual relationship between a medical practitioner and patient.
  5. Define `Abortion’. What is `criminal abortion’? Describe the provisions of the M.T.P. Act of 1971.
  6. Describe the procedure of Coroner’s inquest. How is evidence recorded in a court of law?
  7. Define the Infanticide. How will you distinguish between a live-born and a still-born.
  8. Define `Identity.’ How will you establish the identity of a mutilated, decomposed body?
  9. Define Identity’. How is it established?
  10. Describe the nature of the professional relation between a medical practitioner and his patient.
  11. What precautions should a medical practitioner take to avoid charges of negligence?
  12. Define and discuss `Medical Negligence’. What precautions should a medical practitioner take in order to avoid charges of negligence?
  13. What do you mean by `unnatural sexual offences’? Describe the positive findings in the victim of sodomy.
  14. Define drowning. What are the types of drowning? Describe the post-mortem findings in a case of drowning in sea water.
  15. What is infamous conduct in a professional respect? Mention the circumstances under which the name of a medical practitioner can be erased from the State Medical Register.
  16. What is medical negligence? When does it become criminal in nature? What are the legal remedies available to a patient?
  17. Enumerate the differences between Unnatural sexual offense and sexual perversion. Write the report of the examination of the accused in case of `Sodomy’.
  18. Describe the circumstances under which the acts of a practitioner are called negligent.
  19. The dead body of a young girl is found in a suspended position with a ligature around the neck. How will you establish the cause of death?
  20. What is M.T.P. Act? When, where, by whom and on what grounds can the pregnancy be terminated under this act?
  21. Enumerate Grievous hurt. Describe in detail how an injury certificate is written.
  22. What is infanticide? What are the various acts of omission and commission. How will you establish that the child was born alive?
  23. Define rape. How would you examine a victim of rape? What laboratory investigations will help in establishing identity of the assailant in case of sexual assault?
  24. The dead body of a young female is recovered from a well. It has multiple injuries. Describe the post-mortem examination in such a case.
  25. Mention the various types of `witness’. Describe the procedure for recording evidence in a court of law.
  26. How will you determine the nature of injuries in a case of multiple injuries?
  27. Explain the terms “suffocation”. What are different types of suffocation & postmortem findings?
  28. Enumerate Grievous hurt. How do you determine age of Bruise (contusion).
  29. Compare and contrast (any two pairs).

(a) Dry drowning and classical drowning.

(b) Dying declaration and dying deposition.

(c) Contusion and hypostasis.

  1. Define “Consent”. Name different types of consents. Write in detail about “Informed” consent.

Short Notes

  1. Dry drowning
  2. Imprint abrasion
  3. Contributory negligence
  4. Suicidal cut throat
  5. Locard Principal
  6. Railway Spine
  7. Partial Hanging
  8. Expert Witness
  9. Diatoms
  10. Mummification
  11. Imprint Abrasions
  12. Professional Secrecy
  13. Defloration
  14. Molecular death
  15. Post-mortem lividity
  16. Burking
  17. Incest
  18. Age of contusion
  19. Adipocere
  20. Bestiality
  21. Defense injuries
  22. Magistrate’s quest
  23. Smothering.
  24. Age of viability
  25. Poroscopy
  26. Professional secret
  27. Pugilistic attitude
  28. Dying deposition
  29. Subpoena
  30. Viable infant
  31. P M Caloricity
  32. Mummification
  33. Inquest
  34. Ligature mark on neck
  35. Abrasion collar
  36. Dactylography
  37. Bruise
  38. Hymen
  39. Bestiality
  40. Fabricated injuries
  41. Anthropometry
  42. Hydrostatic test
  43. Privileged communication.
  44. Sexual offences
  45. Professional misconduct
  46. Virgin
  47. Mechanical injuries and their medicolegal importance
  48. Antemortem and Post mortem Burns
  49. Hesitation marks
  50. Medicolegal aspects of identity
  51. Insanity
  52. Determination of time of death
  53. Ante mortem and post mortem incised wound
  54. Cross examination

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Question Bank of Homoeopathic Pharmacy

QUESTION BANK OF HOMOEOPATHIC PHARMACY

Full Questions

  1. What is an ideal vehicle? Write uses, properties & methods of preparation of commonly used solid vehicle in homoeopathy
  2. Describe properties, preparation, & uses or alcohol used in homoeopathic pharmacy.
  3. What are vehicles? Name different vehicles used in Homoeopathic pharmacy
  4. Describe in detail preparation of alcohol.
  5. Name different types of vehicles & describe alcohol in details
  6. Describe different types of alcohol you know in relation to homoeopathic pharmacy
  7. What are the varieties of vehicles used for homoeopathic Medicines State how they are to be selected in preparing medicine?
  8. What are vehicles? Classify them & give advantages & disadvantages of any four commonly used vehicles in homoeopathy.
  9. Give properties & uses of 4 vehicles commonly used in homoeopathic pharmacy
  10. Give preparation, properties, advantages & possible impurities of alcohol / sac lac
  11. Describe the preparation of sac lac. How will you detect impurities in it?
  12. What are vehicles? Give preparation, properties, & uses of Sac lac
  13. What are vehicles? Describe preparation of sugar of milk in homoeopathic pharmacy.
  14. What are globules? How will you prepare globules in homoeopathic pharmacy?
  15. Describe in detail the manufacturing process of globules & their uses.
  16. What are the impurities found in Sugar of milk? Describe in detail process of Staph’s method
  17. How will do prepare distilled water in homoeopathic pharmacy? When is it used in laboratory?
  18. How will you prepare distilled water in homoeopathic pharmacy? What are the impurities found in it?
  19. Name different types of utensils. Describe any 3 in details
  20. Name the instruments & appliances used in pharmacy. How will you clean them ? Describe in detail-Bottles, Water bath, Percolator/
  21. What is Prescription? Describe different parts of prescription. Give examples of two prescriptions
  22. What is prescription writing? Explain validity & utility of prescription writing
  23. What is the scope of ext. application in homoeopathic prescribing? How will you select its ingredients?
  24. What is the scope of ext. Applications in homoeopathic prescribing? How will you prepare arnica ointment
  25. How will you identify, select, collect & preserve a sample of calendula and prepare calendula ointment from it.
  26. Differentiate in detail between trituration or succussion
  27. What are the different sources of homoeopathic drugs? Describe each with example
  28. Explain sources of homoeopathic, drugs with their preservation
  29. What are the different scales in preparing homoeopathic medicines? Describe in detail 50 milliscimal scale
  30. Describe in detail different scales of preparing homoeopathic medicines Describe in detail 50 milliscimal scale
  31. Describe in detail different scales of preparing homoeopathic medicines
  32. Write an essay on drug standarisation
  33. What is standarisation? Describe the various parameters used to standardise a mother tincture
  34. What is standardization? Describe various parameters prepare a standard homoeopathic medicine
  35. What is official sampling describe the process of percolation
  36. Write scope of homoeopathic pharmacy in relation to Materia Medica & Organon of medicine.
  37. Discuss the provisions related to sale & manufacture of homoeopathic medicines
  38. Discuss the professions related to sale & manufacture of homoeopathic medicines
  39. What are nosodes? How are they prepared & preserved in lab.
  40. Describe the preparation of NI & N2 nosodes
  41. How will you proceed to prove a drug which in its natural form produces changes in body? Name few such drugs.
  42. How will you proceed to prove a drug which in its natural form does not effect the vital force? Name few such drugs. ,
  43. What is mother tincture? What is meant by drug power of mother tincture?
  44. Describe preparation of mother tincture from more juice & less juicy plants.
  45. Describe in detail preparation of mother tincture from class II III, IV, V-A with 3 examples of each
  46. Differentiate in detail between mother tincture & mother substance
  47. What is moisture content of plant Describe in detail preparation of mother tincture from dry plant
  48. What are the different methods of knowing moisture content plants? Describe any one of them
  49. What are the different methods of knowing moisture content of plants? How does it help in preparing mother tincture
  50. Why do homoeopaths potentise their medicines? What are the different methods of potentisation
  51. What is jumping potency? How will you convert insoluble substance into liquid potency
  52. Write significance of conversion so solid potency of liquid potency. How will you convert solid potency into liquid potency?
  53. Explain conversion of Cal carb. 6 X to 8 X. Explanation why 7x of this medicine can not be available
  54. How will you prepare liquid potency of cal carb? From this natural sources.
  55. How will you prepare Cal Cab? 1X (first potency) from its natural source?
  56. What is Scilla IC? Describe its preparation & how will you further potentise it.
  57. Give preparation, purification, impurity detection & uses of any one vehicle used for trituration.
  58. Describe the process of trituration. Why do we triturate drugs in homeopathy

Write identifying features, constituents, & various actions or monographs of

  1. Aconite
  2. Cantharis/Spanish Fly
  3. Nux vom/poison nut.
  4. Anacardium orientalis.
  5. Jamal gota/Croton tig.
  6. Hyoscyamus Nig.
  7. Chelidonium
  8. Coffea crud
  9. Calendula
  10. Arsenic alb
  11. Pulsatilla
  12. Colchicum
  13. Abrotanum
  14. Aurum met
  15. Bryonia
  16. Chamomilla
  17. Opium
  18. Lachesis
  19. Drosera
  20. Apis mel
  21. Nux mosh
  22. Carbo veg
  23. Baptisia tinctora
  24. Stramonium
  25. Berberis v.
  26. Sulphur
  27. Arnica
  28. Aloe
  29. Digitalis
  30. Datura
  31. China off.
  32. Sepia
  33. Cina

Short Notes

  1. Maceration
  2. Decantation
  3. Moisture content
  4. Mother tincture
  5. Sources of drugs
  6. Placebo
  7. Nosode
  8. Succussion
  9. Trituration
  10. Fluxion potency
  11. Doctrine of potentisation
  12. Scales of homoeopathy,
  13. Centesimal scale
  14. Pharmacodynamics
  15. Pharmacology
  16. Alcohol
  17. Aqueous solution
  18. Sublimation
  19. Filtration
  20. Remedy
  21. Sublimation
  22. Filtration sources
  23. Vegetable sources
  24. Preservation of drugs
  25. Ideal vehicle
  26. Calendula ointment
  27. Ointment
  28. External applications
  29. Doctrine of signature (with examples)
  30. Active principle
  31. Prescription writing
  32. Jumping potency
  33. Collection of medicinal plants
  34. Official sampling
  35. 50 Milliscimal potency
  36. Sarcodes
  37. Nosodes
  38. Dynamisation
  39. Potentisation
  40. Potency
  41. Pharmacy
  42. Decimal scale
  43. Pharmacopoea
  44. Legislation in Homoeopathy
  45. Distilled water
  46. Distillation
  47. Medicine
  48. Drug
  49. Mortar & Pestle
  50. Chemical balance
  51. Specific gravity
  52. Standardisation
  53. Arnica liniment
  54. Liniment

Differentiate between the following.

  1. Inscription & subscription writing
  2. Cane sugar & Milk
  3. Nosodes & Sarcodes
  4. Centesimal & Decimal scale

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Question Bank of Materia Medica Set-3

MATERIA MEDICA QUESTIONS SET-3

Full Questions

  1. Give the drug picture of : Med, Lyco, Carcinosin, Rhus T, Kali Bi, Bell, Thuja, Lach, Kali C, Bacillinum Sepia, Caust, Cal C, Alum, Phos
  2. Write the short the group symptoms of Magnesium. Describe the drug picture of Mag carb. Compare Mag-Carb, Sulph, Mur, Phos
  3. Describe DP. of Mag C. Detail the Antidotal & Complementary relationship
  4. Write the common group symptoms of Acids. Describe the drug picture of Fluoric acid
  5. Write the group symptoms of Antimony
  6. Write the group symptoms of Halogens. Describe antiscrofulous & antisyphilitic action of Iodium. Discuss its relation with Carbolic Ac
  7. Write the group symptoms of Kali & differentiate the constitution of Kali C & Kali Bi
  8. Write common group symptoms of Ophidia. Describe drug picture of Crotalus Hor.
  9. In  a  given case of common cold the nasal discharge is “thick yellow” discuss the application of Puls, Kali Bi, Kali P. Sil, Arum triph
  10. Outline a CHAM child giving its differentiating features with its counter-part Staph.
  11. What are Nosodes? Write indications & contra-indications of nosodes
  12. Write the leading indication of Sul, Cal, C in psoric miasm
  13. Write the leading indications of Thuja, Med in sycotic miasm
  14. Describe Carb Veg as corpse reviver
  15. Describe Kali Mur as Biochemic Sulphur
  16. Describe Nat Sulph as king of hydro-genoid constitution

Compare & Contrast

  1. MIND – AmbraG & NatM
  2. RESPIRATORY-Euph & AlliumC
  3. SKIN – Sul & Graph
  4. FEMALE – Sep & NuxV
  5. CONVULSIONS-CicV CupM
  6. ŠSUN STROKE-Glon & Natc
  7. TRAUMA-Arn & BellisP
  8. THROAT-MercS & HepS
  9. URINARY-Apis & Canth
  10. HEADACHE-Bell & Bry
  11. JOINTS-Bry & RhusT
  12. RECTAL – Aescul & Collin
  13. G.I.T. – MagM & NatM
  14. HEMORRHAGE-Phos & NitAc

Differentiate the following:

  1. ALLERGY-Ferrum & Bov
  2. ABD. COLIC-Colo & Plb
  3. LIVER-SecCor & ArsA
  4. MENTALS-Phos & Plat
  5. LEUCORRHOEA-Kali Bi & Kreos
  6. CONSTIPATION-Alum & Plat


Short Notes

  1. CONSTITUTION of: AurM, Caps, Cal-Carb, Phos, Sulph, Fl, NatM
  2. BIOPHYSIOLOGICAL ACTION: Kali-P,M,S, Nat-P,M,S
  3. CHANGING MOODS: Alum, Puls Plat
  4. MENTALS: AmbraG, Con, Coff, Caust, Hyosc, Iod, Lach, NatC,  Puls, Petr, Sep, Thuj, Verat alb, Opium
  5. GLANDS: CarduusM CarbAn, Iod
  6. REDLINE MODALITY: CrotT, CupM, Cycl, Glon
  7. SKIN : Anth, CrotT, CarbAn, Graph, Hydroc, Mez, Maland
  8. HOME SICKNESS : Bry, Caps, Ign
  9. MOTION : Asaf, AdonisV, ArgM, AvenaS, AcalI, Anthr, Bry,  Bacil, Bufo, CarbAn, Cina, Cycl, Cham, EupPerf, Kreos, Med, RhusT, Sab, Lyssin
  10. CANCER : AsterR, CarbAn, Carcin, Condur, Hydras
  11. CONVULSIONS: AsterR, Bufo, Cic, CupM
  12. LIVER: Chel, China, NatS, MerS
  13. FEMALE: AmbraG, CoccI, CrocS, Grap, NuxM
  14. CARDIAC: Ado, Cact, Crat, Kal, LithC, Digitalis, Gels
  15. HAEMORRHAGES: Acal, Coll, Caulo, CrocS, Mell
  16. C.N.S. : Agar, ArtV, CupM, Cic, Hell, Lyssin
  17. RESPIRATORY: Ars, AmmM, Bry, Brom, CorRub, Dros, Dig, Meph, Phos, Spong, Sep, Lyco, AntT
  18. ASTHMA: AntArs, Blatta, lobelia
  19. COUGH: AntArs, CorR,
  20. BACKACHE : AescH, KaliC, NatM
  21. RHEUMATISM:  Arn, Colch, Calp, LithC, Led, Puls, Phyt, LacC, RhusT, Sul, Rad.br.
  22. POLYURIA: AmmM, Apis, AcetAc, CalArs, NatS
  23. G.I.T.: Phos, VertA, Abies Can
  24. ABD. COLIC : Bism, Coloc, Lyco, MagP, Plump, Spig
  25. FATIGUE : AvenaS
  26. TRAUMA : BellisP
  27. RECTAL : MagM
  28. ULCER : MercS
  29. INSOMNIA : Coff
  30. FILARIASIS: Hydras
  31. CAR SICKNESS: CoccI
  32. SCROFULA : CarbAn
  33. SEX : Calad
  34. GENERALS : CrocS
  35. DIPHTHERIA: Dipt
  36. TYPHOID: Bapt
  37. HEADACHE : Glon
  38. DIABETES: AcetAc
  39. BREAST : LacC
  40. CHARACTERISTIC SYMPTOMS OF: Aeth,  Agnus,  AbiesC., AmbraG, AntArs, Apocy, Acal, BerbV, Bov, Caps, chinaArs, CarboA, Caust, Con, CrocS, Coca, Dulc, Dios, Fl.Ac, Helonias, KaliBr, LacD, Lyssin, Melli, MercS, NuxM, NatC, Spong,Thuja, VertA, ArumT, Borax, Cinchona, Can. Ind, Medor, Lith. Carb.
  41. PRESCRIPTIVE TOTALITY OF: ArsI, Cyclamen, HepS, NuxV, VertA, Maland.

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Question Bank of Materia Medica Set-2

MATERIA MEDICA QUESTION SET-2

Compare & Contrast

  1. Merc Sol. & Hep. Sulph in Throat complaints
  2. China & Gels in Fever
  3. Digitals & Acetic Acid in Dropsy
  4. Cantharis & Apis Mel in Urinary  complaints
  5. Ammonium Mur & Bromium in Coryza
  6. Conium & Phytolacca in indurations of Glands
  7. Nux  Vomica & Merc Sol in Rectal symptoms
  8. Ammonium  Mur & Bovista in Menstrual disorders
  9. Acetic  Acid  & Apis in Urinary symptoms
  10. Nux. Vom & Pulsatilla in Gastric disorders.
  11. CactG & Digitals in Heart
  12. China and Gels in Fever
  13. Ammonium Mur & Arsenic Iod. in Coryza
  14. Alumina & Platina in GIT
  15. Lycopodium & Gelsemium in Mind
  16. Nux.Moschata & Ambra Gr. in Hysteria
  17. Nat. Mur & Nat Carb. in Headache
  18. Anacardium & Phosphorus in Mental.
  19. Mercuris & Apis Mel in Throat
  20. Apis Mel & Apocynum in Dropsy
  21. Conium & Phytolacca in Glands
  22. Aloes & Podophyllum in Diarrhoea
  23. Ignatia & Lachesis in Throat trouble
  24. Cantharis & Berb. Vul in Renal colic
  25. Ant. Tart & Ipecac in cough
  26. Bryonia & Nux vomica in Constipation
  27. Colocynth & Mag. Phos in Colic
  28. Bryonia & Conium  in Vertigo
  29. Cactus & Gelsemium in Cardiac Manifestation
  30. Ipecac &  Ant. Tart in Respiratory complaints
  31. Veratrum Album & Camphor in Cholera
  32. Puls & Sep in Female
  33. Alumina & Opium in Constipation
  34. Lycopodium & Phosphorus in Respiratory field
  35. Phytolacca and Bromium in Glandular pathology
  36. Acetic acid & Apis Urinary
  37. Ambra gr  & Nat m in mentals
  38. Amm C, Sec C, Bov, Plat Menses.


Differentiate

  1. Opium, Alumina, phos – GIT
  2. Cardiac symptoms of Aur met. Cactus, Dig, Gels
  3. Marasmus of Abrot, BC, NM
  4. Lycopodium & Sepia – Renal colic
  5. Bromium and Ars. Iod – Asthma
  6. Lycopodium & Conium – Urinary disorders
  7. Mercury & Lachesis – Throat complaint
  8. Sepia & Conium – Urinary symptoms
  9. Ammonium mur & Bovista – Mental disorders
  10. Bovista & Ferr Met – Allergies
  11. Gelsemium & Pulsatilla – Fever
  12. Nat  mur & Petroleum  – Skin eruption
  13. Cinchona officinalis & Nat.Carb – Fever

Short Notes

  1. Marasmus – Abrotanum, Bar. C.
  2. Oedema – Apis, Apo, Digit, Cinch
  3. Abdomen – Thuja
  4. Heart – Cactus, Dig
  5. Collapse- Veratrum Alb, Camphor, Carb V
  6. Headache – Nat Mur
  7. Physical generals – Petroleum,  Ferr met
  8. Geriatric Age – Con
  9. Cough – Con
  10. Cholera – Agar
  11. Sexual Disorders – Agnus
  12. Whooping  Cough – Drosera
  13. Rectum – Silicea
  14. Pneumonia – Phos
  15. Liver Symptoms – Chelidonium, Podo
  16. Psychosis – Lach
  17. Constipation – Alumina, Opium, Platina
  18. Asthma – Ars. Alb, Kali. C, CV, AntT., Ip
  19. Eczema – Graphites, Pet
  20. Causation – Conium, RT
  21. Destructive Dimensions – Kali Bich
  22. CNS – Gels, Agar
  23. Suppurations – Sil
  24. Bleeding – Lach
  25. Diarrhoea Podo, Nat S
  26. Eyes – Euph
  27. Typhoid condition – Hyos, Bapt
  28. Food Allergies – Ferr met.
  29. Breast disorders – Con, Phyt, Bor, Bry
  30. Urinary Symp – Apis, Canth, Con, Lyco.
  31. Gastric Symptoms – Nux, Vom, Chel, Bis, Sep, Lyco, Kali Bi, Nat C.
  32. Sciatica – Kali Bichromicum, Colocynth, Magnesium Phosphorus, Phytolacca, Amm mur.
  33. Rheumatism – Causticum, Kali-Carb., Rhus-tox, Pulsatilla, Cal. P., Cimic, Phyt
  34. Dysentry – Merc-Sol., Canth, Kali-Bich, Bryonia, Merc. Cor, Nux-Vomica, Ipecac
  35. Children – Calcium Phosphorus, Silicea, Borax, Chamomilla, Cina, Aeth, Calc, Bar. C.
  36. Fever – Belladonna, Aconite, Arnica, Baptisia, Aethusa, Cinch.
  37. Skin Symptoms – Graphites, Silicea, Bovista, Petroleum, Ars-Iod.
  38. Mentals – Anac, Anacardium, Nat-carb, Platina, Phosphorus, Hellebores, Cantharis, Nat-mur, Aur M, Verat alb
  39. Modalities – Nitric Acid, Dulcamara, Bapt-Tinct., Colchicum, Chel, Aco, Cal. P.
  40. Respiratory symptoms – Antim tart, Carbo veg, Ipecac, Hepar Sulph, Amm C, Dros, Ars I, Bromium, Lyc, Spong, Phos, Ars Alb
  41. Causation and modalities – Lycopodium, Colocynth, Spon, Phos, Nat M.
  42. Anacardium – Split Personality
  43. Platina – Lilliputian hallucination.
  44. Sulphur – Personality

Full Questions

  1. Describe drug picture under following heading: Constitution, Physical generals, Causation, Mentals, Modalities, and Characteristic Particulars.
  2. Calc-carb, Baryta-carb, Phosphorus, Ferrum-met, Aconitum Napellus, Opium, Platina, Sepia, Sul.
  3. Leading Indications:-
  4. Actea Racemosa
  5. Agnus Castus
  6. Chelidonium
  7. Ammonium Carb
  8. Nitric acid
  9. Causticum
  10. Calc. F.
  11. Pulsatilla
  12. Phosphorus
  13. Platina
  14. Merc. Sol
  15. Calc. Ars.
  16. Secale Cor
  17. Ignatia
  18. Opium
  19. Lyco
  20. Lachesis
  21. Arg nit
  22. Ars alb.
  23. Hyos
  24. NV
  25. Describe the drug picture of Lachesis or Lycopodium and give important differentiating features of them in a tabular form. Compare & contrast : mentals, Reproductive, throat
  26. Describe in detail the Drug picture of SEPIA and compare with PULSATILLA. Give the main generalities of each and their differentiating points in mentals.
  27. Describe the leading indications of Sepia an Platina and differentiate them in mentals and rectal symptoms
  28. Give briefly the general sphere of action of Pulsatilla and how will you differentiate it in general with Nux-vomica
  29. Give broad generalisation of: Natrum mur and Silicea and give their differentiation
  30. Give broad generalisation of Sepia and NatM and give their differentiation.
  31. Give broad generalisation of Lycopodium and Lachesis and give their differentiation
  32. Give broad generalisation of Sepia and Nux-Vomica and give their differentiation.

Compare:

  1. Nux-Vom and Sepia
  2. Canth and Apis M.
  3. Lycopodium and Lachesis
  4. Give the Pathophysiology of Opium
  5. Describe leading indication of Lyco & NV & Compare & Contrast them in mentals, renal, GIT.
  6. Give only five leading indications each of Apis, Belladonna. Compare and Contrast them with Mentals, Urine, Stool, Females.
  7. Give only five leading indication each of Gelsemium and Bryonia. Compare and Contrast them with three indication of Head, Throat, Female Extremities

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MATERIA MEDICA QUESTION SET-1

MATERIA MEDICA QUESTION SET-1

Full Questions

Give the “Drug Picture” of the following drugs:

  1. Arsenic alb
  2. Aurum met
  3. Bryonia
  4. Baryta carb
  5. Calc.C.
  6. Carbo veg
  7. Causticum
  8. Graphites
  9. Gelsemium
  10. Kali carb
  11. Lachesis
  12. Lycopodium
  13. Merc sol
  14. Nux vom
  15. Natrum mur
  16. Nitric acid
  17. Pulsatilla
  18. Rhus tox
  19. Sulphur
  20. Silica
  21. Thuja

Short Notes

Give the Generalities of

  1. Bryonia
  2. Cina
  3. Lycopodium
  4. Nitric acid
  5. Sulphur

Give the Leading Indications of:

  1. Arsenic alb
  2. Ant. Crud
  3. Ant. Tart
  4. Argentum nit
  5. Abrotanum
  6. Aethusa
  7. Baryta carb
  8. Calc. Carb.
  9. Causticum
  10. Carbo veg
  11. Graphites
  12. Ipecac
  13. Kali carb
  14. Lycopodium
  15. Natrum mur
  16. Nitric acid
  17. Pulsatilla
  18. Rhus tox
  19. Sulphur
  20. Thuja
  21. Baptisia

Other Short Notes

  1. Give the leading indications of Kali bi & compare Merc c. Merc.s & Nux v in dysentry
  2. Give the guiding indications of Bell & compare delirium of Bell., Hyosc., & Verat alb
  3. Climacteric irritability of Lachesis & compare it with Puls
  4. Indicate finer composition of Graphites & Silicea & differentiate their skin symptoms
  5. Write the mental, physical generals & modalities of Kali carb, Lachesis, Ars alb.
  6. Explain Baryta carb is an idiotic child
  7. Thuja is king of sycotic
  8. Ant. Tart. is a death rattle
  9. Causticum is an important consideration in paralysis

Give Biochemic indications of these drugs

  1. Calc Flour
  2. Calc Phos
  3. Calc Sulph
  4. Ferr Phos
  5. Kali Mur
  6. Kali Phos
  7. Kali Sulph
  8. Mag Phos
  9. Nat Mur
  10. Nat Phos
  11. Nat Sulph
  12. Silicea
  13. Give Biochemic indications of Kali mur in upper respiratory tract infection, Nat phos in gastric complaints
  14. Nat phos in allergic disorders
  15. Mag phos in colic
  16. Ferr phos in fever

Compare & contrast:

  1. Puls & Nat mur in mentals
  2. Arnica & Ledum in trauma
  3. Baryta C & Cal C in children disorders
  4. Ipecac Ant tart in respiratory disorders
  5. Ant C & Puls in gastric complains
  6. Nitric acid & Aesc in rectal complaints
  7. Colo & Mag phos in colic
  8. Carbo veg & Sec cor in collapse
  9. Borax & Nitric acid in mouth complaints.
  10. Biochemic & homoeopathic system of medicine
  11. Aconite & Ars alb in mentals
  12. Arnica & Rhus tox in injuries
  13. Spongia & Drosera in cough
  14. Hepar S & Merc s. in throat complaints
  15. ArsA & Apis in skin-mucus membrane.
  16. Bryonia & Rhus tox in joint pains
  17. Graph & Sulphur in skin disorder
  18. Aconite & Bell in fevers

Give indications of:

  1. Urinary symptoms: Apis, Berb V, Lyco
  2. Fever: Aconite, Bell, Bapt, Gels, Hell, Hyos, Puls, Nux V
  3. Injuries: Arn, Calendula, Rhus T
  4. Female disorders :Kali C, puls, Sec C
  5. Diarrhoea: Aloe, Podo
  6. Gastric complaints: Arg N, Ant C, Aeth, China, Ipec, Sulp.
  7. Irritability: Cina Cham
  8. Tenesmus/Dysentry :Merc cor
  9. Colic :Colo
  10. Pain: Aco, Cham, Ledum
  11. Catarrhal symptoms :Allium c, Euph
  12. Respiratory symptoms: Amm c, Ant t, Allium c, Dulc, Drosera, Ipec, Kali bi
  13. Cough: Spongia, Drosera
  14. Coryza: Euphr
  15. Rheumatism: Colch, Ledum, Puls, Rhus t
  16. Joint involvement: Caust, Ledum, Puls, Rhus t
  17. Skin(Mucous membrane):Apis, Ars, Graph, Hepar s, Nit acid, Sil, Sec C, Thuj
  18. Rectal complaints: Aloe, Aesc, Graph, Nit acid
  19. Piles: Aesc, Ign
  20. Headache: Bry, Sil.
  21. Collapse: Verat alb
  22. Oral cavity: Merc sol
  23. Dentition: Podo
  24. Eye symptoms: Euphr
  25. Child: Ant c, Abrot, Cina, Calc c, Cham
  26. Child milestones: Baryta c
  27. Destructive dimensions: Kali bi, Merc s
  28. Causation(A/F):Caust, Calc c
  29. S.O.A: Calendula, Kali c
  30. Modalities: Bry, Borax, Caust, China, Calc C, Merc S, Thuja
  31. Antidote: Bell, Ipec
  32. Delirium: Nat mur, Thuja, Bell, Bry
  33. Sensation as if: Thuja, Verat alb, Ign
  34. Insanity: Arg nig, Aurum met, Hyosc, Kali phos, Lach, Lyco, Nit acid,
  35. Mentals: Puls, Sulph, Thuja

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QUESTIONS BANK OF PATHOLOGY

QUESTIONS BANK OF PATHOLOGY

Full Questions

  1. Define Hypersensitivity. Discuss various types of hypersensitivity reactions giving examples.
  2. Discuss Etiology, Pathology and complications of Cirrhosis of Liver.
  3. Define repair. Discuss various factors modifying the process of repair.
  4. Define neoplasm. Discuss the laboratory diagnosis of neoplasm
  5. Enumerate the organism causing infective endocarditis. Describe the pathology and laboratory investigation of the same.
  6. What are the serological reactions? Discuss the importance of serological reaction in diagnosis of various diseases.
  7. Describe briefly aetiology, pathology and laboratory investigation of RHEUMATIC FEVER
  8. Define NEPHROTIC SYNDROME. Discuss the pathogenesis, pathology and laboratory investigation of nephrotic syndrome
  9. Enumerate Immune complex diseases with special reference to their pathogenic mechanism
  10. Enumerate the causes of ulcerative lesions in the intestinal tract. Discuss the pathogenesis pathology and laboratory investigations of gastric carcinoma.
  11. Define and differentiate an exudate and transudate. Describe the cellular response in acute Inflammation.
  12. What is neoplasm? Describe the modes of spread of a tumour. What is the difference between benign and malignant tumours?
  13. Nine years old child coming with history of fever, puffiness of face and Oedema feet.
  14. Give possible differential diagnosis, with laboratory diagnosis and gross and microscopic appearance.
  15. What is GRANULOMA? Name some granulomas. Describe the pathogenesis, the gross and microscopic features of any one of them.
  16. What is thrombus? Discuss the mechanism of thrombus formation and its fate and sequelae. Mention its common varieties.
  17. Enumerate the lesion in the diabetic Kidney and discuss the pathogenesis pathology and laboratory investigations of acute Pyelonephritis.
  18. Define Oedema. Describe its mechanism of formation. Differentiate Nephritic Oedema and Nephrotic Oedema.
  19. What is Glomerulonephritis? Discuss the pathogenesis, pathology and laboratory investigations.
  20. Define Immunity. What are the various types of immune reactions and the diseases produced by them?
  21. Define an embolus. What are different types of emboli and discuss the fate of any one embolus.
  22. Define shock. Discuss the pathogenesis and its effects on various organs.
  23. Define Infarction. Give an account of the pathogenesis of infarction with special reference of myocardial infarction.
  24. What is pneumonia? Enumerate the different types and discuss the pathology of any one of them.
  25. Define oedema. Describe the pathogenesis of oedema. Distinguish between a transudate and exudate.
  26. Define Degeneration and Infiltration. Give a detail account of Amyloid degeneration.
  27. Describe aetiology, pathology, and laboratory investigation of Rheumatic heart diseases.
  28. Define Hyperemia. Describe the types and organ changes in chronic passive congestion.
  29. Discuss the aetiology, pathology lesion and complication of atherosclerosis.
  30. Define cirrhosis. Give the aetiopathogenesis of the lesion, the gross and microscopic features.
  31. What is inflammation? Describe the pathology of an inflammatory response and its sequelae.
  32. Discuss the aetiopathogenesis of cardiac and renal oedema.
  33. Enumerate the common ulcers in the G.I.T. and discuss the pathology of the `PEPTIC ULCER’.
  34. Discuss the mechanism of autoimmune diseases with examples.
  35. Define Erosion and Ulcer. Discuss the pathogenesis, gross and microscopic appearance and laboratory investigation of ULCERATIVE COLITIS.
  36. Define Fatty degeneration. Discuss the pathogenesis, gross and microscopic appearance of organs showing fatty degeneration.
  37. What is Oedema? Discuss the pathogenesis of cardiac and renal oedema.

Short Notes

  1. Zenkers Hyaline Degeneration
  2. Amoebic Liver Abscess
  3. Post Necrotic Cirrhosis
  4. Tuberculosis Lymphadenitis
  5. Amyloid Kidney
  6. Special stains for amyloid
  7. Aspiration cytology
  8. Flea Bitten Kidney
  9. Dermoid Cyst
  10. Mucinous degeneration
  11. Spread of tumours.
  12. C.P.C. Lung.
  13. Caseous necrosis.
  14. Chemotaxis.
  15. Fatty degeneration.
  16. Osteogenic sarcoma.
  17. Caseous necrosis.
  18. Ulcers on tongue.
  19. Hyperthyroidism.
  20. Prostatitis.
  21. Splenic Infarct
  22. Chemical carcinogens
  23. Serum Enzymes in myocardial infarction
  24. Arthus phenomenon.
  25. Syphilitic aortitis
  26. Dystrophic calcification.
  27. Aneurysm
  28. Exfoliative Cytology
  29. Obstructive Jaundice
  30. Pyogenic Osteomyelitis
  31. Lepromatous Leprosy
  32. Cell mediated immunity
  33. Macrophage
  34. Tuberculoma
  35. Fat Necrosis
  36. T. B. Pyelonephritis
  37. Gas gangrene
  38. Leucoplakia
  39. Pulmonary Embolism
  40. Dysplasia
  41. Lymphatic permeation
  42. Frozen section
  43. Atrophy
  44. Carcinoma in situ
  45. Giant cells tumour & bone
  46. Pap Smear
  47. Basal cell carcinoma
  48. Pale infarct
  49. Laboratory Diagnosis of Neoplasia.
  50. Fine needle aspiration biopsy
  51. Chemical mediator of Inflammation.
  52. Laboratory Investigation of infertility
  53. Laboratory investigations of infective hepatitis.
  54. Rodent Ulcer.
  55. Gross appearance of liver fatty degeneration.

MICROBIOLOGY & CLINICAL PATHOLOGY.

Full Questions

  1. Enumerate the organisms causing food poisoning. Discuss the morphology cultural characteristic and pathogenesity of any one. Outline the laboratory diagnosis.
  2. Enumerate the parasites seen in the peripheral blood smear. Write the morphology, pathogenesity and laboratory diagnosis of any one.
  3. Describe the morphology, cultural characteristics, and antigenecity in staphylococci. Enumerate the lesion produced and the laboratory diagnosis.
  4. What are spirochetes? Enumerate the Spirochetes you know. Describe the laboratory diagnosis of syphilis.
  5. Enumerate the parasites infecting the central nervous system and discuss the life cycle and laboratory diagnosis of anyone.
  6. Describe the life cycle, pathogenesity and laboratory diagnosis of infestation due to ascaris lumbricoides.
  7. What is anaerobiasis? Describe the morphology, cultural characteristics, animal and human pathogenecity of any one anaerobic organism.
  8. Classify Haemolytic anaemias. Discuss the pathogenesis of thalassaemias, and differentiate between iron deficiency and sideroblastic anaemia.
  9. What is the difference between VIRUS, PROTOZOA, and BACTERIA? Discuss the life cycle of TAENIA SAGINATA and differentiate between T. Saginata and T. Solium.
  10. Enumerate the PUS forming organisms. Discuss the morphology, cultural characteristics, and antigenecity pathogensis of any one of them.
  11. Describe the morphology pathogenecity and laboratory investigation of infestation due to W. BANCROFTI.
  12. Enumerate the extra intestinal parasites. Describe the life cycle of ankylostoma duodenale and differentiate it from nectar Americana.
  13. Enumerate the Organisms causing diarrhoea. Describe the morphology, cultural characteristics, pathogenesis, and antigenic composition of any one of them.
  14. Enumerate the cause of ulcerative lesions in intestinal tract. Discuss how you will differentiate the lesions with their gross and microscopic appearance.
  15. Classify anaemias. Discuss the aetiopathogenesis of Haemolytic anaemias. Describe the blood picture of sickle cell anaemia.
  16. Enumerate the extra intestinal parasites. Describe the life cycle of ankylostoma duodenale and differentiate it from nectar Americana.
  17. Enumerate the Organisms causing meningitis. Describe the morphology, cultural characteristics, antigen composition, and pathogenesis of any one of them.
  18. Classify Leukaemias. Describe the blood picture and bone marrow in chronic myeloid leukaemia. Differentiate between acute myeloid and acute lymphoblastic leukaemia.
  19. Enumerate the organisms causing pneumonia. Describe morphology, cultural characteristics, antigenic composition and pathogenesity of any one of them.
  20. What is Haemophilia? Classify, describe the pathogenesis and laboratory investigations of haemophilia.
  21. Which parasites cause cystic lesions in humans? Describe Pathology and Laboratory diagnosis of Hydatid Cyst.
  22. Define Leukaemia. Discuss acute blast cell Leukaemia.
  23. What is symbiosis, definitive host, intermediate host? Discuss the pathogenesis and life cycle of E. Histolytica.
  24. Describe the life cycle pathogenesity and laboratory diagnosis of infestation due to P. Vivax.
  25. Describe the peripheral blood and bone marrow picture of acute myeloid leukaemia.
  26. Describe the laboratory investigation to diagnose a case of Megaloblastic anaemia.
  27. Discuss the laboratory diagnosis of diabetes mellitus.
  28. Define anaemia. Discuss nutritional anaemias.
  29. Investigate a case of mis-matched blood transfusion.
  30. Describe morphology cultural characteristics Pathogenecity and laboratory investigation of GONOCOCCI.
  31. Enumerate the organism causing sexually transmitted diseases. Discuss the morphology, cultural characteristics, and pathology of Treponema Pallidium.
  32. Define Haemolytic Anaemia. Discuss the difference with respect to presentation, pathology and laboratory diagnosis of thalassaemia iron deficiency anaemia and sideroblastic anaemia.
  33. Discuss the preparation, sterilization and advantages of solid liquid and enriched media.
  34. Enumerate and discuss the various reactions which occur during blood transfusion and mention the indication of blood transfusion.
  35. Enumerate gram positive bacilli. Describe the Morphology, Cultural characters and laboratory diagnosis of C. diphtheriae.

Short Notes

  1. Hazards of blood transfusions
  2. A.I.D.S.
  3. Virus causing human cancer
  4. Ketonuria
  5. Leukemoid reaction
  6. Spores
  7. Ova in stools
  8. Parasites found in blood
  9. Haematuria.
  10. R A Factor
  11. Exfoliative cytology
  12. Significance of specific gravity of urine.
  13. Atypical
  14. Mycobacteria.
  15. Bacteriod
  16. L.F.T. in obstructive jaundice
  17. Urine in acute pyelonephritis
  18. T & B lymphocytes
  19. C.S.F.in pyogenic meningitis.
  20. Criteria in selection of a blood donor
  21. Laboratory diagnosis of enteric fever
  22. Laboratory diagnosis of iron deficiency.
  23. Spores.
  24. Stool in acute amoebic dysentery.
  25. Bacteriophage.
  26. Widal test.
  27. Endotoxin /Exotoxin.
  28. Complement.
  29. Laboratory diagnosis of hydatid cyst
  30. Selective media
  31. Pregnancy Test
  32. Sterilisation by dry heat
  33. Laboratory diagnosis of nephrotic syndrome.
  34. Multiple Myeloma.
  35. Bacteriophage.
  36. Ovarian function test.
  37. Bone Marrow
  38. Hypersplenism.
  39. V.D.R.L.
  40. Protienuria
  41. Laboratory diagnosis of acute diarrhoea
  42. Foetal Hb
  43. Laboratory diagnosis of P. U. O.
  44. Mantoux Test
  45. Serological tests for syphilis
  46. Haemophilia.
  47. Antigen
  48. Thyroid function test
  49. Laboratory investigation of Diabetes-Mellitus
  50. Hospital Infection
  51. Flagella
  52. Glucose Sterilization
  53. Metachromatic stains
  54. Thrombocytopenia
  55. Bacterial toxins

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QUESTION BANK OF PHYSIOLOGY

QUESTION BANK OF PHYSIOLOGY

C.V.S.

Full Questions.

  1. Define cardiac cycle & describe various events taking place in it
  2. Describe volume changes during cardiac cycle
  3. Describe cardiac cycle.
  4. Describe left ventricular pressure & volume changes
  5. Describe various phases of cardiac cycle in correlation with the left ventricular pressure changes
  6. What is cardiac output? Enumerate different methods used to estimate it Describe any one method in details
  7. Enumerate various factors affecting it
  8. Enumerate different parts of junctional tissues of heart Describe in details production & propagation of cardiac impulse,
  9. What is heart rate? Give its physiological variations& describe how it is regulated
  10. Describe regulation of blood volume & describe any one method to measure it clinically
  11. Define Electrocardiogram. Describe the different components of a normal E.C.G. recorded in lead II
  12. Define Blood pressure Explain short & long term regulation of blood pressure
  13. What is blood pressure? Describe how it is measured clinically Enumerate the physiological variations in blood pressure.
  14. What is blood pressure?
  15. Explain role of Sino aortic reflex in regulation of B.P.
  16. What is Sino aortic reflex? Describe how it is studied experimentally. Enumerate its effects on cardio-respiratory mechanisms
  17. What is shock? Describe compensatory & non-compensatory mechanisms operating in circulatory shock.
  18. Cerebral circulation
  19. Coronary circulation
  20. Heart sounds
  21. First heart sound
  22. Junctional tissues of heart
  23. Cardiac action potential
  24. Auscultatory areas of heart
  25. Neural control of blood pressure
  26. Action potential in ventricular muscle
  27. Volumes changes in left ventricle
  28. Pressure changes in left ventricle
  29. Pressure changes in left ventricle during systole
  30. Pressure changes in left ventricle during cardiac cycle

Short Notes

  1. Pulmonary circulation
  2. Arterial pulse
  3. Venous place tracing
  4. A.V.Node
  5. S.A.Node
  6. Sino aortic reflex
  7. Baro receptor reflex
  8. P-R. Interval
  9. Apex beat
  10. J.V.P.
  11. Einthoven’s law

Haematology

Full Questions

  1. What are different leucocytes” Describe the structure & functions of each type.
  2. Give physiological variations (i) of each type. (ii) in total W.B.C. Count
  3. Describe leucopoiesis. What are the functions of leucocytes?
  4. Name different blood groups. Describe how blood groups are determined? Briefly describe their clinical impotence
  5. Name different blood groups. How are they determined? Describe the hazards of mismatched blood transfusion
  6. What are different blood groups? Explain their physiological importance.
  7. Describe the synthesis, functions& fate of Hemoglobin
  8. What is erythropoesis?” Describe the different stages of erythropoesis & its regulation
  9. Name different haemostatic mechanisms & describe the process of coagulation of blood in detail
  10. What is haemostasis? What are different mechanisms of haemostasis? Briefly describe intrinsic & extrinsic pathway of blood coagulation
  11. Describe in different defense mechanisms of body, with special reference to role of lymphocyctes in immunity
  12. What is immunity? Describe various types of immunity & their role in defense
  13. Describe the composition, mechanism of formation & course of circulation of lymph
  14. Describe the structure & functions of spleen
  15. Describe the physiology of spleen
  16. What is pH of blood? Explain its regulation
  17. State normal value of blood volume. Describe the dye dilution method for measuring blood volume. Explain how it is regulated
  18. Describe regulation of blood volume & describe any one method to measure it clinically

Short Notes

  1. Viscosity of blood
  2. Anemia
  3. Anti-coagulants
  4. Lymph gland
  5. Rh. Blood group
  6. Rh. Factor
  7. Neutrophils
  8. T lymphocyte
  9. Erythropoietin
  10. Hemophilia
  11. Phlebogram
  12. Plasmapheresis
  13. Reticulo endothelial system
  14. Absorption of iron
  15. Platelets
  16. Thrombocytes
  17. Hazards of mismatched blood transfusion
  18. Measurement of blood volume
  19. Megaloblastic Anemia
  20. Arnett count maturation factor
  21. Function of lymph
  22. Rh. Incompatibility
  23. Functions of plasma proteins
  24. Plasma proteins
  25. Functions of R.B.C.
  26. Functions of W.B.C.
  27. Functions of spleen
  28. Measurement of total body fluid
  29. Capillary fluid exchange
  30. Maturation factors
  31. Maturation factors of R.B.C.
  32. PH regulation of blood volume
  33. Fibrinolysis

Nervous System

Full Questions

  1. Enumerate different descending tracts. Describe in detail origin, course & termination of pyramidal tracts. Give differences it & extra pyramidal systems.
  2. Compare pyramidal & extra pyramidal systems. Briefly describe pyramidal tract.
  3. Describe physiology of pyramidal tract in details
  4. Describe the course of pyramidal tracts & mention the effects of its section in the internal capsule & in spinal cord-at various levels
  5. Describe the physiology of limbic system
  6. Enumerate the ascending tracts seen in thoracic segment of spinal cord & explain pathway of touch sensation from left leg to cerebral cortex
  7. Describe the pathway of touch sensation from right great toe to cortex; describe the connections & functions of hypothalamus
  8. What is reflex action? Describe different properties of reflex action. Compare them with properties of condition reflex
  9. What is reflex action? Describe different properties of reflex action. What is the physiological importance of reflex action?
  10. Describe the structure & function of synapse. Explain their different. Properties, Describe structure of synapse. Explain mechanism of synaptic transmission Name its different properties
  11. Classify receptors. Describe their properties.
  12. Describe & classify receptor organ & describe their properties.
  13. Describe the structure of neuro muscular function & describe the process of neuromuscular junction.
  14. What is posture? Describe the different the different reflex mechanisms involved in achieving & maintaining the upright posture
  15. Describe connections & functions of hypothalamus

Short Notes

  1. Membrane potential
  2. Pyramid pathway
  3. International tremors
  4. Decerebrate rigidity
  5. Parietal lobe
  6. Electromyogram
  7. Salutatory conduction
  8. Mechanism of E.P.S.P.
  9. Functions of prefrontal lobe
  10. Functions frontal lobe
  11. Functions of hypothalamus
  12. Properties of synapse
  13. Prefrontal lobectomy
  14. Brown Sequard syndrome
  15. Cerebrospinal fluid
  16. Give differences between: Epinephrine & norepinephrin
  17. Functions of cerebellum
  18. Classification of nerve fibers
  19. Properties of nerve fibers
  20. Compound action potential
  21. Conduction of nerve impulse
  22. Velocity of conduction of nerve impulse
  23. Action potential in nerve fiber
  24. Resting membrane potential
  25. Golgi tendon apparatus
  26. Neuro-muscular junction
  27. Effects of posterior nerve-root section
  28. Mechanism of secondary active transport
  29. Mechanism of neuro-muscular transmission
  30. Wallerian degeneration
  31. Functions of hypothalamus
  32. Wallerian degeneration& regeneration

Respiratory system

Full Questions

  1. Describe the transport of oxygen from lungs to tissue cells
  2. Describe the transport of oxygen in atmosphere to the tissue cells
  3. Describe the transport of carbon dioxide from tissue to lungs
  4. Describe chemical control of respiration
  5. Describe chemical regulation of respiration
  6. Describe neural regulation of respiration
  7. Describe the different types of hypoxias
  8. Name different volumes & capacities of lungs & describe how they are measured
  9. Describe different volumes & capacities of lungs & their physiological significance
  10. Enumerate different pulmonary function tests & describe how functional residual; volume is measured
  11. What is acclimatization? Discussion its effects on body.
  12. Describe the structure of respiratory membrane. Describe the process of change of gases through it.

Short Notes

  1. Bhor’s effect
  2. Lung capacities
  3. Surfactant
  4. Alveolar air
  5. Acclimatization
  6. Asphyxia
  7. Cyanosis
  8. Haldane effect
  9. Respiratory membrane
  10. Transport of carbon dioxide
  11. Oxygen dissociation curve
  12. Lung volumes & capacities
  13. Functional residual capacity
  14. Herring Bruer reflex
  15. Timed vital capacity
  16. Vital capacity
  17. Compliance of lung
  18. Dead space air

Endocrine System

Full Questions

  1. Enumerate the hormones secreted by anterior pituitary & describe how their secretions are regulated
  2. Enumerate the hormones secreted by anterior pituitary & describe functions of growth hormone
  3. Describe physiology of growth hormone
  4. Describe physiology of posterior pituitary hormones
  5. Describe synthesis, functions of posterior pituitary hormones.
  6. Describe synthesis, function, & regulations of thyroxin
  7. Describe how blood calcium level is regulated
  8. Describe role of parathyroid hormone in regulating serum calcium levels.
  9. Describe structure & functions of adrenal medulla
  10. Name hormones secreted by adrenal cortex & explain how aldosterone secretion is regulated. Enumerate its functions
  11. Name hormones saturated by adrenal cortex. Describe functions & metabolic action of gluco-corticoids
  12. Describe the actions of gluco-corticoids on body & describe the regulation of gluco corticoids secretion
  13. Describe the physiology of estrogens
  14. Describe the physiology of menstrual cycle
  15. Describe the various phases of menstrual cycle & their hormonal regulation
  16. Describe the physiology of lactation
  17. Describe the role of placenta during pregnancy
  18. Enumerate various pregnancy tests. Describe in detail the immunological test
  19. Describe the process of spermatogenesis & its control
  20. Describe the functions of testosterone & explain how its secretion is regulated

Short Notes

  1. Thyroxin
  2. Growth hormone
  3. A D H
  4. Glycogen
  5. Parathormone
  6. Ovulation
  7. Oxytocin
  8. Myxoedema
  9. Aldosterone
  10. Pregnancy test
  11. Hormones of post pituitary
  12. Blood Glucose level
  13. Menstrual cycle
  14. Functions of placenta
  15. Spermatogenesis
  16. Lactation
  17. Puberty
  18. Acromegaly
  19. Gigantism

Special senses

Full Questions

  1. Describe the physiology of colors vision
  2. Describe the trichromatic theory of color vision & explain color blindness
  3. Describe Photochemistry of vision
  4. Describe the visual pathway. Explain the effects of damage at various levels
  5. What is accommodation? Describe the mechanism of accommodation for near & far vision. Mention the pathway of accommodation
  6. Enumerate different errors of refraction. Describe them in detail with their methods of correction.
  7. Describe the structure & functions of cochlea
  8. Describe the structure & functions of organ of Corti
  9. Describe the structure & functions of vestibular apparatus
  10. Describe the role of middle ear & internal ear in hearing
  11. What is conduction & nerve deafness? Describe the methods used to differentiate them
  12. Explain theories of frequency analysis
  13. Describe the auditory pathway. What are its peculiarities?

Short Notes

  1. Hypermetropia
  2. Myopia
  3. Night blindness
  4. Color vision
  5. Auditory pathway
  6. Pathway of smell
  7. Conduction deafness
  8. Light reflex
  9. Accommodation reflex
  10. Papillary reflex
  11. Triple response
  12. Errors of refraction
  13. Middle ear deafness
  14. Cochlear micro phonic potential
  15. Taste sensation
  16. Aqueous humour
  17. Dark adaptation
  18. Olfactory pathway
  19. Vestibular pathway
  20. Functions of atricle
  21. Functions of middle ear
  22. Deafness

Miscellaneous

Full Questions

  1. Describe the chemical changes during mechanical activity of skeletal muscle
  2. Describe the electro microscopic structure of sarcomere & explain the mechanism of skeletal muscle contraction
  3. Describe the structure of functions of muscle spindle
  4. Describe various mechanisms of heat gain & heat loss of the body & how temperature is regulated
  5. Describe the mechanism of regulation of body temperature with special reference to role of skin

Short Notes

  1. Muscle spindle
  2. Muscle tetanus
  3. Tetany
  4. Fatigue
  5. Fever
  6. Sweating
  7. Shivering
  8. Functions of skin
  9. Sarcomere
  10. Structure of sarcomere
  11. Hypothalamic thermostat
  12. Thermostatic center
  13. Thermal change during skeletal muscle contraction
  14. Mechanism of heat gain by body
  15. Factors affecting tension development in skeletal muscle
  16. Excitation contraction coupling
  17. Tetanic contraction of muscle
  18. Tetanus in skeletal muscle
  19. Role of Ca in muscle contraction
  20. Staircase phenomena in skeletal muscle
  21. Isotonic & isometric contraction
  22. Strength duration curve
  23. Structure & functions of skin
  24. Properties of skeletal muscle
  25. Sweat glands
  26. Thermoregulation by skin
  27. Ratchet theory of muscle contraction

Urinary System

Full Questions

  1. Describe the renal mechanism of regulation of water & electrolytes
  2. Describe the role of kidney in regulation of electrolytes & water balance in the body
  3. Name renal functions tests. Describe various plasma clearance tests Explain in details any one clearance test
  4. What is G.F.R.? What are the different factors affecting it? How is it measured?
  5. Describe mechanism of concentration & dilution of urine
  6. Describe the structure & function of nephron.
  7. Draw & describe parts of nephron. Briefly explain the functions of loop of Henle
  8. Explain the functions of the proximal tubule of nephron
  9. Describe the formation of urine
  10. Describe how renal circulation help kidneys to perform their function
  11. Describe the role of kidney in regulation of acid-base balance
  12. Describe the acid-base balance & its regulation
  13. Describe the process of filling & emptying of urinary bladder

Short Notes

  1. Chloride shift
  2. Rennin
  3. G.F.R.
  4. Counter current mechanism
  5. Emptying of urinary bladder
  6. Cystometrogram
  7. Obligatory urine volume
  8. Juxta-glomerular apparatus
  9. Distal convoluted tubule
  10. Micturation
  11. Insulin clearance test
  12. Urea clearance test
  13. P.A.H clearance test
  14. Peculiarities of renal circulation
  15. Auto regulation of renal blood flow
  16. Renal regulation of blood pressure
  17. Action of ADH of renal tubules
  18. Functions of proximal convoluted tubules

G. I. T.

Full Questions

  1. Describe composition, functions & regulation of pancreatic juice
  2. Describe composition, functions & regulation of gastric juice
  3. Describe composition, functions & regulation o& mechanism of salivary secretion
  4. Name different constituents of succus entericus. Describe the secretion, regulation, & functions of each constituent.
  5. Give an account of composition, formation, & functions of bile
  6. Enumerate the liver function tests. Describe the functions of bile salts
  7. Name the G.I.T. Hormones & describe their functions
  8. Describe functions of stomach.
  9. Describe process of deglutination
  10. Describe process of emptying of stomach
  11. Describe the different movements of small intestine

Biochemistry

Full Questions

  1. Classify proteins. Describe its digestion & absorption in G.I.T.
  2. Classify fats. Describe its digestion & absorption in G.I.T.
  3. Classify carbohydrates Describe its digestion & absorption in G.I.T.
  4. Classify proteins & give the physiological role of essential amino acids in body
  5. Describe digestion, absorption, & metabolism of fats
  6. What are lipids? Classify them & describe how they are digested & absorbed in body
  7. What is balanced diet? Describe how balanced diet for adult pregnant lady is calculated
  8. Prescribe a balanced diet for an adult female
  9. Describe how balanced diet for a medical college student is calculated
  10. Describe the principles of prescribing a balanced diet. Prescribe a suitable diet for a lactating mother
  11. Describe the glycolytic pathway
  12. What is B.M.R? How is measured? Describe the factors affecting it
  13. Describe how blood glucose level is regulated in the body
  14. Describe metabolic actions of insulin. Describe regulation of insulin secretion 091
  15. Enumerate sources of iron. Describe the functions of iron in the body. Briefly explain how iron is absorbed & stored in the body.
  16. Describe TCA cycle & give its significance
  17. Classify vitamins. Give the sources, daily requirements & physiological importance of each vitamin
  18. Enumerate fat soluble vitamins & describe the detail vitamin A that Prevents night blindness
  19. Enumerate water soluble vitamins. Give their sources, physiology functions, effects of deficiency of them
  20. Give the sources physiological role and daily requirement of vitamin A
  21. Give the sources physiological role and daily requirement of vitamin B complex
  22. Give the sources physiological role and daily requirement of vitamin D
  23. Describe the beta-oxidation of palmitic acid in detail

Short Notes

  1. Vitamin A
  2. Vitamin C
  3. Vitamin B12
  4. Vitamin B3
  5. Thiamine
  6. Niacin
  7. Trypsinogen
  8. Gastrin Secretion
  9. Defecation
  10. Rhodopsin cycle
  11. Glycogenolysis
  12. Pancreatic juice
  13. Pancreatic enzymes
  14. B.M.R
  15. Enterokinase
  16. Cholecystokinin
  17. T.C.A. Cycle
  18. Kreb’s Cycle
  19. Insulin
  20. Isoenzymes
  21. Iron absorption
  22. Iron metabolism
  23. Bile salts
  24. Deglutition
  25. D.N.A.
  26. Active transport
  27. Na Co-transport
  28. R.N.A.
  29. Lactic dehydrogenase
  30. Functions of large intestine
  31. Entero-hepatic circulation of bile salts
  32. Factors affecting enzyme activity
  33. Vitamin D
  34. Deglutition reflex
  35. Absorption of amino acids
  36. Essential amino acids
  37. Facilitated amino acids
  38. Essential fatty acids
  39. Gastro colic reflex
  40. Entero gastric reflex
  41. Regulation of salivary secretion
  42. Role of calcium in body
  43. Absorption of fats
  44. Succus entericus
  45. Liver function tests
  46. Glucose tolerance test
  47. Hormones of G.I.T
  48. Glycolytic pathways
  49. Functions of gastric juice
  50. Gastric analysis
  51. Absorption of carbohydrates
  52. Movements of large intestine
  53. Simple diffusion
  54. Facilitated diffusion
  55. Beta oxidation of fats
  56. Embeden Meyeroff’s Pathway
  57. Pavlov’s pouch
  58. A.T.P.
  59. Functions of saliva
  60. Cyclical A.M.P.
  61. Movements of small intestine
  62. Role of Vitamin A in vision

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