List of top Veterinary Science Questions on Veterinary Pharmacology asked in ICAR AIEEA (PG)

Match List-I with List-II.

\[ \begin{array}{|c|l|c|l|} \hline \textbf{List-I} & & \textbf{List-II} & \\ \hline A & \text{Thebaine} & I & \textit{Strophanthus gratus} \\ B & \text{d-Tubocurarine} & II & \text{Semi-synthetic Opioid} \\ C & \text{Ouabain} & III & \textit{Papaver somniferum} \\ D & \text{Etorphine} & IV & \textit{Chondrodendron tomentosum} \\ \hline \end{array} \] 
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Given below are two statements:
Statement (I): The time of drug concentration above minimum inhibitory concentration ($T > \text{MIC}$) is important for clinical success in case of treatment with beta lactam antibiotics.
Statement (II): Carbapenems are sensitive to extended spectrum beta lactamases (ESBL).
In light of the above statements, choose the most appropriate answer from the options given below.
Given below are two statements, one is labelled as Assertion (A) and other one labelled as Reason (R).
Assertion (A): Tetracyclines inhibit protein synthesis and exhibit broad spectrum bactericidal effect.
Reason (R): Tetracyclines bind to 30 S subunit and inhibit the binding of aminoacyl-tRNA to A-site.
In light of the above statements, choose the correct answer from the options given below.
Arrange the adverse effects of Chloramphenicol, Tetracyclines, Aminoglycosides and Sulfadiazine in correct order
(A). Keratoconjunctivitis sicca
(B). Teeth discoloration
(C). Ashen-gray skin discoloration
(D). Deafness
Choose the correct answer from the options given below:
Anaerobic bacteria are intrinsically resistant to
Which of the following statement regarding Cytochrome P450 enzymes is incorrect?
A 70 kg calf was given a drug X at a dose of 100 mg/kg body weight. The half-life of the drug X is 10 hours and its initial plasma concentration is 1.9 mg/ml. True statement about drug X is/are
(A). Clearance is around 0.02 litre/hour
(B). Volume of distribution is around 3.68 L
(C). Elimination rate constant is 0.0693
(D). Clearance is around 0.2 litre/hour
Choose the correct answer from the options given below:
Which of the following statements are not correct about first order kinetics?
(A). Clearance remains constant
(B). Fixed amount of the drug is eliminated
(C). Half-life increases with dose
(D). Decrease in clearance with increasing dose
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The positive inotropic effect of digitalis is due to inhibition of $Na^+/K^+$ ATPase pump in cardiac muscle cell membrane leading to
Which one of the following diuretics does not require its presence in the renal tubular lumen for its pharmacological effects?
All of the following antidiabetic drugs act by enhancing insulin secretion except
Which of the following antiepileptic drugs acts by affecting the levels of GABA?
Which of the following statements are not true about Type B adverse drug reactions?
(A). Qualitatively abnormal responses to the drug
(B). Predictable from the drug's known pharmacological or toxicological effects
(C). Generally dose-dependent
(D). Usually common
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Match List-I with List-II
{|l|l|} List-I (Condition) & List-II (Drug used)
(A). Cyanide Poisoning & (I). Calcium Disodium Edetate
(B). Lead poisoning & (II). Sodium Thiosulphate
(C). Trypanosomosis & (III). Isometamidium Chloride
(D). Hepatozoon canis infection & (IV). Imidocarb Dipropionate

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Dogs with which of the following mutation are predisposed to increased sensitivity to ivermectin and moxidectin ?
Match List-I with List-II
List-I
(A). Morphine
(B). Buprenorphine
(C). Butorphanol
(D). Naloxone
List-II
(I). Opioid antagonist
(II). Opioid agonist-antagonist
(III). Partial opioid agonist
(IV). Opioid agonist
Choose the correct answer:
Which of the following effects are least observed with systemic administration of glycopyrrolate?
Which of the following effects is not associated with the administration of anticholinergic agents?

Match List-I with List-II

List-I (Target)List-II (Agent)
(A) Na, K -2Cl symporter(I) Frusemide
(B) Na-Cl symporter(II) Triamterene
(C) Renal epithelial Na channel(III) Acetazolamide
(D) Carbonic anhydrase(IV) Chlorothiazide

Match List-I with List-II

List-I (Name of drugs)List-II (Characteristics)
(A) Saline(I) Surface active agent
(B) Propylene glycol(II) Mucolytic agent
(C) Bromohexin(III) Diluent mucokinetic agent
(D) Iodide(IV) Bronchomucotropic agent
Arrange the below listed cephalosporins in the order of first to fourth generation
(A) Ceftriaxone
(B) Cephalexin
(C) Cefuroxime
(D) Cefepime
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Main source of Digitoxin is:
All of these are pro-drugs except
Consider the classification of anti-arrhythmic drugs
(A) Quinidine is a class I anti-arrhythmic drug
(B) Amiodarone is a class IV anti-arrhythmic drug
(C) Propranolol is a class ii anti-arrhythmic drug
(D) Lignocaine is a class I anti-arrhythmic drug
Choose the correct answer from the options given below:
Arrange the routes of drug administration in the sequence that offer bioavailability from low to high:
(A) Intramuscular route
(B) Intravenous route
(C) Topical route
(D) Subcutaneous route
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