Pharmacology & Toxicology Class Test | Pharmacology & Toxicology DPEE Test

This test is Improve for Pharmacy exam like Diploma in Pharmacy exit exam MCQs (DPEE), GPAT, & other competitive exam. Pharmacology & Toxicology Class Test | Pharmacology & Toxicology DPEE Test

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Pharmacology & Toxicology MCQs for DPEE | D.Pharma Exit Exam Most Important Question 2022-23

1 / 50

Pilocarpine is classified as

2 / 50

Antidote of atropine is

3 / 50

Major adverse effect of clonidine is

4 / 50

All of the following statement related to neostigmine are correct except

5 / 50

Acetylcholine and physostigmine are examples of……………… type drug interaction.

6 / 50

Local anesthetics produce:

7 / 50

Which of the following is CYP450 enzyme inhibitor?

8 / 50

Atropine is used prior the administration of a general Anesthetics agent due to become it

9 / 50

Phentolamine is competitive antagonism of

10 / 50

Which of the following drug may cause cycloplegia when used topically in the eye?

11 / 50

Which of the following receptor shows the slowest response?

12 / 50

Most common Phase -2nd reaction is

13 / 50

Most serious adverse effect of antithyroid drug, propylthiouracil is

14 / 50

Atropine blocks the muscarinic actions of acetylcholine by

15 / 50

Activation of alpha-2 receptors in the pancreatic islets causes

16 / 50

In the treatment of myasthenia gravis, the best agent for distinguishing between myashenic crisis and cholinergic crisis, given intravenously is

17 / 50

Bioassays are carried out to:

18 / 50

Sweating is inhibited by

19 / 50

Which of the following a is directly acting sympathomimetic agent?

20 / 50

Beta agonist used in bronchial asthma exert action by

21 / 50

Undesirable effects of oral contraceptives include all except

22 / 50

………………drug having highest volume of distribution.

23 / 50

Neostigmine effectively antagonizes skeletal muscle relaxation produced by

24 / 50

Morphine affects the eyes by:

25 / 50

Following are the chloride channel blocker
(P) Amiloride (Q) Cadmium
(R) Picrotoxin. (S) Ketamine

26 / 50

Drug having high affinity but low intrinsic activity is called

27 / 50

Spironolactone is a prodrug and its active metabolite is

28 / 50

Drug of the following drugs. Does not cross the blood-brain barrier?

29 / 50

Serious unwanted effect of epinephrine is

30 / 50

Muscarinic receptor M4 are mainly located at

31 / 50

In urinary incontinence following drug is widely used:

32 / 50

In belladonna poisoning convulsions can be controlled by

33 / 50

Which of the following agent irreversibly bound with acetyl cholinesterase.

34 / 50

Most of the drug is absorbed through

35 / 50

Ganglionic blocking agent may cause all of the following except

36 / 50

Mechanism of action of organic phosphate parathion is

37 / 50

In the bioassay the conviction activity in mice is observed during……………use.

38 / 50

Tolbutamide is contraindicated in

39 / 50

Antidote of organo phosphorus poisoning is

40 / 50

All of the following may enhance the action of sulfonylureas except

41 / 50

Darifenacin is a

42 / 50

Drug of choice in the treatment of cardiogenic shock is

43 / 50

Isolated rabbit jejunum is used

44 / 50

Neostigmine may cause all of the following except

45 / 50

Epinephrine is added to local anaesthetics

46 / 50

Alcuronium is a semisynthetic derivative with similar properties of

47 / 50

Action of D-tubocurarine is

48 / 50

Drug of choice in motion sickness is

49 / 50

Hormones that increase cyclic AMP in the larger organ include all except

50 / 50

Atropine over Dosage may cause all of the following except

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