2011 pharma Flashcards

1
Q

Which of the following properties of the drugs is an indicator of drug safety?
A. Low therapeutic index
B. High therapeutic index

A

B. High therapeutic index

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2
Q
Which group of drugs produces its effect without binding to a receptor or a macromolecular substance?
A. Aspirin 
B. Alcohol
C. Antacids
D. Penicillin
A

C. Antacids

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3
Q

which if the following statements is true regarding the routes of administration?
A. Gastric motility affects the absorption of a drug if administered orally
B. Oral drugs have 100% bioavailability
C. IV drugs can cross the blood-brain barrier
D. Intramuscular administration is not good for unconscious patients

A

A. Gastric motility affects the absorption of a drug if administered orally

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4
Q

In which type of toxicity can we use chelating agents?
A. Alcohol poisoning
B. Heavy metal toxicity
C. Drug overdose

A

B. Heavy metal toxicity

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5
Q

What is the likely cause of drug accumulation in the elderly?
A. Elevated renal function
B. Declined renal function
C. Elevated liver function

A

B. Declined renal function

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6
Q

What should be accounted for when administering an antibiotic that is extensively metabolized?
A. Hepatic function
B. Renal function

A

A. Hepatic function

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7
Q

A patient suffers from a polymorphism in one of the CYP450 enzymes, which makes him a poor metabolizer of drugs metabolized by that enzyme. What is the effect on the response if a drug metabolized by that enzyme is administered?
A. Low response
B. Increased toxicity

A

B. Increased toxicity

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8
Q

Which of the following is true regarding facilitated diffusion?
A. ATP is required
B. From low to high concentration
C. A carrier is required

A

C. A carrier is required

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9
Q

A person suffered a morphine overdose. The concentration of the drug in his system is 32 mg/L. How long will it take for the concentration of the drug to drop to 2mg/L, the safe concentration if the half-life of the drug is 6 hours?
A. 24 hours
B. 16 hours
C. never

A

A. 24 hours

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10
Q

The activation of which receptor induces lipolysis?
A. α2
B. β3
C. β2

A

B. β3

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11
Q

What is the rate limiting step of noradrenaline synthesis?
A. Dopamine to nonepinephrine
B. Tyrosine to DOPA
C. DOPA to dopamine

A

B. Tyrosine to DOPA

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12
Q

What is the β2 agonist that is used in the treatment of asthma by inducing bronchodilation?
A. Salbutamol
B. Dobutamine
C. Clonidine

A

A. Salbutamol

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13
Q

Salicylate is a weak acidic drug with a pka of 3.0. It was administered orally and reached the stomach where the pH was 3.0. What will be the percentage of the ionized salicylate acid?
A. 75%
B. 90%
C. 50%

A

C. 50%

pH = pKa + log [A-] /[HA]

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14
Q

Calculate the half-life of a drug with volume of distribution of 80L and a clearance rate of 1.386 L/hour
A. 50 hours
B. 40 hours
C. 30 hours

A

B. 40 hours

use Cl=Vd x Ke and T1/2= 0.693/ke

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15
Q

What do we call decreased response to a drug because of frequent exposure?

A

Desensitization

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16
Q

Which of the following is a selective α1 antagonist used for the treatment of hypertension?
A. propranolol
B. prazosin
C. Atenolol

A

B. prazosin

17
Q

Which of the following is true regarding renal clearance?
A. Acidification of urine enhances the reabsorption of aspirin
B. The rate of clearance in women is higher than men

A

A. Acidification of urine enhances the reabsorption of aspirin

18
Q

Which of the following best describes idiosyncratic reactions?
A. Normal and predictable
B. Bizarre and unpredictable
C. Occurs for a majority of people

A

B. Bizarre and unpredictable

19
Q
Which of the following is involved in Phase-II metabolism?
A. Sulfation
B. Oxidation
C. Hydrolysis
D. Reduction
A

A. Sulfation

20
Q

What is a pharmacokinetic drug interaction?

A

Displacement of a drug from albumin by another drug

21
Q

50 mg of drug A and 10 mg of drug B have the same effect. Which of the following statements is true?
A. Drug A is more potent than drug B
B. Drug B is more potent that drug A
C. This question is not stupid

A

B. Drug B is more potent that drug A

22
Q

which of the following drugs can be used for the treatment of organophosphate poisoning?
A. Gentamycin
B. Atropine
C. Hemicholinium

A

B. Atropine

23
Q

What is the mechanism of action of hemicholinium?
A. Inhibits Ach storage
B. Inhibits Ach release
C. Inhibits the uptake of choline

A

C. Inhibits the uptake of choline

24
Q

If a drug binds to a receptor but it does not result in a response, the drug is said to be a/an:

a. agonist
b. antagonist
c. synergistic drug

A

b. antagonist

25
Q

Which of the following is a characteristic of type A (augmented) reactions?

a. Related to the pharmacological action of the drug
b. Unrelated to pharmacological actions of the drug
c. only occur after prolonged treatment

A

a. Related to the pharmacological action of the drug

26
Q

What is the mechanism of action of vinca alkaloids?

a. Tyrosine kinase inhibitor
b. Angiogenesis inhibitor
c. Prevent the polymerization of tubulin

A

c. Prevent the polymerization of tubulin

27
Q

What is an adverse effect of suxamethonium?

a. hyperkalemia
b. malignant hypothermia
c. tachycardia

A

a. hyperkalemia

28
Q

When is carbachol contraindicated?

a. hypothyroidism
b. peptic ulcer
c. low sodium

A

b. peptic ulcer

the question is basically asking “why are muscarinic agonists contraindicated?”

29
Q

What receptor does Mivacurium act on?

a. Nicotinic receptor
b. Muscarinic receptor

A

a. Nicotinic receptor