2011 pharma Flashcards
Which of the following properties of the drugs is an indicator of drug safety?
A. Low therapeutic index
B. High therapeutic index
B. High therapeutic index
Which group of drugs produces its effect without binding to a receptor or a macromolecular substance? A. Aspirin B. Alcohol C. Antacids D. Penicillin
C. Antacids
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. Gastric motility affects the absorption of a drug if administered orally
In which type of toxicity can we use chelating agents?
A. Alcohol poisoning
B. Heavy metal toxicity
C. Drug overdose
B. Heavy metal toxicity
What is the likely cause of drug accumulation in the elderly?
A. Elevated renal function
B. Declined renal function
C. Elevated liver function
B. Declined renal function
What should be accounted for when administering an antibiotic that is extensively metabolized?
A. Hepatic function
B. Renal function
A. Hepatic function
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
B. Increased toxicity
Which of the following is true regarding facilitated diffusion?
A. ATP is required
B. From low to high concentration
C. A carrier is required
C. A carrier is required
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. 24 hours
The activation of which receptor induces lipolysis?
A. α2
B. β3
C. β2
B. β3
What is the rate limiting step of noradrenaline synthesis?
A. Dopamine to nonepinephrine
B. Tyrosine to DOPA
C. DOPA to dopamine
B. Tyrosine to DOPA
What is the β2 agonist that is used in the treatment of asthma by inducing bronchodilation?
A. Salbutamol
B. Dobutamine
C. Clonidine
A. Salbutamol
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%
C. 50%
pH = pKa + log [A-] /[HA]
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
B. 40 hours
use Cl=Vd x Ke and T1/2= 0.693/ke
What do we call decreased response to a drug because of frequent exposure?
Desensitization