Category: General Pharmacology

A. Is healthy
B. With mild systemic disease
C. With severe systemic disease
D. None of the above

A. Tetracycline
B. Cimetidine
C. Rifampicin
D. Phenobarbitone

A. It is the proportion (fraction) of unchanged drug that reaches the systemic circulation
B. Biovailability of an orally administered drug can be calculated by comparing the area under cure (o-a) after oral and intravenous (IV) administration
C. Low oral biovailability always and necessarily mean poor absorption
D. Biovailability can be determined from plasma concentration or urinary excretion data

A. Super sensitivity
B. Idiosyncrasy
C. Hyper sensitivity
D. Hyper acidity

A. Volume of distribution
B. Clearance
C. Rate of administration
D. Half life

A. Idosyncrasy
B. Toxicity
C. Side effect
D. None of the above

A. 48
B. 24
C. 12
D. 3

A. Drug toxicty
B. Drug potency
C. Drug safety
D. Drug’s Lethal effect

A. Physical dependence
B. Psychological dependence
C. Addiction
D. Habituation

A. Indifference
B. Synergy
C. Antagonism
D. Bacterial symbiosis