- (A) Purity of Enzyme
- (B) Physiological role
- (C) Half life enzymes drug complex
- (D) Affinity
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- (A) 48
- (B) 24
- (C) 12
- (D) 3
- (A) The proto type member of a class of drugs
- (B) The oldest member of a class of drugs
- (C) An inactive drug that is transformed in the body to an active metabolite
- (D) A drug that is stored in body tissues and is then gradually released in the direction
- (A) Idosyncrasy
- (B) Toxicity
- (C) Side effect
- (D) None of the above
- (A) Passive diffusion
- (B) Active transport
- (C) Facilitated trasnsport
- (D) Filtration
- (A) 84%
- (B) 93%
- (C) 80.5%
- (D) 4.75%
- (A) prevents or bypasses first pass effects
- (B) Easy to administer
- (C) Lipid soluble
- (D) Can be spitted out with signs of toxicity
- (A) Tetracycline
- (B) Cimetidine
- (C) Rifampicin
- (D) Phenobarbitone
- (A) Volume of distribution
- (B) Clearance
- (C) Rate of administration
- (D) Half life
- (A) Morphine
- (B) Nitroglycerine
- (C) Propranolol
- (D) Salicylates

