- (A) Are more common than first order kinetics
- (B) Decrease in concentration exponentially with time
- (C) Have a half – life independent of dose
- (D) Show a plot of drug concentration versus time that is linear
Medical Mcqs
- (A) Phenytoin
- (B) Phenabarbtion
- (C) Erythromycin
- (D) Digoxin
- (A) Genetic component
- (B) Psychological component
- (C) Psysiological component
- (D) Nutritional component
- (A) Physical dependence
- (B) Psychological dependence
- (C) Addiction
- (D) Habituation
- (A) Amiodarone
- (B) Phenytoin
- (C) Verapamil
- (D) Disorpyamide
- (A) Indifference
- (B) Synergy
- (C) Antagonism
- (D) Bacterial symbiosis
- (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) Range of disease in which the drug beneficial
- (B) Maximal intensity of response that can be produced by the drug
- (C) The therapeutic does range of the drug
- (D) The therapeutic index of the drug
- (A) Anti-hypertensives
- (B) Anti-diabetics
- (C) Anticoagulants
- (D) Anti-fibrinolytics
- (A) Aminoglycoside
- (B) Vancomycin
- (C) Calcium channel blocker
- (D) Metronidazole
