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EACH STATEMENT MUST BE ANSWERED EITHER BY WRITING ‘T’ FOR ‘TRUE’ OR ‘F’ FOR
‘FALSE’ BESIDES IT.
b) Pharm................................ interaction
c) Pharm................................. interaction
d) Pharm................................. interaction
88) Complete the following:
a) Precipitation of Thiopental by S............
b) Precipitation of B............................... by Soda bicarb.
c) Inactivation of Catecholamines due to alkalinisation by S..... b.....
d) Two drugs may interact chemically to form a toxic compound. Eg. Desflurane
has been shown to interact with dry s..................... or B............................ to
produce CO & heat.
89) Drug interaction
a) If NO is allowed prolonged contact with O2, it forms Nitrogen dioxide (NO2),
which can produce Pulmonary edema & alveolar hemorrhage T
Alteration of absorption may occur because
b) Direct chemical or physical interaction between drugs in the body T
c) One drug alters physiological mechanism governing absorption of the second T
d) Eg :- oral antidiarrheal drugs (kaolin, pectin) absorb d................ & prevents its
absorption.
90) Drug interaction
a) Antacids reduce absorption of acidic drugs like Midazolam. T
b) In 10% 0f patients receive digoxin 20% or more of the administered dose is
metabolized by the intestinal flora F
c) Oral Tetracycline can be inactivated by chelation if given together with antacids
containing polyvalent cation ( Mg++, Ca++). T
d) Delay of gastric emptying produced by drugs such as Opioids & Anticholinergics
may not reduce the absorption of orally administered drugs. F
91) Drug interaction
a) Prolongation of action of Infiltrated LA by addition of ..........................
Distribution
b) Drugs which decrease cardiac output ( beta blockers, vasodilators) decrease the
arterial concentration of other drugs in highly perfused tissues such as brain &
myocardium F
c) Such drugs augments the effects of drugs such as Propofol, Thiopental & Volatile
anesthetics T
d) Drug induced changes in pH in a particular body region or fluid compartment can
alter the distribution of other drugs by “ion traping”. T
92) Distribution
a) Acidic drugs are unionised at acidic pH T
b) Basic drugs are also unionised at basic pH T
c) And it is only the ionised fraction of the drug which is able to cross the lipid
membranes. F
d) Drugs decreasing the gastric acidity increase gastric absorption of acidic drugs
such as Midazolam F
93) Distribution
a) lipid soluble basic drugs such as Fentanyl can diffuse into stomach from
bloodstream T
b) It is only the unbound fraction of drug that is available for crossing membrane T
c) It is only the bound fraction of drug that is available for crossing membrane F
d) So protein bound, potentially toxic drugs like Warfarin, Phenytoin may not be
displaced by other highly bound drugs F
94) Protein binding
a) The body acts as a buffer against large change in unbound fraction T
b) Any unbound drug in plasma is slowly distributed into peripheral tissues F
Metabolism
c) Administration of Neostigmine intensifies & prolongs the effect of Scoline, by
inhibiting Pseudocholinestrase. T
d) Monoamide oxidase acts to regulate the presynaptic pool of acetylcholine
available for synaptic transmission. F
95) MAOI
a) MAO inhibitors (Phenelzine, Tranylcypromine & Selegiline) are mainly used for
T/t of refractory depression & other mood disorders T
b) MAOI increase the amount of presynaptic transmitter released by Ephedrine,
Amphetamine. T
c) Directly acting sympathomimetics such as Epinephrine, Norepinephrine &
Phenylephrine are affected more by MAOI F
d) Serotonin syndrome may occur in patients taking MAOI who are administered
Meperidine T
96) Hepatic Biotransformation
The removal of drug from the body by hepatic biotransformation is a function of 2
independent variables
a) Hepatic blood flow T
b) Intrinsic clearance T
c) Hepatic blood flow is the rate enhancing factor in hepatic clearance F
d) Clearance is decreased by drugs or factors which decrease hepatic blood flow
such as Beta blockers T
97) Clearance
a) Hepatic enzyme activity is the rate limiting factor in hepatic clearance. T
b) Stimulation or inhibition of enzyme activity do not have direct effect on
metabolism. F
c) Protein binding does not affects clearance F
d) The most important subfamily being CYP3A T
98) Drug elimination
a) Organic anions & cations are actively secreted by separate transporters in the
renal glomeruli. F
b) The cation system handles elimination of Atropine , Isoproterenol , Neostigmine
& Meperidine. T
c) - The anion system is involved in elimination of Salicylates , Penicillin,
cephalosporin & most of potent diuretics. T
d) A weak acid like Phenobarbital (pKa 7.4 ) is largely unionised when urinary pH is 3
F
99) Drug Elimination
a) If the urine pH is raised to 8 or 9 by SodaBicarb ; most of the drug becomes
ionised T
b) If the urine pH is raised to 8 or 9 by SodaBicarb reabsorption decreases &
clearance increases T
c) For a weak base the reverse is true i.e. excretion can be promoted by
acidification of urine T
d) Active tubular secretion occurs in the distal tubules F