Deck 1: Cardiovascular Drugs
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Deck 1: Cardiovascular Drugs
1
In cardiac glycoside, position of ?- unsaturated lactone ring is
A)C - 3
B)C - 14
C)C - 17
D)C - 23
A)C - 3
B)C - 14
C)C - 17
D)C - 23
C - 17
2
Activity of cardiac glycoside depends to a great extent on
A)23rd carbonyl oxygen
B)C - 3 OH
C)Side chain at C - 14
D)Side chain at C - 17
A)23rd carbonyl oxygen
B)C - 3 OH
C)Side chain at C - 14
D)Side chain at C - 17
23rd carbonyl oxygen
3
Angiotensin II causes rise in blood pressure by:
A)Direct vasoconstriction
B)Releasing adrenaline from adrenal medulla
C)Increasing central sympathetic tone
D)All of the above
A)Direct vasoconstriction
B)Releasing adrenaline from adrenal medulla
C)Increasing central sympathetic tone
D)All of the above
All of the above
4
Digitalis slows the heart in congestive heart failure by:
A)Increasing vagal tone
B)Decreasing sympathetic overactivity
C)Direct depression of sinoatrial node
D)All of the above
A)Increasing vagal tone
B)Decreasing sympathetic overactivity
C)Direct depression of sinoatrial node
D)All of the above
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5
Methyldopa is
A)Parasympathomimetic
B)Parasympatholytic
C)Sympathomimetic
D)Sympatholytic
A)Parasympathomimetic
B)Parasympatholytic
C)Sympathomimetic
D)Sympatholytic
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6
Losartan is
A)Renin release blocker
B)ACE inhibitor
C)Angiotension I blocker
D)Angiotension II blocker
A)Renin release blocker
B)ACE inhibitor
C)Angiotension I blocker
D)Angiotension II blocker
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7
IUPAC name of Dobutamine is
A)4-(2-{[4-(4-hydroxyphenyl)butan-2-yl]amino}ethyl)benzene-1,2-diol
B)4-(2-{[4-(4-hydroxyphenyl)butan-2-yl]amino}methyl)benzene-1,2-diol
C)4-(2-{[4-(4-hydroxyphenyl)propan-2-yl]amino}ethyl)benzene-1,2-diol
D)4-(2-{[4-(4-hydroxyphenyl) propan -2-yl]amino}methyl)benzene-1,2-diol
A)4-(2-{[4-(4-hydroxyphenyl)butan-2-yl]amino}ethyl)benzene-1,2-diol
B)4-(2-{[4-(4-hydroxyphenyl)butan-2-yl]amino}methyl)benzene-1,2-diol
C)4-(2-{[4-(4-hydroxyphenyl)propan-2-yl]amino}ethyl)benzene-1,2-diol
D)4-(2-{[4-(4-hydroxyphenyl) propan -2-yl]amino}methyl)benzene-1,2-diol
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8
1-[4-(2-methoxyethyl)phenoxy]-3-[(propan-2-yl)amino]propan-2-ol is IUPAC name of
A)Atenolol
B)Metoprolol
C)Captopril
D)Hydralazine
A)Atenolol
B)Metoprolol
C)Captopril
D)Hydralazine
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9
Hydralazine is synthesized from
A)2-formyl benzoic acid and Hydrazine
B)Methacrylic acid
C)2-azidoethanol
D)o-nitro toluene
A)2-formyl benzoic acid and Hydrazine
B)Methacrylic acid
C)2-azidoethanol
D)o-nitro toluene
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10
The principal action common to all class I antiarrhythmic drugs is:
A)Na+ channel blockade
B)K+ channel opening
C)Depression of impulse conduction
D)Prolongation of effective refractory period
A)Na+ channel blockade
B)K+ channel opening
C)Depression of impulse conduction
D)Prolongation of effective refractory period
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11
Identify high ceiling diuretic.
A)Chlorthiazide
B)Furosemide
C)Spironolactone
D)Amiloride
A)Chlorthiazide
B)Furosemide
C)Spironolactone
D)Amiloride
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12
_____________ is carboxylic acid moiety containing.
A)Captopril
B)Enalapril
C)Fosinopril
D)Bepridil
A)Captopril
B)Enalapril
C)Fosinopril
D)Bepridil
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13
Given structure is of
A)Captopril
B)Enalapril
C)Fosinopril
D)Bepridil
A)Captopril
B)Enalapril
C)Fosinopril
D)Bepridil
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14
_____________ is sulfhydryl moiety containing.
A)Captopril
B)Enalapril
C)Fosinopril
D)Bepridil
A)Captopril
B)Enalapril
C)Fosinopril
D)Bepridil
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15
Given drug is
A)? blocker
B)? blocker
C)K+ channel blocker
D)Ca++ channel blocker
A)? blocker
B)? blocker
C)K+ channel blocker
D)Ca++ channel blocker
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16
The antiarrhythmic drug which decreases both rate of depolarization (phase 0) as well as rate of repolarization (phase 3) of myocardial fibres is:
A)Lignocaine
B)Propranolol
C)Quinidine
D)Verapamil
A)Lignocaine
B)Propranolol
C)Quinidine
D)Verapamil
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17
The following drug is used to reduce the frequency of angina pectoris as well as to terminate an acute attack:
A)Isosorbide dinitrate
B)Pentaerythritol tetranitrate
C)Diltiazem
D)Dipyridamole
A)Isosorbide dinitrate
B)Pentaerythritol tetranitrate
C)Diltiazem
D)Dipyridamole
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18
Blood flow in the following vascular bed generally decreases under the influence of glyceryl trinitrate:
A)Coronary
B)Cutaneous
C)Renal
D)Cranial
A)Coronary
B)Cutaneous
C)Renal
D)Cranial
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19
Phase II in cardiac action potential is
A)Fast depolarization
B)Partial repolarization
C)Plateau
D)Repolarization
A)Fast depolarization
B)Partial repolarization
C)Plateau
D)Repolarization
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20
In HMG-CoA-Reductase Inhibitors, Lactone ring may be substituted at
A)C- 15
B)C- 16
C)C-17
D)C -18
A)C- 15
B)C- 16
C)C-17
D)C -18
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21
2-(diethylamino)-N-(2,6-dimethylphenyl) Acetamide is IUPAC name of
A)Flecainide
B)Atenolol
C)Verapamil
D)Lignocaine
A)Flecainide
B)Atenolol
C)Verapamil
D)Lignocaine
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22
Select the organic nitrate which undergoes minimal first-pass metabolism in the liver:
A)Glyceryl trinitrate
B)Isosorbide dinitrate
C)Isosorbide mononitrate
D)Erythrityl tetranitrate
A)Glyceryl trinitrate
B)Isosorbide dinitrate
C)Isosorbide mononitrate
D)Erythrityl tetranitrate
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23
The primary mechanism of beneficial effect of glyceryl trinitrate in classical angina pectoris is:
A)Increase in total coronary blood flow
B)Redistribution of coronary blood flow
C)Reduction of cardiac preload
D)Reduction of cardiac afterload
A)Increase in total coronary blood flow
B)Redistribution of coronary blood flow
C)Reduction of cardiac preload
D)Reduction of cardiac afterload
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24
Organic nitrates relax vascular smooth muscle by:
A)Increasing intracellular cyclic GMP
B)Increasing intracellular cyclic AMP
C)Decreasing intracellular cyclic AMP
D)Both 'A' and 'C' are correct
A)Increasing intracellular cyclic GMP
B)Increasing intracellular cyclic AMP
C)Decreasing intracellular cyclic AMP
D)Both 'A' and 'C' are correct
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25
Nitrate tolerance is least likely to develop with the use of:
A)Sustained release oral glyceryl trinitrate
B)Sublingual glyceryl trinitrate
C)Transdermal glyceryl trinitrate
D)Oral pentaerythritol tetranitrate
A)Sustained release oral glyceryl trinitrate
B)Sublingual glyceryl trinitrate
C)Transdermal glyceryl trinitrate
D)Oral pentaerythritol tetranitrate
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