|
1. which
of the following is a type b (unpredictable) adverse
drug reaction:
a.
side effect
b.
toxic effect
c.
idiosyncrasy
d. physical dependence
|
C
|
|
2. drugs
producing allergic reactions generally act as:
a.
complete antigens
b.
haptenes
c.
antibodies
d. mediators
|
B
|
|
3. which
of the following is the only life saving measure in
case of anaphylactic shock:
a.
intravenous hydrocortisone hemisuccinate
b.
intravenous chlorpheniramine maleate
c.
intramuscular adrenaline hydrochloride
d. intravenous glucose-saline
|
C
|
|
4. intradermal
drug sensitivity tests can detect the presence of following type of
hypersensitivity:
a.
type i (anaphylactic)
b.
type ii (cytolytic)
c.
type iii (retarded)
d. all of the above
|
a
|
|
the
most vulnerable period of pregnancy for the
causation
of foetal malformations due to drugs is:
a.
18-55 days of gestation
b.
56-84 days of gestation
c.
second trimester
d. 36 weeks onwards
|
A
|
|
functional
proteins that are target of drug action
i.enzymes
ii.transporters
iii.ion
channels
iv.receptors
correct
a.i,ii,iii
b.ii,iv
c.i,ii
d.i,ii,iii,iv
|
D
|
|
5. which
of the following drug is a competitive inhibitor of enzyme but non equilibrium type
a.physostigmine
compete with acetycholine for cholinesterase
b.sulfonamide
compete with paba for bacterial folate synthase
c.allopurinol
compete with hypoxanthenes for xanthine oxidase
d.organophosphate
compete with acetylcholine for cholinestrase
|
D
|
|
6. which
of the following drug is not a non competitive inhibitor of enzyme
a.acetazolamide
inhibit carbonic anhydrase
b.disulfiram
inhibit aldehyde dehydrogenase
c.digoxin
inhibit na k atpase
d
captopril inhibit ace enzyme
|
D
|
|
7. select
the drug act through ion channel
a.ethosuximide
b.amiloride
c.both
a nd b
d.none
of these
|
C
|
|
select
the drug act through transporters
i.fluoxetine
ii.phenytoin
iii.furosemide
iv.desipramine
correct
a.i,ii,iii
b.i,iii,iv
c.ii,iii,iv
d.i,ii,iii,iv
|
b
|
|
select
the wrong statement
a.competitive
antagonist have high affinity and high
intrinsic activity
b.partial
agonist have affinity and sub maximal intrinsic activity
c.inverse
agonist have affinity but intrinsic activity with a minus sign
d.agonist
have both high affinity and maximal
intrinsic
activity
|
A
|
|
8. select
the partial agonist
a.naloxone
b.pentazocine
c.atropine
d.morphine
|
B
|
|
9. select
the competitive antagonist
a.propranolol
b.atropine
c.naloxone
d.all
of these
|
D
|
|
10. select
the following which act through enzyme linked receptors
a.insulin
b.epidermal
growth factor
c.both
of these
d.gaba-a
|
C
|
|
11. which
of the following is ion channel receptor
i.gaba,glycine
ii.nmda,5-ht3
iii.nicotinic
cholinergic
iv.5-ht1,dopamine
correct
a.i,ii,iii,iv
b.i,ii,iii
c.ii,iii,iv
d.i,ii,iv
|
b
|
|
12. which
of the following is a g protein coupled receptor, act through ip3 dag pathway
a.muscarinic-1
b.muscarinic-2
c.muscarinic-3
d.all
a,b,c
e.
both a and c
|
e
|
|
13. histamine
is a g coupled protein receptor,which of the following statement is true
a.h-2
act through adenylyl cyclase pathway by increasing camp
b.h-1
act through ip3 dag pathway
c.
h-2 act through adenylyl cyclase pathway by decreasing camp
d.both
a and b
|
d
|
|
14. select
the ligand act through ip3 dag pathway(gpcr)
a.5-ht2
b.5-ht1
c.5-ht3
d.all
of these
|
a
|
|
15. vit-a
and d act through
a.gpcr
b.ion
channel
c.nuclear
receptor
d.enzyme
linked receptor
|
c
|
|
16. select
the intracellular receptor
a.gpcr
b.ion
channel
c.nuclear
receptor
d.enzyme
linked receptor
|
c
|
|
17. A
receptor which itself has enzymatic property is:
a.
insulin receptor
b.
progesterone receptor
c.
thyroxine receptor
d. glucagon receptor
|
a
|
|
18. ‘drug
efficacy’ refers to:
a.
the range of diseases in which the drug is
beneficial
b.
the maximal intensity of response that can
be
produced by the drug
c.
the dose of the drug needed to produce half
maximal
effect
d.
the dose of the drug needed to produce therapeutic
effect
|
b
|
|
19. which
of the following is always true:
a.
a more potent drug is more efficacious
b.
a more potent drug is safer
c.
a more potent drug is clinically superior
d.
a more potent drug can produce the same
response at lower doses
|
d
|
Monday, 17 July 2017
Target GPAT-2018 General Pharmacology Series- 4
Saturday, 15 July 2017
Target GPAT-2018 General Pharmacology Series-3
|
41
|
which
of the following statement is correct
i.erytromycin,ampicillin,rifampin,
attain high concentation in bile
ii.lithium,rifampin
secreted in saliva and sweat
iii.basic
drugs are more concentrated in milk as compare to acidic drugs
iv.acidic
drugs are more concentrated in milk as compared to basic drugs
right
statement is
a.i,ii,iii
b.i,ii,iv
c.ii,iii
only
d.i,ii
only
|
a
|
|
42
|
which of the following drugs is most likely to be
absorbed from the stomach:
a.
morphine sulfate
b.
diclofenac sodium
c.
hyoscine hydrobromide
d. quinine dihydrochloride
|
b
|
|
43
|
which of the following is a weakly acidic drug:
a.
atropine sulfate
b.
chloroquine phosphate
c.
ephedrine hydrochloride
d. phenytoin sodium
|
d
|
|
44
|
the blood-brain barrier, which restricts entry of
many drugs into brain, is constituted by:
a.
p-glycoprotein efflux carriers in brain
capillary
cells
b.
tight junctions between endothelial cells of
brain
capillaries
c.
enzymes present in brain capillary walls
d. all of the above
|
d
|
|
45
|
weakly acidic drugs:
a.
are bound primarily to alpha 1 acid glycoprotein in
plasma
b.
are excreted faster in alkaline urine
c.
are highly ionized in the gastric juice
d. do not cross blood-brain barrier
|
b
|
|
46
|
which of the following cytochrome p450 isoenzymes
is involved in the metabolism of largest number of drugs in human beings and
has been implicated in some dangerous drug interactions:
a.
cyp 3a4/5
b.
cyp 2c9
c.
cyp 2e1
d. cyp 1a2
|
a
|
|
47
|
which of the following cytochrome p450 isoenzymes
is involved in the metabolism of 2nd
largest number of drugs in human beings
a.
cyp 3a4/5
b.
cyp 2d6
c.
cyp 2e1
d. cyp 1a2
|
b
|
|
48
|
the plasma half life of penicillin-g is longer in
the new
born because their:
a.
plasma protein level is low
b.
drug metabolizing enzymes are immature
c.
glomerular filtration rate is low
d.
tubular transport mechanisms are not well
developed
|
d
|
|
49
|
when the same dose of a drug is repeated at half
life
intervals, the steady-state (plateau) plasma drug
concentration
is reached after:
a.
2–3 half lives
b.
4–5 half lives
c.
6–7 half lives
d. 8–10 half lives
|
b
|
|
50
|
monitoring plasma drug concentration is useful
while
using:
a.
antihypertensive drugs
b.
levodopa
c.
lithium carbonate
d. mao inhibitors
|
c
|
|
51
|
a partial agonist can antagonise the effects of a
full agonist because it has:
a.
high affinity but low intrinsic activity
b.
low affinity but high intrinsic activity
c.
no affinity and low intrinsic activity
d. high affinity but no intrinsic activity
|
a
|
|
52
|
when therapeutic effects decline both below and
above
a narrow range of doses, a drug is said to
exhibit:
a.
ceiling effect
b.
desensitization
c.
therapeutic window phenomenon
d. nonreceptor mediated action
|
c
|
|
53
|
which of the following is always true:
a.
a more potent drug is more efficacious
b.
a more potent drug is safer
c.
a more potent drug is clinically superior
d.
a more potent drug can produce the same
response at lower doses
|
d
|
|
54
|
if the effect of combination of two drugs is
equal to
the sum of their individual effects, the two
drugs are
exhibiting:
a.
potentiation
b.
synergism
c.
cross tolerance
d. antagonism
|
b
|
|
55
|
the antidotal action of sodium nitrite in cyanide
poisoning is based on:
a.
physical antagonism
b.
chemical antagonism
c.
physiological antagonism
d. noncompetitive antagonism
|
b
|
|
56
|
the following is a competitive antagonist of gaba
but a noncompetitive antagonist of diazepam:
a.
picrotoxin
b.
muscimol
c.
flumazenil
d. bicuculline
|
d
|
|
57
|
fixed dose combination formulations are not
necessarily appropriate for:
a.
drugs administered in standard doses
b.
drugs acting by the same mechanism
c.
antitubercular drugs
d. antihypertensive drugs
|
b
|
|
58
|
which adverse drug effect is more common in
children
than in adults:
a.
isoniazid induced neuropathy
b.
chlorpromazine induced muscle dystonia
c.
digoxin induced cardiac arrhythmia
d. penicillin hypersensitivity
|
b
|
|
59
|
the following drug adverse effect is specially
noted in men compared to women:
a.
tardive dyskinesia due to neuroleptics
b.
levodopa induced abnormal movements
c.
ampicillin induced loose motions
d. ketoconazole induced loss of libido
|
d
|
|
60
|
which of the following adverse drug reactions is
due to a specific genetic abnormality:
a.
tetracycline induced sunburn like skin lesions
b.
quinidine induced thrombocytopenia
c.
metoclopramide induced muscle dystonia
d. primaquine induced massive haemolysis
|
d
|
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