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61 Cards in this Set

  • Front
  • Back
How are NSAIDs metabolized?
undergo hepatic metabolism and conjugation followed by renal excretion of inactive metabolites
Which of the following are NSAIDs not indicated for?

a. to induce closure of clinically significant patent ductus arteriosus in premature infants when usual treatments are ineffective

b. dysmenorhea

c. sedation
sedation
What class of drug am I:
reversibly inhibits COX-1 and COX-2 enzymes resulting in decreased formation of prostaglandins
NSAIDs
What drug am I:
irreversibly inhibits COX-1 and COX-2 and thus formation of throboxane A2 resulting in inhibition of platelet aggregation
aspirin
In the pathway of arachidonic acid release and metabolims, what enzyme is responsible for arachidonic acid release?
phospholipase A2
List the following in the correct order of the arachidonic acid release and metabolism pathway.

a. arachidonic acid metabolized by Cox and Lox
b. arachidonic acid released by phospholipase A2
c. Formation of prostaglandins, thromboxane, and leukotrienes
1. arachidonic acid is released by phopholipase A2
2. arachidonic acid is metabolized by Cox and Lox
3. formation of prostaglandins, throboxane, and leukotrienes
prostaglandins, prostacylin and throboxane are formed from the metabolism of arachidonic acid by this enzyme
COX
HETEs, leukotrienes and lipoxins are formed from the metabolism of arachidonic acid by this ezyme
lipooxygenase (LOX)
Which isoform of COX am I:
constitutive
responsible for the formation of eicosaniods important for homeostatis
COX-1
Which isoform of COX am I:
constitutive only in small amounts in certain tissues
inducible at the site of inflammation
COX-2
Which isoform of COX is undesireable?
COX-2
This isoform of COX is important for homeostatic functions, GI tract, renal tract, platelet function, and macrophage differentiation
COX-1
Inhibition of this isoform of COX is undesirable
COX-1
Which of the following drugs have greater COX-2 selectivity?

indomethacin
aspirin
naproxen
ibuprofen
nabumetone
diclofenac
celecoxib
nabumetone
diclofenac
celecoxib
Which of the following have higher selectivity for COX-1?

indomethacin
aspirin
naproxen
ibuprofen
nabumetone
diclofenac
celecoxib
indomethacin
aspirin
naproxen
ibuprofen
What are the risk factors for an NSAID adverse effect?
advanced age
history of previous ulcer
high dose of NSAID
use of multiple NSAID
What type of NSAID (Cox-2 selective or non selective) is associated with reduced risk of GI irritation?
COX-2 selective
What agents can be given with NSAIDs to reduce risk of GI ulcer?
H2 blocker
PPI
misoprostol
Inhibiting which cox isoform will result in decreased renal function?
cox-1
cox-2
inhibition of which cox isoform will result in inhibition of PGI2 thus leading to increased platelet aggregation?
cox-2
inhibition of this cox isoform results in inhibition of throboxane A2 leading to decreased platelet aggregation
cox-1
Use of this drug in children with a viral illness is associated with Reye's sydrome (liver damage and encephalopathy)
aspirin
Which of the following have increased risk of MI and storke if used following CABG surgery?

a. meclofenamate
b. indomethacin
c. celecoxib
c. celecoxib
Which of the following is NOT true regarding NSIADs?

a. NSAIDs delay bone healing after fractures
b. COX-2 inhibitors increase surgical bleeding
c. Aspirin and NSAIDs induce exacerbation of asthma
d. NSAIDs have increased toxicity in the elderly
Cox-2 inhibitors increase surgical bleeding is not true

Cox-2 increase aggregation thus decrease bleeding
Cox-1 decrease aggregation thus increase bleeding
What are the box warnings for NSAIDs?
cardiovascular events
GI events
What drug am I:
NSAID-like drug
less efficacy than NSAIDs
have analgesic and antipyretic effects
do not have anti-inflammatory effects
apap
What adverse effects can patients have if they have an acute overdose of apap?
hepatic failure
renal failure
Liver toxicity of apap is due to the accumulation of this metabolite
NAPQI
What drug am I:
increase concentration of GSH (glutathione ) to convert NAPQI to safe conjugate metabolite
N-acetylcysteine
This drug is used as the antidote for acute overdose of apap
N-acetylcyteine
What am I:
systemic disease caused by the build up of uric acid in the joints
gout
This is the time between two gouty arthritic attacks
intercritical period
This is the rate limiting step in the formation of uric acid
xanthine oxidase
List the following in the correct order of the uric acid pathway

a. purines form hypoxanthine
b. xanthine oxidase converts xanthine to uric acid
b. xanthine oxidase converts hypoxanthine to xanthine
1. purine form hypoxanthine
2. xanthine oxidase converts hypoxanthine into xanthine
3. xanthine oxidase converts xanthine into uric acid
a defect in purine metabolism resuting in uric acid overproduction is term...
overproducers
impaired renal clearance of uric acid is term...
undersecretors
acute gouty arthritic attacks are caused by deposition of _____ in the synovium of the joints.
monosodium urate crystals
the inflammatory reaction of gout is a result of _______ bursting and releasing it's contents.
leukocytes
In acute gouty attacks, urate crystals undergo phagocytosis by ________
polymorphomuclear leukocytes
Which of the following are NOT used for the treatment of acute gouty arthritic attacks?

a. NSAID
b. colchicine
c. corticosteroids
d. allopurinol
d. allopurinol
What is colchicine indicated for?
prophylaxis of recurrent episode of gouty arthritis attacks and terminatio of gouty attacks
What drug am I:
produce antiinflammatory effect by binding to the intracellular protein tubulin thereby preventing it's polymerization into microtubules leading to "inhibition of leukocytes migration and phagocytosis"
colchicine
What adverse effect of colchine would warrant termination of treatment?
diarrhea
Which of the following are not used for gout during the intercritical period?

propencid
sulfinpyrazone
allopurinol
febuxostat
indomethacin
indomethacin
Which of the following are not xanthine oxidase inhibitors?

allopurinol
propencid
febuxostat
propencid
propencid and sulfinpyrazone fall under this class of drugs for gout drug therapy
uricosuric agents
What are uricosuric agents indicated for?
undersecretors
When can uricosuric agents be started?
must wait at least 2-3 weeks after an acute attack
What type of patients should not use uricosuric agents?
overproducers of uric acid
What class of drug am I:
competitively inhibits reabsorption of uric acid at the proximal convoluted tubule thereby promoting its excretion and reducing serum uric acid levels
uricosuric agents
uricosuric agent increase plasma levels of these drugs by competively inhibiting their renal tubular secretion
weak organic acids (B-lactam antibiotics)
What are the ADR of uricosuric agents?
GI irritation
uric acid stones
Which of the following are NOT true regarding uricosuric agents?

a. maintain adequate hydration to minimize possibility of stone formation
b. titirate dose upward slowly to minimize possibility of stone formation
c. do not use with patients with CrCl <50
d. use with aspirin or aspirin-containing substances
use with aspirin or aspirin-containing substace is NOT true

should avoid use with aspirin due to antagonistic effect
What are xanthine oxidase inhibitors indicated for?
chronic management of hyperuricemia in patients with gout
This drug is an isomer of hypoxanthine and competitively inhibits xanthine oxidase
allopurinol
allopurinol is metabolized into this compound which is also a competitive inhibitor of xanthine oxidase
oxypurinol
This drug is a non-purine, non-competitive inhibitor of xanthine oxidase
febuxostat
which of the following are NOT ADRs of xanthine oxidase inhibitors?

a. cardiovascular
b. GI discomfort
c. rash
d. liver function abnormalities
a. cardiovascular
xanthine oxidase inhibitors increase the serum level of these agents
azathioprine
6-mercaptopurine
Concomittant administration of these agents with allopurinol increase risk of rash
ampicillin or amoxicillin
Which of the following is NOT true regarding xanthine oxidase inhibitors?

a. to reduce the risk of precipitating an acute gout attack, titrate dose upward slowly
b. patient with renal insufficiency do not require dose adjustments
c. allopurinol is the standard care therapy for gout in the intercritical period
patients with renal insufficiency do not require dose adjustment is NOT true

patients with renal insufficiency requires dose adjustment