STEP 1 Uworld Drugs Part 2 Flashcards

1
Q

Nitroprusside

A

IV vasodilator (arteriolar and venous) used for rapid BP control in hypertensive emergency. Metabolized to nitric oxide and cyanide ions (toxic)

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2
Q

Mesna

A

sulfhydryl that binds and inactivates toxic acrolein in urine from nitrogen-mustard based chemotherapy –> prevents hemorrhagic cystitis

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3
Q

Phenytoin

A

long acting anticonvulsant –> reduce ability of sodium channels to recover from inactivation –> decrease neuronal high frequency firing (administered with lorazepam for status epilepticus)

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4
Q

Clindamycin

A

Binds 50s ribosomal sub-unit in bacteria and disrupts protein synthesis - acting against oral anaerobes and aerobic gram (+),

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5
Q

BosENtan

A

competitively antagonizes ENdothelin-1 receptors –> decreases pulmonary vascular resistance

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6
Q

Naloxone

A

pure opioid receptor antagonist, greatest affinity for he mu receptor, competes with narcotics and displaces them form opioid receptors (though binds mu, kappa, and delta)

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7
Q

Anastrozole

A

aromatase inhibitor, decreases the synthesis of estrogen from androgens

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8
Q

Phencyclidine (PCP)

A

primarily a N-methyl-D-aspartate (NMDA) receptor antagonist (also does inhibit some re-uptake of biogenic amines). Causes psychosis, hallucinations, violent trauma, ataxia, and horizontal nystagmus.

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9
Q

Cyproheptadine

A

first generation histamine antagonist with nonspecific 5-HT1 and 5-HT2 receptor antagonistic properties, may treat serotonin syndrome

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10
Q

Enoxaparin

A

low molecular weight heparin (LMWH) that binds and activates antithrombin III (AT III). Activated AT III binds and inhibits factor Xa (no conversion of prothrombin to thrombin).

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11
Q

Caspofungin

A

Echinocadin anti-fungal that blocks glucan synthesis inhibiting cell wall synthesis.

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12
Q

Benztropine

A

centrally acting antimuscarinic agent, often used in drug induced parkinsonionism if the antipsychotic cannot be reduced (In such a situation, levodopa should not be used as it can precipitate psychosis)

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13
Q

6-Mercaptopurine

A

cytotoxic purine analog that inhibits de-novo purine synthesis. It is activated by hypoxanthine-guanic phosphoribosyl transferase (HGPRT) and inactivated by xanthine oxidase (XO) and thiopurine methyltransferase (TPMT)

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14
Q

Mifepristone

A

progesterone antagonist –> necrosis of uterine decidua –> pregnancy termination

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15
Q

Diphenoxylate

A

Opioid anti-diarrheal drug that binds mu opiate receptors in the gut to slow motility (combine with atropine to discourage abuse)

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16
Q

Valproate

A

anticonvulsant and mood stabilizer, blocks voltage-gated sodium channels and enhances GABA synthesis and release (tx: bipolar, absence, myoclonic, generalized tonic-clonic seizures)

17
Q

Argatroban

A

direct thrombin inhibitor (Tx: heparin-induced thrombocytopenia)

18
Q

Fibrates (gemfibrozil, tenofibrate)

A

activates peroxisome proliferator-activated receptor alpha (PPAR-a) which decreases hepatic VLDL production and increases LPL activity

19
Q

Omega-3 fatty acids

A

lower triglycerides by decreasing production of VLDL and apolipoprotein B

20
Q

Digoxin

A

slows ventricular rate during AF by increasing parasympathetic vagal tone which leads to inhibition of AV nodal conduction (occurs via inhibition of Na/K ATPase pump)

21
Q

Terbinafine

A

inhibits synthesis of fungal membrane ergosterol by inhibiting squalene epoxidase

22
Q

Abciximab

A

GP IIb/IIIa receptor antagonist that inhibits binding of this receptor to fibrinogen

23
Q

Ribavirin

A

nucleoside antimetabolite drug that interferes with duplication of viral genetic material (tx: hepatitis C and RSV)

24
Q

Thiazolinediones

A

bind peroxisome proliferator-activated receptor-gamma (PPAR-y) which forms a heterodimer complex with the retinoid X receptor –> transcriptional regulation of genes for lipid and glucose metabolism

25
Q

Bosentan

A

endothelin-receptor competitive antagonist –> blocks endothelin (a vasoconstrictor and stimulates endothelial proliferation) –> lowers pulmonary arterial pressure (tx: idiopathic PAH)

26
Q

Dobutamine

A

B-adrenergic agonist (B1 > B2 > a1) –> Gs –> increases cAMP. Positive ionotropic effect and positive chronotropic effect.

27
Q

Olanzapine

A

second generation antipsychotic that blocks dopamine receptors in the CNS, blocks seretonin receptors 5-HT 2A, blocks H1 histamine receptors, and blocks a-1 receptors

28
Q

Tamoxifen

A

selective estrogen receptor modulator (SERM) - competitive inhibitor of estrogen binding, mixed agonist/antagonist action (however, it has a stimulator effect at endometrial tissue –> risk of endometrial hyperplasia and cancer)

29
Q

Gabapentin

A

anticonvulsant that inhibits presynaptic voltage-gated calcium channels which inhibits fusion and release of neurotransmitter vesicles

30
Q

Cilostazol

A

phosphodiesterase inhibitor that inhibits platelet aggregation and acts as a direct arterial vasodilator