STEP 1 Uworld Drugs Part 2 Flashcards
Nitroprusside
IV vasodilator (arteriolar and venous) used for rapid BP control in hypertensive emergency. Metabolized to nitric oxide and cyanide ions (toxic)
Mesna
sulfhydryl that binds and inactivates toxic acrolein in urine from nitrogen-mustard based chemotherapy –> prevents hemorrhagic cystitis
Phenytoin
long acting anticonvulsant –> reduce ability of sodium channels to recover from inactivation –> decrease neuronal high frequency firing (administered with lorazepam for status epilepticus)
Clindamycin
Binds 50s ribosomal sub-unit in bacteria and disrupts protein synthesis - acting against oral anaerobes and aerobic gram (+),
BosENtan
competitively antagonizes ENdothelin-1 receptors –> decreases pulmonary vascular resistance
Naloxone
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)
Anastrozole
aromatase inhibitor, decreases the synthesis of estrogen from androgens
Phencyclidine (PCP)
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.
Cyproheptadine
first generation histamine antagonist with nonspecific 5-HT1 and 5-HT2 receptor antagonistic properties, may treat serotonin syndrome
Enoxaparin
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).
Caspofungin
Echinocadin anti-fungal that blocks glucan synthesis inhibiting cell wall synthesis.
Benztropine
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)
6-Mercaptopurine
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)
Mifepristone
progesterone antagonist –> necrosis of uterine decidua –> pregnancy termination
Diphenoxylate
Opioid anti-diarrheal drug that binds mu opiate receptors in the gut to slow motility (combine with atropine to discourage abuse)
Valproate
anticonvulsant and mood stabilizer, blocks voltage-gated sodium channels and enhances GABA synthesis and release (tx: bipolar, absence, myoclonic, generalized tonic-clonic seizures)
Argatroban
direct thrombin inhibitor (Tx: heparin-induced thrombocytopenia)
Fibrates (gemfibrozil, tenofibrate)
activates peroxisome proliferator-activated receptor alpha (PPAR-a) which decreases hepatic VLDL production and increases LPL activity
Omega-3 fatty acids
lower triglycerides by decreasing production of VLDL and apolipoprotein B
Digoxin
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)
Terbinafine
inhibits synthesis of fungal membrane ergosterol by inhibiting squalene epoxidase
Abciximab
GP IIb/IIIa receptor antagonist that inhibits binding of this receptor to fibrinogen
Ribavirin
nucleoside antimetabolite drug that interferes with duplication of viral genetic material (tx: hepatitis C and RSV)
Thiazolinediones
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
Bosentan
endothelin-receptor competitive antagonist –> blocks endothelin (a vasoconstrictor and stimulates endothelial proliferation) –> lowers pulmonary arterial pressure (tx: idiopathic PAH)
Dobutamine
B-adrenergic agonist (B1 > B2 > a1) –> Gs –> increases cAMP. Positive ionotropic effect and positive chronotropic effect.
Olanzapine
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
Tamoxifen
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)
Gabapentin
anticonvulsant that inhibits presynaptic voltage-gated calcium channels which inhibits fusion and release of neurotransmitter vesicles
Cilostazol
phosphodiesterase inhibitor that inhibits platelet aggregation and acts as a direct arterial vasodilator