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Med School Drugs
Drugs
| Questions | Answers |
|---|---|
| Nafcillin class | B-lactam anti-microbial |
| Nafcillin action | bind PBPs; block peptidoglycan cross-linkage preventing cell wall formation |
| dicloxicillin class | B-lactam anti-microbial |
| dicloxicillin action | bind PBPs; block peptidoglycan cross-linkage preventing cell wall formation |
| amoxicillin class | B-lactam anti-microbial |
| amoxicillin action | bind PBPs; block peptidoglycan cross-linkage preventing cell wall formation |
| Ceflacor class | B-lactam anti-microbial |
| Ceflacor action | bind PBPs; block peptidoglycan cross-linkage preventing cell wall formation |
| Cephalexin class | B-lactam anti-microbial |
| Cephalexin action | bind PBPs; block peptidoglycan cross-linkage preventing cell wall formation |
| aminoglycoside class | aminoglycoside |
| aminoglycoside action | protein synthesis 30S inhibitors; inhibit formation of initiation complex; cause mRNA misreading |
| Albuterol class | adrenergic agonist |
| Albuterol action | B2-receptor agonist; bronchodilator |
| Acetylcysteine class | mucolytic |
| Acetylcysteine action | break disulfide bonds in mucus; decrease mucus viscosity |
| Trimethoprim class | anti-bacterial agent |
| Trimethoprim action | inhibit dihydrofolate reductase; together: inhibit folic acid synthesis, which eventually disrupts DNA synthesis |
| Recombinant human DNAse therapy class | antimucus agent |
| Recombinant human DNAse therapy action | DNAse degrades DNA, which causes the mucus to loosen |
| Ovral-28 class | contraceptive; estrogens, progestin |
| Ovral-28 action | suppression of gonadotropins (FSH & LH) |
| NPH class | Antidiabetic |
| NPH action | intermediate acting insulin |
| Human regular insulin class | Antidiabetic, hypoglycemic |
| Human regular insulin action | acts as normal insulin does |
| Mefoxitin class | B-lactam anti-microbial |
| Mefoxitin action | bind PBPs; block peptidoglycan cross-linkage prevent cell wall formation |
| Phenergan class | anti-emetics; antivertigo |
| Phenergan action | relief of motion sickness, anti-nausea |
| Metformin class | diabetic agent |
| Metformin action | inhibit hepatic gluconeogenesis |
| Aspirin class | NSAID |
| Aspirin action | irreversibly inhibits cyclooxygenase (COX 1 & 2); decrease prostaglandin synthesis |
| Simvastatin class | antihyperlipidemic |
| Simvastatin action | inhibit HMG-CoA reductase; increase LDL receptors |
| Exenatide class | Antidiabetic agent; insulin mimic |
| Exenatide action | enhance glucose-dependent insulin secretion |
| Lisinopril class | antihypertensive agent |
| Lisinopril action | inhibit angiotensin-converting enzyme |
| Heparin class | anti-coagulant |
| Heparin action | accelerate action of antithrombin III |
| Coumadin (Warfarin) class | anti-coagulant |
| Coumadin (Warfarin) action | inhibit Vitamin K-dependent gamma-carboxylation of factors II, VII, IX, and protein C and protein S |
| Lactated ringers class | electrolyte replacement |
| Lactated ringers action | induce blood volume increase |
| Morphine sulfate class | analgesic, narcotic |
| Morphine sulfate action | opioid receptor agonist which leads to hyperpolarization and decreased activity of neural cells |
| Atorvastatin class | antihyperlipidemic |
| Atorvastatin action | inhibit HMG CoA reductase, and thus increase in the concentration of LDL receptors |
| Atenelol class | antiadrenergics, B-blocker |
| Atenelol action | selective B1-receptor antagonist, thus heart rate and contractility are decreased |
| Cefazolin class | B-lactam anti-microbial |
| Cefazolin action | bind PBPs; block peptidoglycan cross-linkage prevent cell wall formation |
| Gentamicin class | antibiotic, aminoglycosides |
| Gentamicin action | protein synthesis inhibitor; binds to the 30S bacterial ribosomal unit and inhibits the formation of the initiation complex, thus causing mRNA misreading |
| Oxycodon class | analgesic, narcotic |
| Oxycodon action | opioid receptor agonist; to hyperpolarization and decreased activity of neural cells |
| Ibuprofen class | NSAID |
| Ibuprofen action | irreversible inhibitor of COX (1 & 2), and thus, decreases prostaglandin synthesis |
| Ciprofloxacin class | antibiotic fluoroquinolone |
| Ciprofloxacin action | inhibit bacterial gyrase and causing cell death; binds to gyrase after DNA strand breakage, preventing the reconnecting action, and leaving DNA fragments |
| Prednisone class | corticosteroid |
| Prednisone action | suppress inflammation and the normal immune response, induce apoptosis of lymphocytes |
| Acetaminophen class | non-narcotic analgesic, antipyretic |
| Acetaminophen action | Act on hypothalmic heat regulating center for antipyresis, elevates pain threshold |
| Methotrexate class | antineoplastic |
| Methotrexate action | Inhibits dihydrofolate reductase preventing the formation of actvie folate disrupting DNA production |
| Imitrex class | Vascular headache suppressant |
| Imitrex action | Selective agonist at specific vascular serotonin receptors causing vasoconstriction in large intracranial arteries |
| Nitroglycerin class | Vasodilator |
| Nitroglycerin action | Relaxation of vascular smooth muscle causes peripheral pooling |