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USMLE
Pharm 5
| Question | Answer |
|---|---|
| Toxicity of amantadine | Ataxia + dizziness+ slurred speech ("Amantadine causes problems with cerebellA") |
| Two antiviral medications that inhibits influenza neuraminidase, both used for influenza A and B | Zanamivir, Oseltamivir |
| Antiviral - inhibits synthesis of guanine nucleotides by competitively inhibiting IMP dehydrogenase, used for treatment of RSV and chronic hep C | Ribavirin |
| Toxicity for Ribavirin | Severe teratogen, Hemolytic anemia |
| This antiviral medication preferentially inhibits viral DNA polymerase when phosphorylated by viral thymidine kinase | Acyclovir |
| Antiviral medication used for treatment of VZV, HSV, EBV, mucocutaneous and genital herpes lesions, prophylaxis in immunocompromised patients | Acyclovir |
| Toxicity for acyclovir | Delirium, Tremor, Nephrotoxicity |
| Antiviral drug - works by phosphorylation viral kinase, preferentially inhibits CMV DNA polymerase, drug of choice for CMV especialy in immunocopromised patients | Ganciclovir |
| Which drug is more toxic - acyclovir or ganciclovir to host enzymes | Ganciclovir |
| Ganciclovir toxicity | Leukopenia, Neutropenia, Thrombocytopenia, Renal toxicity |
| Viral DNA polymerase inhibitor that binds to the pyrophosphate binding site of the enzyme. Does not require activation by viral kinase | FOSCARNET = pyroFOSphate analog |
| Antiviral drug used for treatment of CMV retinitis in immunocompromised patients when ganciclovir fails | FOSCARNET |
| Patient is on foscarnet for CMV retinitis, which toxicity could be suspected? | Nephrotoxicity |
| Saquinavir, ritonavir, indinavir, nelfinavir, aprenavir - class of drugs | HIV therapy, protease inhibitors - inhibit assembly of new virus by blocking protease enzyme |
| HIV patient is taking anti HIV drugs, develops GI intolerance - nausea, diarrhea, hyperglycemia, lipid abnormalities, thrombocytopenia - which drugs was he taking? | PROTEASE INHIBITORS |
| Zidovudine (AZT), didanosine, zalcitobine, stavudine, lamivudine, abacavir - what class of drugs | Reverse transcriptase inhibitors, nucleosides |
| Name non-nucleosides reverse transcriptase inhibitors | Nevirapine, Delavirdine, Efavirenz |
| Toxicity associated with reverse transcriptase inhibitors | Bone marrow suppression (neutropenia, anemia), Peripheral neuropathy, Lactic acidosis (nucleosides), Megaloblastic anemia, Rash (non-nucleosides) |
| Highly active antiretroviral therapy (HAART) generally entails combination of? | Protease inhibitors + reverse transcriptase inhibitors |
| Which antiretroviral drug is used during pregnancy to reduce risk of fetal transmission | AZT |
| Patient on anti HIV therapy develops megaloblastic anemia - which drug most likely caused it | AZT |
| When is HAART initiated? | When patients have low CD4 counts (<500 cell/mm3) or high viral load |
| Glycoproteins from human leukocytes that block various stages of viral RNA and DNA synthesis, used for treatment of chronic hep B and C, Kaposis sarcoma Name drug and what toxicity associated with it | Interferons, Neutropenia |
| Antiparasitic drug from onchocerciasis | Ivermectin (rIVER blindness treated with IVERmectin) |
| Antiparasitic drug used to treat nematode/roundworm (pinworm, whipworm) infections | Mebendazole/thiabendazole |
| Antiparasitic drugs used to treat giant roundowrm (ascaris), hookworm (Necator/Ancylostoma) and pinworm (Enterobius) | Pyrantel pamoate |
| Antiparasitic used to treat trematode/fluke (shistosomes, Paragonimus, Clonorchis) and cysticercosis | Praziquantel |
| Niclosamide is used to treat? | Cestode/tapeworm, infections except cysticercosis |
| Drug of choice for leishmaniasis | Pentavalent antimony |
| Name anti malaria drugs | Chloroquine, Quinine, Mefloquine, Atovaquone, Proguanil |
| Name drug used for treatment of latent hypnozoite (liver) forms of malaria (Plasmodium vivax, P.ovale) | Primaquine |
| Drug of choice against giardiasis, amoebic dysentery, bacteria vaginitis, Trichomonas | Metronidazole |
| Drug of choice for Chagas disease, American trypanosomiasis (trypanosoma cruzi) | Nifurtimox |
| Drug of choice for African trypanosomiasis (sleeping sickness) | Suramin |
| Cholinomimetic used for postoperative and neurogenic ileus and urinary retention - activates bowel and bladder smooth muscle | BETHANECHOL |
| Direct agonist, cholinomimetic used for treatment of glaucoma, activates ciliary muscle of eye (open angle), pupillary sphincter (narrow angle) | Carbachol, pilocarpine |
| Anticholinesterase, used in treatment of postoperative and neurogenic ileus and urinary retention, myasthenia gravis, reversal of neuromuscular junction blockade (postoperative), increases endogenous Ach | Neostigmine |
| Anticholinesterase used in treatment of myasthenia gravis - increases endogenous Ach, increases strength | Pyridostigmine |
| This anticholinesterase is used for diagnosis of myasthenia gravis (extremely short acting), increases endogenous Ach | Edrophonium |
| Anticholinesterase, used in treatment of glaucoma (crosses BBB to CNS) and atropine overdose, increases endogenous Ach | Physostigmine |
| Anticholinergic, used for treatment of glaucoma, increases endogenous Ach | Echothiophate |
| Name symptoms of cholinesterase inhibitor poisoning | (“DUMBBELSS”): Diarrhea, Urination, Miosis, Bronchospasm, Bradycardia, Excitation of skeletal muscle, Lacrimation, Sweating, Salivation (also abdominal cramping) |
| Name substances that can lead to cholinesterase inhibitor poisoning | Parathion and other organophosphates |
| Antidote used in treatment of organophosphate poisoning | Atropine (muscarinic antagonist) plus pralidoxime (chemical antagonist used to regenerate active cholinesterase) |