| Hint | Answer |
|---|
| Neurotoxin taken up by dopaminergic cells that kills them | |
| Best drug for the treatment of superficial yeast infection | |
| Drug that is analgesic and antipyretic and can be used in kids with viral infections | |
| This class of drug causes irreversible ototoxicity | |
| IM form of penicillin G is prepared with ____________________ (two compounds) which allows it to be more slowly released and therefore remain at a steady state longer in the blood. | |
| Class of drug: Memantine HCl | |
| Class of drug: Norafloxacin | |
| Bind to 50s rRNA and inhibits formation or peptide bond | |
| Drug used for TB treatement that interferes with the folic acid pathway because it looks like p-ABA | |
| This compound retards the renal excretion of penecillin | |
| Carbenicillin is particularly effective against this organism | |
| Rapid Excretion/Slow Excretion/Poorly Absorbed: Sulfamerazine | |
| Celecoxib may reduce the effectiveness of what other drug class | |
| Rapid Excretion/Slow Excretion/Poorly Absorbed: Sulfamethoxypyridazine | |
| Drug that crystallizes in the urine if the urine isn't an alkaline pH. | |
| Piperacillin is penicillinase: Sensitive or Resistant | |
| Vancomycin has the potential to cause possibly irreversible _____toxicity | |
| More potent, longer lasting COMT inhibitor | |
| Cloxacillin is penicillinase: Sensitive or Resistant | |
| This drug binds to tubulin in leukocytes preventing their migration and phagocytosis | |
| Sulfonamide with particular specificity for P. carinii, Shigella, Salmonella, Serratia | |
| Infliximab and etanercept target this cytokine | |
| Drug that reduces the adverse effects of L-dopa by preventing its peripheral conversion to dopamine by peripheral dopa decarboxylase. This drug does not cross the blood-brain barri | |
| Sensitive members are suppressed thereby removing inhibitory effects. Overgrowth and repopulation with resistant organisms may occur that, in turn lead to infection. | |
| Class of Drug: Saquinavir | |
| Drug that competes with xanthine oxidase to reduce uric acid production. | |
| Disease modifying anti-rheumatic drug that can decrease neutrophil chemotaxis and reduce function of macrophages and lymphocytes | |
| Dopamine agonists have (more/less) side effects than L-dopa | |
| Class of Drug: benztropine mesylate | |
| _____________ dose aspirin has antipyretic and analgesic effects. (Low or High) | |
| Changes shape of 30s rRNA and causes mRNA to be read incorrectly | |
| Rapid Excretion/Slow Excretion/Poorly Absorbed: Succinylsulfathiazole | |
| This NSAID is used to treat gout and manage patent ductus arteriosis | |
| Bacteriostatic or Bactericidal: Tetracyclines | |
| Anti-fungal agent that is used primarily topically and is particularly effective against vaginal candidiasis | |
| Dicloxacillin is penicillinase: Sensitive or Resistant | |
| Inhibits protein synthesis by binding to the 50S ribosome, blocking peptide formation at either A or P site. | |
| Genus of bacteria against which spectinomycin is particularly effective. | |
| Most important side effect of ethambutol | |
| Class of drug: pamipexol | |
| Plasmodium species associated with the most serious complications and death | |
| Rapid Excretion/Slow Excretion/Poorly Absorbed: Sulfamethazine | |
| Most common organ that experiences injury as a side effect of pyrazinamide | |
| Streptogramins bind to which ribosomal subunit | |
| Class of drug: primidone | |
| Bacteria can upregulate this compound to overcome/become resistant to sulfonamides | |
| Prostaglandins that produce vasodilatory effects and promote edema | |
| Class of drug: Gentamicin | |
| Class of drug: Gatifloxacin | |
| Quinolones are most effective against this type of bacteria (gram positive or gram negative) | |
| All the antiviral nucleotide analogs are effective against this virus | |
| Enzyme that celecoxib selectively inhibits | |
| Severity of migraine treated by narcotics | |
| Triptan with lowest rate of 24-hour relapse and highest percent of migraine-free patients after 24 hours | |
| Prostaglandins that stimulate gastric mucosal secretion | |
| Bacteriostatic or Bactericidal: Vancomycin | |
| Streptogramins are effective against what type of bacteria: gram positive or gram negative | |
| Class of drugs that prolong GABA-mediated chloride channel openings and do some blockade of voltage-dependent sodium channels | |
| Drug used in the treatment of TB that causes hemolytic anemia in patients with glucose-6-phosphate deficiency | |
| This drug is widely distributed through the tissues as demonstrated by orange-red color of the urine, feces, saliva, sputum, tears and sweat but this indicate a problem. | |
| Rapid Excretion/Slow Excretion/Poorly Absorbed: Sulfadiazine | |
| Bacteriostatic agent that reversibly binds to the 50S subunit of the bacterial 70S ribosome resulting in supression of peptidyl transferase activity. Peptide bond formation is inhi | |
| Penicillin G is acid: Labile or Stable | |
| Bacteriostatic or Bactericidal: Isoniazid with 'resting' organisms | |
| Class of Drug: Indinavir | |
| Used in gouty arthritis if colchicine cannot be tolerated | |
| Class of drug: Moxifloxacin | |
| Class of drug associated with yellow brown staining and fluorescence of teeth | |
| If pyroxidine is not given concurrently with isoniazid there is a potential for this condition to arise | |
| Last line of defense against gram+ organisms | |
| Most effective antiviral in treating hepatitis B and hepatitis C | |
| Ticarcillin is particularly effective against this organism | |
| Mega spectrum penicillin that is very active against Pseudomonas | |
| Prepared combination of clavulanic acid and amoxicillin | |
| Resistance will occur if any TB drug is given alone: true or false | |
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