cimetidine (Also cimetidines) : Related Words Words similar in meaning to cimetidine
- cimetidine«
- stomach«
- tagamet«
- peptic ulcer«
- cyp1a2«
- histamine blocker«
- metiamide«
- cyp2d6«
- gastric antacid«
- male«
- cyp3a4«
- antacid«
- inhibit«
- burimamide«
- antiacid«
- impotence«
- drug«
- alkalizer«
- histamine«
- cyp450 enzyme«
- alkaliser«
- heartburn«
- h2 receptor antagonist«
- cyp2e1«
- antagonist«
- nα-guanylhistamine«
- acid«
- chronic calcific tendinitis«
- effect«
- histamine h2 receptor antagonist«
- h2 receptor«
- famotidine«
- ranitidine«
- treatment«
- cyp2c19«
- antiandrogen«
- cyp2c9«
- quinidine«
- tramadol«
- creatinine«
- gynecomastia«
- hepatotoxicity«
- tricyclic antidepressant«
- drug interaction«
- blood level«
- estradiol«
- glaxosmithkline«
- compound«
- testosterone«
- shoulder«
- interaction«
- weak antiandrogen activity«
- universal inhibitor«
- unacceptable nephrotoxicity«
- tubular creatinine secretion«
- specific competitive antagonist«
- sk team«
- sk scientist«
- similar guanidine analogue«
- prototypical histamine h2 receptor antagonist«
- potent cytochrome p450«
- partial h2 receptor antagonist«
- nitrogenous waste buildup«
- new frontier science park research facility«
- imidazole ring nitrogen atom«
- hypothetical h2 receptor«
- human flavin«
- h2 receptor antagonist program«
- extreme plasma level«
- estrogen potentiator«
- drug biotransformations«
- cyp450 oxidative system«
- cyp450 isoforms«
- cyp2d6 substrate desipramine«
- cyp2c9 substrate tolbutamide«
- cyp1a2 substrate theophylline«
- creatinine accumulation«
- creatine breakdown«
- complexed heme«
- cimetidine treatment«
- aminotransferase activity«
- inhibition«
- traditional antihistamine«
- rational drug design approach«
- potential clinical importance«
- glaxo lab«
- metabolism«
- |publisher = american chemical society |work = national historic chemical landmark |accessdate= june«
- u.s. drug market«
- subsequent toxicity«
- stomach acid secretion«
- metabolic inactivation«
- antimalarial medication hydroxychloroquine«
- discovery«
- histamine receptor antagonist«
- histamine h2-receptor«
- fewer drug interaction«
- cytochrome p450 pathway«
- c. robin ganellin«
- receptor model«
- pepcid«
- fmo1«
- cyp3a4 substrate«
- common wart«
- ultimate discovery«
- rational drug«
- international historic chemical landmark«
- cyp2d6 substrate«
- benzoquinone imine«
- unproven benefit«
- paracetamol toxicity«
- arthroscopic lavage«
- psychoactive medication«
- histamine h2 receptor«
- american chemical society national historic chemical landmark«
- hepatic blood flow«
- significant drug interaction«
- fmo3«
- therapy«
- massive overdoses«
- calcific tendinitis«
- zolmitriptan«
- stomach acid production«
- napqi«
- sir james w. black«
- nebivolol«
- moderate inhibitor«
- azole antifungal«
- sparteine«
- irreversible inhibition«
- james w. black«
- dermatological disease«
- blockbuster drug«
- zantac«
- cyp450«
- h2-receptor antagonist«
- flecainide«
- terfenadine«
- temporary decrease«
- prescription product«
- monooxygenases«
- blind clinical trial«
- metabolic byproduct«
- metabolization«
- design lead«
- timolol«
- loratadine«
- design structure«
- hormonal effect«
- androgenic alopecia«
- symptom«
- interstitial nephritis«
- cytochrome p450 system«
- chronic administration«
- galactorrhea«
- steroid injection«
- oxidative metabolism«
- nortriptyline«
- beneficial role«
- acid production«
- procainamide«
- desipramine«
- prestige brand«
- scale clinical trial«
- renal excretion«
- prolactin level«
- fluorouracil«
- isoenzymes«
- gastric acid secretion«
- counter medicine«
- yamanouchi«
- fatal overdose«
- estrogenic activity«
- reversible inhibitor«
- mirtazapine«
- calcium deposit«
- effective agent«
- prodrugs«
- smithkline beecham«
- thiourea«
- complete disappearance«
- mental confusion«
- imipramine«
- amenorrhea«
- proton pump inhibitor«
- estrogen level«
- mechanism«
- hirsutism«
- sildenafil«
- metformin«
- itraconazole«
- amiodarone«
- agranulocytosis«
- angioedema«
- pethidine«
- dihydrotestosterone«
- gabapentin«
- potential«
- uremia«
- propranolol«
- enzyme inhibitor«
- theophylline«
- stomach acid«
- liver function«
- ketoconazole«
- tamoxifen«
- tentative evidence«
- androgen receptor«
- urticaria«
- opioid analgesic«
- cytochrome p450«
- lidocaine«
- phenytoin«
- carbamazepine«
- potent inhibitor«
- oxycodone«
- erythromycin«
- scale study«
- sex hormone«
- selective serotonin reuptake inhibitor«
- muscle pain«
- warfarin«
- low ph«
- acetaminophen«
- term treatment«
- paracetamol«
- active metabolite«
- development«
- sexual dysfunction«
- methadone«
- oral administration«
- erectile dysfunction«
- codeine«
- opioids«
- broad array«
- drug discovery«
- pka«
- kline«
- libido«
- acne«
- pharmacology«
- colorectal cancer«
- benzodiazepine«
- transient«
- acetyl«
- estrogen«
- active site«
- constipation«
- toxicology«
- existence«
- harlow«
- american chemical society«
- metabolite«
- dizziness«
- country«
- secretion«
- structure«
- inhibitor«
- placebo«
- omeprazole«
- alkali«
- base«
- Tagamet«
- 2-hydroxylation«
- Zantac«
- Tums«
- Rolaids«
- Prilosec«
- Pepto-bismal«
- Pepcid«
- Mylanta«
- Maalox«
- Bromo-seltzer«
- Brioschi«
- Alka-seltzer«
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