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| (sigh-MET-ih-deen) |
Tagamet, Tagamet HB, Apo-Cimetidine, Novocimetine, Nu-Cimet, Peptol |
| Class: Histamine H2 antagonist |
Action Reversibly and competitively blocks histamine at H2 receptors, particularly those in gastric parietal cells, leading to inhibition of gastric acid secretion.
Indications Management of duodenal ulcer; treatment of gastroesophageal reflux disease, including erosive esophagitis; therapy for benign gastric ulcer; treatment of pathologic hypersecretory conditions; prevention of upper GI bleeding. Unlabeled use(s): Prevention of aspiration pneumonia and stress ulcers; herpes virus infection; chronic idiopathic urticaria; anaphylaxis (relieves dermatologic symptoms only); dyspepsia; used before anesthesia to prevent aspiration pneumonitis; to treat hyperparathyroidism and to control secondary hyperparathyroidism in chronic hemodialysis patient; treatment of chronic viral warts in children.
Contraindications Hypersensitivity to cimetidine or other H2 antagonists.
Duodenal Ulcer (Active)
ADULTS: PO 800 mg at bedtime for 4 to 6 weeks. ALTERNATE REGIMENS PO 300 mg qid w/meals and at bedtime or 400 mg bid. MAINTENANCE THERAPY PO 400 mg at bedtime.
Active Benign Gastric Ulcer
ADULTS: PO 800 mg at bedtime.
Gastroesophageal Reflux Disease
ADULTS: PO 1600 mg daily in divided doses (800 mg or 400 mg) for 12 weeks, although some patients may require chronic therapy.
Pathologic Hypersecretory Conditions
ADULTS: PO 300 mg qid w/meals and at bedtime. If needed, 300 mg doses may be given more often (maximum 2400 mg/day).
Prevention of Upper GI Bleeding
ADULTS: Continuous IV infusion of 50 mg/hr. For hospitalized patients with pathologic hypersecretory conditions or intractable ulcers, or patients unable to take PO medication. USUAL DOSE: IM/IV 300 mg q 6 h to 8 h (maximum 2400 mg/day).
Antacids, anticholinergics, metoclopramide: May decrease absorption of cimetidine. Benzodiazepines, caffeine, calcium channel blockers, carbamazepine, chloroquine, labetalol, lidocaine, metoprolol, metronidazole, moricizine, pentoxifylline, phenytoin, propranolol, quinidine, quinine, sulfonylureas, theophyllines, triamterene, tricyclic antidepressants, warfarin: Cimetidine may reduce metabolism and increase serum concentration and pharmacologic/toxic effects of these drugs. Carmustine: Bone marrow toxicity may be enhanced. Cigarette smoking: Reversed cimetidine’s effects on suppression of nocturnal gastric secretion. Ferrous salts, indomethacin, fluconazole, ketoconazole, tetracyclines: Cimetidine may decrease absorption of these drugs. Hydantoins: Hydantoin levels may increase. Narcotic analgesics: Toxic effects (eg, respiratory depression) may be increased. Procainamide: Levels of procainamide and its active metabolite may increase. Tocainide: Cimetidine may decrease the pharmacologic effects of tocainide.
Lab Test Interferences None well documented.
CV: Cardiac arrhythmias. CNS: Headache; somnolence; fatigue; dizziness; confusional states; hallucinations. DERM: Exfoliative dermatitis or erythroderma; alopecia; rash; erythema multiforme; epidermal necrolysis. GI: Diarrhea. GU: Impotence; loss of libido. RESP: Bronchospasm. OTHER: Gynecomastia; hypersensitivity reactions; transient pain at injection site; reversible exacerbation of joint symptoms with preexisting arthritis, including gouty arthritis.
Pregnancy: Category B. Lactation: Excreted in breast milk. Children: Safety and efficacy not established. Elderly: May have reduced renal function; decreased clearance may occur. Renal function impairment: Decreased clearance may occur; reduced dosage may be needed. Hepatic function impairment: Use caution; decreased clearance may occur. Hypersensitivity: Rare cases of anaphylaxis have occurred as well as rare episodes of hypersensitivity. Gastric malignancy: Symptomatic relief with cimetidine does not preclude gastric malignancy. Antiandrogenic effect: Gynecomastia, especially in patients treated for pathologic hypersecretory states may occur. Rapid IV administration: Has been followed by rare instances of cardiac arrhythmias and hypotension. Reversible CNS effects: Mental confusion, agitation, psychosis, depression, anxiety, hallucinations and disorientation have occurred, predominantly in severely ill patients. Advanced age and pre-existing liver or renal disease appear to be contributing factors.
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