Search Results for "Metabolic"
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Searched for Metabolic. Results 561 to 570 of 1064 total matches.
Nimodipine for Cerebral Vasospasm Subarachnoid Hemorrhage
The Medical Letter on Drugs and Therapeutics • May 19, 1989 (Issue 792)
(about 12%) is due to extensive first-pass hepatic metabolism. The drug
is excreted in bile and urine ...
Cerebral arterial spasm frequently causes ischemic neurological damage after subarachnoid hemorrhage from a ruptured intracranial aneurysm. Nimodipine (Nimotop - Miles), a 1,4-dihydropyridine calcium-entry blocker, was recently approved by the US Food and Drug Administration (FDA) for oral treatment of such patients; an intravenous preparation is available only for investigational use.
Clozapine for Schizophrenia
The Medical Letter on Drugs and Therapeutics • Jan 12, 1990 (Issue 809)
metabolized, and the metabolites are excreted in urine and feces. The elimination half-life after multiple ...
Clozapine (Clozaril - Sandoz), a dibenzodiazepine antipsychotic drug that has been available in Europe for many years, was recently approved for marketing by the US Food and Drug Administration. Because of its toxicity, the labeling for clozapine recommends using the drug only for schizophrenic patients who have not responded adequately to standard antipsychotic drugs or have had intolerable adverse effects.
Bepridil for Angina Pectoris
The Medical Letter on Drugs and Therapeutics • May 31, 1991 (Issue 845)
a peak in one to
two hours. The drug is extensively metabolized in the liver, and its metabolites ...
Bepridil hydrochloride (Vascor - McNeil Pharmaceutical/Wallace Laboratories), a calcium-channel blocking agent chemically unrelated to verapamil (Calan, and others), nifedipine (Procardia, and others), or other drugs in this class, was recently approved by the US Food and Drug Administration for oral treatment of chronic stable angina pectoris. Because of its potential adverse effects, the labeling recommends reserving the drug for patients who fail to respond optimally to or are intolerant of other antianginal agents.
Ondansentron To Prevent Vomiting After Cancer Chemotherapy
The Medical Letter on Drugs and Therapeutics • Jun 28, 1991 (Issue 847)
activity and therefore is unlikely to have adverse extrapyramidal effects. It is extensively metabolized ...
Ondansetron (on dan' se tron; Zofran - Glaxo), a serotonin (5-hydroxytryptamine) antagonist, was recently marketed in the USA for intravenous use to prevent nausea and vomiting due to cancer chemotherapy. An oral formulation is available in many other countries.
Sertraline For Treatment Of Depression
The Medical Letter on Drugs and Therapeutics • May 15, 1992 (Issue 870)
%) to protein. It is extensively metabolized in the liver, mainly to Ndesmethylsertraline, which has little ...
Sertraline (Zoloft - Roerig), a serotonin reuptake inhibitor, was recently approved for marketing by the US Food and Drug Administration for treatment of depression. Another serotonin reuptake inhibitor, fluoxetine (Prozac), is prescribed more frequently in the USA than any other antidepressant (Medical Letter, 32:83, 1990).
Ticlopidine
The Medical Letter on Drugs and Therapeutics • Jul 10, 1992 (Issue 874)
. Ticlopidine is rapidly and extensively
metabolized in the liver and excreted in the urine. It has a half-life ...
hydrochloride (Ticlid - Syntex), a platelet aggregation inhibitor that has been available in Europe for more than a decade, was recently approved by the U.S. Food and Drug Administration to decrease the risk of thrombotic stroke in men and women who have had premonitory signs of stroke or have had a completed thrombotic stroke. The manufacturer is promoting the drug for patients intolerant to aspirin or with conditions for which aspirin has not been approved (previous thrombotic stroke; transient ischemic attacks in women). The drug has also been used for prevention of myocardial ...
Finasteride for Benign Prostatic Hypertrophy
The Medical Letter on Drugs and Therapeutics • Sep 04, 1992 (Issue 878)
metabolized, probably in the liver, and excreted in urine and stool,
with a mean plasma half-life of about ...
Finasteride (Proscar - Merck) has now been approved by the US Food and Drug Administration (FDA) for oral treatment of benign prostatic hyperplasia. A 4-aza-steroid, the drug is a specific inhibitor of steroid 5 -reductase, the enzyme that catalyzes conversion of testosterone to dihydrotestosterone. Dihydrotestosterone is required for development and maintenance of prostatic hypertrophy (JS Tenover, Endocrinol Metab Clin North Am, 20:893, 1991).
Zolpidem For Insomnia
The Medical Letter on Drugs and Therapeutics • Apr 30, 1993 (Issue 895)
is metabolized in the liver and eliminated mainly in urine; the half-life, usually about 2.5
hours, is prolonged ...
Zolpidem (Ambien - Searle), an imidazopyridine hypnotic available in Europe for several years, was recently approved by the US Food and Drug Administration for short-term treatment of insomnia.
Topical Minoxidil for Baldness: A Reappraisal
The Medical Letter on Drugs and Therapeutics • Jan 21, 1994 (Issue 914)
to the manufacturer,
have serum concentrations close to 50% of those with the oral drug. Minoxidil is metabolized ...
Minoxidil 2% topical solution (Rogaine - Upjohn) has been available in the USA since 1988 for treatment of androgenetic alopecia (Medical Letter, 29:87, 1987). Although available only by prescription, it is advertised on television to the general public.
Fluvastatin for Lowering Cholesterol
The Medical Letter on Drugs and Therapeutics • May 27, 1994 (Issue 923)
— Fluvastatin taken orally is almost completely absorbed, but due to
extensive first-pass metabolism ...
Fluvastatin (Lescol - Sandoz), an HMG-CoA reductase inhibitor, was recently marketed in the USA for treatment of hypercholesterolemia. A synthetic mevalonolactone derivative, it is chemically distinct from previously available drugs in this class.
