Search Results for "Metabolic"
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Searched for Metabolic. Results 461 to 470 of 1064 total matches.
Ophthalmic Levocabastine for Allergic Conjunctivitis
The Medical Letter on Drugs and Therapeutics • Apr 15, 1994 (Issue 920)
.
The remainder is metabolized to the acylglucuronide and excreted in the urine (KL Dechant and KL
Goa, Drugs, 41 ...
A 0.05% ophthalmic solution of levocabastine hydrochloride (Livostin - Iolab), a histamine H 1 -receptor antagonist, has been approved by the US Food and Drug Administration for treatment of seasonal allergic conjunctivitis. The new drug is a cyclohexylpiperidine derivative with no structural relationship to any other antihistamine.
Aprotinin To Decrease Bleeding in Cardiac Surgery
The Medical Letter on Drugs and Therapeutics • Jun 10, 1994 (Issue 924)
disappears rapidly from the circulation and is metabolized by lysosomal activity in the kidney ...
Aprotinin (Trasylol - Miles), an inhibitor of fibrinolysis first identified in 1930, was recently approved by the US Food and Drug Administration for intravenous use in high-risk coronary artery bypass graft (CABG) surgery to decrease bleeding and the need for transfusion. Inhibitors of fibrinolysis previously available in the USA include aminocaproic acid (Amicar, and others) and tranexamic acid (Cyklokapron - Medical Letter, 29:89, 1987).
Yohimbine for Male Sexual Dysfunction
The Medical Letter on Drugs and Therapeutics • Dec 23, 1994 (Issue 938)
, with an elimination half-life of 0.6
hours. Virtually none of the drug is found in urine and its metabolic fate ...
Yohimbine hydrochloride, a presynaptic 2 -adrenergic receptor antagonist available by prescription in the USA (Yocon, Yohimex, and others), is advertised for treatment of impotence and has been used as an aphrodisiac. A pre-1938 drug, yohimbine has never been approved for marketing by the US Food and Drug Administration.
Methotrexate and Misoprostol for Abortion
The Medical Letter on Drugs and Therapeutics • Apr 26, 1996 (Issue 973)
undergoes minimal metabolism in the liver and is excreted in urine, with a half-life of 8 to 15 hours ...
Recent articles in the press have suggested that in early pregnancy, an intramuscular (IM) injection of methotrexate (Folex, and others), a folic acid antagonist, and oral or vaginal administration of misoprostol (Cytotec), a prostaglandin, offers a medical alternative to a surgically induced abortion. Methotrexate is approved by the US Food and Drug Administration for use in rheumatoid arthritis, psoriasis and various types of cancer, including choriocarcinoma, and has also been used to terminate ectopic pregnancies. Misoprostol is approved for prevention of gastric ulcers induced by...
Anastrozole for Metastatic Breast Cancer
The Medical Letter on Drugs and Therapeutics • Jul 05, 1996 (Issue 978)
a maximum within two hours. The drug is extensively
metabolized in the liver, and the metabolites ...
Anastrozole (Arimidex - Zeneca), a selective nonsteroidal aromatase inhibitor, has been approved by the US Food and Drug Administration (FDA) for treatment of postmenopausal women with advanced breast cancer that has progressed during treatment with tamoxifen (Nolvadex, and others).
Reteplase (Retavase)
The Medical Letter on Drugs and Therapeutics • Feb 28, 1997 (Issue 995)
for anistreplase. The drug is metabolized in the liver and excreted in urine.
CLINICAL STUDIES — An open-label ...
Reteplase (Retavase - Boehringer Mannheim), a recombinant protein derivative of human tissue plasminogen activator (t-PA), has been marketed in the USA for thrombolysis in patients with acute myocardial infarction.
Cabergoline for Hyperprolactinemia
The Medical Letter on Drugs and Therapeutics • Jun 20, 1997 (Issue 1003)
tract and extensively metabolized in the liver to inactive products. The parent drug and its ...
Cabergoline (Dostinex - Pharmacia & Upjohn), an ergot alkaloid derivative recently marketed for treatment of hyperprolactinemia, is a selective D2 dopamine agonist that inhibits prolactin-secreting cells in the pituitary. Bromocriptine (Parlodel - Sandoz), the drug most commonly used for this condition, is also a D2 agonist, but affects D1 receptors as well.
Bromfenac for Analgesia
The Medical Letter on Drugs and Therapeutics • Oct 10, 1997 (Issue 1011)
than with other NSAIDs. Bromfenac
is metabolized in the liver and excreted in urine. The half-life ...
Bromfenac sodium (Duract - Wyeth-Ayerst), a nonsteroidal anti-inflammatory drug (NSAID), has been approved by the US Food and Drug Administration (FDA) and is being heavily advertised as an alternative to narcotics for short-term treatment of pain.
Irbesartan for Hypertension
The Medical Letter on Drugs and Therapeutics • Jan 30, 1998 (Issue 1019)
concentrations in two hours. The drug is metabolized in the liver, mainly by
CYP2C9, and excreted in bile ...
Irbesartan (Avapro - Sanofi/Bristol-Myers Squibb) is the third angiotensin II receptor antagonist to become available in the USA for oral treatment of hypertension. Losartan (Cozaar) and valsartan (Diovan) were marketed earlier. Eprosartan (Teveten - SmithKline Beecham) has been approved by the FDA but not marketed.
SAMe For Depression
The Medical Letter on Drugs and Therapeutics • Nov 05, 1999 (Issue 1065)
reactions in human metabolism (T Bottiglieri et al, Drugs, 48:137, 1994). It
is available by prescription ...
S-adenosyl-methionine (SAM; SAMe; ademetionine; adomet), an endogenous compound synthesized from methionine and adenosine-triphosphate (ATP), has been marketed in stores and on the internet as a dietary supplement to promote "emotional well being."
