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Searched for Metabolic. Results 281 to 290 of 1086 total matches.

Drugs for Psychotic Disorders

   
The Medical Letter on Drugs and Therapeutics • Dec 19, 2016  (Issue 1510)
are not at risk for bronchospasm.19 ADVERSE EFFECTS — Movement disorders, metabolic effects, and other adverse ...
Oral antipsychotic drugs used for treatment of schizophrenia, schizoaffective disorder, delusional disorder, and other manifestations of psychosis or mania are listed in Table 1. Parenteral antipsychotic drugs used for treatment of these disorders are listed in Table 2.
Med Lett Drugs Ther. 2016 Dec 19;58(1510):160-4 |  Show IntroductionHide Introduction

Drugs for Alcohol Use Disorder

   
The Medical Letter on Drugs and Therapeutics • Dec 13, 2021  (Issue 1639)
pleasurable. Pharmacokinetics – Naltrexone is metabolized in the liver and excreted in urine. The major ...
Consumption of alcohol has increased during the COVID-19 pandemic. The Diagnostic and Statistical Manual for Mental Disorders, 5th edition (DSM-5) defines alcohol use disorder (AUD; previously called alcohol dependence) as meeting ≥2 of the 11 criteria listed in Table 1 in the past year. The lifetime prevalence of AUD in the US population has been estimated to be about 30%. Despite this high prevalence and the associated morbidity, mortality, and costs, only 3 drugs are FDA-approved for treatment of the disorder.
Med Lett Drugs Ther. 2021 Dec 13;63(1639):193-8 |  Show IntroductionHide Introduction

Foscarnet

   
The Medical Letter on Drugs and Therapeutics • Jan 10, 1992  (Issue 861)
minimal metabolism and is excreted in the urine. The serum elimination half-life is about three to five ...
Phosphonoformic acid or foscarnet (Foscavir - Astra), a synthetic antiviral drug, has now been approved by the US Food and Drug Administration for intravenous (IV) treatment of cytomegalovirus (CMV) retinitis in patients with AIDS. CMV retinitis occurs in up to 30% of patients with AIDS and often causes blindness (MD de Smet and RB Nussenbatt, JAMA, 266:3019, Dec 4, 1991).
Med Lett Drugs Ther. 1992 Jan 10;34(861):3-4 |  Show IntroductionHide Introduction

Enoxacin - A New Fluoroquinolone

   
The Medical Letter on Drugs and Therapeutics • Nov 13, 1992  (Issue 883)
, and myometrium may be higher than those in blood. Enoxacin is partly metabolized in the liver and excreted ...
Enoxacin (en ox' a sin; Penetrex - Rh ne-Poulenc Rorer), a fluoroquinolone antimicrobial for oral use, has now been marketed in the USA for treatment of urinary tract infections and uncomplicated urethral or cervical gonorrhea.
Med Lett Drugs Ther. 1992 Nov 13;34(883):103-5 |  Show IntroductionHide Introduction

Mibefradil--A New Calcium-Channel Blocker

   
The Medical Letter on Drugs and Therapeutics • Nov 07, 1997  (Issue 1013)
concentrations within one to two hours. It is metabolized in the liver by esterase-catalyzed hydrolysis ...
Mibefradil dihydrochloride (Posicor - Roche), a chemically distinct nondihydropyridine calcium-channel blocker, has been approved by the US Food and Drug Administration (FDA) and is being heavily promoted as the first T-type calcium-channel blocker for treatment of hypertension and chronic stable angina.
Med Lett Drugs Ther. 1997 Nov 7;39(1013):103-5 |  Show IntroductionHide Introduction

Propecia and Rogaine Extra Strength for Alopecia

   
The Medical Letter on Drugs and Therapeutics • Feb 27, 1998  (Issue 1021)
is well absorbed from the gastrointestinal tract, metabolized in the liver and excreted in urine ...
Two new formulations of existing drugs were recently approved by the FDA for treatment of male androgenetic alopecia. Finasteride, a steroid 5alpha-reductase inhibitor previously marketed in a 5-mg tablet as Proscar for treatment of benign prostatic hyperplasia (Medical Letter, 34:83, 1992), has now been approved in a 1-mg tablet as Propecia (Merck) for oral treatment of men with male pattern hair loss. Minoxidil, a peripheral vasodilator used to treat hypertension, was previously available over the counter in a 2% topical solution (Rogaine, and others) for treatment of androgenetic alopecia...
Med Lett Drugs Ther. 1998 Feb 27;40(1021):25-7 |  Show IntroductionHide Introduction

Rofecoxib for Osteoarthritis and Pain

   
The Medical Letter on Drugs and Therapeutics • Jul 02, 1999  (Issue 1056)
or the extent of absorption. Rofecoxib is metabolized in the liver, mainly by reduction, and the metabolites ...
Rofecoxib, a selective COX-2 inhibitor, has been approved by the FDA for treatment of osteoarthritis, acute pain and menstrual pain.
Med Lett Drugs Ther. 1999 Jul 2;41(1056):59-62 |  Show IntroductionHide Introduction

Esomeprazole (Nexium)

   
The Medical Letter on Drugs and Therapeutics • Apr 30, 2001  (Issue 1103)
of esomeprazole peak in about 1.5 hours. The drug undergoes less first-pass hepatic metabolism than omeprazole ...
Esomeprazole magnesium (Nexium - AstraZeneca), the S-isomer of omeprazole (Prilosec), is the fifth benzimidazole proton pump inhibitor to become available in the United States. Omeprazole, which was the first, is going off patent this year.
Med Lett Drugs Ther. 2001 Apr 30;43(1103):36-7 |  Show IntroductionHide Introduction

Gleevec (STI-571) For Chronic Myeloid Leukemia

   
The Medical Letter on Drugs and Therapeutics • Jun 11, 2001  (Issue 1106)
administration and highly protein bound in plasma. The drug is metabolized in the liver, primarily by CYP3A4 ...
Imatinib mesylate (STI-571; Gleevec - Novartis), an oral tyrosine kinase inhibitor, has received accelerated approval from the FDA for treatment of all phases of chronic myeloid leukemia (CML) after interferon has failed.
Med Lett Drugs Ther. 2001 Jun 11;43(1106):49-50 |  Show IntroductionHide Introduction

Alosetron (Lotronex) revisited

   
The Medical Letter on Drugs and Therapeutics • Aug 05, 2002  (Issue 1136)
in a future issue of The Medical Letter. PHARMACOLOGY — Alosetron is extensively metabolized in the liver ...
The FDA recently announced that it will permit reintroduction of alosetron hydrochloride (Lotronex - GlaxoSmithKline) for treatment of irritable bowel syndrome (IBS). The drug was previously withdrawn from the market because of severe gastrointestinal toxicity. The reintroduced drug will have a 50% lower starting dose, a narrower indication and some other marketing restrictions (www.fda.gov/cder/drug/infopage/lotronex/lotronex.htm).
Med Lett Drugs Ther. 2002 Aug 5;44(1136):67-8 |  Show IntroductionHide Introduction