Search Results for "Metabolic"
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Searched for Metabolic. Results 511 to 520 of 1052 total matches.

Growth-Hormone-Releasing-Factor for Growth Hormone Deficiency

   
The Medical Letter on Drugs and Therapeutics • Jan 01, 1999  (Issue 1043)
. Sermorelin has a plasma half-life of about 12 minutes. No data are available on its metabolism or excretion ...
Sermorelin acetate, a synthetic form of human growth-hormone-releasing factor has been approved by the FDA for treatment of idiopathic growth hormone deficiency in children with growth failure.
Med Lett Drugs Ther. 1999 Jan 1;41(1043):2-3 |  Show IntroductionHide Introduction

Mometasone Furoate Nasal Spray for Allergic Rhinitis

   
The Medical Letter on Drugs and Therapeutics • Feb 12, 1999  (Issue 1046)
of mometasone appears to be minimal, and the absorbed drug is extensively metabolized by the liver. Serum ...
An intranasal spray formulation of the topical corticosteroid mometasone furoate, marketed for treatment of seasonal and perennial allergic rhinitis, has been advertised on television directly to the public.
Med Lett Drugs Ther. 1999 Feb 12;41(1046):16-7 |  Show IntroductionHide Introduction

Miglitol for Type 2 Diabetes Mellitus

   
The Medical Letter on Drugs and Therapeutics • May 21, 1999  (Issue 1053)
and other monosaccharides. Unlike acarbose, miglitol is absorbed from the gastrointestinal tract. It is not metabolized ...
Miglitol, an oral alpha-glucosidase inhibitor similar to acarbase, is now available for treatment of type 2 diabetes.
Med Lett Drugs Ther. 1999 May 21;41(1053):49-50 |  Show IntroductionHide Introduction

A New Conjugated Estrogen

   
The Medical Letter on Drugs and Therapeutics • Jul 30, 1999  (Issue 1058)
concentration in plasma within 4 to 16 hours. Conjugated estrogens, like endogenous estrogens, are metabolized ...
A new synthetic conjugated estrogen product (Cenestin - Duramed) was recently approved by the US Food and Drug Administration for treatment of vasomotor symptoms due to estrogen deficiency.
Med Lett Drugs Ther. 1999 Jul 30;41(1058):67-70 |  Show IntroductionHide Introduction

Alosetron (Lotronex) For Treatment of Irritable Bowel Syndrome

   
The Medical Letter on Drugs and Therapeutics • Jun 26, 2000  (Issue 1081)
by about 25% and lowers plasma concentrations of the drug. Alosetron is extensively metabolized ...
Alosetron hydrochloride (Lotronex - Glaxo Welcome), a selective serotonin receptor antagonist, has received FDA approval for treatment of irritable bowel syndrome (IBS) in women whose primary bowel symptom is diarrhea.
Med Lett Drugs Ther. 2000 Jun 26;42(1081):53-4 |  Show IntroductionHide Introduction

Cevimeline (Evoxac) For Dry Mouth

   
The Medical Letter on Drugs and Therapeutics • Aug 07, 2000  (Issue 1084)
from the gastrointestinal tract, reaching peak concentrations in about 90 minutes without food. The drug is metabolized ...
Cevimeline hydrochloride, an acetylcholine derivative, has been approved by the FDA for treatment of dry mouth symptoms caused by Sjogren's syndrome. Presumably it could also be used to treat radiation-induced xerostomia in patients with head and neck cancer. Pilocarpine hydrochloride is FDA-approved for both indications
Med Lett Drugs Ther. 2000 Aug 7;42(1084):70 |  Show IntroductionHide Introduction

Eflornithine Cream For Facial Hair Reduction

   
The Medical Letter on Drugs and Therapeutics • Oct 02, 2000  (Issue 1089)
concentration at steady state is about 10 ng/ml. The drug is not metabolized and is excreted unchanged in urine ...
Eflornithine hydrochloride cream 13.9% (Vaniqa - Bristol-Myers Squibb) has been approved by the FDA for reduction of unwanted facial hair in women.
Med Lett Drugs Ther. 2000 Oct 2;42(1089):96 |  Show IntroductionHide Introduction

Anakinra (Kineret) For Rheumatoid Arthritis

   
The Medical Letter on Drugs and Therapeutics • Feb 18, 2002  (Issue 1124)
10% unchanged, with a terminal half-life of about 6 hours. The site of metabolism is unknown. Plasma ...
Anakinra (Kineret - Amgen), an interleuken-1 (IL-1) receptor antagonist, has been approved by the FDA for treatment of moderately to severly active rheumatoid arthritis in adults who have failed at least one disease-modifying anti-rheumatic drug(DMARD) such as methotrexate (Medical Letter 2000; 24:57).
Med Lett Drugs Ther. 2002 Feb 18;44(1124):18-9 |  Show IntroductionHide Introduction

In Brief: Sevelamer-Based Phosphate Binders

   
The Medical Letter on Drugs and Therapeutics • Feb 25, 2008  (Issue 1280)
, Renvela will replace Renagel, which has been shown to induce or exacerbate metabolic acidosis ...
Sevelamer carbonate (Renvela – Genzyme), a buffered form of the anion-exchange resin sevelamer hydrochloride (Renagel – Genzyme),1 has been approved by the FDA for use in patients with chronic kidney disease on dialysis. According to the manufacturer, Renvela will replace Renagel, which has been shown to induce or exacerbate metabolic acidosis in patients on dialysis. Two randomized, crossover studies found the two sevelamer salts equivalent in their ability to lower serum phosphate.2,3 Patients taking the carbonate had higher serum bicarbonate concentrations and fewer gastrointestinal...
Med Lett Drugs Ther. 2008 Feb 25;50(1280):13 |  Show IntroductionHide Introduction

Low-Dose Doxepin (Silenor) for Insomnia

   
The Medical Letter on Drugs and Therapeutics • Oct 04, 2010  (Issue 1348)
fasting, 6.5 hours with a meal Metabolism Hepatic by CYP2C19 and CYP2D6; to a lesser extent CYP1A2 ...
The FDA has approved a new low-dose formulation of the tricyclic antidepressant doxepin (Silenor – Somaxon) for treatment of insomnia associated with sleep maintenance. The manufacturer claims that this dose retains the hypnotic effect of doxepin, without typical tricyclic adverse effects. Doxepin is available generically in higher-strength capsules and in a liquid formulation.
Med Lett Drugs Ther. 2010 Oct 4;52(1348):79-80 |  Show IntroductionHide Introduction