Search Results for "Gastrointestinal"
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Searched for Gastrointestinal. Results 311 to 320 of 424 total matches.
Sparfloxacin and Levofloxacin
The Medical Letter on Drugs and Therapeutics • Apr 25, 1997 (Issue 999)
— All fluoroquinolones occasionally can cause skin rashes or gastrointestinal disturbances. Central-nervous-system ...
Sparfloxacin (Zagam - Rh ne-Poulenc Rorer) and levofloxacin (Levaquin - Ortho-McNeil) are the newest fluoroquinolone antimicrobials to be approved by the US Food and Drug Administration. Sparfloxacin in a once-daily oral preparation is being marketed for treatment of community-acquired pneumonia and acute bacterial exacerbations of chronic bronchitis. Levofloxacin, which is the active stereoisomer of ofloxacin (Floxin), is available for either oral or parenteral use; it is approved for oncedaily treatment of community-acquired pneumonia, acute exacerbations of chronic bronchitis,...
Troglitazone for Non-Insulin-Dependent Diabetes Mellitus
The Medical Letter on Drugs and Therapeutics • May 23, 1997 (Issue 1001)
Both acarbose and metformin cause abdominal discomfort and other usually mild gastrointestinal
effects ...
Troglitazone (Rezulin - Parke-Davis), the first of a new class of thiazolidinedione derivatives ('glitazones') for diabetes, has been marketed for oral treatment of noninsulin- dependent diabetes mellitus (NIDDM) in patients who take more than 30 units of insulin daily and still have a glycosylated hemoglobin concentration (HbA1c) of 8.5% or higher.
Carvedilol for Heart Failure
The Medical Letter on Drugs and Therapeutics • Sep 26, 1997 (Issue 1010)
absorption from the gastrointestinal tract can be
delayed if it is taken with meals. The drug is extensively ...
Carvedilol (Coreg - SmithKline Beecham and Boehringer-Mannheim), a betaadrenergic and alpha-adrenergic blocker approved by the FDA for treatment of hypertension in 1995, but not marketed at that time, has now been approved and marketed for treatment of mild or moderate (NYHA class II or III) heart failure stabilized on other drugs. It is being promoted as an add-on drug that reduces the morbidity and mortality of the disease.
Mibefradil--A New Calcium-Channel Blocker
The Medical Letter on Drugs and Therapeutics • Nov 07, 1997 (Issue 1013)
.
PHARMACOKINETICS — Mibefradil is rapidly absorbed from the gastrointestinal tract,
achieving peak plasma ...
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.
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...
Linezolid (Zyvox)
The Medical Letter on Drugs and Therapeutics • May 29, 2000 (Issue 1079)
and completely absorbed from the gastrointestinal tract, reaching peak plasma concentrations in 1 to 2 hours ...
Linezolid, the first of a new class of antibiotics, the oxazolidinones, has been marketed for treatment of infection due to vancomycin-resistant Enterococcus faecium, nosocomial and community-acquired pueumonia due to Staphylococcus aureus or penicillin-sucsceptible Streptococcus pneumoniae, and skin and skin structure infections, including those due to methicillin-resistant S. aureus (MRSA).
Over-the-counter (OTC) Cough Remedies
The Medical Letter on Drugs and Therapeutics • Mar 19, 2001 (Issue 1100)
and constipation. Dextromethorphan in usual doses does not
cause sedation or gastrointestinal disturbances ...
The number of cough remedies available in the USA continues to multiply, but most products contain the same or similar ingredients in varying combinations. Most acute coughs do not require treatment with drugs, especially in children, and suppression of a productive cough may be harmful.
Nateglinide For Type 2 Diabetes
The Medical Letter on Drugs and Therapeutics • Apr 02, 2001 (Issue 1101)
, and sometimes causes diarrhea and
other gastrointestinal symptoms.
Rosiglitazone and pioglitazone decrease ...
Nateglinide (Starlix), a new meglitinide oral glucose-lowering agent, has been approved by the FDA.
New Treatments for Actinic Keratoses
The Medical Letter on Drugs and Therapeutics • Jun 24, 2002 (Issue 1133)
for upper gastrointestinal hemorrhage found that 4 had been applying a
diclofenac gel formulation ...
Several new treatments are now available for actinic keratoses (AKs), scaly pink papules commonly found on sun-exposed areas of the face, scalp, forearms and dorsal surface of the hands, particularly in the elderly. Some AKs regress spontaneously, but a few may progress to squamous cell carcinoma; the risk of progression has been estimated to be about 0.25% to 1% per year (EWB Jeffes III and EH Tang, Am J Clin Dermatol 2000; 1:167).
Alosetron (Lotronex) revisited
The Medical Letter on Drugs and Therapeutics • Aug 05, 2002 (Issue 1136)
gastrointestinal toxicity. The reintroduced drug will have a 50% lower starting dose, a narrower indication ...
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).