Search Results for "activate"
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Searched for activate. Results 291 to 300 of 1334 total matches.
Dehydroepiandrosterone (DHEA)
The Medical Letter on Drugs and Therapeutics • May 09, 2005 (Issue 1208)
One 24-week placebo-controlled study in
120 women with active SLE found that DHEA 200
mg/d reduced ...
Dehydroepiandrosterone (DHEA), an endogenous adrenal steroid, is marketed as a dietary supplement in the US. It is widely promoted to reverse the effects of aging (loss of muscle, memory and libido) and has been used by athletes as a substitute for anabolic steroids. DHEA is banned by the International Olympic Committee, National Collegiate Athletic Association, National Football League and other sports organizations, but it was specifically exempted from becoming a controlled substance in the Anabolic Steroid Control Act of 2004.
Abatacept (Orencia) for Rheumatoid Arthritis
The Medical Letter on Drugs and Therapeutics • Feb 27, 2006 (Issue 1229)
of T-cell activation, has been approved by the
FDA for treatment of moderate to severe rheumatoid ...
Atacept (Orencia - Bristol-Myers Squibb), an inhibitor of T-cell activation, has been approved by the FDA for treatment of moderate to severe rheumatoid arthritis (RA) in patients who have not responded to one or more disease-modifying anti-rheumatic drugs (DMARDs).
Fesoterodine (Toviaz) for Overactive Bladder
The Medical Letter on Drugs and Therapeutics • May 04, 2009 (Issue 1311)
, with or
without food, and rapidly hydrolyzed to its active moiety
5-hydroxymethyl tolterodine, which is also ...
The FDA has approved the marketing of fesoterodine (Toviaz - Pfizer), a muscarinic receptor antagonist, for treatment of overactive bladder. It is the sixth antimuscarinic drug approved for this indication.
Risankizumab (Skyrizi) - An IL-23 Antagonist for Crohn's Disease
The Medical Letter on Drugs and Therapeutics • Dec 26, 2022 (Issue 1666)
of moderately
to severely active Crohn’s disease (CD) in adults.
Risankizumab was approved earlier ...
The injectable interleukin (IL)-23 antagonist
risankizumab-rzaa (Skyrizi – Abbvie) has been
approved by the FDA for treatment of moderately
to severely active Crohn's disease (CD) in adults.
Risankizumab was approved earlier for treatment of
plaque psoriasis and psoriatic arthritis.
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.
Ticlopidine
The Medical Letter on Drugs and Therapeutics • Jul 10, 1992 (Issue 874)
by inhibiting the adenosine
diphosphate (ADP) pathway for platelet activation. Unlike aspirin, ticlopidine does ...
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 ...
Sotalol for Cardiac Arrhythmias
The Medical Letter on Drugs and Therapeutics • Apr 02, 1993 (Issue 893)
) and also has beta-adrenergicblocking activity (Class II), was recently approved by the US Food and Drug ...
Sotalol (hydrochloride (Betapace -Berlex; Sotacor -Bristol Laboratories of Canada), an antiarrhythmic drug that prolongs repolarization (Class III) and also has beta-adrenergic-blocking activity (Class II), was recently approved by the US Food and Drug Administration (FDA) for oral treatment of life-threatening ventricular arrhythmias.
Venlafaxine - A New Antidepressant
The Medical Letter on Drugs and Therapeutics • Jun 10, 1994 (Issue 924)
of the
drug is about five hours and of a major active metabolite is about 11 hours. The drug and its active ...
Venlafaxine hydrochloride (Effexor - Wyeth-Ayerst) was recently approved by the US Food and Drug Administration for treatment of depression. An aminomethyl-benzyl- cyclohexanol, it is chemically related to bupropion (Wellbutrin).
Tacrolimus FK506 Organ Transplants
The Medical Letter on Drugs and Therapeutics • Sep 16, 1994 (Issue 931)
) and other
immunosuppressive drugs.
ACTIVITY AND PHARMACOKINETICS — Tacrolimus is a bacteria-derived macrolide ...
Tacrolimus (Prograf - Fujisawa), previously called FK506 (Medical Letter, 33:94, 1991), has been approved by the US Food and Drug Administration for primary prevention of organ rejection in patients receiving liver transplants. The drug has also been used as rescue therapy for organ graft rejection unresponsive to cyclosporine (Sandimmune) and other immunosuppressive drugs.
Tramadol - A New Oral Analgesic
The Medical Letter on Drugs and Therapeutics • Jul 07, 1995 (Issue 952)
Administration for oral
treatment of moderate to moderately severe pain. Despite some opioid activity, tramadol ...
Tramadol hydrochloride (Ultram - Ortho-McNeil), a centrally-acting analgesic marketed in Germany since 1977, was recently approved by the US Food and Drug Administration for oral treatment of moderate to moderately severe pain. Despite some opioid activity, tramadol has not been scheduled as a controlled substance.