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Searched for establish. Results 441 to 450 of 654 total matches.

Aspirin for Prevention of Myocardial Infarction

   
The Medical Letter on Drugs and Therapeutics • Feb 17, 1995  (Issue 942)
. For primary prevention in low-risk patients, more studies are required to establish whether the beneficial ...
Aspirin is now widely used for antithrombotic prophylaxis in patients who have had angina pectoris or a myocardial infarction and has also been tried in healthy people to prevent myocardial infarction. Recent studies have focused on increasingly lower doses of the drug. The use of aspirin in patients who have had transient ischemic attacks or strokes will not be discussed here.
Med Lett Drugs Ther. 1995 Feb 17;37(942):14-6 |  Show IntroductionHide Introduction

Terbinafine for Onychomycosis

   
The Medical Letter on Drugs and Therapeutics • Aug 16, 1996  (Issue 981)
has been established, however, between in vitro activity and clinical effectiveness (YM Clayton, Br J Dermatol, 130 ...
Terbinafine (Lamisil - Sandoz), an allylamine synthetic antifungal, previously available in the USA in a topical formulation (Medical Letter, 35:76, 1993) has now been marketed for oral use in the treatment of fungal nail infections caused by dermatophytes. Oral terbinafine has been available in Europe since 1992.
Med Lett Drugs Ther. 1996 Aug 16;38(981):72-4 |  Show IntroductionHide Introduction

Troglitazone for Non-Insulin-Dependent Diabetes Mellitus

   
The Medical Letter on Drugs and Therapeutics • May 23, 1997  (Issue 1001)
. The safety and effectiveness of long-term use of troglitazone remain to be established. THE MEDICAL LETTER ...
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.
Med Lett Drugs Ther. 1997 May 23;39(1001):49-51 |  Show IntroductionHide Introduction

Mibefradil--A New Calcium-Channel Blocker

   
The Medical Letter on Drugs and Therapeutics • Nov 07, 1997  (Issue 1013)
any advantage over older calcium-channel blockers remains to be established. Syncope has occurred ...
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

Two New Antiplatelet Drugs for Angioplasty and Acute Coronary Syndromes

   
The Medical Letter on Drugs and Therapeutics • Sep 11, 1998  (Issue 1035)
of cardiac events associated with acute coronary syndromes; direct comparisons are needed to establish which ...
Two new platelet glycoprotein IIb/IIIa receptor antagonists have been approved for marketing by the US Food and Drug Administration (FDA). Eptifibatide (ep ti fi' ba tyde; Integrilin - Cor, Key) is approved for use in acute coronary syndromes (unstable angina or non-Q-wave myocardial infarction) or percutaneous coronary intervention (angioplasty or atherectomy). Tirofiban (tye roe fye' ban; Aggrastat - Merck) is approved for acute coronary syndromes, but not for angioplasty without an acute coronary syndrome. Abciximab (ReoPro), a monoclonal antibody glycoprotein IIb/IIIa receptor...
Med Lett Drugs Ther. 1998 Sep 11;40(1035):89-90 |  Show IntroductionHide Introduction

Rofecoxib for Osteoarthritis and Pain

   
The Medical Letter on Drugs and Therapeutics • Jul 02, 1999  (Issue 1056)
gastrointestinal bleeding than older NSAIDs remain to be established. THE MEDICAL LETTER (ISSN 1523-2859 ...
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

Tenecteplase (TNKase) for Thrombolysis

   
The Medical Letter on Drugs and Therapeutics • Nov 13, 2000  (Issue 1092)
has not been established. PHARMACOKINETICS — Tenecteplase, a variant of alteplase with three amino acid substitutions ...
Tenecteplase, a recombinant variant of human tissue plasminogen activator, is now available for thrombolysis in patients with acute myocardial infarction.
Med Lett Drugs Ther. 2000 Nov 13;42(1092):106-8 |  Show IntroductionHide Introduction

Over-the-counter (OTC) Cough Remedies

   
The Medical Letter on Drugs and Therapeutics • Mar 19, 2001  (Issue 1100)
has not been established. Prescription guaifenesin products are available in 600 mg to 1.2 gm strengths (Humibid LA ...
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.
Med Lett Drugs Ther. 2001 Mar 19;43(1100):23-5 |  Show IntroductionHide Introduction

Twinrix: A Combination Hepatitis A and B Vaccine

   
The Medical Letter on Drugs and Therapeutics • Aug 06, 2001  (Issue 1110)
or severity with subsequent doses of the vaccine. Safety in pregnancy has not been established. 68 ...
A vaccine to prevent both Hepatitis A and Hepatitis B (Twinrix), previously licensed in Canada and Europe, is now available in the US for adults.
Med Lett Drugs Ther. 2001 Aug 6;43(1110):67-8 |  Show IntroductionHide Introduction

Alosetron (Lotronex) revisited

   
The Medical Letter on Drugs and Therapeutics • Aug 05, 2002  (Issue 1136)
. than with placebo. The safety and efficacy of alosetron have not been established in men. ADVERSE ...
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