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Searched for establish. Results 581 to 590 of 655 total matches.

Airsupra: An Inhaled Albuterol/Budesonide Combination for Asthma

   
The Medical Letter on Drugs and Therapeutics • Mar 18, 2024  (Issue 1698)
alone in children or adolescents with asthma remains to be established. Albuterol/budesonide ...
The FDA has approved Airsupra (AstraZeneca), a metered-dose inhaler containing the short-acting beta2-agonist (SABA) albuterol and the inhaled corticosteroid (ICS) budesonide, for use as needed for treatment or prevention of bronchoconstriction and to reduce the risk of exacerbations in patients ≥18 years old with asthma. Airsupra is the first combination of a SABA and an ICS to become available in the US. It is not approved for use as maintenance therapy.
Med Lett Drugs Ther. 2024 Mar 18;66(1698):41-3   doi:10.58347/tml.2024.1698a |  Show IntroductionHide Introduction

Oral Contraceptives

   
The Medical Letter on Drugs and Therapeutics • May 15, 2000  (Issue 1078)
Mellemkjær et al, BMJ, 319:390, 1999). Cause and effect have not been established (MA Lewis et al, Hum ...
Two types of oral contraceptives are available in the USA: combination oral contraceptives that contain both an estrogen and a progestin, and progestin-only contraceptives, or "mini-pills."Used as directed, all oral contraceptives marketed in the USA are similarly effective in preventing pregnancy.
Med Lett Drugs Ther. 2000 May 15;42(1078):42-4 |  Show IntroductionHide Introduction

Ropinirole for Restless Legs Syndrome

   
The Medical Letter on Drugs and Therapeutics • Aug 01, 2005  (Issue 1214)
used for this indication remains to be established. 1. CJ Earley. Restless legs syndrome. N Engl J ...
Ropinirole (Requip - GlaxoSmithKline), a dopamine agonist already available for treatment of Parkinson's disease, is now the first drug approved by the FDA for treatment of moderate to severe restless legs syndrome (RLS).
Med Lett Drugs Ther. 2005 Aug 1;47(1214):62-4 |  Show IntroductionHide Introduction

Statins for High-Risk Patients without Heart Disease or High Cholesterol

   
The Medical Letter on Drugs and Therapeutics • Jan 02, 2006  (Issue 1225)
remains to be established. In high-risk patients without diabetes and without a history of coronary ...
The FDA recently approved the use of atorvastatin (Lipitor) to reduce the risk of heart attack and stroke in patients without heart disease who have type 2 diabetes plus other risk factors, with or without hypercholesterolemia. The agency also approved the drug's use to reduce the risk of stroke in high-risk nondiabetic patients without heart disease, whether or not they have hypercholesterolemia. Similar indications were previously approved for simvastatin (Zocor).
Med Lett Drugs Ther. 2006 Jan 2;48(1225):1-2 |  Show IntroductionHide Introduction

Coenzyme Q10

   
The Medical Letter on Drugs and Therapeutics • Feb 27, 2006  (Issue 1229)
to be established. 15 Other conditions – In one randomized, double-blind, 12-week study in 97 patients ...
Coenzyme Q10, a fat-soluble antioxidant also known as ubidecarenone, ubiquinone and CoQ10, is marketed as a dietary supplement in the US, both as a single ingredient and in various combination products.
Med Lett Drugs Ther. 2006 Feb 27;48(1229):19-20 |  Show IntroductionHide Introduction

Lybrel - A Continuous Oral Contraceptive

   
The Medical Letter on Drugs and Therapeutics • Jul 30, 2007  (Issue 1266)
. Whether prolonged amenorrhea could have an adverse effect on fertility also remains to be established ...
Lybrel (Wyeth) is the first FDA-approved low-dose combination oral contraceptive taken 365 days a year without a placebo or pill-free interval. All tablets contain low doses of levonorgestrel (0.09 mg) and ethinyl estradiol (20 mcg). Most oral contraceptives are packaged as a 21/7 cycle (21 days of active tablets and 7 days of placebo), resulting in 13 withdrawal bleeding episodes each year. Two formulations are taken for 24 days followed by 4 days of inert tablets (Yaz and Loestrin 24). Two others (Seasonique and Seasonale) have a 91-day cycle with only 4 withdrawal bleeds per...
Med Lett Drugs Ther. 2007 Jul 30;49(1266):61-2 |  Show IntroductionHide Introduction

Metformin/Repaglinide (PrandiMet) for Type 2 Diabetes

   
The Medical Letter on Drugs and Therapeutics • Jun 01, 2009  (Issue 1313)
to be established, but only this combination (because of the repaglinide component) carries instructions to skip ...
A new fixed-dose tablet (PrandiMet - Novo Nordisk) combining metformin (Glucophage, and others) and repaglinide (Prandin) has been approved by the FDA for treatment of type 2 diabetes in patients already taking both metformin and repaglinide, or for patients not adequately controlled on either drug alone.
Med Lett Drugs Ther. 2009 Jun 1;51(1313):41-3 |  Show IntroductionHide Introduction

Drugs for Female Sexual Dysfunction

   
The Medical Letter on Drugs and Therapeutics • Dec 13, 2010  (Issue 1353)
of local estrogen use in women with breast cancer is not established; one study found no increase ...
Sexual complaints related to desire, arousal, orgasm and painful intercourse are common in women. Since the last Medical Letter article on this subject, some new information has become available.
Med Lett Drugs Ther. 2010 Dec 13;52(1353):100-2 |  Show IntroductionHide Introduction

Oral Semaglutide (Rybelsus) for Type 2 Diabetes

   
The Medical Letter on Drugs and Therapeutics • Oct 21, 2019  (Issue 1583)
benefits of oral semaglutide remain to be established. Glucophage exenatide dulaglutide Byetta Bydureon ...
An oral formulation of the glucagon-like peptide-1 (GLP-1) receptor agonist semaglutide (Rybelsus – Novo Nordisk) has been approved by the FDA for once-daily treatment of type 2 diabetes in adults. Semaglutide, which has been available in a subcutaneously-injected formulation (Ozempic) since 2017, is the first GLP-1 receptor agonist to become available for oral administration; the 4 other GLP-1 receptor agonists currently available in the US are administered by subcutaneous (SC) injection.
Med Lett Drugs Ther. 2019 Oct 21;61(1583):166-8 |  Show IntroductionHide Introduction

Lumateperone (Caplyta) for Schizophrenia

   
The Medical Letter on Drugs and Therapeutics • Jul 27, 2020  (Issue 1603)
antipsychotics remains to be established. Until long-term data or results of headto- head trials become ...
The FDA has approved lumateperone (Caplyta — Intracellular Therapies), an oral second-generation antipsychotic, for once-daily treatment of schizophrenia in adults. It is the 13th second-generation antipsychotic drug to be approved by the FDA for this indication.
Med Lett Drugs Ther. 2020 Jul 27;62(1603):113-6 |  Show IntroductionHide Introduction