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Searched for Drug. Results 761 to 770 of 2581 total matches.

In Brief: Higher-Dose Semaglutide (Ozempic) for Type 2 Diabetes

   
The Medical Letter on Drugs and Therapeutics • May 16, 2022  (Issue 1650)
of the drug do not achieve the desired A1C goal.1,2 An oral formulation of semaglutide (Rybelsus ...
The FDA has approved a higher-dose injectable formulation of the long-acting glucagon-like peptide-1 (GLP-1) receptor agonist semaglutide (Ozempic) for treatment of type 2 diabetes in adults. A single SC injection of the new 8 mg/3 mL formulation delivers 2 mg of semaglutide.
Med Lett Drugs Ther. 2022 May 16;64(1650):79 |  Show IntroductionHide Introduction

Rasagiline (Azilect) for Parkinson's Disease

   
The Medical Letter on Drugs and Therapeutics • Dec 04, 2006  (Issue 1249)
Letter ® On Drugs and Therapeutics Volume 48 (Issue 1249/1250) December 4/18, 2006 ...
Rasagiline (Azilect - Teva), a monoamine oxidase-type B (MAO-B) inhibitor, was recently approved by the FDA for once-daily oral treatment of Parkinson's disease (PD). It can be taken alone for treatment of early disease or with levodopa/carbidopa (Sinemet, and others) for advanced disease. Selegiline (Eldepryl, and others), the first MAO-B inhibitor marketed in the US, has been available since 1988; a new lower-dose disintegrating tablet (Zelapar) was recently approved.
Med Lett Drugs Ther. 2006 Dec 4;48(1249):97-9 |  Show IntroductionHide Introduction

Addendum: Timing of Levothyroxine

   
The Medical Letter on Drugs and Therapeutics • Feb 01, 2016  (Issue 1487)
The Medical Letter® on Drugs and Therapeutics Volume 58 (Issue 1487) February 1, 2016 Published ...
In our October 26, 2015 article on drugs for hypothyroidism (Med Lett Drugs Ther 2015; 57:147), we said that levothyroxine should be taken on an empty stomach with a full glass of water 30-60 minutes (60 is preferable) before breakfast. We should have added that taking the drug consistently at bedtime, at least 3 hours after the last meal, is an alternative that some patients may find more convenient.
Med Lett Drugs Ther. 2016 Feb 1;58(1487):18 |  Show IntroductionHide Introduction

Amlodipine - A New Calcium-Channel Blocker

   
The Medical Letter on Drugs and Therapeutics • Oct 30, 1992  (Issue 882)
The Medical Letter  On Drugs and Therapeutics www.medletter.com Published by The Medical ...
Amlodipine (am loe' di peen) besylate (Norvasc - Pfizer), a dihydropyridine calcium-channel blocker, has been approved by the US Food and Drug Administration for once-daily oral treatment of hypertension, chronic stable angina, and vasospastic (Prinzmetal's) angina.
Med Lett Drugs Ther. 1992 Oct 30;34(882):99-100 |  Show IntroductionHide Introduction

Mirtazapine - A New Antidepressant

   
The Medical Letter on Drugs and Therapeutics • Dec 20, 1996  (Issue 990)
The Medical Letter  On Drugs and Therapeutics www.medletter.com Published by The Medical ...
Mirtazapine (mir taz a peen; Remeron - Organon) has been approved by the US Food and Drug Administration for treatment of depression. A tetracyclic piperazinoazepine, it is an analog of mianserin, an antidepressant available in Europe, but is structurally unrelated to antidepressants previously available in the USA.
Med Lett Drugs Ther. 1996 Dec 20;38(990):113-4 |  Show IntroductionHide Introduction

Budesonide Turbuhaler for Asthma

   
The Medical Letter on Drugs and Therapeutics • Jan 16, 1998  (Issue 1018)
The Medical Letter  On Drugs and Therapeutics www.medletter.com Published by The Medical ...
The FDA has approved marketing of the corticosteroid budesonide in an oral inhalatoin powder formulation (Pulmicort Turbuhaler - Astra) for maintenance treatment of asthma in adults and children at least six years old. Budesonide has been available in the USA as an intranasal spray (Rhinocort) for treatment of allergic rhinitis since 1994 and has been used for inhalation treatment of asthma in Canada and Europe for ten years.
Med Lett Drugs Ther. 1998 Jan 16;40(1018):15-6 |  Show IntroductionHide Introduction

Deferasirox (Exjade): A New Iron Chelator

   
The Medical Letter on Drugs and Therapeutics • Apr 24, 2006  (Issue 1233)
Letter ® On Drugs and Therapeutics IN THIS ISSUE Volume 48 (Issue 1233) April 24, 2006 ...
Deferasirox (Exjade - Novartis), an oral chelating agent, recently received accelerated approval from the FDA as an orphan drug for oral treatment of chronic iron overload due to blood transfusions (transfusional hemosiderosis) in patients >2 years old. Deferasirox is a tridentate (2 molecules of deferasirox bind to one atom of iron) chelating agent with high affinity for iron. It has much lower affinity for zinc and copper.
Med Lett Drugs Ther. 2006 Apr 24;48(1233):35-6 |  Show IntroductionHide Introduction

Tapinarof Cream (Vtama) for Atopic Dermatitis

   
The Medical Letter on Drugs and Therapeutics • Mar 03, 2025  (Issue 1723)
with tapinarof cream than with Table 1. Some Topical Nonsteroidal Drugs for Atopic Dermatitis FDA-Approved ...
Tapinarof 1% cream (Vtama – Dermavant), an aryl hydrocarbon receptor (AhR) agonist, has been approved by the FDA for topical treatment of atopic dermatitis in patients ≥2 years old. Tapinarof is the first AhR agonist to be approved in the US for this indication. It was approved in 2022 for treatment of plaque psoriasis in adults.
Med Lett Drugs Ther. 2025 Mar 3;67(1723):37-8   doi:10.58347/tml.2025.1723c |  Show IntroductionHide Introduction

In Brief: Safety of Quinine

   
The Medical Letter on Drugs and Therapeutics • Nov 01, 2010  (Issue 1350)
The Medical Letter® On Drugs and Therapeutics Volume 52 (Issue 1350) November 1, 2010 ...
Qualaquin, the only formulation of quinine sulfate available in the US, is approved only for treatment of uncomplicated malaria, but most prescriptions for its use are written for treatment or prevention of nocturnal leg cramps. The FDA recently issued a warning about its safety.Between April 2005 and October 2008, 38 cases of serious or life-threatening adverse effects of quinine were reported to the FDA. Twenty-one of these patients had thrombocytopenia and required hospitalization. Two deaths were reported: one from hemolysis and the other from thrombotic thrombocytopenic purpura (TTP)....
Med Lett Drugs Ther. 2010 Nov 1;52(1350):88 |  Show IntroductionHide Introduction

In Brief: Low-Dose Indomethacin (Tivorbex) for Pain

   
The Medical Letter on Drugs and Therapeutics • Jul 21, 2014  (Issue 1447)
The Medical Letter® on Drugs and Therapeutics Objective Drug Reviews Since 1959 Volume 56 July ...
The same pharmaceutical company (Iroko) that recently marketed low-dose diclofenac (Zorvolex) for treatment of mild to moderate acute pain1 has now received approval from the FDA to market a low-dose oral formulation of indomethacin (Tivorbex) for the same indication. Tivorbex is available in 20- and 40-mg capsules; conventional immediate-release indomethacin capsules contain 25 mg and 50 mg of the drug.The rationale for this new product is the same as the one offered for Zorvolex: the drug is formulated as submicron particles that increase surface area, leading to faster dissolution and...
Med Lett Drugs Ther. 2014 Jul 21;56(1447):64 |  Show IntroductionHide Introduction