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Searched for Drug. Results 1721 to 1730 of 2610 total matches.

A Long-Acting Depot Formulation of Testosterone (Aveed)

   
The Medical Letter on Drugs and Therapeutics • Mar 31, 2014  (Issue 1439)
The Medical Letter® On Drugs and Therapeutics Published by The Medical Letter, Inc. • 145 ...
The FDA has approved testosterone undecanoate (Aveed – Endo), an injectable depot formulation, for use in men with hypogonadism who require testosterone replacement therapy.
Med Lett Drugs Ther. 2014 Mar 31;56(1439):26-8 |  Show IntroductionHide Introduction

Reslizumab (Cinqair) for Severe Eosinophilic Asthma

   
The Medical Letter on Drugs and Therapeutics • Jun 20, 2016  (Issue 1497)
The Medical Letter® on Drugs and Therapeutics Volume 58 (Issue 1497) June 20, 2016 Published ...
The FDA has approved reslizumab (Cinqair – Teva), a humanized interleukin-5 (IL-5) antagonist monoclonal antibody, for add-on maintenance treatment of severe asthma in adults who have an eosinophilic phenotype. It is the second IL-5 antagonist to be approved in the US; mepolizumab (Nucala) was approved for the same indication in 2015.
Med Lett Drugs Ther. 2016 Jun 20;58(1497):81-2 |  Show IntroductionHide Introduction

Sugammadex (Bridion) for Rapid Reversal of Neuromuscular Blockade

   
The Medical Letter on Drugs and Therapeutics • Aug 29, 2016  (Issue 1502)
The Medical Letter® on Drugs and Therapeutics Volume 58 (Issue 1502) August 29, 2016 Published ...
The FDA has approved sugammadex (Bridion – Merck), a selective relaxant binding agent, for reversal of rocuronium- or vecuronium-induced neuromuscular blockade in adult surgical patients. It is the first selective relaxant binding agent to be approved in the US. Sugammadex has been available in the European Union, Japan, and elsewhere for several years. Previous FDA reviews of sugammadex did not result in approval because of concerns about a risk of anaphylaxis and other hypersensitivity reactions with its use.
Med Lett Drugs Ther. 2016 Aug 29;58(1502):112-3 |  Show IntroductionHide Introduction

Ciprofloxacin/Fluocinolone (Otovel) for Otitis Media with Tympanostomy Tubes

   
The Medical Letter on Drugs and Therapeutics • Dec 05, 2016  (Issue 1509)
Clinical Trials Median Time Otorrhea Drug to Cessation Cessation Rate Regimen of Otorrhea at Day 22 ...
The FDA has approved Otovel (Arbor), a combination of the fluoroquinolone antibiotic ciprofloxacin 0.3% and the corticosteroid fluocinolone acetonide 0.025%, for otic treatment of acute otitis media with tympanostomy tubes (AOMT) in children ≥6 months old. It is the second fluoroquinolone/corticosteroid combination to be approved for this indication; ciprofloxacin 0.3%/dexamethasone 0.1% (Ciprodex) has been available for many years. In December 2015, a suspension of ciprofloxacin 6% (Otiprio) was approved for otic treatment of bilateral otitis media with effusion in children...
Med Lett Drugs Ther. 2016 Dec 5;58(1509):153-5 |  Show IntroductionHide Introduction

Imvexxy - Another Estradiol Vaginal Insert for Dyspareunia

   
The Medical Letter on Drugs and Therapeutics • Sep 10, 2018  (Issue 1555)
randomized to receive Table 1. Some Drugs for Vulvovaginal Atrophy (VVA) Drug Available Formulations Usual ...
The FDA has approved an estradiol softgel vaginal insert (Imvexxy – TherapeuticsMD) for treatment of postmenopausal women with moderate to severe dyspareunia due to vulvovaginal atrophy (VVA). Imvexxy is the second estradiol vaginal insert to be approved in the US; Vagifem, an intravaginal tablet formulation, was the first. Vagifem and Imvexxy are both available in inserts containing 10 mcg of estradiol; Imvexxy is also available in a 4-mcg strength.
Med Lett Drugs Ther. 2018 Sep 10;60(1555):147-8 |  Show IntroductionHide Introduction

Avacincaptad Pegol (Izervay) for Geographic Atrophy in Age-Related Macular Degeneration

   
The Medical Letter on Drugs and Therapeutics • Jan 22, 2024  (Issue 1694)
through 18 months of treatment.9 The drug did not signifi cantly reduce loss of visual acuity in either ...
The FDA has approved the complement C5 inhibitor avacincaptad pegol (Izervay – Iveric) for intravitreal treatment of geographic atrophy (GA) secondary to age-related macular degeneration (AMD). Avacincaptad pegol is the second complement inhibitor to be approved in the US for this indication; pegcetacoplan (Syfovre), a complement C3 and C3b inhibitor, was approved earlier.
Med Lett Drugs Ther. 2024 Jan 22;66(1694):15-6   doi:10.58347/tml.2024.1694d |  Show IntroductionHide Introduction

In Brief: Does Acetaminophen Increase Blood Pressure?

   
The Medical Letter on Drugs and Therapeutics • Apr 18, 2011  (Issue 1362)
The Medical Letter® On Drugs and Therapeutics Volume 53 (Issue 1362) April 18, 2011 ...
A recent article in Circulation reported that acetaminophen (Tylenol, and others; paracetamol outside the US) increased blood pressure in patients with coronary artery disease. This conclusion was based on a randomized, placebo-controlled crossover trial in 33 patients; acetaminophen 1 g three times daily for 2 weeks was associated with statistically significant increases in blood pressure of 2.9 mmHg systolic and 2.2 mmHg diastolic.1NSAIDs can increase blood pressure; the mechanism is thought to be inhibition of cyclooxygenase leading to decreased renal prostaglandin activity. Acetaminophen...
Med Lett Drugs Ther. 2011 Apr 18;53(1362):29 |  Show IntroductionHide Introduction

COVID-19 Update: Evusheld Unlikely to Neutralize XBB.1.5 Omicron Variant (online only)

   
The Medical Letter on Drugs and Therapeutics • Feb 06, 2023  (Issue 1669)
cases in the week ending January 14, 2023, up from 7% of cases 4 weeks earlier.4 1. FDA. Drug safety ...
The FDA has warned that the investigational long-acting monoclonal antibodies tixagevimab and cilgavimab (Evusheld – AstraZeneca) are unlikely to neutralize the XBB.1.5 Omicron variant of SARS-CoV-2. Evusheld is available under an Emergency Use Authorization (EUA) for IM pre-exposure prophylaxis of COVID-19 in persons ≥12 years old who weigh ≥40 kg and have either a history of a severe adverse reaction that prevents their vaccination against COVID-19 or moderate or severe immune compromise.
Med Lett Drugs Ther. 2023 Feb 6;65(1669):e25   doi:10.58347/tml.2023.1669e |  Show IntroductionHide Introduction

In Brief: Hyperthermia with Scopolamine Patches

   
The Medical Letter on Drugs and Therapeutics • Jun 30, 2025  (Issue 5114)
drug, is FDA-approved for prevention of nausea and vomiting associated with motion sickness ...
The FDA has required a new warning in the label for the scopolamine transdermal patch (Transderm-Scōp, and generics) about a risk of serious or fatal hyperthermia. Scopolamine, an anticholinergic drug, is FDA-approved for prevention of nausea and vomiting associated with motion sickness or recovery after surgery in adults; it is often used off-label to reduce drooling in children and adolescents with neurologic disorders.
Med Lett Drugs Ther. 2025 Jun 30;67(5114):1   doi:10.58347/tml.2025.5114a |  Show IntroductionHide Introduction

Finasteride and Minoxidil for Alopecia Revisited

   
The Medical Letter on Drugs and Therapeutics • Nov 21, 2005  (Issue 1222)
Letter ® On Drugs and Therapeutics IN THIS ISSUE Volume 47 (Issue 1222) November 21, 2005 ...
Finasteride and minoxidil continue to be the only drugs approved by the FDA to treat alopecia. Since these agents have different mechanisms of action, some clinicians have used both to treat hair loss in men.
Med Lett Drugs Ther. 2005 Nov 21;47(1222):95-6 |  Show IntroductionHide Introduction