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Searched for action. Results 31 to 40 of 338 total matches.

Comparison Table: Triptans for Migraine (online only)

   
The Medical Letter on Drugs and Therapeutics • Jun 12, 2023  (Issue 1678)
Nasal: 2.5, 5 mg/0.1 mL nasal spray Onset of Action 30-60 min 30-60 min ~2 hrs 1-3 hrs 30-60 min Tabs ...
View the Comparison Table: Triptans for Migraine
Med Lett Drugs Ther. 2023 Jun 12;65(1678):e97-9   doi:10.58347/tml.2023.1678b |  Show IntroductionHide Introduction

Ruxolitinib (Opzelura) for Atopic Dermatitis

   
The Medical Letter on Drugs and Therapeutics • Jan 24, 2022  (Issue 1642)
to moderate AD. It is modestly effective for short-term treatment.5 MECHANISM OF ACTION — The pathogenesis ...
The FDA has approved a 1.5% topical cream formulation of the Janus kinase (JAK) inhibitor ruxolitinib (Opzelura – Incyte) for short-term, non-continuous chronic treatment of mild to moderate atopic dermatitis (AD) in non-immunocompromised patients ≥12 years old whose disease has not been adequately controlled with other topical prescription drugs. Ruxolitinib is the first JAK inhibitor to be approved for topical use and the first to be approved in the US for treatment of AD. An oral formulation of ruxolitinib (Jakafi) is approved for treatment of myelofibrosis, polycythemia...
Med Lett Drugs Ther. 2022 Jan 24;64(1642):12-3 |  Show IntroductionHide Introduction

In Brief: A New Torsemide Formulation (Soaanz) for Edema (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024  (Issue 1709)
hours Duration of action 6-8 hours 6-8 hours Mean increase in potassium 12.7 mEq 5-15 mEq excretion ...
The FDA has approved Soaanz (Sarfez), a new formulation of the loop diuretic torsemide, for treatment of edema associated with heart failure or renal disease in adults. Torsemide has been available generically for years for treatment of hypertension and treatment of edema due to heart failure, renal disease, or hepatic disease. According to the manufacturer, Soaanz tablets are formulated to provide a gradual and sustained diuresis, lowering the risk of excessive urination and hypokalemia.
Med Lett Drugs Ther. 2024 Aug 19;66(1709):e141   doi:10.58347/tml.2024.1709h |  Show IntroductionHide Introduction

In Brief: Removal of Suicidality Warning from GLP-1 Agonists for Weight Management

   
The Medical Letter on Drugs and Therapeutics • Feb 16, 2026  (Issue 1748)
evaluation of reports of suicidal thoughts or actions in patients taking a certain type of medicines ...
The FDA has requested the removal of the suicidal behavior and ideation warning from the labels of the 3 glucagon-like peptide-1 (GLP-1) receptor agonists approved for chronic weight management: liraglutide (Saxenda), semaglutide (Wegovy), and tirzepatide (Zepbound). The warning was initially included in the labels of these drugs based on an increased risk of suicidal behavior and ideation observed with older weight loss drugs.
Med Lett Drugs Ther. 2026 Feb 16;68(1748):32   doi:10.58347/tml.2026.1748e |  Show IntroductionHide Introduction

Nalmefene Nasal Spray (Opvee) for Reversal of Opioid Overdose

   
The Medical Letter on Drugs and Therapeutics • Oct 16, 2023  (Issue 1687)
. Unlike naloxone, nalmefene has a longer duration of action than many opioid analgesics, which could ...
The FDA has approved an intranasal formulation of the opioid antagonist nalmefene (Opvee – Indivior) for emergency treatment of known or suspected opioid overdose in persons ≥12 years old. Nalmefene, which is available by prescription, is the second opioid antagonist to become available as a nasal spray for this indication; the first was naloxone, which is now available for sale over the counter (Narcan, and generic). Other nasal spray formulations of naloxone and injectable formulations of nalmefene and naloxone are available by prescription (see Table 2).
Med Lett Drugs Ther. 2023 Oct 16;65(1687):166-7   doi:10.58347/tml.2023.1687b |  Show IntroductionHide Introduction

DaxibotulinumtoxinA (Daxxify) for Frown Lines (online only)

   
The Medical Letter on Drugs and Therapeutics • Jul 22, 2024  (Issue 1707)
OF ACTION — Botulinum toxin type A, which is produced by Clostridium botulinum, blocks neuromuscular ...
The FDA has approved daxibotulinumtoxinA-lanm (Daxxify – Revance), an acetylcholine release inhibitor and neuromuscular blocking agent, for temporary improvement in the appearance of moderate to severe glabellar (frown) lines associated with corrugator and/or procerus muscle activity. Daxxify is the fifth botulinumtoxin type A product to be approved in the US for this indication (see Table 1). It is also approved for treatment of cervical dystonia in adults
Med Lett Drugs Ther. 2024 Jul 22;66(1707):e121-2   doi:10.58347/tml.2024.1707g |  Show IntroductionHide Introduction

Nalmefene Autoinjector (Zurnai) for Reversal of Opioid Overdose

   
The Medical Letter on Drugs and Therapeutics • Jan 19, 2026  (Issue 1746)
is not possible, a single IM or SC dose of 1 mg is an alternative, but the onset of action may be delayed ...
Zurnai (Purdue), an autoinjector formulation of the opioid antagonist nalmefene, has been approved by the FDA for intramuscular (IM) or subcutaneous (SC) emergency treatment of known or suspected opioid overdose in persons ≥12 years old. Naloxone, another opioid antagonist, has been available in single-use syringes for years. Both nalmefene and naloxone are also available in nasal sprays; some naloxone nasal sprays (Narcan, and others) are available over the counter.
Med Lett Drugs Ther. 2026 Jan 19;68(1746):10-2   doi:10.58347/tml.2026.1746b |  Show IntroductionHide Introduction

In Brief: Melphalan (Hepzato) for Uveal Melanoma (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 04, 2023  (Issue 1684)
of multiple myeloma. MECHANISM OF ACTION — Melphalan is an alkylating agent that binds to the N7 position ...
...
Med Lett Drugs Ther. 2023 Sep 4;65(1684):e148   doi:10.58347/tml.2023.1684d |  Show IntroductionHide Introduction

COVID-19 Updates

   
The Medical Letter on Drugs and Therapeutics • Feb 21, 2022  (Issue 1644)
(Veklury) for COVID-19. Med Lett Drugs Ther 2020; 62:186. 2. FDA News Release. FDA takes actions ...
The IV antiviral drug remdesivir (Veklury – Gilead) has been available for treatment of COVID-19 in hospitalized patients since 2020. Now, the FDA has approved remdesivir for treatment of mild to moderate COVID-19 in outpatients ≥12 years old who weigh ≥40 kg and are at high risk for progression to severe disease, including hospitalization or death; they also issued an Emergency Use Authorization (EUA) allowing its use in any other high-risk outpatient who weighs ≥3.5 kg.
Med Lett Drugs Ther. 2022 Feb 21;64(1644):31-2 |  Show IntroductionHide Introduction

Relyvrio for ALS

   
The Medical Letter on Drugs and Therapeutics • Nov 28, 2022  (Issue 1664)
. MECHANISM OF ACTION ― The exact mechanism of action of sodium phenylbutyrate/taurursodiol in ALS ...
The FDA has approved Relyvrio (Amylyx), a fixed-dose combination of sodium phenylbutyrate and taurursodiol, for treatment of amyotrophic lateral sclerosis (ALS). Sodium phenylbutyrate (Buphenyl, and others) has been available by prescription for years for treatment of urea cycle disorders. Taurursodiol (tauroursodeoxycholic acid), a derivative of ursodiol, is an over-the-counter bile acid supplement claimed to have neuroprotective benefits. Relyvrio is the third drug to be approved in the US for treatment of ALS; riluzole (Rilutek, and others) and edaravone (Radicava, Radicava...
Med Lett Drugs Ther. 2022 Nov 28;64(1664):190-1 |  Show IntroductionHide Introduction