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Searched for data. Results 121 to 130 of 372 total matches.

Gepirone (Exxua) for Depression

   
The Medical Letter on Drugs and Therapeutics • Jun 24, 2024  (Issue 1705)
AND LACTATION — No adequate data on gepirone use during pregnancy are available. In animal studies, gepirone ...
The FDA has approved an oral extended-release formulation of gepirone (Exxua – Fabre-Kramer), a selective 5-HT1A receptor agonist, for treatment of major depressive disorder (MDD) in adults. Gepirone was originally developed decades ago for treatment of anxiety and depression, but it was not approved by the FDA for such use. Gepirone is structurally related to buspirone, which is FDA-approved for treatment of anxiety.
Med Lett Drugs Ther. 2024 Jun 24;66(1705):97-9   doi:10.58347/tml.2024.1705a |  Show IntroductionHide Introduction

Qlosi — Pilocarpine 0.4% Ophthalmic Solution for Presbyopia

   
The Medical Letter on Drugs and Therapeutics • Jan 06, 2025  (Issue 1719)
after ocular administration. No adequate data are available on the use of pilocarpine 0.4% ophthalmic ...
The FDA has approved pilocarpine 0.4% preservativefree ophthalmic solution (Qlosi – Orasis) for treatment of presbyopia in adults. Pilocarpine 1.25% ophthalmic solution (Vuity) was approved in 2021 for the same indication. Pilocarpine 1%, 2%, and 4% ophthalmic solutions (Isopto Carpine, and others) have been available for years for treatment of glaucoma, but local (e.g., blurry vision and instillation-site pain) and systemic (e.g., sweating and GI disturbances) adverse effects have limited their use.
Med Lett Drugs Ther. 2025 Jan 6;67(1719):5-6   doi:10.58347/tml.2025.1719b |  Show IntroductionHide Introduction

Risankizumab (Skyrizi) for Ulcerative Colitis

   
The Medical Letter on Drugs and Therapeutics • Nov 11, 2024  (Issue 1715)
). No adequate data on risankizumab use in pregnant women are available. Increased fetal/infant loss occurred ...
The injectable interleukin (IL)-23 antagonist risankizumab-rzza (Skyrizi – Abbvie), previously approved by the FDA for treatment of Crohn's disease (CD), has now been approved for treatment of moderately to severely active ulcerative colitis (UC) in adults. Risankizumab is the first IL-23 antagonist to be approved for treatment of both CD and UC. It is also approved for treatment of plaque psoriasis and psoriatic arthritis.
Med Lett Drugs Ther. 2024 Nov 11;66(1715):182-4   doi:10.58347/tml.2024.1715d |  Show IntroductionHide Introduction

A Renal Indication for Semaglutide (Ozempic)

   
The Medical Letter on Drugs and Therapeutics • Mar 03, 2025  (Issue 1723)
(based on animal data; no corroborating human data). These drugs are contraindicated in patients ...
The injectable glucagon-like peptide-1 (GLP-1) receptor agonist semaglutide (Ozempic – Novo Nordisk) has been approved by the FDA to reduce the risk of sustained eGFR decline, end-stage kidney disease, and cardiovascular death in adults with type 2 diabetes and chronic kidney disease (CKD). It is the first GLP-1 receptor agonist to be approved in the US for this indication.
Med Lett Drugs Ther. 2025 Mar 3;67(1723):38-40   doi:10.58347/tml.2025.1723d |  Show IntroductionHide Introduction

Lenacapavir (Yeztugo) for HIV Pre-Exposure Prophylaxis

   
The Medical Letter on Drugs and Therapeutics • Aug 18, 2025  (Issue 1735)
intercourse (because of insufficient data). Both combinations have significantly decreased the rate of HIV ...
The FDA has approved oral and injectable formulations of the HIV-1 capsid inhibitor lenacapavir (Yeztugo – Gilead) for pre-exposure prophylaxis (PrEP) to reduce the risk of sexually acquired HIV-1 in at-risk adolescents and adults. Lenacapavir is the first drug to be approved for this indication that is given twice-yearly; other drugs approved for this indication are given once daily or once every 2 months. Lenacapavir was approved in 2022 as Sunlenca for use with other antiretroviral drugs to treat multidrug-resistant HIV-1 infection (MDR-HIV) in heavily treatment-experienced...
Med Lett Drugs Ther. 2025 Aug 18;67(1735):132-4   doi:10.58347/tml.2025.1735c |  Show IntroductionHide Introduction

Donidalorsen (Dawnzera) for Prevention of Hereditary Angioedema Attacks

   
The Medical Letter on Drugs and Therapeutics • Jan 19, 2026  (Issue 1746)
) have been effective in patients with normal C1INH levels, but data are limited.8 MECHANISM OF ACTION ― Donidalorsen ...
Donidalorsen (Dawnzera – Ionis), a subcutaneously injected prekallikrein-directed antisense oligonucleotide, has been approved by the FDA for prevention of hereditary angioedema (HAE) attacks in patients ≥12 years old. It is the first RNA-targeted drug to be approved in the US for this indication.
Med Lett Drugs Ther. 2026 Jan 19;68(1746):12-4   doi:10.58347/tml.2026.1746c |  Show IntroductionHide Introduction

In Brief: Suspension of Johnson & Johnson COVID-19 Vaccine Lifted (online only)

   
The Medical Letter on Drugs and Therapeutics • May 17, 2021  (Issue 1624)
of TTS, but after completing a data review that identified a further 9 cases associated ...
On April 23, 2021, on advice from the Advisory Committee on Immunization Practices (ACIP), the FDA and CDC recommended that use of the Johnson & Johnson adenovirus-based COVID-19 vaccine resume despite its association with development of thrombosis with thrombocytopenia syndrome (TTS). Administration of the vaccine had been paused on April 13 because of 6 reports of TTS, but after completing a data review that identified a further 9 cases associated with the formulation, the agencies concluded that the benefits of the vaccine outweighed its risks. About 7.98 million doses of the...
Med Lett Drugs Ther. 2021 May 17;63(1624):e1 |  Show IntroductionHide Introduction

In Brief: Over-the-Counter Narcan Nasal Spray

   
The Medical Letter on Drugs and Therapeutics • May 01, 2023  (Issue 1675)
of opioid overdose. Approval of the OTC sale of Narcan was based on data demonstrating that the drug ...
The FDA has approved the over-the-counter (OTC) sale of Narcan (Emergent), a nasal spray that delivers 4 mg of the opioid antagonist naloxone. Narcan nasal spray has been available by prescription since 2015 for emergency treatment of opioid overdose. Generic formulations of Narcan have also been approved; the manufacturers of these products will be required to switch them to OTC status and amend their labeling accordingly. Kloxxado, an 8-mg naloxone nasal spray, remains available only by prescription.
Med Lett Drugs Ther. 2023 May 1;65(1675):72   doi:10.58347/tml.2023.1675e |  Show IntroductionHide Introduction

In Brief: Wezlana — An Ustekinumab Biosimilar Interchangeable with Stelara

   
The Medical Letter on Drugs and Therapeutics • Jul 22, 2024  (Issue 1707)
to psoriatic arthritis, Crohn's disease, and ulcerative colitis based on available data.1-3 According ...
The FDA has approved ustekinumab-auub (Wezlana – Amgen), an interchangeable biosimilar product similar to the interleukin-12 and -23 antagonist Stelara, for treatment of the same indications as Stelara (see Table 1). Wezlana is the first Stelara biosimilar to be approved in the US.
Med Lett Drugs Ther. 2024 Jul 22;66(1707):119   doi:10.58347/tml.2024.1707e |  Show IntroductionHide Introduction

In Brief: Low-Dose Chlorthalidone (HemiClor) for Hypertension

   
The Medical Letter on Drugs and Therapeutics • Jul 21, 2025  (Issue 1733)
- mg formulation was based on data from an 8-week double-blind trial in 1714 adults with hypertension ...
The FDA has approved a 12.5-mg tablet formulation of the thiazide-like diuretic chlorthalidone (HemiClor – Ingenus) for treatment of hypertension. Chlorthalidone has been available for years in 15-, 25-, and 50-mg tablets (Thalitone, and generics) and in fixed-dose combinations with azilsartan medoxomil (Edarbyclor) and atenolol (Tenoretic, and generics).
Med Lett Drugs Ther. 2025 Jul 21;67(1733):118   doi:10.58347/tml.2025.1733e |  Show IntroductionHide Introduction