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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 Introduction Hide 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 Introduction Hide 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 Introduction Hide 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 Introduction Hide 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 Introduction Hide 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 Introduction Hide 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...
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 Introduction Hide 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 Introduction Hide 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 Introduction Hide Introduction
