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