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Searched for data. Results 211 to 220 of 372 total matches.
A Fixed-Dose Combination of Meloxicam and Rizatriptan (Symbravo) for Migraine
The Medical Letter on Drugs and Therapeutics • Apr 28, 2025 (Issue 1727)
arteriosus and
persistent pulmonary hypertension in the neonate and
should be avoided.
No adequate data ...
The FDA has approved Symbravo (Axsome), an oral
fixed-dose combination of the nonsteroidal anti-inflammatory
drug (NSAID) meloxicam and the
5-HT1B/1D receptor agonist (triptan) rizatriptan (Maxalt,
and generics), for acute treatment of migraine with or
without aura in adults. It is the second combination
of an NSAID and a triptan to be approved for migraine
treatment. An oral fixed-dose combination of
sumatriptan and naproxen (Treximet, and generics) is
approved for use in patients ≥12 years old.
Med Lett Drugs Ther. 2025 Apr 28;67(1727):68-70 doi:10.58347/tml.2025.1727b | Show Introduction Hide Introduction
Drugs and Devices for Weight Management
The Medical Letter on Drugs and Therapeutics • May 30, 2022 (Issue 1651)
with no history of seizures. Unlike phentermine
alone, Qsymia is FDA-approved for use beyond 3
months. Data ...
Adults with a body mass index (BMI) between 25
and 29.9 kg/m2 are considered overweight. Those
with a BMI ≥30 are considered obese. The initial
recommendation for any weight loss effort is to
achieve a 5-10% reduction in weight, which has been
associated with a reduction in the risk of developing
type 2 diabetes, hypertension, and dyslipidemia. Diet,
exercise, and behavior modification are the preferred
methods for losing weight, but long-term weight
maintenance can be difficult. Several drugs and
devices are FDA-approved for weight reduction and
maintenance of weight...
Lipid-Lowering Drugs
The Medical Letter on Drugs and Therapeutics • Sep 19, 2022 (Issue 1659)
dose of ezetimibe. The
drug has been detected in the milk of lactating rats.
No data are available ...
Cholesterol management guidelines from the
American College of Cardiology/American Heart
Association Task Force were last published in 2019.
Drugs for Irritable Bowel Syndrome
The Medical Letter on Drugs and Therapeutics • Feb 03, 2025 (Issue 1721)
, garlic,
milk, yogurt, wheat, high-fructose corn syrup, and
artificial sweeteners. Data on the efficacy ...
Irritable bowel syndrome (IBS) is a common disorder
characterized by recurrent abdominal pain and altered
bowel habits, often accompanied by bloating. IBS
is classified by its predominant bowel symptom:
constipation (IBS-C), diarrhea (IBS-D), mixed type
(IBS-M), or unclassified (IBS-U). Since the exact cause
of IBS is unknown, the goal of treatment is symptom
control. Some over-the-counter (OTC) products and
prescription drugs for IBS are listed in Tables 1-4. The
safety of these drugs during pregnancy and lactation
is described in Table 5 (online only).
Med Lett Drugs Ther. 2025 Feb 3;67(1721):17-24 doi:10.58347/tml.2025.1721a | Show Introduction Hide Introduction
Avapritinib (Ayvakit) for GIST
The Medical Letter on Drugs and Therapeutics • Feb 08, 2021 (Issue 1617)
) February 8, 2021
No data are available on the presence of avapritinib
in human breast milk or on its ...
The FDA has approved the oral tyrosine kinase
inhibitor avapritinib (Ayvakit – Blueprint Medicines)
for treatment of unresectable or metastatic gastrointestinal
stromal tumors (GISTs) harboring a
platelet-derived growth factor receptor alpha
(PDGFRA) D842V or other PDGFRA exon 18 mutation.
Avapritinib is the first drug to be approved for this
indication in the US.
Difelikefalin (Korsuva) for Chronic Kidney Disease-Associated Pruritus
The Medical Letter on Drugs and Therapeutics • Feb 07, 2022 (Issue 1643)
AND LACTATION — No data are
available on the use of difelikefalin in pregnant or
lactating women. In animal ...
Difelikefalin (Korsuva – Vifor), an IV kappa opioid
receptor (KOR) agonist, has been approved by the
FDA for treatment of moderate to severe pruritus
associated with chronic kidney disease (CKD) in
adults on hemodialysis. It is the first drug to be
approved for this indication and the first KOR agonist
to become available in the US. Difelikefalin has not
been studied in patients on peritoneal dialysis.
Zimhi - A Higher-Dose Injectable Naloxone for Opioid Overdose
The Medical Letter on Drugs and Therapeutics • Apr 18, 2022 (Issue 1648)
. No
clinical data are available on when to use this higher
dose of the drug. Higher doses can increase ...
The FDA has approved a higher-dose injectable
formulation of the opioid antagonist naloxone
(Zimhi – Adamis) for emergency treatment of opioid
overdose. A single IM or SC injection of the new
formulation delivers 5 mg of naloxone; injectable
formulations that deliver 0.4 mg or 2 mg of the drug
have been available for years. Naloxone is also
available in intranasal formulations for the same
indication (see Table 1).
Idecabtagene Vicleucel (Abecma) for Multiple Myeloma (online only)
The Medical Letter on Drugs and Therapeutics • Nov 14, 2022 (Issue 1663)
and is not recommended for use during
pregnancy or while breastfeeding. There are no data
on the presence ...
The FDA has approved idecabtagene vicleucel
(Abecma – BMS), a B-cell maturation antigen (BCMA)-directed genetically-modified cellular product, for
treatment of relapsed or refractory multiple myeloma in
adults who received ≥4 prior lines of therapy, including
a proteasome inhibitor, an immunomodulatory drug,
and an anti-CD38 monoclonal antibody. Abecma is
an individualized cellular product prepared from the
patient’s own T cells, which are genetically modified
to express chimeric antigen receptors (CAR) and
then infused back into the patient. Ciltacabtagene
autoleucel...
Pirtobrutinib (Jaypirca): A Fourth Bruton's Tyrosine Kinase Inhibitor for Mantle Cell Lymphoma (online only)
The Medical Letter on Drugs and Therapeutics • Feb 20, 2023 (Issue 1670)
week after the last dose.
No data are available on the effects of pirtobrutinib
on the breastfed ...
The Bruton's tyrosine kinase (BTK) inhibitor
pirtobrutinib (Jaypirca – Lilly) has received
accelerated approval from the FDA for treatment of
relapsed or refractory mantle cell lymphoma (MCL) in
adults who received ≥2 prior lines of systemic therapy,
including a BTK inhibitor. Accelerated approval was
based on the response rate. The BTK inhibitors
ibrutinib (Imbruvica), acalabrutinib (Calquence),
and zanubrutinib (Brukinsa) are also approved for
treatment of MCL.
Med Lett Drugs Ther. 2023 Feb 20;65(1670):e35-6 doi:10.58347/tml.2023.1670f | Show Introduction Hide Introduction
In Brief: Cardiovascular Outcomes with Bempedoic Acid (Nexletol)
The Medical Letter on Drugs and Therapeutics • Apr 17, 2023 (Issue 1674)
– Esperion) in 2020,1
cardiovascular outcomes data in statin-intolerant
patients have become available ...
Since our initial review of the oral lipid-lowering
adenosine triphosphate-citrate lyase (ACL) inhibitor
bempedoic acid (Nexletol – Esperion) in 2020,
cardiovascular outcomes data in statin-intolerant
patients have become available.
Med Lett Drugs Ther. 2023 Apr 17;65(1674):62-3 doi:10.58347/tml.2023.1674b | Show Introduction Hide Introduction