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Searched for data. Results 41 to 50 of 372 total matches.
In Brief: Label Changes for Menopausal Hormone Therapy Products
The Medical Letter on Drugs and Therapeutics • Feb 16, 2026 (Issue 1748)
product labels will now include data
from the WHI trials in women 50-59 years old along ...
The FDA has requested the removal of some boxed
warnings from the labels of vaginal and systemic
menopausal hormone therapy (MHT) products. The
warnings were initially added in 2003 based on the
results of two placebo-controlled Women's Health
Initiative (WHI) trials evaluating the use of systemic
hormones for primary prevention of coronary heart
disease (CHD) in postmenopausal women 50-79
years old.
Med Lett Drugs Ther. 2026 Feb 16;68(1748):30-1 doi:10.58347/tml.2026.1748d | Show Introduction Hide Introduction
Semaglutide (Wegovy) for Weight Loss
The Medical Letter on Drugs and Therapeutics • Jul 12, 2021 (Issue 1628)
tumors (based on animal data; no
corroborating human data). The drug is contraindicated
in patients ...
The injectable glucagon-like peptide-1 (GLP-1)
receptor agonist semaglutide, previously approved
by the FDA as Ozempic to treat type 2 diabetes and
to reduce the risk of major adverse cardiovascular
events in adults with type 2 diabetes and established
cardiovascular disease, has now been approved in
a higher dose as Wegovy (Novo Nordisk) for chronic
weight management in adults with or without type 2
diabetes who have a body mass index (BMI) ≥30 kg/m2
or a BMI ≥27 kg/m2 and ≥1 weight-related comorbidity
(e.g., hypertension, dyslipidemia). An oral formulation
of semaglutide...
Prenatal Acetaminophen Use and Autism
The Medical Letter on Drugs and Therapeutics • Dec 08, 2025 (Issue 1743)
STUDIES — Data from observational studies
evaluating whether acetaminophen exposure in utero ...
Acetaminophen has been considered the drug
of choice for treatment of fever and pain during
pregnancy for decades, but a recent announcement
by the US Department of Health and Human Services
(HHS) has prompted discussion about its effects on
fetal neurodevelopment and the risk of autism.
Med Lett Drugs Ther. 2025 Dec 8;67(1743):193-5 doi:10.58347/tml.2025.1743a | Show Introduction Hide Introduction
Treatment of Clostridioides difficile Infection
The Medical Letter on Drugs and Therapeutics • Sep 06, 2021 (Issue 1632)
) September 6, 2021
mortality, but the data are mixed.11,12 If ileus is present,
administration ...
Clostridioides (formerly Clostridium) difficile infection
(CDI) is the most common infectious cause of
healthcare-associated diarrhea in adults. Guidelines
on management of CDI have recently been updated.
Three Drugs for Atopic Dermatitis (Adbry, Cibinqo, and Rinvoq)
The Medical Letter on Drugs and Therapeutics • Apr 03, 2023 (Issue 1673)
AND LACTATION — Limited data are
available on the safety of tralokinumab during
pregnancy. Human IgG ...
The subcutaneously injected interleukin-13 (IL-13)
antagonist tralokinumab-ldrm (Adbry – Leo) and
the oral Janus kinase (JAK) inhibitors abrocitinib
(Cibinqo – Pfizer) and upadacitinib (Rinvoq – Abbvie)
have been approved by the FDA for treatment of
moderate to severe atopic dermatitis.
Med Lett Drugs Ther. 2023 Apr 3;65(1673):51-5 doi:10.58347/tml.2023.1673b | Show Introduction Hide Introduction
Drugs for Gout
The Medical Letter on Drugs and Therapeutics • Oct 30, 2023 (Issue 1688)
has been associated with an increased risk of
miscarriage, but the data are weak. Use of an
NSAID beginning at 30 ...
Drugs for gout are used to reduce the pain and
inflammation of acute flares, decrease the frequency
of exacerbations, and lower serum urate levels to
prevent recurrent flares, development of tophi, and
joint damage.
Med Lett Drugs Ther. 2023 Oct 30;65(1688):169-75 doi:10.58347/tml.2023.1688a | Show Introduction Hide Introduction
Drugs for Opioid Use Disorder
The Medical Letter on Drugs and Therapeutics • Sep 04, 2023 (Issue 1684)
/day with Zubsolv). Data supporting the efficacy of doses >24 mg/day are limited.
3. Approved ...
Opioid use disorder is a chronic, relapsing disease with
physical and psychiatric components. It is associated
with economic hardship, social isolation, incarceration,
increased rates of blood-borne infections such as HIV
and viral hepatitis, adverse pregnancy outcomes, and
increased mortality. According to the NIH, there were
80,411 deaths involving an opioid in the US in 2021,
more than in any previous year. Several guidelines on
the management of opioid use disorder are available;
all recommend maintenance pharmacotherapy as the
standard of care.
Med Lett Drugs Ther. 2023 Sep 4;65(1684):137-44 doi:10.58347/tml.2023.1684a | Show Introduction Hide Introduction
Comparison Chart: Some Drugs for HFrEF
The Medical Letter on Drugs and Therapeutics • May 26, 2025 (Issue 1729)
of hospitalization for heart failure in patients with HFrEF, but it does not reduce mortality. Data on the benefits ...
View the Comparison Chart: Some Drugs for HFrEF
Med Lett Drugs Ther. 2025 May 26;67(1729):e1-15 doi:10.58347/tml.2025.1729b | Show Introduction Hide Introduction
In Brief: Abemaciclib (Verzenio) for Early Breast Cancer
The Medical Letter on Drugs and Therapeutics • Dec 13, 2021 (Issue 1639)
Data beyond 3 years are
not available.
Another CDK 4/6 Inhibitor – In a trial (Penelope-B)
in 1250 ...
The oral cyclin-dependent kinase (CDK) 4/6 inhibitor
abemaciclib (Verzenio – Lilly), which was approved
by the FDA in 2017 for treatment of hormone receptor
(HR)-positive, human epidermal growth factor
receptor 2 (HER2)-negative advanced or metastatic
breast cancer, has now been approved for use in
combination with endocrine therapy (tamoxifen or
an aromatase inhibitor) for adjuvant treatment of
patients with HR-positive, HER2-negative, node-positive,
early breast cancer at high risk of recurrence
and a Ki-67 score ≥20%.
Efgartigimod alfa (Vyvgart) for Myasthenia Gravis
The Medical Letter on Drugs and Therapeutics • Apr 18, 2022 (Issue 1648)
; concomitant use is not recommended.
PREGNANCY AND LACTATION — No data are available
on the use ...
Efgartigimod alfa-fcab (Vyvgart – Argenx), a first-in-class neonatal Fc receptor (FcRn) antagonist,
has been approved by the FDA for IV treatment of
generalized myasthenia gravis in adults who are
anti-acetylcholine receptor (AChR) antibody positive.
The IV complement inhibitor eculizumab (Soliris) was
approved for the same indication in 2017.
