Search Results for "Pregnancy"
Search again or select article below to purchase. Single article price: $45. Order 3 or more at one time and receive a 10% discount.
Sort by relevance | Sort by date
Searched for Pregnancy. Results 111 to 120 of 355 total matches.
Emrosi — Low-Dose, Biphasic Oral Minocycline for Rosacea
The Medical Letter on Drugs and Therapeutics • Jan 20, 2025 (Issue 1720)
.
PREGNANCY AND LACTATION — Because of their
adverse effects on tooth and bone development,
tetracyclines ...
Emrosi (Journey), an oral, low-dose, biphasic-release
formulation of the tetracycline antibiotic minocycline,
has been approved by the FDA for once-daily
treatment of inflammatory lesions of rosacea (papules
and pustules) in adults. Low-dose, biphasic-release
doxycycline (Oracea, and generics) has been available
for years for treatment of papulopustular rosacea.
Med Lett Drugs Ther. 2025 Jan 20;67(1720):10-1 doi:10.58347/tml.2025.1720b | Show Introduction Hide Introduction
Dupilumab (Dupixent) for COPD
The Medical Letter on Drugs and Therapeutics • Jan 20, 2025 (Issue 1720)
should
be avoided in patients being treated with dupilumab.
PREGNANCY AND LACTATION — Dupilumab ...
The FDA has approved the subcutaneously injected
interleukin (IL)-4 receptor alpha antagonist dupilumab
(Dupixent – Sanofi/Regeneron) for add-on maintenance
treatment of adults with inadequately controlled
chronic obstructive pulmonary disease (COPD) and an
eosinophilic phenotype. Dupilumab is the first biologic
drug to be approved in the US for this indication. It has
been available for years for treatment of asthma, atopic
dermatitis, chronic rhinosinusitis with nasal polyps,
eosinophilic esophagitis, and prurigo nodularis.
Med Lett Drugs Ther. 2025 Jan 20;67(1720):11-3 doi:10.58347/tml.2025.1720c | Show Introduction Hide Introduction
Drugs for Asthma
The Medical Letter on Drugs and Therapeutics • Nov 25, 2024 (Issue 1716)
and for as long as 24
hours after administration.
PREGNANCY — Poorly controlled asthma symptoms
and acute ...
The goal of asthma treatment is to control symptoms,
prevent exacerbations, and maintain normal lung
function. Management of acute exacerbations in the
emergency department is not discussed here.
Med Lett Drugs Ther. 2024 Nov 25;66(1716):185-92 doi:10.58347/tml.2024.1716a | Show Introduction Hide Introduction
Nonopioid Drugs for Pain
The Medical Letter on Drugs and Therapeutics • Mar 07, 2022 (Issue 1645)
) in some
patients.7
Pregnancy – Occasional use of oral acetaminophen
during pregnancy is generally ...
Nonopioid drugs can be used in the treatment of
many nociceptive and neuropathic pain conditions.
For severe pain, especially severe chronic cancer
pain, use of opioids may be necessary. Noninvasive
nonpharmacologic treatments, including physical
and psychological therapies, have been shown to
improve pain and function in patients with some
common chronic pain conditions and are unlikely
to cause serious harms. A multimodal approach to
analgesic therapy can increase pain control while
reducing opioid use and adverse effects.
FDA Authorizes Johnson & Johnson COVID-19 Vaccine
The Medical Letter on Drugs and Therapeutics • Mar 22, 2021 (Issue 1620)
guidance on management of
anaphylaxis risk related to COVID-19 vaccination.7
PREGNANCY AND LACTATION ...
On February 27, 2021, the FDA issued an Emergency
Use Authorization (EUA) for the Johnson & Johnson
adenovirus-based vaccine for prevention of COVID-19
in persons ≥18 years old. It is the third COVID-19
vaccine to become available in the US and the first to
require only a single dose. Two-dose mRNA-based
vaccines manufactured by Pfizer-BioNTech and
Moderna received EUAs in December 2020.
Vericiguat (Verquvo) for Heart Failure
The Medical Letter on Drugs and Therapeutics • Mar 08, 2021 (Issue 1619)
-5 (PDE5)
inhibitors such as sildenafil (Viagra, and others) is not
recommended.
PREGNANCY ...
The FDA has approved vericiguat (Verquvo – Merck),
an oral soluble guanylate cyclase (sGC) stimulator,
to reduce the risk of hospitalization for heart failure
and cardiovascular (CV) death following a worsening
heart failure event (hospitalization for heart failure or
treatment with IV diuretics as an outpatient) in patients
with symptomatic chronic heart failure and left
ventricular ejection fraction (LVEF) <45%. Vericiguat
is the second sGC stimulator to be marketed in the
US. Riociguat (Adempas), which is FDA-approved
for treatment of pulmonary arterial hypertension...
Evinacumab (Evkeeza) for Homozygous Familial Hypercholesterolemia
The Medical Letter on Drugs and Therapeutics • May 03, 2021 (Issue 1623)
, and
nausea. Anaphylaxis occurred in one patient who
received the drug.
PREGNANCY AND LACTATION — Evinacumab ...
The FDA has approved evinacumab-dgnb (Evkeeza –
Regeneron), an angiopoietin-like 3 (ANGPTL3) inhibitor,
for adjunctive IV treatment of homozygous familial
hypercholesterolemia (HoFH) in patients ≥12 years
old. Evinacumab is the first ANGPTL3 inhibitor to be
approved in the US.
Comparison Table: H2-Receptor Antagonists and PPIs (online only)
The Medical Letter on Drugs and Therapeutics • Apr 04, 2022 (Issue 1647)
use
Pregnancy: Generally safe, but
no adequate human studies in
pregnant women
May decrease serum ...
View the Comparison Table: H2-Receptor Antagonists and PPIs
Semaglutide (Wegovy) for Weight Loss
The Medical Letter on Drugs and Therapeutics • Jul 12, 2021 (Issue 1628)
of oral drugs in
the small intestine.
PREGNANCY AND LACTATION — Administration of
semaglutide ...
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...
Penbraya: A Pentavalent Meningococcal Vaccine
The Medical Letter on Drugs and Therapeutics • Mar 18, 2024 (Issue 1698)
the 30 days after vaccination.
PREGNANCY AND LACTATION — Penbraya has not
been studied in pregnant ...
The FDA has licensed Penbraya (Pfizer), a pentavalent
polysaccharide conjugate meningococcal
vaccine, for prevention of invasive meningococcal
disease caused by Neisseria meningitidis
serogroups A, B, C, W, or Y (MenABCWY) in persons
10-25 years old. Penbraya is the only meningococcal
vaccine that contains all five of these serogroups.
Two quadrivalent polysaccharide conjugate
meningococcal vaccines containing serogroups A,
C, W, and Y (MenACWY; Menveo, MenQuadfi) and
two meningococcal serogroup B vaccines (MenB;
Bexsero, Trumenba) are available in the US (see
Table...
Med Lett Drugs Ther. 2024 Mar 18;66(1698):43-5 doi:10.58347/tml.2024.1698b | Show Introduction Hide Introduction