Search Results for "viral"
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Searched for viral. Results 11 to 20 of 47 total matches.
Maribavir (Livtencity) for Cytomegalovirus Infection (online only)
The Medical Letter on Drugs and Therapeutics • Nov 28, 2022 (Issue 1664)
strains.1,2
MECHANISM OF ACTION — Maribavir inhibits CMV
pUL97 kinase, resulting in inhibition of viral ...
Maribavir (Livtencity – Takeda), an oral cytomegalovirus
(CMV) pUL97 kinase inhibitor, has been
approved by the FDA for treatment of post-transplant
CMV infection refractory to standard antiviral therapy
in patients ≥12 years old who weigh at least 35 kg.
Dupilumab (Dupixent) for COPD
The Medical Letter on Drugs and Therapeutics • Jan 20, 2025 (Issue 1720)
with placebo) were
viral infection, headache, and nasopharyngitis.
DRUG INTERACTIONS — Use of live vaccines ...
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
In Brief: Guillain-Barré Syndrome with the Johnson & Johnson COVID-19 Vaccine
The Medical Letter on Drugs and Therapeutics • Aug 09, 2021 (Issue 1630)
in the US. In many cases, GBS
occurs following a viral or bacterial infection, including
COVID-19.4 The syndrome ...
On July 12, 2021, the FDA added a warning to the
Fact Sheet for the Johnson & Johnson (Janssen)
adenovirus-based COVID-19 vaccine about an
increased risk of Guillain-Barré syndrome (GBS)
following administration of the product.
Fitusiran (Qfitlia) for Hemophilia A and B
The Medical Letter on Drugs and Therapeutics • Jul 07, 2025 (Issue 1732)
with hemophilia A or B with and without inhibitors.
▶ Adverse Effects: Most common were bacterial and viral ...
Fitusiran (Qfitlia – Sanofi), a subcutaneously injected,
antithrombin-directed, small interfering ribonucleic
acid (siRNA), has been approved by the FDA for routine
prophylaxis to prevent or reduce the frequency of
bleeding episodes in patients ≥12 years old who have
hemophilia A with or without factor VIII inhibitors or
hemophilia B with or without factor IX inhibitors. It
is the first antithrombin-lowering therapy to become
available in the US for treatment of hemophilia.
Med Lett Drugs Ther. 2025 Jul 7;67(1732):110-1 doi:10.58347/tml.2025.1732c | Show Introduction Hide Introduction
Teplizumab (Tzield) to Delay Onset of Type 1 Diabetes
The Medical Letter on Drugs and Therapeutics • Jan 09, 2023 (Issue 1667)
in 0.9% of
patients treated with the drug. Serious bacterial and
viral infections have been reported ...
Teplizumab-mzwv (Tzield – Provention Bio), an anti-CD3 monoclonal antibody, has been approved by the
FDA to delay the onset of stage 3 type 1 diabetes
in patients ≥8 years old who have stage 2 type 1
diabetes. It is the first drug to become available in the
US that delays the onset of type 1 diabetes.
Med Lett Drugs Ther. 2023 Jan 9;65(1667):7-8 doi:10.58347/tml.2023.1667c | Show Introduction Hide Introduction
In Brief: New Warning for the RSV Vaccines Arexvy and Abrysvo
The Medical Letter on Drugs and Therapeutics • Feb 17, 2025 (Issue 1722)
in the US; the syndrome is more
common in men and in those >50 years old. In many
cases, GBS occurs following a viral ...
The FDA has required a new warning in the labels of the
recombinant respiratory syncytial virus (RSV) vaccines
Arexvy (GSK) and Abrysvo (Pfizer) about an increased
risk of Guillain-Barré syndrome (GBS) within 42 days
of administration of either vaccine. Both vaccines
are FDA-approved to prevent lower respiratory tract
disease (LRTD) caused by RSV in adults.Abrysvo is
also approved for use in pregnant women at 32-36
weeks' gestation to prevent RSV-associated LRTD in
their infants from birth through 6 months of age.
Med Lett Drugs Ther. 2025 Feb 17;67(1722):31-2 doi:10.58347/tml.2025.1722d | Show Introduction Hide Introduction
Rilonacept (Arcalyst) for Recurrent Pericarditis
The Medical Letter on Drugs and Therapeutics • Sep 06, 2021 (Issue 1632)
— Pericarditis can result from infectious
and noninfectious causes, including viral infections,
tuberculosis ...
Rilonacept (Arcalyst – Kiniksa), an interleukin-1 (IL-1)
antagonist that has been available for years for
treatment of cryopyrin-associated periodic syndromes,
has now been approved by the FDA for treatment
of recurrent pericarditis and prevention of further
recurrences in patients ≥12 years old. It is the first drug
to be approved in the US for this indication. Anakinra
(Kineret), an IL-1 receptor antagonist FDA-approved for
treatment of rheumatoid arthritis, has been used off-label
for years for treatment of recurrent pericarditis.
In Brief: Booster Doses of mRNA-Based COVID-19 Vaccines for All Adults
The Medical Letter on Drugs and Therapeutics • Dec 27, 2021 (Issue 1640)
primary dose primary dose
vp = viral particles
1. CDC. COVID-19 vaccine booster shots. November 29, 2021 ...
On November 19, the FDA expanded the Emergency Use
Authorizations (EUAs) for the mRNA-based COVID-19
vaccines manufactured by Pfizer/BioNTech (Comirnaty)
and Moderna (Spikevax) to include administration
of a booster dose for all adults ≥18 years old after
primary immunization with either the same COVID-19
vaccine or a different one. Booster doses of these
vaccines were previously authorized only for select
populations (age ≥65 years or persons at high risk for
severe COVID-19). The EUA for the adenovirus-based
vaccine manufactured by Johnson & Johnson was
amended in October 2021...
Delayed-Release Budesonide (Tarpeyo) for Primary Immunoglobulin A Nephropathy
The Medical Letter on Drugs and Therapeutics • May 16, 2022 (Issue 1650)
,
bacterial, systemic viral or parasitic infections, or
ocular herpes simplex.
The Medical Letter ® Vol. 64 ...
The FDA has approved Tarpeyo (Calliditas), a delayed-release
capsule formulation of the corticosteroid
budesonide, to reduce proteinuria in adults with
primary immunoglobulin A nephropathy (IgAN; also
called Berger's disease) who are at risk of rapid
disease progression. It is the fi rst drug to be approved
in the US for this indication. Oral formulations
of budesonide have been available for years for
treatment of inflammatory bowel disease.
Upadacitinib (Rinvoq) for Giant Cell Arteritis
The Medical Letter on Drugs and Therapeutics • Jul 21, 2025 (Issue 1733)
be screened for
tuberculosis (TB) and viral hepatitis, and a complete
blood count should be performed ...
The oral Janus kinase (JAK) inhibitor upadacitinib
(Rinvoq – Abbvie) has been approved by the FDA
for treatment of giant cell arteritis. Upadacitinib
was approved earlier for treatment of rheumatoid
arthritis, psoriatic arthritis, ankylosing spondylitis,
nonradiographic axial spondyloarthritis, atopic dermatitis,
ulcerative colitis, and Crohn's disease.
Med Lett Drugs Ther. 2025 Jul 21;67(1733):114-5 doi:10.58347/tml.2025.1733b | Show Introduction Hide Introduction
