Search Results for "viral"
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 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.
Med Lett Drugs Ther. 2022 Nov 28;64(1664):e193-4 |  Show IntroductionHide Introduction

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 IntroductionHide 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.
Med Lett Drugs Ther. 2021 Aug 9;63(1630):121 |  Show IntroductionHide Introduction

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 IntroductionHide 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 IntroductionHide 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 IntroductionHide 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.
Med Lett Drugs Ther. 2021 Sep 6;63(1632):143-4 |  Show IntroductionHide Introduction

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...
Med Lett Drugs Ther. 2021 Dec 27;63(1640):201-2 |  Show IntroductionHide Introduction

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.
Med Lett Drugs Ther. 2022 May 16;64(1650):76-7 |  Show IntroductionHide Introduction

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 IntroductionHide Introduction