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Searched for activate. Results 251 to 260 of 1345 total matches.

Two Neuraminidase Inhibitors for Treatment of Influenza

   
The Medical Letter on Drugs and Therapeutics • Oct 08, 1999  (Issue 1063)
− Medical Letter, 35:109, 1993). Their use has been limited by lack of activity against influenza B, rapid ...
Zanamivir, a neuraminidase inhibitor taken by inhalation, has been approved by the FDA for treatment of influenza. Oseltamivir phosphate, an oral neuraminidase inhibitor, will probably be approved soon.
Med Lett Drugs Ther. 1999 Oct 8;41(1063):91-3 |  Show IntroductionHide Introduction

Lopinavir/Ritonavir: A Protease-inhibitor Combination

   
The Medical Letter on Drugs and Therapeutics • Jan 08, 2001  (Issue 1095)
is a potent inhibitor of CYP3A4 activity and raises lopinavir plasma levels. When used in combination ...
Lopinavir/ritonavir is the first fixed-dose combination of protease inhibitors approved by the FDA for the treatment of HIV infection. It is being marketed for use with other drugs in adults and children more than six months old. Lopinavir is a new drug available only in this combination. Ritonavir is often used with other protease inhibitors to raise their plasma concentrations.
Med Lett Drugs Ther. 2001 Jan 8;43(1095):1-2 |  Show IntroductionHide Introduction

Bamlanivimab and Etesevimab for Post-Exposure Prophylaxis of COVID-19

   
The Medical Letter on Drugs and Therapeutics • Oct 18, 2021  (Issue 1635)
activity than bamlanivimab alone, the FDA presumed it to be effective based on the results of BLAZE-2 Part ...
In February 2021, the FDA issued an Emergency Use Authorization (EUA) for the investigational monoclonal antibodies bamlanivimab and etesevimab (Lilly) for use together to treat mild to moderate COVID-19 in persons ≥12 years old who weigh ≥40 kg and are at high risk of progression to severe disease or hospitalization. The FDA has now expanded this EUA to allow use of the antibodies together for post-exposure prophylaxis of COVID-19 in such persons if they are not fully vaccinated against COVID-19 or are unlikely to have an adequate immune response to full vaccination and have...
Med Lett Drugs Ther. 2021 Oct 18;63(1635):163-4 |  Show IntroductionHide Introduction

Tapinarof Cream (Vtama) for Atopic Dermatitis

   
The Medical Letter on Drugs and Therapeutics • Mar 03, 2025  (Issue 1723)
dermatitis. Tapinarof binds to and activates the AhR, resulting in downregulation of proinflammatory ...
Tapinarof 1% cream (Vtama – Dermavant), an aryl hydrocarbon receptor (AhR) agonist, has been approved by the FDA for topical treatment of atopic dermatitis in patients ≥2 years old. Tapinarof is the first AhR agonist to be approved in the US for this indication. It was approved in 2022 for treatment of plaque psoriasis in adults.
Med Lett Drugs Ther. 2025 Mar 3;67(1723):37-8   doi:10.58347/tml.2025.1723c |  Show IntroductionHide Introduction

Ozanimod (Zeposia) for Multiple Sclerosis

   
The Medical Letter on Drugs and Therapeutics • Aug 24, 2020  (Issue 1605)
disease, and active secondary progressive MS (SPMS). It is the third oral S1P receptor modulator ...
The FDA has approved ozanimod (Zeposia – Celgene), a sphingosine 1-phosphate (S1P) receptor modulator, for treatment of adults with relapsing forms of multiple sclerosis (MS), including clinically isolated syndrome (initial neurological episode), relapsing-remitting disease, and active secondary progressive MS (SPMS). It is the third oral S1P receptor modulator to be approved in the US for treatment of relapsing forms of MS; siponimod (Mayzent) is also indicated for use in adults, and fingolimod (Gilenya) is approved for use in patients ≥10 years old.
Med Lett Drugs Ther. 2020 Aug 24;62(1605):132-4 |  Show IntroductionHide Introduction

In Brief: Clopidogrel and Omeprazole

   
The Medical Letter on Drugs and Therapeutics • Nov 29, 2010  (Issue 1352)
with the activation of clopidogrel and diminish its antiplatelet effect, increasing the risk of cardiovascular events ...
Use of a proton pump inhibitor (PPI) to protect against gastrointestinal (GI) bleeding in patients taking the antiplatelet agent clopidogrel (Plavix) may interfere with the activation of clopidogrel and diminish its antiplatelet effect, increasing the risk of cardiovascular events.1 A randomized, placebo-controlled trial (COGENT) has found that use of the PPI omeprazole in patients taking clopidogrel in addition to aspirin decreased the incidence of GI bleeding without increasing the risk of a cardiovascular event, but the number of cardiovascular events was small and the formulation of...
Med Lett Drugs Ther. 2010 Nov 29;52(1352):93 |  Show IntroductionHide Introduction

Elderberry for Influenza

   
The Medical Letter on Drugs and Therapeutics • Feb 25, 2019  (Issue 1566)
of influenza have been conducted to date. Elderberry appears to have some activity against influenza virus ...
Patients may ask about taking elderberry for prevention and treatment of influenza. Products containing elderberry are promoted for relief of cold and flu symptoms and as an immune system booster.
Med Lett Drugs Ther. 2019 Feb 25;61(1566):32 |  Show IntroductionHide Introduction

Ruxolitinib (Opzelura) for Atopic Dermatitis

   
The Medical Letter on Drugs and Therapeutics • Jan 24, 2022  (Issue 1642)
of AD involves the JAK-signal transducer and activator of transcription (STAT) pathway; inhibition ...
The FDA has approved a 1.5% topical cream formulation of the Janus kinase (JAK) inhibitor ruxolitinib (Opzelura – Incyte) for short-term, non-continuous chronic treatment of mild to moderate atopic dermatitis (AD) in non-immunocompromised patients ≥12 years old whose disease has not been adequately controlled with other topical prescription drugs. Ruxolitinib is the first JAK inhibitor to be approved for topical use and the first to be approved in the US for treatment of AD. An oral formulation of ruxolitinib (Jakafi) is approved for treatment of myelofibrosis, polycythemia...
Med Lett Drugs Ther. 2022 Jan 24;64(1642):12-3 |  Show IntroductionHide Introduction

Atorvastatin - A New Lipid-lowering Drug

   
The Medical Letter on Drugs and Therapeutics • Mar 28, 1997  (Issue 997)
increase in hepatic LDL-receptor activity and may also decrease hepatic production of LDL cholesterol ...
Atorvastatin (Lipitor - Parke-Davis), an HMG-CoA reductase inhibitor (or 'statin'), was recently approved by the US Food and Drug Administration for treatment of primary hypercholesterolemia and mixed dyslipidemia. A single stereoisomer of a pyrrole derivative, the new drug is chemically different from other statins.
Med Lett Drugs Ther. 1997 Mar 28;39(997):29-31 |  Show IntroductionHide Introduction

Which Beta-Blocker?

   
The Medical Letter on Drugs and Therapeutics • Feb 05, 2001  (Issue 1097)
catecholamines, have intrinsic sympathomimetic activity (ISA) and tend to slow heart rate less. Beta-blockers ...
Some classes of drugs include so many agents that hospital formulary committees, managed care organizations and individual practitioners may find it difficult to choose among them. Fifteen beta-adrenergic receptor antagonists (beta-blockers) are now marketed for systemic use in the USA. One or more have been approved by the FDA for use in hypertension and eight other indications.
Med Lett Drugs Ther. 2001 Feb 5;43(1097):9-11 |  Show IntroductionHide Introduction