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Searched for activate. Results 241 to 250 of 1329 total matches.
Felbamate
The Medical Letter on Drugs and Therapeutics • Nov 26, 1993 (Issue 910)
of seizures associated with the Lennox-Gastaut syndrome, a severe epileptic encephalopathy.
ACTIVITY ...
Felbamate (Felbatol - Wallace Laboratories), a phenyl dicarbamate structurally similar to meprobamate (Equanil, and others), was recently approved by the US Food and Drug Administration for use alone or with other drugs in adults with partial seizures with or without secondary generalization. It was also approved for use in addition to other drugs in children with the multiple types of seizures associated with the Lennox-Gastaut syndrome, a severe epileptic encephalopathy.
Nefazodone for Depression
The Medical Letter on Drugs and Therapeutics • Apr 14, 1995 (Issue 946)
Neuropharmacol, 16:S45, 1993). The clinical significance of this activity is unknown.
The Medical Letter, Vol ...
Nefazodone (Serzone - Bristol-Myers Squibb) was recently approved by the US Food and Drug Administration for treatment of depression. A phenylpiperazine, nefazodone is chemically related to trazodone (Desyrel, and others).
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.
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.
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...
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 Introduction Hide 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.
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...
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.
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...