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Searched for activate. Results 141 to 150 of 1334 total matches.
Clobazam (Onfi) for Lennox-Gastaut Syndrome
The Medical Letter on Drugs and Therapeutics • Mar 05, 2012 (Issue 1385)
to an active
metabolite, which is primarily metabolized
by CYP2C19
Elimination 82% in urine (primarily ...
Clobazam (Onfi – Lundbeck), an oral benzodiazepine, has been approved by the FDA for adjunctive treatment of seizures associated with Lennox-Gastaut syndrome (LGS) in patients ≥2 years old. It has been available in Canada (Frisium) and other countries for years for treatment of anxiety and many types of epilepsy.
Efgartigimod alfa (Vyvgart) for Myasthenia Gravis
The Medical Letter on Drugs and Therapeutics • Apr 18, 2022 (Issue 1648)
from baseline in the
Myasthenia Gravis Activities of Daily Living score
during the first treatment cycle ...
Efgartigimod alfa-fcab (Vyvgart – Argenx), a first-in-class neonatal Fc receptor (FcRn) antagonist,
has been approved by the FDA for IV treatment of
generalized myasthenia gravis in adults who are
anti-acetylcholine receptor (AChR) antibody positive.
The IV complement inhibitor eculizumab (Soliris) was
approved for the same indication in 2017.
In Brief: Dabrafenib (Tafinlar) and Trametinib (Mekinist) for Glioma (online only)
The Medical Letter on Drugs and Therapeutics • Apr 17, 2023 (Issue 1674)
dabrafenib capsules or
trametinib tablets.
MECHANISM OF ACTION — BRAF V600E mutations
activate the mitogen ...
The oral kinase inhibitors dabrafenib (Tafinlar –
GSK) and trametinib (Mekinist – Novartis) have been
approved by the FDA for use together for a sixth
indication: treatment of low-grade glioma (LGG)
with a BRAF V600E mutation in patients ≥1 years old
who require systemic therapy. This combination is
the first systemic therapy to be approved in the US
for first-line treatment of LGG with a BRAF V600E
mutation in pediatric patients. The FDA also approved
new oral formulations of both drugs for patients
who are unable to swallow dabrafenib capsules or
trametinib...
Med Lett Drugs Ther. 2023 Apr 17;65(1674):e75-6 doi:10.58347/tml.2023.1674i | Show Introduction Hide Introduction
Mesalamine For Ulcerative Colitis
The Medical Letter on Drugs and Therapeutics • May 20, 1988 (Issue 766)
to sulfapyridine and 5ASA in the intestine, is effective both for treatment of active disease and in maintaining ...
Mesalamine (Rowasa - Reid-Rowell), probably better known as 5-aminosalicylic acid (5-ASA) and also called mesalazine in some other countries, was recently marketed in the USA as an enema for treatment of mild to moderate distal ulcerative colitis, including ulcerative proctosigmoiditis and ulcerative proctitis.
Nizatidine (Axid)
The Medical Letter on Drugs and Therapeutics • Aug 12, 1988 (Issue 772)
and Drug
Administration for treatment of active duodenal ulcer and for maintenance therapy after healing ...
Nizatidine (Axid - Lilly), a new H2-receptor antagonist similar to cimetidine (Tagamet), ranitidine (Zantac) and famotidine (Pepcid), was recently approved by the US Food and Drug Administration for treatment of active duodenal ulcer and for maintenance therapy after healing. Cimetidine, ranitidine and famotidine are also approved for treatment of pathological hypersecretory conditions such as Zollinger- Ellison syndrome; cimetidine is approved in addition for treatment of gastric ulcers.
Betaxolol for Hypertension
The Medical Letter on Drugs and Therapeutics • Jun 29, 1990 (Issue 821)
drug is
beta
1
(cardio)-selective with no intrinsic sympathomimetic (partial agonist) activity ...
Betaxolol (Kerlone - Searle), an oral beta-adrenergic blocker, was recently approved by the US Food and Drug Administration for once-daily treatment of hypertension. The new drug is beta 1 (cardio)-selective with no intrinsic sympathomimetic (partial agonist) activity. It is also available in a topical formulation for treatment of glaucoma (Betoptic - Medical Letter, 28:45, 1986). Beta-blockers currently available in the USA for treatment of hypertension are listed in the table below.
Lamotrigine For Epilepsy
The Medical Letter on Drugs and Therapeutics • Mar 17, 1995 (Issue 944)
of patients with intractable epilepsy, new drugs with antiepileptic activity are usually tried
first ...
Lamotrigine (la mo tri jeen; Lamictal - Burroughs Wellcome), a phenyltriazine derivative, has been approved by the US Food and Drug Administration for use in addition to other antiepileptic drugs in adults with partial seizures. Since this diagnostic category includes the largest number of patients with intractable epilepsy, new drugs with antiepileptic activity are usually tried first for this indication. Lamotrigine was first marketed abroad in 1990 and is now available in more than 50 other countries.
Vardenafil (Levitra) for Erectile Dysfunction
The Medical Letter on Drugs and Therapeutics • Sep 29, 2003 (Issue 1166)
.
ACTIVITY — Vardenafil, like sildenafil, is a selective phosphodiesterase type 5 (PDE5) inhibitor ...
Vardenafil (Levitra -Bayer) is the second oral drug approved by the FDA for treatment of erectile dysfunction. Sildenafil (Viagra - Medical Letter 1998; 40:51), the first oral drug, has been available for 5 years. Pharmacokinetics, effectiveness, adverse effects, dosage and cost of the new drug are reviewed. Whether it offers any benefits over sildenafil is discussed.
Ophthalmic Azithromycin (AzaSite)
The Medical Letter on Drugs and Therapeutics • Feb 11, 2008 (Issue 1279)
are not active against the
gram-negative organisms that cause a small percentage of these infections. Polymyxin ...
The FDA has approved azithromycin 1% ophthalmic solution (AzaSite - Inspire) for treatment of bacterial conjunctivitis in patients > 1 year old. It is formulated, according to the manufacturer, in a controlled-release delivery system that keeps the drug in the eye for several hours.
Dimethyl Fumarate (Tecfidera) for Multiple Sclerosis
The Medical Letter on Drugs and Therapeutics • Jun 10, 2013 (Issue 1418)
has not been established.
It has been shown to activate an antioxidant
response pathway (Nrf2) thought to be the primary ...
The FDA has approved dimethyl fumarate (Tecfidera –
Biogen Idec), formerly called BG-12, for treatment of
relapsing forms of multiple sclerosis (MS). It is the
third oral drug to be approved in recent years for this
indication.