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Searched for activate. Results 301 to 310 of 1329 total matches.
Tovorafenib (Ojemda) for Pediatric Low-Grade Glioma (online only)
The Medical Letter on Drugs and Therapeutics • Jun 10, 2024 (Issue 1704)
glioma harboring an
activating RAF alteration is ongoing.
ADVERSE EFFECTS — In the FIREFLY-1 trial ...
Tovorafenib (Ojemda – Day One), a type II RAF kinase
inhibitor, has received accelerated approval from the
FDA for treatment of patients ≥6 months old with
relapsed or refractory pediatric low-grade glioma
harboring a BRAF fusion or rearrangement or a BRAF
V600 mutation. Tovorafenib is the first systemic
treatment to be approved in the US for pediatric
low-grade gliomas with BRAF fusions. Accelerated
approval of tovorafenib was based on response rates
and duration of response.
Med Lett Drugs Ther. 2024 Jun 10;66(1704):e97-8 doi:10.58347/tml.2024.1704f | Show Introduction Hide Introduction
Saxagliptin (Onglyza) for Type 2 Diabetes
The Medical Letter on Drugs and Therapeutics • Nov 02, 2009 (Issue 1324)
hrs (active metabolite)
Metabolism Hepatic by CYP3A4/5 to active metabolite
(half as potent ...
Saxagliptin (Onglyza - Bristol-Myers Squibb), the second oral dipeptidyl peptidase-4 (DPP-4) inhibitor to be marketed in the US, has been approved by the FDA for treatment of adults with type 2 diabetes.
Cefiderocol (Fetroja) - A New IV Cephalosporin for Complicated UTI
The Medical Letter on Drugs and Therapeutics • May 04, 2020 (Issue 1597)
stability against
beta-lactamases.4,5
SPECTRUM OF ACTIVITY — Cefiderocol has no clinically
relevant ...
The FDA has approved cefiderocol (Fetroja – Shionogi),
a new IV cephalosporin antibiotic, for treatment of
complicated urinary tract infections (UTI) caused by
susceptible gram-negative bacteria in adults who
have limited or no alternative treatment options.
Pharmaceutical Drug Overdose
Treatment Guidelines from The Medical Letter • Sep 01, 2006 (Issue 49)
pneumonia. Perforation of the esophagus,
laryngospasm and hypoxia can occur.
Activated charcoal (AC ...
Every pharmaceutical drug is a dose-dependent poison. This article describes the clinical presentation and treatment of some dangerous overdoses commonly reported in adults.
Timing of Remdesivir for COVID-19
The Medical Letter on Drugs and Therapeutics • Oct 19, 2020 (Issue 1609)
analog that inhibits viral
replication by binding to RNA-dependent RNA
polymerase. It is active against ...
Remdesivir (Veklury – Gilead), an investigational
antiviral drug administered by IV infusion, is now
available through an FDA Emergency Use Authorization
(EUA) for treatment of COVID-19 in all hospitalized
patients. An earlier EUA limited use of the drug to
patients hospitalized with severe disease.
In Brief: Anktiva for Bladder Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Jun 24, 2024 (Issue 1705)
of the
drug to its receptor causes proliferation and activation
of natural killer (NK) and CD8+ killer ...
Nogapendekin alfa inbakicept-pmln (Anktiva –
ImmunityBio), a first-in-class interleukin-15 (IL15)
receptor agonist, has been approved by the FDA for
use with Bacillus Calmette-Guérin (BCG) for treatment
of patients with BCG-unresponsive nonmuscle
invasive bladder cancer (NMIBC) with carcinoma in
situ with or without papillary tumors. Such patients
generally undergo bladder tumor resection, followed
by intravesical BCG treatment, but treatment failure
and cancer recurrence are common. The adenoviral
vector-based intravesical gene therapy nadofaragene
firadenovec-vncg (Adstiladrin)...
Med Lett Drugs Ther. 2024 Jun 24;66(1705):e105-6 doi:10.58347/tml.2024.1705e | Show Introduction Hide Introduction
Antiviral Drugs
Treatment Guidelines from The Medical Letter • Mar 01, 2013 (Issue 127)
acyclovir therapy (400 mg
three times daily) beginning at week 36 to pregnant
women with active recurrent ...
The drugs of choice for treatment of viral infections
(other than HIV) and their dosages are listed in Tables
1-6 on the pages that follow. Some of the indications
and dosages recommended here have not been
approved by the FDA. Vaccines used for the prevention
of viral infections are discussed elsewhere.
Olsalazine
The Medical Letter on Drugs and Therapeutics • Nov 16, 1990 (Issue 831)
available in the USA.
PHARMACOLOGY — 5-ASA is active topically in the colon, but not systemically. Given ...
Olsalazine sodium (Dipentum - Pharmacia), a dimer (two molecules linked by an azo bond) of 5-aminosalicylic acid, was recently approved by the US Food and Drug Administration for oral use to maintain remission of ulcerative colitis in adult patients who cannot tolerate sulfasalazine (Azulfidine; and others).
Gabapentin - A New Anticonvulsant
The Medical Letter on Drugs and Therapeutics • Apr 29, 1994 (Issue 921)
with antiepileptic activity are generally tried first for this indication.
PREVIOUSLY AVAILABLE DRUGS ...
Gabapentin (Neurontin - Parke-Davis), a cyclohexane acetic acid derivative, has been approved by the US Food and Drug Administration for use in addition to other antiepileptic drugs in patients with partial (focal) seizures with or without secondary generalization. Since this diagnostic category includes the largest number of patients with intractable epilepsy, new drugs with antiepileptic activity are generally tried first for this indication.
Treatment of Hypothermia
The Medical Letter on Drugs and Therapeutics • Dec 23, 1994 (Issue 938)
.
Hypothermia associated with exhaustion during outdoor sports activities can occur even at relatively mild ...
This winter physicians in many area may see patients suffering from hypothermia. Old age, lack of adequate housing, drug overdose and alcohol ingestion are often prediposing factors, but hypothermia also occurs in healthy young people after prolonged exposure to cold due to incapacitating trauma or cold water immersion. Hypothermia associated with exhaustionduring outdoor sports activities can occur even at relatively mild temperatures.