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Searched for activate. Results 511 to 520 of 1329 total matches.

In Brief: Lisocabtagene Maraleucel (Breyanzi) for Large B-Cell Lymphoma (online only)

   
The Medical Letter on Drugs and Therapeutics • Jun 26, 2023  (Issue 1679)
to CD19 proteins on the surface of B cells, promoting T-cell activation and proliferation and secretion ...
The FDA has approved lisocabtagene maraleucel (Breyanzi – BMS) for treatment of adults with large B-cell lymphoma (LBCL), including diffuse large B-cell lymphoma (DLBCL) not otherwise specified, high-grade B-cell lymphoma, primary mediastinal large B-cell lymphoma, or follicular lymphoma grade 3B who have disease refractory to first-line chemoimmunotherapy, relapsed within 12 months of or after first-line chemoimmunotherapy, are not eligible for hematopoietic stem cell transplantation due to comorbidities or age, or have relapsed or refractory disease after ≥2 lines of...
Med Lett Drugs Ther. 2023 Jun 26;65(1679):e104-5   doi:10.58347/tml.2023.1679f |  Show IntroductionHide Introduction

Opill — An OTC Oral Contraceptive

   
The Medical Letter on Drugs and Therapeutics • Sep 18, 2023  (Issue 1685)
with an increase in the risk of breast cancer.8,9 DRUG INTERACTIONS — Drugs that induce hepatic enzyme activity ...
The FDA has approved Opill (Perrigo), a progestin-only oral contraceptive that contains norgestrel, for sale over the counter (OTC). Opill is the first oral contraceptive to be approved in the US for sale without a prescription. Approval of OTC Opill is intended to increase access to effective contraception and reduce the rate of unintended pregnancies.
Med Lett Drugs Ther. 2023 Sep 18;65(1685):151-2   doi:10.58347/tml.2023.1685c |  Show IntroductionHide Introduction

Iloprost (Aurlumyn) for Frostbite

   
The Medical Letter on Drugs and Therapeutics • Jul 22, 2024  (Issue 1707)
frostbite are lacking. Treatment with tissue plasminogen activator (tPA) plus low-molecular-weight heparin ...
The FDA has approved Aurlumyn (Eicos Sciences), an IV formulation of the prostacyclin analog iloprost, to reduce the risk of digit amputation in adults with severe frostbite. Iloprost is the first drug to be approved by the FDA for treatment of severe frostbite; it has been used off-label for this indication in the EU and elsewhere for decades. In the US, iloprost is also available as an inhaled formulation (Ventavis) for treatment of pulmonary arterial hypertension.
Med Lett Drugs Ther. 2024 Jul 22;66(1707):114   doi:10.58347/tml.2024.1707b |  Show IntroductionHide Introduction

Two New Intra-Articular Injections for Knee Osteoarthritis

   
The Medical Letter on Drugs and Therapeutics • Aug 27, 2018  (Issue 1554)
because they can cause precipitation of sodium hyaluronate. Any strenuous activities or prolonged weight ...
The FDA has approved a single-injection hyaluronic acid gel (Durolane – Bioventus) and an extended-release (ER) formulation of the synthetic corticosteroid triamcinolone acetonide (Zilretta – Flexion) for intra-articular (IA) treatment of osteoarthritic knee pain.
Med Lett Drugs Ther. 2018 Aug 27;60(1554):142-4 |  Show IntroductionHide Introduction

Tafenoquine (Arakoda; Krintafel) for Malaria

   
The Medical Letter on Drugs and Therapeutics • Jul 01, 2019  (Issue 1575)
hypnozoite stage in the liver.2 ACTIVITY — Tafenoquine is an 8-aminoquinoline antimalarial that acts ...
The oral antimalarial tafenoquine succinate, a long-acting analog of primaquine, has been approved by the FDA in 2 different strengths. Arakoda (100-mg tablets; Sixty Degrees) is indicated for the prophylaxis of malaria in adults. Krintafel (150-mg tablets; GSK) is indicated for the prevention of relapse (radical cure) of Plasmodium vivax malaria in patients ≥16 years old undergoing treatment for acute P. vivax infection.
Med Lett Drugs Ther. 2019 Jul 1;61(1575):101-4 |  Show IntroductionHide Introduction

Drugs for Bacterial Infections

   
Treatment Guidelines from The Medical Letter • Jul 01, 2013  (Issue 131)
. Ceftaroline fosamil, a new IV cephalosporin with activity against MRSA, may be effective as monotherapy ...
The text that follows reviews some common bacterial infections and their empiric treatment pending the results of culture and susceptibility testing. The recommendations made here are based on the results of susceptibility studies, clinical trials, and the opinions of Medical Letter reviewers. Tables 1 and 2 list the usual dosages of antibacterial drugs.
Treat Guidel Med Lett. 2013 Jul;11(131):65-74 |  Show IntroductionHide Introduction

In Brief: Oral Propranolol for Infantile Hemangiomas

   
The Medical Letter on Drugs and Therapeutics • Oct 31, 2011  (Issue 1376)
is not known, but is thought to be related to down-regulation of the RAF mitogen-activated protein kinase ...
The surprising observation that oral administration of the beta-blocker propranolol (Inderal, and others) can stop the growth and rapidly cause the involution of disfiguring or life-threatening infantile hemangiomas1 has quickly led to a series of confirmatory observations and now a controlled trial. The mechanism of this effect is not known, but is thought to be related to down-regulation of the RAF mitogen-activated protein kinase signaling pathway resulting in inhibition of vascular endothelial growth factor (VEGF) and apoptosis in capillary endothelial cells. The response of infantile...
Med Lett Drugs Ther. 2011 Oct 31;53(1376):88 |  Show IntroductionHide Introduction

COVID-19 Update: Dosing Interval for Tixagevimab/Cilgavimab (Evusheld) (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 08, 2022  (Issue 1656)
modeling data, which suggest that tixagevimab and cilgavimab retain activity against currently circulating ...
The FDA has amended its Emergency Use Authorization (EUA) for the investigational long-acting monoclonal antibodies tixagevimab and cilgavimab (Evusheld – AstraZeneca) to recommend repeat dosing every 6 months in patients who require ongoing protection against COVID-19. Evusheld is authorized for IM pre-exposure prophylaxis of COVID-19 in persons ≥12 years old who weigh ≥40 kg and have either a history of a severe adverse reaction that prevents their vaccination against COVID-19 or moderate or severe immune compromise
Med Lett Drugs Ther. 2022 Aug 8;64(1656):e122-3 |  Show IntroductionHide Introduction

Transdermal Selegiline (Emsam)

   
The Medical Letter on Drugs and Therapeutics • May 22, 2006  (Issue 1235)
by CYP2B6, CYP2C9 and CYP3A4/5; metabolites are only weakly active. 4 Only small amounts of the drug ...
The FDA recently approved the monoamine oxidase inhibitor (MAOI) selegiline in a transdermal (patch) formulation (Emsam - Bristol-Myers Squibb/Somerset) for treatment of major depressive disorder. Selegiline is also available in an oral formulation (Eldepryl, and others) for treatment of Parkinson's disease.
Med Lett Drugs Ther. 2006 May 22;48(1235):41-2 |  Show IntroductionHide Introduction

Vorinostat (Zolinza) for Cutaneous T-cell Lymphoma

   
The Medical Letter on Drugs and Therapeutics • Mar 12, 2007  (Issue 1256)
transcriptional activation, resulting in cell cycle arrest, differentiation, and apoptosis. 4 HDAC inhibitors ...
Vorinostat (Zolinza - Merck), an oral histone deacetylase (HDAC) inhibitor, has received accelerated approval from the FDA for treatment of skin manifestations of cutaneous T-cell lymphoma (CTCL) that is persistent, progressive or recurrent after two systemic therapies. The most common types of CTCL are mycosis fungoides and SΘzary syndrome, the leukemic form of mycosis fungoides.
Med Lett Drugs Ther. 2007 Mar 12;49(1256):23-4 |  Show IntroductionHide Introduction