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Searched for 1. Results 1911 to 1920 of 2621 total matches.

Imetelstat (Rytelo) for Myelodysplastic Syndromes (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 30, 2024  (Issue 1712)
earlier this year for the same indication in patients ≥12 years old.1 Key Points: Betibeglogene ...
The FDA has approved imetelstat (Rytelo – Geron), a first-in-class telomerase inhibitor, for treatment of low- to intermediate-1 risk myelodysplastic syndromes (MDS) in adults with transfusion-dependent anemia requiring 4 or more red blood cell (RBC) units over 8 weeks who have not responded to, are no longer responding to, or are ineligible for erythropoiesis-stimulating agents (ESAs).
Med Lett Drugs Ther. 2024 Sep 30;66(1712):e169-70   doi:10.58347/tml.2024.1712d |  Show IntroductionHide Introduction

Acoramidis (Attruby) for Transthyretin Amyloid Cardiomyopathy

   
The Medical Letter on Drugs and Therapeutics • Mar 17, 2025  (Issue 1724)
to be approved in the US for this indication; tafamidis (Vyndaqel, Vyndamax) was approved in 2019.1 Table 1 ...
The FDA has approved acoramidis (Attruby – BridgeBio), an oral transthyretin stabilizer, to reduce cardiovascular-related hospitalization and cardiovascular death in adults with wild-type or variant (hereditary) transthyretin amyloid cardiomyopathy (ATTR-CM). Acoramidis is the second transthyretin stabilizer to be approved in the US for this indication; tafamidis (Vyndaqel, Vyndamax) was approved in 2019.
Med Lett Drugs Ther. 2025 Mar 17;67(1724):45-6   doi:10.58347/tml.2025.1724c |  Show IntroductionHide Introduction

Linvoseltamab (Lynozyfic) for Multiple Myeloma (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 18, 2025  (Issue 1735)
are given subcutaneously, were approved earlier.1,2 Key Points: Linvoseltamab (Lynozyfic) ▶ Description ...
Linvoseltamab (Lynozyfic – Regeneron), a bispecific B-cell maturation antigen (BCMA)-directed CD3 T-cell engager, has received accelerated approval from the FDA for intravenous treatment of relapsed or refractory multiple myeloma in adults who had received ≥4 prior lines of therapy, including a proteasome inhibitor, an immunomodulatory drug, and an anti-CD38 monoclonal antibody. Accelerated approval was based on the response rate and durability of response. Linvoseltamab is the third bispecific BCMA-directed CD3 T-cell engager to be approved for this indication; teclistamab...
Med Lett Drugs Ther. 2025 Aug 18;67(1735):e136-7   doi:10.58347/tml.2025.1735h |  Show IntroductionHide Introduction

Focalin XR for ADHD

   
The Medical Letter on Drugs and Therapeutics • Mar 23, 2009  (Issue 1308)
of clinical practice. 1 Recently the FDA approved a labeling change that apparently permits Novartis ...
Short-acting methylphenidate (MPH) is effective for treatment of attention-deficit/hyperactivity disorder (ADHD), but its 3-5 hour duration of action usually requires mid-day dosing in school, which children may find disruptive or stigmatizing.
Med Lett Drugs Ther. 2009 Mar 23;51(1308):22-4 |  Show IntroductionHide Introduction

Dexamethasone Bacterial Meningitis In Children

   
The Medical Letter on Drugs and Therapeutics • Jan 27, 1989  (Issue 784)
occurred in 12 patients (14%) treated with placebo and one (1%) treated with dexamethasone ...
A recent report in the New England Journal of Medicine suggested that in children with bacterial meningitis, adding the corticosteroid dexamethasone (Decadron; and others) to antibiotic treatment could decrease the incidence of moderate or severe hearing loss.
Med Lett Drugs Ther. 1989 Jan 27;31(784):6-7 |  Show IntroductionHide Introduction

Flutamide For Prostate Cancer

   
The Medical Letter on Drugs and Therapeutics • Jul 28, 1989  (Issue 797)
hepatitis (W Hart and BH Stricker, Ann Intern Med, 110:943, June 1, 1989). In one study, diarrhea was more ...
Flutamide (Eulexin - Schering), an oral antiandrogen, is now available in the USA for treatment of metastatic prostate cancer. Flutamide is recommended by the manufacturer only for use concurrently with an analog of luteinizing hormone-releasing hormone (LHRH) such as leuprolide (Lupron - Medical Letter, 27:71, 1985).
Med Lett Drugs Ther. 1989 Jul 28;31(797):72 |  Show IntroductionHide Introduction

Ovral As A 'Morning-After' Contraceptive

   
The Medical Letter on Drugs and Therapeutics • Oct 20, 1989  (Issue 803)
to prevent pregnancy in 0 to 7.4% of women, with a pooled failure rate of 1.8% (M Fasoli et al ...
High doses of various hormones have been used for many years to prevent pregnancy after unprotected coitus. Diethylstilbestrol (DES), a synthetic estrogen, was once approved for this purpose by the US Food and Drug Administration (Medical Letter 15:58, 1973), but no drug is now approved for such use. Ovral, an oral contraceptive containing 50 g of the estrogen ethinyl estradiol and 0.5 mg of the progestin norgestrel, has been recommended as a 'morning-after' pill by some physicians (RA Hatcher et al, Contraceptive Technology 1988-1989, 14th ed., New York:Irvington, 1988, page...
Med Lett Drugs Ther. 1989 Oct 20;31(803):93-4 |  Show IntroductionHide Introduction

Masoprocol for Multiple Actinic Keratoses

   
The Medical Letter on Drugs and Therapeutics • Oct 15, 1993  (Issue 907)
applied only the vehicle, the mean number of lesions decreased from 13.4 to 11.1. Among the patients who ...
Masoprocol cream 10% (meso-nordihydroguiaretic acid, Actinex - Reed and Carnrick) is now available in the USA for topical treatment of actinic keratoses.
Med Lett Drugs Ther. 1993 Oct 15;35(907):97-8 |  Show IntroductionHide Introduction

The Female Condom

   
The Medical Letter on Drugs and Therapeutics • Dec 24, 1993  (Issue 912)
— According to the manufacturer, each Reality condom will cost family planning clinics about $1 ...
A condom for women (Reality - Wisconsin Pharmacal) to prevent pregnancy and sexually transmitted diseases, including AIDS, has been approved for marketing by the US Food and Drug Administration (FDA). Already available in many family planning clinics, it will be available in pharmacies in a few months.
Med Lett Drugs Ther. 1993 Dec 24;35(912):123-4 |  Show IntroductionHide Introduction

Riluzole for Amyotrophic Lateral Sclerosis

   
The Medical Letter on Drugs and Therapeutics • Dec 08, 1995  (Issue 963)
. The premarketing supply is limited; the manufacturer (1-800-798-7425) has enough on hand to treat 3,000 ...
The US Food and Drug Administration (FDA) has approved 'early access' use of riluzole (Rilutek - Rh ne-Poulenc Rorer) for treatment of amyotrophic lateral sclerosis (ALS). is the first drug to become available for treatment of this condition. The premarketing supply is limited; the manufacturer (1-800-798-7425) has enough on hand to treat 3,000 of the 25,000 patients with the disease in the USA, and those 3,000 have already been selected through a lottery. Similar arrangements have been made in several European countries. Riluzole is not available commercially in any country.
Med Lett Drugs Ther. 1995 Dec 8;37(963):113-4 |  Show IntroductionHide Introduction