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Searched for vol. Results 951 to 960 of 1584 total matches.

Vibrant – An Oral Vibrating Capsule for Chronic Idiopathic Constipation

   
The Medical Letter on Drugs and Therapeutics • May 01, 2023  (Issue 1675)
straining, stool consistency, and quality of life, compared to placebo.7 The Medical Letter ® Vol. 65 ...
The Vibrant orally administered vibrating capsule (Vibrant Gastro), an FDA-cleared medical device, is now available by prescription for treatment of adults with chronic idiopathic constipation (CIC) who have not experienced relief of their bowel symptoms by using laxative therapies at the recommended dosage for at least one month. It is the first drug-free treatment to be authorized by the FDA for this indication.
Med Lett Drugs Ther. 2023 May 1;65(1675):65-7   doi:10.58347/tml.2023.1675a |  Show IntroductionHide Introduction

Cariprazine (Vraylar) for Adjunctive Treatment of Depression

   
The Medical Letter on Drugs and Therapeutics • May 29, 2023  (Issue 1677)
be considered first. The Medical Letter ® Vol. 65 (1677) May 29, 2023 85 ADVERSE EFFECTS — In clinical trials ...
The FDA has approved the second-generation antipsychotic drug cariprazine (Vraylar — Abbvie) for adjunctive treatment of major depressive disorder (MDD) in adults. Cariprazine was previously approved for treatment of schizophrenia and bipolar depression, and for acute treatment of manic or mixed episodes associated with bipolar I disorder.
Med Lett Drugs Ther. 2023 May 29;65(1677):84-6   doi:10.58347/tml.2023.1677c |  Show IntroductionHide Introduction

Brexpiprazole (Rexulti) for Agitation in Alzheimer's Dementia

   
The Medical Letter on Drugs and Therapeutics • Jun 26, 2023  (Issue 1679)
effective than placebo. The Medical Letter ® Vol. 65 (1679) June 26, 2023 100 Table 1. Brexpiprazole ...
The FDA has approved the oral second-generation antipsychotic drug brexpiprazole (Rexulti – Otsuka/Lundbeck) for once-daily treatment of agitation associated with dementia due to Alzheimer's disease (AD). Brexpiprazole is the first drug to be approved in the US for this indication. It is also approved for treatment of schizophrenia and as an adjunct to antidepressants for treatment of major depressive disorder.
Med Lett Drugs Ther. 2023 Jun 26;65(1679):99-101   doi:10.58347/tml.2023.1679b |  Show IntroductionHide Introduction

Sotagliflozin (Inpefa) for Heart Failure

   
The Medical Letter on Drugs and Therapeutics • Jul 24, 2023  (Issue 1681)
:129. The Medical Letter ® Vol. 65 (1681) July 24, 2023 for use during the second and third ...
The FDA has approved sotagliflozin (Inpefa – Lexicon), an oral sodium-glucose cotransporter 1 and 2 (SGLT1/2) inhibitor, to reduce the risk of hospitalization for heart failure (HF), urgent HF visits, and cardiovascular death in adults with either HF (with any left ventricular ejection fraction [LVEF]) or type 2 diabetes, chronic kidney disease (CKD), and other cardiovascular risk factors. Sotagliflozin is the first dual SGLT1/2 inhibitor to be approved in the US. Unlike SGLT2 inhibitors, it is not FDA-approved to improve glycemic control in adults with type 2 diabetes....
Med Lett Drugs Ther. 2023 Jul 24;65(1681):114-6   doi:10.58347/tml.2023.1681b |  Show IntroductionHide Introduction

Zavegepant (Zavzpret) for Acute Treatment of Migraine

   
The Medical Letter on Drugs and Therapeutics • Jul 24, 2023  (Issue 1681)
antagonists, for acute treatment of migraine. The Medical Letter ® Vol. 65 (1681) July 24, 2023 117 ...
The FDA has approved zavegepant nasal spray (Zavzpret – Pfizer) for acute treatment of migraine with or without aura in adults. Zavzpret is the first nasal spray formulation of a calcitonin gene-related peptide (CGRP) receptor antagonist ("gepant") to become available in the US.
Med Lett Drugs Ther. 2023 Jul 24;65(1681):116-8   doi:10.58347/tml.2023.1681c |  Show IntroductionHide Introduction

Roflumilast Foam (Zoryve) for Seborrheic Dermatitis

   
The Medical Letter on Drugs and Therapeutics • Apr 15, 2024  (Issue 1700)
Letter ® Vol. 66 (1700) April 15, 2024 58 Table 3. Some Topical Products for Seborrheic Dermatitis1 ...
The FDA has approved a 0.3% foam formulation of the phosphodiesterase-4 (PDE4) inhibitor roflumilast (Zoryve – Arcutis) for topical treatment of seborrheic dermatitis in patients ≥9 years old. Roflumilast is the first PDE4 inhibitor to be approved in the US for this indication. It is also available in a 0.3% cream formulation (Zoryve) for treatment of plaque psoriasis and in an oral formulation (Daliresp, and generics) for treatment of chronic obstructive pulmonary disease. A 0.15% cream formulation for treatment of atopic dermatitis in patients ≥6 years old will be reviewed...
Med Lett Drugs Ther. 2024 Apr 15;66(1700):57-9   doi:10.58347/tml.2024.1700a |  Show IntroductionHide Introduction

Elafibranor (Iqirvo) for Primary Biliary Cholangitis

   
The Medical Letter on Drugs and Therapeutics • Dec 23, 2024  (Issue 1718)
. The major active metabolite of elafibranor. The Medical Letter ® Vol. 66 (1718) December 23, 2024 203 ...
Elafibranor (Iqirvo – Ipsen), a peroxisome proliferator-activated receptor (PPAR) agonist, has been granted accelerated approval by the FDA for treatment of primary biliary cholangitis (PBC) in adults. It is indicated for use in combination with ursodeoxycholic acid (ursodiol, UDCA; Urso, and others) in patients with an inadequate response to UDCA alone and as monotherapy in those unable to tolerate UDCA.
Med Lett Drugs Ther. 2024 Dec 23;66(1718):202-4   doi:10.58347/tml.2024.1718b |  Show IntroductionHide Introduction

A New RSV Vaccine (mResvia) for Adults ≥60 Years Old

   
The Medical Letter on Drugs and Therapeutics • Oct 14, 2024  (Issue 1713)
. The Medical Letter ® Vol. 66 (1713) October 14, 2024 167 Table 3. Risk Factors for Severe RSV Disease ...
TThe FDA has licensed mResvia (Moderna), an mRNA respiratory syncytial virus (RSV) vaccine, for prevention of lower respiratory tract disease (LRTD) caused by RSV in adults ≥60 years old. It is the first mRNA vaccine to be licensed in the US for this indication. Two recombinant RSV vaccines, Arexvy and Abrysvo, are also available for prevention of RSV LRTD. Arexvy is approved for use in adults ≥50 years old. Abrysvo is approved for use in adults ≥60 years old and in pregnant women to prevent RSV LRTD in their infants.
Med Lett Drugs Ther. 2024 Oct 14;66(1713):166-8   doi:10.58347/tml.2024.1713d |  Show IntroductionHide Introduction

Shield — A Blood Test for Colorectal Cancer Screening

   
The Medical Letter on Drugs and Therapeutics • Jun 09, 2025  (Issue 1730)
polyps CRC = colorectal cancer; CT = computed tomography The Medical Letter ® Vol. 67 (1730) June 9 ...
The FDA has approved Shield (Guardant), a DNA blood test, for colorectal cancer (CRC) screening in average-risk adults ≥45 years old. Shield is the second blood-based DNA test to be approved for CRC screening; ColoHealth (formerly Epi proColon) was approved in 2016.
Med Lett Drugs Ther. 2025 Jun 9;67(1730):90-2   doi:10.58347/tml.2025.1730b |  Show IntroductionHide Introduction

Aztreonam/Avibactam (Emblaveo) for Complicated Intra-Abdominal Infections

   
The Medical Letter on Drugs and Therapeutics • Feb 16, 2026  (Issue 1748)
prohibited. For further information call: 800-211-2769 The Medical Letter ® Vol. 68 (1748) February 16 ...
The FDA has approved Emblaveo (Abbvie), an intravenously administered fixed-dose combination of the monobactam antibacterial drug aztreonam and the beta-lactamase inhibitor avibactam, for use with metronidazole to treat complicated intra-abdominal infections (cIAIs) in adults.
Med Lett Drugs Ther. 2026 Feb 16;68(1748):25-7   doi:10.58347/tml.2026.1748a |  Show IntroductionHide Introduction