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Searched for vol. Results 201 to 210 of 395 total matches.

Tramadol Oral Solution (Qdolo) for Pain

   
The Medical Letter on Drugs and Therapeutics • May 31, 2021  (Issue 1625)
increase tramadol levels and the risk of seizures. Concurrent 84 The Medical Letter ® Vol. 63 (1625 ...
The opioid agonist tramadol is now available in an oral solution (Qdolo – Athena Bioscience) for management of pain severe enough to require an opioid and for which alternative treatment options are inadequate. Tramadol has been available for years in immediate-release tablets and capsules, extended-release capsules (Ultram, and others), and in a fixed-dose combination tablet with acetaminophen (Ultracet, and generics).
Med Lett Drugs Ther. 2021 May 31;63(1625):83-4 |  Show IntroductionHide Introduction

Setmelanotide (Imcivree) for Rare Genetic Forms of Obesity (online only)

   
The Medical Letter on Drugs and Therapeutics • Jul 26, 2021  (Issue 1629)
The Medical Letter ® Vol. 63 (1629) July 26, 2021 DOSAGE, ADMINISTRATION, AND COST — Setmelanotide ...
The FDA has approved setmelanotide (Imcivree – Rhythm), a subcutaneously injected melanocortin 4 (MC4) receptor agonist, for chronic weight management in patients ≥6 years old with obesity due to pro-opiomelanocortin (POMC) deficiency, proprotein subtilisin/kexin type 1 (PCSK1) deficiency, or leptin receptor (LEPR) deficiency.
Med Lett Drugs Ther. 2021 Jul 26;63(1629):e3-4 |  Show IntroductionHide Introduction

Xywav - A Mixed-Salt Oxybate Oral Solution for Idiopathic Hypersomnia

   
The Medical Letter on Drugs and Therapeutics • Dec 27, 2021  (Issue 1640)
of Xywav costs $5110. The Medical Letter ® Vol. 63 (1640) December 27, 2021Medical Letter 1. E ...
Xywav (Jazz), an oral solution that contains calcium, magnesium, potassium, and sodium oxybates, has been approved by the FDA for treatment of idiopathic hypersomnia in adults. It is the first drug to be approved in the US for this indication. Xywav was approved in 2020 for treatment of excessive daytime sleepiness or cataplexy in patients ≥7 years old with narcolepsy. It contains about 92% less sodium than sodium oxybate oral solution (Xyrem), which has been available in the US for years for use in patients ≥7 years old with narcolepsy.
Med Lett Drugs Ther. 2021 Dec 27;63(1640):207-8 |  Show IntroductionHide Introduction

A Drug-Eluting Contact Lens for Allergic Conjunctivitis

   
The Medical Letter on Drugs and Therapeutics • Apr 18, 2022  (Issue 1648)
; they can be reinserted after 10 minutes. The Medical Letter ® Vol. 64 (1648) April 18, 2022 61 ...
The FDA has approved Acuvue Theravision with Ketotifen (Johnson & Johnson Vision Care), a daily-wear, disposable, vision-correcting soft contact lens that releases the H1-antihistamine ketotifen, for prevention of ocular itch due to allergic conjunctivitis in contact lens users. This is the first approval for a drug-eluting contact lens. Ketotifen eye drops (Alaway, Zaditor, and others) are available over the counter.
Med Lett Drugs Ther. 2022 Apr 18;64(1648):60-1 |  Show IntroductionHide Introduction

Vazalore - A New Aspirin Formulation

   
The Medical Letter on Drugs and Therapeutics • May 02, 2022  (Issue 1649)
to immediate- release or enteric-coated aspirin, and it costs much more. The Medical Letter ® Vol. 64 (1649 ...
The FDA has approved an over-the-counter (OTC) liquid-filled capsule formulation of aspirin (Vazalore – PLx Pharma). The manufacturer has been heavily promoting Vazalore with claims of fast, predictable absorption and antiplatelet activity and improved gastrointestinal safety compared to existing OTC aspirin formulations.
Med Lett Drugs Ther. 2022 May 2;64(1649):70-1 |  Show IntroductionHide Introduction

In Brief: Higher-Dose Semaglutide (Ozempic) for Type 2 Diabetes

   
The Medical Letter on Drugs and Therapeutics • May 16, 2022  (Issue 1650)
, randomised, phase 3B trial. Lancet Diabetes Endocrinol 2021; 9:563. The Medical Letter ® Vol. 64 (1650 ...
The FDA has approved a higher-dose injectable formulation of the long-acting glucagon-like peptide-1 (GLP-1) receptor agonist semaglutide (Ozempic) for treatment of type 2 diabetes in adults. A single SC injection of the new 8 mg/3 mL formulation delivers 2 mg of semaglutide.
Med Lett Drugs Ther. 2022 May 16;64(1650):79 |  Show IntroductionHide Introduction

Alpelisib (Vijoice) for PIK3CA-Related Overgrowth Spectrum (online only)

   
The Medical Letter on Drugs and Therapeutics • Nov 14, 2022  (Issue 1663)
® Vol. 64 Published online November 14, 2022 1. G Canaud et al. LBA23 EPIK-P1: retrospective chart ...
The oral kinase inhibitor alpelisib (Vijoice – Novartis) has been approved by the FDA for treatment of patients ≥2 years old with severe manifestations of PIK3CA-related overgrowth spectrum (PROS) who require systemic treatment. Alpelisib is the first drug to be approved in the US for this indication. It was also approved in 2019 as Piqray for use in combination with fulvestrant for treatment of certain types of breast cancer.
Med Lett Drugs Ther. 2022 Nov 14;64(1663):e186-7 |  Show IntroductionHide Introduction

Neratinib (Nerlynx) for Metastatic HER2-Positive Breast Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • Nov 14, 2022  (Issue 1663)
with neratinib and for at least one month after the last dose. e193 The Medical Letter ® Vol. 64 Published ...
The oral tyrosine kinase inhibitor neratinib (Nerlynx – Puma Biotechnology) has been approved by the FDA for use in combination with capecitabine (Xeloda, and generics) for treatment of advanced or metastatic human epidermal growth factor receptor 2 (HER2)-positive breast cancer in adults who received ≥2 prior anti-HER2-based regimens for metastatic disease. It was previously approved for use as monotherapy for extended adjuvant treatment of adults with early-stage, HER2-positive breast cancer following adjuvant trastuzumab (Herceptin)-based therapy. HER2 is overexpressed in...
Med Lett Drugs Ther. 2022 Nov 14;64(1663):e192-3 |  Show IntroductionHide Introduction

In Brief: Zanubrutinib (Brukinsa) for CLL or SLL (online only)

   
The Medical Letter on Drugs and Therapeutics • Feb 20, 2023  (Issue 1670)
) for CLL or SLL e34 The Medical Letter ® Vol. 65 Published online February 20, 2023 1. CS Tam et al ...
The Bruton's tyrosine kinase (BTK) inhibitor zanubrutinib (Brukinsa), which was previously approved by the FDA for treatment of mantle cell lymphoma, Waldenström's macroglobulinemia, and relapsed or refractory marginal zone lymphoma, has now been approved for treatment of chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) in adults. The BTK inhibitors ibrutinib (Imbruvica) and acalabrutinib (Calquence) were approved earlier for treatment of CLL and SLL.
Med Lett Drugs Ther. 2023 Feb 20;65(1670):e33-4   doi:10.58347/tml.2023.1670e |  Show IntroductionHide Introduction

In Brief: OTC Ivermectin for Head Lice

   
The Medical Letter on Drugs and Therapeutics • Jun 26, 2023  (Issue 1679)
to ivermectin is rare.6 The Medical Letter ® Vol. 65 (1679) June 26, 2023Medical Letter Table 1. Some OTC ...
Topical ivermectin lotion 0.5% (Sklice, and generics), which has been available by prescription since 2012, is now FDA-approved for sale over the counter (OTC) for treatment of head lice in patients ≥6 months old. Ivermectin is also available by prescription as a 1% cream (Soolantra) approved for topical treatment of inflammatory lesions of rosacea and in oral tablets (Stromectol, and generics) for treatment of various parasitic infections.
Med Lett Drugs Ther. 2023 Jun 26;65(1679):103-4   doi:10.58347/tml.2023.1679e |  Show IntroductionHide Introduction