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Searched for days. Results 471 to 480 of 486 total matches.

Miudella — A Lower-Dose Copper IUD

   
The Medical Letter on Drugs and Therapeutics • Jun 09, 2025  (Issue 1730)
an etonogestrel implant or another IUD can have the Miudella IUD inserted on the same day the implant or IUD ...
Miudella (Sebela), a copper intrauterine device (IUD), has been approved by the FDA for prevention of pregnancy for up to 3 years. Miudella is the second copper IUD to be approved in the US; ParaGard, which contains more copper and is approved for up to 10 years of use, was approved in 1984. Four hormonal IUDs (Mirena, Liletta, Skyla, Kyleena) that release the progestin levonorgestrel are also available for pregnancy prevention (see Table 2).
Med Lett Drugs Ther. 2025 Jun 9;67(1730):89-90   doi:10.58347/tml.2025.1730a |  Show IntroductionHide Introduction

Cologuard Plus — An At-Home Stool DNA Test for Colorectal Cancer Screening

   
The Medical Letter on Drugs and Therapeutics • May 12, 2025  (Issue 1728)
hours (6 days) of collection (an increase from 72 hours with Cologuard). A positive result should ...
The FDA has approved Cologuard Plus (Exact Sciences), a new at-home multitarget stool DNA test, for colorectal cancer (CRC) screening in average-risk adults ≥45 years old. Cologuard, the first FDA-approved multitarget stool DNA test, has been available since 2014.
Med Lett Drugs Ther. 2025 May 12;67(1728):73-5   doi:10.58347/tml.2025.1728a |  Show IntroductionHide Introduction

Sarilumab (Kevzara) for Polymyalgia Rheumatica

   
The Medical Letter on Drugs and Therapeutics • May 13, 2024  (Issue 1702)
(prednisone 15-20 mg/day or equivalent) are used for initial treatment of PMR; symptoms typically resolve ...
The FDA has approved the interleukin (IL)-6 inhibitor sarilumab (Kevzara – Sanofi/Regeneron) for treatment of polymyalgia rheumatica (PMR) in adults who had an inadequate response to corticosteroids or cannot tolerate a corticosteroid taper. Sarilumab is the first biologic drug to be approved for treatment of PMR; it was previously approved for treatment of rheumatoid arthritis.
Med Lett Drugs Ther. 2024 May 13;66(1702):77-8   doi:10.58347/tml.2024.1702c |  Show IntroductionHide Introduction

Comparison Chart: Some Available Insulins for Type 2 Diabetes (online only)

   
The Medical Letter on Drugs and Therapeutics • Dec 08, 2025  (Issue 1743)
to be administered at the same time each day ▪ Similar to insulin glargine 100 units/mL in A1C lowering ...
View the Comparison Chart: Some Available Insulins for Type 2 Diabetes
Med Lett Drugs Ther. 2025 Dec 8;67(1743):e201-4   doi:10.58347/tml.2025.1743d |  Show IntroductionHide Introduction

In Brief: Finerenone (Kerendia) for Diabetic Kidney Disease

   
The Medical Letter on Drugs and Therapeutics • Jan 23, 2023  (Issue 1668)
hepatic impairment (Child-Pugh C). A 30-day supply of Kerendia costs $597.60.7 CONCLUSION — Addition ...
Recently published guidelines from the American Diabetes Association (ADA) and the Kidney Disease: Improving Global Outcomes (KDIGO) Diabetes Work Group recommend addition of the oral nonsteroidal mineralocorticoid receptor antagonist (MRA) finerenone (Kerendia) to standard treatment in patients with type 2 diabetes and chronic kidney disease (CKD).
Med Lett Drugs Ther. 2023 Jan 23;65(1668):15-6   doi:10.58347/tml.2023.1668e |  Show IntroductionHide Introduction

Mirikizumab (Omvoh) for Ulcerative Colitis

   
The Medical Letter on Drugs and Therapeutics • Mar 18, 2024  (Issue 1698)
; subcutaneous Metabolism Catabolism into small peptides and amino acids Half-life 9.3 days (in patients ...
The FDA has approved the interleukin (IL)-23 antagonist mirikizumab-mrkz (Omvoh – Lilly) for treatment of moderately to severely active ulcerative colitis (UC) in adults. Mirikizumab is the first selective IL-23 antagonist to be approved for this indication. Ustekinumab (Stelara), an IL-12/23 antagonist, was approved for treatment of UC in 2019. The IL-23 antagonist risankizumab (Skyrizi) is approved for treatment of Crohn's disease.
Med Lett Drugs Ther. 2024 Mar 18;66(1698):46-7   doi:10.58347/tml.2024.1698c |  Show IntroductionHide Introduction

Donanemab (Kisunla) for Alzheimer's Disease

   
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024  (Issue 1709)
-dose vials Route Intravenous Metabolism Proteolysis Half-life ~12.1 days AD = Alzheimer's Disease ...
Donanemab-azbt (Kisunla – Lilly), an IV amyloid beta-directed monoclonal antibody, has been approved by the FDA for treatment of Alzheimer's disease (AD). The label states that the drug should only be started in patients with mild cognitive impairment (MCI) or mild dementia. Donanemab is the third IV amyloid beta-directed monoclonal antibody to be marketed in the US. Lecanemab (Leqembi – Biogen/Eisai) was approved by the FDA in 2023 for the same indication as donanemab. Aducanumab (Aduhelm – Lilly) was granted accelerated approval in 2021, but it was withdrawn from the market...
Med Lett Drugs Ther. 2024 Aug 19;66(1709):129-31   doi:10.58347/tml.2024.1709a |  Show IntroductionHide Introduction

A Renal Indication for Semaglutide (Ozempic)

   
The Medical Letter on Drugs and Therapeutics • Mar 03, 2025  (Issue 1723)
intervals to 0.5 mg and then to 1 mg once weekly. The wholesale acquisition cost (WAC) for a 28-day supply ...
The injectable glucagon-like peptide-1 (GLP-1) receptor agonist semaglutide (Ozempic – Novo Nordisk) has been approved by the FDA to reduce the risk of sustained eGFR decline, end-stage kidney disease, and cardiovascular death in adults with type 2 diabetes and chronic kidney disease (CKD). It is the first GLP-1 receptor agonist to be approved in the US for this indication.
Med Lett Drugs Ther. 2025 Mar 3;67(1723):38-40   doi:10.58347/tml.2025.1723d |  Show IntroductionHide Introduction

Sebetralstat (Ekterly) for Treatment of Hereditary Angioedema Attacks

   
The Medical Letter on Drugs and Therapeutics • Feb 16, 2026  (Issue 1748)
, and laryngeal mucosa. Attacks generally last for 2-5 days and are less likely to be fatal now that effective ...
Sebetralstat (Ekterly – Kalvista), an oral plasma kallikrein inhibitor, has been approved by the FDA for treatment of acute hereditary angioedema (HAE) attacks in patients ≥12 years old. It is the first oral drug to be approved in the US for this indication. The intravenous C1 esterase inhibitors (C1INHs) Berinert and Ruconest, the subcutaneous plasma kallikrein inhibitor ecallantide (Kalbitor), and the subcutaneous bradykinin B2 receptor antagonist icatibant (Firazyr) have been available for years for on-demand treatment of HAE attacks; all of these drugs except ecallantide can...
Med Lett Drugs Ther. 2026 Feb 16;68(1748):29-30   doi:10.58347/tml.2026.1748c |  Show IntroductionHide Introduction

Oriahnn for Fibroid-Associated Heavy Menstrual Bleeding

   
The Medical Letter on Drugs and Therapeutics • Apr 05, 2021  (Issue 1621)
not be used for more than 24 months because of the risk of irreversible bone loss. The cost of 28 days ...
Oriahnn (Abbvie), a fixed-dose combination of the gonadotropin-releasing hormone (GnRH) receptor antagonist elagolix, the estrogen estradiol, and the progestin norethindrone acetate copackaged with elagolix alone, has been approved by the FDA for oral treatment of heavy menstrual bleeding associated with uterine leiomyomas (fibroids) in premenopausal women. It is the first product to be approved in the US for this indication. Elagolix (Orilissa) has been available since 2018 for treatment of moderate to severe pain associated with endometriosis. The GnRH receptor antagonist...
Med Lett Drugs Ther. 2021 Apr 5;63(1621):51-2 |  Show IntroductionHide Introduction