Search Results for "days"
Search again or select article below to purchase. Single article price: $45. Order 3 or more at one time and receive a 10% discount.
Sort by relevance | Sort by date
Searched for days. Results 1781 to 1790 of 1856 total matches.

Extended-Release Amantadine (Gocovri) for Dyskinesia in Parkinson's Disease

   
The Medical Letter on Drugs and Therapeutics • Dec 04, 2017  (Issue 1535)
(eGFR) ...
The FDA has approved an extended-release (ER) capsule formulation of amantadine (Gocovri – Adamas) for once-daily treatment of levodopa-induced dyskinesia in patients with Parkinson's disease (PD). It is the first product to be approved in the US for this indication. Immediate-release (IR) amantadine has been used off-label for years to manage levodopa-induced dyskinesia.
Med Lett Drugs Ther. 2017 Dec 4;59(1535):198-200 |  Show IntroductionHide Introduction

Shingrix - An Adjuvanted, Recombinant Herpes Zoster Vaccine

   
The Medical Letter on Drugs and Therapeutics • Dec 04, 2017  (Issue 1535)
daily activities occurred in 17% of persons who received Shingrix and persisted for a mean of 2 days ...
The FDA has approved an adjuvanted, recombinant varicella zoster virus (VZV) vaccine (Shingrix – GSK) for prevention of herpes zoster (shingles) in adults ≥50 years old. Shingrix is the second herpes zoster vaccine to be approved in the US; Zostavax, a live-attenuated VZV vaccine approved for the same indication, has been available since 2006.
Med Lett Drugs Ther. 2017 Dec 4;59(1535):195-6 |  Show IntroductionHide Introduction

Fiasp - Another Insulin Aspart Formulation for Diabetes

   
The Medical Letter on Drugs and Therapeutics • Jan 01, 2018  (Issue 1537)
or at room temperature; drug stored at room temperature should be discarded after 28 days. CONCLUSION ...
The FDA has approved Fiasp (Novo Nordisk), a new formulation of insulin aspart, to improve glycemic control in adults with diabetes. Fiasp is described by the manufacturer as faster-acting than conventional insulin aspart (Novolog).
Med Lett Drugs Ther. 2018 Jan 1;60(1537):6-7 |  Show IntroductionHide Introduction

Baricitinib (Olumiant) for Rheumatoid Arthritis

   
The Medical Letter on Drugs and Therapeutics • Jul 16, 2018  (Issue 1551)
PO once/d 4095.60 1. Approximate WAC for 30 days’ treatment at the usual adult dosage. WAC ...
The FDA has approved the Janus kinase (JAK) inhibitor baricitinib (Olumiant – Lilly) for oral treatment of adults with moderately to severely active rheumatoid arthritis (RA) that has not responded adequately to one or more tumor necrosis factor (TNF) inhibitors. Baricitinib is the second JAK inhibitor to be approved for treatment of RA; tofacitinib (Xeljanz, Xeljanz XR) was the first.
Med Lett Drugs Ther. 2018 Jul 16;60(1551):120-1 |  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

More New Drugs for HIV and Associated Infections

   
The Medical Letter on Drugs and Therapeutics • Feb 14, 1997  (Issue 994)
and Cost — The initial dosage of nevirapine is 200 mg once daily for the first 14 days to decrease ...
Four new drugs have become available in the USA for HIV infection or its complications. Nevirapine (Viramune - Roxane), intravenous cidofovir (Vistide - Gilead), and amphotericin B oral suspension (Fungizone Oral Suspension - Bristol-Myers Squibb) have been approved by the US Food and Drug Administration; nelfinavir (Viracept - Agouron) is currently available only through an "Expanded Access Program."
Med Lett Drugs Ther. 1997 Feb 14;39(994):14-6 |  Show IntroductionHide Introduction

Diagnostic Tests for HIV

   
The Medical Letter on Drugs and Therapeutics • Aug 29, 1997  (Issue 1008)
) or seven days. Negative results are available from a recorded message; patients with positive results ...
Diagnostic tests for human immunodeficiency virus (HIV) infection use four approaches: identification of antibodies to viral proteins, detection of viral antigens, detection of viral nucleic acids, and culturing the virus (CJ Schleupner in GL Mandell et al, eds, Principles and Practice of Infectious Diseases, 4th ed, New York:Churchill Livingstone, 1995, page 1253). In recent years, the FDA has approved the use of a 10- minute blood test, two home collection kits, and office tests that use urine and oral secretions to diagnose HIV infection. One home test, Confide (Johnson & Johnson), was...
Med Lett Drugs Ther. 1997 Aug 29;39(1008):81-3 |  Show IntroductionHide Introduction