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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.
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.
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).
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.
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 Introduction Hide 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 Introduction Hide 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 Introduction Hide 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 Introduction Hide 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."
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...