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 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 Introduction Hide 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 Introduction Hide 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 Introduction Hide 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 Introduction Hide 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 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
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 Introduction Hide 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...
