Search Results for "1"
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 1. Results 1191 to 1200 of 2716 total matches.
iDose TR — A Travoprost Implant for Glaucoma
The Medical Letter on Drugs and Therapeutics • Apr 29, 2024 (Issue 1701)
; Durysta, an intracameral implant
containing the prostaglandin analog bimatoprost,
was the first.1 ...
The FDA has approved iDose TR (Glaukos), an
intracameral implant containing the prostaglandin
analog (PGA) travoprost, for reduction of intraocular
pressure (IOP) in patients with open-angle glaucoma
or ocular hypertension. Travoprost is also available
as a topical ophthalmic solution (Travatan Z, and
generics) for the same indication. iDose TR is the
second ocular implant to become available in the US
for this indication; Durysta, an intracameral implant
containing the prostaglandin analog bimatoprost,
was the first.
Med Lett Drugs Ther. 2024 Apr 29;66(1701):70-1 doi:10.58347/tml.2024.1701d | Show Introduction Hide Introduction
Iloprost (Aurlumyn) for Frostbite
The Medical Letter on Drugs and Therapeutics • Jul 22, 2024 (Issue 1707)
to assess vascular flow to the affected area. Frostbite is classified according to severity from grade 1 ...
The FDA has approved Aurlumyn (Eicos Sciences),
an IV formulation of the prostacyclin analog iloprost,
to reduce the risk of digit amputation in adults
with severe frostbite. Iloprost is the first drug to be
approved by the FDA for treatment of severe frostbite;
it has been used off-label for this indication in the EU
and elsewhere for decades. In the US, iloprost is also
available as an inhaled formulation (Ventavis) for
treatment of pulmonary arterial hypertension.
Med Lett Drugs Ther. 2024 Jul 22;66(1707):114 doi:10.58347/tml.2024.1707b | Show Introduction Hide Introduction
Comparison Chart: Some Drugs for Irritable Bowel Syndrome with Diarrhea (IBS-D) (online only)
The Medical Letter on Drugs and Therapeutics • Feb 03, 2025 (Issue 1721)
)
5.8 g/teaspoon powder; 5.8 g
packets; 1.8 g caps; 2 g wafers
$29.00
10-35 g/day in 2-3 divided ...
View the Comparison Chart: Some Drugs for Irritable Bowel Syndrome with Diarrhea (IBS-D)
Med Lett Drugs Ther. 2025 Feb 3;67(1721):e1-3 doi:10.58347/tml.2025.1721f | Show Introduction Hide Introduction
Imlunestrant (Inluriyo) for Advanced Breast Cancer
The Medical Letter on Drugs and Therapeutics • Jan 19, 2026 (Issue 1746)
receptor (ER)-positive, human epidermal
growth factor receptor 2 (HER2)-negative, estrogen
receptor 1 ...
The FDA has approved imlunestrant (Inluriyo – Lilly),
an oral estrogen receptor antagonist, for treatment
of estrogen receptor (ER)-positive, human epidermal
growth factor receptor 2 (HER2)-negative, estrogen
receptor 1 (ESR1)-mutated advanced or metastatic
breast cancer in adults who had disease progression
following at least one prior line of endocrine therapy.
Imlunestrant is the second oral selective estrogen
receptor degrader (SERD) to be approved in the US for
treatment of breast cancer; elacestrant (Orserdu) was
approved in 2023.
Med Lett Drugs Ther. 2026 Jan 19;68(1746):14-5 doi:10.58347/tml.2026.1746d | Show Introduction Hide Introduction
Ensitrelvir (Xocova) for Post-Exposure Prophylaxis of COVID-19
The Medical Letter on Drugs and Therapeutics • Jul 20, 2026 (Issue 1759)
mg PO on day 1 (taken within 72 hours of
exposure), followed by 125 mg on days 2-5
▶ Cost: A 5-day ...
The FDA has approved ensitrelvir (Xocova – Shionogi), a SARS-CoV-2 main protease inhibitor, for postexposure prophylaxis
of COVID-19 in patients ≥12 years old who had contact with
an infected individual. Ensitrelvir is the first oral antiviral
drug to be approved in the US for this indication. The parenteral
monoclonal antibody combinations bamlanivimab and
etesevimab and casirivimab and imdevimab (REGEN-COV)
are no longer authorized for postexposure prophylaxis of
COVID-19 in the US.
Med Lett Drugs Ther. 2026 Jul 20;68(1759):113-4 doi:10.58347/tml.2026.1759a | Show Introduction Hide Introduction
Drugs for Overactive Bladder
The Medical Letter on Drugs and Therapeutics • Mar 20, 2023 (Issue 1672)
of dietary irritants such as
alcohol and caffeine, should be tried first.1,2
ANTICHOLINERGIC DRUGS ...
In overactive bladder, involuntary bladder contractions
due to detrusor overactivity result in urinary
urgency, frequency, nocturia, and incontinence.
The prevalence of the disorder increases with age.
Nonpharmacologic treatment, including bladder
training, urge suppression, pelvic floor muscle
exercises, constipation management, modification of
fluid intake, and avoidance of dietary irritants such as
alcohol and caffeine, should be tried first.
Med Lett Drugs Ther. 2023 Mar 20;65(1672):41-5 doi:10.58347/tml.2023.1672a | Show Introduction Hide Introduction
Tickborne Encephalitis and Dengue Vaccines (online only)
The Medical Letter on Drugs and Therapeutics • Nov 19, 2018 (Issue 1560)
; 0 and 1-7 months for TBE-Moscow); a rapid
schedule of EnceVir (0 and 1-2 months) can be used ...
No vaccines against tickborne encephalitis (TBE) or
dengue are available in the US, but vaccines have been
licensed in some other countries.
Aripiprazole with Digital Ingestion Tracking (Abilify MyCite)
The Medical Letter on Drugs and Therapeutics • Jan 28, 2019 (Issue 1564)
for maintenance treatment of nonadherent
patients (Abilify Maintena, Aristada).1
INGESTION TRACKING — Cuprous ...
Monitoring adherence of psychiatric patients to
oral medication may be especially difficult. The
FDA has approved Abilify MyCite (Otsuka/Proteus),
an aripiprazole tablet with an embedded sensor
that tracks when patients take the medication. It is
indicated for treatment of adults with schizophrenia,
bipolar disorder, or major depressive disorder. Abilify MyCite is the first drug with a digital ingestion tracking
system to be approved in the US.
In Brief: Prevention of Meningococcal B Disease
The Medical Letter on Drugs and Therapeutics • Dec 09, 2013 (Issue 1431)
to be immunogenic,
and appears to be safe.1 Its efficacy has not been
established clinically, but laboratory ...
An outbreak (8 cases to date) of meningococcal disease at Princeton University caused by Neisseria meningitidis serogroup B has led the FDA and CDC to permit importation and investigational use (at Princeton University only) of a meningococcus B vaccine (4CMenB; Bexsero – Novartis) that has not been approved in the US. Bexsero has been approved for use in the European Union and in Australia.THE VACCINE — Until recently, no serogroup B vaccine was widely available because the polysaccharide capsule of the B serogroup, unlike those of the other main meningococcal serogroups (A, C, Y, and...
In Brief: Uridine Triacetate (Xuriden) for Hereditary Orotic Aciduria (online only)
The Medical Letter on Drugs and Therapeutics • Mar 28, 2016 (Issue 1491)
(estimated birth
prevalence: ...
The FDA has approved the pyrimidine analog uridine triacetate (Xuriden [zur' uh den] – Wellstat Therapeutics) for treatment of hereditary orotic aciduria, a rare autosomal recessive disorder (estimated birth prevalence: <1:1,000,000) in infants and children caused by a deficiency in uridine 5'-monophosphate (UMP) synthase. This deficiency prevents synthesis of uridine nucleotides and causes developmental delays, failure to gain weight, hematologic abnormalities, and excessive urinary excretion of orotic acid, which can lead to urinary obstruction.1 Xuriden is the first drug to be approved...
