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Searched for Drug. Results 1391 to 1400 of 2663 total matches.
Epsolay - A Benzoyl Peroxide Cream for Rosacea
The Medical Letter on Drugs and Therapeutics • Feb 06, 2023 (Issue 1669)
%) or
severe (11%) papulopustular rosacea. In both trials,
patients were randomized to apply the drug or its ...
Epsolay (Galderma), a 5% benzoyl peroxide cream,
has been approved by the FDA for treatment of
inflammatory lesions of rosacea in adults. It is the first
product containing benzoyl peroxide to be approved
in the US for treatment of rosacea. Benzoyl peroxide
formulations approved for acne have been used off-label
to treat rosacea for years, but itching and burning
have limited their use.
Med Lett Drugs Ther. 2023 Feb 6;65(1669):21-2 doi:10.58347/tml.2023.1669c | Show Introduction Hide Introduction
Vutrisiran (Amvuttra) for Transthyretin Amyloid Cardiomyopathy
The Medical Letter on Drugs and Therapeutics • Jun 23, 2025 (Issue 1731)
of ATTR-CM. These drugs bind to
transthyretin tetramers, slowing their dissociation and
the formation ...
The FDA has approved vutrisiran (Amvuttra – Alnylam), a
subcutaneously injected small interfering RNA (siRNA),
to reduce cardiovascular hospitalizations, urgent heart
failure visits, and cardiovascular death in adults with
wild-type or variant transthyretin amyloid cardiomyopathy
(ATTR-CM). Vutrisiran is the first siRNA to be
approved in the US for this indication; it was approved
earlier for treatment of polyneuropathy associated with
hereditary transthyretin-mediated amyloidosis.
Med Lett Drugs Ther. 2025 Jun 23;67(1731):102-4 doi:10.58347/tml.2025.1731b | Show Introduction Hide Introduction
In Brief: Lisdexamfetamine (Vyvanse) for Binge Eating Disorder
The Medical Letter on Drugs and Therapeutics • Mar 16, 2015 (Issue 1464)
The Medical Letter®
on Drugs and Therapeutics
Objective Drug Reviews Since 1959
Volume 57 (Issue ...
Lisdexamfetamine dimesylate (Vyvanse), a prodrug of dextroamphetamine previously approved for treatment of attention-deficit/hyperactivity disorder, has now been approved for treatment of moderate-to-severe binge eating disorder (recurrent episodes of compulsive overeating without purging) in adults.FDA approval of lisdexamfetamine for this indication was based on two unpublished, 12-week trials, summarized in the package insert, that randomized patients with moderate-to-severe binge eating disorder to lisdexamfetamine 30 mg/day, which was titrated to 50 mg or, if needed, 70 mg, or to placebo....
COVID-19 Update: Remdesivir (Veklury) FDA-Approved for Children <12 Years Old (online only)
The Medical Letter on Drugs and Therapeutics • Jun 13, 2022 (Issue 1652)
Remdesivir (Veklury) FDA-Approved for Children ...
IV antiviral drug remdesivir (Veklury) has now been FDA-approved for treatment of COVID-19 in patients ≥28 days old who weigh ≥3 kg and are either hospitalized or at high risk for progression to severe disease. Remdesivir was already FDA-approved for these indications in patients ≥12 years old who weigh ≥40 kg; it was available under an Emergency Use Authorization (EUA) for younger or lighter patients. Remdesivir is the first drug to be FDA-approved for treatment of COVID-19 in children <12 years old.
In Brief: Pembrolizumab (Keytruda) for Cancers with Biomarkers (online only)
The Medical Letter on Drugs and Therapeutics • Jan 01, 2018 (Issue 1537)
with
a fluoropyrimidine, oxaliplatin, and irinotecan. This is
the first approval of a cancer drug based solely ...
The immune checkpoint inhibitor pembrolizumab (Keytruda – Merck), a programmed death receptor-1 (PD-1) inhibitor, has been granted accelerated approval by the FDA for use in adults and children who have unresectable or metastatic microsatellite-instability-high (MSI-H) or mismatch-repair-deficient (dMMR) solid tumors that have progressed following treatment, and do not have any satisfactory alternative treatment options. For metastatic colorectal cancer, the indication is limited to tumors that have progressed following combination treatment with a fluoropyrimidine, oxaliplatin, and...
In Brief: Wezlana — An Ustekinumab Biosimilar Interchangeable with Stelara
The Medical Letter on Drugs and Therapeutics • Jul 22, 2024 (Issue 1707)
of the drug is not yet available, but will presumably be less expensive than Stelara. The wholesale ...
The FDA has approved ustekinumab-auub (Wezlana –
Amgen), an interchangeable biosimilar product similar
to the interleukin-12 and -23 antagonist Stelara, for
treatment of the same indications as Stelara (see
Table 1). Wezlana is the first Stelara biosimilar to be
approved in the US.
Med Lett Drugs Ther. 2024 Jul 22;66(1707):119 doi:10.58347/tml.2024.1707e | Show Introduction Hide Introduction
Treatment of Xerostomia
The Medical Letter on Drugs and Therapeutics • Jul 29, 1988 (Issue 771)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical ...
Xerostomia, dry mouth due to decreased or absent saliva, is a common problem, particularly among elderly patients. Decreased salivary flow can be due to many different conditions, including drug therapy, Sj gren's syndrome (keratoconjunctivitis sicca) or radiation of the salivary glands.
Ibuprofen vs. Acetaminophen in Children
The Medical Letter on Drugs and Therapeutics • Dec 15, 1989 (Issue 807)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical ...
Since the implication of aspirin in Reye's syndrome, acetaminophen (Tylenol; and others) has become the standard drug for symptomatic treatment of fever and pain in children. Ibuprofen, a nonsteroidal anti-inflammatory drug (NSAID) available for many years in tables (Mortin; Advil; and others), has now become available in a suspension. The suspension will be sold by presecription for treatment of fever or arthritis in children.
Felodipine - Calcium-Channel Blocker For Hypertension
The Medical Letter on Drugs and Therapeutics • Dec 13, 1991 (Issue 859)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical ...
Felodipine (Plendil - Merck), an extended-release preparation of a dihydropyridine calcium-channel blocker was recently marketed in the USA for oral treatment of hypertension. An immediate-release formulation is available in some other countries.
Captopril for Diabetic Nephropathy
The Medical Letter on Drugs and Therapeutics • May 27, 1994 (Issue 923)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical Letter ...
Captopril (Capoten - Bristol-Myers Squibb), an angiotensin-converting enzyme (ACE) inhibitor previously available for treatment of hypertension, has now been approved by the US Food and Drug Administration (FDA) for treatment of diabetic nephropathy in patients with insulin-dependent diabetes mellitus (IDDM). Diabetic nephropathy is the most common cause of end-stage renal disease in the United States.
