Search Results for "days"
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Searched for days. Results 51 to 60 of 1911 total matches.
Toremifene and Letrozole for Advanced Breast Cancer
The Medical Letter on Drugs and Therapeutics • Apr 10, 1998 (Issue 1024)
Aminoglutethimide − Cytadren (Novartis) 250 mg PO qid 135.43
* Cost to the pharmacist for 30 days’ treatment based ...
The antiestrogen toremifene (Fareston - Schering) and the selective aromatase inhibitor letrozole (Femara - Novartis) have been approved by the FDA for treatment of advanced breast cancer in postmenopausal women.
Valacyclovir (Valtrex) for Oral Herpes
The Medical Letter on Drugs and Therapeutics • Nov 11, 2002 (Issue 1143)
(Valtrex − GlaxoSmithKline) was recently approved by the FDA for one-day
oral treatment of patients ...
Valacyclovir (Valtrex - GlaxoSmithKline) was recently approved by the FDA for one-day oral treatment of patients at least 12 years old with orolabial herpes simplex infections. The drug was previously approved for treatment and suppression of genital herpes and for treatment of herpes zoster (shingles).
Timing of Remdesivir for COVID-19
The Medical Letter on Drugs and Therapeutics • Oct 19, 2020 (Issue 1609)
with remdesivir than with placebo
(median 10 vs 15 days), a statistically significant
difference. Kaplan-Meier ...
Remdesivir (Veklury – Gilead), an investigational
antiviral drug administered by IV infusion, is now
available through an FDA Emergency Use Authorization
(EUA) for treatment of COVID-19 in all hospitalized
patients. An earlier EUA limited use of the drug to
patients hospitalized with severe disease.
Escitalopram (Lexapro) for Depression
The Medical Letter on Drugs and Therapeutics • Sep 30, 2002 (Issue 1140)
(Forest) 40 mg once/day $ 69.00
Escitalopram − Lexapro (Forest) 10 mg once/day 66.71**
Fluoxetine ...
Escitalopram (Lexapro - Forest), the active S-enantiomer of racemic citalopram (Celexa - Forest), a selective serotonin reuptake inhibitor (SSRI), was recently approved by the FDA for treatment of depression. The manufacturer plans to stop promoting Celexa in favor of Lexapro; Celexa will continue to be available for patients already taking it.
An EUA for Baricitinib (Olumiant) for COVID-19
The Medical Letter on Drugs and Therapeutics • Dec 28, 2020 (Issue 1614)
received baricitinib
4 mg or placebo once daily for 14 days or until hospital
discharge, in addition ...
The oral Janus kinase (JAK) inhibitor baricitinib
(Olumiant – Lilly) has been granted an FDA Emergency
Use Authorization (EUA) for treatment of confirmed or
suspected COVID-19 in hospitalized patients ≥2 years
old who require supplemental oxygen, mechanical
ventilation, or extracorporeal membrane oxygenation
(ECMO); the EUA requires that baricitinib be used
in combination with the IV antiviral drug remdesivir
(Veklury). Baricitinib has been available for treatment
of rheumatoid arthritis since 2018. Remdesivir was
recently approved by the FDA for treatment of COVID-19
in...
Expanded Table: Some Drugs for Altitude Illness, Jet Lag, and Motion Sickness (online only)
The Medical Letter on Drugs and Therapeutics • Oct 07, 2019 (Issue 1582)
– generic 125, 250 mg tabs 125 mg bid (started the day before
ascent and continued at high altitude
for 2 ...
View the Expanded Table: Some Drugs for Altitude Illness, Jet Lag, and Motion Sickness
Oral Semaglutide (Wegovy) for Weight Loss
The Medical Letter on Drugs and Therapeutics • Feb 02, 2026 (Issue 1747)
, a 30-day supply of Wegovy
25-mg tablets costs $299.
▶ Conclusion: Once-daily use of oral Wegovy ...
The FDA has approved an oral tablet formulation of
the glucagon-like peptide-1 (GLP-1) receptor agonist
semaglutide (Wegovy) for chronic weight management
in adults. It is the first oral GLP-1 receptor agonist to
be approved in the US for weight management. An
injectable formulation of Wegovy was approved for
the same indication in 2021.1 The injectable GLP-1
receptor agonist liraglutide (Saxenda, and generic)
and the injectable glucose-dependent insulinotropic
polypeptide (GIP)/GLP-1 receptor agonist tirzepatide
(Zepbound) are also FDA-approved for chronic weight
management (see...
Med Lett Drugs Ther. 2026 Feb 2;68(1747):17-8 doi:10.58347/tml.2026.1747a | Show Introduction Hide Introduction
Two New Drugs for Skin and Skin Structure Infections
The Medical Letter on Drugs and Therapeutics • Aug 18, 2014 (Issue 1449)
, 600 mg vials 600 mg q12h 5-14 days
Teflaro (Forest) $126.30
Dalbavancin3 – 500 mg vials 1000 mg x 1 ...
The FDA has approved two new drugs for treatment
of adults with acute bacterial skin and skin structure
infections caused by susceptible gram-positive
bacteria. Dalbavancin (Dalvance – Durata) is a long-acting
intravenous (IV) lipoglycopeptide antibiotic
similar to telavancin (Vibativ). Tedizolid phosphate
(Sivextro – Cubist) is an IV and oral oxazolidinone
antibacterial drug similar to linezolid (Zyvox). A
third IV antibiotic, oritavancin (Orbactiv), recently
approved by the FDA for the same indication, will be
reviewed in a future...
Omadacycline (Nuzyra) - A New Tetracycline Antibiotic
The Medical Letter on Drugs and Therapeutics • May 20, 2019 (Issue 1572)
or moxifloxacin;
patients could be switched to the respective oral
formulation after 3 days to complete a total ...
The FDA has approved omadacycline (Nuzyra – Paratek),
a semisynthetic tetracycline derivative, for once-daily
IV and oral treatment of community-acquired bacterial
pneumonia (CAP) and acute bacterial skin and skin
structure infections (ABSSSIs) in adults.
Botulinum Toxin for Chronic Migraine
The Medical Letter on Drugs and Therapeutics • Jan 24, 2011 (Issue 1356)
headache days/month for >3 months). It is the first
drug approved for treatment of this indication. Botox ...
The FDA has approved injection of onabotulinumtoxinA
(Botox – Allergan) for prevention of
headaches in adult patients with chronic migraine (≥15
headache days/month for ≥3 months). It is the first
drug approved for treatment of this indication. Botox is
also FDA-approved for treatment of upper limb spasticity,
axillary hyperhidrosis, cervical dystonia, blepharospasm
and strabismus, and for cosmetic
reduction of wrinkles.
