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Searched for days. Results 151 to 160 of 1849 total matches.
Lybrel - A Continuous Oral Contraceptive
The Medical Letter on Drugs and Therapeutics • Jul 30, 2007 (Issue 1266)
Publication
Lybrel (Wyeth) is the first FDA-approved low-dose
combination oral contraceptive taken 365 days ...
Lybrel (Wyeth) is the first FDA-approved low-dose combination oral contraceptive taken 365 days a year without a placebo or pill-free interval. All tablets contain low doses of levonorgestrel (0.09 mg) and ethinyl estradiol (20 mcg). Most oral contraceptives are packaged as a 21/7 cycle (21 days of active tablets and 7 days of placebo), resulting in 13 withdrawal bleeding episodes each year. Two formulations are taken for 24 days followed by 4 days of inert tablets (Yaz and Loestrin 24). Two others (Seasonique and Seasonale) have a 91-day cycle with only 4 withdrawal bleeds per...
Drugs for Cognitive Loss and Dementia
The Medical Letter on Drugs and Therapeutics • Aug 22, 2022 (Issue 1657)
subjects,
donepezil exposure with the 10 mg/day transdermal
formulation was similar to that with 10-mg ...
Alzheimer's disease (AD) is the most common
cause of dementia, but cognitive decline is also
associated with other neurological conditions such
as Parkinson's disease, dementia with Lewy bodies,
vascular dementia, and frontotemporal dementia.
Fluoxetine (Prozac) Revisited
The Medical Letter on Drugs and Therapeutics • Sep 07, 1990 (Issue 826)
of fluoxetine reach a peak within six to 12 hours, and
norfluoxetine peaks within one to three days ...
In the short time since fluoxetine (Prozac - Lilly) first became available in the USA (Medical Letter, 30:45, 1988), it has become the most frequently prescribed of all antidepressants. Some recent reports, however, have questioned its safety.
An EUA for Bebtelovimab for Treatment of COVID-19
The Medical Letter on Drugs and Therapeutics • Mar 21, 2022 (Issue 1646)
confirmatory testing for SARS-CoV-2 infection within
the previous 3 days. BLAZE-4 was completed before ...
The investigational monoclonal antibody
bebtelovimab (LY-CoV1404 – Lilly) has been granted
an FDA Emergency Use Authorization (EUA) for IV
treatment of mild to moderate COVID-19 in patients
≥12 years old who weigh ≥40 kg and are at high
risk of progressing to severe disease, including
hospitalization and death, and for whom alternative
treatment options are unavailable or inappropriate.
Bebtelovimab is active against the Omicron variant of
SARS-CoV-2; sotrovimab (VIR-7831) is the only other
monoclonal antibody currently available for treatment
of COVID-19 that is active...
Sertraline For Treatment Of Depression
The Medical Letter on Drugs and Therapeutics • May 15, 1992 (Issue 870)
one day.
EFFECTIVENESS — An eight-week double-blind, placebo-controlled multicenter trial including ...
Sertraline (Zoloft - Roerig), a serotonin reuptake inhibitor, was recently approved for marketing by the US Food and Drug Administration for treatment of depression. Another serotonin reuptake inhibitor, fluoxetine (Prozac), is prescribed more frequently in the USA than any other antidepressant (Medical Letter, 32:83, 1990).
Pantroprazole (Protonix)
The Medical Letter on Drugs and Therapeutics • Jul 24, 2000 (Issue 1083)
INHIBITORS
Drug Dosage
1
Formulation Cost
2
Lansoprazole − Prevacid (Tap) 30 mg/day capsule $116.41 ...
Pantoprazole, the fourth benzimidazole proton pump inhibitor to become available in the United States, has been marketed for short-term oral treatment of erosive gastroesophageal reflux disease (GERD).
Vibrant – An Oral Vibrating Capsule for Chronic Idiopathic Constipation
The Medical Letter on Drugs and Therapeutics • May 01, 2023 (Issue 1675)
at night
between 9 and 10 pm and was preprogrammed to
begin vibrating at noon the next day; it was active ...
The Vibrant orally administered vibrating capsule
(Vibrant Gastro), an FDA-cleared medical device, is
now available by prescription for treatment of adults
with chronic idiopathic constipation (CIC) who have
not experienced relief of their bowel symptoms
by using laxative therapies at the recommended
dosage for at least one month. It is the first drug-free
treatment to be authorized by the FDA for this
indication.
Med Lett Drugs Ther. 2023 May 1;65(1675):65-7 doi:10.58347/tml.2023.1675a | Show Introduction Hide Introduction
Fluoxetine For Depression
The Medical Letter on Drugs and Therapeutics • Apr 22, 1988 (Issue 764)
. The elimination halflife is one to three days for fluoxetine and seven to 15 days for norfluoxetine (L Lemberger ...
Fluoxetine (Prozac - Dista), a phenylpropylamide, is the first serotonin-reuptake blocker introduced in the USA for treatment of . It is being promoted as causing fewer adverse effects than other antidepressants. Claims of greater safety and patient tolerability have often been made for new non-tricyclic antidepressants in recent years, but unpredicted adverse effects have emerged with widespread use, including priapism with trazodone (Desyrel - Medical Letter, 26:35, 1984) and fatal hemolytic anemia with nomifensine (Merital - Medical Letter, 27:73, 1985).
Famciclovir for Herpes Zoster
The Medical Letter on Drugs and Therapeutics • Oct 28, 1994 (Issue 934)
lesions was five days with either dosage of the drug and seven days with placebo. There was no difference ...
Famciclovir (Famvir - SmithKline Beecham) is now available in the USA for oral treatment of acute uncomplicated herpes zoster (shingles). The manufacturer claims that use of the drug reduces the duration of postherpetic neuralgia. Famciclovir is similar to acyclovir (Zovirax - Burroughs Wellcome), which has been the drug of choice for treatment of varicella-zoster and herpes simplex virus infections (Medical Letter, 36:27, 1994).
Perampanel (Fycompa) for Epilepsy
The Medical Letter on Drugs and Therapeutics • Feb 03, 2014 (Issue 1435)
with food)
Time to steady state 2-3 wks (5-7 days with enzyme-inducing AEDs)
Metabolism Primary oxidation ...
Perampanel (per am’ pa nel; Fycompa – Eisai), a first-in-class noncompetitive AMPA receptor antagonist, has
been approved by the FDA for adjunctive treatment of
partial-onset seizures in patients ≥12 years old. New
drugs for epilepsy are often initially approved by the
FDA as adjunctive treatment for partial seizures.