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Searched for v. Results 171 to 180 of 220 total matches.
Metaglip and Avandamet for Type 2 Diabetes
The Medical Letter on Drugs and Therapeutics • Dec 23, 2002 (Issue 1146)
by 1.0% and 1.2%, compared
to metformin-placebo (V Fonseca et al, JAMA 2000; 283:1695). Another 26-week ...
Two new fixed-dose combinations are now available for management of type 2 diabetes. Metaglip (Bristol-Myers Squibb), a combination of metformin and glipizide, is approved for initial therapy or as second-line treatment when control is not adequate on metformin or a sulfonylurea alone. Avandamet (GlaxoSmithKline), a combination of metformin and rosiglitazone, is approved by the FDA only as second-line therapy for patients who are not well controlled on metformin alone, or are already taking both metformin and rosiglitazone. Glucovance (Bristol-Myers Squibb), a combination of metformin and...
Gemifloxacin (Factive)
The Medical Letter on Drugs and Therapeutics • Sep 20, 2004 (Issue 1192)
for 5 days compared
with sequential therapy with I.V. ceftriaxone/oral cefuroxime (maxiGEMIFLOXACIN ...
Gemifloxacin (Factive - Oscient), a new oral fluoroquinolone antibiotic, has been approved by the FDA for 5 days' treatment of acute bacterial exacerbations of chronic bronchitis (ABECB) and 7 days' treatment of mild to moderate community-acquired pneumonia (CAP) in adults. For the next 6-8 months it will only be available, presumably for commercial reasons, in states east of the Rocky Mountains.
Bepotastine (Bepreve) - An Ophthalmic H1-Antihistamine
The Medical Letter on Drugs and Therapeutics • Feb 08, 2010 (Issue 1331)
conjunctivitis. Immunol
Allergy Clin North Am 2008; 28:43.
2. V Yaylali et al. Comparative study of 0.1 ...
Bepotastine besilate 1.5% ophthalmic solution (Bepreve - ISTA Pharmaceuticals), an H1-antihistamine, has been approved by the FDA for topical treatment of itching associated with allergic conjunctivitis in patients ≥2 years old. Bepotastine was first developed in an oral systemic formulation and has been used as such for treatment of allergic rhinitis in Japan.
Ezogabine (Potiga) for Epilepsy
The Medical Letter on Drugs and Therapeutics • Aug 20, 2012 (Issue 1397)
as a
Schedule V controlled substance. The drug is classified
as category C (risk cannot be ruled out) for use ...
The FDA has approved ezogabine (ee-ZOE-ga-been;
Potiga – GSK/Valeant) for oral adjunctive treatment of
partial-onset seizures in adults. Ezogabine is available
in Europe as retigabine (Trobalt).
Ponesimod (Ponvory) for Multiple Sclerosis
The Medical Letter on Drugs and Therapeutics • Aug 09, 2021 (Issue 1630)
with an
increased risk of SARS-CoV-2 infection or development
of severe COVID-19, but data are limited.9 In one ...
The FDA has approved ponesimod (Ponvory –
Janssen), a sphingosine 1-phosphate (S1P) receptor
modulator, for treatment of adults with relapsing forms
of multiple sclerosis (MS), including clinically isolated
syndrome (initial neurological episode), relapsing-remitting
disease, and active secondary progressive
MS (SPMS). Ponesimod is the fourth oral S1P receptor
modulator to be approved in the US for once-daily
treatment of relapsing forms of MS; ozanimod
(Zeposia) and siponimod (Mayzent) are also approved
for use in adults, and fingolimod (Gilenya) is indicated
for use in patients...
Drugs for Cardiac Arrhythmias
Treatment Guidelines from The Medical Letter • Jun 01, 2007 (Issue 58)
of drugs varies with the clinical setting (V Fuster et al, ACC/AHA/ESC Guidelines. J Am Coll Cardiol 2006 ...
The drugs of choice for treatment of common cardiac arrhythmias are listed in Tables 1 and 2. Some drugs are recommended for indications that have not been approved by the FDA.
Vaccines for Travelers
The Medical Letter on Drugs and Therapeutics • Nov 19, 2018 (Issue 1560)
by
toxigenic V. cholerae serogroup O1, including areas
with cholera activity within the last year ...
Persons planning to travel outside the US should be
up to date on routine vaccines and, depending on their
destination, duration of travel, and planned activities,
may also receive certain travel-specific vaccines.
Tickborne encephalitis and dengue vaccines, which
are not available in the US, are reviewed in a separate
article available online. Detailed advice for travel to
specific destinations is available from the Centers for
Disease Control and Prevention (CDC) at www.cdc.gov/travel/destinations/list. Recommendations for
administration of vaccines as part of routine...
Drugs for Anxiety Disorders
The Medical Letter on Drugs and Therapeutics • Aug 07, 2023 (Issue 1682)
as a schedule
V controlled substance because of reports of euphoria
associated with its use. Gabapentin ...
Anxiety disorders (generalized anxiety disorder,
panic disorder, social anxiety disorder, and various
phobias) are the most common form of psychiatric
illness. They can be treated effectively with cognitive
behavioral therapy (CBT) and/or pharmacotherapy.
Med Lett Drugs Ther. 2023 Aug 7;65(1682):121-8 doi:10.58347/tml.2023.1682a | Show Introduction Hide Introduction
Pregabalin (Lyrica) for Fibromyalgia
The Medical Letter on Drugs and Therapeutics • Sep 24, 2007 (Issue 1270)
— Pregabalin is a Schedule V
controlled substance. Adverse effects in clinical trials
have included dizziness ...
Pregabalin (Lyrica - Pfizer) is the first drug approved by the FDA for management of fibromyalgia. When it was first marketed, pregabalin, which is structurally similar to gabapentin (Neurontin, and others), was approved for treatment of neuropathic pain associated with postherpetic neuralgia and diabetic peripheral neuropathy and for adjunctive treatment of partial onset seizures in adults with epilepsy. It has also been prescribed off-label for other types of neuropathic pain such as sciatica.
Cannabidiol (Epidiolex) for Epilepsy
The Medical Letter on Drugs and Therapeutics • Nov 05, 2018 (Issue 1559)
the absence of
euphoria.7 It has been classified as a schedule V
controlled substance by the DEA.
CLINICAL ...
The FDA has approved cannabidiol oral solution
(Epidiolex – Greenwich Biosciences) for treatment
of seizures associated with Dravet syndrome or
Lennox-Gastaut syndrome in patients ≥2 years old.
Cannabidiol (CBD) is a cannabinoid constituent of
the marijuana plant (Cannabis sativa). It is the first
natural marijuana product to be approved by the FDA
for any indication and the first drug to be approved in
the US for treatment of Dravet syndrome. Stiripentol
(Diacomit), which is not a marijuana product, was also
recently approved by the FDA for treatment of Dravet
syndrome in...