Search Results for "treatment guidelines"
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Searched for treatment guidelines. Results 301 to 310 of 424 total matches.
Apixaban (Eliquis) - A New Oral Anticoagulant for Atrial Fibrillation
The Medical Letter on Drugs and Therapeutics • Feb 04, 2013 (Issue 1409)
Apixaban (Eliquis) — A New Oral
Anticoagulant for Atrial Fibrillation
STANDARD TREATMENT — Atrial ...
The FDA has approved apixaban (Eliquis – Bristol-Myers Squibb/Pfizer), an oral direct factor Xa inhibitor,
for prevention of stroke and systemic embolism in
patients with nonvalvular atrial fibrillation. It is the third
new oral anticoagulant to be approved for this indication
as an alternative to warfarin.
Antiviral Drugs for Seasonal Influenza for 2024-2025
The Medical Letter on Drugs and Therapeutics • Dec 09, 2024 (Issue 1717)
illness.1,3
Guidelines for treatment of community-acquired
pneumonia (CAP) recommend antiviral treatment ...
Influenza is generally a self-limited illness, but
pneumonia, respiratory failure, and death can occur,
especially in persons at increased risk for influenza
complications (see Table 1). Updated information on
influenza activity and antiviral resistance is available
from the CDC at cdc.gov/flu.
Med Lett Drugs Ther. 2024 Dec 9;66(1717):193-8 doi:10.58347/tml.2024.1717a | Show Introduction Hide Introduction
Resmetirom (Rezdiffra) for Metabolic Dysfunction-Associated Steatohepatitis
The Medical Letter on Drugs and Therapeutics • Apr 29, 2024 (Issue 1701)
, has received accelerated
approval from the FDA for treatment of noncirrhotic
nonalcoholic steatohepatitis ...
Resmetirom (Rezdiffra – Madrigal), a thyroid hormone
receptor-beta agonist, has received accelerated
approval from the FDA for treatment of noncirrhotic
nonalcoholic steatohepatitis (NASH) with moderate
to advanced fibrosis in adults. NASH has recently
been renamed metabolic dysfunction-associated
steatohepatitis (MASH). Resmetirom is the first drug
to be approved in the US for this indication.
Med Lett Drugs Ther. 2024 Apr 29;66(1701):65-6 doi:10.58347/tml.2024.1701a | Show Introduction Hide Introduction
In Brief: Extended-Release Amoxicillin for Strep Throat
The Medical Letter on Drugs and Therapeutics • Mar 09, 2009 (Issue 1307)
-daily
treatment of pharyngitis or tonsillitis caused by
Streptococcus pyogenes in adults and children ...
The FDA has approved an extended-release formulation of amoxicillin (Moxatag – MiddleBrook) for once-daily treatment of pharyngitis or tonsillitis caused by Streptococcus pyogenes in adults and children ≥12 years old. Approval was based on an unpublished study that found once-daily treatment with Moxatag 775 mg for 10 days non-inferior to penicillin V 250 mg four times a day for 10 days in eradication of S. pyogenes.For decades, the drug of choice for oral treatment of streptococcal pharyngitis in adolescents and adults has been penicillin V 250 mg taken three or four times a day.1...
Drugs for Psoriatic Arthritis
The Medical Letter on Drugs and Therapeutics • Dec 30, 2019 (Issue 1588)
arthritis.1 Updated guidelines for treatment
of psoriatic arthritis have recently been published.2 ...
Psoriatic arthritis is a chronic inflammatory
arthropathy associated with psoriasis. A recent review
found that about 20% of patients with psoriasis have
psoriatic arthritis. Updated guidelines for treatment
of psoriatic arthritis have recently been published.
Eloctate for Hemophilia A
The Medical Letter on Drugs and Therapeutics • Oct 12, 2015 (Issue 1479)
factor VIII (produced ▶ Treatment and prophylaxis of bleeding 14.7 hrs N.A.4
(Octapharma) in human ...
The FDA has approved Eloctate (Biogen), a recombinant
factor VIII Fc fusion protein with an extended half-life,
for use in adults and children with hemophilia
A. Eloctate is indicated for control and prevention of
bleeding episodes, perioperative management, and
routine prophylaxis to prevent or reduce the frequency
of bleeding episodes. It is the first antihemophilic factor
VIII Fc fusion protein to be approved for hemophilia A.
Nalmefene - Long-Acting Injectable Opioid Antagonist
The Medical Letter on Drugs and Therapeutics • Oct 27, 1995 (Issue 960)
in patients with end-stage renal failure or with hepatic disease. Guidelines for use in children and neonates ...
Nalmefene (Revex - Ohmeda), an i methylene analog of naltrexone (Trexan), is a long-acting opioid antagonist that has been approved by the US Food and Drug Administration for reversal of postoperative opioid drug effects, including respiratory depression, sedation and hypotension and for management of known or suspected opioid overdose in the emergency department. The only other opioid antagonists available in the USA are naloxone (Narcan), which is also injectable but has a short duration of action, and naltrexone, which has a long duration of action but is marketed only for oral...
Choice of Drugs for Heparin-Induced Thrombocytopenia
The Medical Letter on Drugs and Therapeutics • May 28, 2012 (Issue 1391)
publications have made somewhat different recommendations
on its treatment.1-3
HIT — Antibody-mediated severe ...
A reader has asked us to review the choice of drugs for
heparin-induced thrombocytopenia (HIT), a prothrombotic
state with high morbidity and mortality. Three recent
publications have made somewhat different recommendations
on its treatment.
Ozenoxacin 1% Cream (Xepi) for Impetigo
The Medical Letter on Drugs and Therapeutics • Apr 22, 2019 (Issue 1570)
of ozenoxacin (Xepi – Cutanea), a nonfluorinated
quinolone antibiotic, for treatment of impetigo caused ...
The FDA has approved a 1% cream formulation
of ozenoxacin (Xepi – Cutanea), a nonfluorinated
quinolone antibiotic, for treatment of impetigo caused
by Staphylococcus aureus or Streptococcus pyogenes
in patients ≥2 months old.
Varenicline (Chantix) Warnings: Risk Versus Benefit
The Medical Letter on Drugs and Therapeutics • Jul 14, 2008 (Issue 1290)
and attempted suicide.
6
CLINICAL TRIALS — In clinical trials with varenicline,
no increase in treatment ...
The nicotine receptor partial agonist varenicline (Chantix - Pfizer) appears to be the most effective drug available to treat tobacco dependence, but the FDA has added a warning to the package insert about neuropsychiatric symptoms and exacerbations of preexisting psychiatric illness associated with its use. Agitation, hostility, depressed mood, suicidal ideation and suicidal behavior have been reported as postmarketing adverse events in patients who took varenicline and stopped smoking and in those who took the drug and continued to smoke.