Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Charlene M. Flowers"'
Publikováno v:
Neurology. 90:e1548-e1552
ObjectiveTo evaluate acute acalculous cholecystitis (AAC) as a potential safety risk for patients treated with alemtuzumab.MethodsThe Food and Drug Administration Adverse Event Reporting System and the medical literature were searched for cases of AA
Autor:
Yi Tsong, Min Chen, Feng Zhou, David A. Flockhart, Denise Toyer, Curtis Rosebraugh, Charlene M. Flowers, Ann Corken Mackey, Peter K. Honig
Publikováno v:
Pharmacoepidemiology and Drug Safety. 12:97-101
Purpose Evaluate whether a 15-minute lecture intervention will improve adverse drug reaction reporting quality on standard MedWatch forms. Methods Seventy-eight 4th-year medical students were randomized to intervention ‘Group-A’ or non-interventi
Publikováno v:
Alimentary Pharmacology & Therapeutics.
Aliment Pharmacol Ther 31, 1028–1035 Summary Background Natalizumab is a recombinant monoclonal antibody approved for the treatment of patients with multiple sclerosis and patients with Crohn’s disease. Because of its immunosuppressive effects, n
Publikováno v:
Pediatric neurology. 37(2)
Oxcarbazepine, a carbamazepine analog, was approved for use as an antiepileptic agent in the United States in 2000. A search of the United States Food and Drug Administration's Adverse Event Reporting System identified nine cases of oxcarbazepine-ass
Publikováno v:
New England Journal of Medicine. 354:773-774
To the Editor: Thirty-one case reports of new-onset seizures associated with off-label use of tiagabine (Gabitril) have prompted the addition of a boldface warning to the product label.1 (Tiagabine is approved by the Food and Drug Administration [FDA
Publikováno v:
Mayo Clinic Proceedings. 78:730-731