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FDA is aware of cases where patients have used LifeScan OneTouch Ultra test strips with their Abbott Precision Xtra blood glucose meters.
As a result, the meters recorded lower-than-expected blood glucose levels, which can have serious clinical ...
Written by Food and Drug Adminstration (FDA): Patient Safety News · Filed Under FDA: News/Recalls
FDA has issued an advisory about the danger of mistakenly swallowing Spiriva (tiotropium bromide inhalation powder) and Foradil (formoterol fumarate inhalation powder) inhalation capsules. These capsules are intended to be used with inhalation devic...
Written by Food and Drug Adminstration (FDA): Patient Safety News · Filed Under FDA: News/Recalls
In a recent Public Health Notification, FDA informed healthcare professionals about new data on mortality rates associated with the AneuRx Stent Graft System. This endovascular graft, made by Medtronic, is used as an alternative to open surgery in p...
Written by Food and Drug Adminstration (FDA): Patient Safety News · Filed Under FDA: News/Recalls
FDA and Tibotec Therapeutics are alerting healthcare professionals about the risk of hepatotoxicity associated with the antiretroviral drug Prezista (darunavir). Prezista, co-administered with ritonavir and other antiretroviral agents, is used to tr...
Written by Food and Drug Adminstration (FDA): Patient Safety News · Filed Under FDA: News/Recalls
Talecris Biotherapeutics has revised the directions for administering some of the company's immune globulin products -- ones that come in uncalibrated prefilled 2 mL syringes with fixed needles. The products are HyperRABâ„¢ S/D , which is an anti-rabi...
Written by Food and Drug Adminstration (FDA): Patient Safety News · Filed Under FDA: News/Recalls
Roche Laboratories has updated information on neuropsychiatric events for Tamiflu (oseltamivir phosphate), a drug that's used to treat or prevent influenza in patients 1 year and older.
The revised labeling reminds practitioners that some patients...
Written by Food and Drug Adminstration (FDA): Patient Safety News · Filed Under FDA: News/Recalls
Biogen Idec and Elan Pharmaceuticals are warning healthcare professionals about reports of clinically significant liver injury in patients taking Tysabri (natalizumab). Tysabri is a monoclonal antibody used to treat certain patients with relapsing f...
Written by Food and Drug Adminstration (FDA): Patient Safety News · Filed Under FDA: News/Recalls
FDA is cautioning healthcare professionals, patients and caregivers about the unsafe use of Tussionex Pennkinetic Extended-Release Suspension. This product is a long-acting cough suppressant containing hydrocodone, a narcotic antitussive, and chlorp...
Written by Food and Drug Adminstration (FDA): Patient Safety News · Filed Under FDA: News/Recalls
FDA recently licensed a new treatment for hemophilia A called Xyntha. Xyntha, which is made by Wyeth Pharmaceuticals, is a genetically engineered version of factor VIII, a protein essential for blood clotting that is decreased or absent in patients ...
Written by Food and Drug Adminstration (FDA): Patient Safety News · Filed Under FDA: News/Recalls
NEW YORK -- Young children who live in city neighborhoods with tree-lined streets are less likely to develop asthma, but the actual protective factor remains unknown, researchers said.
Written by MedPageToday.com - Latest medical news and health news plus CME for physicians and healthcare professionals · Filed Under Medical News
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