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 FDA Information - May 16, 2008
| The Food and Drug Administration warned the medical community on Friday regarding heparin after learning that some of the facilities still had supplies of the contaminated blood thinner. A large number of hospitals, medical societies and pharmaceutical organizations were warned despite a recall by the California Department of Health and the FDA's own recall monitoring. Baxter International Inc., the largest supplier of heparin, also showed gaps in the recall response | | An electronic pillbox meant to aid the elderly people in taking their medicines on time is a useful tool in old age, new research reveals. The pill box not only beeps at the appointed drug-taking time but also announces the number of pills to take and how to take them. Manufactured by Santa Barbara, Calif.-based company Lifetechniques, the interactive pillbox was given to a group of patients between the ages of 65 and 84. All the patients were following a prescription regimen of at least four medications | | Insulin pumps used by teens to treat Type 1 diabetes have been linked to injuries and even deaths, a study by the U.S. Food and Drug Administration (FDA) has found. The FDA advised parents to keep a watch on their children's use of pumps, as many times the devices fail to function properly | | The U.S. Food and Drug Administration said Wednesday that a generic version of a popular name brand antidepressant is both safe and effective, despite recent consumer complaints The federal agency reviewed the generic version of Wellbutrin manufactured by Teva after some patients reported their depression returned when they switched from the brand name drug Wellbutrin XL to the generic pharmaceutical. Some patients also complained of headaches, anxiety and other side effects | | The U.S. Food and Drug Administration (FDA) is advising consumers not to purchase or consume Total Body Formula, a dietary supplement after dangerously high amounts of the mineral selenium was found in them. The Centers for Disease Control and Prevention (CDA), the FDA and state health departments are investigating more than a hundred cases of acute poisoning from the products. The selenium found in them was as much as 200 times or more the amount listed on the products' labels | |
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