AED failures may lead to cardiac arrest deaths A lot more than 1,000 cardiac arrest deaths over 15 years are linked to the failure of automated exterior defibrillators ; battery failure accounted for nearly one-quarter of the failures. Researchers analyzed reviews to the Food and Medication Administration about all adverse events linked to use of an AED between January 1993 and October 2008. Related StoriesNew article provides information on handling mid-air wellness crisesParamedic care enhances survival for paediatric patients who suffer cardiac arrest outside of hospitalStudy: EMS-initiated CPR for out-of-hospital cardiac arrest should be performed for 35 minutesProblems with pads and connectors accounted for 23.7 % of the failures and battery power problems accounted for 23.2 % of the failures.Actavis data files ANDA for generic version of Neupro Actavis plc today confirmed that it offers filed an Abbreviated New Drug Software with the U.S. Food and Medication Administration seeking approval to market Rotigotine Extended-launch Transdermal Film, 1 mg/24 hr, 2mg/24 hr, 3 mg/24hr, 4 mg/24 hr, 6mg/24hr, and 8 mg/24 hr. UCB, Inc., UCB Manufacturing Ireland Limited, UCB Pharma GmbH and LTS Lohmann Therapie-Systeme AG filed match against Actavis' on August 21 subsidiaries, 2014 in the U.S. District Court for the District of Delaware wanting to prevent Actavis from commercializing its ANDA item prior to the expiration of certain U.S. Patents. The lawsuit was filed beneath the provisions of the Hatch-Waxman Act, resulting in a stay of last FDA authorization of Actavis' ANDA for 30 weeks from the day the plaintiffs received see of Actavis' ANDA filing or until final resolution of the problem before the courtroom, whichever occurs sooner, at the mercy of any other exclusivities.S.