Chemar Posted November 17, 2007 Report Share Posted November 17, 2007 I am not sure if this news has already been posted http://www.newsweek.com/id/70847 Link to comment Share on other sites More sharing options...
kim Posted November 17, 2007 Report Share Posted November 17, 2007 Cheri, I'm not sure if this has been posted here either as I have posted and discussed this at length in a couple of other places. This is a page, I know I have posted here before. I hope everyone takes some time to scan as often as pssible. It has headlines, updated daily with news regarding vaccines and a lot of the propaganda that is being foisted on parents. There are numerous artcles relating to the story you just linked to. http://www.vaccinationnews.com/Opening.htm I can't tell you how dangerous I feel this practice is, especially in light of the issues that our kids deal with. There are so many unknowns in relationship to the immune system and surrounding TS/tics. I would gladly spend time in jail, than see my boys injected with aluminum, multiple antigens, and to borrow a phrase from another mom, over my cold, lifeless ,dead body...mercury There is no one in this household, that will be receiving any type of vaccine in this lifetime. Link to comment Share on other sites More sharing options...
kim Posted November 24, 2007 Report Share Posted November 24, 2007 cross post from autism info...thanks Tereasa FDA: Flu Drugs Affecting Kids' Behavior 11:36 PM PST, November 23, 2007 http://www.latimes. com/news/ nationworld/ nation/wire/ ats-ap_health10n ov23,1,716696. story WASHINGTON — Government health regulators recommended adding label precautions about neurological problems seen in children who have taken flu drugs made by Roche and GlaxoSmithKline. The Food and Drug Administration on Friday released its safety review of Roche's Tamiflu and Glaxo's Relenza. Next week, an outside group of pediatric experts is scheduled to review the safety of several such drugs when used in children. FDA began reviewing Tamiflu's safety in 2005 after receiving reports of children experiencing neurological problems, including hallucinations and convulsions. Twenty-five patients under age 21 have died while taking the drug, most of them in Japan. Five deaths resulted from children "falling from windows or balconies or running into traffic." There have been no child deaths connected with Relenza, but regulators said children taking the drug have shown similar neurological problems. While FDA said it isn't clear whether the problems are directly related to the drugs, it recommends adding language about the possible side effects to labeling for physicians who prescribe Tamiflu and Relenza. Besides being a drug side effect, the agency said the behaviors alternately could result from an unusual strain of flu or a rare genetic reaction to the drug. Company representatives were not immediately available for comment. * - - * New Warnings Urged For Flu Drugs' Labels By Christopher Lee Washington Post Staff Writer Saturday, November 24, 2007; A02 http://www.washingt onpost.com/ wp-dyn/content/ article/2007/ 11/23/AR20071123 01658.html Food and Drug Administration experts are recommending new label warnings about possible dangerous psychiatric side effects of influenza drugs Tamiflu and Relenza, according to FDA documents. The documents, posted on the agency's Web site yesterday, were prepared for a meeting Tuesday of the FDA's Pediatric Advisory Committee. Studies revealed 596 cases in which patients who took Tamiflu experienced "neuropsychiatric events" such as delirium, delusions or hallucinations. The episodes sometimes led to impulsive behavior and self-injury. Tamiflu is made by Roche Holdings. The problems tended to occur within 24 hours of first taking the drug, and the majority were in patients younger than 21, mostly in Japan, according to the documents. In five cases involving pediatric patients, the reported delirium resulted in death, and there were three reports of suicide in adults. "In the remaining reports of delirium with impulsive behavior and self-injury, patients were attempting to flee or escape from windows or balconies and were unsuccessful in their efforts," the FDA documents say. "In addition, there were a few patients who became aggressive or violent and/or performed acts that were injurious to themselves (e.g. banging head against wall) or others (e.g. child tried to strangle mother)." Tamiflu, available in pill and syrup form, can treat the symptoms of seasonal influenza. In a bird flu pandemic, many experts believe the drug could help reduce the length and severity of symptoms. Safety concerns about Tamiflu arose two years ago after reports of 12 deaths and 32 cases of psychiatric problems in children in Japan. Labeling for Tamiflu in the United States notes that self-injury and delirium have occurred primarily among pediatric patients. Now FDA regulators are recommending that U.S. labeling be updated to note that "fatalities have occurred in adult and pediatric patients in Japan, the onset may be abrupt, and fatal events have occurred even while the patient was being monitored." Regulators cautioned that no causal link has been established between the drug and the abnormal behavior, and that delirium and other problems can be complications of influenza itself. Roche spokesman Terry Hurley said reports of abnormal behavior were "infrequent. " "If the FDA concludes that it is valuable to place additional details on the label with regard to specific adverse event reports, then Roche is open to that consideration, " Hurley said in a statement. Regarding Relenza, an antiviral drug by GlaxoSmithKline that is in the same class as Tamiflu, FDA experts said studies turned up 115 cases of psychiatric problems, including 74 cases in patients younger than 21. Seventy percent were from Japan. No potentially related fatalities were reported. Because Relenza, which is inhaled by mouth, is not easily absorbed, experts said the problems probably were related to the influenza rather than the treatment. Nevertheless, they recommended updating Relenza's label to note that "postmarketing reports of hallucinations, delirium and abnormal behavior have been observed in patients" receiving the drug for treatment of influenza. The label currently does not warn of psychiatric side effects. Glaxo spokesman Jeff McLaughlin said, "A review of clinical trial data and postmarketing reports demonstrated no evidence of a causal association between Relenza and neuropsychiatric adverse events." William Schaffner, chairman of the Department of Preventive Medicine at Vanderbilt University School of Medicine in Nashville, said the proposed warnings are "prudent and appropriate. " Schaffner noted that in Japan, where Tamiflu and Relenza are used not just to treat influenza but to prevent it, some children are on the drugs for as long as seven weeks. In the United States, the drugs primarily are used to treat illness, and children typically are on them for five days or less. "We still don't know whether there is a causal relationship between the exposure to these events and the drugs," he said, "but we use these drugs differently than they do in Japan." Post a Comment View all comments that have been posted about this article. * The material in this post is distributed without profit to those who have expressed a prior interest in receiving the included information for research and educational purposes.For more information go to: http://www4. law.cornell. edu/uscode/ 17/107.html http://oregon. uoregon.edu/ ~csundt/document s.htm If you wish to use copyrighted material from this email for purposes that go beyond 'fair use', you must obtain permission from the copyright owner. Link to comment Share on other sites More sharing options...
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