Guest guest Posted June 9, 2006 Report Share Posted June 9, 2006 atracyphd2 Thu, 8 Jun 2006 20:37:36 EDT [drugawareness] UK's MHRA: Wyeth's Effexor May Raise Overdose Risks Keep in mind that Andrea Yates was taking high doses of Effexor (450mgs) and was dropped by 150mgs to the maximum dose previously considered safe of 300mgs just two days before she drowned her five small children. Effexor withdrawal is deadly to the brain and the body throwing both into shock. These new warnings concern heart risks of Effexor. Dr. Candace Pert, who headed the brain chemistry department at NIH for 13 years and helped discover the serotonin binding process making the SSRI antidepressants possible, warned of the serious heart risks of the SSRIs and SNRIs eight years ago. She spoke out publicly calling these drugs " monsters " - monsters she is alarmed to have been connected to their development in any way. Ann Blake Tracy, Ph.D., Executive Director, International Coalition For Drug Awareness Web site: _www.drugawareness.org_ (http://www.drugawareness.org/) Author: Prozac: Panacea or Pandora? - Our Serotonin Nightmare & CD or audio tape on safe withdrawal: " Help! I Can't Get Off My Antidepressant! " (800-280-0730) The Medicines and Healthcare products Regulatory Agency said in a statement that severely depressed patients taking doses of 300 milligrams or more a day of Effexor, also known as venlafaxine, should be supervised by specialists. Doctors will be alerted to risks for heart patients and people with hypertension, the MHRA said. _http://www.therapeuticsdaily.com/news/article.cfm?contenttype=sentryarticle & c ontentvalue=931312 & channelID=30_ (http://www.therapeuticsdaily.com/news/article.cfm?contenttype=sentryarticle & con\ tentvalue=931312 & channelID=30) Wyeth's Effexor May Raise Overdose Risks For Some-MHRA Dow Jones - May. 31, 2006 (http://ad.doubleclick.net/jump/TherapeuticsDaily/cns_cat;sz=300x250;ord=[timest\ amp]?) LONDON -(Dow Jones)- Wyeth (WYE) antidepressant drug Effexor may raise overdose risks for some patients, a U.K. regulatory review said Wednesday. The Medicines and Healthcare products Regulatory Agency said in a statement that severely depressed patients taking doses of 300 milligrams or more a day of Effexor, also known as venlafaxine, should be supervised by specialists. Doctors will be alerted to risks for heart patients and people with hypertension, the MHRA said. " We are writing to healthcare professionals to ensure they are fully informed of the updated information on Effexor to allow them to make informed prescribing decisions, said Dr. June Raine, the agency's director, in the statement released on the agency's Web site. " Patients already taking Effexor should make a routine appointment with their doctor, so that their treatment can be reviewed, " Raine said, adding: " For most patients, no changes to their treatment will be needed. " The warnings, which will also be included in a patient information leaflet packaged with drug, include a suggestion that patients review their treatment with their doctors. The drug will be available in a smaller pack sizes too, the agency said. Web sites: http://www.mhra.gov.uk/home www.wyeth.com/ -By Sten Stovall, Dow Jones Newswires; +44 207 842 9292; sten.stoval (END) Dow Jones Newswires May 31, 2006 13:54 ET (17:54 GMT) Quote Link to comment Share on other sites More sharing options...
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