Jere Beasley Report May 3, 2011 Our firm has committed financially to help a group of independent filmmakers in the creation of a documentary that would shed light on the harmful side effects of the HPV vaccine, Gardasil. Titled “One More Girl,” the documentary will share the stories of individuals and families devastated following a […]
Gardasil – The Grim Reaper – Mounting Injuries Last as Long as Vaccine Efficacy
By Leslie Carol Botha April 25, 2011 PR Log FOR IMMEDIATE RELEASE PRLog (Press Release) – Apr 25, 2011 – It is becoming hard to comprehend why the United States government; FDA, CDC and the NCI have blatantly turned their backs on the thousands of families whose daughters and sons […]
Gold Law Firm, LLC Files Gardasil Vaccine Complaint
PR Web
Massachusetts Law Firm files Gardasil Injury Petition under the National Vaccine Injury Compensation Program. Many are now aware of Compensation Program and the deadlines that must be met in order to qualify.
Wellesley Hills, MA (PRWEB) April 25, 2011
Gold law Firm, LLC attorney Howard S Gold recently filed a Gardasil vaccine complaint on behalf of a now 21-year old Massachusetts woman, who has a chronic, autoimmune disorder. The case, filed in The Court of Federal Claims in Washington, D.C., seeks recovery under the National Vaccine Injury Compensation Program.
SANEVax – Our Daughters Should Not Be Experiments for The Drug Industry
Child Health Safety Posted on April 20, 2011 by childhealthsafety SANEVax News Release Parents of Daughters & Women Injured from Gardasil React to FDA Decision Why are medical consumers the medical experiments? Safety and efficacy studies should be conducted for all intended age intended before market release. On April 7, 2011 the media broke the news […]
Parents of Daughters ; Women Injured from Gardasil React to FDA Decision
Why are medical consumers the medical experiments? Safety and efficacy studies should be conducted for all intended age groups before market release. SANE Vax Inc. April 19, 2011. PR Log. On April 7, 2011 the media broke the news about the U.S. FDA’s ruling against Merck’s supplemental biologics license application (sBLA) for an indication […]
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