FOR IMMEDIATE RELEASE: June 23, 2009
Judicial Watch | Contact: 202-646-5188
New FDA Records Obtained by Judicial Watch Indicate 28 Deaths
Related to Gardasil in 2008
Records Document 6,723 Adverse Reactions in 2008,
Including 1,061 Considered “Serious” and 142 Considered “Life Threatening”
(Washington, DC) — Judicial Watch, the public interest group that investigates and prosecutes government corruption, announced today that it has obtained records from the Food and Drug Administration (FDA) documenting 28 deaths in 2008 associated with Gardasil, the vaccination for human papillomavirus (HPV), up from the 19 deaths in 2007. The total number of Gardasil-related deaths is 47 since the vaccine was approved in 2006. Overall, the FDA documented 6,723 “adverse events” related to Gardasil in 2008, of which 1,061 were considered “serious,” and 142 considered “life threatening.”
The following are several “adverse events” documented by the FDA’s Vaccine Adverse Event Reporting System (VAERS)”:
- “15 months from the completion of the GARDASIL HPV vaccination, I had full blown cervical cancer. My oncologist would like to do a hysterectomy at this time, but [as I have] always wanted children, I have chosen to wait . . . I have two of the [strains] that the shot is suppose to prevent . . . I now have cervical cancer and I am left wondering what role the GARDASIL HPV vaccination played in the hasty onset.” (ID: 319836)
- “After receiving her second dose of GARDASIL … she could crawl but … needed to use crutches or a wheel chair … She was experienced problems breathing and had ‘super migraines’ that never went away … She had swelling in her face, jaw and wrists. The patient was diagnosed with GUILLAIN-BARRE syndrome, myelin sheath degeneration and peripheral neuropathy. Patient was hospitalized twice … patient has not recovered from symptoms.” (ID: 318052)
- A 19-year-old girl with no medical history immediately experienced side effects after receiving the Gardasil vaccine. Within eleven days her symptoms included “Aggression, Arthralgia, Complex partial seizures, Confusional state, Convulsion, Crying, Dizziness, Epilepsy, Fatigue, Feeling abnormal, Grand mal convulsion, Immediate post-injection reaction, Irritability, Myalgia, Nausea, Pain, Postictal state, Somnolence, Syncope, Tremor, and Unresponsive to stimuli.” (ID: 320598)
- “Two weeks after the third dose, the patient developed a complication. She was taken to the hospital by ambulance but passed away during the transport from an unknown cause…Upon arrival in ER unresponsive, pupils fixed and dilated, no cardiac activity. Resuscitation unsuccessful and patient expired.” (ID: 314769)
The FDA VAERS reports show that since last June, 235 cases detailed permanent disability. There were also 29 new cases of Guillain-Barre Syndrome, and 147 cases of “spontaneous abortions,” or miscarriages, when the vaccine was given to pregnant women.
Moreover, 62 girls developed warts after receiving the vaccine. This development is of particular concern because Gardasil, which is designed to prevent two strains of genital warts, is not supposed to react with other HPV strains. However, not only did previously healthy women experience genital warts after the vaccination, but 21 girls developed warts on other areas, most commonly the face, hands and feet, and in one case, “all over her body.” (ID: 330671)
Of the 47 reported deaths, 41 occurred within a month of receiving the vaccine and of those deaths, 17 were within two weeks of receiving the vaccine. In most of the deaths the cause is still unknown.
“The FDA is supposed to be a guardian of public health, and yet the agency continues to turn a blind eye to what seems to be an extremely serious public health problem. The public relations push for Gardasil by Merck, politicians and public health officials needs to pause so that these adverse reactions can be further studied,” said Judicial Watch President Tom Fitton. “The already serious problems associated with Gardasil seem to be getting worse. No one should require this vaccine for young children.”
These reports can be read in full at http://www.judicialwatch.org
Jill S. Farrell Director of Public Affairs
Judicial Watch501 School St, SW, Suite 700
Washington, DC 20024
Direct 202.646.5188
Judicial Watch, Inc. is a constitutionally conservative, nonpartisan educational foundation that promotes transparency, accountability and integrity in government, politics and the law.
An update for the 2024 - 2025 flu season will be coming soon.
Any update for the 2024 flu?
Based on your articles and the experience of Cardinal Burke I received the Covid vaccinations tp protect myself and those…
James, Entyvio (Natalizumab) was pre-clinically tested in animal models (Guinea Pig) and is produced in Chinese Hamster Ovary (CHO) cell…
Jose, Any info on monoclonal treatments for other diseases? How about Entyvio? Used for ulcerative colitis?
Debbi, you are most welcome! And thank you for your kind words.
Thank you for the information in your article and the responses you made in the comments. God bless you.
Elisha, I have yet to research a psychotropic drug that was developed using fetal cell lines or fetal tissue of…
Dorothy, Actonel/risedronate sodium was not developed or tested, nor is it manufactured using aborted fetal cell lines or tissues of…
Hi, I appreciate your research and response. In your research do all psychotropic medications have fetal cells or MRC-5 fetal…
Vorrei sapere se gli anticorpi monoclonali per curare l'emicrania sono etici. Grazie.
Is risedronate sodium or actonel tested or derived from aborted fetal cells.
Andrew, the Tdap shots are ethically developed, tested and produced. There's a note at the bottom of the chart informing…
Anyone know about ethics and safety of Tdap for older kids and adults? I did not see it on the…
Thank you very much. I greatly appreciate your help and all the great work you do. God bless you all,…