WDDTY’s campaign against Gardasil is reliant on accepting that al events in the Vaccine Adverse Event Reporting System (VAERS) database are caused by the vaccine. This particularly applies to adverse events.
Two reports from VAERS reported by Reuben at The Poxes Blog demonstrate the fallacy if this approach:
Information has been received from a licensed practical nurse concerning a 19 year old female patient with penicillin allergy who on 09-NOV-2010 was vaccinated with the first dose of GARDASIL without incident. At 09:00 on 01-MAR-2011 the patient received a dose of GARDASIL (Lot# 666597/0768Z, Expiration: 17-OCT-2011) (dose, strength and therapy route were unspecified). A lot check has been initiated. Concomitant therapy included SEASONIQUE and ZYRTEC. In January 2011, the patient experienced mononuceleosis. At 13:26 on 01-MAR-2011, the patient was involved in an automobile accident and suffered some bumps and bruises. The patient was not hospitalized. At the time of report, the patient was recovering. Therapy was not discontinued. There was no lab diagnostics. The patient sought medical attention. Bumps, bruises and automobile accident were considered to be life threatening by the reporter. Additional information has been requested.
VAERS report for an HPV vaccine (ID 418957-1)
We received on 12 FEB 2008 from a healthcare professional the following information: A 7-year-old male patient, born on 21 JUN 2000 was vaccinated with FLUVIRIN (batch no. unknown) on 19 NOV 2007. The patient was killed in an automobile traffic accident on 01 FEB 2008. The subject had participated in a clinical trial sponsored by MedImmune. FLUVIRIN was used in that trial as a control, and Novartis Vaccine & Diagnostics (NVD) has donated the FLUVIRIN, but other than that has not been involved. Although the event did not occur during the duration of the trial, and the investigator did not see any causal relationship to the vaccination with FLUVIRIN, he reported the event to the IRB and NVD because the child had died.
VAERS report ID 308661-1
A consumer reported that her 36 year old husband received a dose of FluMist on an unspecified date in 2003. On 12/13/03, he experienced dizziness and was subsequently involved in a car accident. The reporter indicated that the event was life-threatening. No additional information was available at the time of this report.
VAERS report ID 214473-1
Information has been received from a study concerning a patient (age and gender not reported) who was vaccinated with a dose of PROQUAD (date, dose, route not reported). It was reported that the patient died due to drowning (date not reported). This is one of several reports from the same source. Additional information has been requested.
VAERS report ID 331195-1
No data obtained. Parents are awaiting final autopsy report and the death certificate. These will not be produced until a final toxicology report is obtained. All of this is per the coroner. Autopsy states cause of death as undetermined. Death certificate states cause of death due to cerebral laceration w/open skull fracture due to an automobile accident.
VAERS report ID 168749-1
VAERS is an excellent system. It exists to document and analyse problems with vaccines, and its mere existence is proof that SCAM proponents are wrong when they claim that medical science is in denial about vaccine risks. No, it really isn’t – vaccine risks are tiny, but they are taken entirely seriously because very large numbers of patients are involved and the treatment is prophylactic – it is rightly considered important to be extra careful when treating people who are not actually ill at the time.