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Dangers of Gardasil Starting to Emerge

On May 22, 2007, five schoolgirls from Sacred Heart Girls College in suburban Melbourne, Australia, were rushed to hospital after being injected with Gardasil, the latest mandatory cervical cancer vaccine. Shortly after the vaccination, twenty-six girls were seen at the campus medical clinic. Five were admitted to hospital: two were kept overnight for dizziness; one had temporary paralysis and loss of speech. The condition of the other two was not known. (1)

In the United States, symptoms similar to those experienced by Australian girls have been reported to the Vaccine Adverse Events Reporting System (VAERS). Since the vaccine’s approval in June 2006, at least 1,600 adverse events have been reported. Here are some examples taken directly from the VAERS report pages:

“Immediately after the injection, the patient complained of severe pain at the site. Fell off the table and passed out for about 10-15 seconds. Hyperventilation. Complaint of headaches, blurred vision; the vision test was normal. Vomiting x 1 in the parking lot and speech was momentarily inarticulate. Sent to the ER where her neurological exam was normal except for the recall word “coffee instead of coughing” and saying “begotten instead of tired.”

“A patient was vaccinated with a first dose of HPV vaccine. Subsequently, as the patient left the examination room, the patient passed out. The patient recovered shortly after fainting.

“A 14-year-old woman was vaccinated with Gardasil. The patient was reported to be sitting on a bench. When the nurse left the room, the patient apparently passed out and eventually fell off the bench. It was reported that he was unsure if the patient had broken her nose but there was blood. At the time of this report, the outcome of the events was unknown.

VAERS is a passive surveillance system and depends on voluntary reporting by clinicians and parents of serious health problems after vaccination. Although VAERS reports do not prove causation, they can provide a warning system that a vaccine may cause health problems.

It has been estimated that less than 10%, or even as few as 1-4%, of adverse reactions to a prescription drug or vaccine are reported.(2) If only 1% of all adverse reactions associated with Gardasil are reported for VAERS, there could have been up to 160,000 acute health issues from the vaccine in less than a year. Long-term neurological or immune system complications are completely unknown. It is not certain that any of these vaccinated children will develop fertility problems, cancer or damage to their genes, which Merck admits in its leaflet has not been studied.

John Iskander, of the Center for Disease Control’s Office of Immunization Safety, said: “There’s absolutely no reason to think there’s anything in this vaccine that will make people more likely to faint”. (3) Despite its assurances, some ingredients in the vaccine may cause dizziness and fainting.

Histidine, an amino acid, is easily converted into another amino acid, histamine, when it enters the body. When released, histamine causes redness, swelling, itching and allergic reactions leading to widening of capillaries, lowering of blood pressure… people may pass out. The vaccine also contains Polysorbates 80, an agent used in creams, ointments, lotions, and multiple medical preparations, including vitamin oils and anti-cancer agents. Polysorbate 80 can cause life-threatening reactions including anaphylaxis, characterized by a sudden drop in blood pressure, hives, difficulty breathing… people may faint. (4)

Fainting after vaccination can have serious consequences. An article published in the Archives of Pediatric and Adolescent Medicine (1997), reviewed the 697 reports of syncope (fainting) that occurred after vaccination and were reported to VAERS between 1990 and 1995. Over 97% of events occurred within 30 minutes of a vaccination, establishing a causal relationship. Of these, six patients suffered serious head injuries, including skull fracture, cerebral hemorrhage and cerebral contusion. Three of these patients required brain surgery and two were left with significant residual neurological deficits between six months and two years after follow-up. (5) Dizziness and fainting after vaccination should not be taken lightly.

As for children in Australia, the vaccination program is expected to continue in June. “The college is confident that this vaccination program is safe to offer to students,” said Christopher Dalton, the school’s principal. “We will be working with the Victoria Department of Social Services and Monash Town Immunization Services in planning the immunization program.”

The assumption is that sickness and dizziness are “normal reactions” to a vaccine. The overriding theme for Australians is that “We have a vaccine, and we will use it”. For baby girls in the United States, watchful waiting is advised.

________________________________________

REFERENCES

(1) “Disease-related vaccine”. [http://www.news.com.au/story/0],23599,21774793-2,00.html

(2) Braun M. Vaccine Adverse Event Reporting System (VAERS): utility and limitations. John’s Hopkins Bloomburg School of Public Health. http://www.vaccinesafety.edu/VAERS.htm

(3) The CDC states that Gardasil side effects are minor, additional warning labels are unnecessary. February 26, 2007 http://www.medicalnewstoday.com/medicalnews.php?newsid=63651

(4) Coors, EA. Polysorbate 80 in medicinal products and non-immunological anaphylactoid reactions. Ann Allergy Asthma Immunol. 2005 Dec;95(6):593-9. PMID: 16400901

(5) Braun MM, et al. Syncope after vaccination. Arch Pediatr Adolesc Med 1997;151:255-9.

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