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You are here: Home / NEWS . . . . . . . . / Science & Medicine / Cancer / SaneVax urges FDA and NCI to establish a reliable HPV genotyping test for virology-based cervical cancer prevention in patient care

SaneVax urges FDA and NCI to establish a reliable HPV genotyping test for virology-based cervical cancer prevention in patient care

January 19, 2011 By Norma Leave a Comment

By:  Norma Erickson

06 November 2010

Last Tuesday, the SaneVax team sent a letter to Dr. Margaret Hamburg, FDA Commissioner, and Dr. Harold E. Varmus, Director of the National Cancer Institute (NCI), requesting the establishment of a reliable human papillomavirus (HPV) genotyping test to support the national virology-based cervical cancer prevention program for patient care.

To date, American medical consumers must rely on one of two FDA approved HPV tests. One of them generated two to four times the number of positive results as the other, and no one knows which, if either, of the tests are accurate.

The SaneVax team believes American medical consumers have the right to the most reliable testing available. Science has made accurate HPV genotyping available to humanity, but the FDA has not to date approved reliable HPV genotyping for American medical consumers.

Read the letter here.

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Filed Under: Cancer, FDA, NCI, World News Tagged With: cervical cancer prevention, FDA, medical consumers, NCI, reliable HPV genotyping test

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HPV Vaccine VAERS Reports

Description 12/14/2019  TOTAL
Disabled 3,092
Deaths 523
Did Not Recover 13,072
Abnormal Smear 695
Cervical Cancer 186
Infertility 52
Life-threatening 1,001
Emergency Room 15,419
Hospitalized 6,448
Extended Hosp. Stay 304
Serious 9,497
Total Adverse Events 64,270

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