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Merck Announces New FDA-Approved Guidelines for HPV Vaccine

by Reshma Anand on  December 16, 2015 at 2:35 PM Corporate News   - G J E 4
The U.S. Food and Drug Administration (USFDA) has released a new set of guidelines for the use of already approved Recombinant Human Papillomavirus 9-valent Vaccine in males.
Merck Announces New FDA-Approved Guidelines for HPV Vaccine
Merck Announces New FDA-Approved Guidelines for HPV Vaccine
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US-based Merck Pharmaceuticals vaccine GARDASIL 9 has announced the age expansion for its use in males approved by the USFDA. The vaccine can now be used in males from 16 through 26 years of age.

‘GARDASIL 9, Merck’s Human Papilloma Vaccine can now be administered to males from 16 through 26 years of age to prevent oral cancer, precancerous lesions and genital warts.’
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The vaccine prevents oral cancer caused by HPV types (16, 18, 31, 33, 45, 52 and 58), precancerous or dysplastic lesions caused by HPV types (6, 11, 16, 18, 31, 33, 45, 52 and 58) and genital warts caused by HPV types 6 and 11.

GARDASIL 9 has been already approved by the USFDA for use in boys 9 through 15 years of age for the prevention of these diseases. Similarly, the vaccine can prevent cervical, vulvar, vaginal, and anal cancers caused by HPV types when administered to girls and young women 9 through 26 years of age.

GARDASIL 9 is contraindicated in individuals with hypersensitivity, including severe allergic reactions to yeast, or after a previous dose of GARDASIL 9 or GARDASIL [Human Papillomavirus Quadrivalent (Types 6, 11, 16, and 18) Vaccine, Recombinant].

Source: Medindia
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