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Publications:

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(10/19/05) Petition to the FDA to require a black box warning for erectile dysfunction drugs (VIAGRA, CIALIS, LEVITRA) to warn of the potential for irreversible vision loss (HRG Publication #1753)

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(6/5/00) Letter to Center for Drug Evaluation and Research urging the Food and Drug Administration (FDA) to reject the approval of Uprima (apomorphine). (HRG Publication #1522)

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(8/27/98) Letter to the Medicines Control Agency, United Kingdom, urging them to require important warnings on labeling of sildenafil/Viagra. (HRG Publication #1454)

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(8/24/98) Letter to the Therapeutic Products Program in Canada urging them to require important warnings on the labeling of sildenafil/Viagra. (HRG Publication #1452)

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(8/20/98) Letter to the Food and Drug Administration urging them to immediately convene an advisory committee to review various serious problems related to the use of sildenafil/Viagra. (HRG Publication #1451)

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(7/1/98) Petition to the Food and Drug Administration to change the labeling and other sources of information on sildenafil/Viagra to reflect problems with the drug. (HRG Publication #1445)


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