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Testosterone Supplements Require Further Testing, FDA Declares

Testosterone supplements have been approved by the Food and Drug Administration (FDA) to treat only certain, and relatively rare, medical conditions that slow or halt natural production of the hormone ...
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FDA Issues Warning About Using Testosterone Products; Requires Labeling Change to Inform of Possible Increased Risk of Heart Attack and Stroke

The FDA today released the following safety alert on its website. Please contact us immediately if you have been using testosterone products for low testosterone due to aging and have experienced any ...
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FDA Meets to Assess Low-T Health Risks

If you are currently or considering undergoing testosterone replacement therapy, stay tuned. In a combined meeting with two advisory committees, the FDA will be spending today and tomorrow assessing ...
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David Ratner Appointed to Low-T MDL Trial Committee

David Ratner, Managing Partner of Morelli Law Firm, has been selected to serve as a member of the Multidistrict Litigation (MDL) Trial Committee for the litigation against testosterone replacement ...
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FDA Unwilling to Include Black Box Warnings on Testosterone Replacement Therapy Drugs

The US Food and Drug Administration denied a citizen petition Wednesday from advocacy group Public Citizen demanding the agency to notify consumers of possible cardiovascular risks stemming from use ...
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JPML Creates All Testosterone Product MDL

On June 6, 2014, the Judicial Panel on Multidistrict Litigation (JPML) created an all testosterone product MDL in the Northern District of Illinois before Judge Kennelly. This decision was made on the ...
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