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Virginia Agencies Investigating Reports of Illness among Men Who Took Dietary Supplement V8

Posted on September 16, 2019

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OFFICE OF COMMUNICATIONS, Contact: Elaine Lidholm, www.vdacs.virginia.gov

For Release: Aug. 22, 2019

Contact: Elaine Lidholm, 804.786.7686

Virginia Agencies Investigating Reports of Illness among Men Who Took Dietary Supplement V8

(Richmond, Va.) – The Virginia Department of Agriculture and Consumer Services (VDACS) is advising consumers not to purchase or use a product sold under the name V8, which is a supplement promoted for male sexual enhancement. As of Aug. 21, 2019, the Virginia Department of Health (VDH) had received three reports in the metro Richmond area of patients experiencing severe hypoglycemia (very low blood sugar) after taking V8 pills. The patients required emergency care.

Symptoms of hypoglycemia include irritability, anxiety, shakiness, hunger, profuse sweating and/or a racing heartbeat. Anyone experiencing severe hypoglycemia should seek immediate medical attention. Individuals and healthcare professionals should contact one of Virginia’s three Poison Control Centers at 800.222.1222 about adverse events and side effects to products.

Preliminary laboratory analysis has identified several compounds within the pills that could result in severe hypoglycemia. Testing is ongoing. The U.S. Food and Drug Administration (FDA) has reported an emerging trend of over-the-counter products containing hidden active ingredients that are harmful.

VDH, VDACS, the VCU Poison Center and the Division of Consolidated Laboratory Services are collaborating on this investigation. VDACS Food Safety Specialists are actively seeking this product at convenience stores and other retail locations and will remove and destroy any product located.

Clinicians should report adverse events or side effects to FDA’s MedWatch Safety Information and Adverse Reporting Program.

Photo available from VDACS on request.

MedWatch link: www.accessdata.fda.gov/scripts/medwatch/

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