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Friday, April 19, 2024

FDA warns against giving probiotics to preterm babies after infant’s death

U.S. Food and Drug Administration is advising against using probiotic products for preterm infants due to potentially fatal health risks. The news comes weeks after the agency announced it wasinvestigating the death of a preterm babythat was given a probiotic in the hospital, which ultimately caused the child’s death.

“Probiotic products contain live organisms such as bacteria or yeast and are commonly marketed as foods, including as dietary supplements,” the agency said in anews releaseThursday.

The FDA said preterm infants who are given probiotics are at risk of “invasive, potentially fatal disease, or infection, caused by the bacteria or yeast” contained in the products.

In addition to recently sending a letter to health care providers about these risks, the agency has also issued twowarning letters to companies for illegally selling these types of products.

“Adverse events in any infant following the use of a probiotic are a concern to the FDA. We especially want to make clear that products containing live microorganisms may present serious risks to preterm infants in hospital settings,” Dr. Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research, said in the news release.

“With today’s message, we want to warn parents, caregivers and healthcare providers that if these products are used for the prevention or treatment of disease, they have not undergone the agency’s rigorous premarket process to evaluate their safety, effectiveness and quality for these medical uses,” Marks said.

The FDA says these products have been associated with “more than two dozen other reported adverse events in the United States since 2018.”

The most recent death followed use of Evivo with MCT Oil, a probiotic manufactured by California-based Infinant Health (formerly Evolve BioSystems Inc.). The product is now recalled.

Infinant Health, Inc received one of the FDA’s warning letters; the other was sent to Abbott Laboratories on Tuesday for its product, Similac Probiotic Tri-Blend.

“Abbott has agreed to discontinue sales of its Similac Probiotic Tri-Blend product and is working with the FDA to take additional corrective actions,” the FDA’s release says.

The FDA previously noted that no probiotics have been approved for use as a drug or biological product in babies, meaning probiotics are not subject to the “agency’s rigorous manufacturing and testing standards” for other medications regulated by the FDA.

Probiotics are allowed to be sold in the U.S. as dietary supplements, bypassing the FDA’s higher bar for drug and biologics approvals.

-Alexander Tin contributed to this report.

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