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Medical Daily
Medical Daily
Health
Dorothy Brooks

As FDA Weighs Wider Peptide Access, Adverse Event Reports and Two Las Vegas Intubations Sharpen Safety Questions

Nearly three months after an FDA advisory panel voted to ease restrictions on six unapproved peptides, the agency still has not issued a final decision. In the meantime, a KFF Health News investigation published Oct. 13 describes people who say BPC-157 and similar products left them with migraines, eye pain, fatigue, and months of anxiety.

The report also points to entries in the FDA's adverse event database. They include a 36-year-old woman hospitalized in December after taking BPC-157 for weight control and a skin condition, and a 48-year-old man who was hospitalized with a condition described as life-threatening after peptide use. These reports are voluntary and unverified, so they cannot prove a peptide caused the harm.

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