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More alarming still are reports of users contracting HIV, hepatitis B and C, and serious eye infections from contaminated injections

The GDS-15 was completed by 34 patients (17 per group), with median scores initially at 2.0 in the loading dose group and 3.5 in the no loading dose group, which adjusted to 2.5 and 2.0 respectively after 90 days

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Why it was included in the FDA ban The agency cited a lack of human trials and the risk for immune reactions and peptide impurities with injectable Thymosin Beta 4