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User 3, recovering from a complete ACL and LCL rupture at 21 years old, used 500mcg split as 250mcg every 12 hours and discontinued at day 40

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Reporting issues to the FDA FDA encourages health care professionals, patients, and compounders to report adverse events or quality problems with these or any medications to FDAs MedWatch Adverse Event Reporting program: Complete and submit the report online