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Adverse events were predominantly gastrointestinal and generally mild to moderate

This guide explains the process within the EU and patient requirements

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If you suspect an adverse reaction to either supplement, you can report it through the MHRA Yellow Card Scheme (yellowcard.mhra.gov.uk)

If you receive a damaged or incorrect shipment, you must notify us within 24 hours of delivery with photographic documentation

Compared with the HFD group, Retatrutide treatment did not upregulate Ucp1, Cidea or Prdm16