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According to Sahpra, inspectors uncovered extensive regulatory failures during the raid, including what it described as the illegal importation of active pharmaceutical ingredients (APIs), inadequate sterile manufacturing conditions and the absence of proper analytical testing to confirm product quality, potency and purity

This overlap creates potential challenges in distinguishing medication side effects from disease flares, which could delay appropriate escalation of IBD therapy

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These events were generally mild to moderate in severity and included: Nausea often accompanying changes in bowel habits, particularly after dose escalation Diarrhoea loose or watery stools, sometimes with urgency Vomiting less common but reported, especially at higher doses Constipation occurring in some individuals, reflecting the variable effect on gut motility Abdominal discomfort or bloating a sensation of fullness or cramping Flatulence increased wind, which can accompany altered digestion Gastrointestinal adverse events were the most common reason for discontinuation in the Phase 2 trial, occurring in approximately 510% of participants depending on dose group

Whether it is taken as a pre-workout or post workout, it shows great effects on the body