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Therefore, the combined intervention may exhibit a time window effect, with 6 weeks potentially representing an optimal threshold
The most commonly reported adverse events (observed in greater than 5% of clinical trial participants) were nausea, diarrhea, vomiting, constipation, abdominal pain, dyspepsia, injection-site reactions, fatigue, hypersensitivity reactions, eructation, hair loss and gastroesophageal reflux disease
Always consult a qualified healthcare provider before starting, adjusting, or stopping any medication
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