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FMI's analysis of the GLP-1 receptor agonist market in North America consists of country-wise assessment including the United States and Canada

Unlike regulators in India and China, the FDA does not require most generic drug makers to conduct human clinical trials if they can demonstrate that the generic version is chemically equivalent to the original drug

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The most frequently reported adverse effects of GLP-1 receptor agonists are gastrointestinal in nature, including nausea, vomiting, diarrhea, constipation, and abdominal discomfort