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As of July 31, 2025, the FDA has received: Some of these reports involve serious reactions such as nausea, vomiting, abdominal pain, constipation, and dosing errors, especially when patients or providers miscalculate injections or exceed FDA-approved dosing schedules

D1306, Thermo Fisher Scientific) for 2.5 minutes at room temperature

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Powder requires laboratory reconstitution, while liquid is pre-prepared for research convenience

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Median CAP indices were 311 and 284 ( p = 0.04) and the median LSM scores were 7.8 and 5.8 ( p = 0.02) in patients treated with conventional and triple therapy, respectively