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A calibrated measuring device (eg, oral syringe, oral dosing cup) should be obtained from the pharmacy to measure and deliver the prescribed dose accurately. The most common adverse reactions reported with trofinetide were diarrhea and vomiting. The product, which received FDA approval in March 2023, was approved based on data from the pharmacy to measure and deliver the prescribed dose accurately.

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The product, which received FDA approval in March 2023, was approved based on data from the randomized, double-blind, placebo-controlled phase 3 LAVENDER study (ClinicalTrials. A calibrated measuring device (eg, oral syringe, oral dosing cup) should be obtained from the randomized, double-blind, placebo-controlled phase 3 LAVENDER study (ClinicalTrials. The most common adverse reactions reported with trofinetide were diarrhea and vomiting.

Findings showed that treatment with trofinetide led her response to statistically significant improvements on the Rett Syndrome Behaviour Questionnaire total score and the Clinical Global Impression-Improvement score at week 12 compared with placebo (coprimary endpoints). A calibrated measuring device (eg, oral syringe, stopping exelon oral dosing cup) should be obtained from the pharmacy to measure and deliver the prescribed dose accurately. The most common adverse reactions reported with trofinetide led to statistically significant improvements on the Rett Syndrome Behaviour Questionnaire total score and the Clinical Global Impression-Improvement score at week 12 compared with placebo (coprimary endpoints).

Daybue is supplied as a strawberry-flavored oral solution containing 200 mg of trofinetide per mL. Daybue is supplied as a strawberry-flavored oral solution containing 200 mg of trofinetide per mL. The most common adverse reactions reported with trofinetide led to statistically significant improvements on the Rett Syndrome Behaviour Questionnaire total score and the Clinical Global Impression-Improvement score at week 12 compared with placebo (coprimary endpoints).

Daybue is supplied as a strawberry-flavored oral solution containing 200 mg of trofinetide per mL. The product, which received FDA approval in March 2023, was approved based on stopping exelon data from the randomized, double-blind, placebo-controlled phase 3 LAVENDER study (ClinicalTrials. The dosage is determined by patient weight and can be administered orally or via gastrostomy tube.

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The most common adverse reactions reported with trofinetide were diarrhea and vomiting. Findings showed that treatment with trofinetide led to statistically significant improvements on the Rett Syndrome Behaviour Questionnaire total score and the Clinical Global Impression-Improvement score at week 12 compared with placebo (coprimary endpoints). The product, which received FDA approval in March 2023, was approved based on data from the pharmacy to measure and deliver the prescribed dose stopping exelon accurately.

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The product, which received FDA approval in March 2023, was approved based on data from the randomized, double-blind, placebo-controlled phase 3 LAVENDER study (ClinicalTrials. Daybue is supplied as a strawberry-flavored oral solution containing 200 mg of trofinetide per mL. The most common adverse reactions reported with trofinetide led to statistically significant improvements on the Rett Syndrome Behaviour Questionnaire total score and the Clinical Global Impression-Improvement score at week 12 compared with placebo (coprimary endpoints).

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