Viloxazine moderate dose associated with good ADHD outcomes

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Autor principal: Alison Knopf
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Publicado: Wiley 2024
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author Alison Knopf
author_facet Alison Knopf
Alison Knopf
collection Wiley Open Access
contents Viloxazine moderate dose associated with good ADHD outcomes Alison Knopf The Brown University Child & Adolescent Psychopharmacology Update Attention‐deficit hyperactivity disorder (ADHD) is treated by medications, most recently, by viloxazine (Qelbree). Researchers in China looked at clinical trials to try to determine the best dose. Viloxazine was associated with better outcomes than placebo, with a bell‐shaped response curve suggesting that doses greater than 400 mg or greater than 7 mg/kg might not be linked to greater efficacy. Ascent curves tapered off about weeks 4 to 6. The curve for only 100 mg/d declined more rapidly, while the curves for 200 mg/dl and 400 mg/dl declined more gradually. In terms of adverse effects, there was a higher risk of discontinuation with viloxazine compared to placebo. The discontinuation rates due to adverse effects was 4.15% in the viloxazine group. 10.1002/cpu30925 http://onlinelibrary.wiley.com/termsAndConditions#vor
doi_str_mv 10.1002/cpu30925
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institution Wiley Open Access
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publishDate 2024
publisher Wiley
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spellingShingle Viloxazine moderate dose associated with good ADHD outcomes
Alison Knopf
The Brown University Child & Adolescent Psychopharmacology Update
Viloxazine moderate dose associated with good ADHD outcomes Alison Knopf The Brown University Child & Adolescent Psychopharmacology Update Attention‐deficit hyperactivity disorder (ADHD) is treated by medications, most recently, by viloxazine (Qelbree). Researchers in China looked at clinical trials to try to determine the best dose. Viloxazine was associated with better outcomes than placebo, with a bell‐shaped response curve suggesting that doses greater than 400 mg or greater than 7 mg/kg might not be linked to greater efficacy. Ascent curves tapered off about weeks 4 to 6. The curve for only 100 mg/d declined more rapidly, while the curves for 200 mg/dl and 400 mg/dl declined more gradually. In terms of adverse effects, there was a higher risk of discontinuation with viloxazine compared to placebo. The discontinuation rates due to adverse effects was 4.15% in the viloxazine group. 10.1002/cpu30925 http://onlinelibrary.wiley.com/termsAndConditions#vor
title Viloxazine moderate dose associated with good ADHD outcomes
topic The Brown University Child & Adolescent Psychopharmacology Update
url https://onlinelibrary.wiley.com/doi/10.1002/cpu30925