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Home News

Drug Maker Recalls ADHD Medicine Over Label Mixup

by Matthew
January 31, 2024
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Drug Maker Recalls ADHD Medicine Over Label Mixup
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Why it matters:
The voluntary recall of an ADHD and narcolepsy medication, Zenzedi, is concerning because the wrong pills, an antihistamine called carbinoxamine maleate, were found in packages of the medication. Patients who unknowingly consume the antihistamine instead of Zenzedi could experience undertreatment of their symptoms and adverse reactions.

What they are saying:
The FDA warns that patients who take carbinoxamine maleate instead of Zenzedi will experience undertreatment of their symptoms and an increased risk of accidents or injuries. Adverse events from consuming the antihistamine include drowsiness, sleepiness, central nervous system depression, increased eye pressure, enlarged prostate urinary obstruction, and thyroid disorder.

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The big picture:
The recall of Zenzedi comes at a time when there is a nationwide shortage of medications used to treat ADHD. Many manufacturers of the ADHD drug Adderall have been experiencing production delays, leaving patients struggling to fill their prescriptions.

What to watch:
Patients who have purchased packages of the recalled lot of Zenzedi should return any remaining pills to the place of purchase. Those who have taken the mislabeled medication and are experiencing adverse reactions are encouraged to see their doctor. It will be important to monitor the impact of the recall on patients who rely on ADHD medication and whether the shortage will worsen as a result.

My take:
The mix-up in packaging is a serious concern, as patients who depend on Zenzedi may be unknowingly taking the wrong medication and experiencing undertreatment of their symptoms. It is crucial for patients and healthcare professionals to stay vigilant and ensure that the correct medications are being prescribed and dispensed. The nationwide shortage of ADHD medication adds another layer of difficulty for patients who already struggle to access their necessary treatments. Prompt action from pharmaceutical companies and regulators is necessary to address these issues and prevent potential harm to patients.

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Tags: ADHDAzurity PharmaceuticalsBig PharmaFDAhealthmedicationnarcolepsynewspillsprescription drugsrecallZenzedi
Matthew

Matthew

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