FDA issues alert for Tussionex cough med
The U.S. Food and Drug Administration (FDA) has issued an alert on
the correct and safe use of Tussionex Pennkinetic Extended-Release
Suspension. The FDA has received numerous reports of adverse
reactions--including deaths--due to the misuse of Tussionex in
children younger than age six, or because patients took the drug
more frequently than every 12 hours. The potent cough medication,
which combines the opioid hydrocodone and the antihistamine
chlorpheniramine, is only approved for use in children and adults
ages 6 and older and for use every 12 hours.
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