FDA reviews safety of children's cold medicines
Agency to decide whether over-the-counter remedies need new regulation
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NEW YORK - U.S. health regulators said Friday they have been reviewing the safety of over-the-counter children’s cough and cold medications, especially for those under age 2.
“We have been looking at this issue internally with regard to the safety and efficacy of cough, cold products in children,” said Dr. Charles Ganley, head of the Food and Drug Administration’s Office of Nonprescription Products.
The FDA said it could not yet determine whether new regulations would result from the safety review, according to a report in the New York Times Friday.
A group of pediatricians and public health officials asked the agency Thursday to bar drug manufacturers from marketing such remedies as Toddler’s Dimetapp, Infant Triaminic and Little Colds to children under 6.
A recent study by the federal Centers for Disease Control and Prevention showed that more than 1,500 children under 2 had experienced serious health problems — and three died — after taking common cold medicines in 2004 and 2005. The American College of Chest Physicians last year recommended avoiding using cough and cold medicines in children, especially young ones.
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The president of the Consumer Healthcare Products Association, which represents companies that sell over-the-counter cold drugs, noted that the medicines had FDA approval and had been used for decades. They should be taken only in recommended doses, association president Linda A. Suydam said.
The pediatricians who petitioned the FDA Thursday acknowledged that children’s cold medicines were generally safe in recommended doses, but they said overdoses were common because many children were given more than one medicine, among other reasons. They also questioned the drugs’ effectiveness in children.
Many cold and cough drugs won FDA approval decades ago, when the agency’s standards were less strict, The Times reported.
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