Pediatricians Warn FDA on Cold Medicines
Friday, October 19, 2007; 1:08 AM
WASHINGTON -- Cold and cough medicines given to infants and toddlers work no better than dummy pills and can be dangerous, pediatricians seeking to curb their use told government health advisers Thursday.
The doctors told the Food and Drug Administration advisers that the over-the-counter medicines shouldn't be given to children younger than 6 because they don't help them and aren't safe. Such a prohibition would go beyond last week's drug industry move to eliminate sales of the nonprescription drugs targeted at children under 2.
The group petitioned the FDA seeking in part a government statement saying the medications shouldn't be used in older children as well. The expert advisers began a two-day meeting to consider the issue. The FDA has yet to act, in part pending a recommendation expected late Friday from the joint panel of outside experts in pediatrics and nonprescription drugs, said the agency's Dr. Joel Schiffenbauer.
The medicines have been marketed for use in children for decades, with drug companies spending $50 million a year on heart-tugging ads in parenting magazines and elsewhere. Still, it has long been acknowledged there are little or no data from studies in the very young to show the medicines are safe and work. Worse, some studies suggest the medicines are no better than dummy pills in treating cold and cough symptoms in young children, the petitioners said.
"When a treatment is ineffective, its risks _ if not zero _ always will exceed its benefits," said Dr. Michael Shannon, a Children's Hospital Boston pediatrician and Harvard Medical School professor who was another of the petitioners.
The drug industry, meanwhile, maintains the widely used medicines are safe and work but can lead to death and injury from overdoses or misuse in infants. It estimates children receive 3.8 billion doses of the medicines a year.
"The vast majority of consumers are using these medicines properly and serious adverse events are rare," said Linda Suydam, president of the Consumer Healthcare Products Association, which represents makers of over-the-counter drugs.
The meeting opened a week after drug makers pulled from sale oral cough and cold medicines for children under 2. The labels on those medicines had recommended parents "ask a doctor" before giving them to children that young _ advice that seemingly did little to rein in their use.
"We all have a lot of friends who call up their pediatricians and the pediatricians tell them to take the drugs," said panelist Ralph D'Agostino, a Boston University public health and statistics expert.
The drug industry now says simply that the medicines shouldn't be used in that age group. The petitioners, including Baltimore city health officials, are pushing to expand that to those under 6.
Some of the drugs _ which include Wyeth's Dimetapp and Robitussin, Johnson & Johnson's Pediacare and Novartis AG's Triaminic products _ have never been tested in children, which a previous FDA panel noted as long ago as 1972.
"Studies in children are few and sparse," said Lolita Lopez, an FDA pediatrician, noting a review found just 11 published over the last half-century. Those studies did not establish the medicines work, Lopez said.