Almost a year after studies showed the diet pill Meridia increases heart attack and stroke risk, U.S. health regulators announced they will consider pulling the Abbott Laboratories‘ drug off the market.
Meridia has been sold since 1997, but data released in November showed patients with heart disease taking the drug had a more than 11 percent chance of cardiovascular risks, compared with 10 percent of those taking a placebo. European regulators pulled the product off the market in January.
However, the FDA said Monday that it is considering a range of options for the drug, including simply adding more warning labels.
A 170-page FDA review posted online contains analyses by half a dozen agency scientists, at least two of whom seem to favor withdrawing the drug. One reviewer points out that the weight-reduction benefits of Meridia, known generically as sibutramine, have not been significant with patients losing an average of 4 percent of their original weight.
“Given the modest decrease in body weight associated with sibutramine and the potentially substantial weight regain with discontinuation of therapy, even a small increase in cardiovascular risk seems unwarranted,” states Dr. Simone Pinheiro, of the agency’s epidemiology division.
In a public hearing Wednesday, an outside panel of experts will weigh in on the course of action FDA should take. The agency is not required to follow the group’s advice, although it often does.
“It is difficult to discern a credible rationale for keeping this medication on the market,” the journal’s editorial concluded.
Meridia was approved against the majority opinion of FDA’s outside advisers, who highlighted the potential for heart problems. The drug later won approval in Europe, though regulators there called on Abbott to study the drug’s effect on pre-existing heart conditions.
The research involved about 10,700 overweight or obese people 55 or older who had heart disease, diabetes or both and were treated for about 3 1/2 years. According to results issued late last year, patients taking Meridia had a slightly higher risk of heart attack, stroke or other fatal heart problems than those taking placebo.
European regulators withdrew the drug from the market on the results, while the FDA bolstered the drug’s warning label, underscoring the risks to patients with heart problems. In the U.S., the drug is contraindicated for patients with a history of heart disease, though prescribers do not always follow such guidelines.
A large portion of the FDA’s analysis issued Monday analyzes data from the 10,000-patient study. Since trial enrollees already had a history of heart disease, several scientists said it was difficult to parse out which heart problems were caused by the drug.
But another FDA reviewer points out that deaths continue to be reported with the drug in young patients with no history of heart problems.
“Young people without known risk factors, aside from obesity, have died shortly after initiating sibutramine therapy,” states the review from the FDA’s Office of Surveillance and Epidemiology, which monitors adverse events reported with drugs.
Abbott spokesman Scott Davies said Monday that the average age of U.S. Meridia users is 44, so any adverse events reported with the drug would be among relatively young patients. Mr. Davies said the North Chicago-based company will use Wednesday’s meeting to suggest “risk-management measures to ensure that the drug is used in the appropriate patient population.”View Entire Story
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