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American drug and European regulators had two different reactions this week to data on an obesity medication. The raw data from the study states that people with certain health disorders who took the prescription diet drug Meridia had increased heart attacks, strokes and other cardiovascular problems than people getting a placebo. The European Medicines Agency advised physicians and pharmacists to stop prescribing and dispensing European equivalents of the drug Meridia. The Food and Drug Administration, looking at the similar study data on Thursday, took a less forceful step and asked Abbott Laboratories, the maker of Meridia, to put a stronger warning on its label.

The F.D.A. said the new warning should state that the drug was not to be used by people who have a history of heart attacks or strokes, or who have uncontrolled high blood pressure. buy phentermine

Abbott, which that manufactures Meridia in Europe under different brand names, including ECtiva and Reductil indicated Friday that it would comply with the F.D.A.’s labeling request and with the European advisory by suspending sales of the drugs in Europe.

Meridia contains the active ingredient sibutramine, which acts by increasing neurotransmitter activity in the brain, helping people to feel full after a meal and thereby reducing their food intake. The company said the medication was safe and effective when used in appropriate patients.

We believe there are many number of patients who will benefit from Meridia, Dr. Eugene Sun, vice president for the development and global pharmaceutical research at Abbott. The company’s global sales of Meridia drugs last year were about $300 million, although usage in the United States has been declining for years.

The study, called the Scout trial, is indeed necessary for the field of obesity as a whole because its findings contradict what has been the long-held presumption — that weight-loss medications are more than just cosmetic. buy phentermine online