WASHINGTON - The Food and Drug Administration warned patients yesterday that using large amounts of a Johnson & Johnson foot-ulcer medication could heighten their risk of dying from cancer.
The FDA added its most serious warning to the company's cream medication Regranex, which is prescribed to treat severe foot and leg ulcers in diabetics. The new boxed warning states that patients who used three or more tubes of Regranex over a 20-month period were five times more likely to die of cancer.
When patients used smaller amounts of the cream, the FDA said their chances of developing cancer were no higher than patients who had never used the drug.
The findings come from a long-term analysis of records from health-care providers comparing 1,600 patients who took Regranex with 2,800 patients who did not, according to the FDA.
The new label, which is outlined in a black box, advises doctors to use caution when prescribing the drug to patients with malignancies.
Regranex is a man-made version of a substance produced by the human body that helps heal ulcers. Because the drug causes cells to divide more rapidly, the FDA said Johnson & Johnson closely monitored patients for reports of cancer, which spreads through uncontrolled cell division.
The FDA in March said it was reviewing the drug's links to cancer.
A spokeswoman for New Brunswick, N.J.-based Johnson & Johnson said the company cooperated with the FDA on the new label and was "committed to getting the information out to physicians and patients."
About 750,000 people have used the drug since it was approved by the FDA in 1997. It is marketed by Ethicon Inc., a subsidiary of Johnson & Johnson.
Shares of the parent company fell $1.20 yesterday to close at $65.76.