FDA: More risks from anemia drugs

The FDA dealt another blow to embattled anemia drugs [1] yesterday. The agency revealed two new studies that show cancer patients may be more likely to die while using Amgen's blockbuster drugs Aranesp and Epogen (also sold under the brand name Procrit by Johnson & Johnson).

The drugs, known as erythropoiesis stimulating agents (ESAs), are already under safety review by regulators. In November, new warnings of their cancer risks--that tumors might grow faster and patients may die sooner, according to four other studies--were added to their labels. Other research has shown that ESAs pose increased risk of heart attack, stroke, and heart failure. The risks are greatest with high doses of the drugs, so several months ago, Medicare limited reimbursement to lower doses. Some insurers followed suit.

Now, according to an FDA statement, the agency "may take additional action." If regulators further restrict the drugs, Amgen would be deeply wounded [2]. ESAs account for more than half the company's profits.

- see the FDA release [3]
- get details [4] about the newly released data
- read the article [5] from the Los Angeles Times

Related Articles:
Amgen in new talks over ESA safety. Report [6]
Analyst: Anemia drug warnings 'not bad'. Report [7]
Amgen income hammered as anemia drug use drops. Report [8]
Amgen, J&J win a round in anemia controversy. Report [9]