The Food and Drug Administration yesterday warned physicians to consider alternatives to the popular arthritis drug Celebrex because of new evidence that it can more than double...
The Food and Drug Administration yesterday warned physicians to consider alternatives to the popular arthritis drug Celebrex because of new evidence that it can more than double the chances of heart attacks and strokes.
The federal agency also said it may soon take other actions, including requiring stronger warnings or even blocking the drug from sale. Coupled with the October removal from the market of a similar drug, Vioxx, the future of the widely used class of painkillers called COX-2 inhibitors is in question.
Most Read Stories
- Seattle hits record high for income inequality, now rivals San Francisco
- Anthony Bourdain brought 'Parts Unknown' to Seattle — here's where he ate
- A Washington county that went for Trump is shaken as immigrant neighbors start disappearing VIEW
- Seattle’s crazy restaurant boom | PNW Magazine VIEW
- Seattle-Dublin nonstop flights to begin in May 2018
The FDA warning came hours after Celebrex manufacturer Pfizer issued a statement saying that a study of the drug’s efficacy as a cancer treatment found evidence of increased cardiovascular risk. Pfizer, however, gave no indication it would withdraw the drug, which the company says 27 million Americans take.
The study’s findings added to growing concerns about the effectiveness of the FDA’s system for assessing risks of new drugs and for monitoring dangerous side effects in medications it has approved.
“Right now we have a situation where the public is left wondering when the next shoe might drop when it comes to drug safety,” said Sen. Charles Grassley, R-Iowa, who held hearings last month on the problems with Vioxx, manufactured by Merck. “At this point, no one can say with confidence whether the worst drug-safety problems are behind us or ahead of us.”
But Dr. John Jenkins, director of the FDA’s Office of New Drugs, said discovery of problems with Celebrex indicates the system is working.
“I don’t see this as a failure of the system,” Jenkins said. “This is how drug development, drug approval and post-market monitoring is done, not only in the United States, but in all countries that have a regulatory system.”
Dr. Joseph Feczko, president of worldwide development for Pfizer, said in a statement that doctors “should factor this new information” and weigh it against the risks of other painkilling drugs.
But patient groups voiced concern about the continued use of Celebrex and related drugs.
The Arthritis Foundation issued a statement urging caution in the use of any COX-2 inhibitor.
The consumer-advocacy group Public Citizen said the findings should lead to the withdrawal of the drug.
“This is a doomed class of drugs,” said Dr. Sidney Wolfe, Public Citizen’s director of health research. “They will be taken off the market. It’s a matter of when, not whether.”
Celebrex and other COX-2 inhibitors were developed to be a stomach-friendly alternative to anti-inflammatory medicines such as aspirin, ibuprofen and naproxen. Taken long term, the older medicines can cause stomach bleeding and gastric problems.
The new COX-2 inhibitors became tremendous money makers because they are used as maintenance drugs, taken on a daily basis by millions of people worldwide. They sell for as much as $3 a pill.
The older medicines, by comparison, sell for pennies a pill in generic versions sold in supermarkets and drug stores.
Two COX-2 drugs, Celebrex and Bextra, were expected to account for $5 billion of Pfizer’s estimated 2005 sales of $55 billion, said Sena Lund, a market analyst for Cathay Financial in New York.
Some researchers suspected COX-2 inhibitors might be reducing the body’s production of a protein that prevents blood platelets from clumping together, possibly leading to a stroke or heart attack.
Evidence of the risk in Celebrex surfaced in a Pfizer study, conducted by the National Cancer Institute, to determine if high doses of the drug could prevent formation of certain precancerous colon polyps.
Dr. Ernest Hawk of the institute said the study, which has been going on for nearly three years, involved 2,000 patients, divided into three groups. Some were given a placebo. Others were given 400 or 800 milligrams of Celebrex a day.
The usual dose for arthritis patients ranges from 100 to 200 milligrams daily for those suffering from osteoarthritis to 200 to 400 milligrams daily for rheumatoid arthritis.
As concerns were being raised about Vioxx, the cancer institute brought in a special team of cardiac experts to evaluate its Celebrex data.
They found six cases of such adverse effects in the placebo group, 15 cases in the lower-dose Celebrex group and 20 cases in the higher-dose group. The risk of adverse effects was 2.5 times greater in the lower-dose group and 3.4 times greater in the higher-dose group, Hawk said.
The cancer institute halted the Celebrex study, and the National Institutes of Health yesterday ordered a review of more than 40 studies involving COX-2 inhibitors.
Pfizer, however, said the cancer study was out of step with other evidence showing Celebrex is safe.
There is a “large body of data that we and others have accumulated over time, in which an increased risk of serious cardiovascular events in arthritis patients, even at higher-than-recommended doses, had not been seen,” Feczko said in a statement.
Indeed, there was some confusion in the medical world over the study’s findings.
Researchers who have studied Vioxx said the FDA needs more information to reach a conclusion on Celebrex.
“I was caught by complete surprise,” said Dr. Gurkirpal Singh at Stanford Medical School. “Everything with Celebrex was pointing in the direction that it had a small cardio-protective effect.”
Singh said he would be “very cautious” about prescribing Celebrex to patients at this point, although he did not think there was enough information to pull the drug from the market.
Another researcher, Dr. Bruce Psaty of the University of Washington, said the latest episode reinforces criticisms that the FDA’s drug-review and -approval process is flawed.
The FDA had planned to convene an advisory committee in February to discuss COX-2 inhibitors.
The agency now may have to act sooner.
Bextra, a newer COX-2 inhibitor that 7 million people worldwide have used, also drew criticism yesterday with the release of a letter from three physicians at the Vanderbilt University School of Medicine warning doctors against prescribing the medicine “except in extraordinary circumstances.”
The letter, to be published in Thursday’s edition of the New England Journal of Medicine, was released early because of Pfizer’s Celebrex announcement.
The doctors said previous findings of an increased risk for heart-bypass patients taking Bextra were serious enough to call into question the drug’s safety for other people.
Information on the number of people who have taken Celebrex and Bextra was provided by The Washington Post.