FDA Pulls Darvon and Companion Drug Due to Heart
FRIDAY, Nov. 19 (HealthDay News) -- The opioid-based painkillers
Darvon and Darvocet are being withdrawn from the U.S. market
because they've been linked to serious and potentially deadly heart
rhythms, federal officials said Friday.
The U.S. Food and Drug Administration said Xanodyne
Pharmaceuticals -- which makes Darvon and Darvocet -- is
voluntarily taking the drugs off the market. The active ingredient
in these drugs is propoxyphene. The agency has also asked the
makers of generic versions of propoxyphene to remove them from the
"We have recently completed our review of a new clinical trial that was designed to assess the impact of propoxyphene on the electrical activity of the heart," Dr. John Jenkins, director of FDA's Office of New Drugs, Center for Drug Evaluation and Research, said during a Friday press conference. The trial showed propoxyphene can cause potentially serious or even deadly heart rhythm problems, called arrhythmias, he said.
"We concluded the pain benefits of propoxyphene no longer outweighed the heart risk and that propoxyphene should no longer be sold in the United States," Jenkins said.
In 2009, the European Medicines Agency recommended withdrawing
the drug across the European Union. A phased withdrawal is under
way, the FDA said.
Dr. Gerald Dal Pan, director of the FDA's Office of Surveillance
and Epidemiology, said the agency is asking doctors to stop
"We are advising patients who are currently taking the drug not to stop taking propoxyphene right away. You still need to manage your pain. Instead, we urge you to contact your health care professional as soon as possible to discuss switching to another pain-management therapy," he said.
Dal Pan said patients taking the drug who experience heart
palpitations, dizziness or light-headedness should contact their
doctor right away.
People who stop the drug suddenly may experience withdrawal
effects, such as nausea, diarrhea, anxiety and shivering, he said.
"That's why this should be done under the supervision of a medical
professional," he added.
Dal Pan said that the heart effects of propoxyphene aren't
cumulative, so once the drug is stopped the risk should go
In 2009, approximately 10 million people in the United States
were taking propoxyphene, he said. The most widely prescribed
version was Darvocet, he noted.
Propoxyphene was approved by the FDA in 1957, is sold by
prescription under various names, including Darvon, or in
combination with acetaminophen (Darvocet).
The FDA said it had been asked twice since 1978 to take
propoxyphene off the market, but until now the agency believed the
drug's benefits outweighed the risks.
In 2009, an FDA advisory committee voted 14 to 12 to remove the
drug from the market.
Despite that 2009 recommendation, the FDA left the drug
available, but required a new boxed warning on the label, alerting
patients and doctors of the risk of a fatal overdose. The agency
also required Xanodyne to conduct a new safety study of
propoxyphene's impact on the heart.
Results of that study showed significant changes to the heart's
electrical activity, which can increase the risk for serious
abnormal heart rhythms that have been linked to serious adverse
effects, including sudden death, the FDA said.
In a news release issued after the FDA announcement, Dr. Sidney
Wolfe, director of Public Citizen's Health Research Group, said:
"The announcement by the U.S. Food and Drug Administration that
propoxyphene-containing products are finally going to be taken off
the market -- because of dangers previously known and acted upon,
with bans announced in the U.K. almost six years ago, and in
Europe, almost 1.5 years ago -- is a serious indictment of the
FDA's long-lasting unwillingness to protect people in this country
from a deadly but barely effective painkiller."
Dr. William O'Neill, executive dean for clinical affairs at the
University of Miami Miller School of Medicine, said he had a
problem with the way the FDA handled drug withdrawals, recalls and
"I'm a little annoyed, because what always happens with these drug recalls is that they tell patients to see their doctor, which puts the onus on doctors to help each individual patient make a decision about the benefit of the drug versus the potential side effects," O'Neill said.
Practicing physicians have no basis to make an informed
decision, because they have not seen that data on which the FDA
made its decision, O'Neill said. "I have no way of getting that
information; it's not in any published journal," he said. "I have
to infer from the nanny state that this is what's best -- I know
what's right -- without being able to determine whether the drug is
of value or not."
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