Washington Post Staff Writer
Wednesday, June 11, 2003; Page A14
The British government warned doctors yesterday against prescribing the
antidepressant Paxil to children, spurring the U.S. Food and Drug Administration
to confirm that it is conducting its own investigation into the safety of the
drug for younger patients.
The British warning said the medicine appeared to increase the risk of
suicide or suicidal thinking among children with depression.
The U.S. agency is examining the same studies that Paxil's manufacturer
submitted to British authorities.
"There is data that has come to light that may be noteworthy," said an FDA
official yesterday, speaking on the condition of anonymity. "We will take
whatever action is deemed appropriate to protect the public health."
The FDA official gave no timetable for a decision, but said, "when you have a
serious question like this, you want to do the analysis as quickly as possible."
The British warning was issued after an independent group of scientists and
regulators concluded that the risks of Paxil, which is marketed as Seroxat in
Britain, outweighed its benefits among children and adolescents with depression.
"There is an increase in the rate of self-harm and potentially suicidal
behavior in this age group, when Seroxat is used for depressive illness," said a
statement from the Medicines and Healthcare products Regulatory Agency. "It has
become clear that the benefits of Seroxat in children for the treatment of
depressive illness do not outweigh these risks."
Paxil is one of a group of medicines called selective serotonin reuptake
inhibitors (SSRIs) used to treat depression, anxiety and other psychiatric
disorders. Charges that the drugs increase the risk of suicide have dogged the
medicines since the first SSRI, Prozac, was introduced in the late 1980s.
Regulators and most psychiatrists have maintained that the medicines are
safe, even though some doctors have said the drugs have a dangerous profile.
Although many patients say they have benefited from the medicines, others say
they have been harmed, have launched large advocacy campaigns against the drugs
over the Internet and have filed lawsuits.
Paxil is not approved for use among children in the United States or Britain,
but doctors have written thousands of "off-label" prescriptions for it.
Off-label prescriptions are uses of FDA-approved drugs for purposes other than
those approved by the agency.
Mary Anne Rhyne, a spokeswoman for GlaxoSmithKline, the manufacturer of
Paxil, said that of about 28 million prescriptions for Paxil last year, less
than 10 percent, possibly less than 5 percent, were written for children.
Alan Metz, vice president for clinical development for the company, said that
British authorities had overreacted, drawing conclusions from small statistical
differences.
Metz said the company had submitted data to both British and U.S. regulators
supporting Paxil's safety and effectiveness among children and adolescents. Nine
studies compared Paxil with dummy pills among 1,200 children who suffered from
depression, obsessive-compulsive disorder and social anxiety disorder.
He said 33 children had shown signs of mood swings that included suicidal
thinking and suicide attempts. In that number, the rate was about 1 percent to 2
percent in the group taking placebos, and about 2 percent to 3.5 percent in the
group taking the medicine, he said.
In its warning yesterday, the British health agency said that children taking
Paxil should not discontinue treatment without medical supervision. It added
that "patients over 18 years and those who are benefiting from Seroxat should
not be frightened into stopping their medication."
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