Birth-control patch may raise clot risk
ST. LOUIS, Missouri (AP) --
A new study shows that women using the Ortho Evra
birth-control patch have double the risk of developing
blood clots than those who take the pill, the Food and
Drug Administration said Friday.
But the agency said the
results are preliminary and do not require immediate
action other than advising women to discuss the risk
with their doctor.
The results of the study,
and another that found no increased risk, were made
public Thursday by the patch's manufacturer.
"The results are
preliminary and further evaluation is necessary to
understand what these results mean," Dr. Daniel Shames,
director of the division of reproductive and urological
drug products at FDA, said at a briefing.
The finding comes from one
of two studies comparing the patch and pill, said Ortho
Women's Health & Urology, maker of the once-a-week
patch. The Raritan, New Jersey-based company is owned by
Johnson & Johnson.
Last year an investigation
by The Associated Press, citing federal death and injury
reports, found higher rates of blood clots in women
using the patch.
The first study found no
increased risk of clots but the interim results from the
second study suggested a twofold increase in the risk of
venous thromboembolic events, or clots in the legs and
lungs, in women using the patch, Ortho said.
However, because the
confidence intervals of the results for the two forms of
contraceptive overlap, there actually may be no
increased risk from the patch or it may be more than
twice, Shames said at a briefing.
He said the risk of a
nonfatal blood clot is about one per year in 10,000
women not using a contraceptive. For those using a
hormonal contraceptive such as the patch or pill the
risk rises to between three and five, he said.
"These are fairly unusual
events," said Shames. He noted that in preapproval
testing of the patch on about 3,000 women there were two
reports of blood clots, but one involved a woman who
had had surgery.
The ongoing studies also
are looking at the risk of heart attacks and strokes
among users of the two types of contraception. Currently
there is no difference but the numbers are small and it
will take another 18 months to see if a difference
occurs, Shames said.
The company said that the
risk of clots remains rare and that they have been
reported as a potential risk of all hormonal
contraceptives.
Release of the interim
results comes four months after the Food and Drug
Administration warned women that the increased levels of
hormones released by the patch put them at higher risk
of blood clots and other serious side effects. Ortho
said it shared the results of the latest studies with
the FDA.
Additions to the patch
label made in November warned women that they would be
exposed to about 60 percent more estrogen than those who
use birth-control pills.
Since the patch went on
sale in 2002, more than 4 million women have used it.
The investigation by The
Associated Press found that patch users die and suffer
blood clots at a rate three times higher than women
taking the pill. About a dozen women died in 2004 from
blood clots believed linked to use of the patch, the AP
reported. Dozens more suffered strokes and other
clot-linked problems.
Health officials warn that
women who smoke should not use the patch, since smoking
increases the risk of stroke and heart attack.