Injectible
contraceptive being recalled because of lack of potency
A subpotent dose
may not be effective in preventing pregnancy
10/10/2002
WASHINGTON (AP) -- A type of contraceptive injected once a month
is being recalled because some doses may not be potent enough, the
manufacturer announced Thursday.
A subpotent dose may not be effective in preventing pregnancy.
Pharmacia Corporation of Peapack, N.J., said the recall covers
Lunelle monthly contraceptive in prefilled syringes.
As many as 100,000 women could be affected by the recall,
covering products distributed between January and October of this
year, the Food and Drug Administration reported.
The recall does not include the form of Lunelle packed in vials,
the company said, but only the prefilled syringes which constitute
the majority of the market.
When the drug won approval in 2000, the company said it was 99
percent effective.
Pharmacia spokeswoman Caroline Bullock said the company has not
seen any increase in unintended pregnancies among users of the drug.
Women who used the contraceptive may not be aware if they
received the prepacked form or that drawn from a vial. Pharmacia
urged women who have been using Lunelle to contact their physician
about another form of contraception and begin using an additional
barrier form of contraception in the meantime.
Lunelle is an alternative to another injectible contraceptive,
called Depo-Provera, that lasts three months. Like many
birth-control pills, it works through a combination of the hormones
progestin and estrogen.
Women taking the contraceptive injection still have monthly
menstrual cycles.
Pharmacia said patients can call 1-888-691-6813 for more
information. Healthcare professionals can call 1-800-323-4204.
On the Net:
Lunelle
(Copyright 2002 by The Associated Press. All Rights Reserved.)