"The U.S. Food and Drug Administration today announced that it has approved an amended application submitted by Teva Women's Health, Inc. to market Plan B One-Step (active ingredient levonorgestrel) for use without a prescription by women 15 years"...
Overdosage can result if more than six capsules of the NORPLANT (levonorgestrel implants (unavailable in us)) SYSTEM are in situ. All implanted NORPLANT (levonorgestrel implants (unavailable in us)) SYSTEM capsules should be removed before inserting a new set of NORPLANT (levonorgestrel implants (unavailable in us)) SYSTEM capsules. Overdosage may cause fluid retention with its associated effects and uterine bleeding irregularities.
- Active thrombophlebitis or thromboembolic disorders. There is insufficient information regarding women who have had previous thromboembolic disease.
- Undiagnosed abnormal genital bleeding.
- Known or suspected pregnancy.
- Acute liver disease; benign or malignant liver tumors.
- Known or suspected carcinoma of the breast.
- History of idiopathic intracranial hypertension.
- Hypersensitivity to levonorgestrel or any of the other components of the NORPLANT (levonorgestrel implants (unavailable in us)) SYSTEM.
Last reviewed on RxList: 1/5/2009
This monograph has been modified to include the generic and brand name in many instances.
Additional Norplant Information
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