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Plan B® is composed of progestin-only (levonorgestrel) tablets. Levonorgestrel is well-trusted and has been commonly used in many birth control pills for over 35 years. Plan B® also has a superior tolerability profile compared to the Yuzpe regimen (levonorgestrel and ethinyl estradiol); in a clinical trial, 23% of women taking Plan B® experienced nausea and 5.6% experienced vomiting. Plan B® is safe and well tolerated. Some women may experience mild side effects, similar to those of regular birth control pills. The most common include: nausea, abdominal pain, fatigue, headache, menstrual changes, dizziness, breast tenderness, vomiting, and diarrhea. After taking Plan B®, they should be informed that their next period may be heavier or lighter, earlier or later. In a clinical trial, the majority of women (87%) had their menstrual period at the expected time or within ±7 days. Patients should be advised that if their period is more than one week late, they may be pregnant. If your patient experiences severe abdominal pain, she may have an ectopic pregnancy and should seek immediate medical attention. |
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| Important Safety Information: | For more information about Plan B®, call 1-800-330-1271 |
Important Safety Information: Plan B® is indicated to prevent pregnancy following unprotected intercourse or contraceptive failure. Plan B® is contraindicated in women with known or suspected pregnancy, hypersensitivity to any component of the product. Plan B® is not recommended for routine use as a contraceptive, because it isn't as effective. Plan B® is not effective in terminating an existing pregnancy. Plan B® does not protect against HIV infection and other sexually transmitted infections (STIs). Menstrual bleeding may be heavier or lighter, earlier or later after taking Plan B®. If menses is delayed beyond one week, the patient may be pregnant. Severe abdominal pain may signal a tubal (ectopic) pregnancy. Common side effects associated with the use of Plan B® include nausea, abdominal pain, fatigue, headache, menstrual changes, dizziness, breast tenderness, vomiting, and diarrhea. Your patients are encouraged to report any negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088. |
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