sexually transmitted diseases

Description

The I Am Generess program has teamed up with the Rape, Abuse & Incest National Network (RAINN) to support their fight against sexual violence. This video explains how RAINN, the world's largest anti-sexual violence organization, works to help victims of sexual violence, prevent future attacks, and bring rapists to justice. I Am Generess is a charitable giving program that makes financial donations to organizations that help women. For every Generess® Fe prescription filled, you can donate $5 worth of coins to a participating women's charity. See complete terms and conditions at https://www.generess.com/. Important Safety Information GENERESS FE is an estrogen/progestin COC indicated for use by women to prevent pregnancy. You should not use GENERESS FE if you are over 35 and smoke as it increases the risk of having serious heart-related events. You should not use GENERESS FE if you are at high risk of blood clots, if you have abnormal uterine bleeding, breast or liver cancer, liver disease, high blood pressure, or uncontrolled high blood cholesterol. Treatment with GENERESS FE should be stopped if you have a blood clot, and at least 4 weeks before and through 2 weeks after major surgery. You should not take GENERESS FE any earlier than 4 weeks after having a baby and should not take GENERESS FE if you are breastfeeding. If you experience yellowing of the skin due to problems with your liver, you should stop taking GENERESS FE. If you are pre-diabetic or diabetic, your doctor should monitor you while using GENERESS FE, and should evaluate you if you have any significant change in headaches or irregular menstrual bleeding. The most common adverse events associated with the use of GENERESS FE included nausea/vomiting, headaches/migraine, depression/mood complaints, pain with menstrual bleeding, acne, increased weight, breast pain/tenderness and anxiety. GENERESS FE will not protect against HIV infection (AIDS) or other sexually transmitted diseases. Please see full Prescribing Information at http://pi.watson.com/prescribing_info.asp?type=pi&product_group=1706&uid= You are encouraged to report negative side effects of prescription drugs to the FDA. Visit http://www.fda.gov/medwatch, or call 1-800-FDA-1088.