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Side effects from neplan birth control
Side effects from neplan birth control







side effects from neplan birth control

Nexplanon is super effective - in fact, fewer than 1% of people who use it for one year will get pregnant. What are the benefits of the birth control implant, Nexplanon? With so many other types of birth control out there, we’re bringing you the pros and cons of the implant to help you make an informed choice. Since there’s only one option for the contraceptive implant, you only need to use your decision-making muscles to figure out if this birth control option is the right method for you. The pros, cons, and the good-to-knows about the implant While Implanon is still used in other countries, Nexplanon is the only birth control implant available in the US. Implanon, Nexplanon's predecessor, was discontinued in the US in 2014, and the Nexplanon implant is its updated version. Nexplanon is currently approved for use for three years, but there is evidence that it can be used for up to five years (but don't prolong use of your implant without first talking with a health care professional). Once implanted, it releases a low-yet-steady dose of progestin (a synthetic progesterone) and prevents pregnancy by:

#Side effects from neplan birth control skin#

It's placed under the skin of your upper arm by your healthcare provider. Nexplanon, a long-acting method of contraception, is a small, trim, flexible plastic rod, about the size of a matchstick. All products being used in the study are FDA-approved for contraception.A tiny birth control implant method with huge results Of note, the primary risk with COC use is related to the estrogen which can increase the risk of venous thromboembolic disease. We would not expect any increase in side effects by adding a contraceptive implant to COC users. The systemic hormone exposure with a contraceptive implant is minimal relative to a COC. The study intervention (study drug) is the contraceptive implant. No blood draws will occur during this study.ĭata to be collected by study staff include demographics, past medical and gynecologic history, prior and current contraceptive use, and reason for using COC (contraception, medical or both).īecause women are being enrolled who are already currently using COCs or who plan to start COCs, the COC is not a study drug. No surveys will be used that the subject fills out herself. Study participation will be complete after the 6 month follow-up visit. The ENG implant will be removed upon request at any time during the study.Ī phone call will occur approximately 1 week prior to the 3 and 6 month visits to check status and remind subject of the scheduled visit. At the 1 and 3 month visits, additional diaries will be dispensed as needed. The subject will inform the study staff if she is using her COC and if she wants to continue use of her COC and ENG implant. Adverse events will be determined by inquiry and diary review. The diary will be reviewed and a copy made to keep with the source documentation. A diary will be dispensed for the subject to document daily bleeding, COC use and adverse events.įollow-up A follow-up visit will occur at 1 month (+1 week) and 3 and 6 months (+2 weeks). Eligible subjects will receive a prescription for the desired COC (if needed) and have a Nexplanon contraceptive implant placed. A urine pregnancy test will be performed.

side effects from neplan birth control

After obtaining informed consent, subjects will be screened for entry criteria. Subjects will also need to review the package label information for Nexplanon and sign the FDA-required Nexplanon consent. The consent form will include a standardized description of the side effects and bleeding profile of COCs and the implant. As part of informed consent, subjects will be educated that there is little data available on the adverse effects of combined COC and ENG implant use. The investigators expect that most women will be recruited while in the office who decide to initiate COCs or are continuing COC use-these women will be offered the ability to talk to research staff about the study. Potential participants must be women currently COCs or intending to initiate COCs at the time of the office visit. The investigators will recruit women being seen in a UC Davis medical office or who contact our research office. Why Should I Register and Submit Results?.









Side effects from neplan birth control