
NEXPLANON®
Searching for efficient non-uterine long-acting reversible contraception for your patients? Order NEXPLANON® intended for use as a contraceptive measure to prevent pregnancy. It is the only non-uterine LARC that is over 99% effective. NEXPLANON® comes in the form of a small (about the size of a matchstick), thin, and flexible birth control implant which is placed discreetly just under the skin on the inner side of a patient’s non-dominant upper arm by a trained healthcare professional.
We Bring the Best Solutions to You. Register Now
Join us in discovering the perfect medical and aesthetic solutions for your clinic. By registering, you'll receive personalized consultations that connect you with an extensive selection of products– tailored to your clinic's distinctive needs and aspirations.
What is NEXPLANON® Used For and How Does It Work?
NEXPLANON®, radiopaque etonogestrel implant 68mg, is not an intrauterine device (IUD) and it doesn’t contain estrogen. It is an implant that is placed in a patient's arm. NEXPLANON® is a prescription birth control for the prevention of pregnancy. It may last up to 3 years. What does it mean when we say that it is over 99% effective? That means less than 1 pregnancy per 100 women who used NEXPLANON® for 1 year.How to Administer For Best Results?
It should be inserted subdermally to ensure palpability immediately post-insertion. Failure to do so may result in undetected implantation failure, leading to unintended pregnancies. Additionally, keep in mind that incorrectly removed implants may result in continued effects of etonogestrel, potentially leading to compromised fertility, ectopic pregnancy, or persistence or occurrence of adverse drug reactions. NEXPLANON® is administered subdermally just under the skin at the inner side of the non-dominant upper arm. NEXPLANON must be removed no later than by the end of the third year. Read our comprehensive article on Nexplanon Side Effects.Before You Buy: Essential Considerations
NEXPLANON should not be utilized in the following cases:- Women with known or suspected pregnancy.
- Those with a current or past history of thrombosis or thromboembolic disorders.
- Individuals with liver tumors, benign or malignant, or active liver disease.
- Women experiencing undiagnosed abnormal genital bleeding.
- Those with known or suspected breast cancer, personal history of breast cancer, or other progestin-sensitive cancer, whether present or in the past.
- Individuals who have experienced allergic reactions to any component of NEXPLANON.