BOXED WARNING Risk of complications due to improper insertion and removal; available only through a restricted program (NEXPLANON REMS) with required provider training.
FDA dosing
Population
Start
Target
Max
Prevention of pregnancy for up to 5 years
Women of reproductive potential
Insert one implant subdermally at inner side of non-dominant upper arm
Remove no later than the end of the fifth year; may replace at removal
Renal Undefined
Hepatic Undefined
Efficacy does not depend on daily/weekly/monthly administration; must be removed by end of the fifth year.
Instructions
Insert subdermally just under the skin at the inner non-dominant upper arm by a trained provider; confirm by palpation immediately after insertion
Rule out pregnancy before insertion; timing depends on prior contraceptive use
Remove/replace by end of fifth year; locate non-palpable implants by imaging before removal
Contraindications
Known or suspected pregnancy
Current or past history of thrombosis or thromboembolic disorders
Liver tumors, benign or malignant, or active liver disease
Undiagnosed abnormal uterine bleeding
Known or suspected breast cancer, personal history of breast cancer, or other progestin-sensitive cancer, now or in the past
Cautions
Insertion/removal complications — pain, paresthesia, migration (including to pulmonary vessels); may require surgical removal
Changes in menstrual bleeding patterns
Ectopic pregnancy possibility
Thrombotic and other vascular events — remove if thrombosis occurs