What is the dosage and administration of Nexplanon (etonogestrel)?

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Nexplanon Dosage and Administration

Device Specifications and Dosing

Nexplanon is a single-rod subdermal implant containing 68 mg of etonogestrel that provides effective contraception for up to 3 years. 1, 2, 3

  • The implant is 4 cm long, made of ethylene vinyl acetate copolymer (non-absorbable material), and contains 15 mg of barium sulfate for radiographic visualization 2
  • It releases approximately 120 μg of etonogestrel daily (the active metabolite) 1
  • The device comes pre-loaded in a sterile applicator for single-use insertion 3

Insertion Timing and Technique

Timing of Insertion

The implant can be inserted at any time if it is reasonably certain the woman is not pregnant. 1

Optimal timing based on clinical scenario: 1

  • Within first 5 days of menstrual bleeding: No backup contraception needed
  • Day 6 or later of menstrual cycle: Requires 7 days of backup contraception (abstinence or barrier method)
  • Postpartum (breastfeeding): Can insert anytime ≥1 month postpartum without backup if amenorrheic and fully/nearly fully breastfeeding; otherwise requires 7 days backup 1
  • Postpartum (not breastfeeding): Can insert immediately or anytime; if ≥21 days postpartum and menstrual cycles have not returned, requires 7 days backup contraception 1
  • Post-abortion: Can insert within first 7 days (including immediately) without backup contraception needed 1

Insertion Procedure

Mean insertion time is approximately 0.5-1.1 minutes. 3, 4

  • Position the applicator needle subdermally in the inner aspect of the non-dominant upper arm 3
  • Withdraw the cannula, leaving the implant rod in place 3
  • Insertion complications are extremely rare (0.3% incidence) 3

Duration of Use and Removal

The implant provides effective contraception for 3 years and must be removed or replaced after this period. 1, 2, 4

Removal Procedure

  • Mean removal time is approximately 2.6-3.5 minutes 3, 4
  • Use the "pop out" technique involving a 2-mm incision 3
  • Removal complications are rare (0.2% incidence) 3
  • Return to normal menstrual cycles and fertility is rapid after removal 4

Efficacy

Nexplanon has a failure rate of less than 1 per 100 woman-years, with no pregnancies reported in major clinical trials. 1, 5, 4

  • In one U.S. study with 474 woman-years of exposure, zero pregnancies occurred 4
  • Continuation rate at 12 months is approximately 93.8% 6

Common Pitfalls to Avoid

Do not confuse the timing requirements for backup contraception—the critical threshold is whether insertion occurs within the first 5 days versus day 6 or later of the menstrual cycle. 1

  • Failure to provide adequate counseling about expected bleeding pattern changes is the most common reason for discontinuation (13% of users) 4
  • Most women experience infrequent bleeding patterns (most common) rather than frequent bleeding (least common), with amenorrhea rates of 14-20% during months 4-24 4
  • Deep insertion should be avoided as it complicates removal 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Implant site Nexplanon reaction?

BMJ case reports, 2015

Research

Insertion and removal of Implanon: practical considerations.

The European journal of contraception & reproductive health care : the official journal of the European Society of Contraception, 2000

Guideline

Management of Primary Dysmenorrhea with Nexplanon

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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