Ballicules.com

Etonogestrel implant

NEXPLANON

What it isSubdermal progestin agonist that suppresses ovulation and thickens cervical mucus; long-acting contraception.

Why this oneIt removes daily adherence and fertility returns promptly after removal, without estrogen-related thrombosis risk.

What limits itUnpredictable bleeding is the chief reason for removal; insertion can injure nerves or vessels, and enzyme inducers reduce efficacy.

FDA label

BOXED WARNING Risk of complications due to improper insertion and removal; available only through a restricted program (NEXPLANON REMS) with required provider training.
FDA dosingPopulationStartTargetMax
Prevention of pregnancy for up to 5 yearsWomen of reproductive potentialInsert one implant subdermally at inner side of non-dominant upper armRemove 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

Contraindications

Cautions

Adverse reactions

Pregnancy Contraindicated in pregnancy; remove the implant if pregnancy is to be maintained.

Lactation Small amounts of etonogestrel present in milk; can reduce milk production; no significant adverse effects observed in breastfed infants.

NO BOXED WARNINGS

Classes and tags

Clinical profile

Direct muscarinic antagonism0 / 4

Mechanism of action: Etonogestrel implant ballicule

Etonogestrel implant ballicule: receptor binding, kinetics and half-life diagram

Open Etonogestrel implant in the interactive console ↗