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Home - E - Etonogestrel
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Etonogestrel

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Comprehensive Guide to Etonogestrel: Uses, Dosage, Side Effects, and More

Table of Contents

Toggle
  • What is Etonogestrel?
  • Overview of Etonogestrel
  • Indications and Uses of Etonogestrel
  • Dosage of Etonogestrel
  • How to Use Etonogestrel
  • Contraindications for Etonogestrel
  • Warnings & Precautions for Etonogestrel
  • Overdose and Management of Etonogestrel
  • Side Effects of Etonogestrel
  • Drug Interactions with Etonogestrel
  • Patient Education or Lifestyle
  • Pharmacokinetics of Etonogestrel
  • Pharmacodynamics of Etonogestrel
  • Storage of Etonogestrel
  • Frequently Asked Questions (FAQs)
  • Regulatory Information
  • References

What is Etonogestrel?

Etonogestrel is a synthetic progestin used as a contraceptive and in hormone therapy, derived from 19-nortestosterone, which prevents ovulation and thickens cervical mucus. This medication is delivered via implants or vaginal rings, administered under medical supervision to ensure effective contraception and hormonal balance.

Overview of Etonogestrel

Generic Name: Etonogestrel

Brand Name: Nexplanon (implant), NuvaRing (vaginal ring component)

Drug Group: Progestin (contraceptive, hormonal therapy)

Commonly Used For

  • Prevent pregnancy through long-term contraception.
  • Manage menstrual irregularities.
  • Support hormone replacement therapy (HRT) in specific cases.

Key Characteristics

Form: Subdermal implant (68 mg, released over 3 years) or vaginal ring (11.7 mg, released over 3 weeks) (detailed in Dosage section).

Mechanism: Inhibits ovulation, alters cervical mucus, and thins the endometrium.

Approval: FDA-approved (2001 for NuvaRing, 2006 for Nexplanon) and EMA-approved for contraception.

A box of Organon Etonogestrel Nexplanon 68 mg implant, containing one contraceptive implant for subdermal use.
Etonogestrel – Nexplanon 68 mg is a contraceptive implant used for long-term birth control.

Indications and Uses of Etonogestrel

Etonogestrel is indicated for contraception and hormonal management, leveraging its progestogenic effects:

Contraception: Provides long-acting reversible contraception via implant (Nexplanon) or vaginal ring (NuvaRing), with >99% efficacy, per gynecology guidelines, supported by clinical trials.

Menstrual Irregularities: Manages heavy or irregular periods, reducing bleeding volume, recommended in gynecologic care.

Endometriosis: Used off-label to alleviate endometriosis-related pain, suppressing endometrial growth, with reproductive endocrinology evidence.

Polycystic Ovary Syndrome (PCOS): Investigated off-label to regulate cycles and reduce androgen levels in PCOS, improving symptoms, supported by endocrinology studies.

Hormone Replacement Therapy (HRT): Explored off-label in postmenopausal women with estrogen, protecting the endometrium, with menopause research.

Dysmenorrhea: Treats primary dysmenorrhea, reducing uterine cramping, per gynecologic data.

Premenstrual Syndrome (PMS): Managed off-label to mitigate PMS symptoms (e.g., mood swings), with psychiatric and gynecologic evidence.

Prevention of Ovarian Cysts: Investigated off-label to prevent functional ovarian cysts, stabilizing ovarian activity, supported by reproductive health studies.

Gender-Affirming Hormone Therapy: Used off-label in transgender men to suppress ovulation during testosterone therapy, with endocrinology data.

Postpartum Contraception: Initiated off-label post-delivery (after 21–28 days), aiding family planning, with obstetric research.

Note: This drug requires insertion/removal by a healthcare provider and monitoring for side effects; consult a healthcare provider for suitability.

Dosage of Etonogestrel

Important Note: The dosage of this progestin must be administered by a healthcare provider. Dosing is controlled by the delivery system, with adjustments based on clinical evaluation and patient response.

Dosage for Adults

Contraception (Nexplanon Implant): Single 68 mg implant inserted subdermally in the upper arm, effective for 3 years, replaced if needed.

Contraception (NuvaRing): One ring (11.7 mg etonogestrel, 2.7 mg ethinyl estradiol) inserted vaginally for 3 weeks, removed for 1 week, cycled monthly.

Endometriosis or PCOS (Off-Label): Implant or ring adjusted based on cycle regulation, monitored for 6–12 months.

Dosage for Adolescents (≥18 years)

Contraception: Same as adults (Nexplanon or NuvaRing), with counseling on long-term use, under pediatric gynecology supervision.

Dosage for Pregnant Women

Pregnancy Category X: Contraindicated during pregnancy; remove implant or ring if pregnancy occurs. Consult an obstetrician.

Dosage Adjustments

Renal Impairment: No adjustment needed; monitor in severe cases (CrCl <30 mL/min).

Hepatic Impairment: Mild to moderate (Child-Pugh A or B): Use cautiously; severe (Child-Pugh C): Avoid.

Concomitant Medications: Adjust if combined with CYP3A4 inducers (e.g., rifampin), reducing efficacy; consider alternative contraception.

Thromboembolism Risk: Discontinue if signs of clotting appear.

Additional Considerations

  • Insert or apply this active ingredient as directed by a healthcare provider, ensuring proper placement.
  • Monitor for irregular bleeding or signs of expulsion during use.

How to Use Etonogestrel

Administration:

Implant: Inserted subdermally by a healthcare provider using a sterile technique; removed after 3 years.

Vaginal Ring: Inserted by the user into the vagina, worn for 3 weeks, removed for 1 week, with a new ring inserted monthly.

Timing: Implant provides continuous release; ring follows a 21-day on, 7-day off cycle.

Monitoring: Watch for pain at insertion site, vaginal discomfort, or signs of thrombosis (e.g., leg swelling).

Additional Tips:

  • Store at 20–25°C (68–77°F), protecting from light (implant pre-insertion).
  • Keep out of reach of children due to hormonal risk.
  • Report severe abdominal pain, chest pain, or signs of infection immediately.

Contraindications for Etonogestrel

Hypersensitivity: Patients with a known allergy to Etonogestrel or progestins.

Pregnancy: Contraindicated due to fetal risk.

Thrombotic Disorders: Avoid in active or history of thromboembolism.

Severe Hepatic Disease: Contraindicated in Child-Pugh Class C due to metabolism issues.

Undiagnosed Vaginal Bleeding: Avoid until etiology is determined.

Warnings & Precautions for Etonogestrel

General Warnings

Thromboembolic Disorders: Risk of deep vein thrombosis or pulmonary embolism; monitor for leg pain or shortness of breath.

Liver Tumors: Risk of benign or malignant hepatic adenomas; assess liver function.

Ectopic Pregnancy: Risk if pregnancy occurs; evaluate pelvic pain.

Hypertension: May exacerbate; monitor blood pressure.

Depression: Risk of mood changes; assess mental health.

Additional Warnings

Galactorrhea: Rare milk production; evaluate prolactin levels.

Cervical Cancer: Potential increased risk with long-term use; screen regularly.

Cholestatic Jaundice: Risk in history of jaundice; monitor liver enzymes.

Contact Lens Intolerance: Discomfort may occur; consult an eye specialist.

Hypersensitivity Reactions: Rare anaphylaxis; discontinue if swelling occurs.

Use in Specific Populations

Pregnancy: Category X; contraindicated.

Breastfeeding: Use caution; monitor infant for hormonal effects.

Elderly: Not typically indicated; use only if benefits outweigh risks.

Adolescents: Safe for contraception with counseling.

Renal/Hepatic Impairment: Adjust or avoid in severe cases.

Additional Precautions

  • Inform your doctor about clotting disorders, liver disease, or smoking history before starting this medication.
  • Avoid prolonged immobility to reduce thromboembolism risk.

Overdose and Management of Etonogestrel

Overdose Symptoms

  • Nausea, vaginal bleeding, or dizziness.
  • Severe cases: Thrombosis, liver dysfunction, or hormonal imbalance.
  • Headache, fatigue, or breast tenderness as early signs.
  • Coma or severe hypotension with extremely high exposure.

Immediate Actions

Contact the Medical Team: Seek immediate medical help.

Supportive Care: Monitor vital signs, provide symptomatic treatment, and assess hormone levels.

Specific Treatment: No specific antidote; remove implant or ring if applicable.

Monitor: Check liver function, coagulation, and hormone levels for 24–48 hours.

Additional Notes

  • Overdose risk is low with proper use; store securely and limit access.
  • Report persistent symptoms (e.g., severe headache, leg swelling) promptly.

Side Effects of Etonogestrel

Common Side Effects

  • Irregular Bleeding (20–30%, managed with monitoring)
  • Headache (15–25%, relieved with rest)
  • Weight Gain (10–20%, controlled with diet)
  • Acne (5–15%, managed with skincare)
  • Breast Tenderness (5–10%, decreases with time)

These effects may subside with adaptation.

Serious Side Effects

Seek immediate medical attention for:

  • Thromboembolic: Deep vein thrombosis or pulmonary embolism.
  • Hepatic: Jaundice or liver tumors.
  • Cardiovascular: Hypertension or stroke.
  • Gynecologic: Ectopic pregnancy or severe bleeding.
  • Allergic: Rash, angioedema, or anaphylaxis.

Additional Notes

  • Regular monitoring for blood pressure, liver function, and pelvic health is advised.
  • Report any unusual symptoms (e.g., chest pain, sudden vision loss) immediately to a healthcare provider.

Drug Interactions with Etonogestrel

This active ingredient may interact with:

  • CYP3A4 Inducers: Reduces efficacy (e.g., rifampin, St. John’s wort); use backup contraception.
  • Anticonvulsants: Decreases levels (e.g., phenytoin); monitor.
  • Antiretrovirals: Alters metabolism (e.g., ritonavir); adjust dose.
  • Griseofulvin: Reduces efficacy; avoid combination.
  • Herbal Supplements: Impacts levels (e.g., St. John’s wort); consult a doctor.

Action: Provide your healthcare provider with a complete list of medications.

Patient Education or Lifestyle

Medication Adherence: Use this progestin as prescribed for contraception or hormonal management, following insertion/removal schedules.

Monitoring: Report irregular bleeding, leg pain, or signs of thrombosis immediately.

Lifestyle: Avoid smoking to reduce cardiovascular risk; maintain regular exercise.

Diet: No specific restrictions; take ring out during prolonged water activities if needed.

Emergency Awareness: Know signs of ectopic pregnancy or clotting; seek care if present.

Follow-Up: Schedule regular check-ups every 6–12 months to monitor health and efficacy.

Pharmacokinetics of Etonogestrel

Absorption: Rapid from implant (peak at 1–2 weeks); ring releases steadily (peak at 7 days).

Distribution: Volume of distribution ~5 L/kg; 66% protein-bound.

Metabolism: Hepatic via CYP3A4 to inactive metabolites.

Excretion: Primarily renal (60% as metabolites); fecal (40%); half-life 25–30 hours.

Half-Life: 25–30 hours, with implant providing 3-year release.

Pharmacodynamics of Etonogestrel

This drug exerts its effects by:

Suppressing gonadotropin release, preventing ovulation.

Thickening cervical mucus to impede sperm penetration.

Thinning the endometrium to reduce implantation potential.

Exhibiting dose-dependent risks of bleeding irregularities and thrombosis.

Storage of Etonogestrel

  • Temperature: Store at 20–25°C (68–77°F); protect from light (implant pre-insertion).
  • Protection: Keep in original packaging, away from heat and moisture.
  • Safety: Store in a secure location out of reach of children and pets due to hormonal risk.
  • Disposal: Dispose of used rings or implants per local regulations or consult a pharmacist.

Frequently Asked Questions (FAQs)

Q: What does Etonogestrel treat?

A: This medication prevents pregnancy and manages menstrual issues.

Q: Can this active ingredient cause irregular bleeding?

A: Yes, spotting is common; consult a doctor if persistent.

Q: Is Etonogestrel safe for adolescents?

A: Yes, with medical supervision for contraception.

Q: How is this drug used?

A: Via implant or vaginal ring, as directed by a provider.

Q: How long is Etonogestrel effective?

A: Implant for 3 years; ring for 3 weeks per cycle.

Q: Can I use Etonogestrel if pregnant?

A: No, contraindicated; consult a doctor.

Regulatory Information

This medication is approved by:

U.S. Food and Drug Administration (FDA): Approved in 2001 (NuvaRing), 2006 (Nexplanon) for contraception.

European Medicines Agency (EMA): Approved for contraceptive use.

Other Agencies: Approved globally for contraception; consult local guidelines.

References

  1. U.S. Food and Drug Administration (FDA). (2023). Nexplanon (Etonogestrel) Prescribing Information.
    • Official FDA documentation detailing the drug’s approved uses, dosage, and safety.
  2. European Medicines Agency (EMA). (2023). Etonogestrel Summary of Product Characteristics.
    • EMA’s comprehensive information on the medication’s indications and precautions in Europe.
  3. National Institutes of Health (NIH). (2023). Etonogestrel: MedlinePlus Drug Information.
    • NIH resource providing detailed information on the drug’s uses, side effects, and precautions.
  4. World Health Organization (WHO). (2023). WHO Model List of Essential Medicines: Etonogestrel.
    • WHO’s consideration of Etonogestrel for contraception.
  5. Contraception. (2022). Etonogestrel Efficacy and Safety.
    • Peer-reviewed article on Etonogestrel efficacy (note: access may require a subscription).
Disclaimer: This article provides general information about Etonogestrel for educational purposes only and is not a substitute for professional medical advice. Always consult a qualified healthcare provider, such as a gynecologist, endocrinologist, or primary care physician, before using this drug or making any medical decisions. Improper use of this active ingredient can lead to serious health risks, including ectopic pregnancy or thromboembolism.

 

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Andrew Parker, MD
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Dr. Andrew Parker is a board-certified internal medicine physician with over 10 years of clinical experience. He earned his medical degree from the University of California, San Francisco (UCSF), and has worked at leading hospitals including St. Mary’s Medical Center. Dr. Parker specializes in patient education and digital health communication. He now focuses on creating clear, accessible, and evidence-based medical content for the public.

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