Jadelle (levonorgestrel implant)
Pronunciation: juh-DEL (jadelle); lee-vo-nor-JES-trel (levonorgestrel).
- Generic name
- levonorgestrel (subdermal implant)
- Drug class
- Progestin-only long-acting reversible contraceptive (LARC) implant
- Form
- Two flexible rods (43 mm x 2.5 mm), each containing 75 mg levonorgestrel (150 mg total)
- Route
- Subdermal (under the skin)
- Legal status
- Prescription-only, inserted and removed by a trained clinician
Availability and supply rules vary by country
Trade names by country: United States · Canada · New Zealand
Australia: · Full directory
What levonorgestrel (subdermal implant) is and how it works
Jadelle is a prescription-only contraceptive implant: two small, flexible rods inserted just under the skin of the upper arm by a trained clinician, releasing a steady low dose of the hormone levonorgestrel to prevent pregnancy for up to 5 years. (1) (3)
Jadelle must be inserted and removed by a clinician trained in the specific technique -- it is not something you place or remove yourself. Changes to your monthly bleeding pattern are common and expected, especially in the first year; discuss any bleeding changes that concern you with your prescriber rather than assuming something is wrong.
Mechanism of action: how levonorgestrel (subdermal implant) works
Levonorgestrel is a synthetic progestin released continuously from the silicone rods, suppressing the luteinising hormone surge (inhibiting ovulation) and thickening cervical mucus to impede sperm penetration; endometrial changes may also contribute to contraceptive effect. (1)
What levonorgestrel (subdermal implant) is used for
Long-term contraception (pregnancy prevention)
Used to prevent pregnancy for up to 5 years per insertion. It works mainly by preventing ovulation and thickening cervical mucus so sperm cannot easily reach an egg. It does not protect against sexually transmitted infections. (1) (3)
Before taking levonorgestrel (subdermal implant)
Do not take / not appropriate for
- Do not have Jadelle inserted if you are pregnant or think you might be pregnant. (all countries where marketed) (1)
- Do not have Jadelle inserted if you have current or past blood clots (such as deep vein thrombosis or pulmonary embolism), acute liver disease or liver tumours, undiagnosed abnormal vaginal bleeding, or known or suspected breast cancer. (all countries where marketed) (1)
Tell your clinician about
- Any history of blood clots, liver disease, or breast cancer.
- Any unexplained vaginal bleeding that has not been diagnosed.
- All other medicines and supplements you take, especially rifampin, certain anticonvulsant medicines (such as phenytoin or carbamazepine), some HIV medicines, or St John's Wort -- these can reduce how well Jadelle prevents pregnancy.
- Your body weight, since evidence reviewed by New Zealand's regulator suggests efficacy may decline somewhat with higher body weight over the full 5-year period.
- Pregnancy plans or breastfeeding.
How to take levonorgestrel (subdermal implant)
- Jadelle is inserted by a clinician trained in the specific technique, typically within the first 7 days after the start of your period, into the inner upper arm.
- The implant provides continuous contraception for up to 5 years; your clinician will advise you on your specific removal or replacement date.
- If you weigh more than about 60 kg, discuss with your clinician whether removal after 4 years, rather than waiting the full 5 years, may be a reasonable option based on New Zealand regulatory safety review findings.
- Use an additional barrier method (such as condoms) if you are told your current medicines might reduce Jadelle's effectiveness.
Procedures and treatment changes
Tell the treating team before surgery, procedures, or any medicine change. Do not alter treatment without the responsible clinician. (1) (2) (3) (4)
Missed dose
There is no daily dose to miss with an implant. Contact your clinician if you are due for removal or replacement and are unsure of the correct timing, or if you are concerned the implant may no longer be effective (for example, after taking a medicine that can reduce its effectiveness).
Overdose
Overdose in the usual sense does not apply to an implant, since it releases a steady low dose. Contact your clinician if you have concerns about the implant's position, or seek urgent medical attention for any severe symptoms such as significant arm pain, numbness, or signs of infection at the insertion site. (1)
Side effects
Side effects and their urgency vary; report severe, persistent, or concerning symptoms.
Changes in menstrual bleeding pattern -- including irregular bleeding, spotting, prolonged bleeding, or absent periods -- especially in the first year; this is common and expected.
What to notice: Changes in menstrual bleeding pattern -- including irregular bleeding, spotting, prolonged bleeding, or absent periods -- especially in the first year; this is common and expected.
What to do: Discuss persistent or troublesome symptoms with the treating clinician or pharmacist. (1)
Breast tenderness, weight gain, acne or skin blemishes, and vaginal discharge.
What to notice: Breast tenderness, weight gain, acne or skin blemishes, and vaginal discharge.
What to do: Discuss persistent or troublesome symptoms with the treating clinician or pharmacist. (1)
Pain, bruising, or discomfort at the insertion or removal site.
What to notice: Pain, bruising, or discomfort at the insertion or removal site.
What to do: Discuss persistent or troublesome symptoms with the treating clinician or pharmacist. (1)
Serious warnings
Signs of a blood clot (deep vein thrombosis or pulmonary embolism) — emergency
Symptoms: Swelling, pain, or warmth in a leg; sudden shortness of breath; chest pain; or coughing up blood.
Action: Seek emergency medical help immediately. (1)
Signs of infection at the insertion or removal site — urgent
Symptoms: Increasing redness, warmth, swelling, pus, or fever near the implant site.
Action: Contact your clinician promptly for assessment and treatment. (1)
Signs of possible ectopic pregnancy — emergency
Symptoms: Severe lower abdominal or pelvic pain, with or without vaginal bleeding, especially if you think you might be pregnant.
Action: Seek emergency medical help immediately -- there is a higher relative risk of ectopic pregnancy if pregnancy occurs while the implant is in place, and this can be life-threatening. (1)
Arm numbness, tingling, or an implant that feels like it has moved or cannot be felt under the skin — high caution
Symptoms: Numbness, tingling, or inability to feel one or both rods where they were inserted.
Action: Contact your clinician promptly -- rare cases of implant migration have been reported and may need imaging to locate the implant before removal. (1)
Interactions
- Rifampin (an antibiotic) can significantly reduce Jadelle's contraceptive effectiveness. (1)
- Certain anticonvulsant (anti-seizure) medicines, such as phenytoin and carbamazepine, can reduce effectiveness. (1)
- Some HIV medicines and the herbal supplement St John's Wort can also reduce effectiveness by increasing the breakdown of levonorgestrel in the liver. (1)
- If you are prescribed any of these interacting medicines, discuss with your clinician whether you need an additional or alternative contraceptive method. (1)
Pregnancy, breastfeeding, kidney/liver function, age
Pregnancy
Jadelle must not be inserted during pregnancy. If pregnancy is suspected while the implant is in place, contact a clinician promptly -- there is a higher relative risk of ectopic pregnancy in this situation. (1) (2) (3) (4)
Breastfeeding
Progestin-only contraceptives are generally considered compatible with breastfeeding; discuss timing of insertion after delivery with your prescriber. (1) (2) (3) (4)
Children
Not intended for use before the start of menstruation; not studied in this population per the sources reviewed. (1) (2) (3) (4)
Elderly
Not typically used in postmenopausal women; not specifically addressed in the sources reviewed. (1) (2) (3) (4)
Hepatic_impairment
Contraindicated in acute liver disease or liver tumours -- tell your prescriber about any liver problems. (1) (2) (3) (4)
Renal_impairment
Not specifically addressed in the sources reviewed -- tell your prescriber about any kidney problems. (1) (2) (3) (4)
Source_ids
Monitoring
Before starting
- Pregnancy test if there is any possibility of pregnancy
- Review of personal/family history of blood clots, liver disease, and breast cancer
- Review of current medicines for hepatic-enzyme-inducing interactions
- Body weight, given the New Zealand regulatory signal about efficacy duration
During treatment
- Periodic review of bleeding pattern and any concerns.
- Checking the insertion site for signs of infection, migration, or difficulty locating the rods.
- Discussion of replacement or removal timing, including possible earlier removal (around 4 years) for women weighing more than 60 kg.
Storage
Jadelle rods are stored and handled by the clinician/pharmacy before insertion, per the product's specific storage instructions (typically room temperature, protected from excessive heat). Patients do not store the medicine themselves once it is inserted.
Professional information
Clinician-facing context only, sourced from the current FDA-approved US labeling and New Zealand Medsafe sources reviewed; verify against the current full label/data sheet before prescribing.
United States (FDA-approved labeling; not currently commercially marketed)
Indication: Contraception, up to 5 years
Dose summary: Two 75 mg levonorgestrel rods (150 mg total) inserted subdermally in the inner upper arm within 7 days of menses onset; release rate approx. 100 mcg/day at month 1, declining to ~40 mcg/day at 12 months and ~30 mcg/day at 24 months and beyond.
Renal context: Not established in the source reviewed. (1)
New Zealand
Indication: Contraception, up to 5 years (4 years reasonable in women >60 kg per MARC review)
Dose summary: Two 75 mg levonorgestrel rods inserted subdermally; Pharmac-subsidised.
Renal context: Not established in the source reviewed. (3) (4)
Hepatic guidance
Contraindicated in acute liver disease or hepatic tumours; hepatic enzyme induction by other drugs reduces circulating levonorgestrel and contraceptive efficacy.
Overdose note
Not applicable in the conventional sense given continuous low-dose release; clinical concerns instead relate to insertion depth, migration, and correct localisation prior to removal (imaging may be required if rods cannot be palpated). (1)
Frequently asked questions
Is Jadelle available in the US, UK, Europe, Canada, Australia, and New Zealand?
Jadelle holds FDA approval in the United States but has not been commercially marketed/distributed there. It is genuinely approved, marketed, and government-subsidised in New Zealand. Despite thorough research, no evidence of marketing authorisation was found for the United Kingdom, the European Union, Canada, or Australia -- Jadelle is used mainly through international and donor-funded family-planning programmes in more than 60 other countries rather than as a retail product in those 4 markets. (1) (2) (3)
Will irregular bleeding with Jadelle go away?
Changes in bleeding pattern -- including irregular bleeding, spotting, or absent periods -- are common, especially in the first year, and often settle over time. Still, discuss any bleeding changes that concern you with your prescriber. (1)
Does my weight affect how well Jadelle works?
New Zealand's medicines regulator reviewed evidence suggesting contraceptive efficacy may decline somewhat with higher body weight over the full 5-year period. For women weighing more than 60 kg, discussing removal after 4 years rather than waiting the full 5 years is a reasonable option to raise with your prescriber. (4)
What is the mechanism of action of levonorgestrel (subdermal implant)?
Levonorgestrel is a synthetic progestin released continuously from the silicone rods, suppressing the luteinising hormone surge (inhibiting ovulation) and thickening cervical mucus to impede sperm penetration; endometrial changes may also contribute to contraceptive effect. (1)
References
- JADELLE (levonorgestrel implants) for subdermal use -- FDA-approved labeling, NDA 020544s010U.S. Food and Drug Administration (accessdata.fda.gov), approved labeling · United States · dated 2016-01-01 · accessed 2026-07-29 · source 1
- Jadelle US market availability statusWikipedia summary of FDA/manufacturer history, cross-checked against rxlist.com and Federal Register · United States · dated 2026-01-01 · accessed 2026-07-29 · source 2
- Jadelle New Zealand Data Sheet and Consumer Medicine InformationMedsafe (New Zealand regulator) · New Zealand · dated 2025-11-21 · accessed 2026-07-29 · source 3
- Jadelle and the Impact of WeightMedsafe Prescriber Update -- Medicines Adverse Reactions Committee (MARC) · New Zealand · dated 2016-06-01 · accessed 2026-07-29 · source 4
Brand names by country
Single-ingredient levonorgestrel (subdermal implant) names are shown separately by country. Product availability, strengths, and supply rules can change; combination products are not included here.
Priority countries
United States
- My Way1.5 mg · lupin pharmaceuticals,inc.
- PostDay One-Step1.5 mg.5mg, 1.5 mg · rapha pharmaceuticals, inc.
- Julie1.5 mg · julie products inc
- Plan B One-Step1.5 mg · foundation consumer healthcare llc
- My Choice TM1.5 mg · proficient rx lp
- Morning After1.5 mg.5mg · rapha pharmaceuticals, inc.
- Morning After Pill1.5 mg · cadence health inc
- Julie Morning After Pill1.5 mg · julie products inc.
- Option 21.5 mg · l. perrigo company
- Skyla13.5 mg · bayer healthcare pharmaceuticals inc.
Canada
- PLAN B
- MIRENA
- NEXT CHOICE
- OPTION
- JAYDESS
- CONTINGENCY ONE
- BACKUP PLAN ONESTEP
- KYLEENA