Lutera Side Effects
Generic name: ethinyl estradiol / levonorgestrel
Medically reviewed by Drugs.com. Last updated on Mar 1, 2025.
Note: This document contains side effect information about ethinyl estradiol / levonorgestrel. Some dosage forms listed on this page may not apply to the brand name Lutera.
For healthcare professionals
Applies to ethinyl estradiol / levonorgestrel: oral tablet, oral tablet chewable, transdermal film.
General adverse events
The most frequently reported side effects were headache, heavy/irregular vaginal bleeding, nausea/vomiting, acne, dysmenorrhea, weight increased, mood changed, anxiety/panic attack, breast pain, and migraines.[Ref]
Genitourinary
- Very common (10% or more): Irregular/heavy uterine bleeding (up to 17%), menorrhagia (up to 11.6%), breast pain (up to 11.2%), dysmenorrhea (up to 11%), breakthrough bleeding/spotting
- Common (1% to 10%): Breast tenderness/discomfort, vaginitis, candidiasis, breast enlargement, breast secretion, breast tension, intermenstrual bleeding/metrorrhagia
- Uncommon (0.1% to 1%): Breast enlargement, breast hypertrophy, menstrual flow changed
- Rare (less than 0.1%): Breast discharge, vaginal discharge, amenorrhea
- Frequency not reported: Uterine myoma, temporary infertility, cervical erosion changed, cervical secretion changed, diminution in lactation
- Postmarketing reports: Menstrual flow reduced, withdrawal bleeding missed, post pill amenorrhea[Ref]
Cardiovascular
- Uncommon (0.1% to 1%): Blood pressure increased
- Rare (less than 0.1%): Venous thromboembolism, arterial thromboembolism
- Frequency not reported: Deep vein thrombosis, hypertension, myocardial infarction, varicose veins exacerbated, thrombophlebitis, cerebral vascular disease, mitral valve prolapse
- Postmarketing reports: Thrombosis[Ref]
Nervous system
- Very common (10% or more): Headache (up to 33%)
- Common (1% to 10%): Migraine, dizziness
- Very rare (less than 0.01%): Chorea exacerbated
- Frequency not reported: Loss of consciousness, epilepsy, Sydenham's chorea, transient ischemic attack, ischemic stroke, hemorrhagic stroke, stroke, cerebral hemorrhage, cerebral thrombosis[Ref]
Local
- Common (1% to 10%): Application site disorder (transdermal system)
Gastrointestinal
- Very common (10% or more): Nausea/vomiting (up to 11%)
- Common (1% to 10%): Abdominal pain/cramps, diarrhea
- Very rare (less than 0.01%): Pancreatitis
- Frequency not reported: Crohn's disease, ulcerative colitis, bloating, mesenteric thrombosis
- Postmarketing reports: Abdominal distention[Ref]
Oncologic
- Rare (less than 0.1%): Benign liver tumor, malignant liver tumor, breast cancer[Ref]
Hepatic
- Rare (less than 0.1%): Cholestatic jaundice
- Very rare (less than 0.01%): Gallbladder disease, gallbladder disease exacerbated
- Frequency not reported: Cholecystitis, cholelithiasis, Budd-Chiari syndrome
- Postmarketing reports: Liver function disturbance[Ref]
Hematologic
- Frequency not reported: Hemolytic uremic syndrome[Ref]
Psychiatric
- Common (1% to 10%): Mood changed, mood swings/alteration/affect lability, depression, anxiety/panic attack, nervousness, libido decreased, libido increased, depression
- Frequency not reported: Major depressive disorder, suicide attempt, depressed mood, crying, major depression, affective disorder, depression suicidal, dysthymic disorder
- Postmarketing reports: Insomnia[Ref]
Immunologic
- Rare (less than 0.1%): Hypersensitivity reaction, anaphylactic/anaphylactoid reaction
- Very rare (less than 0.01%): Systemic lupus erythematosus exacerbated[Ref]
Ocular
- Rare (less than 0.1%): Contact lens intolerance
- Very rare (less than 0.01%): Retinal vein thrombosis
- Frequency not reported: Cataract, corneal curvature changed/steepening
- Postmarketing reports: Optic neuritis[Ref]
Metabolic
- Common (1% to 10%): Appetite increased, fluid retention/edema
- Uncommon (0.1% to 1%): Appetite decreased, serum lipid levels changed, hypertriglyceridemia
- Rare (less than 0.1%): Glucose tolerance changed
- Frequency not reported: Tolerance to carbohydrates reduced[Ref]
Dermatologic
- Common (1% to 10%): Acne
- Uncommon (0.1% to 1%): Urticaria, rash, chloasma
- Rare (less than 0.1%): Erythema nodosum, erythema multiforme, hereditary angioedema exacerbated
- Frequency not reported: Herpes gestationis, hirsutism, alopecia, melasma
- Postmarketing reports: Alopecia, itching, angioedema[Ref]
Other
- Common (1% to 10%): Weight gain, weight changed, flu syndrome
- Rare (less than 0.1%): Weight decreased
- Very rare (less than 0.01%): Porphyria exacerbated
- Frequency not reported: Ectopic pregnancy, spontaneous abortion, porphyria, congenital anomaly, cystitis-like syndrome
- Postmarketing reports: Chest pain, fatigue, malaise, edema peripheral, pain, serum folate decreased[Ref]
Musculoskeletal
- Common (1% to 10%): Back pain
- Frequency not reported: Systemic lupus erythematosus
- Postmarketing reports: Muscle spasm, pain in extremity[Ref]
Renal
- Frequency not reported: Pulmonary embolism
- Postmarketing reports: Pulmonary thrombosis[Ref]
See also:
References
1. (2001) "Product Information. Triphasil (ethinyl estradiol-levonorgestrel)." Wyeth-Ayerst Laboratories
2. Cerner Multum, Inc. "UK Summary of Product Characteristics."
3. Cerner Multum, Inc. "Australian Product Information."
4. (2017) "Product Information. Alesse-28 (ethinyl estradiol-levonorgestrel)." Wyeth-Ayerst Canada Inc
5. (2017) "Product Information. Quartette (91 Day) (ethinyl estradiol-levonorgestrel)." Teva Pharmaceuticals USA
6. (2017) "Product Information. LoSeasonique (ethinyl estradiol-levonorgestrel)." Teva Pharmaceuticals USA
7. (2017) "Product Information. Seasonale (ethinyl estradiol-levonorgestrel)." Barr Pharmaceuticals Inc
8. (2017) "Product Information. Seasonique (ethinyl estradiol-levonorgestrel)." Teva Pharmaceuticals USA
9. (2021) "Product Information. Twirla (ethinyl estradiol-levonorgestrel)." Agile Therapeutics, Inc.
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Further information
Lutera side effects can vary depending on the individual. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Note: Medication side effects may be underreported. If you are experiencing side effects that are not listed, submit a report to the FDA by following this guide.