Tarina Fe 1/20 Side Effects: Common, Severe, Long Term

Generic name: ethinyl estradiol / norethindrone

Medically reviewed by Drugs.com. Last updated on Mar 31, 2024.

Note: This document provides detailed information about Tarina Fe 1/20 Side Effects associated with ethinyl estradiol / norethindrone. Some dosage forms listed on this page may not apply specifically to the brand name Tarina Fe 1/20.

Applies to ethinyl estradiol / norethindrone: oral capsule liquid filled, oral tablet, oral tablet chewable.

Other dosage forms:

• oral tablet, oral tablet chewable

Serious side effects of Tarina Fe 1/20

Along with its needed effects, ethinyl estradiol/norethindrone may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.

Check with your doctor immediately if any of the following side effects occur while taking ethinyl estradiol/norethindrone:

Other side effects of Tarina Fe 1/20

Some side effects of ethinyl estradiol / norethindrone may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.

Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:

For healthcare professionals

Applies to ethinyl estradiol / norethindrone: oral capsule, oral tablet, oral tablet chewable, oral tablet disintegrating.

General adverse events

The most frequently reported side effects were headache, vaginal candidiasis, nausea, menstrual cramps, breast tenderness, abdominal pain, mood changes, bacterial vaginitis, acne, irregular uterine bleeding, and weight gain.^[Ref]

Genitourinary

• Common (1% to 10%): Vaginal candidiasis, menstrual cramps, breast tenderness, bacterial vaginitis, abnormal/irregular bleeding, metrorrhagia, irregular menstruation, menorrhagia, vaginal hemorrhage, breast pain, dysmenorrhea, vaginal hemorrhage, dysfunctional uterine bleeding
• Frequency not reported: Ovarian vein thrombosis, vaginitis, amenorrhea, breakthrough bleeding, breast enlargement, breast secretion, cervical erosion changed, cervical secretion, menstrual flow changed, diminution in lactation, spotting, temporary infertility after discontinuation of treatment, premenstrual syndrome, uterine fibroid disease exacerbated
• Postmarketing reports: Vaginal infection, pollakiuria, dysuria, ovarian cyst, pelvic pain, ovarian cyst rupture, pelvic fluid collection, nipple pain, nipple discharge, galactorrhea, fibrocystic breast change, breast disorder, breast mass, uterine leiomyomata size increased, cervical ectropion changed, endometrial hyperplasia, ovarian cyst, uterine enlargement^[Ref]

Cardiovascular

• Uncommon (0.1% to 1%): Blood pressure increased
• Frequency not reported: Deep vein thrombosis, myocardial infarction, hypertension, arterial thromboembolism, thrombophlebitis
• Postmarketing reports: Coronary artery thrombosis, palpitation, tachycardia, angina pectoris, hot flush, heart rate irregular^[Ref]

Gastrointestinal

• Common (1% to 10%): Nausea/vomiting, abdominal pain
• Frequency not reported: Abdominal cramps, bloating, colitis, dyspepsia, inflammatory bowel disease, Crohn's disease, ulcerative colitis, mesenteric thrombosis
• Postmarketing reports: Constipation, pancreatitis^[Ref]

Nervous system

• Common (1% to 10%): Headache
• Frequency not reported: Migraine, dizziness, cerebral hemorrhage, cerebral thrombosis
• Postmarketing reports: Loss of consciousness, hyperesthesia, paresthesia, hypoesthesia, somnolence, sensory disturbance, transient ischemic attack, ischemic stroke, chorea, epilepsy exacerbated, dementia, hemiparesis^[Ref]

Oncologic

• Frequency not reported: Hepatic adenoma, hepatic carcinoma, benign liver tumor
• Postmarketing reports: Hemangioma of liver, breast cancer, ovarian cancer, endometrial cancer, uterine cancer^[Ref]

Endocrine

• Postmarketing reports: Hypothyroidism, hyperthyroidism^[Ref]

Psychiatric

• Common (1% to 10%): Mood swing, depression, mood changed, anxiety
• Frequency not reported: Nervousness
• Postmarketing reports: Insomnia, suicidal ideation, panic attack, libido changed, homicidal ideation, dissociation, bipolar disorder, mood disturbed, irritability^[Ref]

Dermatologic

• Common (1% to 10%): Acne
• Frequency not reported: Hirsutism, loss of scalp hair, melasma, chloasma, erythema multiforme, erythema nodosum, hemorrhagic eruption, photosensitivity, pruritus
• Postmarketing reports: Alopecia, generalized rash, allergic rash, skin discoloration, urticaria, angioedema, night sweats, angioedema, hirsutism, skin burning sensation, generalized erythema^[Ref]

Hepatic

• Frequency not reported: Liver disease, gallbladder disease, cholestatic jaundice, Budd-Chiari syndrome
• Postmarketing reports: Cholelithiasis, cholecystitis^[Ref]

Hematologic

• Frequency not reported: Hemolytic uremic syndrome
• Postmarketing reports: Anemia^[Ref]

Immunologic

• Postmarketing reports: Hypersensitivity reaction, anaphylactic/anaphylactoid reaction^[Ref]

Ocular

• Frequency not reported: Corneal curvature change/steepening, contact lens intolerance, cataracts, retinal thrombosis
• Postmarketing reports: Vision blurred, vision impaired, corneal thinning, fungal infection, transient blindness^[Ref]

Respiratory

• Frequency not reported: Pulmonary embolism
• Postmarketing reports: Asthma exacerbated, dyspnea^[Ref]

Musculoskeletal

• Frequency not reported: Leg cramp, backache
• Postmarketing reports: Myalgia, arthralgia, back pain^[Ref]

Metabolic

• Common (1% to 10%): Weight fluctuation
• Frequency not reported: Tolerance to carbohydrates reduced
• Postmarketing reports: Appetite increased, appetite decreased, diabetes mellitus, hypoglycemia, hypocalcemia, triglycerides increased, blood glucose abnormal^[Ref]

Other

• Common (1% to 10%): Cervical smear abnormal, weight gain, edema
• Frequency not reported: Fatigue, porphyria, Vitamin B6 deficient
• Postmarketing reports: Weight decreased, peripheral edema, malaise, chest pain^[Ref]

Renal

• Frequency not reported: Renal function impaired
• Postmarketing reports: Cystitis-like syndrome^[Ref]

Further information

Tarina Fe 1/20 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.

Some side effects may not be reported. You may report them to the FDA.

Medical Disclaimer