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Estinyl Side Effects, and Drug Interactions - Ethinyl Estradiol

Estinyl Side Effects, and Drug Interactions - Ethinyl Estradiol

SIDE EFFECTS

(See WARNINGS regarding induction of neoplasia, adverse effects on the fetus, increased incidence of gallbladder disease, the adverse effects similar to those of oral contraceptives, including thromboembolism.) The following additional adverse reactions have been reported with estrogenic therapy, including oral contraceptives:

Genitourinary system: Breakthrough bleeding, spotting, change in menstrual flow: dysmenorrhea; premenstrual-like syndrome; amenorrhea during and after treatment, increase in size of uterine fibromyomata; vaginal candidiasis; change in cervical eversion and in degree of cervical secretion; cystitis-like syndrome.

Breasts: Tenderness, enlargement, secretion.

Gastrointestinal: Nausea, vomiting; abdominal cramps, bloating; cholestatic jaundice.

Skin: Chloasma or melasma which may persist when drug is discontinued; erythema multiforme; erythema nodosum; hemorrhagic eruption; loss of scalp hair; hirsutism.

Eyes: Steepening of corneal curvature; intolerance to contact lenses.

CNS: Headache, migraine, dizziness; mental depression; chorea.

Miscellaneous: Increase or decrease in weight; reduced carbohydrate tolerance; aggravation of porphyria; edema; changes in libido.

DRUG INTERACTIONS

Certain endocrine and liver function tests may be affected by estrogen-containing oral contraceptives. The following similar changes may be expected with larger doses of estrogen:

Increased sulfobromophthalein retention; increased prothrombin and factors VII, VIII, IX, and X; decreased antithrombin 3; increased norepinephrine-induced platel et aggregation; increased thyroid binding globulin (TBG) leading to increased circulating total thyroid hormone, as measured by PBI, T4 by column, or T4 by radioimmunoassay. Free T3 resin uptake is decreased, reflecting the elevated TBG; free T4 concentration is unaltered: impaired glucose tolerance; decreased pregnanediol excretion; reduced response to metyrapone test; reduced serum folate concentration; increased serum triglyceride and phospholipid concentration.

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