Ethinyl oestradiol (Estrogens ( ** ) @ - (FDC- List )
Drug Name:Ethinyl oestradiol (Estrogens ( ** ) @ - (FDC- List )
List Of Brands:
Indication Type Description:
Drug Interaction
Indication
Adverse Reaction
Contra-Indications
Dosages/ Overdosage Etc
Patient Information
Pharmacology/ Pharmacokinetics
Drug Interaction:
Indication:
Female hypogonadism, Breast Cancer
Adverse Reaction:
Prolonged and continous use predisposes to endometrial hyperplasia and malinancy.
Thrombosis, hypertension, liver tumors. Ca breast.
Nausea, vomiting, disturbance of menstrual
cycle,fluid retension, discomfort in breast,
weight gain, increased appetite, increased tendency for vaginal candidiasis,
mental depression, alteration in libido,
rashes, alopecia, hirsutism,gynaecomastia and impotence.
Contra-Indications:
Uterine,liver & mammary carcinoma,thromboembolic disorders. Pregnancy, undiagnosed
vaginal bleeding.
Special precautions:
H/O cholestatic jaundice,impaired liver function CVS disease.
Dosages/ Overdosage Etc:
Female hypogonadism, Breast Cancer
Dosage:
Usual dosage range is 0.02 to 1.5mg/day. The effective dose may be as low as 0.02mg
every other day.
Patient Information:
1. Patient information is available with products
2. Diabetic patients- Notify physician if any of the following occur. Pain in the groin or calves of the leg, sharp chest pain,or sudden shortness of breath, abnormal vaginal bleeding, missed menstrual period or suspected pregnancy lumps in the breast, sudden severe headache, dizziness or fainting, vision or speech disturbance,weakness or numbness in the arm or leg, severe abdominal pain, yellowing of the skin or eyes, severe depression
3. May cause photosensitivity (sensitivity to sunlight). Avoid prolonged exposure to the sun and other ultraviolet light.
Use sunscreens and wear protective clothing until tolerance is determined
Pharmacology/ Pharmacokinetics:
Pharmacology:
Although six different natural estrogens have been isolated from the human female, only three are present insignificant quantities - Estradiol, estrone, and estriol. The most potent secretory product of the ovary, estradiol is rapidly oxidised to estrone. Hydration of estrone produces the much weaker estriol. The estrogenic potency of estradiol is 12 times
estrones and 80 times estriols
Pharmacokinetics:
Absorptrion of most natural estrogens and their derivatives from the GI tract is complete. The limited oral effectiveness of natural estrogens and their esters is due to their metabolism. About 80% of estradiol is bound to sex hormone binding globulin, most of the rest is loosely bound to albumin and about 2% is unbound. Estrone is highly bound to protein as it circulates in the blood primarily as a conjugate with sulfate.