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Indication & Dosage
 
 
Oral
HRT
Adult:  In menopausal women: 10-20 mcg daily in conjunction with a progestogen in women with uterus.
 
Oral
FEMALE HYPOGONADISM
Adult: 10-50 mcg daily in a cyclical regimen.
 
Oral
PALLIATIVE TREATMENT OF BREAST CARCINOMA
Adult: In postmenopausal women: 0.1-1 mg tid.
 
Oral
PALLIATIVE TREATMENT OF PROSTATIC CARCINOMA
Adult: 0.15-3 mg daily.
 
Oral
AS PART OF COMBINED ORAL CONTRACEPTIVE
Adult: As the oestrogenic component of combined oral contraceptive: 20-40 mcg/day.
   
Administration May be taken with or without food.
   
Precautions Asthma; epilepsy; migraine; DM; cardiac or renal dysfunction; hepatic disease; familial defects of lipoprotein metabolism. Increased risk of endometrial cancer in unopposed oestrogen therapy. Increased risk of gallbladder disease in women on postmenopausal oestrogens. Large doses may increase CV risk, BP, risk of thrombophlebitis and pulmonary embolism.
   
Potentially Life-threatening 
Adverse Drug Reactions
Oedema, hypertension; dizziness; headache; thromboembolism; cholestatic jaundice; nausea, vomiting; disturbance of menstrual cycle; fluid retention, discomfort in breast, wt gain/loss; increased appetite, increased tendency for vag candidiasis; mental depression; alteration in libido; rashes; alopoecia, hirsutism; gynaecomastia and impotence.
   
Adverse Drug Reactions Endometrial cancer (prolonged use).
   
Interactions

Antibiotics (ampicillin, tetracycline, sulphonamides and chloramphenicol) can cause intermenstrual bleeding or failure of contraception. Reduced efficacy of antihypertensives or hypoglycaemic drugs.

CYP1A2 and CYP3A4 inducers such as aminoglutethimide, carbamazepine, phenobarbital, and rifampin may decrease the effects of estradiol. May enhance the effects of hydrocortisone and prednisolone when used together. Altered anticoagulant effect when used with dicoumarol.

   
   
 

 

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