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The NSCLCs account for 80% of all lung cancers and can be further subdivided into squamous-cell carcinoma, large-cell carcinoma and adenocarcinoma (which includes bronchioloalveolar-cell carcinoma [BAC] Pharmacologic management of asthma aims to control symptoms, prevent exacerbations and provide the best possible pulmonary function with minimal medications, side effects and risk factors. Insomnia, hormones released in the body are involved in certain aspects of homeostasis, including regulating the circadian rhythms established by the SCN of the hypothalamus. Gastrointestinal stromal tumours (GISTs) are the most common mesenchymal tumours of the gastrointestinal (GI) tract.
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Medicine information : FEMOSTON
 
Drug class description :  Oestrogens / progestogens.
Generic Name :  Estradiol [oestradiol], dydrogesterone
Presentation :  Femoston 1/10: Estradiol 1 mg (14 white tablets); estradiol 1 mg , dydrogesterone 10 mg (14 grey tablets). Femoston 2/10: Estradiol 2 mg (14 orange tablets); estradiol 2 mg , dydrogesterone 10 mg (14 yellow tablets). Femoston 2/20: Estradiol 2 mg (14 orange tablets); estradiol 2 mg , dydrogesterone 20 mg (14 blue tablets).
Indications :  Femoston 1/10: Relief of menopausal symptoms in women with a uterus. Femoston 2/10, Femoston 2/20: Relief of menopausal symptoms. Prevention of osteoporosis.
Adult Dosage :  Femoston 1/10: Initially 1 Femoston 1/10 daily without break starting with white tablets. Start by fifth day of menstruation if present or at any time if not. If control of symptoms is not achieved, change to Femoston 2/10. Should rare breakthrough bleeding or inadequate progestational response occur, change to Femoston 2/20. Femoston 2/10, Femoston 2/20: 1 Femoston 2/10 daily without break starting with orange tabs. Start by fifth day of menstruation if present or at any time if not. Should rare breakthrough bleeding or inadequate progestational response occur, change to Femoston 2/20.
Child Dosage :  Not applicable.
Contra Indications :  Cancer of breast, genital tract or other oestrogen-dependent bleeding. Active deep vein thrombosis, thromboembolic disorders or a history of confirmed venous thromboembolism. Acute or chronic liver disease. Dubin-Johnson or Rotor syndromes. Pregnancy, lactation. Cerebral vascular accident.
Special Precautions :  A thorough examination is required before commencing therapy and at regular intervals thereafter. In cases of continuing abnormal and/or irregular bleeding, a diagnostic endometrial biopsy should be performed. Women of child bearing potential should use non-hormonal contraceptive methods. HRT is associated with an increased risk of venous thromboembolism (VTE). If risk factors present (personal or family history, severe obesity), weigh benefits against risks. An increased risk of being diagnosed with breast cancer has been reported with HRT. Monitor patients with epilepsy, migraine, diabetes, cardiac failure, multiple sclerosis, hypertension, porphyria, haemoglobinopathies, otosclerosis, a history of liver disease, uterine fibroids or history of endometriosis.
Interactions :  Liver enzyme inducing drugs.
Adverse Reactions :  Nausea, breast tenderness, abdominal pain, dysmenorrhoea, bloating, oedema, nausea, skin reactions, haemoglobinopathies, headache, dizziness. REASONS FOR IMMEDIATE DISCONTINUATION OF TREATMENT: Occurence of migraine-type headaches for the first time, frequent severe headaches, acute visual disturbances, signs of thrombophlebitis or thromboembolism, or any other possible prodromal symptoms of vascular occlusion. Rise in blood pressure. Jaundice. Pregnancy. Discontinue four weeks before major elective surgery and during immobilisation entailing risk of thrombosis.
Manufacturer :  Solvay
Drug Availability :  (POM)
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