Description
Directions for use and dosage
- Intravenously, irrespective of meals.
- The recommended dose of Letrozole is 2.5 mg once daily, long-term. As prolonged adjuvant therapy, treatment should be continued for 5 years (not longer than 5 years).
- Letrozole should be discontinued if signs of disease progression occur.
- No dose adjustment is required in elderly patients.
- No dose adjustment is required for hepatic or renal impairment (CK ≥10 ml/min). However, in cases of severe hepatic impairment (Child-Pugh class C), patients should be kept under constant observation.
Undesirable effects
- headache, dizziness, weakness, depression, increased fatigue (including weakness and anxiety)
- Nausea, vomiting, indigestion, constipation, diarrhoea, changes in appetite, decreased or increased body weight, hypercholesterolaemia, anorexia, thirst
- peripheral oedema
- leucorrhoea, vaginal bleeding, vaginal bleeding, breast pain
- skin rash (including erythematous and papular macular rash, vesicular rash, psoriasis-like rash), hot flashes, alopecia areata.
- dyspnoea, cough
- superficial and deep vein thrombophlebitis, tachycardia, increased blood pressure, thromboembolism.
- musculoskeletal pain (including shoulder, back, leg and bone pain), joint pain, muscle pain, osteoporosis, bone fractures
- increased sweating, thinning hair
- increased urination, urinary tract infections
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