Description
Contraindications to the use of letrozole
- Endocrine conditions specific to the reproductive period;
- pregnancy;
- lactation (breastfeeding);
- Infancy (efficacy and safety in children has not been established);
- hypersensitivity to the components of the drug.
Caution: the drug should be used in cases of lactase deficiency, lactase intolerance, glucose-galactose malabsorption syndrome. There are no data on the use of letrozole in patients with a CK < 30 ml/min (the ratio of potential risk to expected treatment effect should be carefully considered before prescribing the drug to such patients).
Method of administration
- The drug is taken orally, irrespective of meals.
- The recommended dose of letrozole is 2.5 mg once/day, daily, long-term (for 5 years or until relapse).
- As extended adjuvant therapy, treatment should be continued for 4 years (not more than 5 years).
- Letrozole should be discontinued if there are signs of disease progression.
- In patients with end-stage or metastatic cancer, treatment with letrozole should be continued as long as there is tumour progression.
- No dose adjustment of letrozole 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 require continuous medical supervision.
- Use of letrozole during pregnancy and lactation
Contraindicated use during pregnancy and lactation (breastfeeding).
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