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- ANASOMA 1 FILM-COATED TABLETS 1MG [SIN16621P]
ANASOMA 1 FILM-COATED TABLETS 1MG [SIN16621P]
Active ingredients: ANASOMA 1 FILM-COATED TABLETS 1MG
Product Info
ANASOMA 1 FILM-COATED TABLETS 1MG
[SIN16621P]
Product information
Active Ingredient and Strength | ANASTROZOLE - 1 MG |
Dosage Form | TABLET, FILM COATED |
Manufacturer and Country | EUGIA PHARMA SPECIALITIES LIMITED - INDIA |
Registration Number | SIN16621P |
Licence Holder | APOTHECA MARKETING PTE LTD |
Forensic Classification | PRESCRIPTION ONLY MEDICINES |
Anatomical Therapeutic Chemical (ATC) code | L02BG03 |
Therapeutic indications
Anastrozole is indicated for the:
Treatment of advanced breast cancer in postmenopausal women with hormone receptor positive or hormone receptor unknown locally advanced or metastatic breast cancer. Efficacy has not been demonstrated in oestrogen receptor negative patients unless they had a previous positive clinical response to tamoxifen.
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
The recommended dose of Anastrozole for adults including the elderly is one 1 mg tablet once a day.
Special populations
Paediatric population
Anastrozole is not recommended for use in children and adolescents.
Renal impairment
No dose change is recommended in patients with mild or moderate renal impairment.
Hepatic impairment
No dose change is recommended in patients with mild hepatic disease.
Method of administration
Anastrozole should be taken orally.
CONTRAINDICATIONS
Anastrozole is contraindicated in:
premenopausal women.
pregnant or lactating women.
patients with severe renal impairment (creatinine clearance less than 20ml/min).
patients with moderate or severe hepatic disease.
patients with known hypersensitivity to anastrozole or to any of the excipients as listed under “List of excipients”.
Oestrogen-containing therapies should not be co-administered with Anastrozole as they would negate its pharmacological action.
Concurrent tamoxifen therapy.
