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Powder for suspension for injection, sustained release formulation.
Therapeutic indications
• Treatment of patients with locally advanced, non-metastatic prostate cancer, as an alternative to surgical castration.
• Treatment of metastatic prostate cancer.
• As adjuvant treatment to radiotherapy in patients with high-risk localised or locally advanced prostate cancer.
• As neoadjuvant treatment prior to radiotherapy in patients with high-risk localised or locally advanced prostate cancer.
• As adjuvant treatment to radical prostatectomy in patients with locally advanced prostate cancer at high risk of disease progression.
• Treatment of endometriosis.
• Treatment of uterine fibroids prior to surgery or when surgery is not appropriate.
• As adjuvant treatment in combination with tamoxifen or an aromatase inhibitor, of endocrine responsive early stage breast cancer in women at high risk of recurrence who are confirmed as pre-menopausal after completion of chemotherapy
Features
Nature and contents of container
• A type I, 5 mL capacity glass vial with an elastomer stopper and an aluminium cap containing the powder.
• Type I, 3 mL capacity glass ampoule containing 2 mL of the suspension vehicle.
• Box containing 1 vial and 1 ampoule with 1 syringe and 2 needles.
Special precautions for storage
• Do not store above 25°C. Keep the container in the outer carton.
Shelf life
• The product should be used immediately after reconstitution.
| Presentation | Vial |
| Presentation | Vial |
| Pack size | 1 |
| Presentation | Vial |
