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Adverse event reporting information is available at the bottom of this webpage.

Resources

Prostate Cancer

Decapeptyl® (triptorelin) SR 3 mg, Decapeptyl® (triptorelin) 3-month 11.25 mg and Decapeptyl® (triptorelin) 6-month 22.5 mg therapeutic indications.

Decapeptyl® (triptorelin) SR and Decapeptyl® (triptorelin) 3-month are indicated for:

  • Management of advanced prostatic carcinoma.

Decapeptyl® (triptorelin) 6-month is indicated for:

  • Treatment of locally advanced or metastatic.
  • Hormone-dependent prostate cancer.

Information About Decapeptyl®

Efficacy & Tolerability

Support for Your Patients

Contact your Ipsen representative

To access relevant information about Prostate Cancer, please choose one of the following options:

Adverse events should be reported.
Reporting forms and information can be found at www.hpra.ie or e-mail medsafety@hpra.ie.
The HPRA can also be contacted on +353 16764971. Adverse events should also be reported to Ipsen via email at pharmacovigilance.uk-ie@ipsen.com or phone on +353 1 8098256.

Reporting of side effects:
If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in the package leaflet. You can also report side effects directly to the HPRA. Reporting forms and information can be found at www.hpra.ie or email medsafety@hpra.ie. Adverse events should also be reported to Ipsen via email at pharmacovigilance.uk-ie@ipsen.com or phone on +353 1 8098256. By reporting side effects, you can help provide more information on the safety of this medicine.