Anapen^®

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Advice

Reporting suspected adverse reactions after authorisation of the medical
product is important. It allows continued monitoring of the benefit/risk
balance of the medicinal product.

Adverse events should be reported by contacting your Doctor, Pharmacist, or Nurse, or directly via the HPRA website, email address, or telephone number. Additional HPRA information on how to report including forms for ADR submission can be found via the HPRA link below:

W: HPRA Patient Reporting of Side Effects link

E: medsafety@hpra.ie

T: (01) 676 4971

Adverse events and complaints etc can also be sent directly to Bioprojet UK Limited c/o Bioprojet Pharma via the Contact Us Page - For any other
questions, please use the contact us form.

Further Information

If you have a medical or product query and are based in the Republic of Ireland, please call 016869342 (free phone number). For any other questions please use the contact us form

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