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PP-E1A-IRL-0016. Date of Preparation April 2024.

Adverse events should be reported. Report an adverse event to your national reporting system (HPRA Pharmacovigilance)
 

Adverse events should also be reported to Pfizer Medical Information on 1800 633 363

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This site is intended only for healthcare professionals resident in the Republic of Ireland. If you are a member of the public wishing to access information on a specific medicine, please visit https://www.medicines.ie

 

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PP-UNP-IRL-0832. October 2024
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PP-UNP-IRL-0832. October 2024