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Explore guides and other downloadable resources that offer additional information about PAXLOVID for you and your patients.
Materials may be downloaded for sharing with patients but should NOT be shown directly to patients on this website. Access to this website is intended for Republic of Ireland healthcare professionals only.
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▼ This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions. See section 4.8 of the SmPC for how to report adverse reactions.
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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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PP-UNP-IRL-0784. June 2024