UK: Adverse Event Reporting
Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard.
If you wish to directly notify BPL, Adverse events should be reported to Kedrion Global Pharmacovigilance office by email to farmacovigilanza@kedrion.com or call to: +44 (0) 20 8957 2622 / +44 208 957 2200
BPL Mexico: Adverse Event Reporting / Reportar Eventos Adversos
Envíe informes de efectos secundarios a:
Tel +52 (55) 53350985
BPL GmbH, Germany: Adverse Event Reporting and Medical Enquiries
Nebenwirkdungsmeldungen richten senden Sie bitte an
FAX +49 (0) 2408 956 8072
Tel +49 (0) 2408 146 0245
US: Adverse Event Reporting and Medical Enquiries
To report an adverse event you think may be related to a BPL product, contact us at
855-3KDRION (855-353-7466) or to
For general product or questions about reimbursement, contact us at
844-4BPLUSA (844-427-5872)