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At Fresenius Kabi, we welcome your questions, comments and requests.

To report any adverse event (also known as side effects) that might be related to a Fresenius Kabi pharmaceutical product or medical device, please contact us by using below offered contact details. These requests will be processed immediately.

Company Related ​Inquiries:

Tel: +353 1 8413030
Unit 3B Fingal Bay Business Park Balbriggan, Co.Dublin, Ireland

Adverse E​vents:​

Adverse events must be reported.

Reporting forms and information can be found at:
https://yellowcard.mhra.gov.uk/ (for UK residents)

http://www.hpra.ie/homepage/medicines/safety-information/reporting-suspected-side-effects (for residents of the Republic of Ireland)

Adverse events should also be reported to Fresenius Kabi Ltd.
Phone: +44 (0)1928 533612 (please use only for reporting adverse events)
E-mail: pharmacovigilance.gb@fresenius-kabi.com

▼ This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. You can help by reporting any side effects you may get. If you experience any side effects, talk to your doctor, pharmacist or nurse. This includes any side effects not listed in the package leaflet. You can also report side effects directly via the Yellow Card Scheme at www.mhra.gov.uk/yellowcard (for UK residents) or see http://www.hpra.ie/homepage/medicines/safety-information/reporting-suspected-side-effects (for residents of the Republic of Ireland). By reporting side effects, you can help provide more information on the safety of this medicine.

  • KabiCare has been developed and funded by Fresenius Kabi Ltd. IDACIO is a registered trademark of Fresenius Kabi Ltd.

019/KABICARE/FKUK-IRL April 2020 

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For general product information about IDACIO (adalimumab) for members of the public, please refer to the Patient Information Leaflet and the Summary of Product Characteristics(SmPC).

If you have any questions, please consult your healthcare professional team.

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