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*The statement ‘First and only once-daily, oral advanced treatment for Crohn's disease’ is valid as of November 2022.
▼ 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.
REFERENCE
- RINVOQ Summary of Product Characteristics.
[Affiliates to insert local adverse events reporting websites]
ALL-RNQG-220167 Date of preparation: November 2022
Adverse events should also be reported to AbbVie on GBPV@abbvie.com