Adverse Events
Adverse events should be reported. Reporting forms and information can be found at www.hpra.ie/homepage/about-us/report-an-issue.
Adverse events should also be reported to Boehringer Ingelheim Drug Safety on 1850 946100.
For Republic of Ireland healthcare
professionals only
FOR PREVENTION OF STROKE OR SYSTEMIC EMBOLISM IN ADULT PATIENTS WITH NON-VALVULAR ATRIAL FIBRILLATION,
PLUS ONE OR MORE RISK FACTORS1,2
Stroke prevention in atrial fibrillation
For prevention of stroke or systemic embolism in adult patients with nonvalvular atrial fibrillation, plus one or more risk factors1,2
Adverse events should be reported. Reporting forms and information can be found at www.hpra.ie/homepage/about-us/report-an-issue.
Adverse events should also be reported to Boehringer Ingelheim Drug Safety on 1850 946100.
References: