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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does PRADAXA Cause Adverse event? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Adverse event have been filed in association with PRADAXA. This represents 0.1% of all adverse event reports for PRADAXA.

5
Reports of Adverse event with PRADAXA
0.1%
of all PRADAXA reports
1
Deaths
4
Hospitalizations

How Dangerous Is Adverse event From PRADAXA?

Of the 5 reports, 1 (20.0%) resulted in death, 4 (80.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.

Is Adverse event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PRADAXA. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does PRADAXA Cause?

Gastrointestinal haemorrhage (907) Anaemia (332) Haemorrhage (311) Haemorrhagic anaemia (286) Cerebrovascular accident (218) Coagulopathy (215) Renal failure acute (193) Lower gastrointestinal haemorrhage (135) Fall (127) Cerebral haemorrhage (125)

What Other Drugs Cause Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which PRADAXA Alternatives Have Lower Adverse event Risk?

PRADAXA vs PRALATREXATE PRADAXA vs PRALSETINIB PRADAXA vs PRAMIPEXOLE PRADAXA vs PRAMIPEXOLE\PRAMIPEXOLE PRADAXA vs PRAMLINTIDE

Related Pages

PRADAXA Full Profile All Adverse event Reports All Drugs Causing Adverse event PRADAXA Demographics