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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 ELIQUIS Cause Subdural haematoma? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Subdural haematoma have been filed in association with ELIQUIS. This represents 0.6% of all adverse event reports for ELIQUIS.

8
Reports of Subdural haematoma with ELIQUIS
0.6%
of all ELIQUIS reports
1
Deaths
5
Hospitalizations

How Dangerous Is Subdural haematoma From ELIQUIS?

Of the 8 reports, 1 (12.5%) resulted in death, 5 (62.5%) required hospitalization, and 1 (12.5%) were considered life-threatening.

Is Subdural haematoma Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ELIQUIS. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does ELIQUIS Cause?

Haemorrhage (79) Gastrointestinal haemorrhage (72) Dizziness (65) Rash (51) Epistaxis (49) Headache (49) Dyspnoea (41) Adverse event (40) Diarrhoea (37) Contusion (34)

What Other Drugs Cause Subdural haematoma?

RIVAROXABAN (1,423) ASPIRIN (1,181) APIXABAN (1,025) WARFARIN (1,012) CLOPIDOGREL BISULFATE (809) DABIGATRAN ETEXILATE (648) IBRUTINIB (342) HEPARIN (201) ENOXAPARIN (156) CYCLOPHOSPHAMIDE (146)

Which ELIQUIS Alternatives Have Lower Subdural haematoma Risk?

ELIQUIS vs ELOSULFASE ALFA ELIQUIS vs ELOTUZUMAB ELIQUIS vs ELOXATIN ELIQUIS vs ELRANATAMAB ELIQUIS vs ELRANATAMAB-BCMM

Related Pages

ELIQUIS Full Profile All Subdural haematoma Reports All Drugs Causing Subdural haematoma ELIQUIS Demographics