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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 ACALABRUTINIB Cause Subdural haematoma? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Subdural haematoma have been filed in association with ACALABRUTINIB (CALQUENCE). This represents 0.1% of all adverse event reports for ACALABRUTINIB.

14
Reports of Subdural haematoma with ACALABRUTINIB
0.1%
of all ACALABRUTINIB reports
5
Deaths
6
Hospitalizations

How Dangerous Is Subdural haematoma From ACALABRUTINIB?

Of the 14 reports, 5 (35.7%) resulted in death, 6 (42.9%) required hospitalization, and 4 (28.6%) 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 ACALABRUTINIB. However, 14 reports have been filed with the FAERS database.

What Other Side Effects Does ACALABRUTINIB Cause?

Death (1,857) Fatigue (536) Headache (534) Product dose omission issue (349) Diarrhoea (320) Fall (289) Malignant neoplasm progression (285) Contusion (270) Dyspnoea (259) Pneumonia (244)

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 ACALABRUTINIB Alternatives Have Lower Subdural haematoma Risk?

ACALABRUTINIB vs ACAMPROSATE ACALABRUTINIB vs ACARBOSE ACALABRUTINIB vs ACCUTANE ACALABRUTINIB vs ACEBUTOLOL ACALABRUTINIB vs ACECLOFENAC

Related Pages

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