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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 ENCORAFENIB Cause Subdural haematoma? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Subdural haematoma have been filed in association with ENCORAFENIB (BRAFTOVI). This represents 0.1% of all adverse event reports for ENCORAFENIB.

6
Reports of Subdural haematoma with ENCORAFENIB
0.1%
of all ENCORAFENIB reports
1
Deaths
6
Hospitalizations

How Dangerous Is Subdural haematoma From ENCORAFENIB?

Of the 6 reports, 1 (16.7%) resulted in death, 6 (100.0%) required hospitalization, and 1 (16.7%) 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 ENCORAFENIB. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does ENCORAFENIB Cause?

Death (1,004) Off label use (989) Nausea (758) Fatigue (685) Diarrhoea (574) Neoplasm progression (548) Pyrexia (539) Product use in unapproved indication (506) Vomiting (429) Rash (414)

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 ENCORAFENIB Alternatives Have Lower Subdural haematoma Risk?

ENCORAFENIB vs ENDOXAN ENCORAFENIB vs ENDOXAN BAXTER ENCORAFENIB vs ENDOXAN INJ ENCORAFENIB vs ENDOXAN , POUDRE POUR ENCORAFENIB vs ENFORTUMAB VEDOTIN

Related Pages

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