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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 NINTEDANIB Cause Subdural haematoma? 18 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Subdural haematoma have been filed in association with NINTEDANIB. This represents 0.1% of all adverse event reports for NINTEDANIB.

18
Reports of Subdural haematoma with NINTEDANIB
0.1%
of all NINTEDANIB reports
3
Deaths
17
Hospitalizations

How Dangerous Is Subdural haematoma From NINTEDANIB?

Of the 18 reports, 3 (16.7%) resulted in death, 17 (94.4%) required hospitalization, and 1 (5.6%) 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 NINTEDANIB. However, 18 reports have been filed with the FAERS database.

What Other Side Effects Does NINTEDANIB Cause?

Diarrhoea (9,103) Nausea (4,198) Dyspnoea (3,080) Decreased appetite (2,832) Death (2,790) Weight decreased (2,628) Vomiting (2,524) Fatigue (2,511) Cough (2,193) Idiopathic pulmonary fibrosis (1,905)

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 NINTEDANIB Alternatives Have Lower Subdural haematoma Risk?

NINTEDANIB vs NINTEDANIB ESYLATE NINTEDANIB vs NIRAPARIB NINTEDANIB vs NIRMATRELVIR\RITONAVIR NINTEDANIB vs NIROGACESTAT NINTEDANIB vs NIROGACESTAT HYDROBROMIDE

Related Pages

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