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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 OSIMERTINIB 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 OSIMERTINIB (TAGRISSO). This represents 0.1% of all adverse event reports for OSIMERTINIB.

14
Reports of Subdural haematoma with OSIMERTINIB
0.1%
of all OSIMERTINIB reports
1
Deaths
8
Hospitalizations

How Dangerous Is Subdural haematoma From OSIMERTINIB?

Of the 14 reports, 1 (7.1%) resulted in death, 8 (57.1%) required hospitalization, and 3 (21.4%) 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 OSIMERTINIB. However, 14 reports have been filed with the FAERS database.

What Other Side Effects Does OSIMERTINIB Cause?

Death (10,423) Malignant neoplasm progression (2,920) Diarrhoea (1,408) Drug resistance (1,026) Fatigue (819) Rash (772) Decreased appetite (706) Drug ineffective (627) Dyspnoea (621) Nausea (610)

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 OSIMERTINIB Alternatives Have Lower Subdural haematoma Risk?

OSIMERTINIB vs OSPEMIFENE OSIMERTINIB vs OSPHENA OSIMERTINIB vs OVINE DIGOXIN IMMUNE FAB OSIMERTINIB vs OXACILLIN OSIMERTINIB vs OXALIPLATIN

Related Pages

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