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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 KARDEGIC 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 KARDEGIC. This represents 4.0% of all adverse event reports for KARDEGIC.

6
Reports of Subdural haematoma with KARDEGIC
4.0%
of all KARDEGIC reports
3
Deaths
4
Hospitalizations

How Dangerous Is Subdural haematoma From KARDEGIC?

Of the 6 reports, 3 (50.0%) resulted in death, 4 (66.7%) required hospitalization, and 2 (33.3%) 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 KARDEGIC. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does KARDEGIC Cause?

Anaemia (18) Haematoma (16) Melaena (9) Drug interaction (7) International normalised ratio increased (7) Diarrhoea (6) Fall (6) Gastrointestinal haemorrhage (6) Interstitial lung disease (6) Pancreatitis acute (6)

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 KARDEGIC Alternatives Have Lower Subdural haematoma Risk?

KARDEGIC vs KEPPRA KARDEGIC vs KETAMINE KARDEGIC vs KETOCONAZOLE KARDEGIC vs KETOPROFEN KARDEGIC vs KETOPROFEN LYSINE

Related Pages

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