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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 FIBRINOGEN HUMAN Cause Cerebral infarction? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Cerebral infarction have been filed in association with FIBRINOGEN HUMAN (TachoSil). This represents 1.7% of all adverse event reports for FIBRINOGEN HUMAN.

7
Reports of Cerebral infarction with FIBRINOGEN HUMAN
1.7%
of all FIBRINOGEN HUMAN reports
5
Deaths
4
Hospitalizations

How Dangerous Is Cerebral infarction From FIBRINOGEN HUMAN?

Of the 7 reports, 5 (71.4%) resulted in death, 4 (57.1%) required hospitalization.

Is Cerebral infarction Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for FIBRINOGEN HUMAN. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does FIBRINOGEN HUMAN Cause?

Foetal exposure during pregnancy (40) No adverse event (38) Off label use (38) Drug ineffective (34) Hypotension (31) Foetal anaemia (27) Foetal growth restriction (27) Haemorrhage in pregnancy (26) Anaphylactic shock (25) Maternal exposure during pregnancy (25)

What Other Drugs Cause Cerebral infarction?

RIVAROXABAN (1,367) APIXABAN (937) DABIGATRAN ETEXILATE (713) ASPIRIN (535) EDOXABAN (419) CLOPIDOGREL BISULFATE (315) PEMBROLIZUMAB (295) BEVACIZUMAB (269) METHOTREXATE (265) NIVOLUMAB (262)

Which FIBRINOGEN HUMAN Alternatives Have Lower Cerebral infarction Risk?

FIBRINOGEN HUMAN vs FIBRINOGEN HUMAN\HUMAN THROMBIN FIBRINOGEN HUMAN vs FIBRINOGEN HUMAN\THROMBIN HUMAN FIBRINOGEN HUMAN vs FIDAXOMICIN FIBRINOGEN HUMAN vs FILGOTINIB FIBRINOGEN HUMAN vs FILGRASTIM

Related Pages

FIBRINOGEN HUMAN Full Profile All Cerebral infarction Reports All Drugs Causing Cerebral infarction FIBRINOGEN HUMAN Demographics