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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 APROTININ\CALCIUM\FIBRINOGEN HUMAN\HUMAN THROMBIN Cause Hypersensitivity? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Hypersensitivity have been filed in association with APROTININ\CALCIUM\FIBRINOGEN HUMAN\HUMAN THROMBIN. This represents 75.0% of all adverse event reports for APROTININ\CALCIUM\FIBRINOGEN HUMAN\HUMAN THROMBIN.

9
Reports of Hypersensitivity with APROTININ\CALCIUM\FIBRINOGEN HUMAN\HUMAN THROMBIN
75.0%
of all APROTININ\CALCIUM\FIBRINOGEN HUMAN\HUMAN THROMBIN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Hypersensitivity From APROTININ\CALCIUM\FIBRINOGEN HUMAN\HUMAN THROMBIN?

Of the 9 reports, and 9 (100.0%) were considered life-threatening.

Is Hypersensitivity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for APROTININ\CALCIUM\FIBRINOGEN HUMAN\HUMAN THROMBIN. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does APROTININ\CALCIUM\FIBRINOGEN HUMAN\HUMAN THROMBIN Cause?

Anaphylactic reaction (11) Haemothorax (11) Shock haemorrhagic (11) Adverse reaction (9) Anaphylactic shock (9) Angiopathy (9) Back pain (9) Blood pressure increased (9) Emphysema (9) Epistaxis (9)

What Other Drugs Cause Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Related Pages

APROTININ\CALCIUM\FIBRINOGEN HUMAN\HUMAN THROMBIN Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity APROTININ\CALCIUM\FIBRINOGEN HUMAN\HUMAN THROMBIN Demographics