Does FACTOR XIII CONCENTRATE Cause Hypersensitivity? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Hypersensitivity have been filed in association with FACTOR XIII CONCENTRATE. This represents 3.2% of all adverse event reports for FACTOR XIII CONCENTRATE.
5
Reports of Hypersensitivity with FACTOR XIII CONCENTRATE
3.2%
of all FACTOR XIII CONCENTRATE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Hypersensitivity From FACTOR XIII CONCENTRATE?
Of the 5 reports, 1 (20.0%) required hospitalization, and 3 (60.0%) 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 FACTOR XIII CONCENTRATE. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does FACTOR XIII CONCENTRATE Cause?
Drug ineffective (25)
No adverse event (20)
Haemorrhage (12)
Device issue (9)
Off label use (8)
Product preparation issue (8)
Product use in unapproved indication (8)
Abortion spontaneous (7)
Exposure during pregnancy (7)
Factor xiii inhibition (7)
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)
Which FACTOR XIII CONCENTRATE Alternatives Have Lower Hypersensitivity Risk?
FACTOR XIII CONCENTRATE vs FAM-TRASTUZUMAB DERUXTECAN-NXKI
FACTOR XIII CONCENTRATE vs FAMCICLOVIR
FACTOR XIII CONCENTRATE vs FAMOTIDINE
FACTOR XIII CONCENTRATE vs FAMOTIDINE\IBUPROFEN
FACTOR XIII CONCENTRATE vs FARICIMAB