Does FACTOR XIII CONCENTRATE Cause Product preparation issue? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product preparation issue have been filed in association with FACTOR XIII CONCENTRATE. This represents 5.2% of all adverse event reports for FACTOR XIII CONCENTRATE.
8
Reports of Product preparation issue with FACTOR XIII CONCENTRATE
5.2%
of all FACTOR XIII CONCENTRATE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product preparation issue From FACTOR XIII CONCENTRATE?
Of the 8 reports.
Is Product preparation issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FACTOR XIII CONCENTRATE. However, 8 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 use in unapproved indication (8)
Abortion spontaneous (7)
Exposure during pregnancy (7)
Factor xiii inhibition (7)
Deep vein thrombosis (5)
What Other Drugs Cause Product preparation issue?
ONABOTULINUMTOXINA (677)
COAGULATION FACTOR IX HUMAN\COAGULATION FACTOR VII HUMAN\COAGULATION FACTOR X HUMAN\PROTEIN C\PROTEIN S HUMAN\PROTHROMBIN (252)
HUMAN C1-ESTERASE INHIBITOR (238)
SOMATROPIN (200)
INCOBOTULINUMTOXINA (174)
STIRIPENTOL (129)
TESAMORELIN (119)
ABATACEPT (115)
INFLIXIMAB (101)
ABOBOTULINUMTOXINA (91)
Which FACTOR XIII CONCENTRATE Alternatives Have Lower Product preparation issue 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