Does FACTOR XIII CONCENTRATE Cause Device issue? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Device issue have been filed in association with FACTOR XIII CONCENTRATE. This represents 5.8% of all adverse event reports for FACTOR XIII CONCENTRATE.
9
Reports of Device issue with FACTOR XIII CONCENTRATE
5.8%
of all FACTOR XIII CONCENTRATE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device issue From FACTOR XIII CONCENTRATE?
Of the 9 reports.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FACTOR XIII CONCENTRATE. However, 9 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)
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)
Deep vein thrombosis (5)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which FACTOR XIII CONCENTRATE Alternatives Have Lower Device 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