Does COAGULATION FACTOR IX RECOMBINANT HUMAN Cause Device issue? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Device issue have been filed in association with COAGULATION FACTOR IX RECOMBINANT HUMAN. This represents 4.0% of all adverse event reports for COAGULATION FACTOR IX RECOMBINANT HUMAN.
43
Reports of Device issue with COAGULATION FACTOR IX RECOMBINANT HUMAN
4.0%
of all COAGULATION FACTOR IX RECOMBINANT HUMAN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device issue From COAGULATION FACTOR IX RECOMBINANT HUMAN?
Of the 43 reports.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for COAGULATION FACTOR IX RECOMBINANT HUMAN. However, 43 reports have been filed with the FAERS database.
What Other Side Effects Does COAGULATION FACTOR IX RECOMBINANT HUMAN Cause?
Haemarthrosis (318)
Haemorrhage (261)
No adverse event (97)
Traumatic haemorrhage (62)
Fall (61)
Drug ineffective (60)
Muscle haemorrhage (54)
Arthralgia (52)
Contusion (52)
Product preparation issue (39)
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 COAGULATION FACTOR IX RECOMBINANT HUMAN Alternatives Have Lower Device issue Risk?
COAGULATION FACTOR IX RECOMBINANT HUMAN vs COAGULATION FACTOR IX RECOMBINANT HUMAN\ISOPROPYL ALCOHOL
COAGULATION FACTOR IX RECOMBINANT HUMAN vs COAGULATION FACTOR VIIA RECOMBINANT HUMAN
COAGULATION FACTOR IX RECOMBINANT HUMAN vs COBAMAMIDE
COAGULATION FACTOR IX RECOMBINANT HUMAN vs COBICISTAT
COAGULATION FACTOR IX RECOMBINANT HUMAN vs COBICISTAT\DARUNAVIR ETHANOLATE