Does ANTI-INHIBITOR COAGULANT COMPLEX Cause Product storage error? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product storage error have been filed in association with ANTI-INHIBITOR COAGULANT COMPLEX (FEIBA). This represents 0.8% of all adverse event reports for ANTI-INHIBITOR COAGULANT COMPLEX.
11
Reports of Product storage error with ANTI-INHIBITOR COAGULANT COMPLEX
0.8%
of all ANTI-INHIBITOR COAGULANT COMPLEX reports
8
Deaths
8
Hospitalizations
How Dangerous Is Product storage error From ANTI-INHIBITOR COAGULANT COMPLEX?
Of the 11 reports, 8 (72.7%) resulted in death, 8 (72.7%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANTI-INHIBITOR COAGULANT COMPLEX. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does ANTI-INHIBITOR COAGULANT COMPLEX Cause?
Haemorrhage (380)
Treatment failure (135)
Drug ineffective (129)
Therapy partial responder (104)
Haemarthrosis (92)
Acquired haemophilia (77)
Pre-existing disease (74)
Death (59)
Factor viii inhibition (56)
Anti factor viii antibody positive (49)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which ANTI-INHIBITOR COAGULANT COMPLEX Alternatives Have Lower Product storage error Risk?
ANTI-INHIBITOR COAGULANT COMPLEX vs ANTIHEMOPHILIC FACTOR HUMAN
ANTI-INHIBITOR COAGULANT COMPLEX vs ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT
ANTI-INHIBITOR COAGULANT COMPLEX vs ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT RESIDUES 743-1636 DELETED
ANTI-INHIBITOR COAGULANT COMPLEX vs ANTIHEMOPHILIC FACTOR, PEGYLATED HUMAN SEQUENCE RECOMBINANT
ANTI-INHIBITOR COAGULANT COMPLEX vs ANTIHEMOPHILIC FACTOR PORCINE, B-DOMAIN TRUNCATED RECOMBINANT