Does ANTIHEMOPHILIC FACTOR HUMAN Cause Device issue? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Device issue have been filed in association with ANTIHEMOPHILIC FACTOR HUMAN. This represents 4.5% of all adverse event reports for ANTIHEMOPHILIC FACTOR HUMAN.
36
Reports of Device issue with ANTIHEMOPHILIC FACTOR HUMAN
4.5%
of all ANTIHEMOPHILIC FACTOR HUMAN reports
1
Deaths
1
Hospitalizations
How Dangerous Is Device issue From ANTIHEMOPHILIC FACTOR HUMAN?
Of the 36 reports, 1 (2.8%) resulted in death, 1 (2.8%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANTIHEMOPHILIC FACTOR HUMAN. However, 36 reports have been filed with the FAERS database.
What Other Side Effects Does ANTIHEMOPHILIC FACTOR HUMAN Cause?
Haemarthrosis (118)
Haemorrhage (112)
Drug ineffective (69)
No adverse event (64)
Epistaxis (43)
Acquired haemophilia (41)
Arthralgia (40)
Fall (37)
Pre-existing disease (36)
Therapy partial responder (36)
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 ANTIHEMOPHILIC FACTOR HUMAN Alternatives Have Lower Device issue Risk?
ANTIHEMOPHILIC FACTOR HUMAN vs ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT
ANTIHEMOPHILIC FACTOR HUMAN vs ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT RESIDUES 743-1636 DELETED
ANTIHEMOPHILIC FACTOR HUMAN vs ANTIHEMOPHILIC FACTOR, PEGYLATED HUMAN SEQUENCE RECOMBINANT
ANTIHEMOPHILIC FACTOR HUMAN vs ANTIHEMOPHILIC FACTOR PORCINE, B-DOMAIN TRUNCATED RECOMBINANT
ANTIHEMOPHILIC FACTOR HUMAN vs APALUTAMIDE