Does DEVICE Cause Injection site reaction? 58 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 58 reports of Injection site reaction have been filed in association with DEVICE. This represents 0.5% of all adverse event reports for DEVICE.
58
Reports of Injection site reaction with DEVICE
0.5%
of all DEVICE reports
1
Deaths
7
Hospitalizations
How Dangerous Is Injection site reaction From DEVICE?
Of the 58 reports, 1 (1.7%) resulted in death, 7 (12.1%) required hospitalization, and 1 (1.7%) were considered life-threatening.
Is Injection site reaction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 58 reports have been filed with the FAERS database.
What Other Side Effects Does DEVICE Cause?
Blood glucose increased (2,114)
Device issue (1,417)
Product use issue (1,076)
Intercepted product preparation error (1,033)
Wrong technique in product usage process (935)
Device leakage (795)
Injection site pain (751)
Syringe issue (634)
Product quality issue (567)
Drug ineffective (488)
What Other Drugs Cause Injection site reaction?
ETANERCEPT (9,962)
ADALIMUMAB (4,375)
NALTREXONE (4,360)
DUPILUMAB (4,129)
GLATIRAMER (3,317)
IXEKIZUMAB (1,701)
METHOTREXATE (1,663)
TIRZEPATIDE (1,389)
TOCILIZUMAB (1,343)
CERTOLIZUMAB PEGOL (1,253)
Which DEVICE Alternatives Have Lower Injection site reaction Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN