Does DEVICE Cause Dermatitis contact? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Dermatitis contact have been filed in association with DEVICE. This represents 0.2% of all adverse event reports for DEVICE.
20
Reports of Dermatitis contact with DEVICE
0.2%
of all DEVICE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Dermatitis contact From DEVICE?
Of the 20 reports, 3 (15.0%) required hospitalization.
Is Dermatitis contact Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 20 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 Dermatitis contact?
TREPROSTINIL (1,834)
DUPILUMAB (358)
HUMAN IMMUNOGLOBULIN G (345)
ADALIMUMAB (321)
EPOPROSTENOL (190)
ETANERCEPT (170)
NICOTINE (163)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (160)
AMBRISENTAN (147)
CHLORHEXIDINE\ISOPROPYL ALCOHOL (146)
Which DEVICE Alternatives Have Lower Dermatitis contact Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN