Does DEVICE Cause Intentional product misuse? 148 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 148 reports of Intentional product misuse have been filed in association with DEVICE. This represents 1.2% of all adverse event reports for DEVICE.
148
Reports of Intentional product misuse with DEVICE
1.2%
of all DEVICE reports
1
Deaths
13
Hospitalizations
How Dangerous Is Intentional product misuse From DEVICE?
Of the 148 reports, 1 (0.7%) resulted in death, 13 (8.8%) required hospitalization.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 148 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which DEVICE Alternatives Have Lower Intentional product misuse Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN