Does DEVICE Cause Product storage error? 187 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 187 reports of Product storage error have been filed in association with DEVICE. This represents 1.5% of all adverse event reports for DEVICE.
187
Reports of Product storage error with DEVICE
1.5%
of all DEVICE reports
0
Deaths
13
Hospitalizations
How Dangerous Is Product storage error From DEVICE?
Of the 187 reports, 13 (7.0%) required hospitalization, and 1 (0.5%) were considered life-threatening.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 187 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 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 DEVICE Alternatives Have Lower Product storage error Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN