Does DEVICE Cause Product dose omission? 170 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 170 reports of Product dose omission have been filed in association with DEVICE. This represents 1.3% of all adverse event reports for DEVICE.
170
Reports of Product dose omission with DEVICE
1.3%
of all DEVICE reports
10
Deaths
43
Hospitalizations
How Dangerous Is Product dose omission From DEVICE?
Of the 170 reports, 10 (5.9%) resulted in death, 43 (25.3%) required hospitalization, and 1 (0.6%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 170 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 dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which DEVICE Alternatives Have Lower Product dose omission Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN