Does DEVICE Cause Blood glucose increased? 2,114 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,114 reports of Blood glucose increased have been filed in association with DEVICE. This represents 16.6% of all adverse event reports for DEVICE.
2,114
Reports of Blood glucose increased with DEVICE
16.6%
of all DEVICE reports
5
Deaths
161
Hospitalizations
How Dangerous Is Blood glucose increased From DEVICE?
Of the 2,114 reports, 5 (0.2%) resulted in death, 161 (7.6%) required hospitalization, and 13 (0.6%) were considered life-threatening.
Is Blood glucose increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 2,114 reports have been filed with the FAERS database.
What Other Side Effects Does DEVICE Cause?
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)
Dyspnoea (482)
What Other Drugs Cause Blood glucose increased?
INSULIN LISPRO (31,969)
INSULIN GLARGINE (19,234)
DULAGLUTIDE (9,119)
INSULIN HUMAN (8,704)
INSULIN ASPART (4,743)
METFORMIN (4,038)
EXENATIDE (3,363)
INSULIN DEGLUDEC (2,644)
SEMAGLUTIDE (2,240)
TIRZEPATIDE (2,240)
Which DEVICE Alternatives Have Lower Blood glucose increased Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN