Does DEVICE Cause Blood glucose decreased? 374 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 374 reports of Blood glucose decreased have been filed in association with DEVICE. This represents 2.9% of all adverse event reports for DEVICE.
374
Reports of Blood glucose decreased with DEVICE
2.9%
of all DEVICE reports
1
Deaths
43
Hospitalizations
How Dangerous Is Blood glucose decreased From DEVICE?
Of the 374 reports, 1 (0.3%) resulted in death, 43 (11.5%) required hospitalization, and 4 (1.1%) were considered life-threatening.
Is Blood glucose decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 374 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 Blood glucose decreased?
INSULIN LISPRO (6,439)
INSULIN GLARGINE (4,552)
INSULIN HUMAN (2,587)
DULAGLUTIDE (1,671)
INSULIN ASPART (1,421)
METFORMIN (1,103)
SEMAGLUTIDE (1,009)
INSULIN DEGLUDEC (983)
TIRZEPATIDE (813)
EXENATIDE (809)
Which DEVICE Alternatives Have Lower Blood glucose decreased Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN