Does DEVICE Cause Glycosylated haemoglobin increased? 231 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 231 reports of Glycosylated haemoglobin increased have been filed in association with DEVICE. This represents 1.8% of all adverse event reports for DEVICE.
231
Reports of Glycosylated haemoglobin increased with DEVICE
1.8%
of all DEVICE reports
0
Deaths
26
Hospitalizations
How Dangerous Is Glycosylated haemoglobin increased From DEVICE?
Of the 231 reports, 26 (11.3%) required hospitalization, and 3 (1.3%) were considered life-threatening.
Is Glycosylated haemoglobin increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 231 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 Glycosylated haemoglobin increased?
DULAGLUTIDE (2,691)
INSULIN GLARGINE (2,649)
INSULIN LISPRO (2,482)
METFORMIN (1,539)
INSULIN HUMAN (1,008)
EXENATIDE (921)
SEMAGLUTIDE (818)
EMPAGLIFLOZIN (743)
TIRZEPATIDE (555)
INSULIN ASPART (550)
Which DEVICE Alternatives Have Lower Glycosylated haemoglobin increased Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN