Does INSULIN GLULISINE Cause Device issue? 58 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 58 reports of Device issue have been filed in association with INSULIN GLULISINE (Apidra). This represents 1.7% of all adverse event reports for INSULIN GLULISINE.
58
Reports of Device issue with INSULIN GLULISINE
1.7%
of all INSULIN GLULISINE reports
0
Deaths
8
Hospitalizations
How Dangerous Is Device issue From INSULIN GLULISINE?
Of the 58 reports, 8 (13.8%) required hospitalization, and 2 (3.4%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN GLULISINE. However, 58 reports have been filed with the FAERS database.
What Other Side Effects Does INSULIN GLULISINE Cause?
Blood glucose increased (736)
Hypoglycaemia (417)
Hyperglycaemia (280)
Drug ineffective (277)
Blood glucose decreased (194)
Blood glucose abnormal (162)
Diabetes mellitus inadequate control (156)
Malaise (147)
Glycosylated haemoglobin increased (140)
Dizziness (138)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which INSULIN GLULISINE Alternatives Have Lower Device issue Risk?
INSULIN GLULISINE vs INSULIN HUMAN
INSULIN GLULISINE vs INSULIN LISPRO
INSULIN GLULISINE vs INSULIN LISPRO-AABC
INSULIN GLULISINE vs INSULIN NOS
INSULIN GLULISINE vs INSULIN PORK\INSULIN PURIFIED PORK