Does INSULIN HUMAN Cause Suspected product quality issue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Suspected product quality issue have been filed in association with INSULIN HUMAN (Humulin N). This represents 0.0% of all adverse event reports for INSULIN HUMAN.
7
Reports of Suspected product quality issue with INSULIN HUMAN
0.0%
of all INSULIN HUMAN reports
0
Deaths
3
Hospitalizations
How Dangerous Is Suspected product quality issue From INSULIN HUMAN?
Of the 7 reports, 3 (42.9%) required hospitalization, and 1 (14.3%) were considered life-threatening.
Is Suspected product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN HUMAN. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does INSULIN HUMAN Cause?
Blood glucose increased (8,704)
Blood glucose decreased (2,587)
Drug ineffective (2,464)
Incorrect dose administered (1,949)
Visual impairment (1,402)
Hypoglycaemia (1,350)
Wrong technique in product usage process (1,163)
Glycosylated haemoglobin increased (1,008)
Blood glucose abnormal (900)
Maternal exposure during pregnancy (865)
What Other Drugs Cause Suspected product quality issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (64)
LEVOTHYROXINE (37)
HUMAN IMMUNOGLOBULIN G (32)
ESTRADIOL (30)
ONABOTULINUMTOXINA (30)
SODIUM (30)
CLONAZEPAM (29)
AFLIBERCEPT (27)
INSULIN GLARGINE (27)
IOPROMIDE (25)
Which INSULIN HUMAN Alternatives Have Lower Suspected product quality issue Risk?
INSULIN HUMAN vs INSULIN LISPRO
INSULIN HUMAN vs INSULIN LISPRO-AABC
INSULIN HUMAN vs INSULIN NOS
INSULIN HUMAN vs INSULIN PORK\INSULIN PURIFIED PORK
INSULIN HUMAN vs INTERFERON