Does INSULIN HUMAN Cause Product dose omission issue? 345 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 345 reports of Product dose omission issue have been filed in association with INSULIN HUMAN (Humulin N). This represents 1.3% of all adverse event reports for INSULIN HUMAN.
345
Reports of Product dose omission issue with INSULIN HUMAN
1.3%
of all INSULIN HUMAN reports
1
Deaths
72
Hospitalizations
How Dangerous Is Product dose omission issue From INSULIN HUMAN?
Of the 345 reports, 1 (0.3%) resulted in death, 72 (20.9%) required hospitalization, and 2 (0.6%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN HUMAN. However, 345 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 Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which INSULIN HUMAN Alternatives Have Lower Product dose omission 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