Does INSULIN HUMAN Cause Incorrect product administration duration? 157 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 157 reports of Incorrect product administration duration have been filed in association with INSULIN HUMAN (Humulin N). This represents 0.6% of all adverse event reports for INSULIN HUMAN.
157
Reports of Incorrect product administration duration with INSULIN HUMAN
0.6%
of all INSULIN HUMAN reports
0
Deaths
20
Hospitalizations
How Dangerous Is Incorrect product administration duration From INSULIN HUMAN?
Of the 157 reports, 20 (12.7%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN HUMAN. However, 157 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which INSULIN HUMAN Alternatives Have Lower Incorrect product administration duration 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