Does INSULIN LISPRO Cause Incorrect product administration duration? 479 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 479 reports of Incorrect product administration duration have been filed in association with INSULIN LISPRO (Humalog KwikPen). This represents 0.6% of all adverse event reports for INSULIN LISPRO.
479
Reports of Incorrect product administration duration with INSULIN LISPRO
0.6%
of all INSULIN LISPRO reports
0
Deaths
59
Hospitalizations
How Dangerous Is Incorrect product administration duration From INSULIN LISPRO?
Of the 479 reports, 59 (12.3%) 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 LISPRO. However, 479 reports have been filed with the FAERS database.
What Other Side Effects Does INSULIN LISPRO Cause?
Blood glucose increased (31,969)
Incorrect dose administered (8,318)
Blood glucose decreased (6,439)
Drug ineffective (5,411)
Visual impairment (4,654)
Underdose (3,156)
Drug dose omission (3,063)
Glycosylated haemoglobin increased (2,482)
Blood glucose abnormal (2,460)
Malaise (2,204)
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)
DICLOFENAC (362)
OMEPRAZOLE (302)
ALENDRONATE (287)
Which INSULIN LISPRO Alternatives Have Lower Incorrect product administration duration Risk?
INSULIN LISPRO vs INSULIN LISPRO-AABC
INSULIN LISPRO vs INSULIN NOS
INSULIN LISPRO vs INSULIN PORK\INSULIN PURIFIED PORK
INSULIN LISPRO vs INTERFERON
INSULIN LISPRO vs INTERFERON ALFA-2A