Does INSULIN LISPRO Cause Wrong patient received product? 334 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 334 reports of Wrong patient received product have been filed in association with INSULIN LISPRO (Humalog KwikPen). This represents 0.4% of all adverse event reports for INSULIN LISPRO.
334
Reports of Wrong patient received product with INSULIN LISPRO
0.4%
of all INSULIN LISPRO reports
1
Deaths
20
Hospitalizations
How Dangerous Is Wrong patient received product From INSULIN LISPRO?
Of the 334 reports, 1 (0.3%) resulted in death, 20 (6.0%) required hospitalization, and 2 (0.6%) were considered life-threatening.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INSULIN LISPRO. However, 334 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 Wrong patient received product?
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
LAMOTRIGINE (112)
Which INSULIN LISPRO Alternatives Have Lower Wrong patient received product 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