Does INSULIN LISPRO Cause Product dose omission issue? 1,492 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,492 reports of Product dose omission issue have been filed in association with INSULIN LISPRO (Humalog KwikPen). This represents 1.9% of all adverse event reports for INSULIN LISPRO.
1,492
Reports of Product dose omission issue with INSULIN LISPRO
1.9%
of all INSULIN LISPRO reports
2
Deaths
157
Hospitalizations
How Dangerous Is Product dose omission issue From INSULIN LISPRO?
Of the 1,492 reports, 2 (0.1%) resulted in death, 157 (10.5%) required hospitalization, and 8 (0.5%) 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 LISPRO. However, 1,492 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 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 LISPRO Alternatives Have Lower Product dose omission issue 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