Does CEFUROXIME AXETIL Cause Incorrect product storage? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Incorrect product storage have been filed in association with CEFUROXIME AXETIL (Cefuroxime axetil). This represents 0.5% of all adverse event reports for CEFUROXIME AXETIL.
13
Reports of Incorrect product storage with CEFUROXIME AXETIL
0.5%
of all CEFUROXIME AXETIL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product storage From CEFUROXIME AXETIL?
Of the 13 reports.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CEFUROXIME AXETIL. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does CEFUROXIME AXETIL Cause?
Drug hypersensitivity (442)
Diarrhoea (328)
Rash (297)
Vomiting (287)
Anxiety (265)
Fatigue (258)
Dizziness (251)
Dyspnoea (244)
Abdominal pain (242)
Pruritus (235)
What Other Drugs Cause Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
Which CEFUROXIME AXETIL Alternatives Have Lower Incorrect product storage Risk?
CEFUROXIME AXETIL vs CELEBREX
CEFUROXIME AXETIL vs CELECOXIB
CEFUROXIME AXETIL vs CELIPROLOL
CEFUROXIME AXETIL vs CELLCEPT
CEFUROXIME AXETIL vs CEMIPLIMAB