Does CEFUROXIME Cause Wrong product administered? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Wrong product administered have been filed in association with CEFUROXIME (Cefuroxime sodium). This represents 0.1% of all adverse event reports for CEFUROXIME.
6
Reports of Wrong product administered with CEFUROXIME
0.1%
of all CEFUROXIME reports
1
Deaths
5
Hospitalizations
How Dangerous Is Wrong product administered From CEFUROXIME?
Of the 6 reports, 1 (16.7%) resulted in death, 5 (83.3%) required hospitalization, and 1 (16.7%) were considered life-threatening.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CEFUROXIME. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does CEFUROXIME Cause?
Dyspnoea (476)
Drug ineffective (386)
Condition aggravated (326)
Anaphylactic reaction (319)
Off label use (319)
Rash (303)
Drug hypersensitivity (287)
Pyrexia (287)
Diarrhoea (259)
Anaphylactic shock (234)
What Other Drugs Cause Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which CEFUROXIME Alternatives Have Lower Wrong product administered Risk?
CEFUROXIME vs CEFUROXIME AXETIL
CEFUROXIME vs CELEBREX
CEFUROXIME vs CELECOXIB
CEFUROXIME vs CELIPROLOL
CEFUROXIME vs CELLCEPT