Does CEFUROXIME Cause Product complaint? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Product complaint have been filed in association with CEFUROXIME (Cefuroxime sodium). This represents 0.3% of all adverse event reports for CEFUROXIME.
16
Reports of Product complaint with CEFUROXIME
0.3%
of all CEFUROXIME reports
0
Deaths
12
Hospitalizations
How Dangerous Is Product complaint From CEFUROXIME?
Of the 16 reports, 12 (75.0%) required hospitalization, and 2 (12.5%) were considered life-threatening.
Is Product complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CEFUROXIME. However, 16 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 Product complaint?
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417)
ALBUTEROL (2,291)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826)
FLUTICASONE\SALMETEROL (1,601)
MEPOLIZUMAB (1,296)
FLUTICASONE (1,112)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108)
BELIMUMAB (1,079)
SUMATRIPTAN (718)
NICOTINE (700)
Which CEFUROXIME Alternatives Have Lower Product complaint Risk?
CEFUROXIME vs CEFUROXIME AXETIL
CEFUROXIME vs CELEBREX
CEFUROXIME vs CELECOXIB
CEFUROXIME vs CELIPROLOL
CEFUROXIME vs CELLCEPT