Does CEFUROXIME Cause Product quality issue? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product quality issue have been filed in association with CEFUROXIME (Cefuroxime sodium). This represents 0.2% of all adverse event reports for CEFUROXIME.
12
Reports of Product quality issue with CEFUROXIME
0.2%
of all CEFUROXIME reports
1
Deaths
2
Hospitalizations
How Dangerous Is Product quality issue From CEFUROXIME?
Of the 12 reports, 1 (8.3%) resulted in death, 2 (16.7%) required hospitalization, and 3 (25.0%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CEFUROXIME. However, 12 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which CEFUROXIME Alternatives Have Lower Product quality issue Risk?
CEFUROXIME vs CEFUROXIME AXETIL
CEFUROXIME vs CELEBREX
CEFUROXIME vs CELECOXIB
CEFUROXIME vs CELIPROLOL
CEFUROXIME vs CELLCEPT