Does CEFIDEROCOL Cause Incorrect product administration duration? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Incorrect product administration duration have been filed in association with CEFIDEROCOL (Fetroja). This represents 1.2% of all adverse event reports for CEFIDEROCOL.
8
Reports of Incorrect product administration duration with CEFIDEROCOL
1.2%
of all CEFIDEROCOL reports
6
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product administration duration From CEFIDEROCOL?
Of the 8 reports, 6 (75.0%) resulted in death.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CEFIDEROCOL. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does CEFIDEROCOL Cause?
Death (136)
Drug resistance (66)
Treatment failure (63)
Drug ineffective (54)
Off label use (52)
Pneumonia (33)
Septic shock (32)
Acute kidney injury (30)
Multiple organ dysfunction syndrome (30)
Pathogen resistance (30)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which CEFIDEROCOL Alternatives Have Lower Incorrect product administration duration Risk?
CEFIDEROCOL vs CEFIXIME
CEFIDEROCOL vs CEFMETAZOLE
CEFIDEROCOL vs CEFOPERAZONE
CEFIDEROCOL vs CEFOPERAZONE\SULBACTAM
CEFIDEROCOL vs CEFOTAXIME