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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does CEFIDEROCOL Cause Condition aggravated? 21 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Condition aggravated have been filed in association with CEFIDEROCOL (Fetroja). This represents 3.2% of all adverse event reports for CEFIDEROCOL.

21
Reports of Condition aggravated with CEFIDEROCOL
3.2%
of all CEFIDEROCOL reports
15
Deaths
6
Hospitalizations

How Dangerous Is Condition aggravated From CEFIDEROCOL?

Of the 21 reports, 15 (71.4%) resulted in death, 6 (28.6%) required hospitalization, and 3 (14.3%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CEFIDEROCOL. However, 21 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which CEFIDEROCOL Alternatives Have Lower Condition aggravated Risk?

CEFIDEROCOL vs CEFIXIME CEFIDEROCOL vs CEFMETAZOLE CEFIDEROCOL vs CEFOPERAZONE CEFIDEROCOL vs CEFOPERAZONE\SULBACTAM CEFIDEROCOL vs CEFOTAXIME

Related Pages

CEFIDEROCOL Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated CEFIDEROCOL Demographics