Does ANIDULAFUNGIN Cause Condition aggravated? 37 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 37 reports of Condition aggravated have been filed in association with ANIDULAFUNGIN (ERAXIS). This represents 5.3% of all adverse event reports for ANIDULAFUNGIN.
37
Reports of Condition aggravated with ANIDULAFUNGIN
5.3%
of all ANIDULAFUNGIN reports
22
Deaths
11
Hospitalizations
How Dangerous Is Condition aggravated From ANIDULAFUNGIN?
Of the 37 reports, 22 (59.5%) resulted in death, 11 (29.7%) required hospitalization, and 1 (2.7%) 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 ANIDULAFUNGIN. However, 37 reports have been filed with the FAERS database.
What Other Side Effects Does ANIDULAFUNGIN Cause?
Drug ineffective (234)
Multiple organ dysfunction syndrome (108)
Off label use (85)
Candida infection (61)
Death (57)
Neutropenia (53)
Pneumonia (49)
Septic shock (45)
Sepsis (42)
Drug resistance (37)
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 ANIDULAFUNGIN Alternatives Have Lower Condition aggravated Risk?
ANIDULAFUNGIN vs ANIFROLUMAB
ANIDULAFUNGIN vs ANIFROLUMAB-FNIA
ANIDULAFUNGIN vs ANTHOXANTHUM ODORATUM POLLEN\DACTYLIS GLOMERATA POLLEN\LOLIUM PERENNE POLLEN\PHLEUM PRATENSE POLLEN\POA PRATENSIS POLLEN
ANIDULAFUNGIN vs ANTI-INHIBITOR COAGULANT COMPLEX
ANIDULAFUNGIN vs ANTIHEMOPHILIC FACTOR HUMAN