Does COLISTIMETHATE Cause Product dose omission? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product dose omission have been filed in association with COLISTIMETHATE (Colistimethate). This represents 0.7% of all adverse event reports for COLISTIMETHATE.
6
Reports of Product dose omission with COLISTIMETHATE
0.7%
of all COLISTIMETHATE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product dose omission From COLISTIMETHATE?
Of the 6 reports, 5 (83.3%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for COLISTIMETHATE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does COLISTIMETHATE Cause?
Off label use (96)
Acute kidney injury (91)
Condition aggravated (68)
Drug ineffective (48)
Septic shock (40)
Rash maculo-papular (37)
Death (36)
Eosinophilia (35)
Thrombocytopenia (34)
Leukocytosis (33)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which COLISTIMETHATE Alternatives Have Lower Product dose omission Risk?
COLISTIMETHATE vs COLISTIN
COLISTIMETHATE vs COLLAGENASE CLOSTRIDIUM HISTOLYTICUM
COLISTIMETHATE vs COLLAGENASE CLOSTRIDIUM HISTOLYTICUM-AAES
COLISTIMETHATE vs COMBIVENT
COLISTIMETHATE vs COMBIVIR