Does CYCLOSPORINE Cause Incorrect product storage? 203 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 203 reports of Incorrect product storage have been filed in association with CYCLOSPORINE (Verkazia). This represents 0.3% of all adverse event reports for CYCLOSPORINE.
203
Reports of Incorrect product storage with CYCLOSPORINE
0.3%
of all CYCLOSPORINE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Incorrect product storage From CYCLOSPORINE?
Of the 203 reports, 4 (2.0%) required hospitalization.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CYCLOSPORINE. However, 203 reports have been filed with the FAERS database.
What Other Side Effects Does CYCLOSPORINE Cause?
Drug ineffective (11,172)
Off label use (6,860)
Eye irritation (5,806)
Product use in unapproved indication (5,019)
Condition aggravated (2,310)
Eye pain (2,197)
Drug intolerance (2,176)
Pneumonia (2,022)
Pyrexia (2,020)
Treatment failure (1,961)
What Other Drugs Cause Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
Which CYCLOSPORINE Alternatives Have Lower Incorrect product storage Risk?
CYCLOSPORINE vs CYCLOSPORINE A
CYCLOSPORINE vs CYMBALTA
CYCLOSPORINE vs CYNODON DACTYLON POLLEN
CYCLOSPORINE vs CYPROHEPTADINE
CYCLOSPORINE vs CYPROTERONE