Does CYCLOSPORINE Cause Product storage error? 721 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 721 reports of Product storage error have been filed in association with CYCLOSPORINE (Verkazia). This represents 1.1% of all adverse event reports for CYCLOSPORINE.
721
Reports of Product storage error with CYCLOSPORINE
1.1%
of all CYCLOSPORINE reports
5
Deaths
15
Hospitalizations
How Dangerous Is Product storage error From CYCLOSPORINE?
Of the 721 reports, 5 (0.7%) resulted in death, 15 (2.1%) required hospitalization, and 17 (2.4%) were considered life-threatening.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CYCLOSPORINE. However, 721 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 Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which CYCLOSPORINE Alternatives Have Lower Product storage error Risk?
CYCLOSPORINE vs CYCLOSPORINE A
CYCLOSPORINE vs CYMBALTA
CYCLOSPORINE vs CYNODON DACTYLON POLLEN
CYCLOSPORINE vs CYPROHEPTADINE
CYCLOSPORINE vs CYPROTERONE