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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 CYCLOSPORINE Cause Device issue? 34 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Device issue have been filed in association with CYCLOSPORINE (Verkazia). This represents 0.1% of all adverse event reports for CYCLOSPORINE.

34
Reports of Device issue with CYCLOSPORINE
0.1%
of all CYCLOSPORINE reports
0
Deaths
9
Hospitalizations

How Dangerous Is Device issue From CYCLOSPORINE?

Of the 34 reports, 9 (26.5%) required hospitalization, and 17 (50.0%) were considered life-threatening.

Is Device issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CYCLOSPORINE. However, 34 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 Device issue?

ADALIMUMAB (17,630) SOMATROPIN (5,131) PEGFILGRASTIM (5,071) ETANERCEPT (4,143) INSULIN GLARGINE (3,175) EXENATIDE (2,862) LEVONORGESTREL (2,623) CARBIDOPA\LEVODOPA (2,574) GOLIMUMAB (1,827) USTEKINUMAB (1,716)

Which CYCLOSPORINE Alternatives Have Lower Device issue Risk?

CYCLOSPORINE vs CYCLOSPORINE A CYCLOSPORINE vs CYMBALTA CYCLOSPORINE vs CYNODON DACTYLON POLLEN CYCLOSPORINE vs CYPROHEPTADINE CYCLOSPORINE vs CYPROTERONE

Related Pages

CYCLOSPORINE Full Profile All Device issue Reports All Drugs Causing Device issue CYCLOSPORINE Demographics