Cyclosporine Modified

54,387 adverse event reports submitted to the FDA (1994–2026)

This data reflects voluntary reports submitted to the FDA's Adverse Event Monitoring System (AEMS), formerly the FDA Adverse Event Reporting System (FAERS). A report does not mean the medication caused the event. Data may be incomplete or contain errors. Learn more about AEMS. New to this data? Read our guide on how to interpret FDA adverse event reports →
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Top Reported Adverse Events

The most frequently reported events in association with Cyclosporine Modified in the FAERS database. These are events reported by patients taking this medication, not necessarily caused by it. A single report may include multiple events.

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Ranked by frequency of reports, not severity. The most-reported event is not necessarily the most dangerous or the most common in patients taking this drug.

Who Is Reporting

Demographics of patients in FAERS reports that included this information. Not all reports include patient demographics.

By Sex

View reporter sex data as a table
Cyclosporine Modified adverse event reports by reporter sex
SexReports
Male23,272
Female22,143
Unknown495

By Age Group

View age group data as a table
Cyclosporine Modified adverse event reports by reporter age group
Age groupReports
0-177,898
18-346,210
35-497,468
50-6410,921
65-744,647
75+1,665

This shows who filed reports, reflecting who takes this drug and who tends to report, not who is at greatest risk.

Reported Outcomes

Outcomes recorded in FAERS reports that included Cyclosporine Modified. A single report may involve multiple reactions, each with a different outcome. These categories are defined by FDA reporting guidelines, not by PillSignal.

View outcome data as a table
Cyclosporine Modified adverse event reports by reported outcome
OutcomeReports
Other Serious37,149
Hospitalization16,693
Death10,556
Non-Serious5,072
Life-Threatening3,592
Disability1,040

Serious outcomes are far more likely to be reported than mild ones, so this overstates how often outcomes are serious. A recorded death does not mean the drug caused it.

Number of FAERS reports received per quarter for Cyclosporine Modified. Changes in volume may reflect shifts in prescribing rates, media attention, or reporting behavior, not changes in the medication's safety profile.

View report trend as a table
Cyclosporine Modified adverse event reports by year
YearReports
19941
20011
20034
2004881
2005900
20061,027
2007986
20081,677
20091,919
20101,635
20112,284
20121,610
2013732
2014794
2015766
2016956
20171,232
20181,823
20192,553
20203,612
20213,657
20225,362
20235,492
20246,916
20256,087
2026 (partial)1,480

The steep increase around 2004 reflects the FDA's move to electronic submission, not a change in this drug's safety. Trends track reporting volume, not risk.

Medications commonly reported with Cyclosporine Modified

In FDA adverse event reports that mention Cyclosporine Modified, these medications appeared most often in the same report.

This reflects co-occurrence in submitted reports, not evidence of drug interaction or combined risk. People often report several medications taken for the same condition or for unrelated reasons. Talk to a doctor or pharmacist about your specific medications.

Other medications with similar adverse event profiles in FDA FAERS reports.

Data Source

This data is sourced from the FDA's Adverse Event Monitoring System (AEMS), formerly FAERS, via the OpenFDA API. PillSignal is not affiliated with the FDA.

View this data on the FDA website →

Data last updated: June 2026