Tacrolimus

120,503 adverse event reports submitted to the FDA (2004–2026)

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 →
New to FDA adverse event data? Here's how to read these reports →

Top Reported Adverse Events

The most frequently reported events in association with Tacrolimus 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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  • Off Label Use 12,160 reports

    Using a medication for a condition or in a way that the FDA has not officially approved. This is common and often legal, and a report of it does not mean something went wrong. Doctors sometimes prescribe drugs off label based on their judgment.

    Full definition in the glossary →
  • Drug Ineffective 8,568 reports

    A report that the medication did not work as expected for the person taking it. This is a reporting category, not a sign the drug is defective. It simply means someone felt it was not helping their condition.

    Full definition in the glossary →
  • Product Use in Unapproved Indication 5,939 reports

    Using a medication for a condition it is not officially approved to treat. Like off label use, this is a reporting category and does not by itself mean harm occurred.

    Full definition in the glossary →
  • Drug Interaction 5,462 reports

    A report that two or more medications may have affected each other when taken together.

    Full definition in the glossary →
  • Acute Kidney Injury 5,219 reports

    A sudden drop in how well the kidneys are working. It is often temporary and can have many causes.

    Full definition in the glossary →
  • Diarrhoea 4,397 reports

    Loose or watery bowel movements, often frequent. Also spelled diarrhea in American English.

    Full definition in the glossary → See all drugs reporting this event →
  • Transplant Rejection 4,028 reports
  • Cytomegalovirus Infection 3,919 reports

    An infection with a common virus, often called CMV, that can be serious for people with weakened immune systems.

    Full definition in the glossary →
  • Pyrexia 3,745 reports

    The medical term for fever, meaning a raised body temperature.

    Full definition in the glossary → See all drugs reporting this event →
  • COVID-19 3,683 reports

    The illness caused by the SARS-CoV-2 coronavirus.

    Full definition in the glossary →
  • Toxicity to Various Agents 3,549 reports

    A broad reporting category used when the body has a harmful response, sometimes involving more than one substance.

    Full definition in the glossary →
  • Pneumonia 3,445 reports

    An infection that inflames the air sacs in the lungs, which can cause cough, fever, and difficulty breathing.

    Full definition in the glossary →
  • Death 3,332 reports

    A report that the person died. A death appearing in reports for a drug does not mean the drug caused it. Reports record that a death occurred while the medication was being used, which can happen for many unrelated reasons.

    Full definition in the glossary →
  • Post Transplant Lymphoproliferative Disorder 2,802 reports
  • Sepsis 2,781 reports

    A serious, body-wide response to an infection that can become life threatening and needs urgent care.

    Full definition in the glossary →

Browse the full glossary →

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
Tacrolimus adverse event reports by reporter sex
SexReports
Male58,676
Female44,795
Unknown602

By Age Group

View age group data as a table
Tacrolimus adverse event reports by reporter age group
Age groupReports
0-1712,933
18-3413,701
35-4917,779
50-6429,347
65-7414,155
75+3,413

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 Tacrolimus. 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
Tacrolimus adverse event reports by reported outcome
OutcomeReports
Other Serious80,377
Hospitalization47,869
Death19,280
Non-Serious11,275
Life-Threatening10,026
Disability1,446

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 Tacrolimus. 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
Tacrolimus adverse event reports by year
YearReports
2004169
2005219
2006260
2007555
2008951
20091,053
20101,201
20112,206
20122,458
20131,608
20142,523
20153,005
20164,185
20176,099
20189,096
20199,391
202010,997
202110,769
202211,189
202312,610
202413,674
202513,522
2026 (partial)2,763

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 Tacrolimus

In FDA adverse event reports that mention Tacrolimus, 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