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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 ACLIDINIUM Cause Hepatotoxicity? 79 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 79 reports of Hepatotoxicity have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 1.6% of all adverse event reports for ACLIDINIUM.

79
Reports of Hepatotoxicity with ACLIDINIUM
1.6%
of all ACLIDINIUM reports
0
Deaths
79
Hospitalizations

How Dangerous Is Hepatotoxicity From ACLIDINIUM?

Of the 79 reports, 79 (100.0%) required hospitalization.

Is Hepatotoxicity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 79 reports have been filed with the FAERS database.

What Other Side Effects Does ACLIDINIUM Cause?

Dyspnoea (1,706) Device malfunction (1,325) Drug dose omission (996) Asthma (857) Intentional product misuse (745) Chronic obstructive pulmonary disease (697) Wheezing (688) Off label use (620) Product quality issue (557) Device issue (499)

What Other Drugs Cause Hepatotoxicity?

METHOTREXATE (1,917) ACETAMINOPHEN (1,557) LEFLUNOMIDE (829) HYDROXYCHLOROQUINE (715) PREDNISONE (707) RITUXIMAB (702) ETANERCEPT (699) ADALIMUMAB (674) CYCLOPHOSPHAMIDE (632) SULFASALAZINE (613)

Which ACLIDINIUM Alternatives Have Lower Hepatotoxicity Risk?

ACLIDINIUM vs ACLIDINIUM\FORMOTEROL ACLIDINIUM vs ACORAMIDIS ACLIDINIUM vs ACTEMRA ACLIDINIUM vs ACTIQ ACLIDINIUM vs ACTIVATED CHARCOAL

Related Pages

ACLIDINIUM Full Profile All Hepatotoxicity Reports All Drugs Causing Hepatotoxicity ACLIDINIUM Demographics