Does ACLIDINIUM Cause Ill-defined disorder? 41 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 41 reports of Ill-defined disorder have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 0.8% of all adverse event reports for ACLIDINIUM.
41
Reports of Ill-defined disorder with ACLIDINIUM
0.8%
of all ACLIDINIUM reports
0
Deaths
9
Hospitalizations
How Dangerous Is Ill-defined disorder From ACLIDINIUM?
Of the 41 reports, 9 (22.0%) required hospitalization, and 1 (2.4%) were considered life-threatening.
Is Ill-defined disorder Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 41 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 Ill-defined disorder?
ACETAMINOPHEN\OXYCODONE (9,780)
ACETAMINOPHEN\HYDROCODONE (6,159)
TOCILIZUMAB (4,411)
RITUXIMAB (4,220)
ETANERCEPT (4,202)
METHOTREXATE (4,063)
ABATACEPT (3,630)
LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN (3,600)
LEFLUNOMIDE (3,570)
CERTOLIZUMAB PEGOL (3,273)
Which ACLIDINIUM Alternatives Have Lower Ill-defined disorder Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL