Does ACLIDINIUM Cause Product use issue? 184 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 184 reports of Product use issue have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 3.7% of all adverse event reports for ACLIDINIUM.
184
Reports of Product use issue with ACLIDINIUM
3.7%
of all ACLIDINIUM reports
2
Deaths
31
Hospitalizations
How Dangerous Is Product use issue From ACLIDINIUM?
Of the 184 reports, 2 (1.1%) resulted in death, 31 (16.8%) required hospitalization.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 184 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which ACLIDINIUM Alternatives Have Lower Product use issue Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL