Does ACLIDINIUM Cause Unevaluable event? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Unevaluable event have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 0.3% of all adverse event reports for ACLIDINIUM.
14
Reports of Unevaluable event with ACLIDINIUM
0.3%
of all ACLIDINIUM reports
0
Deaths
7
Hospitalizations
How Dangerous Is Unevaluable event From ACLIDINIUM?
Of the 14 reports, 7 (50.0%) required hospitalization, and 1 (7.1%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 14 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 Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which ACLIDINIUM Alternatives Have Lower Unevaluable event Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL