Does ACLIDINIUM Cause Adverse event? 34 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Adverse event have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 0.7% of all adverse event reports for ACLIDINIUM.
34
Reports of Adverse event with ACLIDINIUM
0.7%
of all ACLIDINIUM reports
0
Deaths
11
Hospitalizations
How Dangerous Is Adverse event From ACLIDINIUM?
Of the 34 reports, 11 (32.4%) required hospitalization, and 4 (11.8%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for ACLIDINIUM.
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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which ACLIDINIUM Alternatives Have Lower Adverse event Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL