Does ACLIDINIUM Cause Intentional product misuse? 745 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 745 reports of Intentional product misuse have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 15.0% of all adverse event reports for ACLIDINIUM.
745
Reports of Intentional product misuse with ACLIDINIUM
15.0%
of all ACLIDINIUM reports
4
Deaths
135
Hospitalizations
How Dangerous Is Intentional product misuse From ACLIDINIUM?
Of the 745 reports, 4 (0.5%) resulted in death, 135 (18.1%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 745 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)
Chronic obstructive pulmonary disease (697)
Wheezing (688)
Off label use (620)
Product quality issue (557)
Device issue (499)
Cough (471)
What Other Drugs Cause Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which ACLIDINIUM Alternatives Have Lower Intentional product misuse Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL