Does ACLIDINIUM Cause Intentional device misuse? 346 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 346 reports of Intentional device misuse have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 7.0% of all adverse event reports for ACLIDINIUM.
346
Reports of Intentional device misuse with ACLIDINIUM
7.0%
of all ACLIDINIUM reports
2
Deaths
64
Hospitalizations
How Dangerous Is Intentional device misuse From ACLIDINIUM?
Of the 346 reports, 2 (0.6%) resulted in death, 64 (18.5%) required hospitalization.
Is Intentional device misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 346 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 Intentional device misuse?
BUDESONIDE\FORMOTEROL (1,318)
EXENATIDE (1,254)
BUDESONIDE (292)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (182)
SOMATROPIN (128)
TERIPARATIDE (117)
FORMOTEROL\GLYCOPYRROLATE (103)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (102)
CARBIDOPA\LEVODOPA (100)
LEVONORGESTREL (82)
Which ACLIDINIUM Alternatives Have Lower Intentional device misuse Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL