Does ACLIDINIUM Cause Device failure? 304 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 304 reports of Device failure have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 6.1% of all adverse event reports for ACLIDINIUM.
304
Reports of Device failure with ACLIDINIUM
6.1%
of all ACLIDINIUM reports
1
Deaths
45
Hospitalizations
How Dangerous Is Device failure From ACLIDINIUM?
Of the 304 reports, 1 (0.3%) resulted in death, 45 (14.8%) required hospitalization.
Is Device failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 304 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 Device failure?
EPINEPHRINE (1,344)
SOMATROPIN (1,141)
PEGFILGRASTIM (829)
TREPROSTINIL (713)
BACLOFEN (691)
BUDESONIDE\FORMOTEROL (686)
ETANERCEPT (576)
GOLIMUMAB (487)
LEVONORGESTREL (332)
INSULIN ASPART (271)
Which ACLIDINIUM Alternatives Have Lower Device failure Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL