Does ACLIDINIUM Cause Device use error? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Device use error have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 0.2% of all adverse event reports for ACLIDINIUM.
8
Reports of Device use error with ACLIDINIUM
0.2%
of all ACLIDINIUM reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device use error From ACLIDINIUM?
Of the 8 reports, 2 (25.0%) required hospitalization.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 8 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 use error?
PEGFILGRASTIM (6,001)
ALBUTEROL (5,215)
ALBIGLUTIDE (4,056)
EVOLOCUMAB (4,002)
SOMATROPIN (2,801)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
Which ACLIDINIUM Alternatives Have Lower Device use error Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL