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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ACLIDINIUM Cause Forced expiratory volume decreased? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Forced expiratory volume decreased have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 0.1% of all adverse event reports for ACLIDINIUM.

6
Reports of Forced expiratory volume decreased with ACLIDINIUM
0.1%
of all ACLIDINIUM reports
0
Deaths
5
Hospitalizations

How Dangerous Is Forced expiratory volume decreased From ACLIDINIUM?

Of the 6 reports, 5 (83.3%) required hospitalization.

Is Forced expiratory volume decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 6 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 Forced expiratory volume decreased?

OMALIZUMAB (1,497) ALBUTEROL (344) PREDNISONE (335) MONTELUKAST (274) TIOTROPIUM (236) MEPOLIZUMAB (209) METFORMIN (183) BUDESONIDE\FORMOTEROL (171) BUDESONIDE (150) LEVOFLOXACIN (138)

Which ACLIDINIUM Alternatives Have Lower Forced expiratory volume decreased Risk?

ACLIDINIUM vs ACLIDINIUM\FORMOTEROL ACLIDINIUM vs ACORAMIDIS ACLIDINIUM vs ACTEMRA ACLIDINIUM vs ACTIQ ACLIDINIUM vs ACTIVATED CHARCOAL

Related Pages

ACLIDINIUM Full Profile All Forced expiratory volume decreased Reports All Drugs Causing Forced expiratory volume decreased ACLIDINIUM Demographics