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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 Dyspnoea? 1,706 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,706 reports of Dyspnoea have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 34.4% of all adverse event reports for ACLIDINIUM.

1,706
Reports of Dyspnoea with ACLIDINIUM
34.4%
of all ACLIDINIUM reports
12
Deaths
552
Hospitalizations

How Dangerous Is Dyspnoea From ACLIDINIUM?

Of the 1,706 reports, 12 (0.7%) resulted in death, 552 (32.4%) required hospitalization, and 15 (0.9%) were considered life-threatening.

Is Dyspnoea Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 1,706 reports have been filed with the FAERS database.

What Other Side Effects Does ACLIDINIUM Cause?

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) Cough (471)

What Other Drugs Cause Dyspnoea?

ALBUTEROL (21,856) TREPROSTINIL (16,348) AMBRISENTAN (13,367) PREDNISONE (12,830) BUDESONIDE\FORMOTEROL (11,158) TIOTROPIUM (10,863) ADALIMUMAB (10,547) DUPILUMAB (10,310) FLUTICASONE\SALMETEROL (9,783) MEPOLIZUMAB (9,192)

Which ACLIDINIUM Alternatives Have Lower Dyspnoea Risk?

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

Related Pages

ACLIDINIUM Full Profile All Dyspnoea Reports All Drugs Causing Dyspnoea ACLIDINIUM Demographics