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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 Eosinophil count increased? 55 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of Eosinophil count increased have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 1.1% of all adverse event reports for ACLIDINIUM.

55
Reports of Eosinophil count increased with ACLIDINIUM
1.1%
of all ACLIDINIUM reports
0
Deaths
10
Hospitalizations

How Dangerous Is Eosinophil count increased From ACLIDINIUM?

Of the 55 reports, 10 (18.2%) required hospitalization.

Is Eosinophil count increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 55 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 Eosinophil count increased?

ALBUTEROL (1,359) PREDNISONE (846) BUDESONIDE\FORMOTEROL (719) DUPILUMAB (712) TIOTROPIUM (682) MEPOLIZUMAB (670) MONTELUKAST (504) BUDESONIDE (493) CLOZAPINE (475) FLUTICASONE\SALMETEROL (416)

Which ACLIDINIUM Alternatives Have Lower Eosinophil count increased Risk?

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

Related Pages

ACLIDINIUM Full Profile All Eosinophil count increased Reports All Drugs Causing Eosinophil count increased ACLIDINIUM Demographics