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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 Coronary artery disease? 170 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 170 reports of Coronary artery disease have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 3.4% of all adverse event reports for ACLIDINIUM.

170
Reports of Coronary artery disease with ACLIDINIUM
3.4%
of all ACLIDINIUM reports
1
Deaths
102
Hospitalizations

How Dangerous Is Coronary artery disease From ACLIDINIUM?

Of the 170 reports, 1 (0.6%) resulted in death, 102 (60.0%) required hospitalization, and 7 (4.1%) were considered life-threatening.

Is Coronary artery disease Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 170 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 Coronary artery disease?

ROSIGLITAZONE (4,982) ASPIRIN (807) METFORMIN\ROSIGLITAZONE (738) AVANDIA (667) ROSUVASTATIN (508) TESTOSTERONE (453) PANTOPRAZOLE (422) CLOPIDOGREL BISULFATE (402) ALBUTEROL (391) ADALIMUMAB (353)

Which ACLIDINIUM Alternatives Have Lower Coronary artery disease Risk?

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

Related Pages

ACLIDINIUM Full Profile All Coronary artery disease Reports All Drugs Causing Coronary artery disease ACLIDINIUM Demographics