Does ACLIDINIUM Cause Full blood count abnormal? 202 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 202 reports of Full blood count abnormal have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 4.1% of all adverse event reports for ACLIDINIUM.
202
Reports of Full blood count abnormal with ACLIDINIUM
4.1%
of all ACLIDINIUM reports
1
Deaths
123
Hospitalizations
How Dangerous Is Full blood count abnormal From ACLIDINIUM?
Of the 202 reports, 1 (0.5%) resulted in death, 123 (60.9%) required hospitalization, and 7 (3.5%) were considered life-threatening.
Is Full blood count abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 202 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 Full blood count abnormal?
ALBUTEROL (3,060)
PREDNISONE (2,230)
BUDESONIDE\FORMOTEROL (1,786)
TIOTROPIUM (1,754)
MONTELUKAST (1,529)
MEPOLIZUMAB (1,440)
BUDESONIDE (1,339)
PALBOCICLIB (1,146)
CICLESONIDE (916)
PANTOPRAZOLE (776)
Which ACLIDINIUM Alternatives Have Lower Full blood count abnormal Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL