Does ACLIDINIUM Cause Condition aggravated? 305 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 305 reports of Condition aggravated have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 6.2% of all adverse event reports for ACLIDINIUM.
305
Reports of Condition aggravated with ACLIDINIUM
6.2%
of all ACLIDINIUM reports
2
Deaths
136
Hospitalizations
How Dangerous Is Condition aggravated From ACLIDINIUM?
Of the 305 reports, 2 (0.7%) resulted in death, 136 (44.6%) required hospitalization, and 2 (0.7%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 305 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ACLIDINIUM Alternatives Have Lower Condition aggravated Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL