Does ACLIDINIUM Cause Off label use? 620 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 620 reports of Off label use have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 12.5% of all adverse event reports for ACLIDINIUM.
620
Reports of Off label use with ACLIDINIUM
12.5%
of all ACLIDINIUM reports
5
Deaths
200
Hospitalizations
How Dangerous Is Off label use From ACLIDINIUM?
Of the 620 reports, 5 (0.8%) resulted in death, 200 (32.3%) required hospitalization, and 7 (1.1%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 620 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)
Product quality issue (557)
Device issue (499)
Cough (471)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which ACLIDINIUM Alternatives Have Lower Off label use Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL