Does ACLIDINIUM Cause Product dose omission issue? 261 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 261 reports of Product dose omission issue have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 5.3% of all adverse event reports for ACLIDINIUM.
261
Reports of Product dose omission issue with ACLIDINIUM
5.3%
of all ACLIDINIUM reports
1
Deaths
23
Hospitalizations
How Dangerous Is Product dose omission issue From ACLIDINIUM?
Of the 261 reports, 1 (0.4%) resulted in death, 23 (8.8%) required hospitalization, and 2 (0.8%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 261 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 Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which ACLIDINIUM Alternatives Have Lower Product dose omission issue Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL