Does ACLIDINIUM Cause Drug dose omission? 996 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 996 reports of Drug dose omission have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 20.1% of all adverse event reports for ACLIDINIUM.
996
Reports of Drug dose omission with ACLIDINIUM
20.1%
of all ACLIDINIUM reports
13
Deaths
181
Hospitalizations
How Dangerous Is Drug dose omission From ACLIDINIUM?
Of the 996 reports, 13 (1.3%) resulted in death, 181 (18.2%) required hospitalization, and 6 (0.6%) were considered life-threatening.
Is Drug dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 996 reports have been filed with the FAERS database.
What Other Side Effects Does ACLIDINIUM Cause?
Dyspnoea (1,706)
Device malfunction (1,325)
Asthma (857)
Intentional product misuse (745)
Chronic obstructive pulmonary disease (697)
Wheezing (688)
Off label use (620)
Product quality issue (557)
Device issue (499)
Cough (471)
What Other Drugs Cause Drug dose omission?
ETANERCEPT (10,871)
CINACALCET (8,683)
EVOLOCUMAB (4,914)
ADALIMUMAB (3,993)
INSULIN LISPRO (3,063)
GOLIMUMAB (2,652)
TERIPARATIDE (2,616)
APREMILAST (2,466)
ALBUTEROL (2,309)
FLUTICASONE\SALMETEROL (2,153)
Which ACLIDINIUM Alternatives Have Lower Drug dose omission Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL