Does ACLIDINIUM Cause Product dose omission? 225 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 225 reports of Product dose omission have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 4.5% of all adverse event reports for ACLIDINIUM.
225
Reports of Product dose omission with ACLIDINIUM
4.5%
of all ACLIDINIUM reports
2
Deaths
55
Hospitalizations
How Dangerous Is Product dose omission From ACLIDINIUM?
Of the 225 reports, 2 (0.9%) resulted in death, 55 (24.4%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 225 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?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which ACLIDINIUM Alternatives Have Lower Product dose omission Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL