Does ACLIDINIUM Cause Therapeutic product effect incomplete? 413 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 413 reports of Therapeutic product effect incomplete have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 8.3% of all adverse event reports for ACLIDINIUM.
413
Reports of Therapeutic product effect incomplete with ACLIDINIUM
8.3%
of all ACLIDINIUM reports
1
Deaths
248
Hospitalizations
How Dangerous Is Therapeutic product effect incomplete From ACLIDINIUM?
Of the 413 reports, 1 (0.2%) resulted in death, 248 (60.0%) required hospitalization, and 7 (1.7%) were considered life-threatening.
Is Therapeutic product effect incomplete Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 413 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 Therapeutic product effect incomplete?
ALBUTEROL (8,496)
ADALIMUMAB (6,986)
PREDNISONE (6,709)
METHOTREXATE (6,037)
TOFACITINIB (4,914)
SECUKINUMAB (4,661)
BUDESONIDE\FORMOTEROL (4,392)
TIOTROPIUM (4,327)
MEPOLIZUMAB (4,106)
ETANERCEPT (3,961)
Which ACLIDINIUM Alternatives Have Lower Therapeutic product effect incomplete Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL