Does ACLIDINIUM Cause Device malfunction? 1,325 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,325 reports of Device malfunction have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 26.7% of all adverse event reports for ACLIDINIUM.
1,325
Reports of Device malfunction with ACLIDINIUM
26.7%
of all ACLIDINIUM reports
9
Deaths
260
Hospitalizations
How Dangerous Is Device malfunction From ACLIDINIUM?
Of the 1,325 reports, 9 (0.7%) resulted in death, 260 (19.6%) required hospitalization, and 5 (0.4%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 1,325 reports have been filed with the FAERS database.
What Other Side Effects Does ACLIDINIUM Cause?
Dyspnoea (1,706)
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)
Cough (471)
What Other Drugs Cause Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which ACLIDINIUM Alternatives Have Lower Device malfunction Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL