Does ACLIDINIUM Cause Wrong technique in device usage process? 102 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 102 reports of Wrong technique in device usage process have been filed in association with ACLIDINIUM (Tudorza Pressair). This represents 2.1% of all adverse event reports for ACLIDINIUM.
102
Reports of Wrong technique in device usage process with ACLIDINIUM
2.1%
of all ACLIDINIUM reports
1
Deaths
16
Hospitalizations
How Dangerous Is Wrong technique in device usage process From ACLIDINIUM?
Of the 102 reports, 1 (1.0%) resulted in death, 16 (15.7%) required hospitalization.
Is Wrong technique in device usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM. However, 102 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 Wrong technique in device usage process?
ALBUTEROL (5,380)
SOMATROPIN (4,746)
EXENATIDE (3,255)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,673)
FLUTICASONE\SALMETEROL (2,259)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (2,197)
INSULIN GLARGINE (1,749)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,531)
BUDESONIDE\FORMOTEROL (1,481)
BELIMUMAB (1,347)
Which ACLIDINIUM Alternatives Have Lower Wrong technique in device usage process Risk?
ACLIDINIUM vs ACLIDINIUM\FORMOTEROL
ACLIDINIUM vs ACORAMIDIS
ACLIDINIUM vs ACTEMRA
ACLIDINIUM vs ACTIQ
ACLIDINIUM vs ACTIVATED CHARCOAL