Does ACLIDINIUM\FORMOTEROL Cause Device issue? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Device issue have been filed in association with ACLIDINIUM\FORMOTEROL. This represents 2.3% of all adverse event reports for ACLIDINIUM\FORMOTEROL.
11
Reports of Device issue with ACLIDINIUM\FORMOTEROL
2.3%
of all ACLIDINIUM\FORMOTEROL reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device issue From ACLIDINIUM\FORMOTEROL?
Of the 11 reports, 2 (18.2%) required hospitalization, and 2 (18.2%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACLIDINIUM\FORMOTEROL. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does ACLIDINIUM\FORMOTEROL Cause?
Chronic obstructive pulmonary disease (252)
Wheezing (232)
Bronchiectasis (225)
Gastrooesophageal reflux disease (200)
Dyspnoea (155)
Asthma (148)
Obstructive airways disorder (138)
Therapeutic product effect incomplete (136)
Breath sounds abnormal (118)
Oedema peripheral (110)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which ACLIDINIUM\FORMOTEROL Alternatives Have Lower Device issue Risk?
ACLIDINIUM\FORMOTEROL vs ACORAMIDIS
ACLIDINIUM\FORMOTEROL vs ACTEMRA
ACLIDINIUM\FORMOTEROL vs ACTIQ
ACLIDINIUM\FORMOTEROL vs ACTIVATED CHARCOAL
ACLIDINIUM\FORMOTEROL vs ACTONEL