Does UMECLIDINIUM Cause Adverse event? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Adverse event have been filed in association with UMECLIDINIUM (Anoro Ellipta). This represents 0.6% of all adverse event reports for UMECLIDINIUM.
36
Reports of Adverse event with UMECLIDINIUM
0.6%
of all UMECLIDINIUM reports
0
Deaths
31
Hospitalizations
How Dangerous Is Adverse event From UMECLIDINIUM?
Of the 36 reports, 31 (86.1%) required hospitalization, and 27 (75.0%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UMECLIDINIUM. However, 36 reports have been filed with the FAERS database.
What Other Side Effects Does UMECLIDINIUM Cause?
Dyspnoea (1,817)
Asthma (1,433)
Wheezing (1,111)
Therapeutic product effect incomplete (980)
Cough (913)
Drug ineffective (734)
Loss of personal independence in daily activities (711)
Obstructive airways disorder (654)
Chronic obstructive pulmonary disease (588)
Condition aggravated (580)
What Other Drugs Cause Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which UMECLIDINIUM Alternatives Have Lower Adverse event Risk?
UMECLIDINIUM vs UMECLIDINIUM\VILANTEROL TRIFENATATE
UMECLIDINIUM vs UMIFENOVIR
UMECLIDINIUM vs UNSPECIFIED INGREDIENT
UMECLIDINIUM vs UPADACITINIB
UMECLIDINIUM vs URAPIDIL