Does UMECLIDINIUM Cause Condition aggravated? 580 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 580 reports of Condition aggravated have been filed in association with UMECLIDINIUM (Anoro Ellipta). This represents 9.2% of all adverse event reports for UMECLIDINIUM.
580
Reports of Condition aggravated with UMECLIDINIUM
9.2%
of all UMECLIDINIUM reports
180
Deaths
388
Hospitalizations
How Dangerous Is Condition aggravated From UMECLIDINIUM?
Of the 580 reports, 180 (31.0%) resulted in death, 388 (66.9%) required hospitalization, and 237 (40.9%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UMECLIDINIUM. However, 580 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)
Wrong technique in device usage process (490)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which UMECLIDINIUM Alternatives Have Lower Condition aggravated Risk?
UMECLIDINIUM vs UMECLIDINIUM\VILANTEROL TRIFENATATE
UMECLIDINIUM vs UMIFENOVIR
UMECLIDINIUM vs UNSPECIFIED INGREDIENT
UMECLIDINIUM vs UPADACITINIB
UMECLIDINIUM vs URAPIDIL