Does UMECLIDINIUM Cause Blood count abnormal? 248 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 248 reports of Blood count abnormal have been filed in association with UMECLIDINIUM (Anoro Ellipta). This represents 3.9% of all adverse event reports for UMECLIDINIUM.
248
Reports of Blood count abnormal with UMECLIDINIUM
3.9%
of all UMECLIDINIUM reports
0
Deaths
139
Hospitalizations
How Dangerous Is Blood count abnormal From UMECLIDINIUM?
Of the 248 reports, 139 (56.0%) required hospitalization, and 9 (3.6%) were considered life-threatening.
Is Blood count abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UMECLIDINIUM. However, 248 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 Blood count abnormal?
ALBUTEROL (3,248)
TIOTROPIUM (1,677)
PREDNISONE (1,600)
BUDESONIDE\FORMOTEROL (1,595)
MONTELUKAST (1,264)
PALBOCICLIB (1,169)
MEPOLIZUMAB (1,157)
RUXOLITINIB (1,080)
FLUTICASONE\SALMETEROL (841)
LENALIDOMIDE (701)
Which UMECLIDINIUM Alternatives Have Lower Blood count abnormal Risk?
UMECLIDINIUM vs UMECLIDINIUM\VILANTEROL TRIFENATATE
UMECLIDINIUM vs UMIFENOVIR
UMECLIDINIUM vs UNSPECIFIED INGREDIENT
UMECLIDINIUM vs UPADACITINIB
UMECLIDINIUM vs URAPIDIL