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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does UMECLIDINIUM Cause Full blood count abnormal? 449 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 449 reports of Full blood count abnormal have been filed in association with UMECLIDINIUM (Anoro Ellipta). This represents 7.1% of all adverse event reports for UMECLIDINIUM.

449
Reports of Full blood count abnormal with UMECLIDINIUM
7.1%
of all UMECLIDINIUM reports
66
Deaths
302
Hospitalizations

How Dangerous Is Full blood count abnormal From UMECLIDINIUM?

Of the 449 reports, 66 (14.7%) resulted in death, 302 (67.3%) required hospitalization, and 194 (43.2%) were considered life-threatening.

Is Full blood count abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UMECLIDINIUM. However, 449 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 Full blood count abnormal?

ALBUTEROL (3,060) PREDNISONE (2,230) BUDESONIDE\FORMOTEROL (1,786) TIOTROPIUM (1,754) MONTELUKAST (1,529) MEPOLIZUMAB (1,440) BUDESONIDE (1,339) PALBOCICLIB (1,146) CICLESONIDE (916) PANTOPRAZOLE (776)

Which UMECLIDINIUM Alternatives Have Lower Full blood count abnormal Risk?

UMECLIDINIUM vs UMECLIDINIUM\VILANTEROL TRIFENATATE UMECLIDINIUM vs UMIFENOVIR UMECLIDINIUM vs UNSPECIFIED INGREDIENT UMECLIDINIUM vs UPADACITINIB UMECLIDINIUM vs URAPIDIL

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UMECLIDINIUM Full Profile All Full blood count abnormal Reports All Drugs Causing Full blood count abnormal UMECLIDINIUM Demographics