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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 Sepsis? 215 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 215 reports of Sepsis have been filed in association with UMECLIDINIUM (Anoro Ellipta). This represents 3.4% of all adverse event reports for UMECLIDINIUM.

215
Reports of Sepsis with UMECLIDINIUM
3.4%
of all UMECLIDINIUM reports
197
Deaths
116
Hospitalizations

How Dangerous Is Sepsis From UMECLIDINIUM?

Of the 215 reports, 197 (91.6%) resulted in death, 116 (54.0%) required hospitalization, and 92 (42.8%) were considered life-threatening.

Is Sepsis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UMECLIDINIUM. However, 215 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 Sepsis?

RITUXIMAB (4,043) CYCLOPHOSPHAMIDE (4,041) METHOTREXATE (3,933) ADALIMUMAB (3,169) DEXAMETHASONE (3,150) LENALIDOMIDE (2,956) VINCRISTINE (2,791) DOXORUBICIN (2,740) PREDNISONE (2,634) PREDNISOLONE (2,281)

Which UMECLIDINIUM Alternatives Have Lower Sepsis Risk?

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

Related Pages

UMECLIDINIUM Full Profile All Sepsis Reports All Drugs Causing Sepsis UMECLIDINIUM Demographics