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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 Hypercholesterolaemia? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Hypercholesterolaemia have been filed in association with UMECLIDINIUM (Anoro Ellipta). This represents 0.2% of all adverse event reports for UMECLIDINIUM.

12
Reports of Hypercholesterolaemia with UMECLIDINIUM
0.2%
of all UMECLIDINIUM reports
12
Deaths
11
Hospitalizations

How Dangerous Is Hypercholesterolaemia From UMECLIDINIUM?

Of the 12 reports, 12 (100.0%) resulted in death, 11 (91.7%) required hospitalization, and 11 (91.7%) were considered life-threatening.

Is Hypercholesterolaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UMECLIDINIUM. However, 12 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 Hypercholesterolaemia?

ALENDRONATE (1,607) METHOTREXATE (1,547) TOCILIZUMAB (1,483) ADALIMUMAB (1,479) ABATACEPT (1,410) RITUXIMAB (1,389) PREDNISONE (1,377) INFLIXIMAB (1,338) DICLOFENAC (1,331) LEFLUNOMIDE (1,322)

Which UMECLIDINIUM Alternatives Have Lower Hypercholesterolaemia 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 Hypercholesterolaemia Reports All Drugs Causing Hypercholesterolaemia UMECLIDINIUM Demographics