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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 Hyperlipidaemia? 45 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Hyperlipidaemia have been filed in association with UMECLIDINIUM (Anoro Ellipta). This represents 0.7% of all adverse event reports for UMECLIDINIUM.

45
Reports of Hyperlipidaemia with UMECLIDINIUM
0.7%
of all UMECLIDINIUM reports
45
Deaths
42
Hospitalizations

How Dangerous Is Hyperlipidaemia From UMECLIDINIUM?

Of the 45 reports, 45 (100.0%) resulted in death, 42 (93.3%) required hospitalization, and 42 (93.3%) were considered life-threatening.

Is Hyperlipidaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UMECLIDINIUM. However, 45 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 Hyperlipidaemia?

ALENDRONATE (511) AMLODIPINE (226) DENOSUMAB (204) SITAGLIPTIN (186) METHOTREXATE (184) ROSUVASTATIN (179) PREDNISONE (169) FINASTERIDE (145) MYCOPHENOLATE MOFETIL (141) ASPIRIN (138)

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