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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 DOLUTEGRAVIR Cause Hyperlipidaemia? 23 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Hyperlipidaemia have been filed in association with DOLUTEGRAVIR (Juluca). This represents 0.2% of all adverse event reports for DOLUTEGRAVIR.

23
Reports of Hyperlipidaemia with DOLUTEGRAVIR
0.2%
of all DOLUTEGRAVIR reports
1
Deaths
10
Hospitalizations

How Dangerous Is Hyperlipidaemia From DOLUTEGRAVIR?

Of the 23 reports, 1 (4.3%) resulted in death, 10 (43.5%) required hospitalization, and 1 (4.3%) 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 DOLUTEGRAVIR. However, 23 reports have been filed with the FAERS database.

What Other Side Effects Does DOLUTEGRAVIR Cause?

Foetal exposure during pregnancy (1,036) Exposure during pregnancy (776) Virologic failure (770) Pathogen resistance (586) Maternal exposure during pregnancy (517) Viral mutation identified (510) Treatment failure (453) Drug ineffective (447) Off label use (413) Blood hiv rna increased (410)

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 DOLUTEGRAVIR Alternatives Have Lower Hyperlipidaemia Risk?

DOLUTEGRAVIR vs DOLUTEGRAVIR\LAMIVUDINE DOLUTEGRAVIR vs DOLUTEGRAVIR\LAMIVUDINE\TENOFOVIR DISOPROXIL DOLUTEGRAVIR vs DOLUTEGRAVIR\RILPIVIRINE DOLUTEGRAVIR vs DOMPERIDONE DOLUTEGRAVIR vs DOMPERIDONE\PANTOPRAZOLE

Related Pages

DOLUTEGRAVIR Full Profile All Hyperlipidaemia Reports All Drugs Causing Hyperlipidaemia DOLUTEGRAVIR Demographics