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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 LORLATINIB Cause Dyslipidaemia? 67 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 67 reports of Dyslipidaemia have been filed in association with LORLATINIB (Lorbrena). This represents 1.2% of all adverse event reports for LORLATINIB.

67
Reports of Dyslipidaemia with LORLATINIB
1.2%
of all LORLATINIB reports
5
Deaths
12
Hospitalizations

How Dangerous Is Dyslipidaemia From LORLATINIB?

Of the 67 reports, 5 (7.5%) resulted in death, 12 (17.9%) required hospitalization, and 2 (3.0%) were considered life-threatening.

Is Dyslipidaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LORLATINIB. However, 67 reports have been filed with the FAERS database.

What Other Side Effects Does LORLATINIB Cause?

Death (1,050) Neoplasm progression (633) Off label use (394) Weight increased (306) Hallucination (290) Blood cholesterol increased (281) Dyspnoea (223) Oedema peripheral (198) Oedema (195) Fatigue (188)

What Other Drugs Cause Dyslipidaemia?

OLANZAPINE (230) ROSUVASTATIN (206) ARIPIPRAZOLE (185) METHOTREXATE (175) QUETIAPINE (161) ATORVASTATIN (155) RISPERIDONE (154) METFORMIN (151) TACROLIMUS (149) ZIPRASIDONE (149)

Which LORLATINIB Alternatives Have Lower Dyslipidaemia Risk?

LORLATINIB vs LORMETAZEPAM LORLATINIB vs LORNOXICAM LORLATINIB vs LOSARTAN LORLATINIB vs LOSARTAN\LOSARTAN LORLATINIB vs LOTEPREDNOL ETABONATE

Related Pages

LORLATINIB Full Profile All Dyslipidaemia Reports All Drugs Causing Dyslipidaemia LORLATINIB Demographics