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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 Hepatic function abnormal? 23 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Hepatic function abnormal have been filed in association with LORLATINIB (Lorbrena). This represents 0.4% of all adverse event reports for LORLATINIB.

23
Reports of Hepatic function abnormal with LORLATINIB
0.4%
of all LORLATINIB reports
5
Deaths
14
Hospitalizations

How Dangerous Is Hepatic function abnormal From LORLATINIB?

Of the 23 reports, 5 (21.7%) resulted in death, 14 (60.9%) required hospitalization.

Is Hepatic function abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LORLATINIB. However, 23 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 Hepatic function abnormal?

NIVOLUMAB (1,131) PEMBROLIZUMAB (1,079) METHOTREXATE (1,054) CABOZANTINIB S-MALATE (912) CYCLOPHOSPHAMIDE (824) BEVACIZUMAB (769) PACLITAXEL (603) LENVATINIB (528) ATORVASTATIN (520) CYCLOSPORINE (508)

Which LORLATINIB Alternatives Have Lower Hepatic function abnormal Risk?

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

Related Pages

LORLATINIB Full Profile All Hepatic function abnormal Reports All Drugs Causing Hepatic function abnormal LORLATINIB Demographics