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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 Condition aggravated? 57 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 57 reports of Condition aggravated have been filed in association with LORLATINIB (Lorbrena). This represents 1.0% of all adverse event reports for LORLATINIB.

57
Reports of Condition aggravated with LORLATINIB
1.0%
of all LORLATINIB reports
14
Deaths
16
Hospitalizations

How Dangerous Is Condition aggravated From LORLATINIB?

Of the 57 reports, 14 (24.6%) resulted in death, 16 (28.1%) required hospitalization, and 5 (8.8%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LORLATINIB. However, 57 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which LORLATINIB Alternatives Have Lower Condition aggravated Risk?

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

Related Pages

LORLATINIB Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated LORLATINIB Demographics