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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 Intentional dose omission? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Intentional dose omission have been filed in association with LORLATINIB (Lorbrena). This represents 0.1% of all adverse event reports for LORLATINIB.

7
Reports of Intentional dose omission with LORLATINIB
0.1%
of all LORLATINIB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Intentional dose omission From LORLATINIB?

Of the 7 reports, 1 (14.3%) required hospitalization.

Is Intentional dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LORLATINIB. However, 7 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 Intentional dose omission?

DUPILUMAB (2,269) CERTOLIZUMAB PEGOL (1,253) ADALIMUMAB (845) TOFACITINIB (845) INFLIXIMAB (815) ABALOPARATIDE (623) ETANERCEPT (615) AMBRISENTAN (595) SODIUM OXYBATE (580) CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)

Which LORLATINIB Alternatives Have Lower Intentional dose omission Risk?

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

Related Pages

LORLATINIB Full Profile All Intentional dose omission Reports All Drugs Causing Intentional dose omission LORLATINIB Demographics