Does LORLATINIB Cause Product prescribing error? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product prescribing error have been filed in association with LORLATINIB (Lorbrena). This represents 0.2% of all adverse event reports for LORLATINIB.
9
Reports of Product prescribing error with LORLATINIB
0.2%
of all LORLATINIB reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product prescribing error From LORLATINIB?
Of the 9 reports.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LORLATINIB. However, 9 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 Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which LORLATINIB Alternatives Have Lower Product prescribing error Risk?
LORLATINIB vs LORMETAZEPAM
LORLATINIB vs LORNOXICAM
LORLATINIB vs LOSARTAN
LORLATINIB vs LOSARTAN\LOSARTAN
LORLATINIB vs LOTEPREDNOL ETABONATE