Table 3

Adverse drug events reactions in patients exposed to cancer chemotherapy, excluding neutropenic fever

ATC*DrugAgeAdverse drug eventNaranjo scoreAvoidable?Licensing state
LMethotrexateAdolescentPancreatitis4NoOff-label
LVincristineAdolescentConstipation7NoLicensed
LVincristineChildAtaxia and diarrhoea9NoLicensed
LVincristineChildAtaxia and diarrhoea10NoLicensed
LAsparagines7NoLicensed
LDoxorubicin7NoOff-label
LVincristineAdolescentRetinal haemorrhage7NoLicensed
LCarboplatin9NoUnlicensed
LEtoposideChildVomiting9NoUnlicensed
LCisplatin9NoUnlicensed
LDexrazoxaan9NoOff-label
LDoxorubicinChildAnaemia9NoUnlicensed
LCytarabineTrombopaenia, petechiea9NoOff-label
LMitoxantroneAdolescent9NoUnlicensed
LCytarabineTrombopaenia, petechiea10NoOff-label
LMitoxantroneAdolescent10NoUnlicensed
LMethotrexaat10NoOff-label
LMercaptopurine10NoOff-label
LVincristineChildLeucopaenia10NoOff-label
LVincristineBaby/toddlerConstipation6NoOff-label
  • *Anatomical Therapeutical Chemical (ATC) classification system of the WHO. A, alimentary tract and metabolism; C, cardiovascular system; J, anti-infectives for systemic use; L, antineoplastic and immunomodulating agents; N, nervous system.15

  • Patient age by means of EMeA criteria: preterm, newborn (0–1 month), baby/toddler (1 month–2 years), child (2–11 years), adolescent (12–18 years).

  • Probability measured by Naranjo score: ≤0 Adverse Drug Reactions (ADR) doubtful, 1–4 ADR possible, 5–8 ADR likely, ≥9 ADR certain.11

  • EMeA, European Medicines (Evaluation) Agency.