RISKS OF INCORRECT DOSING OF ORAL ANTI-CANCER MEDICINES
See Cytotoxic drugs p. 938.
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→Appendix 1: talazoparib
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▶Common or very common Alopecia. anaemia. appetite
decreased. asthenia. decreased leucocytes. diarrhoea.
dizziness. gastrointestinal discomfort. headache. nausea.
neutropenia. stomatitis. taste altered. thrombocytopenia
. vomiting
▶Frequency not known Bone marrow depression. neoplasms
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Manufacturer advises
effective contraception in women of childbearing potential
during treatment and for 7 months after receiving the last
dose. Male patients should use effective contraception
during and for at least 4 months after treatment if their
Immune system and malignant disease
partner is pregnant or of childbearing potential. See also
Pregnancy and reproductive function in Cytotoxic drugs
p. 938.
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Manufacturer advises avoid—toxicity in
animal studies. See also Pregnancy and reproductive
function in Cytotoxic drugs p. 938.
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Manufacturer advises avoid during
treatment and for 1 month after last dose—no information
available.
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Manufacturer advises avoid in
moderate or severe impairment unless benefit outweighs
risk (no information available).
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Manufacturer advises avoid if
creatinine clearance less than 30 mL/minute unless benefit
outweighs risk (no information available).
Dose adjustments Manufacturer advises reduce starting
dose to 750 micrograms once daily if creatinine clearance
30–60 mL/minute.
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Manufacturer advises
monitor full blood count before treatment initiation, then
monthly thereafter and as clinically indicated.
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