High Alert
Absorption: IV administration results in complete bioavailability. Well absorbed from IM and SUBQ sites. Absorption follows intrapleural and intraperitoneal administration.
Distribution: Widely distributed; concentrates in skin, lungs, peritoneum, kidneys, and lymphatics.
Half-Life: 2 hr (↑ in renal impairment).
Contraindicated in:
Use Cautiously in:
↑risk of pulmonary toxicity and renal impairment in older adults
.CV: hypotension, peripheral vasoconstriction
Derm: hyperpigmentation, mucocutaneous toxicity, alopecia, erythema, rash, urticaria, vesiculation
GI: anorexia, nausea, stomatitis, vomiting
Hemat: anemia, leukopenia, thrombocytopenia
Local: pain at tumor site, phlebitis at IV site
Neuro: aggressive behavior, disorientation, weakness
Resp: pneumonitis, PULMONARY FIBROSIS
Misc: chills, fever, ANAPHYLACTOID REACTIONS
Drug-drug:
Monitor for anaphylactic (fever, chills, hypotension, wheezing) and idiosyncratic (confusion, hypotension, fever, chills, wheezing) reactions. Keep resuscitation equipment and medications nearby. Patients with lymphoma are at particular risk for idiosyncratic reactions that may occur immediately or several hr after therapy, usually after the 1st or 2nd dose.
Assess for dyspnea and fine rales, the earliest sign and symptom of pulmonary toxicity. Monitor chest x-ray every 12 wk during therapy. If pulmonary changes occur, hold bleomycin to determine if causal. Consider monitoring pulmonary diffusion capacity (DLco) at baseline and monthly during therapy. If DLco<3035% of baseline value, permanently discontinue bleomycin.
Lab Test Considerations:
Carboplatin should be administered in a monitored setting under the supervision of a physician experienced in cancer chemotherapy.
IV Administration: