High Alert
Contraindicated in:
Pregnancy
;Use Cautiously in:
Derm: alopecia, facial flushing, photosensitivity, rash
Endo: gonadal suppression
GI: anorexia, nausea, vomiting, diarrhea, HEPATIC NECROSIS, hepatic vein thrombosis
Hemat: anemia leukopenia thrombocytopenia
Local: pain at IV site, phlebitis at IV site, tissue necrosis
MS: myalgia
Neuro: facial paresthesia, malaise
Misc: ANAPHYLAXIS, fever, flu-like syndrome
Drug-drug:
Malignant Melanoma
Hodgkin Disease
Absorption: IV administration results in complete bioavailability.
Distribution: Widely distributed to tissues; probably concentrates in liver; some CNS penetration.
Half-Life: 5 hr (↑ in renal and hepatic impairment).
(effects on blood counts)
ROUTE | ONSET | PEAK | DURATION |
---|---|---|---|
IV (WBCs) | 1620 days | 2125 days | 35 days |
IV (platelets) | unknown | 16 days | 35 days |
May cause fetal harm. Advise women of reproductive potential to notify health care provider if pregnancy is planned or suspected and to avoid breastfeeding during therapy. Advise patient of the need for a nonhormonal method of contraception.
NDC Code