BOXED WARNING Severe myelosuppression — do not administer to patients with baseline neutrophil count <1,500 cells/mm3
FDA dosing
Population
Start
Target
Max
Metastatic breast cancer
Adults
260 mg/m2 IV over 30 min q3wk
260 mg/m2 q3wk
NSCLC (+ carboplatin)
Adults
100 mg/m2 IV over 30 min days 1, 8, 15 of each 21-day cycle
same
Pancreatic adenocarcinoma (+ gemcitabine)
Adults
125 mg/m2 IV over 30-40 min days 1, 8, 15 of each 28-day cycle
same
Renal No starting-dose adjustment required for renal impairment
Hepatic No adjustment for mild; reduce starting dose for moderate-severe; not recommended if AST >10x ULN or bilirubin >5x ULN
Instructions
Do not substitute for other paclitaxel products
Closely monitor infusion site for extravasation/infiltration
Available strengths
inj 6 mg/mL
Contraindications
Baseline neutrophil count <1,500 cells/mm3
Cautions
Severe myelosuppression / neutropenia
Sensory neuropathy
Sepsis (with gemcitabine)
Pneumonitis
Severe hypersensitivity reactions
Increased toxicity in hepatic impairment
Embryo-fetal toxicity
Adverse reactions
Alopecia
Neutropenia
Sensory neuropathy
Abnormal ECG
Fatigue/asthenia
Myalgia/arthralgia
AST and alkaline phosphatase elevation
Anemia
Nausea
Infections
Diarrhea
Pregnancy Can cause fetal harm based on mechanism and animal findings
Lactation Undefined
Cost
Paclitaxel (TAXOL)
Strength
#/mo
generic $/unit
CostPlus
6 mg/mL
inj
per unit
not offered
NADAC is a voluntary CMS survey of what retail community pharmacies pay for the drugs they stock. Paclitaxel is administered under clinical supervision and dispensed outside retail pharmacies, so it rarely appears on surveyed invoices.