Dose Modification and Reinitiation of Therapy: Bortecade therapy should be withheld at the onset of any Grade 3 non-hematological or Grade 4 hematological toxicities excluding neuropathy as discussed as follows (see Precautions).
Once the symptoms of the toxicity have resolved, Bortecade therapy may be reinitiated at a 25% reduced dose (1.3 mg/m2/dose reduced to 1.0 mg/m2/dose; 1.0 mg/m2/dose reduced to 0.7 mg/m2/dose). The following table contains the recommended dose modification for the management of patients who experience Bortecade-related neuropathic pain and/or peripheral sensory neuropathy (Table 1). Patients with pre-existing severe neuropathy should be treated with Bortecade only after careful risk/benefit assessment. (See Table 1.)

Administration: Bortecade is administered as a 3-5 second bolus intravenous injection through a peripheral or central intravenous catheter followed by a flush with 0.9% sodium chloride solution for injection. The safety and effectiveness of Bortezomib in children has not been established.