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Incompatibilities: This medicinal product must not be mixed with other medicinal products.
Special instructions for use and handling: Prior to administration, VECTIBIX is diluted in 0.9% sodium chloride to a maximum concentration of ≤ 10 mg/mL: VECTIBIX should be inspected visually prior to administration. The solution should be colorless and may contain visible translucent-to-white, amorphous, proteinaceous particulates (which will be removed by in-line filtration). Do not administer VECTIBIX if its appearance is not as described previously.
Do not use a hypodermic needle with a gauge less than a 21-gauge to withdraw the necessary amount of VECTIBIX for a dose of 6 mg/kg or 2.5 mg/kg as appropriate. Do not use needle-free devices (e.g., vial adapters) to withdraw vial contents.
Dilute in 0.9% sodium chloride injection USP/Ph Eur/JP to a maximum concentration of ≤ 10 mg/mL and total volume of 100 mL.
Diluted solution should be mixed by gentle inversion. DO NOT SHAKE.
Discard the vial and any liquid remaining in the vial after the single-use.
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