HPE Managing CINV pocket guide 2019 | Page 59

Additional information for IV administration • Infusion-site reactions: erythema, pruritus, pain, induration and thrombophlebitis • Lower risk of systemic hypersensitivity reactions and infusion-site adverse reactions compared to IV fosaprepitant 41 • Not interchangeable with fosaprepitant IV 7 • Infusion site reactions: majority including thrombophlebitis and vasculitis, reported with concomitant vesicant chemotherapy administration, particularly when associated with extravasation • Should always be diluted and given as a slow intravenous infusion • Not interchangeable with aprepitant IV 7 • No infusion site or anaphylactic reaction related to IV NEPA 72 • Safety profile generally similar to that seen with oral NEPA • IV NEPA may be better tolerated than other NK 1 RAs (clinical trial information: NCT03403712) • Quick onset of infusion-related hypersensitivity reactions (most reactions occur within first few minutes of administration) • Patients should be consulted to determine if they are hypersensitive to any component of the product, including soybean oil • In case of known allergies to legumes, soybean oil or other related allergens (including peanuts), monitor patients closely events (within 1 hour of infusion) compared with fosaprepitant. 7,36,41 An overview of intravenously administered NK 1 RA formulations is presented in Table 1. Netupitant Oral formulation NEPA is an oral fixed combination of the highly selective NK 1 RA netupitant 300mg and the pharmacologically and clinically distinct 5-HT 3 RA, palonosteron 0.5mg. Netupitant is not available as a single agent. Similar to aprepitant, it inhibits CYP3A4, so the possibility of drug–drug interactions must be taken hospitalpharmacyeurope.com | 2019 | 59