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    Therapeutic action

    • Neutralisation of rabies virus at wound sites


    • Prevention of rabies after category III exposure (except in patients who have received a full course of pre-exposure prophylaxis against rabies), in combination with rabies vaccine
    • Prevention of rabies after category II and III exposures in immunocompromised patients (even in patients who have received a full course of pre-exposure prophylaxis against rabies), in combination with rabies vaccine

    Forms and strengths, route of administration

    • Solution for injection, 300 IU in 1 ml ampoule (300 IU/ml) and 1500 IU in 5 ml ampoule (300 IU/ml) for infiltration into and around the wound

    Dosage and duration

    • Child and adult: 20 IU/kg single dose on D0, along with the first dose of rabies vaccine.
    • Infiltrate as much of the dose as possible into and around the wound(s), which has been cleaned beforehand.
    • In the event of multiple wounds, dilute the dose 2 to 3-fold with sterile 0.9% sodium chloride to obtain a sufficient quantity to infiltrate all the sites.
    • If HRIG is not available on D0, administer the first dose of rabies vaccine alone. Administer HRIG as soon as possible between D0 and D7; from D8, it is not necessary to administer rabies immunoglobulin as vaccine-induced antibodies begin to appear.

    Contra-indications, adverse effects, precautions

    • May cause: fever, headache, gastrointestinal disturbances, joint pain, local reactions at the injection site (pain, inflammation); rarely: anaphylactic reactions. 
    • Aspirate prior to injection to confirm that the needle is not in a vein and ensure that the HRIG does not enter a blood vessel (risk of shock).
    • For finger wounds, infiltrate with caution to avoid increased pressure in the tissue compartment.
    • If administered simultaneously with rabies immunoglobulin and other vaccines, use different syringes and injection sites.
    • Pregnancy and breast-feeding: no contra-indication


    • Purified equine rabies immunoglobulin F(ab’)2 fragments may replace HRIG if unavailable. The method of administration is the same but the dose is 40 IU/kg.


    –  Between 2 °C and 8 °C. Do not freeze.