checkAd

     585  0 Kommentare TEZSPIRE approved for self-administration in the US with a new pre-filled pen - Seite 2

    Acute Asthma Symptoms or Deteriorating Disease

    TEZSPIRE should not be used to treat acute asthma symptoms, acute exacerbations, acute bronchospasm, or status asthmaticus.

    Abrupt Reduction of Corticosteroid Dosage

    Do not discontinue systemic or inhaled corticosteroids abruptly upon initiation of therapy with TEZSPIRE. Reductions in corticosteroid dose, if appropriate, should be gradual and performed under the direct supervision of a physician. Reduction in corticosteroid dose may be associated with systemic withdrawal symptoms and/or unmask conditions previously suppressed by systemic corticosteroid therapy.

    Parasitic (Helminth) Infection

    It is unknown if TEZSPIRE will influence a patient’s response against helminth infections. Treat patients with pre-existing helminth infections before initiating therapy with TEZSPIRE. If patients become infected while receiving TEZSPIRE and do not respond to anti-helminth treatment, discontinue TEZSPIRE until infection resolves.

    Live Attenuated Vaccines

    The concomitant use of TEZSPIRE and live attenuated vaccines has not been evaluated. The use of live attenuated vaccines should be avoided in patients receiving TEZSPIRE.

    ADVERSE REACTIONS

    The most common adverse reactions (incidence ≥3%) are pharyngitis, arthralgia, and back pain.

    USE IN SPECIFIC POPULATIONS

    There are no available data on TEZSPIRE use in pregnant women to evaluate for any drug-associated risk of major birth defects, miscarriage, or other adverse maternal or fetal outcomes. Placental transfer of monoclonal antibodies such as tezepelumab-ekko is greater during the third trimester of pregnancy; therefore, potential effects on a fetus are likely to be greater during the third trimester of pregnancy.

    INDICATION

    TEZSPIRE is indicated for the add-on maintenance treatment of adult and pediatric patients aged 12 years and older with severe asthma.

    TEZSPIRE is not indicated for the relief of acute bronchospasm or status asthmaticus.

    Full Prescribing Information including Patient Information and Instructions for Use.

    You may report side effects related to AstraZeneca products by clicking here.

    Notes

    TEZSPIRE pre-filled pen

    TEZSPIRE will be available as a fixed-dose 210mg subcutaneous injection via a pre-filled, single-use auto-injector (the TEZSPIRE pre-filled pen) or via a pre-filled, single-use syringe (the TEZSPIRE pre-filled syringe). Both are administered every four weeks.

    Seite 2 von 6



    Business Wire (engl.)
    0 Follower
    Autor folgen
    TEZSPIRE approved for self-administration in the US with a new pre-filled pen - Seite 2 AstraZeneca and Amgen’s TEZSPIRE (tezepelumab-ekko) has been approved in the US for self-administration in a pre-filled, single-use pen for patients aged 12 years and older with severe asthma. TEZSPIRE is the only biologic approved for severe asthma …