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Prescribing Information Tezspire®▼(tezepelumab)
Adverse Event Reporting
Safety Information

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TEZSPIRE® (tezepelumab): Dosing
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TEZSPIRE® (tezepelumab): dosing & administration

 

See full indication

 

One dose every 28 days in eligible adults and adolescents 12 years and older1:

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Images are not of real patients and have been used for illustrative purposes only.

  • 210 mg every 28 days, no loading dose required 
  • No biomarker restriction (bEOS, IgE and FeNO)
  • Tezspire may be self-administered (after training on technique) or administered by a caregiver

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Refer to SmPC before initiation and for full dosing recommendations.

TEZSPIRE is intended for long-term treatment. A decision to continue the therapy should be made at least annually based on the patient's level of asthma control.1
Patients with a history of anaphylaxis should be monitored for an appropriate time after administration.1

GUIDANCE FOR STORAGE

Store in a refrigerator (2ºC – 8ºC). Keep the pre-filled pen or pre-filled syringe in the outer carton to protect from light. Do not freeze. Do not shake. Do not expose to heat.1

 

TEZSPIRE (tezepelumab) is indicated as an add-on maintenance treatment in adults and adolescents 12 years and older with severe asthma who are inadequately controlled despite high dose inhaled corticosteroids plus another medicinal product for maintenance treatment1

bEOS=blood eosinophils; IgE=immunoglobulin E; FeNO=fractional exhaled nitric oxide

 

  1. Tezspire (tezepelumab). Summary of Product Characteristics. 2022. Available at: https://www.medicines.org.uk/emc/product/14064/smpc (last accessed: November 2024).

GB-56894 | November 2024

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to AstraZeneca by visiting https://contactazmedical.astrazeneca.com/ or by calling ‌‌‌0‌‌‌8‌‌‌‌‌0‌‌‌‌0‌‌‌ ‌‌7‌‌‌‌‌‌8‌‌‌3‌‌‌ ‌‌0‌‌‌‌‌0‌‌‌‌3‌‌‌‌3‌‌‌.

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