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FASENRA SOLUTION FOR INJECTION 30MG/ML (PRE-FILLED SYRINGE) [SIN15683P]
Active ingredients: FASENRA SOLUTION FOR INJECTION 30MG/ML (PRE-FILLED SYRINGE)
Last updated 26 October 2025
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Product Info
FASENRA SOLUTION FOR INJECTION 30MG/ML (PRE-FILLED SYRINGE)
[SIN15683P]
Product information
Active Ingredient and Strength | BENRALIZUMAB - 30 MG/ML |
Dosage Form | INJECTION, SOLUTION |
Manufacturer and Country | ASTRAZENECA PHARMACEUTICALS LP FREDERICK MANUFACTURING CENTER (FMC) (DP INTERMEDIATE) - UNITED STATES |
Registration Number | SIN15683P |
Licence Holder | ASTRAZENECA SINGAPORE PTE LTD |
Forensic Classification | PRESCRIPTION ONLY MEDICINES |
Anatomical Therapeutic Chemical (ATC) code | R03DX10 |
4.1 Therapeutic indication
FASENRA is indicated as an add-on maintenance treatment in adult patients with severe eosinophilic asthma inadequately controlled despite high-dose inhaled corticosteroids plus long-acting β-agonists.
4.2 Posology and method of administration
Posology
The recommended dose is 30 mg of FASENRA by subcutaneous injection every 4 weeks for the first 3 doses, and then every 8 weeks thereafter.
FASENRA is intended for long-term treatment. A decision to continue the therapy should be made at least annually based on disease severity, level of exacerbation control and blood eosinophil counts.
Paediatric population
Available data of FASENRA in adolescents aged 12 to less than 18 years are described in section 5.1, however no posology recommendations can be made – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information.
The safety and efficacy of FASENRA in children aged less than 12 years have not been established.
Elderly patients
No dose adjustment is required for elderly patients (see section 5.2 – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).
Renal and hepatic impairment
No dose adjustment is required for patients with renal or hepatic impairment (see section 5.2 – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).
Method of administration
FASENRA is administered as a subcutaneous injection. In line with clinical practice, monitoring of patients after administration of biologic agents is recommended (see section 4.4, Hypersensitivity Reactions – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).
Administer FASENRA into the thigh, or abdomen. If somebody else administers the injection, the upper arm can also be used. Do not administer into areas where the skin is tender, bruised, erythematous, or hardened.
A patient may self-inject FASENRA or the patient’s caregiver may administer FASENRA if their healthcare professional determines it is appropriate. However, the healthcare professional should ensure appropriate initiation and follow-up of patients. Proper training in subcutaneous injection technique using the prefilled syringe should be provided according to the ‘Instructions for Use’ – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information.
4.3 Contraindications
FASENRA is contraindicated in patients who have known hypersensitivity to benralizumab or any of its excipients (see section 4.4 – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).