FASENRA
Pronunciation: ben-ra-LIZ-yoo-mab


What it isIL-5 receptor monoclonal antibody that depletes eosinophils; severe eosinophilic asthma and EGPA.
Why this oneIt causes near-complete depletion by antibody-dependent cytotoxicity rather than neutralizing IL-5; for asthma, every-eight-week maintenance dosing.
What limits itBenefit tracks eosinophil count. Hypersensitivity can end treatment; treat helminths first and never use it for acute bronchospasm.
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| FDA dosing | Population | Start | Target | Max |
|---|---|---|---|---|
| Severe eosinophilic asthma (add-on maintenance) | Adults & pediatric ≥12 yr | 30 mg SC q4wk ×3 doses | then 30 mg SC q8wk | — |
| Severe eosinophilic asthma (add-on maintenance) | Pediatric 6–11 yr, <35 kg | 10 mg SC q4wk ×3 doses | then 10 mg SC q8wk | — |
| Severe eosinophilic asthma (add-on maintenance) | Pediatric 6–11 yr, ≥35 kg | 30 mg SC q4wk ×3 doses | then 30 mg SC q8wk | — |
| Eosinophilic granulomatosis with polyangiitis (EGPA) | Adults | — | 30 mg SC q4wk | — |
| Hypereosinophilic syndrome (HES) | Adults & pediatric ≥12 yr | — | 30 mg SC q4wk | — |
Renal Undefined
Hepatic Undefined
Available strengths
Pregnancy Insufficient data; monoclonal antibody crosses placenta (3rd trimester).
Lactation No human milk data; IgG present in human milk in small amounts.
| Strength | #/mo | generic $/unit | CostPlus | |
|---|---|---|---|---|
| 30 mg/mL | inj | per unit | not offered |
NO BOXED WARNINGS
Principal riskHypersensitivity reactions; not a rescue for acute asthma