benralizumab
Brand names: Fasenra
Fasenra is a medicine that can help treat severe asthma and EGPA. It works by lowering the number of eosinophils in your blood, which can reduce swelling in your lungs and blood vessels.
What it does
Fasenra is used to treat severe asthma in adults and children 6 years and older when used with other asthma medicines.
Common side effects
Headache, Sore throat, Fever
Key warnings
Serious allergic reactions can happen after you get a Fasenra shot.
How It Works
Fasenra is a special type of antibody that targets a protein called interleukin-5 receptor alpha (IL-5Rα). This protein is found on the surface of eosinophils. By attaching to this protein, Fasenra helps to lower the number of eosinophils in your blood.
How to Take It
Fasenra is given as a shot under the skin (subcutaneous injection). For asthma, adults and children 6 years and older usually get a 10mg or 30mg injection every 4 weeks for the first 3 doses. After that, you will get a shot once every 8 weeks. For EGPA, adults get a 30mg injection once every 4 weeks.
Pregnancy & Breastfeeding
There is not enough information to know if Fasenra will harm your unborn baby. Talk to your doctor if you are pregnant or plan to become pregnant. It is not known if Fasenra passes into breast milk. Talk to your doctor about the best way to feed your baby if you are taking Fasenra.
Missed Dose
If you miss a dose of Fasenra, call your doctor right away to reschedule your injection. Do not double your next dose.
Storage
Store Fasenra in the refrigerator between 36°F and 46°F (2°C and 8°C) in its original carton to protect it from light.
Side Effects (from patient reports)
Based on 12,182 FDA adverse event reports.
FDA Adverse Event Report Analysis
Detailed analysis of 17,680 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2012–2025.
Total Reports
17,680
Death-Related Reports
1,749
Hospitalization Reports
4,130
Top Indication
Asthma
Gender Distribution
Age Distribution
Most Reported Adverse Reactions (FAERS)
| # | Reaction | Reports |
|---|---|---|
| 1 | ASTHMA | 2,775 |
| 2 | DYSPNOEA | 1,802 |
| 3 | DEATH | 1,437 |
| 4 | DRUG INEFFECTIVE | 1,418 |
| 5 | COUGH | 944 |
| 6 | HEADACHE | 874 |
| 7 | PRODUCT DOSE OMISSION ISSUE | 825 |
| 8 | PNEUMONIA | 823 |
| 9 | WHEEZING | 692 |
| 10 | FATIGUE | 592 |
| 11 | MALAISE | 565 |
| 12 | INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION | 536 |
| 13 | ARTHRALGIA | 515 |
| 14 | PYREXIA | 510 |
| 15 | RASH | 486 |
Reactions in Death Reports
Reactions in Hospitalization Reports
Source: FDA FAERS (Adverse Event Reporting System) FDA FAERS (Adverse Event Reporting System) Reports are voluntary and do not establish causation
Serious Warnings
Serious allergic reactions can happen after you get a Fasenra shot. Tell your doctor right away if you have any signs of an allergic reaction, such as hives, swelling, or trouble breathing. Do not stop taking your steroid medicines suddenly when you start Fasenra. Your doctor will lower your steroid dose slowly, if needed. If you have a parasitic infection, it should be treated before you start Fasenra.
Common Questions
What should I tell my doctor before taking Fasenra?
Can Fasenra be used for sudden asthma attacks?
How will I know if Fasenra is working?
Can I stop taking my other asthma medicines while using Fasenra?
How is Fasenra given?
What if I have side effects from Fasenra?
How long will I need to take Fasenra?
Can children take Fasenra?
What does Fasenra look like?
Can I travel with Fasenra?
What are the common side effects of benralizumab?
What drug class is benralizumab?
Is benralizumab safe during pregnancy?
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What the FDA Data Shows for benralizumab
The FDA label for benralizumab (sold under brand names such as Fasenra) classifies it as a prescription-only medication in the Anti-IL-5R Monoclonal Antibody class. Fasenra is used to treat severe asthma in adults and children 6 years and older when used with other asthma medicines. Official labeling lists 3 commonly reported side effects, including Headache, Sore throat, Fever.
Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 12,182 voluntary reports. Interaction data is drawn directly from FDA-approved prescribing information. Acquisition-cost data is surveyed weekly by CMS and updated as manufacturers report changes.
Report counts do not establish causation — a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice — always consult a licensed healthcare provider before starting, stopping, or changing any medication.
Data Sources
Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS).
FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.
Last updated: September 17, 2024
Read our methodology — how this data is sourced, computed, and verified.
All federal data sources used on this page
- FDA Orange Book — approved drug products with therapeutic equivalence. accessdata.fda.gov/cder/ob
- FDA DailyMed — NIH-hosted drug labeling for FDA-approved meds. dailymed.nlm.nih.gov
- FDA Adverse Event Reporting System (FAERS) — post-marketing safety surveillance. fda.gov/drugs/faers
- NLM RxNorm — standardized clinical drug nomenclature. nlm.nih.gov/research/umls/rxnorm
- CMS Medicare Part B Drug Average Sales Price Files — federal drug pricing data. cms.gov/medicare/part-b-drugs/asp
- FDA Drug Shortages Database — current and resolved drug shortage tracking. accessdata.fda.gov/drugshortages