What is Fraizeron? Uses, Side Effects & Expert Tips You Must Know

What is Fraizeron (secukinumab)? When is this biologic medication prescribed? What critical safety information do patients need to know? SignsSymptomsList provides expert insights backed by clinical data and medical guidelines.
Active ingredient: secukinumab
Drug class: Interleukin-17A (IL-17A) inhibitor
Brand alternatives: Cosentyx®
Table of Contents
- What is Fraizeron?
- FDA-Approved Uses
- Contraindications
- Administration Guide
- Dosage Protocols
- Clinical Trial Safety Data
- Drug Interactions
- Patient Safety Checklist
- Special Populations
- Overdose Management
- Missed Dose Protocol
- Storage Requirements
What is Fraizeron? Key Mechanism Explained
Fraizeron contains secukinumab, a monoclonal antibody targeting interleukin-17A (IL-17A). This cytokine plays a central role in inflammatory pathways:
- Blocks IL-17A receptors with 94% target occupancy at 12 weeks[1]
- Reduces production of pro-inflammatory cytokines (IL-6, TNF-α)
- Shows 80% PASI 75 improvement in psoriasis patients vs placebo[2]

FDA-Approved Uses of Fraizeron
Condition | Approval Status | Efficacy Data |
---|---|---|
Moderate-Severe Plaque Psoriasis | First-line biologic | 83% skin clearance (CLEAR study)[3] |
Psoriatic Arthritis | DMARD combination therapy | 67% ACR20 response at 24 weeks[4] |
Ankylosing Spondylitis | After NSAID failure | 61% ASAS40 improvement[5] |
For comprehensive understanding of spondylitis, read: Ankylosing Spondylitis: Diagnosis & Advanced Treatments
Absolute Contraindications
- Active tuberculosis (TB) or untreated latent TB
- History of anaphylaxis to secukinumab
- Concurrent live vaccines (MMR, varicella)
Step-by-Step Administration Guide
- Rotate injection sites (thighs, abdomen, upper arms)
- Use 27-gauge needle for subcutaneous delivery
- Avoid psoriatic lesions by 3cm margin
Dosage Protocols by Condition
Condition | Loading Dose | Maintenance |
---|---|---|
Plaque Psoriasis | 300mg weekly x4 | 300mg monthly |
Psoriatic Arthritis | 150-300mg weekly x4 | 150-300mg monthly |
Ankylosing Spondylitis | 150mg weekly x4 | 150mg monthly |
Dietary considerations for psoriasis patients: Psoriasis Nutrition Guide: 7 Evidence-Based Tips
Safety Profile: Clinical Trial Data (N=3439)
Side Effect | Frequency | Severity |
---|---|---|
Upper Respiratory Infection | 27% | Mild |
Oral Herpes | 14% | Moderate |
Neutropenia | 8% | Reversible |

Critical Drug Interactions
- 🛑 Live vaccines: Avoid for 12 weeks post-treatment
- ⚠️ CYP450 substrates: Potential altered metabolism
6-Point Safety Checklist
- Screen for TB with interferon-gamma test
- Monitor for inflammatory bowel disease onset
- Check CBC monthly for neutropenia
Special Population Guidelines
Group | Recommendation |
---|---|
Pregnancy (Category B) | Discontinue 20 weeks pre-conception |
Lactation | Pump-and-dump for 20 weeks post-dose |
Pediatrics | Not approved <18>18> |
Essential reading: Pregnancy Medication Safety Guide
Overdose Protocol
- Maximum tested dose: 30mg/kg (no severe events)
- Contact Poison Control: +1-800-222-1222
Missed Dose Management
If >7 days late:
1. Administer missed dose immediately
2. Reset schedule from last dose date
Storage Specifications
- Unopened: 2-8°C (do not freeze)
- In-use: 25°C for max 24 hours
References:
[1] IL-17 Inhibition Mechanism Study
[2] FDA Prescribing Information
[3] CLEAR Trial Data 2020