Skyrizi (Risankizumab) – Psoriasis | HongKong DengYue Medicine
- Generic Name/Brand Name: Risankizumab/Skyrizi
- Indications: Psoriasis
- Dosage Form: Injection
- Specification: 150 mg × 1 syringe & 600 mg × 1 vial
Risankizumab Application Scope
Risankizumab is indicated for the treatment of adult patients with moderate to severe plaque psoriasis who are candidates for systemic therapy or phototherapy; active psoriatic arthritis; moderately to severely active Crohn’s disease; and moderately to severely active ulcerative colitis. In China, it was initially approved for adult moderate to severe Crohn’s disease, with potential expansions.

Risankizumab Characteristics
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Ingredients: Risankizumab
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Properties: Sterile, preservative-free solution; colorless to yellow (clear to slightly opalescent); pH 5.7 for most formulations, pH 6.2 for 90 mg/mL.
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Packaging Specification: Subcutaneous: 150 mg/mL single-dose prefilled syringe or pen (1 syringe/pen per carton); 90 mg/mL single-dose prefilled syringe (2 or 4 syringes per carton); 180 mg/1.2 mL (150 mg/mL) single-dose prefilled cartridge with accompanying autoinjector (kit); 360 mg/2.4 mL (150 mg/mL) single-dose prefilled cartridge with accompanying autoinjector (kit). Intravenous: 600 mg/10 mL (60 mg/mL) single-dose vial (1 vial per carton).
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Storage: Store in refrigerator at 36°F-46°F (2°C-8°C); do not freeze; protect from light in original carton; do not shake.
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Expiry Date: The expiration date is stated on individual vial, syringe, pen, or cartridge labels and outer carton after the designation ‘EXP’. Do not use the medicine after this expiration date.
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Executive Standard: U.S. FDA-approved prescribing information; complies with Chinese NMPA standards for approved formulations.
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Approval Number: 国药准字SJ20250008 for subcutaneous injection; JXSS2300052 for injection. U.S. License Number 1889.
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Date of Revision: June 2024 (based on available prescribing information).
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Manufacturer:AbbVie Inc.; in China: AbbVie Pharmaceutical Trading (Shanghai) Co., Ltd.
Guidelines for the Use of Risankizumab
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Dosage and Administration:
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Recommended Dose: Plaque psoriasis and psoriatic arthritis: 150 mg subcutaneous injection at Week 0, Week 4, and every 12 weeks thereafter. Crohn’s disease: Induction: 600 mg intravenous infusion at Week 0, Week 4, and Week 8; Maintenance: 180 mg or 360 mg subcutaneous at Week 12 and every 8 weeks thereafter (use lowest effective dose). Ulcerative colitis: Induction: 1,200 mg intravenous infusion at Week 0, Week 4, and Week 8; Maintenance: 180 mg or 360 mg subcutaneous at Week 12 and every 8 weeks thereafter (use lowest effective dose)
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Administration: Subcutaneous: Administer into thigh or abdomen (upper arm by professional/caregiver); initial doses under supervision, then self-administer after training. Intravenous: Dilute in 5% dextrose or 0.9% sodium chloride; infuse over at least 1 hour (Crohn’s) or 2 hours (ulcerative colitis); do not co-administer with other drugs. Inspect solution before use.
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Missed Dose: Administer as soon as possible, then resume regular schedule. Consult a healthcare professional if needed.
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Adverse Reactions:
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Common Adverse Reactions: Upper respiratory tract infections, headache, fatigue, injection site reactions, tinea infections (plaque psoriasis/psoriatic arthritis); arthralgia, abdominal pain, anemia, pyrexia, back pain, arthropathy, urinary tract infection (Crohn’s/ulcerative colitis maintenance).
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Serious Adverse Reactions: Hypersensitivity reactions (e.g., anaphylaxis); infections (including tuberculosis—screen prior); hepatotoxicity (monitor liver enzymes/bilirubin in IBD patients).
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Contraindications: Serious hypersensitivity to risankizumab-rzaa or any excipients.
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Precautions:
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Evaluate for tuberculosis and complete vaccinations before starting; avoid live vaccines; monitor for infections and hepatotoxicity; train patients on injection technique; rotate injection sites; if overdose occurs, seek medical advice.
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Risankizumab Interactions
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No clinically significant drug interactions with CYP substrates (e.g., caffeine, warfarin); increased infection risk with live vaccines—avoid concurrent use.
Note:
- If there is a new packaging for the drug, the new packaging shall prevail. The above information is sourced from DengYue Medicine.
- This content is for reference only. Prescription drugs must be used under a doctor’s guidance and purchased from authorized sources.









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