Prescription medication · Anti-IL-23 Monoclonal Antibody
risankizumab
Also sold as Skyrizi. Skyrizi is used to treat moderate to severe plaque psoriasis in adults.
Data updated 2026-05-15
- $20211.78
- Brand price (NADAC)
risankizumab (Skyrizi) is a prescription Anti-IL-23 Monoclonal Antibody. Skyrizi is used to treat moderate to severe plaque psoriasis in adults.
Skyrizi is a medicine that can help reduce inflammation in your body. It is used to treat conditions like psoriasis, psoriatic arthritis, Crohn's disease, and ulcerative colitis.
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Drug Pricing (NADAC)
Brand Price
$20211.78/unit
Generic Available
No
Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →
What it does
Skyrizi is used to treat moderate to severe plaque psoriasis in adults.
Common side effects
Upper respiratory infections (like a cold), Headache, Fatigue
Key warnings
Serious allergic reactions, including anaphylaxis, can happen.
The sections below are summarized in plain English from risankizumab's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.
How It Works
Skyrizi is a type of antibody that blocks a protein called interleukin-23 (IL-23). IL-23 causes inflammation in the body. By blocking IL-23, Skyrizi helps to reduce inflammation and the symptoms of certain diseases.
Serious Warnings
Serious allergic reactions, including anaphylaxis, can happen. If you have an infection, tell your doctor. Skyrizi may increase your risk of getting an infection or make an existing infection worse. Your doctor will check you for tuberculosis (TB) before you start Skyrizi. For inflammatory bowel disease, Skyrizi can cause liver problems. Your doctor will check your liver before and during treatment.
Common Questions
What should I tell my doctor before taking Skyrizi?
Can I get vaccines while taking Skyrizi?
What are the symptoms of an allergic reaction?
How often will I need to get injections?
Will Skyrizi cure my condition?
Can I take Skyrizi with other medications?
What if I have side effects?
How long does Skyrizi stay in my system?
Can Skyrizi affect my immune system?
What tests will I need before starting Skyrizi?
What are the common side effects of risankizumab?
What drug class is risankizumab?
What pregnancy or breastfeeding source fields are listed for risankizumab?
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betamethasone
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Betamethasone dipropionate cream is a strong steroid medicine used on the skin.
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Medication Guides
Understanding Drug Interactions
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Generic vs Brand Name Drugs
FDA requirements, cost savings, and when the difference matters
Narrow Therapeutic Index Drugs
FDA bioequivalence and label-record context for narrow therapeutic index medicines
Common Drug Interactions
Dangerous medication combinations and how to protect yourself
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What the FDA Data Shows for risankizumab
The FDA label for risankizumab (sold under brand names such as Skyrizi) classifies it as a prescription-only medication in the Anti-IL-23 Monoclonal Antibody class. Skyrizi is used to treat moderate to severe plaque psoriasis in adults. Official labeling lists 5 commonly reported side effects, including Upper respiratory infections (like a cold), Headache, Fatigue.
Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. Voluntary reports accumulate over the lifetime of a drug and reflect wide-ranging clinical use. Interaction data is drawn directly from FDA-approved prescribing information. NADAC pricing from CMS.
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 are separate source-record fields. This page is a public FDA/CMS registry and does not provide medical, treatment, substitution, or medication-change directions.
Data Sources
Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC).
FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. This registry does not provide medication decisions.
Last updated: September 3, 2025
PlainMeds is rendered directly from FDA openFDA/FAERS extracts, DailyMed labels, and CMS drug-pricing files, no number is typed in by an editor. FAERS counts, recalls, shortages, and price figures on this page are queried live from those federal extracts. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of 2026-05-15. Primary sources: openFDA / FAERS, DailyMed and CMS Part B ASP.
Read our methodology - how this data is sourced, computed, and verified.
Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled from the source snapshot dated . See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a data issue.
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