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What Is Inflectra?

Inflectra is a prescription tumor necrosis factor blocker containing infliximab-dyyb. It is biosimilar to Remicade. Current labeling includes Crohn disease, ulcerative colitis, rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, and plaque psoriasis under indication-specific criteria.

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What Is Inflectra?

Inflectra is a prescription tumor necrosis factor blocker containing infliximab-dyyb. It is biosimilar to Remicade. Current labeling includes Crohn disease, ulcerative colitis, rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, and plaque psoriasis under indication-specific criteria.

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How Does Inflectra Block TNF?

Infliximab-dyyb binds to soluble and transmembrane forms of tumor necrosis factor alpha and inhibits binding to TNF receptors. This reduces inflammatory signaling associated with several immune-mediated diseases.

Who Is Treated With Inflectra?

Inflectra is used in adults with Crohn disease, ulcerative colitis, rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, or plaque psoriasis. Pediatric labeling includes moderately to severely active Crohn disease and ulcerative colitis in patients age 6 and older.

How Is Inflectra Dosed?

Adult and pediatric Crohn disease and ulcerative colitis use 5 mg per kg intravenously at weeks 0, 2, and 6, then every 8 weeks. Rheumatoid arthritis uses 3 mg per kg on the same induction schedule and then every 8 weeks with methotrexate. Ankylosing spondylitis uses 5 mg per kg at weeks 0, 2, and 6, then every 6 weeks.

What Serious Risks Are Linked to Inflectra?

Inflectra carries boxed warnings for serious infections and malignancies. Risks include tuberculosis, invasive fungal infections, bacterial sepsis, lymphoma, and other cancers. Other serious concerns include hepatitis B reactivation, liver toxicity, heart failure, blood-cell abnormalities, neurologic reactions, and serious infusion reactions.

Frequently Asked Questions About Inflectra

Is Inflectra a biosimilar to Remicade?

Yes. Inflectra contains infliximab-dyyb and is biosimilar to Remicade.

What pediatric conditions does Inflectra treat?

Current labeling includes Crohn disease and ulcerative colitis in patients age 6 and older.

What is the standard Crohn disease induction schedule?

The labeled regimen uses 5 mg per kg intravenously at weeks 0, 2, and 6.

Does Inflectra have boxed warnings?

Yes. The boxed warnings concern serious infections and malignancies.

References

Biosimilar Product Information - U.S. Food and Drug Administration. https://www.fda.gov/drugs/biosimilars/biosimilar-product-information. Date Accessed October 2, 2026.

DailyMed - INFLECTRA - infliximab-dyyb injection, powder, lyophilized, for solution. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=37eaca10-d812-48bc-8b8e-b836bfa9968f. Date Accessed October 2, 2026.

FDA Approves Inflectra, a Biosimilar to Remicade. https://www.fda.gov/news-events/press-announcements/fda-approves-inflectra-biosimilar-remicade. Date Accessed October 2, 2026.

Infliximab Injection - MedlinePlus Drug Information. https://medlineplus.gov/druginfo/meds/a604023.html. Date Accessed October 2, 2026.

Purple Book Search - Inflectra. https://purplebooksearch.fda.gov/index.cfm?blaNo=125544&event=productdetails. Date Accessed October 2, 2026.