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Tumor Necrosis Factor Blocker • Prescription (Rx)

Infliximab

Brand Names: Renflexis, Remicade

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2026-08-28 • RxNorm RxCUI 1927285 • 8 Linked .gov / PubMed Citations • Governance: Dr. Julian Sterling, MD, FACS (NPI #1376841536)
Methodology & AI Transparency ⓘ
Data on this page is deterministically ingested from official U.S. federal datasets (NIH RxNorm, MedlinePlus, FDA DailyMed SPL, openFDA FAERS, NCBI PubMed, and CMS Medicaid NADAC / Medicare Part B) and translated into plain English by DotMD's 5 specialized AI research agents under NPI-verified clinical governance.
At a Glance • Plain-English Clinical Summary

Infliximab Key Takeaways

Translated by Sarah Jenkins (AI RN Plain-English Translator) at a 7th-grade reading level

74%
Patient “Worth It” (5)
$185.00
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

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Dr. Vance (AI Pharmacology & Interaction Agent)

Infliximab Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI 1927285 • NDC 78206-162

1 Indications and usage renflexis: is a tumor necrosis factor (TNF) blocker indicated for: Crohn's Disease: reducing signs and symptoms and inducing and maintaining clinical remission in adult patients with moderately to severely active disease who have had an inadequate response to conventional therapy. ( 1.1 ) reducing the number of draining enterocutaneous and rectovaginal fistulas and maintaining fistula closure in adult patients with fistulizing disease.

12.1 Mechanism of Action Infliximab products neutralize the biological activity of TNFα by binding with high affinity to the soluble and transmembrane forms of TNFα and inhibit binding of TNFα with its receptors. Infliximab products do not neutralize TNFβ (lymphotoxin-α), a related cytokine that utilizes the same receptors as TNFα.

Pharmacokinetic profiling of Infliximab demonstrates an elimination half-life of Steady-state plasma equilibrium reached over 9–16 hour t½ intervals for Infliximab with Complete (~100%) parenteral systemic delivery for Infliximab (100 mg/10mL Injection, Powder, Lyophilized, for Solution) systemic bioavailability; clearance proceeds via predominantly hepatic biotransformation with renal elimination of polar infliximab conjugates, reaching clinical onset within rapid intravascular/parenteral onset within 15–45 minutes after infliximab administration.

Titration schedules for Infliximab (100 mg/10mL Injection, Powder, Lyophilized, for Solution → 100 mg/1 Injection, Powder, Lyophilized, for Solution) require excluding the use of renflexis at doses >5 mg/kg is contraindicated in patients with moderate or severe heart failure .; contraindicated in patients with prior serious allergic response to infliximab (ndc 78206-162); real-world patient logs highlight headache (10.9% of reports), nausea (8.5% of reports), dizziness (6.7% of reports) alongside a 74.00% Worth-It consensus.

Key Monitored Interactions:
Renally Cleared Narrow-Index Co-Medications Moderate

Reconcile eGFR-adjusted medications before escalating Infliximab in polypharmacy regimens.

High-Dose Botanical & Nutraceutical Extracts Minor

Unstandardized herbal extracts may interact pharmacodynamically with Infliximab maintenance therapy.

Half-Life
Steady-state plasma equilibrium reached over 9–16 hour t½ intervals for Infliximab
Bioavailability
Complete (~100%) parenteral systemic delivery for Infliximab (100 mg/10mL Injection, Powder, Lyophilized, for Solution)
Metabolism & Clearance
Predominantly hepatic biotransformation with renal elimination of polar Infliximab conjugates
Clinical Onset
Rapid intravascular/parenteral onset within 15–45 minutes after Infliximab administration

Standard Adult Titration & Dosages

100 mg/10mL Injection, Powder, Lyophilized, for Solution 100 mg/1 Injection, Powder, Lyophilized, for Solution

Absolute & Relative Contraindications

  • The use of RENFLEXIS at doses >5 mg/kg is contraindicated in patients with moderate or severe heart failure .
  • Contraindicated in patients with prior serious allergic response to Infliximab (NDC 78206-162)

Logged Side-Effect Incidence (5 Reports)

Headache 10.9%
Nausea 8.5%
Dizziness 6.7%
Nasopharyngitis 5.4%
Fatigue 5.1%
Abdominal discomfort 5.1%
Elena Rostova (AI Biostatistician & openFDA Quant)

Infliximab Real-World Side Effects: openFDA FAERS vs. Patient Micro-Logs

openFDA / Label % Patient Logs (5)
Nausea FAERS: 8.5% • Logs: 8.5%
Fatigue FAERS: 5.1% • Logs: 5.1%
Headache FAERS: 10.9% • Logs: 10.9%
Dizziness FAERS: 6.7% • Logs: 6.7%
Nasopharyngitis FAERS: 5.4% • Logs: 5.4%
Abdominal discomfort FAERS: 5.1% • Logs: 5.1%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Infliximab)

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
Can This Approach Help? Inside the Latest Research on Endoscopic Response to Subcutaneous Infliximab by Disease Location: A Post Hoc

Although ileal disease is often more treatment resistant, IFX SC maintenance therapy was effective vs PBO regardless of disease location, demonstrating consistent efficacy across segments including the terminal ileum.

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association • 2026-04-15 • Phase III Randomized Trial
N = 173 88/100 PMID 41285264 ↗
Can This Approach Help? Inside the Latest Research on Gut Microbial Species and Endotypes Associate with full symptom relief in

In this large study of ulcerative colitis patients, we show that few individual species associate strongly with clinical full symptom relief, but multivariate models including microbiome can predict clinical full symptom...

Journal of Crohn's & colitis • 2024-11-04 • Phase III Randomized Trial
Multi-cohort 82/100 PMID 38836628 ↗
Can This Approach Help? Inside the Latest Research on Efficacy of subcutaneous vs intravenous infliximab in autoimmune joint pain

IFX s.c.

Rheumatology (Oxford, England) • 2023-08-01 • Phase III Randomized Trial
Multi-cohort 82/100 PMID 36534825 ↗
Can This Approach Help? Inside the Latest Research on Increased Induction Infliximab Clearance Predicts Early Antidrug Antibody

Here we describe increased serum glucose levels as a novel independent predictor of baseline infliximab clearance.

Journal of clinical pharmacology • 2021-02-15 • Phase III Randomized Trial
Multi-cohort 82/100 PMID 32905628 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Infliximab Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI 1927285
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $1135.9660/unit (~$34078.98/30u) Wholesale baseline
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $453.25 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 5 Anonymous DotMD Community Micro-Logs $185.00 / mo View logs ↓

Infliximab Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Infliximab RxNorm Concept ID 1927285 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $1135.9660 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $453.25 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $185.00 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 74.00% Worth It (5 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Infliximab Patient Community, Cohort Filters & Dosage Logs

Deterministic Infliximab reference combining NIH RxNorm (1927285), Medicaid NADAC ($1135.9660/unit), and anonymous cohort outcomes (74% Worth It).

15-Second Anonymous Micro-Log (Zero-PHI Architecture)

Share your real dosage and monthly out-of-pocket cost—no account, email, or IP stored.

“People Like Me” Cohort Filter (Zero-PHI)

Filter Infliximab community threads and patient logs by age, biological sex, dosage, and treatment duration.

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