Product image of Inflectra (Infliximab) supplied by GNH India

Inflectra

Active Ingredient:
Infliximab
Origin:
EU

Inflectra (Infliximab)

Infliximab, the active ingredient in Inflectra, is a monoclonal antibody presented as a solution for infusion for intravenous use. It targets inflammatory pathways and is employed to manage autoimmune conditions such as rheumatoid arthritis, Crohn's disease, ulcerative colitis, ankylosing spondylitis, psoriatic arthritis and plaque psoriasis in adult patients.

GNH India supplies Inflectra as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides cold‑chain logistics for biologic products globally.

Manufacturer / TM Owner

Pfizer Europe Ma Eeig

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Indications & Clinical Uses

Inflectra (infliximab) acts on the tumor necrosis factor‑alpha pathway to control inflammation in several autoimmune diseases.

  • Rheumatoid arthritis: reduces joint inflammation, pain and structural damage, improving functional ability.
  • Crohn's disease: induces and maintains remission of intestinal inflammation, decreasing need for surgery.
  • Ulcerative colitis: controls colonic inflammation, helping achieve clinical remission and mucosal healing.
  • Ankylosing spondylitis: alleviates spinal pain and stiffness, slowing radiographic progression.
  • Psoriatic arthritis: diminishes joint swelling and skin lesions, enhancing quality of life.
  • Plaque psoriasis: clears skin plaques and reduces severity scores in moderate to severe cases.

How It Works

  • Infliximab is a chimeric IgG1 monoclonal antibody that binds with high affinity to soluble and transmembrane forms of tumor necrosis factor‑alpha (TNF‑α). By neutralizing TNF‑α, it prevents activation of downstream inflammatory cascades, reduces recruitment of immune cells, and inhibits cytokine production, thereby diminishing systemic and local inflammation associated with autoimmune disorders.

Side Effects

Inflectra may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Infusion‑related reactions such as fever, chills, or flushing.
  • Headache.
  • Nausea or vomiting.
  • Upper respiratory tract infections.

Serious or Rare Side Effects

  • Reactivation of latent tuberculosis or other serious infections.
  • Development of malignancies, including lymphoma.
  • Severe hypersensitivity reactions, including anaphylaxis.

Precautions & Warnings

Before initiating Inflectra therapy, several safety considerations should be evaluated.

  • Screen for latent tuberculosis: perform TB testing and treat if positive before starting.
  • Monitor for infections: watch for signs of bacterial, fungal or viral infections during treatment.
  • Assess cardiac function: avoid use in patients with moderate to severe heart failure.
  • Avoid live vaccines: do not administer live attenuated vaccines while receiving therapy.
  • Pregnancy and lactation: safety data are limited; use only if potential benefit justifies risk.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Inflectra can interact with other medicines, influencing efficacy or safety.

Major Interactions (Avoid)

  • Live vaccines: concurrent use may cause severe infection.
  • Concomitant anti‑TNF agents: combined immunosuppression increases infection risk.
  • Severe heart failure: may exacerbate condition.

Moderate Interactions (Monitor Closely)

  • Azathioprine or 6‑mercaptopurine: may increase risk of bone marrow suppression.
  • Methotrexate: may enhance immunosuppressive effect, requiring blood count monitoring.
  • Corticosteroids: additive infection risk, monitor for signs of infection.

Frequently Asked Questions

Inflectra (infliximab) is prescribed for several autoimmune disorders, including rheumatoid arthritis, Crohn's disease, ulcerative colitis, ankylosing spondylitis, psoriatic arthritis and moderate to severe plaque psoriasis. It is used in adult patients to reduce inflammation and improve disease‑specific outcomes.

Infliximab is a chimeric monoclonal antibody that binds to both soluble and membrane‑bound tumor necrosis factor‑alpha (TNF‑α). By neutralising TNF‑α, it blocks a key pro‑inflammatory cytokine, preventing downstream signalling that drives the chronic inflammation seen in the diseases it treats.

The dosing regimen for Inflectra is individualized by the prescribing clinician based on the specific indication, patient weight, disease severity and response to therapy. The prescriber decides the initial dose, infusion frequency and any subsequent adjustments.

The pregnancy category for infliximab is listed as unknown because limited human data are available. Use during pregnancy or lactation should only occur when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and after careful discussion with a healthcare professional.

To order Inflectra, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, cold‑chain shipping details and any necessary import documentation.

Inflectra is a biosimilar to the reference product Remicade and shares the same mechanism of action as other anti‑TNF biologics such as adalimumab and etanercept. Clinical studies have shown comparable efficacy and safety, while offering potential cost advantages in many markets.

Inflectra should be stored in a refrigerator at 2‑8 °C (36‑46 °F). Keep the vial in its original packaging, protect it from light, and do not freeze or shake the product. Once prepared for infusion, it should be used within the time frame specified by the manufacturer.

Inflectra is given as an intravenous infusion. The initial dose is typically administered over a period of 2 hours, followed by subsequent infusions at intervals determined by the treating physician, often every 6 to 8 weeks depending on the indication and patient response.

The most serious risks include reactivation of latent tuberculosis or other serious infections, development of certain malignancies such as lymphoma, severe heart failure exacerbation, and rare but life‑threatening hypersensitivity reactions like anaphylaxis. Patients should be monitored closely for these events.

Inflectra is contraindicated in patients with known hypersensitivity to infliximab, murine proteins, or any component of the formulation. It should also be avoided in individuals with active serious infections, untreated latent tuberculosis, or moderate to severe heart failure, unless the benefits clearly outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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