GNH USA

Europe — EMA

Inflectra

GNH USA supplies Inflectra (Infliximab), a TNF‑alpha inhibitor for rheumatoid arthritis, Crohn’s disease and ulcerative colitis. Request a quote for supply.

Infliximab

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What is Infliximab?

Infliximab, the active ingredient in Inflectra, is a monoclonal antibody presented as a sterile intravenous solution for infusion use. It targets inflammatory diseases by neutralizing tumor necrosis factor‑alpha and is prescribed for adults with autoimmune conditions. It is indicated for chronic inflammatory disorders and is administered under medical supervision in specialized care settings.

GNH USA 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.

What is Infliximab used for?

Inflectra is a TNF‑alpha inhibitor used to treat several chronic inflammatory diseases. - Rheumatoid arthritis: reduces joint inflammation and slows disease progression. - Crohn's disease: induces and maintains remission of intestinal inflammation. - Ulcerative colitis: helps achieve clinical remission and mucosal healing. - Ankylosing spondylitis: alleviates spinal pain and improves mobility. - Psoriatic arthritis: decreases joint swelling and skin lesions. - Plaque psoriasis: clears skin plaques and reduces scaling.

What are the side effects of Infliximab?

Inflectra may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects: - Infusion‑related reactions: flushing, chills, or shortness of breath during administration. - Headache: mild to moderate intensity, often transient. - Nausea: occasional gastrointestinal upset. - Infections: upper respiratory or urinary tract infections.

Serious or Rare Side Effects: - Severe infections: including opportunistic bacterial, fungal, or viral infections. - Reactivation of latent tuberculosis: may progress to active disease. - Demyelinating disorders: new or worsening neurologic symptoms such as optic neuritis.

What precautions apply to Infliximab?

Before starting Inflectra, clinicians should evaluate patients for factors that could increase risk of complications. - Screen for active infections: perform TB, hepatitis B/C, and HIV testing. - Monitor for latent tuberculosis: consider prophylactic therapy if indicated. - Assess cardiac function: avoid in patients with moderate to severe heart failure. - Update vaccinations: administer required non‑live vaccines before therapy. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Infliximab interact with?

Inflectra can interact with other agents that affect immune function or infection risk.

Major Interactions (Avoid): - Live vaccines: may cause uncontrolled infection; avoid concurrent use. - Antifungal azoles (e.g., ketoconazole): can increase serum infliximab levels, raising toxicity risk.

Moderate Interactions (Monitor Closely): - Methotrexate or other immunosuppressants: heightened infection susceptibility; monitor labs. - Systemic corticosteroids: additive immunosuppression; watch for signs of infection. - NSAIDs: may increase gastrointestinal bleeding risk; assess patient tolerance.

Frequently asked questions

What conditions is Inflectra used to treat?+
Inflectra is indicated for several chronic inflammatory disorders, including rheumatoid arthritis, Crohn's disease, ulcerative colitis, ankylosing spondylitis, psoriatic arthritis, and plaque psoriasis. It works by targeting the inflammatory pathway mediated by tumor necrosis factor‑alpha, helping to control symptoms and prevent disease progression.
How does infliximab, the active ingredient in Inflectra, work?+
Infliximab is a monoclonal antibody that binds specifically to both soluble and membrane‑bound tumor necrosis factor‑alpha (TNF‑α). By neutralizing TNF‑α, it interrupts the cascade of pro‑inflammatory signals that drive autoimmune inflammation, thereby reducing tissue damage and clinical signs of disease.
What is the usual dose of Inflectra?+
The dosing regimen for Inflectra is individualized and determined by the prescribing healthcare professional based on the specific indication, disease severity, patient weight, and response to therapy. Physicians follow approved labeling and clinical guidelines to set the infusion schedule and amount.
Is Inflectra safe to use during pregnancy or while breastfeeding?+
Data on the use of infliximab during pregnancy and lactation are limited. The drug crosses the placenta, especially in the third trimester, and may be present in breast milk. Clinicians weigh potential benefits against risks and generally reserve use for situations where no safer alternatives exist.
How do I order Inflectra from GNH USA?+
To request Inflectra, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, cold‑chain shipping details and necessary import documentation.
How does Inflectra compare with the main alternative drug or class?+
Inflectra is a biosimilar to the reference product Remicade (infliximab). Clinical studies have demonstrated comparable efficacy, safety, and immunogenicity. Compared with other TNF‑alpha inhibitors such as adalimumab or etanercept, infliximab is administered intravenously, allowing controlled dosing in a clinical setting.
What are the storage and handling requirements for Inflectra?+
Inflectra must be stored refrigerated between 2 °C and 8 °C. It should be kept in its original container, protected from light, and must never be frozen or shaken. Prior to infusion, the product is allowed to reach room temperature as directed by the prescribing information.
How is Inflectra administered to patients?+
Inflectra is given as an intravenous infusion in a healthcare facility. The initial dose is usually administered over a period of 2 hours, followed by subsequent infusions at intervals recommended for the specific indication, such as every 6 to 8 weeks for rheumatoid arthritis.
What are the most serious risks to watch for while receiving Inflectra?+
Serious risks include severe infections (including tuberculosis and opportunistic pathogens), reactivation of latent TB, demyelinating diseases, heart failure exacerbation, and rare malignancies. Patients should be monitored closely for signs of infection, neurological changes, or cardiac symptoms throughout therapy.
Who should not use Inflectra?+
Inflectra is contraindicated in individuals with known hypersensitivity to infliximab or any component of the formulation, and in patients with active serious infections, including untreated tuberculosis. Caution is also advised for those with moderate to severe heart failure or a history of demyelinating disorders.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Infliximab
Route
Intravenous Use
Manufacturer
Pfizer Europe Ma Eeig
Origin
EU

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