GNH USA

Europe — EMA

Inflectra

GNH USA supplies Inflectra (Infliximab), a monoclonal antibody (TNF‑alpha inhibitor) for rheumatoid arthritis, Crohn's disease and other inflammatory

Infliximab

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What is Infliximab?

Infliximab, the active ingredient in Inflectra, is a monoclonal antibody (TNF‑alpha inhibitor) presented as a solution for infusion for intravenous use. It treats autoimmune and inflammatory conditions such as rheumatoid arthritis, Crohn's disease, ulcerative colitis, ankylosing spondylitis, psoriatic arthritis and plaque psoriasis.

GNH USA supplies Inflectra as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Infliximab used for?

Inflectra is a biologic that targets the TNF‑alpha pathway, providing disease‑modifying benefits across several inflammatory disorders. - Rheumatoid arthritis: reduces joint inflammation and slows structural damage. - Crohn's disease: induces and maintains remission of intestinal inflammation. - Ulcerative colitis: helps achieve clinical remission and mucosal healing. - Ankylosing spondylitis: improves spinal mobility and reduces pain. - Psoriatic arthritis: decreases joint damage and skin lesions. - Plaque psoriasis: clears skin plaques and reduces disease severity.

What are the side effects of Infliximab?

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

Common Side Effects: - Infusion‑related reactions (fever, chills, flushing, dyspnea). - Upper respiratory tract infections. - Headache. - Nausea.

Serious or Rare Side Effects: - Severe infections such as tuberculosis, sepsis, or opportunistic fungal infections. - Hepatotoxicity, including elevated liver enzymes and hepatitis. - Malignancies, notably lymphoma and other solid tumors. - Exacerbation of congestive heart failure.

What precautions apply to Infliximab?

Before and during treatment with Inflectra, several safety measures should be observed. - Screening for latent TB: perform tuberculin skin test or interferon‑γ release assay prior to initiation. - Monitor for infections: promptly evaluate any signs of bacterial, viral, or fungal infection. - Assess liver function: conduct baseline and periodic hepatic enzyme tests. - Evaluate cardiac status: avoid use in patients with moderate to severe heart failure. - Vaccination: administer required vaccines before therapy; avoid live vaccines while receiving Inflectra. - 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 medicines, influencing safety or effectiveness.

Major Interactions (Avoid): - Live vaccines: concurrent administration may cause uncontrolled infection. - Other potent immunosuppressants (e.g., azathioprine, cyclophosphamide): increase risk of serious infections. - Cytokine‑targeted agents (e.g., anakinra, canakinumab): additive immunosuppression may be hazardous.

Moderate Interactions (Monitor Closely): - Antifungal azoles (ketoconazole, itraconazole): may raise infliximab serum levels. - Live bacterial vaccines (e.g., BCG): consider timing to avoid overlap. - Concomitant corticosteroids: may enhance infection risk; monitor closely.

Frequently asked questions

What conditions is Inflectra used to treat?+
Inflectra is indicated for several immune‑mediated inflammatory diseases, including rheumatoid arthritis, Crohn's disease, ulcerative colitis, ankylosing spondylitis, psoriatic arthritis and plaque psoriasis. In each condition it works to reduce inflammation and modify disease progression.
How does infliximab work in the body?+
Infliximab is a monoclonal antibody that binds tightly to tumor necrosis factor‑alpha (TNF‑α), a key cytokine driving inflammation. By neutralising both soluble and membrane‑bound TNF‑α, it prevents activation of TNF receptors, thereby dampening the inflammatory cascade that underlies the listed autoimmune disorders.
What is the usual dosing schedule for Inflectra?+
The dosing regimen for Inflectra is individualized by the prescribing clinician based on the specific indication, patient weight, disease severity and response to therapy. Healthcare professionals determine the infusion dose, frequency and any subsequent adjustments.
Is Inflectra safe to use during pregnancy or breastfeeding?+
Safety data for infliximab in pregnancy and lactation are limited, and the product carries an unknown pregnancy category. Clinicians should weigh potential benefits against risks and discuss options with the patient. Breastfeeding decisions should also be made in consultation with a healthcare provider.
How do I order Inflectra from GNH USA?+
To place an order, submit an enquiry on the Inflectra product page at gnh-usa.com, specifying the required quantity. GNH USA works with 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 other TNF‑alpha inhibitors?+
Inflectra (infliximab) is a chimeric monoclonal antibody administered intravenously, whereas other TNF‑alpha blockers such as adalimumab or etanercept are fully human or receptor‑fusion proteins given subcutaneously. Clinical efficacy is comparable across many indications, but differences in administration route, dosing frequency and immunogenicity may influence choice.
What are the storage requirements for Inflectra?+
Inflectra must be stored refrigerated at 2‑8 °C. Keep the vials in their original packaging, protect them from light, and do not freeze or shake the solution. If the product reaches room temperature, it should be used promptly and not re‑refrigerated.
How is Inflectra administered to patients?+
Inflectra is supplied as a sterile solution for intravenous infusion. The infusion is performed in a clinical setting by qualified healthcare personnel, typically over a period of 2 hours for the initial dose, with subsequent infusions given at intervals defined by the treating physician.
What are the most serious risks associated with Inflectra?+
The most serious risks include severe infections such as tuberculosis or opportunistic fungal infections, reactivation of hepatitis B, infusion‑related severe reactions, heart failure exacerbation, and rare malignancies like lymphoma. Patients should be monitored closely for any signs of these events.
Who should not receive Inflectra?+
Inflectra is contraindicated in patients with known hypersensitivity to infliximab or any component of the formulation, and in those with active serious infections. Caution is advised for individuals with moderate to severe heart failure, demyelinating disorders, or a history of malignancy.
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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