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Tavneos

Sourced directly from the authorized manufacturer network to ensure authenticity and quality.

Ready to proceed? Start a request for Tavneos on our secure patient portal to submit your prescription, upload documents and track your approval status.

Tavneos

Supplied with complete CDSCO-approved import and customs documentation, including Form 12A & 12B, CDEC, GST Bill of Entry, Commercial Invoice, and Packing List.

Medicine Name: Tavneos
Generic Name (API): Avacopan
Dosage Form & Strength: 10 mg
Route: Oral
Drug Class:

Manufacturer / Innovator:

Switzerland

Regulatory Approval:

  • FDA (US)
  • HC (Canada)
  • EMA (Europe) – revoked August 2026
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    Temperature-controlled logistics ensuring safe, reliable, and timely medicine delivery.

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Understanding Tavneos and Its Medical Uses

Tavneos (avacopan) is an oral complement C5a receptor antagonist approved for the adjunctive treatment of adult patients with severe active anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis — specifically granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA) — used in combination with standard therapy including glucocorticoids.

How Tavneos Works

Tavneos blocks the C5a receptor, part of the complement system that drives inflammation and tissue damage in ANCA-associated vasculitis. By blocking this pathway, Tavneos helps reduce inflammatory activity, allowing for reduced reliance on high-dose glucocorticoids over time.

Approved Patient Population

Tavneos is intended for adults with severe active GPA or MPA as an add-on to standard therapy, not as a standalone treatment, and is typically used to help reduce glucocorticoid exposure during vasculitis management.

Dosage and Administration

The recommended dose of Tavneos is 30 mg (three 10 mg capsules) taken orally twice daily with food.

Warnings and Precautions for Tavneos

Tavneos does not carry a formal FDA boxed warning. However, patients and prescribers should be aware of the following important safety information.

Hepatotoxicity

Serious hepatotoxicity, including cases of vanishing bile duct syndrome, has been reported. Liver function should be monitored before and periodically during treatment.

Serious Hypersensitivity Reactions

Serious hypersensitivity reactions, including angioedema, have been reported. Tavneos should be discontinued if a serious reaction occurs.

Hepatitis B Reactivation

Reactivation of hepatitis B virus has occurred in some patients. Screening for hepatitis B prior to treatment is recommended where appropriate.

Serious Infections

Tavneos may increase susceptibility to infections, particularly when used alongside other immunosuppressive therapies. Patients should be monitored for signs of infection throughout treatment.

How to Access Tavneos in India: A 6-Step Process

Step 1 – Search & request your medicine: The patient or treating doctor submits a request with basic details to initiate the access process.

Step 2 – Verification & eligibility review: The team verifies availability and reviews eligibility against regulatory and clinical requirements to ensure a compliant pathway.

Step 3 – Receive quote & delivery timeline: A transparent quotation is shared, covering medicine cost, logistics, and a clear delivery timeline.

Step 4 – Regulatory approval process: Assistance is provided to secure the approvals and documentation required for legal cross-border access.

Step 5 – Temperature-controlled import & handling: The medicine is sourced and transported under strict GDP-compliant conditions to maintain product integrity.

Step 6 – Secure delivery: The medicine is delivered to the patient or treating hospital, with updates provided at each stage.

Note: From request to delivery, every step is designed to ensure your treatment reaches you safely, compliantly, and without unnecessary delays.

Documentation and Availability of Tavneos

Tavneos is manufactured and marketed by Vifor Fresenius Medical Care Renal Pharma for European markets. It is sourced through authorized distribution channels for patients seeking named-patient import into India.

Required Documentation

Patients typically need a valid prescription from a treating rheumatologist or nephrologist confirming ANCA-associated vasculitis diagnosis. NPP's regulatory team assists in preparing and verifying the documentation needed for a compliant import.

Availability

As an approved therapy for severe active ANCA-associated vasculitis, Tavneos is sourced through authorized channels and imported under GDP-compliant logistics to preserve product quality throughout transit.

Sourcing and Delivery of Tavneos

NPP sources Tavneos directly from authorized pharmaceutical distributors to ensure product authenticity and full traceability. Every shipment is handled under Good Distribution Practice (GDP) conditions from origin to the patient's doorstep.

Storage and Handling

Tavneos should be stored at 20°C to 25°C, with excursions permitted between 15°C and 30°C, and this condition is maintained throughout transit.

Delivery Timelines

Once documentation and regulatory approvals are in place, delivery timelines are communicated transparently at the time of quotation, accounting for import clearance and last-mile logistics to the patient's city.

Availability of Tavneos Across Major Cities in India

Patients across India can access Tavneos through NPP's regulated import pathway, with rheumatology and nephrology specialists in major cities supporting the treatment process.

Mumbai

Leading hospitals in Mumbai support rheumatology and nephrology care coordination and documentation for Tavneos access.

Delhi

Delhi's major hospitals assist patients with prescription support and documentation for Tavneos.

Bangalore

Bangalore's specialist network offers access coordination for eligible vasculitis patients seeking Tavneos.

Chennai

Chennai-based rheumatology specialists coordinate Tavneos access alongside comprehensive vasculitis care.

Hyderabad

Hyderabad's care institutions support patients pursuing Tavneos therapy.

Kolkata

Kolkata's specialist centers help coordinate documentation and treatment access for Tavneos.

Pune

Pune-based specialists assist with prescription support and Tavneos treatment planning.

Ahmedabad

Ahmedabad's specialty hospitals support the import and treatment process for Tavneos.

Kochi

Kochi's specialist units assist patients with the documentation needed for Tavneos access.

Chandigarh

Chandigarh's care centers support Tavneos treatment coordination for patients from North India.

Jaipur

Jaipur's specialists help patients navigate the Tavneos access process.

Lucknow

Lucknow-based centers assist patients pursuing Tavneos therapy.

Bhubaneswar

Bhubaneswar's institutions support access to Tavneos for eligible patients.

Guwahati

Guwahati's specialists help coordinate Tavneos access for patients across the Northeast.

Patients in other cities across India can also access Tavneos through NPP's nationwide coordination network.

Author Details

Nitin Goswami

Written By

Nitin Goswami

Deputy Manager – Content & Social Media, Ikris Pharma Network

Sources: FDA

Dr. Chirag C Shah

Medically Reviewed By

Dr. Chirag C Shah

MBBS

Last Updated: 15 September 2026

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