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List of Oncology Medication For

Arthritis

Rheumatology is a branch of medicine devoted to the evaluation, diagnosis, and management of musculoskeletal disorders or other connective diseases, including arthritis and sort tissue lesions.

If Rheumatology Medicines are not yet approved or available in your area, you may give a request, to get access price in India under a specific brand name through IPN. For assistance and guidance, you can contact us by providing complete details. Our pharmaceutical expert will help you find a suitable and practical solution to your query. To receive comprehensive support, please call us at +91 9891 296 838 (Mr. Tarun) / +91 9811 747 774 (Mr. Neeraj).

Kineret (anakinra) for injection

Kineret (anakinra) – Rheumatoid Arthritis (RA) Therapy in India

Kineret (anakinra) is indicated for treating moderately to severely active Rheumatoid Arthritis (RA) in adults failing other DMARDs, and for rare autoinflammatory conditions like Cryopyrin-Associated Periodic Syndromes (CAPS), including NOMID, and Deficiency of Interleukin-1 Receptor Antagonist (DIRA), plus Still’s Disease (SJIA/AOSD) in specific age groups, working by blocking inflammation-causing interleukin-1. It’s an immunosuppressant that blocks immune chemical messengers.

Brand Name: Kineret
Generic Name: anakinra
Strength: Injection: 100 mg/0.67 mL solution in a single-use prefilled syringe for
subcutaneous injection. Graduated syringe allows for doses between 20 mg and 100 mg.
Manufacturer: Swedish Orphan Biovitrum AB (publ)
Approved By: EMA, USFDA

Source Details: Patient Information.
Kineret must always be used under the supervision of a Registered Medical Practitioner (RMP).

Get access to Kineret in India for treatment of Rheumatoid Arthritis (RA) on a Named Patient Import Basis.

IPN, New Delhi serves as a facilitator for the procurement of specialized drugs on behalf of patients or treating doctors, enabling access to Kineret (anakinra) for injection for personal use. To proceed, the applicant must submit an application in Form 12A along with a valid prescription issued by a Registered Medical Practitioner (RMP).

For any queries, including information regarding imported medicine pricing estimates in India, please contact the IPN Healthcare Support Team via email or at the following numbers: Mobile/WhatsApp: Mr. Tarun: +91 9891 296 838 |  Mr. Neeraj: +91 9811 747 774.

Note: All access is provided strictly on a Named Patient Import Basis and for personal use only, in accordance with Indian regulatory guidelines.

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RINVOQ (upadacitinib) tablets

RINVOQ (upadacitinib) extended-release tablets, for oral use Initial U.S. Approval: 2019

RINVOQ is a prescription medicine used to treat: Adults with moderate to severe rheumatoid arthritis (RA) when 1 or more medicines called tumor necrosis factor (TNF) blockers have been used, and did not work well or could not be tolerated.

Brand Name: RINVOQ
Generic Name: upadacitinib
Strength: • Extended-release tablets: 15 mg, 30 mg, and 45 mg
Manufacturer: AbbVie Inc
Approved By: EMA, USFDA

Source Details: Patient Information

IPN, New Delhi can facilitate patient to import of “RINVOQ (upadacitinib) tablets” in small quantities for personal use. For this applicant is required to make an application in Form 12A, along with the prescription of the Registered Medical Practitioner (RMP). If you have any question, please email IPN healthcare Support Team for RINVOQ (upadacitinib) tablets price list or cost in India. on Mr. Tarun:- +91 9891 296 838 / Mr. Neeraj:- +91 9811 747 774.

Indian Pharma Network (IPN) serves as a legitimate consultant and facilitator situated in New Delhi, India. With over two decades of industry experience, IPN offers extensive coverage across India, including prominent cities such as Mumbai, Delhi, Kolkata, Bhubaneswar, Bangalore, Hyderabad, Chennai, Ahmedbad, Pune, Surat, Visakhapatnam, Jaipur, Lucknow, Nagpur, Indore, Patna, Agartala, Guwahati, Imphal, Kohima, Namchi, Noida, Ghaziabad, Ludhiana, Agra, Varanasi, Srinagar, Amritsar, Jodhpur, Chandigarh, Gurgaon, Gorakhpur, Dehradun, Jammu, Hyderabad, Thiruvananthapuram, Kochi, Coimbatore, Puducherry, Mysuru, Salem, Vellore, Tiruppur, Guntur, Goa, Kolhapur, Mumbai, Nashik, and various other regions in India.

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Rituximab-abbs Injection

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rituximab-abbs injection
for intravenous use Initial U.S. Approval: 2018

Truxima (rituximab) is a medication used for the treatment of follicular lymphoma and diffuse large B-cell Non-Hodgkin’s Lymphoma (NHL); chronic lymphocytic leukemia (CLL); severe active rheumatoid arthritis and granulomatosis with polyangiitis and microscopic polyangiitis.

Facts about rituximab-abbs injection

Disease Indications-Leukemia, Lymphoma, Rheumatoid Arthritis, Granulomatosis , Polyangiitis
Manufacturer-Celltrion Healthcare Hungary Kft, Teva Pharmaceuticals
Usage-Intravenous
Medicine Approved By-European Medical Agency (EMA), Food and Drug Administration (FDA), Health Canada, Therapeutic Goods Administration (TGA), Medsafe (NZ)
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)

Access the best support services globally

If you have a prescription from a Registered Medical Practitioner (RMP), IPN in Delhi can assist you in obtaining access to genuine medication.  Our professional will provide you with a step-by-step guide on how to legally and safely import “Rituximab-abbs Injection” based on the information you provide.

Indian Pharma Network (IPN) serves as a legitimate consultant and facilitator situated in New Delhi, India. With over two decades of industry experience, IPN offers extensive coverage across India, including prominent cities such as Mumbai, Delhi, Kolkata, Bhubaneswar, Bangalore, Hyderabad, Chennai, Ahmedbad, Pune, Surat, Visakhapatnam, Jaipur, Lucknow, Nagpur, Indore, Patna, Agartala, Guwahati, Imphal, Kohima, Namchi, Noida, Ghaziabad, Ludhiana, Agra, Varanasi, Srinagar, Amritsar, Jodhpur, Chandigarh, Gurgaon, Gorakhpur, Dehradun, Jammu, Hyderabad, Thiruvananthapuram, Kochi, Coimbatore, Puducherry, Mysuru, Salem, Vellore, Tiruppur, Guntur, Goa, Kolhapur, Mumbai, Nashik, and various other regions in India.

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Safinamide Tablets

safinamide tablets
for oral use Initial U.S. Approval: 2017

XADAGO is a monoamine oxidase type B (MAO-B) inhibitor indicated as adjunctive treatment to levodopa/carbidopa in patients with Parkinson’s disease (PD) experiencing “off” episodes

Facts about safinamide tablets

Approval Date:  2017
Proprietary Name:  XADAGO (safinamide) tablets
Active Ingredient(s):  safinamide
FDA-approved use:
Dosage Form:  Tablets: 50 mg and 100 mg
Medicine Approved By: Food and Drug Administration (FDA)
Manufacturer: US WorldMeds, LLC,
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)

Access the best support services globally

If you have a prescription from a Registered Medical Practitioner (RMP), IPN in Delhi can assist you in obtaining access to genuine medication.  Our professional will provide you with a step-by-step guide on how to legally and safely import “safinamide tablets” based on the information you provide.

Indian Pharma Network (IPN) serves as a legitimate consultant and facilitator situated in New Delhi, India. With over two decades of industry experience, IPN offers extensive coverage across India, including prominent cities such as Mumbai, Delhi, Kolkata, Bhubaneswar, Bangalore, Hyderabad, Chennai, Ahmedbad, Pune, Surat, Visakhapatnam, Jaipur, Lucknow, Nagpur, Indore, Patna, Agartala, Guwahati, Imphal, Kohima, Namchi, Noida, Ghaziabad, Ludhiana, Agra, Varanasi, Srinagar, Amritsar, Jodhpur, Chandigarh, Gurgaon, Gorakhpur, Dehradun, Jammu, Hyderabad, Thiruvananthapuram, Kochi, Coimbatore, Puducherry, Mysuru, Salem, Vellore, Tiruppur, Guntur, Goa, Kolhapur, Mumbai, Nashik, and various other regions in India.

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Sarilumab Injection

Sarilumab injection, for subcutaneous use InitialU.S.Approval:2017

Generic Name – Kevzara (Sarilumab)
Medicine Type – Injection / Intravenous
Manufacturer Name – Regenore, Sanofi
Approval Year – 2017
Approved by – US Food and Drug Administration (FDA)

Access the best support services globally

If you have a prescription from a Registered Medical Practitioner (RMP), IPN in Delhi can assist you in obtaining access to genuine medication.  Our professional will provide you with a step-by-step guide on how to legally and safely import sarilumab injection” based on the information you provide.

Indian Pharma Network (IPN) serves as a legitimate consultant and facilitator situated in New Delhi, India. With over two decades of industry experience, IPN offers extensive coverage across India, including prominent cities such as Mumbai, Delhi, Kolkata, Bhubaneswar, Bangalore, Hyderabad, Chennai, Ahmedbad, Pune, Surat, Visakhapatnam, Jaipur, Lucknow, Nagpur, Indore, Patna, Agartala, Guwahati, Imphal, Kohima, Namchi, Noida, Ghaziabad, Ludhiana, Agra, Varanasi, Srinagar, Amritsar, Jodhpur, Chandigarh, Gurgaon, Gorakhpur, Dehradun, Jammu, Hyderabad, Thiruvananthapuram, Kochi, Coimbatore, Puducherry, Mysuru, Salem, Vellore, Tiruppur, Guntur, Goa, Kolhapur, Mumbai, Nashik, and various other regions in India.

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SELARSDI (ustekinumab-aekn) Injection

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Brand Name: SELARSDI. Generic Name: (ustekinumab-aekn). It is used to treat plaque psoriasis (PsO), psoriatic arthritis (PsA), Crohn’s disease (CD), ulcerative colitis(UC).

SELARSDI is a human interleukin-12 and -23 antagonist indicated for the treatment of:
Adult patients with:
• moderate to severe plaque psoriasis (PsO) who are candidates for phototherapy or systemic therapy.
• active psoriatic arthritis (PsA).
• moderately to severely active Crohn’s disease (CD).
• moderately to severely active ulcerative colitis.

Brand Name: SELARSDI
Generic Name: ustekinumab-aekn
Strength: • Subcutaneous Injection
Injection: 45 mg/0.5 mL or 90 mg/mL solution in a single-dose prefilled syringe
• Intravenous Infusion
Injection: 130 mg/26 mL (5 mg/mL) solution in a single-dose vial
Manufacturer: Teva Pharmaceuticals
Approved By: EMA, USFDA

Source Details: Patient Information

IPN, New Delhi can facilitate patient to import of “SELARSDI (ustekinumab-aekn) Injection” in small quantities for personal use. For this applicant is required to make an application in Form 12A, along with the prescription of the Registered Medical Practitioner (RMP). If you have any question, please email IPN healthcare Support Team for pharma product cost in India. on Mr. Tarun:- +91 9891 296 838 / Mr. Neeraj:- +91 9811 747 774.

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SIMLANDI (adalimumab-ryvk ) Injection

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Brand Name: SIMLANDI. Generic Name: (adalimumab-ryvk). It is used to treat plaque psoriasis, Crohn’s disease, ulcerative colitis, rheumatoid arthritis, juvenile idiopathic arthritis, psoriatic arthritis, ankylosing spondylitis, hidradenitis suppurativa, and uveitis.

SIMLANDI (adalimumab-ryvk ) Injection is a drug used to treat plaque psoriasis, Crohn’s disease, ulcerative colitis, rheumatoid arthritis, juvenile idiopathic arthritis, psoriatic arthritis, ankylosing spondylitis, hidradenitis suppurativa, and uveitis in certain patients.

Brand Name: SIMLANDI
Generic Name: adalimumab-ryvk
Strength: • Injection: 40 mg/0.4 mL single-dose autoinjector
Manufacturer: Teva Pharmaceuticals
Approved By: EMA, USFDA

Source Details: Patient Information

IPN, New Delhi can facilitate patient to import of “SIMLANDI (adalimumab-ryvk ) Injection” in small quantities for personal use. For this applicant is required to make an application in Form 12A, along with the prescription of the Registered Medical Practitioner (RMP). If you have any question, please email IPN healthcare Support Team for pharma product cost in India. on Mr. Tarun:- +91 9891 296 838 / Mr. Neeraj:- +91 9811 747 774.

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TALTZ (ixekizumab) injection

TALTZ (ixekizumab) – for plaque psoriasis, psoriatic arthritis, ankylosing spondylitis (AS), and non-radiographic axial spondyloarthritis (nr-axSpA) Therapy in India

TALTZ® is a humanized interleukin-17A antagonist indicated for the treatment of: • patients aged 6 years or older with moderate-to-severe plaque psoriasis who are candidates for systemic therapy or phototherapy. • adults with active psoriatic arthritis. • adults with active ankylosing spondylitis.

Brand Name: TALTZ
Generic Name: ixekizumab
Strength: Injection:
• 80 mg/mL solution in a single-dose prefilled autoinjector
• 80 mg/mL solution in a single-dose prefilled syringe
• 40 mg/0.5 mL solution in a single-dose prefilled syringe
• 20 mg/0.25 mL solution in a single-dose prefilled syringe
Manufacturer: Eli Lilly and Company
Approved By: EMA, USFDA

Source Details: Patient Information

Access TALTZ for plaque psoriasis, psoriatic arthritis, ankylosing spondylitis (AS), and non-radiographic axial spondyloarthritis (nr-axSpA)

Ixekizumab, sold under the brand name TALTZ, is available in India. Patients can access this medicine for personal use through authorized channels. IPN, New Delhi serves as a facilitator for the procurement of specialized drugs on behalf of patients or treating doctors. To proceed, the applicant must submit an application with a valid prescription issued by a Registered Medical Practitioner (RMP).

For any queries, including information regarding the cost of the pharmaceutical product in India, please contact the IPN Healthcare Support Team via email or at the following numbers: Mobile/WhatsApp: Mr. Tarun: +91 9891 296 838 |  Mr. Neeraj: +91 9811 747 774.

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