Baricinix 2MG & 4MG (Baricitinib)

Product Name : Baricinix(Baricitinib)
Generic Name : Baricitinib
Formulation : Tablet
Available Pack Size : 30’s Pot
Available Strengths : 2mg & 4mg
Registrations : 08.07.2021

Product Information

Baricinix 2MG & 4MG (Baricitinib) is a selective and reversible JAK1 and JAK2 inhibitor approved to treat moderate to severe active Rheumatoid Arthritis (RA), moderate to severe Atopic Dermatitis, and severe Alopecia Areata in adult patients. It works by partially inhibiting Janus Kinase (JAK1 and JAK2) enzymatic activity, thereby reducing the phosphorylation and activation of Signal Transducers and Activators of Transcription (STATs) that drive inflammation and abnormal immune response. For patients also requiring oncology and specialty medicines, Mediaid Pharmacy provides a full range of internationally sourced treatments. Baricinix is manufactured by Beacon Pharmaceuticals Ltd., Bangladesh and globally supplied by Mediaid Pharmacy with worldwide shipping.

Basic Product Information of Baricinix 2MG & 4MG (Baricitinib)

Brand Name Baricinix (Baricitinib)
Generic Name Baricitinib INN
Drug Class Selective and Reversible JAK1 and JAK2 Inhibitor (Janus Kinase Inhibitor)
Available Strengths 2mg and 4mg
Formulation Film-Coated Tablet
Pack Size 30 Tablets per Pot
Primary Indication Moderate to Severe Active Rheumatoid Arthritis (RA), Atopic Dermatitis, and Alopecia Areata
Regulatory Approvals USFDA Approved (RA, Atopic Dermatitis, Alopecia Areata). EMA Approved (RA and Atopic Dermatitis). FDA Emergency Use Authorization (EUA) for severe COVID-19.
Originator Brand Olumiant by Eli Lilly and Incyte
Manufacturer Beacon Pharmaceuticals Ltd., Mymensingh, Bangladesh
Global Supplier Mediaid Pharmacy Worldwide Shipping Available
Registration Date 08/07/2021
Storage Conditions Store below 30°C in a dry place away from light and moisture. Keep out of the reach of children.

How Baricinix 2MG & 4MG (Baricitinib) Works JAK-STAT Pathway Inhibition

Baricitinib, the active ingredient in Baricinix 2MG & 4MG, is a selective and reversible inhibitor of Janus kinase enzymes JAK1 and JAK2. Janus kinases (JAKs) are intracellular enzymes that transmit signals from the surface of immune cells in response to cytokines and growth factors involved in haematopoiesis, inflammation, and immune function. In autoimmune conditions such as rheumatoid arthritis and atopic dermatitis, these JAK-STAT signalling pathways become chronically overactive, driving sustained inflammation and progressive tissue damage.

Baricitinib works by partially inhibiting JAK1 and JAK2 enzymatic activity with IC50 values of 5.9 nM and 5.7 nM respectively thereby reducing the phosphorylation and activation of Signal Transducers and Activators of Transcription (STATs). By blocking this cascade, Baricinix interrupts the inflammatory signals responsible for joint pain, swelling, stiffness, and tissue destruction in rheumatoid arthritis, and skin inflammation in atopic dermatitis. Baricitinib is selective for JAK1 and JAK2 over JAK3 and TYK2 at therapeutic concentrations, contributing to its focused mechanism and manageable tolerability profile.

Unlike biologic DMARDs administered by subcutaneous or intravenous injection, Baricinix is a convenient once-daily oral film-coated tablet. This oral route of administration offers patients a practical and well-tolerated alternative to injectable therapies without compromising therapeutic efficacy. In the landmark RA-BEAM trial, Baricitinib demonstrated superiority over adalimumab and placebo in ACR20 response rates at Week 12, establishing its clinical value as a front-line advanced therapy option for rheumatoid arthritis. Physicians and patients seeking a broader view of oncology and specialty medicines available through Mediaid Pharmacy can review the full oncology portfolio for additional treatment options.

Approved Indications for Baricinix 2MG & 4MG (Baricitinib)

Baricinix (Baricitinib) 2mg and 4mg is approved for the following clinical indications in adult patients:

Moderate to Severe Rheumatoid Arthritis (RA)

For adult patients with moderate to severe active rheumatoid arthritis who have responded inadequately to or are intolerant of one or more disease-modifying anti-rheumatic drugs (DMARDs). Baricinix may be used as monotherapy or in combination with Methotrexate. Approved by USFDA and EMA.

Atopic Dermatitis

For adult patients with moderate to severe atopic dermatitis whose disease is not adequately controlled with other systemic therapies. Baricitinib has received USFDA and EMA approval for this indication, demonstrating significant reductions in skin inflammation and itch severity.

Alopecia Areata

USFDA-approved for severe alopecia areata in adults. Baricitinib has shown significant hair regrowth in clinical trials for patients suffering from this autoimmune condition that causes patchy or complete hair loss.

Severe COVID-19 (Emergency Use)

Baricitinib received FDA Emergency Use Authorization (EUA) for the treatment of hospitalised adults requiring supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ECMO) due to severe COVID-19.

Key Clinical Benefits of Baricinix (Baricitinib) 2mg and 4mg

Once-Daily Oral Convenience

Baricinix is taken once daily by mouth, with or without food eliminating the need for injections. This oral route of administration improves patient adherence and quality of life compared to subcutaneous biologic therapies.

Multi-Indication Regulatory Approval

USFDA-approved for rheumatoid arthritis, atopic dermatitis, and alopecia areata, with EMA approval for RA and atopic dermatitis, and FDA EUA for severe COVID-19 making Baricinix one of the most broadly approved JAK inhibitors available.

Clinically Proven Symptom Control

In the RA-BEAM trial, Baricitinib achieved superior ACR20 response rates versus adalimumab and placebo at Week 12, and delivered significant reductions in DAS28 disease activity scores, radiographic joint progression, and morning stiffness duration.

Affordable Generic Alternative to Olumiant

Baricinix contains the same active ingredient as Olumiant (Eli Lilly and Incyte) at a significantly lower cost. Patients in both developing and developed markets gain access to the same proven JAK1/JAK2 inhibition mechanism without the financial burden of the originator price.

Methotrexate-Compatible Combination Therapy

Baricinix can be prescribed as monotherapy or combined with Methotrexate for rheumatoid arthritis, giving rheumatologists full flexibility to tailor treatment to individual disease activity profiles and prior DMARD histories.

WHO-GMP and cGMP Certified Manufacturing

Produced by Beacon Pharmaceuticals Ltd. under strict WHO-GMP, cGMP, and ISO-certified manufacturing standards. Every batch of Baricinix meets consistent quality, safety, and bioequivalence requirements validated for international export to Asia, Africa, Europe, and Latin America.

How to Take Baricinix 2MG & 4MG (Baricitinib) Dosage Guidelines

Route of Administration: Oral taken by mouth with or without food at any consistent time of day.

Rheumatoid Arthritis (RA): 4mg once daily is the standard adult dose. A 2mg once-daily dose is appropriate for patients aged 75 years and above, those with a history of chronic or recurrent infections, or patients who have achieved sustained disease control on 4mg and are eligible for dose tapering.

Atopic Dermatitis: 4mg once daily for adults under 65 years. 2mg once daily for patients aged 65 and above. A dose reduction to 2mg once daily may be considered for patients achieving sustained control on 4mg.

Alopecia Areata: 4mg once daily for adults under 65 years. 2mg once daily for patients aged 65 years and above.

Renal Impairment: 2mg once daily is recommended for patients with a creatinine clearance (CrCl) of 30 to 60 mL per minute. Baricinix is not recommended for patients with CrCl below 30 mL per minute.

Hepatic Impairment: No dose adjustment is required in patients with mild or moderate hepatic impairment. Baricinix is not recommended in patients with severe hepatic impairment.

OAT3 Inhibitor Co-Administration: Reduce dose to 2mg once daily when co-administering with strong Organic Anion Transporter 3 (OAT3) inhibitors such as probenecid, as these agents increase Baricitinib plasma exposure.

Paediatric Use: The safety and efficacy of Baricitinib in patients aged 0 to 18 years have not been established. No data are currently available; use is not recommended in this population.

Prescription Medication Pre-Treatment Blood Count Requirements. Treatment with Baricinix should not be initiated in patients with an Absolute Lymphocyte Count (ALC) below 0.5 × 10⁹ cells per litre, an Absolute Neutrophil Count (ANC) below 1 × 10⁹ cells per litre, or a haemoglobin value below the clinically required threshold. Complete blood count (CBC) monitoring is mandatory before treatment initiation and at regular intervals throughout therapy. Always follow your prescribing physician’s instructions.

Clinical Monitoring Requirements During Baricinix Treatment

Regular clinical monitoring is mandatory throughout Baricinix (Baricitinib) treatment. Healthcare providers must monitor for signs of serious bacterial, viral, fungal, and opportunistic infections, as Baricitinib suppresses JAK-STAT immune signalling and reduces immune surveillance capacity. Monitoring parameters include Complete Blood Count (CBC) for lymphopenia, neutropenia, and anaemia; liver function tests (LFTs); lipid panels including LDL and HDL cholesterol (Baricitinib may elevate both); renal function via serum creatinine and estimated GFR; and clinical assessment for signs of venous thromboembolism (VTE), malignancy, and major adverse cardiovascular events (MACE). Patients should report any fever, unusual fatigue, shortness of breath, or signs of infection to their physician without delay.

Drug Interactions and Important Safety Information for Baricinix

Concomitant use of Baricinix with other JAK inhibitors, biologic DMARDs (such as adalimumab, etanercept, or tocilizumab), or potent immunosuppressants including azathioprine and cyclosporine must be avoided. Combining these agents increases the risk of additive immunosuppression, serious infections, and lymphopenia without established clinical benefit.

The Baricinix dose must be reduced to 2mg once daily when co-administered with strong Organic Anion Transporter 3 (OAT3) inhibitors such as probenecid, because OAT3 inhibition increases Baricitinib plasma exposure by approximately 2-fold. Live vaccines must not be administered during Baricinix therapy or shortly before initiating treatment. Patients should inform their prescribing physician of all medications, supplements, and herbal products currently being taken before starting Baricinix.

Side Effects and Precautions of Baricinix (Baricitinib)

Common Side Effects

Upper respiratory tract infections

Nausea

Headache

Elevated blood cholesterol (LDL and HDL)

Acne and folliculitis

Thrombocytosis (elevated platelet count)

Urinary tract infections

Weight gain

Serious Warnings and Precautions

Serious infections including tuberculosis (TB), bacterial, viral, and fungal infections. Screen all patients for latent TB before treatment initiation.

Venous thromboembolism (VTE) including deep vein thrombosis (DVT) and pulmonary embolism (PE). Use with caution in patients at high thrombotic risk.

Major adverse cardiovascular events (MACE) including myocardial infarction and stroke. Use with caution in patients with cardiovascular risk factors or smokers.

Malignancy risk including lymphoma. Avoid in patients with known active malignancy or recent history of malignancy. See our oncology medicines page for specialist cancer treatment options.

Not recommended during pregnancy or breastfeeding. Effective contraception is required during treatment and for at least one week after the final dose.

Live vaccines must not be administered during Baricinix treatment.

Not recommended in patients with severe renal impairment (CrCl <30 mL/min) or severe hepatic impairment.

Who Should Use Baricinix 2MG & 4MG (Baricitinib)?

Baricinix is indicated for adult patients diagnosed with moderate to severe active rheumatoid arthritis who have had an inadequate response or intolerance to one or more DMARDs; adult patients with moderate to severe atopic dermatitis not controlled by conventional systemic therapies; and adult patients with severe alopecia areata. Baricinix is prescribed by rheumatologists, dermatologists, and specialist physicians with experience in managing autoimmune and inflammatory conditions. A thorough pre-treatment medical assessment including complete blood count, renal function, liver function, lipid levels, and screening for latent tuberculosis and hepatitis B and C is required before initiating therapy. Patients with concurrent or historical malignancy should consult their oncologist; Mediaid Pharmacy’s oncology specialty medicines portfolio supports multidisciplinary management across autoimmune and oncology indications.

Manufacturer: Beacon Pharmaceuticals Ltd., Bangladesh

Beacon Pharmaceuticals Ltd. is a leading pharmaceutical manufacturer based in Mymensingh, Bangladesh and the number one oncology and specialty medicine company in the country. Beacon was the first company in Bangladesh to export cancer drugs and currently exports to markets across Asia, Africa, Europe, and Latin America. With more than 200 generic drugs and 65 oncology products in its portfolio, Beacon operates under strict WHO-GMP, cGMP, and ISO-certified manufacturing standards. Baricinix (Baricitinib) 2mg and 4mg is one of Beacon’s internationally recognised specialty autoimmune products, offering a high-quality, bioequivalent, and affordable alternative to Olumiant by Eli Lilly at a fraction of the originator cost. Every batch exported by Beacon meets the quality benchmarks required for approval in regulated international markets.

Global Supplier: Mediaid Pharmacy Worldwide Shipping for Baricinix (Baricitinib)

Mediaid Pharmacy is a trusted global supplier of specialty, autoimmune, and oncology medications. Baricinix (Baricitinib) 2mg and 4mg is available through Mediaid Pharmacy with reliable worldwide shipping to South Asia, the Middle East, Africa, Europe, and beyond. Our team provides full order support including pricing, availability confirmation, documentation, and delivery tracking. Contact Mediaid Pharmacy directly via WhatsApp, phone, or WeChat for enquiries.

Why Choose Baricinix (Baricitinib) from Mediaid Pharmacy?

Baricinix represents a clinically proven advancement in the treatment of autoimmune and inflammatory conditions. As the generic bioequivalent of Olumiant by Eli Lilly and Incyte, Baricinix delivers the same active ingredient Baricitinib with the same proven JAK1 and JAK2 inhibition mechanism, at a dramatically more affordable price point. Manufactured by the internationally trusted Beacon Pharmaceuticals Ltd. under WHO-GMP and cGMP standards, and distributed globally by Mediaid Pharmacy with worldwide shipping, Baricinix gives patients and healthcare providers access to high-quality advanced autoimmune therapy without the financial barrier of brand-name pricing. For patients whose treatment plans also require cancer medicines, Mediaid Pharmacy’s oncology medicines section provides a comprehensive range of specialty oncology products sourced from verified manufacturers. For any patient or physician seeking a proven, affordable, and globally accessible Baricitinib treatment option, Baricinix from Mediaid Pharmacy is the trusted choice.

Frequently Asked Questions About Baricinix 2MG & 4MG (Baricitinib)

What is Baricinix 2MG & 4MG (Baricitinib) used for?

Baricinix (Baricitinib) 2mg and 4mg is a selective JAK1 and JAK2 inhibitor used to treat moderate to severe rheumatoid arthritis, moderate to severe atopic dermatitis, and severe alopecia areata in adults. Baricitinib also received FDA Emergency Use Authorization (EUA) for the treatment of hospitalised adults with severe COVID-19 requiring respiratory support. Baricinix reduces the overactive JAK-STAT immune signals that cause chronic inflammation and tissue damage in these autoimmune conditions.

What is the correct dose of Baricinix (Baricitinib)?

Baricinix is taken orally once daily, with or without food, at any consistent time of day. The standard adult dose for rheumatoid arthritis is 4mg once daily. The 2mg once-daily dose is used for patients aged 75 and above, those with significant renal impairment (CrCl 30–60 mL/min), patients taking strong OAT3 inhibitors, or those who have achieved sustained disease control and are clinically eligible for dose tapering. Always follow your prescribing physician’s exact dosing instructions.

What strengths and pack sizes is Baricinix (Baricitinib) available in?

Baricinix is available in 2mg and 4mg film-coated tablets, each supplied in a pot of 30 tablets. The 4mg strength is the standard recommended dose for most adult patients with rheumatoid arthritis. The 2mg strength is used when a reduced dose is clinically appropriate due to patient age, renal function, specific co-medications, or treatment response.

Is Baricinix the same as Olumiant (Baricitinib by Eli Lilly)?

Yes. Baricinix is the generic equivalent of Olumiant. Both products contain the same active ingredient Baricitinib in the same dosage form and strengths. Baricinix is manufactured by Beacon Pharmaceuticals Ltd. in Bangladesh under WHO-GMP-certified conditions and delivers the same clinical mechanism of JAK1 and JAK2 inhibition as Olumiant, at a significantly lower cost. This makes Baricinix a more financially accessible long-term treatment option for patients worldwide.

What are the side effects of Baricinix (Baricitinib)?

Common side effects of Baricinix include upper respiratory tract infections, nausea, headache, elevated LDL and HDL cholesterol, acne, folliculitis, urinary tract infections, thrombocytosis, and weight gain. Serious but less frequent risks include serious infections (including tuberculosis), venous thromboembolism (VTE), major adverse cardiovascular events (MACE), and malignancy. Always consult your physician for a complete individual risk-benefit assessment before and during treatment.

Can Baricinix be combined with Methotrexate or other DMARDs?

Yes. Baricinix can be used as monotherapy or in combination with Methotrexate for rheumatoid arthritis. However, Baricinix must not be combined with other JAK inhibitors, biologic DMARDs (such as adalimumab or tocilizumab), or potent immunosuppressants such as azathioprine or cyclosporine. These combinations increase immunosuppression and the risk of serious infections. The dose of Baricinix must be reduced to 2mg when co-administered with strong OAT3 inhibitors such as probenecid.

Is Baricinix (Baricitinib) safe during pregnancy or while breastfeeding?

No. Baricinix is not recommended during pregnancy or breastfeeding due to potential risks to the foetus and neonate. Women of childbearing potential must use effective contraception during the full course of Baricinix treatment and for at least one week after the final dose. Consult your physician before starting treatment if you are pregnant, planning to become pregnant, or currently breastfeeding.

Can I order Baricinix 2MG & 4MG (Baricitinib) online with worldwide shipping?

Yes. Mediaid Pharmacy supplies Baricinix (Baricitinib) 2mg and 4mg to patients and healthcare providers globally with worldwide shipping. Contact Mediaid Pharmacy via WhatsApp, phone, or WeChat at +8801773428128, or send an email enquiry to info@mediaidpharmacy.com for pricing, stock availability, and delivery details for your country.

Order Baricinix 2MG & 4MG (Baricitinib) with Worldwide Shipping

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