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METOJECT™ solution for subcutaneous injection 50mg/ml (0.35ml), syringes 1pc

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Table of Contents

METOJECT™ 50mg Solution 0.35ml Buy Online

Metoject Solution for Subcutaneous Injection: A Comprehensive Overview

Managing chronic inflammatory conditions like rheumatoid arthritis can be challenging. Finding the right treatment that effectively manages symptoms while minimizing side effects is crucial for improving quality of life. Metoject, a subcutaneous injection, offers a potential solution for patients seeking effective disease management.

What is Metoject?

Metoject is a methotrexate-based medication administered via subcutaneous injection. Methotrexate is a disease-modifying antirheumatic drug (DMARD) known for its effectiveness in treating various inflammatory conditions. Its precise formulation as Metoject allows for convenient, self-administered weekly doses.

Metoject is primarily indicated for the treatment of active rheumatoid arthritis in adult patients. It’s also used in cases of severe, recalcitrant psoriasis and psoriatic arthritis that haven’t responded adequately to other treatments. The specific dosage and treatment duration are determined by a physician based on individual needs and response.

Metoject is administered subcutaneously, meaning it’s injected under the skin. The recommended initial dose is typically 7.5 mg once weekly. A healthcare professional should supervise the first injection to ensure proper technique. The dose may be adjusted gradually based on the patient’s response and tolerance. Consistent weekly administration is vital for efficacy.

Methotrexate, the active component of Metoject, works by inhibiting the activity of folic acid, a crucial element in cell growth and division. By slowing down the rapid reproduction of cells, it effectively reduces inflammation and the progression of autoimmune diseases. This mechanism is crucial in managing the symptoms of conditions like rheumatoid arthritis and psoriasis.

  • Effective Disease Management: Demonstrates efficacy in reducing inflammation and managing symptoms of rheumatoid arthritis, psoriasis, and psoriatic arthritis.
  • Convenient Administration: Subcutaneous self-injection allows for home administration, enhancing patient convenience and independence.
  • Established Treatment: Methotrexate has a long history of use and a well-established safety profile, providing physicians with substantial clinical data.
  • Potential Side Effects: Like all medications, Metoject carries the risk of side effects, including nausea, fatigue, and gastrointestinal issues. These are usually manageable with appropriate monitoring and adjustments.
  • Requires Medical Supervision: Initial administration and ongoing monitoring by a healthcare professional are essential to ensure safe and effective use.
  • Not a Cure: Metoject manages symptoms and disease progression but does not offer a cure for rheumatoid arthritis or other inflammatory conditions.

Important Considerations

Regular blood tests are necessary to monitor liver function and complete blood counts. Patients should immediately report any unusual symptoms to their healthcare provider. The medication should be used strictly as prescribed by a physician and not stopped abruptly without medical consultation.

Conclusion

Metoject offers a valuable treatment option for individuals with rheumatoid arthritis, psoriasis, and psoriatic arthritis. Its convenient subcutaneous administration and established efficacy make it a significant contribution to managing these chronic inflammatory diseases. However, close monitoring and adherence to the prescribed regimen are essential for safe and effective outcomes.

What is Metoject?

Metoject, a pre-filled syringe containing 0.35ml of a 50mg/ml methotrexate solution, represents a significant advancement in the delivery of this crucial medication. Designed for subcutaneous injection, Metoject offers a convenient and efficient method of administering methotrexate, a cornerstone treatment for various inflammatory conditions. Its single-use syringe format ensures both hygiene and accurate dosage, minimizing the risk of contamination and medication errors. This streamlined approach to administration can significantly improve patient compliance and overall treatment outcomes.

Methotrexate, the active pharmaceutical ingredient in Metoject, is a disease-modifying antirheumatic drug (DMARD). Its mechanism of action involves interfering with the cellular processes that drive inflammation. By targeting specific metabolic pathways, methotrexate effectively reduces the symptoms of autoimmune diseases such as rheumatoid arthritis and psoriasis, improving patients’ quality of life. The precise concentration and pre-filled format of Metoject ensure a consistent and reliable delivery of the therapeutic dose, contributing to its effectiveness and safety profile. The ease of administration distinguishes Metoject from other methotrexate formulations, making it a more accessible and user-friendly option for patients requiring regular treatment.

The development of Metoject reflects a commitment to improving the patient experience in managing chronic inflammatory conditions. The focus on ease of use and precise dosing makes it an important tool in the arsenal of therapies available for these challenging diseases. Metoject’s single-use design contributes to infection control, while the standardized concentration allows for consistent and predictable therapeutic effects. This careful design prioritizes both patient convenience and the assurance of accurate medication delivery, contributing to optimal treatment results.

Indications and Clinical Use

Metoject’s primary clinical application lies in the management of rheumatoid arthritis (RA), a debilitating autoimmune disease characterized by chronic inflammation of the joints. In RA, the body’s immune system mistakenly attacks its own tissues, leading to pain, swelling, and stiffness. Metoject’s active ingredient, methotrexate, effectively suppresses this aberrant immune response, alleviating symptoms and improving joint function. Its use is particularly relevant in adult patients where standard therapies have proven inadequate.

Beyond rheumatoid arthritis, Metoject finds application in the treatment of severe, recalcitrant psoriasis. Psoriasis is a chronic skin condition marked by inflamed, scaly patches. Metoject’s anti-inflammatory properties can significantly reduce the severity of psoriatic lesions, improving both the appearance and the comfort of affected individuals. It’s often considered when other treatments, such as phototherapy or topical medications, have failed to provide sufficient relief. The efficacy of Metoject in psoriasis stems from its ability to modulate the hyperproliferative and inflammatory processes driving the disease.

Furthermore, Metoject is indicated for the treatment of psoriatic arthritis, a form of arthritis associated with psoriasis. This condition combines the joint inflammation characteristic of RA with the skin manifestations of psoriasis. Metoject’s dual action, addressing both the inflammatory and the hyperproliferative aspects of the disease, makes it a valuable therapeutic option for psoriatic arthritis. Its use is generally reserved for cases where the symptoms are severe and unresponsive to other treatments. Careful monitoring and dose adjustment are crucial in optimizing the benefits while minimizing potential side effects, tailored to the individual patient’s response and overall health.

It is important to note that Metoject’s use should always be under the strict supervision of a healthcare professional. The dosage and duration of treatment are determined based on individual patient factors, response to therapy, and potential side effects. Regular monitoring is essential to ensure the safe and effective use of Metoject and to make any necessary adjustments to optimize treatment outcomes. This careful approach ensures that patients receive the maximum benefit from the medication while minimizing risks.

Administration and Dosage

Metoject’s convenient, pre-filled syringe design simplifies administration. The medication is intended for subcutaneous injection, meaning it’s injected under the skin, typically into the thigh or abdomen. This route of administration offers a less invasive alternative to intravenous or intramuscular injections, enhancing patient comfort and reducing the risk of injection site complications. Proper injection technique is crucial for optimal absorption and to minimize discomfort; healthcare professionals should provide thorough instruction on the correct procedure.

Dosage regimens for Metoject are highly individualized and depend on several factors, including the specific condition being treated (rheumatoid arthritis, psoriasis, or psoriatic arthritis), the patient’s overall health, and their response to the medication. While a typical starting dose might be 7.5mg once weekly, this is merely a guideline. A physician will carefully assess each patient’s needs and adjust the dosage accordingly. Regular monitoring of the patient’s condition, along with blood tests to assess liver function and other relevant markers, is essential for determining the appropriate dose and ensuring the safety and efficacy of the treatment.

Dosage adjustments are often made gradually, increasing or decreasing the weekly dose in increments determined by the physician based on clinical response and tolerance. It’s crucial to remember that Methotrexate, the active component of Metoject, has a narrow therapeutic index, meaning that the difference between an effective dose and a toxic dose can be small. Therefore, close monitoring is essential to avoid adverse effects. Patients should meticulously adhere to their prescribed dosage and schedule, consulting their physician immediately should any concerns arise. Consistent administration, according to the prescribed regimen, is key to achieving the desired therapeutic effect and minimizing potential complications. The patient’s active participation in their treatment plan, including careful adherence to the prescribed dosage and schedule, is vital for successful outcomes.

Mechanism of Action

Metoject’s therapeutic effects stem from its active ingredient, methotrexate, a powerful immunosuppressant and anti-inflammatory agent. Methotrexate’s primary mechanism involves inhibiting dihydrofolate reductase (DHFR), a crucial enzyme involved in the synthesis of DNA and RNA. By blocking DHFR, methotrexate disrupts the cell cycle, slowing down the rapid proliferation of cells, a key feature in both rheumatoid arthritis and psoriasis. This effect is particularly relevant in the context of autoimmune diseases, where uncontrolled cell growth and inflammation contribute to disease progression.

The impact of methotrexate extends beyond simple cell cycle inhibition. It also modulates the activity of various immune cells, including T lymphocytes and B lymphocytes, reducing their ability to produce pro-inflammatory cytokines. These cytokines are signaling molecules that drive inflammation and tissue damage in autoimmune diseases. By dampening the inflammatory cascade, methotrexate alleviates symptoms such as joint pain, swelling, and skin lesions associated with rheumatoid arthritis and psoriasis. This multifaceted approach is a key factor in methotrexate’s clinical efficacy.

Furthermore, methotrexate exhibits anti-inflammatory effects through various other pathways. It influences the production of adenosine, a potent anti-inflammatory molecule, and affects the activity of matrix metalloproteinases (MMPs), enzymes involved in tissue breakdown. By inhibiting MMPs, methotrexate helps preserve cartilage and reduce joint damage in rheumatoid arthritis. These multiple mechanisms of action contribute to methotrexate’s ability to effectively manage both the inflammatory and the destructive processes characteristic of these chronic conditions. This complex interplay of actions explains why methotrexate remains a cornerstone treatment for these challenging diseases, despite the development of newer therapies. Its multifaceted approach offers a potent combination of immunosuppression and anti-inflammatory effects, contributing to its long-standing role in managing autoimmune conditions.

Pros of Using Metoject

Metoject offers several key advantages for patients and healthcare providers alike. Its pre-filled, single-use syringe design significantly enhances convenience and reduces the risk of contamination or medication errors often associated with reconstituting powdered medications. This ease of use promotes better patient compliance, leading to improved treatment outcomes. The single-dose format also eliminates the need for handling multiple components, streamlining the injection process and minimizing the potential for errors.

The subcutaneous route of administration, as opposed to intravenous or intramuscular injections, is generally better tolerated by patients. It’s associated with less pain and discomfort at the injection site, contributing to improved patient satisfaction and adherence to the prescribed treatment regimen. This increased comfort level directly translates to better patient compliance, a critical factor in the successful management of chronic conditions like rheumatoid arthritis and psoriasis. The convenience and relative painlessness of subcutaneous injection make it a preferred method for many patients, enhancing their overall treatment experience.

Metoject’s formulation provides a precise and consistent dose of methotrexate, ensuring reliable therapeutic effects. This accuracy is crucial, especially considering the narrow therapeutic index of methotrexate, where the difference between an effective and a toxic dose is relatively small. The pre-filled syringe design eliminates the variability inherent in manual preparation, reducing the chance of medication errors and ensuring consistent drug delivery. This reliability is essential for achieving optimal therapeutic outcomes and minimizing potential side effects, contributing to safer and more effective treatment.

Finally, the established efficacy and safety profile of methotrexate, combined with the improved delivery system of Metoject, make it a valuable therapeutic option for healthcare professionals. Its long history of use provides clinicians with extensive clinical data and experience, underpinning its widespread use in the management of inflammatory conditions. The combination of proven efficacy and enhanced delivery makes Metoject a strong contender in the treatment of rheumatoid arthritis, psoriasis, and psoriatic arthritis.

Cons of Using Metoject

While Metoject offers significant advantages, potential drawbacks warrant consideration. A primary concern is the risk of adverse effects associated with methotrexate. These can range from mild gastrointestinal disturbances like nausea and diarrhea to more serious complications affecting the liver, kidneys, and bone marrow. The frequency and severity of these side effects vary considerably among individuals, necessitating close monitoring by healthcare professionals. Regular blood tests are crucial for early detection of potential problems, allowing for timely intervention and dose adjustment.

Another important consideration is the need for careful patient selection and monitoring. Methotrexate is not suitable for all patients, particularly those with pre-existing liver or kidney disease, significant alcohol consumption, or certain other medical conditions. Pre-treatment assessments are essential to identify individuals who may be at higher risk of adverse effects. Furthermore, ongoing monitoring throughout treatment is crucial to detect any early warning signs of toxicity and to make necessary adjustments to the treatment regimen to minimize risks. This careful approach is vital to ensure the safe and effective use of Metoject.

Furthermore, methotrexate can suppress the immune system, making patients more susceptible to infections. This increased vulnerability necessitates vigilance regarding any signs of infection and prompt medical attention should symptoms arise. Patients should be educated about the importance of maintaining good hygiene practices and reporting any signs of illness to their healthcare provider. This proactive approach helps to minimize the risk of serious complications related to immunosuppression. The potential for immunosuppression necessitates careful consideration of potential risks versus benefits, particularly in patients with a history of infections or weakened immune systems.

Finally, while the pre-filled syringe design enhances convenience, it also means that dose adjustments require a new syringe. This can be a logistical challenge in some situations. While the single-use format promotes sterility and accuracy, the lack of flexibility in dosage within a single syringe may necessitate more frequent dispensing or administration adjustments. Healthcare providers should carefully consider this aspect when prescribing Metoject to ensure appropriate logistical arrangements are in place for patients requiring dose alterations.

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