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Description
Product Overview
Amifostine Injection USP 500 mg is a cytoprotective agent used in oncology supportive care. It is administered prior to certain chemotherapy and radiation treatments to help minimize damage to healthy tissues. This medicine does not treat cancer directly but plays a crucial role in reducing treatment-related side effects under medical supervision.
Key Benefits
1. Helps protect normal cells during chemotherapy and radiation therapy
2. Reduces oxidative stress and tissue damage
3. Supports recovery of healthy tissues
4. Lowers the risk of treatment-related toxicity
5. Enhances overall tolerance to cancer treatment
How It Works
Amifostine is converted into its active form primarily in healthy tissues. This active compound:
-Neutralizes harmful free radicals
-Reduces oxidative damage caused by cancer therapies
-Protects normal cells more effectively than tumor cells
-Assists in minimizing radiation-induced injury
-Administration Guidelines
-Administered by trained healthcare professionals
-Given shortly before chemotherapy or radiation therapy sessions
-Not intended for self-administration
-Dosage and schedule are determined by the treating oncologist
Storage Instructions
-Store as per manufacturer’s recommended temperature
-Keep in original packaging
-Protect from direct sunlight
-Do not freeze
-Maintain a clean and dry storage environment
-Follow proper aseptic handling procedures in healthcare settings
-Missed Dose Information
Since amifostine is administered in clinical settings:
Missed doses are rare
Contact the oncology team immediately if a session is missed
Do not attempt to self-administer
Do not double the next dose
The treatment schedule may be adjusted by the doctor
Available Strength
Amifostine Injection USP 500 mg
Additional strengths may be available depending on manufacturer offerings
Frequently Asked Questions
1. What is amifostine injection used for?
It is used to reduce certain side effects associated with chemotherapy and radiation therapy under medical supervision.
2. Is amifostine a cancer treatment drug?
No, it is a supportive care medicine designed to protect healthy tissues during cancer treatment.
3.Who administers amifostine?
It is administered by qualified healthcare professionals in hospitals or oncology centers.
4. Can it be exported internationally?
Yes, authorized exporters supply Amifostine to licensed hospitals, distributors, and procurement agencies worldwide, subject to regulatory compliance.
5. What documents are provided for export?
Typical documentation may include COA, batch COA, product specifications, manufacturing license, GMP certificate (if applicable), commercial invoice, packing list, and certificate of origin.
Lenakast 10mg Capsule – Product Description
Lenakast 10mg Capsule is a prescription medicine commonly used in the management of allergic conditions, depending on its active ingredient and prescribed indication. It may help relieve symptoms such as sneezing, runny or blocked nose, itching, and watery eyes.
Key Benefits:
Helps manage allergy-related symptoms
May reduce sneezing and nasal irritation
Helps relieve itching and watery eyes
Can support better comfort during allergic episodes
Important: Use Lenakast 10mg Capsule only as directed by a qualified healthcare professional. The exact uses, dosage, precautions, and side effects depend on the medicine's active ingredient and the patient's condition. Avoid self-medication.
Description
Lenangio 10mg Capsule: Advanced Immunomodulatory Therapy for Multiple Myeloma and Myelodysplastic Syndromes
Extensive Product Profile: In-Depth Insights on Lenangio 10mg Capsules
Lenangio 10mg Capsule, manufactured under strict global GMP compliance standards within India, is a highly effective mid-range oral antineoplastic and immunomodulatory treatment. Each capsule contains precisely Lenalidomide ($10text{ mg}$) as its active pharmaceutical ingredient. Lenalidomide is a potent analogue of thalidomide belonging to the chemical class of isoindolones. It is designed to selectively manipulate cellular environments, alter cytokine release, and stimulate defense cells to disrupt blood-based cancers at their core.
1. Clinical Indications & Target Therapeutic Applications
Multiple Myeloma (MM): Used in combination with dexamethasone or as a standalone maintenance therapy following autologous stem cell transplantation (ASCT) for patients with newly diagnosed or relapsed/refractory multiple myeloma. The $10text{ mg}$ strength is highly utilized for strategic dose maintenance or during scheduled step-down titration cycles to control drug toxicity.
Myelodysplastic Syndromes (MDS): Indicated for patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with a specific cytogenetic abnormality—the deletion 5q (del 5q) chromosomal mutation, with or without additional cytogenetic abnormalities.
Mantle Cell Lymphoma (MCL): Prescribed for patients with mantle cell lymphoma whose disease has relapsed or progressed after two prior therapies, one of which must have included bortezomib.
2. Comprehensive Mechanism of Action (MOA)
Cereblon E3 Ubiquitin Ligase Binding: Lenalidomide binds directly to cereblon (CRBN), a component of the cullin-RING E3 ubiquitin ligase enzyme complex. This binding selectively alters the substrate specificity of the ligase, targeting two essential lymphoid transcription factors—IKZF1 (Ikaros) and IKZF3 (Aiolos)—for rapid cellular degradation.
Direct Tumor Suppression & Apoptosis: The destruction of Ikaros and Aiolos causes a down-regulation of crucial survival factors in B-cell malignancies, leading to immediate cell cycle arrest and programmed cell death (apoptosis) in malignant plasma cells.
3. Storage, Stability, and Handling Protocols
Environmental Matrix: Store Lenangio 10mg Capsules in their original moisture-resistant container or blister packaging at controlled room temperature, strictly below 30°C (86°F). Protect the inventory from high ambient steam, humidity, heat, and direct exposure to light.
Administration Matrix: Capsules must be swallowed completely whole with a glass of water, once daily at the same time, either with or without food. Do not crush, chew, open, or break the capsule shell, as direct contact with the internal powder poses handling risks and alters designated absorption rates.
Potential Side Effects of Lenangio 10mg
Severe Myelosuppression: Significant reductions in blood cell counts, leading to severe neutropenia (low white cells increasing susceptibility to infections), thrombocytopenia (low platelets increasing bruising or bleeding hazards), and anemia (causing extreme fatigue and weakness). Regular Complete Blood Counts (CBC) are required before and during treatment.
Venous and Arterial Thromboembolism: Patients treated with Lenalidomide face a significantly increased risk of deep vein thrombosis (DVT), pulmonary embolism (PE), myocardial infarction, and stroke. Prophylactic antithrombotic therapy is highly recommended for most patients.
Description
Lenangio 10mg Capsule: Advanced Immunomodulatory Therapy for Multiple Myeloma and Myelodysplastic Syndromes
Extensive Product Profile: In-Depth Insights on Lenangio 10mg Capsules
Lenangio 10mg Capsule, manufactured under strict global GMP compliance standards within India, is a highly effective mid-range oral antineoplastic and immunomodulatory treatment. Each capsule contains precisely Lenalidomide ($10text{ mg}$) as its active pharmaceutical ingredient. Lenalidomide is a potent analogue of thalidomide belonging to the chemical class of isoindolones. It is designed to selectively manipulate cellular environments, alter cytokine release, and stimulate defense cells to disrupt blood-based cancers at their core.
1. Clinical Indications & Target Therapeutic Applications
Multiple Myeloma (MM): Used in combination with dexamethasone or as a standalone maintenance therapy following autologous stem cell transplantation (ASCT) for patients with newly diagnosed or relapsed/refractory multiple myeloma. The $10text{ mg}$ strength is highly utilized for strategic dose maintenance or during scheduled step-down titration cycles to control drug toxicity.
Myelodysplastic Syndromes (MDS): Indicated for patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with a specific cytogenetic abnormality—the deletion 5q (del 5q) chromosomal mutation, with or without additional cytogenetic abnormalities.
Mantle Cell Lymphoma (MCL): Prescribed for patients with mantle cell lymphoma whose disease has relapsed or progressed after two prior therapies, one of which must have included bortezomib.
2. Comprehensive Mechanism of Action (MOA)
Cereblon E3 Ubiquitin Ligase Binding: Lenalidomide binds directly to cereblon (CRBN), a component of the cullin-RING E3 ubiquitin ligase enzyme complex. This binding selectively alters the substrate specificity of the ligase, targeting two essential lymphoid transcription factors—IKZF1 (Ikaros) and IKZF3 (Aiolos)—for rapid cellular degradation.
Direct Tumor Suppression & Apoptosis: The destruction of Ikaros and Aiolos causes a down-regulation of crucial survival factors in B-cell malignancies, leading to immediate cell cycle arrest and programmed cell death (apoptosis) in malignant plasma cells.
3. Storage, Stability, and Handling Protocols
Environmental Matrix: Store Lenangio 10mg Capsules in their original moisture-resistant container or blister packaging at controlled room temperature, strictly below 30°C (86°F). Protect the inventory from high ambient steam, humidity, heat, and direct exposure to light.
ANTI CANCER MEDICINE
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