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Buy Edaravone (Daiichi Sankyo) Online

DISEASE INDICATIONS: Amyotrophic Lateral Sclerosis (ALS), Cerebral Infarction

MANUFACTURER: Daiichi Sankyo Company Limited

USAGE: Intravenous

MEDICINE APPROVED BY:

Pharmaceuticals and Medical Devices Agency (PMDA)

Edaravone is a medication developed and marketed by Daiichi Sankyo under the trade name Radicava. It is primarily used for the treatment of a specific neurological condition known as amyotrophic lateral sclerosis (ALS), also referred to as Lou Gehrig’s disease.

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Edaravone is a medication developed and marketed by Daiichi Sankyo under the trade name Radicava. It is primarily used for the treatment of a specific neurological condition known as amyotrophic lateral sclerosis (ALS), also referred to as Lou Gehrig’s disease. ALS is a progressive and degenerative disorder that affects nerve cells in the brain and spinal cord, leading to muscle weakness, loss of motor function, and ultimately, severe disability.

Here is a comprehensive description of Edaravone (Radicava):

1. Drug Class and Mechanism of Action: Edaravone is classified as a neuroprotective medication with antioxidant properties. It is believed to work by reducing oxidative stress and inflammation in the central nervous system, which are thought to contribute to the progression of ALS.

2. Indications: Edaravone is specifically indicated for the treatment of amyotrophic lateral sclerosis (ALS) in adults. ALS is a rare and debilitating neurodegenerative disease characterized by the gradual loss of motor neurons, leading to muscle weakness and atrophy, difficulty speaking and swallowing, and eventual paralysis.

3. Dosage and Administration: Edaravone is administered intravenously (IV) and is typically given as a daily infusion over a 10 to 14-day cycle, followed by a 14-day drug-free period. This cycle is repeated for as long as the healthcare provider deems necessary based on the patient’s condition. The treatment is typically administered in a healthcare setting.

4. Effectiveness: Clinical trials have shown that Edaravone can slow the decline in functional abilities associated with ALS. While it is not a cure for the disease, it has been shown to provide some benefit by potentially delaying disease progression and preserving motor function for a period of time.

5. Side Effects: Common side effects of Edaravone may include headache, bruising at the injection site, gait disturbance, and respiratory infections. More serious side effects are rare but may include liver problems, hypersensitivity reactions, and reduced white blood cell counts. It is essential for patients to report any unusual or severe side effects to their healthcare provider promptly.

6. Precautions and Monitoring: Before starting Edaravone treatment, individuals should inform their healthcare provider of their medical history, allergies, and all medications they are taking. Regular monitoring is crucial to assess the medication’s effectiveness and manage potential side effects.

7. Cost and Insurance Coverage: Edaravone is a specialized medication, and its cost can be significant. Insurance coverage and access to the medication may vary depending on individual insurance plans and geographic location. Financial assistance programs may be available for eligible patients.

8. Duration of Treatment: The duration of Edaravone treatment varies depending on the progression of ALS and the patient’s response to therapy. It is typically prescribed for as long as the healthcare provider believes it is providing benefit.

9. Other Therapies: Edaravone is often used as part of a comprehensive treatment plan for ALS, which may include physical therapy, occupational therapy, speech therapy, and supportive care to manage symptoms and improve quality of life.

10. Conclusion: Edaravone (Radicava) is a medication developed by Daiichi Sankyo for the treatment of amyotrophic lateral sclerosis (ALS). It is administered intravenously and is believed to work by reducing oxidative stress and inflammation in the central nervous system, potentially slowing the progression of the disease. While it is not a cure, it can provide some benefit by preserving motor function and delaying the decline in functional abilities associated with ALS. Its use should be closely monitored by healthcare professionals to assess effectiveness and manage potential side effects. It is an important option for individuals living with ALS to consider as part of their treatment plan.

Package

10 vials of 30 mg/20 mL, 10 infusion bags of 30 mg/100 mL

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