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WSC 2025 in Barcelona: Global Solidarity in the Fight Against Stroke Sets a New Direction for Development. New Data on the Role of Succinate-Containing Therapy

In October 2025, the 17th World Stroke Congress (WSC 2025), ​​becoming the largest and most significant international forum in this field. More than 4,000 delegates from 100 countries—leading neurologists, neurosurgeons, rehabilitation specialists, researchers, and patient advocates—united under the auspices of the World Stroke Organization (WSO) to define the future of stroke prevention, treatment, and rehabilitation. The data presented on the role of antioxidant therapy was of particular interest.

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Changes in the instructions for the medical use of Mexidol: a new indication (ADHD) and children's age (6+)

Dear colleagues, we inform you about the inclusion of a new indication - attention deficit syndrome with hyperactivity (ADHD) in children aged 6 to 12 years, including hyperactivity, impaired attention, impulsiveness.

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In/m injections at home - saving time of the procedural office and convenience for young patients

With the high -speed rhythm of life that is now, many patients, especially working age, do not always manage to find time in their dense schedule for visiting the procedural office. Nevertheless, they also get sick and they can also diagnose serious pathologies that will require the purpose of the course of effective therapy, including Injection forms.

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The article “The results of a multicenter double blind randomized placebo-controlled clinical study on assessing the effectiveness and safety of the drug Mexidol in the treatment of attention deficit syndrome in children (mega)”

section "Library""Evidence Base" contains the article "Results of a multicenter, double-blind, randomized, placebo-controlled clinical trial to evaluate the efficacy and safety of Mexidol in the treatment of attention deficit hyperactivity disorder in children (MEGA)."

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The results of a unique and first one kind of international multicenter randomized double-centered placebo-controlled study on the study of the efficiency of consecutive therapy with Mexidol® and Mexidol® Forte 250 in patients with chronic brain ischemia (Memo)

The results of an international, multicenter, randomized, double-blind, placebo-controlled study evaluating the efficacy and safety of sequential therapy with Mexidol® and Mexidol® FORTE 250 in patients with chronic cerebral ischemia (the MEMO study), conducted in full compliance with international ethical and scientific standards for the design and conduct of research involving human subjects (GCP), were published in the Korsakov Journal of Neurology and Psychiatry, 2021; 121(11):7–16, a leading peer-reviewed journal for neurologists and psychiatrists in Russia, recognized by the Higher Attestation Commission (HAC).

 

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Consistent, prolonged therapy - the key to effective treatment

To fully utilize the therapeutic potential of Mexidol®, sequential long-term therapy is recommended (EPICA1, 2017): initially 14 days of injections (saturation phase), followed by a transition to Mexidol® or Mexidol® FORTE 250 tabletsfor 2months (therapeutic effect maximization phase). Therapy is administered 2-3 times per year or during periods of exacerbation.

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News of medicine

Resolution of the Council of Experts "The possibilities of neuroprotective therapy in patients with arterial hypertension and cognitive disorders"

Neuroprotection should be an integral part of the management of patients with hypertension. It is recommended to supplement the drug treatment algorithm for patients with hypertension by including ethylmethylhydroxypyridine succinate (Mexidol®)in the clinical guidelines for "Arterial Hypertension in Adults" (I10/I11/I12/I13/I15, according to ICD-10).

12.11.23
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About the drug Mexidol®

Mexidol® - Bereday care for children's health

NPK PHARMASOFT LLC announces the inclusion of a new indication – attention deficit hyperactivity disorder in children (aged 6 years and over), including hyperactivity, attention deficit, and impulsivity – in the instructions for medical use of the medicinal product Mexidol®film -coated tablets, 125 mg.

03.10.23
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About the drug Mexidol®

Changes in the instructions for the medical use of Mexidol: a new indication (ADHD) and children's age (6+)

Dear colleagues, we inform you about the inclusion of a new indication - attention deficit syndrome with hyperactivity (ADHD) in children aged 6 to 12 years, including hyperactivity, impaired attention, impulsiveness.

12.04.23
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News of medicine

In/m injections at home - saving time of the procedural office and convenience for young patients

With the high -speed rhythm of life that is now, many patients, especially working age, do not always manage to find time in their dense schedule for visiting the procedural office. Nevertheless, they also get sick and they can also diagnose serious pathologies that will require the purpose of the course of effective therapy, including Injection forms.

20.02.23
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News of medicine

The influence of influenza on memory and brain activity

Influenza is an acute infectious disease that affects both the upper and lower respiratory tract, the causative agent of which is the virus.

01.02.23
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About the drug Mexidol®

The article “The results of a multicenter double blind randomized placebo-controlled clinical study on assessing the effectiveness and safety of the drug Mexidol in the treatment of attention deficit syndrome in children (mega)”

section "Library""Evidence Base" contains the article "Results of a multicenter, double-blind, randomized, placebo-controlled clinical trial to evaluate the efficacy and safety of Mexidol in the treatment of attention deficit hyperactivity disorder in children (MEGA)."

31.08.22
Read more
About the drug Mexidol®

The results of a unique and first one kind of international multicenter randomized double-centered placebo-controlled study on the study of the efficiency of consecutive therapy with Mexidol® and Mexidol® Forte 250 in patients with chronic brain ischemia (Memo)

The results of an international, multicenter, randomized, double-blind, placebo-controlled study evaluating the efficacy and safety of sequential therapy with Mexidol® and Mexidol® FORTE 250 in patients with chronic cerebral ischemia (the MEMO study), conducted in full compliance with international ethical and scientific standards for the design and conduct of research involving human subjects (GCP), were published in the Korsakov Journal of Neurology and Psychiatry, 2021; 121(11):7–16, a leading peer-reviewed journal for neurologists and psychiatrists in Russia, recognized by the Higher Attestation Commission (HAC).

 

19.01.22
Read more
About the drug Mexidol®

Consistent, prolonged therapy - the key to effective treatment

To fully utilize the therapeutic potential of Mexidol®, sequential long-term therapy is recommended (EPICA1, 2017): initially 14 days of injections (saturation phase), followed by a transition to Mexidol® or Mexidol® FORTE 250 tabletsfor 2months (therapeutic effect maximization phase). Therapy is administered 2-3 times per year or during periods of exacerbation.

27.08.20
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THE INFORMATION IS INTENDED FOR HEALTHCARE AND PHARMACEUTICAL PROFESSIONALS. THIS INFORMATION IS NOT INTENDED AS A SUBSTITUTE FOR MEDICAL ADVICE.

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