Hot sale good quality Rhodiola Rosea Extract in Hamburg


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Hot sale good quality Rhodiola Rosea Extract in Hamburg Detail:

[Latin Name] Rhodiola Rosea

[Plant Source] China

[Specifications] Salidrosides:1%-5%

Rosavin:3% HPLC

[Appearance] Brown fine powder

[Plant Part Used] Root

[Particle size] 80 Mesh

[Loss on drying] ≤5.0%

[Heavy Metal] ≤10PPM

[Storage] Store in cool & dry area, keep away from the direct light and heat.

[Package] Packed in paper-drums and two plastic-bags inside.

Rhodiola Rosea Extrac11t

[What is Rhodiola Rosea]

Rhodiola Rosea (also known as Arctic root or golden root) is a member of the family Crassulaceae, a family of plants native to the arctic regions of Eastern Siberia. Rhodiola rosea is widely distributed  in Arctic and mountainous regions throughout Europe and Asia. It grows at altitudes of 11,000 to 18,000 feet above sea level.

There are numerous animal and test tube studies showing that rhodiola has both a stimulating and a sedating effect on the central nervous system; enhance physical endurance; improves thyroid, thymus, and adrenal function; protects the nervous system, heart and liver; and has antioxidant and anticancer properties.

Rhodiola Rosea Extrac221t

[Function]

1 Enhancing immunity and delaying aging;

2 Resisting radiation and tumor;

3 Regulating nervous system and metabolism, effectively limiting melancholy feeling and mood, and promoting mental status;

4 Protecting cardiovascular, dilating coronary artery,preventing coronary arteriosclerosis and arrhythmia.


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    medskl.com is a global, free open access medical education (FOAMEd) project covering the fundamentals of clinical medicine with animations, lectures and concise summaries. medskl.com is working with over 170 award-winning medical school professors to provide content in 200+ clinical presentations for use in the classroom and for physician CME.

    Primary Care – Infant and Child Immunization
    Whiteboard Animation Transcript
    with David Scheifele, MD

    https://medskl.com/Module/Index/infant-and-child-immunization

    Modern vaccines are safe and impressively effective, potentially eliminating circulation of most target infections. Immunization allows for protection against a broad range of infections.

    During pregnancy, transplacental passage of maternal IgG antibodies allows for passive protection in the first 6 months of life. This, however, decays rapidly, with little remaining beyond 6 months of age. Thus, early infancy is the ideal time to begin immunization so that active immunity can replace waning passive protection without a period of vulnerability in between.

    To achieve this goal, infants typically require several initial vaccine doses spaced about 8 weeks apart, known as the primary series. It ensures that their immature immune system responds adequately. Adherence to the schedule minimizes infection risks. Depending on the vaccine, a booster dose may be required in the second year of life to reinforce the antibody response and extend protection throughout early childhood; additional booster doses may be needed at 4-6 years and in adolescence to renew and extend protection.

    Immunization schedules vary to some extent across regions and you should become familiar with the schedule used in your region of practice.

    As clinicians, you will often get asked about the safety profiles of childhood vaccines. In general, almost all of these vaccines are well tolerated and cause very mild side effects, such as injection site pain or transient fever. The tangible risks are febrile seizures and hypotonic (fainting) spells, which both have low risk rates and benign outcomes.

    This table lists some of the rare complications associated with vaccines.

    MMR meningitis is mainly attributable to the mumps component and differs among products, being very unlikely with the vaccines used in Canada. Measles encephalitis is a great rarity, seen in a few immunocompromised vaccinees.

    Lastly, presence of certain health conditions will alter immunization recommendations. Children at high risk for invasive pneumococcal infection should get 3 primary doses of the PCV13 vaccine (instead of 2) and should also receive the 23-valent pneumococcal polysaccharide vaccine after age 2, which is not part of the routine schedule. Immunocompromised children should not receive live attenuated vaccines.

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