Remove 2022 Remove Adverse Reactions Remove Immunity
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FDA Approvals: September 2022 Recap

Digital Pharmacist

Date of Approval: 9/30/2022. Common adverse effects include musculoskeletal pain, constipation, diarrhea, fatigue, dry mouth, and abdominal pain , among others. . Date of Approval: 9/29/2022. Common adverse effects noted include diarrhea, abdominal pain, nausea, and upper respiratory tract infection. .

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First chikungunya vaccine approved

European Pharmaceutical Review

In March 2022, Valneva reported final pivotal Phase III data for the vaccine showing a 98.9 As part of the US FDA approval, the FDA stated that the company is required to conduct a postmarketing study to assess the serious risk of severe chikungunya-like adverse reactions following administration of IXCHIQ.

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The 5 Stages of Hashimoto’s Thyroiditis

The Thyroid Pharmacist

This means that our immune system recognizes the thyroid gland as a foreign invader and begins to attack it, eventually leading to the destruction of our thyroid tissue. Left unbalanced, the immune system may go on to attack different parts of the body, leading to the development of other autoimmune conditions.

Immunity 122
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Low Dose Naltrexone and Hashimoto’s

The Thyroid Pharmacist

However, low doses of this medication (hence, low dose naltrexone or LDN), have been found to modulate the immune system and have shown promise in improving cases of autoimmune disease. These include Crohn’s, MS, and Hashimoto’s, as well as other immune system-related conditions such as cancer and HIV/AIDS. Doses of 1.5-4.5

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The 7 Most Common Nutrient Deficiencies in Hashimoto’s

The Thyroid Pharmacist

Most people with Hashimoto’s have deficiencies in these nutrients, and I’ve seen very limited adverse reactions with supplementation (please check the special considerations/cautions sections under each supplement heading to learn about adverse reactions). (12-16). When to Expect to See Benefits: Usually 3 to 5 days.

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BMS Submits Application for Abecma® for Relapsed or Refractory Multiple Myeloma

LifeProNow

In Japan, Abecma was approved for manufacturing and marketing on January 20, 2022, and indicated for patients with relapsed or refractory multiple myeloma who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti-CD38 antibody.

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Developing point-of-care CAR T manufacturing

European Pharmaceutical Review

This is especially important due to the two unique toxicities of CAR T cells, namely CRS and the neurology toxicities that subsequently received the term immune effector cell- associated neurotoxicity syndrome (ICANS). After this incident CAR-related toxicity scales and guidelines were established to prevent adverse reactions.