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PEA (palmitoylethanolamide) is a naturally occurring fatty acid amide with anti-inflammatory and pain-relieving properties, widely used as a supplement for chronic pain.
PEA (palmitoylethanolamide) is a naturally occurring fatty acid amide with anti-inflammatory and pain-relieving properties, widely used as a supplement for chronic pain.
PEA stands for palmitoylethanolamide, a naturally occurring fatty acid amide produced by the human body. It belongs to the group of endogenous lipid mediators and is structurally related to endocannabinoids, but without any psychoactive effects. Small amounts of PEA are also found in foods such as egg yolk, soybeans, and peanuts.
PEA exerts its effects through several key mechanisms:
PEA is used and researched in various medical fields:
PEA is frequently used for chronic pain conditions such as fibromyalgia, back pain, sciatica, and neuropathic pain. Multiple clinical studies have demonstrated a reduction in pain perception with regular use.
The effects of PEA have been particularly well studied in neuropathic pain conditions, for example in diabetic neuropathy or carpal tunnel syndrome, where it shows significant pain-relieving effects.
Due to its anti-inflammatory properties, PEA is also being investigated for inflammatory conditions such as osteoarthritis, irritable bowel syndrome, and chronic inflammatory diseases.
In neurology, PEA is being researched for conditions such as multiple sclerosis, Alzheimer's disease, and Parkinson's disease, as it may influence neuroinflammatory processes.
Clinical studies have commonly used doses of 300 to 1200 mg of PEA per day, divided into two to three administrations. PEA is available as a dietary supplement in capsule or powder form. It is recommended to take PEA with a meal, as it is fat-soluble. Consulting a healthcare professional before starting supplementation is advised.
PEA is generally considered very well tolerated. Clinical studies have reported few serious side effects. Mild gastrointestinal discomfort may occasionally occur. PEA is non-psychoactive and non-habit-forming. Long-term safety data over multiple years remain limited. There are insufficient safety data for pregnant or breastfeeding individuals, so use is not recommended during these periods.
The bioavailability of standard PEA is limited due to its poor water solubility. Newer formulations such as micronized PEA (m-PEA) or ultramicronized PEA (um-PEA) show significantly improved absorption and are preferred in most clinical studies.
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