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Boluoke Canada RNA 60 caps by Researched Nutritionals



 

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Product Code: BOLUOKE-SM-60
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Description
 
BoluokeŽ (lumbrokinase) is the only fully researched oral fibrinolytic supplement on the market. Besides having in vitro studies, animal studies, toxicity studies, and pharmacokinetic studies done, BoluokeŽ has also been put through all phases of clinical trials (including randomized double blind controlled studies) in China. Lumbrokinase has been studied as a treatment for various clinical conditions, including acute, sub-acute, and chronic conditions that are associated with the presence of hypercoagulation and hypoperfusion.

Lumbrokinase is a more potent enzyme preparation than nattokinase. One of the advantages of BoluokeŽ (lumbrokinase) is that it does not interfere with the clotting cascade, but instead, works by reducing fibrinogen and fibrin. BoluokeŽ does not affect INR or aPTT, thus is compatible with CoumadinŽ or heparin.

BoluokeŽ vs. Other Lumbrokinase Products
Comparing other lumbrokinase products to BoluokeŽ is like comparing apples and oranges. BoluokeŽ’s enzymatic strength is standardized against urokinase and t-PA. The imitation products are likely just earthworm protein extract containing little pure lumbrokinase or lumbrokinase of low enzymatic strength. Some companies are making products with 230mg to 250mg of lumbrokinase per capsule and trying to quote BoluokeŽ’s research as their own. BoluokeŽ’s capsules are of 200mg in size, and contain 20mg of lumbrokinase inside each capsule. Most of these other lumbrokinase are unable to distinguish between the weight of the capsule (i.e. 250 mg) and the active lumbrokinase per capsule (BoluokeŽ is 20 mg).

BoluokeŽ is the only fully researched oral fibrinolytic supplement on the market. Besides having in vitro studies, animal studies, toxicity studies, and pharmacokinetic studies done, BoluokeŽ has also been put through all phases of clinical trials (including randomized double blind controlled studies) in China. BoluokeŽ is the only Lumbrokinase that is backed by Phase I – III clinical trials in China, the one that is first used in hospitals in China, and covered by the Chinese National Fundamental Health Insurance.

A common question we receive is about potential side effects of BoluokeŽ. The earthworm has been used in Traditional Chinese Medicine for a few thousand years, and is considered to be one of the safest medicines in the traditional pharmacopoeias. In one of the largest clinic trials of BoluokeŽ involving 16 hospitals and 1560 patients in China, the overall adverse reaction rate was 1.92% (30 cases). 0.58% had skin itching, 0.19% had skin rash, and 1.15% had nausea or diarrhea; no hemorrhage or major side effect was reported. Again, this research pertains only to BoluokeŽ.

It is interesting that other lumbrokinase products cite the clinical results achieved with only BoluokeŽ, confusing the reader into assuming that the research was done on their formulations. However, their products may be very different, and your patients may have very different results.

On the raw material market, the price of lumbrokinase can vary by up to 15 fold, and the enzymatic strengths of various Lumbrokinase also differ greatly. In addition, lumbrokinase is a preparation containing multiple enzyme fractions, and the extraction and purification method determines the composition of the various enzyme fractions. Thus different extraction methods will produce different sub-fractions of lumbrokinase. This is the reason why BoluokeŽ does not significantly change prothrombin time (PT) or activated partial thromboplastin time (aPTT), while other lumbrokinase sources may significantly alter PT or aPTT as shown in studies. No other lumbrokinase product can provide you with this assurance.

BoluokeŽ seems to be beneficial for any illness that has an accompanying hypercoagulable blood state, which has been shown to be present in many chronic illnesses. Some practitioners are also recommending BoluokeŽ for those who choose to be on hormone replacement therapy or birth control pills, and for those who could not tolerate standard preventative pharmaceutical drugs.


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