Description
Solventium Pharmacodynamics
Common osteochondrosis (deposition of salts) is a metabolic disease in which products of disturbed metabolism (so-called salts or slag) are deposited on the surface of bones, most often in the joints. Subsequently, the affected joints can become inflamed, with pain, swelling, and sometimes reddening of the joints. This phenomenon is called metabolic polyarthritis. A common complication of osteochondrosis is an inflammation of nerve roots or the entire nerve trunk (neuralgia, radiculitis, lumbago, sciatica, etc.) of varying localization, often with severe neuralgic pain.
Osteochondrosis of the spine (especially in the cervical and thoracic spine) compresses numerous nerves and blood vessels, which in turn causes or intensifies the so-called vegetovascular dystonia. Exactly this symptom complex (i.e. the combination of osteochondrosis and vegetovascular disorders) is a real killer of modern mankind: according to statistics, its long-term consequences – cardiovascular failure, heart attack and stroke – occupy the first place in the list of causes of death, ahead of even cancer.
The drug “Solvent” specifically affects the metabolism in a regulating and strengthening way. At the same time, salt deposits are dissolved. By treating the cause, the drug eliminates related symptoms and complications (polyarthritis, neuralgia, vegetative-vascular disorders).
“Solventium” regulates calcium metabolism, so it is effective for Osteoporosis, which consists in the fact that in the place where calcium should be, it is absent, and where it should not be, it is deposited in the form of osteochondral hardening.
Experience with Solvent has shown it to be effective (i.e., causes shrinkage and resorption) in benign tumors of all kinds, such as MIOMAs and FIBROADENOMAs.
Indications
In the treatment of osteochondrosis.
Contraindications .
Increased individual sensitivity to the individual components of the drug. Age under 18 years (in the absence of special studies).
Dosage and administration.
- Inside. Dilute 10 drops of the drug in 1/4 cup water and drink in small sips, without swallowing and without drinking anything. The drug is taken twice a day (4 days take, 3 days break). Take 30 minutes before or 30 minutes to one hour after a meal. The course of treatment of 1.5 months. It is possible to repeat courses.
- Occasional short pauses and missed receptions are not very reflected in the overall course of treatment. In the case of a reaction (deterioration) – a break of 7-10 days. The drug is diluted in water (less than a quarter cup) and drunk in small sips without swallowing; the drug may be dripped directly into the mouth. Food weakens the effect, so if possible take half an hour or more before a meal and half an hour or more after a meal.
