INTRODUCTION
Almost every country is seeking new efficient
methods to decrease the sickness rate. Rapid progress in pharmacology gave rise
to the advent of many new highly specific medicaments. They are efficient in treating
some particular diseases and destroying certain activators.
However, modern medicine virtually made no progress
in treating many chronic illnesses whose prevalence rate is steadily rising. This
is because physicians have disregarded the organism’s defensive capacities
for a long time. The situation is aggravated by the fact that modern
drugs are synthesized compounds. Their structure and characteristics do not
correspond to those of natural chemical compounds encoded in the human genetic
apparatus to be consumed with food. Hence, these drugs are perceived by the
human being as xenogenic. As a result, the intake of synthesized compounds brings
about bodily defensive reactions followed by neutralizing and eliminating the
compounds.
The above-mentioned situation gave rise to a rapid
development of complimentary medicine. The latter is based on a well-established idea that the complex
treatment of any disease should take into account an organism’s systemic
reactions. This approach allows nocifencors to be stimulated, not suppressed.
An efficient method for such stimulation is based on
applying both conventional and novel phytopharmaceutical drugs. Many
investigations verified the therapeutic efficiency of nutritive and dietary
supplements. At present, the role of folk medicine and its methods can be
reappraised due to the thorough knowledge of cell biochemistry and complicated
phenomena of the interaction between tissues and organs.
The uncontrolled application of poorly tested and
low-grade preparations discredited the idea of dietary supplements. However, dietary
supplements are often either harmless drug substitutes or fail-safe drug protectors.
These medicaments offer new opportunities to professional medicine for health care.
One can practice a self-care approach because natural medicine is available,
harmless, and easy-to-use.
If physicians give enough informative and
professional support, dietary supplements could resolve many problems. In
particular, dietary supplements can intensify the regenerating processes of the
body after an illness, stimulate autoimmune processes, and improve physical and
intellectual abilities.
Preventive medicine is another important trend in dietary
supplement application. Modern social development is accompanied by the
epidemic of neuroses and environmental hazards. This particularly goes for physical
factors, such as ionizing radiation, nonionizing radiation, and some others.
The
entire system of negative factors causes the intricate development of pathologically changed cells in organs.
As a result, the damaged organs cannot function properly. Generally, an organ
retains normal functioning for some time due to its functional backup. However,
it fails as soon as it has exhausted its strength. This gives rise to various
chronic inflammatory, dystrophic, or malignant
diseases.
Analyzing
the current situation in medical science and practice, one may come to a
conclusion that the 21st century will be the century of
environmental medicine and healthy lifestyle. Recently, many countries have
formed a brand new philosophy of national health. According to this philosophy,
a social and moral priority for health should be a national value in the
individual and collective consciousness. It should be formed using
administrative, financial, judicial, and religious tools. People should be
personally liable for their health.
Today,
the Public Health Service of the Russian Federation has developed and ratified a
concept and branch plan on Healthy
Person’s Health Protection and Support from 2003 to 2010 (the Commandments
of the Public Health Service of the Russian Federation No. 113 and 114, dated
of March 21, 2003). The main idea of the Concept is a model of medical care directed
to preserving a healthy person’s health,
preventing diseases, and developing restorative medicine.
An
important part of the program is dedicated to the development and application of
dietary supplements. It is assumed that newly developed compounds should meet some
requirements to implement the concept of preserving a healthy person’s health.
Apart from generally accepted requirements (such as scientific
verification and harmless application), the compounds need to possess special
properties. The latter should both stimulate nocifensors and enable the immune
system to timely identify microbes and damaged cells. They should also destroy pathological
cells and harmlessly eliminate nascent decay products out of the body.
Discovery of New Properties of Chlorine Herbal Compounds
Many pharmacological companies are searching for the
most efficient medicaments based on natural dietary supplements. Some of the
most efficient drugs use well-known vegetable adaptogenes, such as the ginseng,
eleuterococus, schizandra, and some others. However, these agents produce an
invigorating effect and stimulate nonspecific host defense mechanisms. In
addition, they have to produce a more selective, long-term, and adjustable
effect. Furthermore, these agents should act not only in conjunction with the
bodily defensive mechanisms, but also in conjunction with pathologically
changed cells of the body.
Therefore, Russian scientists paid special attention
to chlorophyll and its derivatives. For the first time, miscible chlorophyll
derivatives were used for medical purposes by Å. Snyder (USA) in 1942. Later, scientists began to use them for the prevention
and treatment of cardiovascular diseases, atherosclerosis, and rheumatoid
arthritis. In 1986, chlorophyll series derivatives were reported to be efficient
in the photodynamic therapy of malignant
diseases.
In experiments in vitro, in which chlorophyll was
produced from Spirulina platensis, a compound called
Radachlorophyll-C was synthesized. This compound revealed a wide range
of unique properties in experiments in
vitro. A microscopic examination was made of killer cells and macrophages biopsied
from oncological patients. It was found that immune cells interacted with
abnormal cells without their attraction or damage. Evidently, acquired immune
deficiency disordered the receptor and biochemical identification processes in pathologically
changed cells. When the Radochlorophyll-C compound was used, it accumulated in
abnormal cells. This initiated a massive “attack” of killer cells and
macrophages on the blastema cells, followed by their damage. Thus, this
compound produced a selective effect on the pathological cells. It also made
them “visible” for the immune cells.
Besides, the Radochlorophyll-C compound had a properly destructive
effect on pathological cells. It interacts with cell oxygen and transfers its
energy to the cell oxygen. This leads to the generation of a new “singlet”
(active) oxygen form. The singlet oxygen brings about intense oxidative
processes that exceed thresholds in pathological cells. This results in their
damage and necrocytosis (cytotoxic properties).
Active oxygen produces a strong antibacterial effect, which is described
in the scientific literature. The successful application of singlet oxygen is
reportedly effective in the treatment of severe staphylococcia, bacillary
carriage, trophic ulcer, and anabrosis were registered. It also suppresses the
growth and development of bacteria in wounds, anaerobic bacteria, and
enteromycosis.
Active oxygen forms initiate many inflammatory reactions and immune processes.
For instance, the high concentration of active oxygen forms inhibits the DNA
synthesis and cell division. It may also activate apoptosis─a programmed
necrocytosis. This prevents the advance of malignant
growth (Wiseman H., Halliwell
B., 1996). It is the ability to cause apoptosis in the abnormal cells which
makes many anticancer drugs to be therapeutic in action. The efficient application
of ozone-containing compounds to cure cancer might be explained by the
above-mentioned process.
It is
necessary to emphasize that Radochlorophyll-C produces a favorable effect on
the increase in the neutrophyl, lymphocyte, and macrophage count of peripheral
blood. Later, this phenomenon was clinically verified at the Moscow
Scientific-Research Institute of Hematology of the Russian Academy of Medical
Sciences and at the N. N. Blokhin Moscow Cancer Centre of the Russian
Academy of Medical Sciences.
Today,
the Radochlorophyll-C compound is used to make different dosage bands and
dietary supplements, such as the “PHOTOSTIM” dietary supplement, for example.
Composition and Characteristics of the Dietary Supplement “Radavita-HB” Basic Components
When developing
an integrated dietary supplement based on phytopharmaceutical products,
scientists assumed that its formula should contain components producing a
cumulative and synergetic effect. Moreover, the supplement should be able to identify
pathological cells different in nature (such as phlogistic, dystrophic, and
neoplastic), destroy them, and
harmlessly eliminate decay products out of the body. The “Radavita-HB”
dietary supplement meets these requirements in full measure. Its composition
runs as follows:
- Radochlorophyll-C;
- holy thistle seeds (mariol);
- vitamin C;
- lactose;
- peppermint leaves;
- bottlebrush herbs;
- dandelion roots;
- solid vitamin E.
The main active agent of the dietary supplement (Radochlorophyll-C) is used:
- to identify xenogenic germs (antigens) and pathological autologous cells
(autoantigens) and to accumulate in them;
- to cause apoptosis (pathological cell destruction through the DNA
inhibition and proteolytic reaction intensification);
- to stimulate acute inflammatory reactions and immune processes in the
body, which helps macrophages destroy all identified antigen structures.
Among the
extra effects of Radochlorophyll-C is metabolism activation, oxygen transport improvement,
and cardiovascular system hypersthenia.
All the
above-mentioned properties can be efficiently used (and they are actually used)
to treat many diseases whose etiology and pathogenesis involve cell damage or pathological
changes in cell structures. Moreover, these properties can be used to prevent
many pathological processes.
Radochlorophyll-C
is a very active compound. Its pharmacological action results in a large number
of intermediate protheolysis products of pathological cells that may cause
autointoxication. Therefore, it is necessary to stimulate the eliminating
systems of all nascent autotoxins of an organism. This is of particular
importance for diseased people who usually reveal disorders in the neutralizing
liver function, excretory kidney function, and gastrointestinal motility.
When developing
an integrated dietary supplement, researchers had to support the eliminating
systems in order to improve bodily detoxication. Thus, an important constituent
of the “Radavita-HB” dietary supplement is the holy thistle or mariol (Silybum marianum). The holy thistle is one
of the strongest natural anti-oxidants. Its flavonoids prevent tissues from
free radicals. Silymarin contained in its leaves is efficient against hepatic diseases.
According
to Quilisch (1944), the holy thistle is efficient in treating hepatic and bile-cyst
diseases. Some other authors also reported the results of their clinical trials.
They noted a favorable effect of the holy thistle on hepatic illnesses, bile-cyst
diseases, as well as on holecystopathies (Ritter,
1941; Unseld, 1941; Schimert, 1948; Schwarzhaupt, 1953; and Spaich, 1978). Schondube (1956) reported a holy thistle tincture to
have a strong choleretic effect. He also reported the positive results of treating
lower limb venous distensibility.
Recent comprehensive
photochemical, experimental-pharmacological, and clinical-pharmacological
studies demonstrated that drugs made of holy thistle seeds produced a strong therapeutic
effect on patients with chronic holecystopathies and posthepatic syndromes.
Experiments with the holy thistle were made on mice, rats, rabbits, and dogs.
They empirically proved the protective properties of the holy thistle for the hepatic
disorders. These properties were associated with silimarin contained in holy
thistle seeds.
Silimarin
was reported to suppress formalin-caused peritonitis and immunologic-caused
polyarthritis (Vogel & Co., 1975).
The protective and therapeutic effect of silibin (a compound contained in
silimarin) on the liver pulp was potentiated because 80% of the used dosage were
eliminated with the bile (Bulles è &Co., 1975). Experiments carried out in
Germany revealed that silimarin affected poisonous substances intoxicating the liver.
It blocked the toxicant permeation to hepatic cells and resolved other poisons
before they came in action. It is the
only natural compound known today to protect hepatic cells and regenerating its
functions.
Besides,
silimarin was also shown to provide the hepatic self-maintenance. In the Pavia
University (Italy), laboratory rats were cut off 70% of their liver. On the
second day, 54.2% more new cells were regenerated in the group treated with the
active compounds of the holy thistle. Three days after the operation, the liver
regeneration amounted to 21.6%.
In the
Max Plank Institute of Biochemistry (Munich), this fact was given a scientific
explanation. It was shown that the effect of holy thistle components on the
liver involved the stabilization of hepatic cell biomembranes, considerable
activation of detoxicative and antioxidant hepatic systems, as well as the
glutathione synthesis intensification. At the same time, they also stimulated the
protein synthesis and regenerating processes in the body. This gave rise to the
regeneration of damaged hepatic cells. Besides, the Saint-Mary-thistle
intensified the bilification and promoted its elimination thus normalizing the
digestive and metabolic processes.
Hence, adding
the holy thistle to the “Radavita-HB” dietary supplement potentiates the
pharmacological effect of Radochlorophyll-C. One component causes the
destruction of pathological cells; another initiates the active neutralizing
and eliminating of decay products by the liver.
To further
potentiate the compound effect of “Radavita-HB”, some other phytogenic
components were also added (such as peppermint leaves, bottlebrush herbs, and
dandelion roots).
Peppermint (Mentha piperita) contains menthol,
flavonoids, ursolic and oleanolic acids, many microelements (such as copper,
manganese, strontium, and some others). Because all these compounds and
substances have pharmacological action, peppermint has been used in the
galenicals and tinctures for many centuries. Peppermint reflectory improves
blood circulation in brain and cardiac vessels. As a spasmolysant, peppermint
is prescribed when a person has spastic phenomena in the gastrointestinal
tract, bile ducts, and pancreatic ducts. A peppermint tincture is used as an
analgetic to treat neurodynia and toothaches. As an antiseptic, it is used to
treat the upper respiratory tract inflammations and stomatitis.
In the
dietary supplement “Radavita-HB,” flavonoids of peppermint complement the
hepatoprotective action of silimarin. They
stimulate the bile-expelling liver
function and the motor function of the gastrointestinal tract.
Dandelion (Taraxacum officinale) roots are rich in polysaccharide inuline. By
fall, about 40% of it is accumulated in dandelion roots. At this period, they
contain up to 18% of saccharides (such as fructose, sucrose, and glucose). Its
roots contain many substances, such as the triterpene compounds, sterols,
caoutchouc, phenol-carbonate acids, tanning agents, flavonoids, lactones, and
fatty oil. As a result of such a composition, dandelion roots provoke appetite,
intensify gastric secretion, and are good cholagogues. Vitamins A, B, C, and E
contained in dandelion roots provide an antioxidant effect on the liver,
pancreas, and bile cyst. Dandelion roots in the form of a decoction are
recommended for the diabetics, since it improves the metabolic activity.
Dandelion roots in the form of a decoction and coffee substitute are also used
as an anti-sclerotic agent. For people with chronic constipations, dandelion
roots are used as an evacuant agent. Dandelion roots are contained in appetizing,
gastric, and diuretic teas.
Bottlebrush herbs (Equisetum arvense) contain alkaloids, saponin, equisetonin,
flavonoids, organic acids, fatty oil, volatile oil, vitamin C, carotene, many
siliceous acid salts, bitter stuff, tanning agents, resins, and polytrimethylcellulose compounds. It was reported
that bottlebrush improves the urine passage, possesses the blood-regenerating
and anti-inflammatory properties, and initiates lead elimination. The siliceous
acid and its salts are part of most organic tissues. They influence ostein and
collagen formations. Silicium contained in the bottlebrush is invigorating in
action. It provides a healthy bone and blood-vessel development.
According
to the abovementioned facts, bottlebrush is used as an emictory and
blood-regenerating agent to treat the inflammatory urinary tract and liver
diseases, vesical calcifications, arthropathy, and
salt exchange damage. As an emictory agent, bottlebrush is also used to treat
the cardiac illnesses accompanied by congestive phenomena as well as to treat
cardiopulmonary diseases. Bottlebrush tincture may irrigate septic wounds,
treat furuncles, trophic ulcers, and some other skin diseases. It is also
recommended that a person should take the bottlebrush agents to treat acute and
chronic lead poisoning.
The
adding of bottlebrush herbs to the “Radavita-HB” dietary supplement is mainly
provided by its diuretic properties. It accelerates the excretory process of proteolysis
products of pathologically changed cells and metabolic substances.
Vitamin C (Acidum ascorbinicum) contained in “Radavita-HB” produces a strong invigorating
effect on the body. Being one of the strongest antioxidants, vitamin C
activates natural nocifensors and helps to cure many diseases. In “Radavita-HB”,
the containing of vitamin C is 60 mg, which is 85% of a daily dose. The
“Radavita-HB” biologically active substances potentiate the invigorating effect
of the vitamin C.
Vitamin E (Tocopheroli acetas) is a vital vitamin,
which influences the functioning of the entire body. According to the data
obtained from literature, vitamin E normalizes the blood pressure, improves the
skin, strengthens the lung, cardiac and nervous tissues, consolidates blood
vessel parietes, particularly capillary tubes, and produces the antibacterial
and antioxidant effects.
“Radavita-HB”
contains 6.0 mg of vitamin E, which is 60% of a daily dose.
The
combination of vitamin C, vitamin E, and the biologically active components in
herbal substances results in a strong invigorating effect for the entire body.
Lactose (milk sugar) is used in the
“Radavita-HB” dietary supplement to maintain lactic-acid bacteria in the body.
They process proteolysis products eliminated by the bile in the
gastrointestinal tract.
The Results of the “Radavita-HB” Dietary Supplements
Clinical Trials
The
clinical trials of the “Radavita-HB” dietary supplement were organized at the
Rheumatology-Oriented General Medicine Department of the Samara Medical
Institute “Reaviz.” The trials were headed by Professor Y. S. Pimenov,
the Head of the Department, Academician of the Academy of Medical and Technical
Sciences, Doctor of Medical Science, and the managing director of the
Diagnostic and Treatment Centre “Zdraviye,” and Y. A. Podkorytov ,
the Doctor of Philosophy in Medical Science.
The
clinical trials of the “Radavita-HB” dietary supplement were carried out for
the following diseases: chronic hepatitis B and C, chronic pancreatitis, chronic
pyelonephritis, severe pneumonias, including septic pneumonia with a burdened
history (drug or alcohol addiction), severe systemic lupus erythematosus with a
multiple organ damage and high activity, incipient infective endocarditis of
the prosthetic valves, pollen fever, HIV infection associated with the early
drug taking, for patients operated after brain tumors, radial, and
polychemotherapy.
A control
group consisted of 20 people: 10 men and 10 women aged between 15 and 65. To
control the efficiency of the dietary supplement, 2 patients with each of the
above-mentioned nosologies received a conventional treatment.
The
efficiency of the dietary supplement in both groups (experimental and control)
was estimated according to the overall health of the patients, blood indices
dynamics (such as general blood analysis, biochemical analysis, and depending
on the clinical entity, immunologic research), X-ray examinations, ultrasound investigations,
computerized tomography (CT), magnetic resonance imaging (MRI), and
electrocardiography. The investigations
were carried out at the admission, 2 weeks after the treatment commencement,
and after the treatment termination.
The
“Radavita-HB” dietary supplement was recommended as a monotherapy, as well as
part of multiple treatment: a person took 1 capsule 3 times a day during 16
days.
Results of the Clinical Trials in Nosological
Groups
In the
chronic viral hepatitis group, 6 people (3 people with hepatitis B and 3 people
with hepatitis C) were examined. All the patients had a moderate process
activity, cholestatic syndrome, assident chronic pancreatitis, and fatty
hepatosis. Computerized tomography showed that one patient had a sclerosing cholangitis with a “soft”
cholesterol calculus in the common bile duct.
The
“Radavita-HB” dietary supplement was added to the treatment course which was
previously rather inefficient. On the 5th to 6th day
after having taken the preparation, the patients had no pains and lower
heaviness in the dextral hypochondrium. As they claimed, they stopped “feeling
their liver.” The feces and emiction became of normal color. In one case, Patient
G., 1968 had stopped taking the drug for about 1 day because of diagnostic
procedures. As a result, the patient’s feces became paler again and his
emiction became darker. After resuming the intake of the “Radavita-HB” dietary
supplement, the patient’s state normalized. This proved the potentiating effect
of “Radavita-HB”.
In
another case, patient T. (1948) with a severe skin itch had an evident clinical
performance. The drug intake stoppage has resulted in skin itch
intensification. After resuming the compound intake, the patient’s state
normalized. This patient revealed another interesting phenomenon. Before the
treatment, computerized tomography found a “soft” calculus in his common bile
duct. After having used the preparation for 15 days, the patient was operated
on for the obstructive jaundice. However, no calculus was observable in his
common bile duct. This fact indicated that the “Radavita-HB” dietary supplement
components were cholelitolitic in action.
After
the treatment, it was found that the patients of the experimental group had an increase
in albumen, a decrease in γ-globulin, thymol, amyolytic enzymes,
and transaminase. These changes were observable to a greater extent as compared
to the control group. The patients with the cholestasis had a greater decrease
in the bilirubin level. The urinary sediment index showed a tendency to
normalize.
Five
patients with the chronic hepatitis had skin itch, exfoliation, and general
weakness alleviation, as well as fissure cicatrisation. These changes were
observable to a greater extent as compared to the control group treated without
the dietary supplement. In general, the treatment of the patients with the
chronic hepatitis complicated by the concomitant pathology in the control group
was more efficient. The “distance” of the clinical improvement dynamics between
the groups was 3 to 4 days.
In the chronic
pancreatitis group, 3 patients were examined. Two of them have passed the
following treatment course: a diet, mesim-forte, pancreatine, contricale,
multivitamins, and the “Radavita-HB” dietary supplement. One patient with the
sequent middle-severity pancreatitis recrudescence was taking the dietary
supplement as a monotherapy. The control group consisted of two patients with a
similar clinical course and the same treatment course without taking the
dietary supplement. It was noticed that in general the including of the
“Radavita-HB” dietary supplement to the treatment course alleviates the patient’s
recuperation process.
The
same patient taking the dietary supplement as a monotherapy also noticed quite
an early subjective recovery. On the 4th day of the dietary
supplement intake, the general weakness reduced, the stool normalized, and the
appetite improved in a week.
Two
patients with acute chronic pyelonephritis with the concomitant chronic
hepatitis C were treated with the “Radavita-HB” dietary supplement in addition
to the rheoferon and ribamidile. The patients were also given the uroseptics.
In the experimental group as well as in the control group, the patients had a
considerably stable emiction and the Nechiporenko probe normalization, even
though they received no uroseptics. This may indicate the fact that the
“Radavita-HB” dietary supplement is anti-inflammatory and uroseptic in action.
Two
patients with double pneumonia were examined. It is necessary to emphasize that
the course of the disease of one of the patients was aggravated by heroin addiction.
In the other patient, the disease was associated with sepsis, accompanied by
the inflammatory endocarditis, and aggravated by a long-term alcohol addiction.
On the 15th day of the antibacterial and detoxication therapy, there
was no positive dynamics. It was decided to include the “Radavita-HB” dietary
supplement to the treatment course (the patient was taking 5 capsules a day).
In 4 days, the situation improved considerably. The patients had less
expectoration, the intoxication indices of urea and creatinine as well as the
body temperature reduced, and the overall health improved.
Although
these two severe pneumonias resulted in the metapneumonic pneumofibrosis, one should take into
consideration a really serious pneumonia run of the patients taking the
“Radavita-HB” dietary supplement, particularly the patient with sepsis. One
could hardly expect the vital end in such a case.
The
similar “additional” effect of the “Radavita-HB” dietary supplement was noticed
in the treatment of two rheumatologic patients (systemic lupus erythematosus and rheumatologic
defects), as well as the patient with the incipient infective endocarditis of
the prosthetic valves. The addition of the “Radavita-HB” dietary supplement to
the treatment course resulted in the body temperature reduction, appetite
improvement, labored breathing and general weakness remission, peripheral blood
indices normalization. Two control patients receiving the conventional
treatment had the above-mentioned changes with a 3-to-4 day delay, as compared
to the experimental group.
To
investigate the influence of “Radavita-HB” on the immune system, this compound
was prescribed as a monotherapy for two HIV positive 22-year-old patients. Both
of them had heroin addiction during 3 years and the positive HIV test during
1.5 years in their anamnesis. They complained about the progressing weight
loss, absence of appetite, suicidal thinking, frequent strong headaches, and
general weakness. There was also amenorrhea during several months. In 2 weeks
after having used the “Radavita-HB” dietary supplement, these women revealed
good appetite, began to gain in weight, and had less depression. Their headaches
were not so frequent and strong, and the overall health improved. In a month,
they exhibited instable periods (menstruation). The data obtained are summed up
in the tables below.
Table 1. Results of the
“Radavita-HB” dietary supplement application in the treatment of HIV patients
|
The most vivid results
|
Patient 1
|
Patient 2
|
|
Dietary supplement + monotherapy
|
Dietary supplement + monotherapy
|
|
Before the treatment
|
After the treatment
|
Before the treatment
|
After the treatment
|
|
Hemoglobin, g/l
|
115
|
117
|
119
|
124
|
|
The erythrocyte contents in the peripheral blood, n×1012
|
4.7
|
5.0
|
4.3
|
4.5
|
|
The leukocyte contents in the peripheral blood, n×109
|
8.1
|
6.2
|
9.4
|
8.1
|
|
ALT, IU/L
|
48
|
36
|
56
|
40
|
|
Total blood protein, g/l
|
56
|
60
|
58
|
61
|
|
Blood Sedimentation Rate (BSR), mm per hour
|
32
|
16
|
24
|
14
|
|
Immunoglobulin M
|
0.33
|
0.31
|
0.28
|
0.29
|
|
Immunoglobulin G
|
0.08
|
0.1
|
0.07
|
0.08
|
|
Immunoglobulin Â
|
1.2
|
1.5
|
2.5
|
2.8
|
|
Phagocytic index
|
33
|
38
|
45
|
49
|
As one
can see from Table 1, some figures tend to increase. It is possible to state
that the dietary supplement produces a slightly immunomodulatory effect and stimulates
the hepatic function.
Both
patients were operated on for the brain
tumor after radiation therapy and chemotherapy. The application of the dietary
supplement in them produced a favorable effect on their recovery. The tumors
had different localizations in the cerebral hemispheres and were verified
as cancerous. The “Radavita-HB” was prescribed in the experimental group as a
monotherapy. Before using it, the patients had severe headaches, motion discoordination,
and hemiparesis phenomena. The BSR was significantly increased in both cases.
The two patients of the control group took nootropics and multivitamins during rehabilitation
treatment.
In a
month, all the patients revealed a better physical state, improved laboratory
indices, and decreased intracranial pressure. However, patients of the experimental
group exhibited a more considerable decrease in the headache rate, headache severity,
and hemiparesis, as compared to the control group. Table 2 shows some
laboratory-clinical indices.
Table 2. Results of the “Radavita-HB” dietary
supplement application in the treatment of patients with CNS pathology
|
Some illustrative indices
|
Patients operated on for the brain tumor (rehabilitation period)
|
|
Control group
(conventional treatment)
|
Experimental group (dietary supplement + monotherapy)
|
|
Before
the treatment
|
After the treatment
|
Before the treatment
|
After the treatment
|
|
Hemoglobin, g/l
|
115
|
120
|
121
|
128
|
|
BSR, mm per hour
|
28
|
14
|
32
|
13
|
|
The erythrocyte contents in the peripheral blood, n×1012
|
4.0
|
4.3
|
3.8
|
4.1
|
|
The leukocyte contents in the peripheral blood, n×109
|
3.6
|
4.4
|
3.1
|
4.8
|
|
Total blood protein, g/l
|
58
|
61
|
61
|
63
|
|
Subjective indices:
Weakness reduction
|
On the 15th day of the therapy
|
On the 9th day of the dietary supplement usage
|
|
Appetite improvement
|
On the 13th day of the therapy
|
On the 7th day of dietary supplement application
|
|
Mood improvement
|
Not observed
|
On the 12th day of dietary supplement application
|
|
Sleep normalization
|
On the 13th day of
dietary supplement application
|
On the 12th day of dietary supplement application
|
Taking
into consideration data shown in Table 2, one may come to a conclusion
that the main difference lays in the subjective indices and the total exchange
dynamics. The latter can be associated with the energizing action of the “Radavita-HB”
dietary supplement.
The
research group of the Samara Medical Institute concluded that it was efficient
to apply the “Radavita-HB” dietary supplement in combination with Radochlorophyll-C
and biologically active phytopharmaceutical components that stimulate an organism’s
eliminatory systems. This makes it possible to facilitate the intensive
antibiotic treatment and chemotherapy. It also enables one to successfully apply
the “Radavita-HB” dietary supplement as a monotherapy in the pathosis
treatment. Thus, the “Radavita-HB”:
- improved overall health, alleviated subjective sensations, improved
mood, mitigated and eliminated pain sensations;
- normalized blood indices (increased albumen and γ-globulin; decreased thymol indices,
amyolytic enzymes, and transaminases) to a greater extent as compared to a conventional
treatment;
- expedited the recovering and regenerating processes of almost all the patients
as compared to a conventional treatment;
- activated the immune system of all the patients, which considerably
shortened the treatment term and improved rehabilitation indices.
Practical Application Guidelines
Pharmacological
action and clinical results obtained enable us to recommend that the “Radavita-HB”
dietary supplement be part of complex treatment of the following diseases:
- Chronic viral hepatitises accompanied by cholestasis, skin itch, and
other skin disorders;
- Chronic pancreatitises, chronic cholecystitises, and bile passage
dyskinesias;
- Severe inflammatory diseases (such as pneumonia, sepsis, HIV infection, and
urinary tract infections);
- Rheumatic diseases;
- Malignant tumors at the rehabilitation period, postsurgical period, after
radiation therapy, or after polychemotherapy;
- Diseases accompanied by drug or alcohol addiction;
- Immune system dysfunction causing autoimmune diseases;
- Hepatic kinesis slackening and motor-evacuative bowel function weakening;
- Viral and bacterial infections at the recovery period;
- Excessive exercise and psychological stress caused by professional
activities and environmental exposures.
Medical Contra-Indications to the “Radavita-HB”
Dietary Supplement Application
Clinical
results showed that the “Radavita-HB” dietary supplement should be used under the
physician’s supervision. Some “Radavita-HB” components can sometimes give rise
to allergic reactions, which are characteristic of any drug compound. In some
cases, the “Radavita-HB” dietary supplement may cause a transient exacerbation
of latent chronic diseases. It is associated with a massive pathological cell
damage and decay product release in blood. Sometimes, the “Radavita-HB” dietary
supplement may cause some discomfort in the epigastric region. Such a situation
may require a timely consultation of the attending physician to examine the patient’s
state, to calm him or her down, and to correct the drug application regimen.
Administration Procedure and Dose Recommendations
- As a prophylactic treatment of a virtually healthy person, one should
take 1 capsule daily after meals during a month;
- As part of the complex treatment of simple chronic diseases, a person
should take 1 capsule 2 to 3 times a day during the treatment course (up to 30
days);
- In more serious cases, a person should take up to 6 capsules a day in 3
to 4 times during 20 days.
The
“Radavita-HB” dietary supplement has a sanitation-and-epidemiological conclusion of the
State Sanitation and Epidemiological Control Council of
the Russian Federation No. 77.99.21.972.Á.000340.10.03 dated of October 31, 2003. This conclusion is based on the
expert judgment of the State Test Centre of the Research Nutrition Institute of the Russian Academy of Medical Sciences No. 72\Ý-1828-03 dated of 11.09.2003.