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Side effects of anavar:
is not very toxic, not very androgenic, mildly anabolic, and pretty mild on the body´s HPTA (Hypothalamic-Testicular-Pituitary-Axis). Those are its 4 major points, and I´d like to examine each one a bit further; as usual, gym-rumors and internet conjecture has made this steroid the subject of many misconceptions.}
Anavar (Oxandrolone) Side Effects:
First of all, and this will come as no surprise to many people, Anavar (oxandrolone) is quite mild on your liver. It´s probably the mildest oral steroid available today. Dosages of up to 80mgs/day are easily tolerated by most men, and most side effects often found with other steroids are not common with ´var (1). For this reason, Anavar is frequently the steroid of choice for many top level female bodybuilders and other athletes.
Anavar DosageDue to its being a mild steroid in every sense of the word, high amounts of Anavar dosage are needed. It binds reasonably well to the AR, but pretty high doses are still needed and I would never suggest doing less than 20mgs/day. In fact, 20-80mgs are needed to start halting AIDS related wasting(1) and recovering weight for burn victims (2) so that´s the range I´d recommend keeping your dosages in concerning this compound. Personally, I´d use 100mgs/day if I were ever going to try this stuff. Any less than this amount (20-100mgs) would be a waste. For women, however, I think 2.5-10mgs/day would suffice. Virilation is not a concern with this compound, as it is only very mildly androgenic (3). Water retention is also virtually nil with it.
Although Anavar is an oral steroid, and has been alpha-alkylated to survive oral ingestion and the first pass through the liver, it´s still relatively mild in that respect too..., the unique chemical configuration of oxandrolone both confers a resistance to liver metabolism as well as noticable anabolic activity. It would also appear that Anavar appears not to exhibit the serious hepatotoxic effects (jaundice, cholestatic hepatitis, peliosis hepatis, hyperplasias and neoplasms) typically attributed to the C17alpha-alkylated AASs. (17) Anavar has even been used successfully in some studies to heal cutaneous wounds (7), or to improve respiratory function (18). Both of these novel properties could make it a good choice for in-season use for boxers, Mixed Martial Arts competitors, and other such athletes.
Anavar and Fat Loss:
Now here´s some interesting stuff for anyone interested primarily in the fat loss properties of this stuff: Anavar may be what we´d call a "fat-burning steroid". Abdominal and visceral fat were both reduced in one study when subjects in the low/normal natural testosterone range used anavar (4). In another study, appendicular, total, and trunk fat were all reduced with a relatively small dose of 20mgs/day (8), and no exercise. In addition, weight gained with ´var may be nearly permanent too. It might not be much, but you´ll stand a good chance of keeping most of it. In one study, subjects maintained their weight (re)gains from anavar for at least 6 months after cessation (2)! Concomitantly, in another study, Twelve weeks after discontinuing oxandrolone, 83% of the reductions in total, trunk, and extremity fat were also sustained (8)! If you´re regaining weight, Anavar will give you nearly permanent gains, and if you are trying to lose fat (and you keep your diet in check), the fat lost with Anavar is basically looks to be nearly permanent. Check this chart out:
Absolute change in total fat mass (A) and trunk fat (B) by dual-energy X-ray absorptiometry from baseline to study week 12 (solid bars) and from baseline to study week 24 (open bars) in the placebo (n = 12) and the oxandrolone (n = 20) study groups. Values are means ± SE. *Significant decrease from baseline, P < 0.001. Significant difference between study groups for change in fat mass from 0 to 12 wk, P < 0.001. (15)(8)
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Celebrex Celebrex is in a class of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). Celebrex works by reducing substances that cause inflammation, pain, and fever in the body.
Celebrex is used to reduce pain, inflammation, and stiffness caused by osteoarthritis, rheumatoid arthritis, and ankylosing spondylitis. Celebrex is also used to reduce the number of adenomatous colorectal polyps in familial adenomatous polyposis (FAP), to treat acute pain, and to treat pain associated with menstruation.
Before taking Celebrex, tell your doctor if you:
- smoke
- drink alcohol
- have an ulcer or bleeding in the stomach
- have liver disease
- have kidney disease
- have coronary artery disease (CAD)
- have arteriosclerotic disease (hardening of the arteries, clogged or blocked arteries)
- have asthma
- have congestive heart failure
- have fluid retention
- have heart disease
- have high blood pressure
- have a coagulation (bleeding) disorder or are taking an anticoagulant (blood thinner) such as warfarin (Coumadin);
- are taking a steroid medicine such as prednisone (Deltasone and others), methylprednisolone (Medrol and others), prednisolone (Prelone, Pediapred, and others), and others
There are no restrictions on food, beverages, or activity while taking Celebrex unless otherwise directed by your doctor.
Notify your doctor immediately if you develop abdominal pain, tenderness, or discomfort; nausea; bloody vomit; bloody, black, or tarry stools; unexplained weight gain; swelling or water retention; fatigue or lethargy; a skin rash; itching; yellowing of the skin or eyes;"flu-like" symptoms; or unusual bruising or bleeding. These symptoms could be early signs of dangerous side effects.
serious side effects:
an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives);
less serious side effects:
- flatulence or diarrhea
- dizziness
- headache
- insomnia.
Before taking Celebrex, tell your doctor if you are taking any of the following drugs:
- aspirin or another salicylate (form of aspirin) such as salsalate (Disalcid), choline salicylate-magnesium salicylate (Trilisate, Tricosal, others), and magnesium salicylate (Doan's, Bayer Select Backache Formula, others);
- an over-the-counter cough, cold, allergy, or pain medicine that contains aspirin, ibuprofen, naproxen, or ketoprofen
- a diuretic (water pill) such as furosemide (Lasix), hydrochlorothiazide (HydroDiuril, others), chlorothiazide (Diuril, others), chlorthalidone (Hygroton, Thalitone), and others
- an angiotensin-converting-enzyme inhibitor (ACE inhibitor) such as benazepril (Lotensin), captopril (Capoten), enalapril (Vasotec), lisinopril (Prinivil, Zestril), moexipril (Univasc), quinapril (Accupril), and others;
- a steroid medicine such as prednisone (Deltasone and others), methylprednisolone (Medrol and others), prednisolone (Prelone, Pediapred, and others), and others
- an anticoagulant (blood thinner) such as warfarin (Coumadin)
- lithium (Eskalith, Lithobid, others)
- fluconazole (Diflucan)
Celebrex is used to:
Relieve the signs and symptoms of osteoarthritis and rheumatoid arthritis in adults.
ViagraSildenafil citrate, sold under the names Viagra. Viagra pills are blue and diamond-shaped with the words "Pfizer" on one side and "VGR xx" (with xx representing 25, 50 or 100, the dose of that pill in milligrams) on the other. Its primary competitors on the market are tadalafil (Cialis), and vardenafil (Levitra).
As with all prescription drugs, proper dosage is at the discretion of a licensed medical doctor. The dose of sildenafil is 25 mg to 100 mg taken once per day between 30 minutes to 4 hours before sexual intercourse.
It is usually recommended to start with a dosage of 50 mg and then lower or raise the dosage as appropriate. The drug is sold in three dosages (25, 50, and 100 mg).
Contraindications include:
When taking nitric oxide donors, organic nitrites and nitrates, such as glyceryl trinitrate, sodium nitroprusside, amyl nitrite ("poppers")
In men for whom sexual intercourse is inadvisable due to cardiovascular risk factors
Severe hepatic impairment (decreased liver function)
Severe impairment in renal function
Hypotension (low blood pressure)
Recent stroke or heart attack
Hereditary degenerative retinal disorders (including genetic disorders of retinal phosphodiesterases)
Amongst sildenafil's serious adverse effects are: priapism, severe hypotension, myocardial infarction, ventricular arrhythmias, sudden death, stroke and increased intraocular pressure.
Common side effects include sneezing, headache, flushing, dyspepsia, prolonged erections, palpitations and photophobia. Visual changes including blurring of vision and a curious bluish tinge have also been reported.
Care should be exercised by patients who are also taking Protease inhibitors for the treatment of HIV. Protease inhibitors inhibit the metabolism of sildenafil, effectively multiplying the plasma levels of sildenafil, increasing the incidence and severity of side-effects. It is recommended that patients using protease inhibitors limit their use of sildenafil to no more than one 25-mg dose every 48 hours.
Some Viagra users have complained of blurriness and loss of peripheral vision.
A small number of men have lost eyesight in one eye some time after taking Viagra, Cialis, or Levitra. This type of vision loss is called non-arteritic anterior ischemic optic neuropathy (NAION). NAION causes a sudden loss of eyesight because blood flow is blocked to the optic nerve.
We do not know at this time if Viagra, Cialis, or Levitra causes NAION. NAION also happens in men who do not take these medicines. People who have a higher chance for NAION include those who:
have heart disease
over 50 years old
have diabetes
have high blood pressure
have high cholesterol
smoke
have certain eye problems
XenicalBrand name for orlistat, Xenical is a wonder drug for people suffering with obesity and fat related syndromes. A potent member of Lipase inhibitor group of drugs, Xenical helps reduce unwanted weight and also maintain the sliced weight from rising up the scales again. Xenical stops the human digestive system from digesting and absorbing certain fat taken through food. This, however, nullifies the chances of calories settling down on the body. Xenical can show results only when it is taken in with controlled and fat free diet. The most beneficial part of Xenical is that it doesn't stop working after it has reduced the weight. It is equally active in maintaining the lowered weight and thus protects the body from getting affected with other obesity related syndromes. Although much safer from other weight reducing drugs available in the market, Xenical has many side effects. So it is in the interest of the users to take this drug regularly on time for the best results.
Xenical Warnings
The effectiveness and dosage of Xenical may vary from person to person depending on the health conditions. Let your doctor know if you are allergic to any Lipase Inhibitor or Xenical in particular. Also don't forget to mention if you are already suffering from any of the following diseases:
High Blood Sugar;
Chronic mal-absorption syndrome;
Gallbladder problems;
Kidney stones;
Anorexia;
Bulimia.
Enlisted in FDA pregnancy category B, Xenical is not expected to cause any severe damage to growing foetus. This drug has not yet been studied on pregnant women, but cause reduction in the amount of vitamins absorbed by our body through food. It is not known whether Xenical passes into mother's breast milk or not. However, women should always consult a doctor before taking up Xenical during pregnancy or breast-feeding stage.
Xenical have not been tested on children and older adults so far. Doctors are, however, not suspecting any harmful effects of this drug on children and aged individuals.
Xenical may not work at its best with all other OTC or prescribed drugs. So it is recommended to tell your doctor before hand if you are taking any of the following drugs before taking up Xenical:
Neoral;
Sandimmune;
Coumadin;
Lipitor;
Baycol;
Lescol;
Mevacor;
Pravachol;
Zocor.
Xenical Side Effects
Intake of Xenical is followed by the appearance of a host of side effects. Although side effects disappear within 2 to 3 days of usage, it is always safer to consult a doctor immediately after the side effects start surfacing. The serious side effects of Xenical include breath trouble, closed throat, swollen lips, tongue, or face etc.
Side effects like fever, body ache, cough, headache, running nose, sneezing, sore throat gas formation with loose motion, oily stool discharge, orange or brown colored oil in your stool are very common and less harmful. . .
Among the uncommon side effects of Xenical, blood in urine, hearing difficulty, urination problem, dental problem, sudden tension, change in menstrual cycle, rectal pain and uneasiness are notable.
Xenical Overdose
So far no cases of Xenical overdose with fatal consequences have been reported. However, prevention is always better than cure. Avoid taking double dose and rush to a doctor immediately after you realize that you have taken a double dose. This is more important as nothing is known about the normal symptoms of Xenical overdose.
Missed dose of Xenical may not be much harmful. Take the missed dose within one hour after a meal. And if you don't remember within 1 hour just skip the last dose and go for the next scheduled one. Be very careful not to take a double dose.
Xenical Usage Guidelines
Rely on your doctor for the best usage guidelines. Normally Xenical is taken in with a full glass of water. Xenical is taken within one hour of the main meal. Make sure not to include more than 30% of fat in your meal. As Xenical may reduce vitamin absorption power of the body, be very careful and particular about taking vitamin supplements prescribed by the drug. Store Xenical at room temperature for best results.
SolcoserylSolcoseryl Jelly:
Skin and mucous tunic regenerating action. Indications: burns, ulcers and venous insufficiency.
Solcoseryl® Jelly:Suitable for wet wounds.
Apply Solcoseryl® Jelly 2-3 times a day until fresh skin tissue has formed. Improves metabolism and accelerates the regeneration of the tissue in cases of surface ulcers.
Contains:
Free of protein extract of cattle blood.
To date no side effects have been observed. After application of Solcoseryl® Jelly an unpleasant stinging may occur for a short time.
Solcoseryl® Ointment:
Suitable for dry wounds. Continue with Solcoseryl® Ointment to obtain complete epithlisation.
Solcoseryl ointment:
Solkoseril is an extract of the cattle blood, but is free of protein. This product improves the metabolism and accelerates of the regeneration of the tissue in cases of surface ulcers caused by oxygen deprivation, gangrene, bedsores, burns, radiation ulcers, and skin grafts.
Recommended dosage:
In cases of bedsores apply gel until a scab emerges and then use ointment until the new skin surface appears. For burns use either gel or ointment. Normal course of treatment depends on the body's healing process, but usually lasts from 4 to 8 weeks. Use of the gel may irritate or burn the skin, but these side effects do not require interruption of therapy.
RoaccutaneHow does it work?
Roaccutane capsules contain the active ingredient isotretinoin. (NB. Isotretinoin capsules are also available without a brand name, ie as the generic medicine.) Isotretinoin belongs to a group of medicines known as retinoids, which are derivatives of vitamin A. Isotretinoin taken by mouth works by reducing the production of the skin's natural oil (sebum).
Acne occurs due to an excessive production of sebum from over-active sebaceous glands in the skin. The sebum blocks the sebaceous glands, which prevents the oil from flowing freely out and causes an accumulation of sebum under the skin. The bacteria associated with acne thrive in these conditions. They feed on the sebum, and produce waste products and fatty acids that irritate the sebaceous glands, making them inflamed and causing spots.
Isotretinoin decreases the size and activity of the sebaceous glands in the skin, which reduces the amount of sebum that is produced. This stops the glands becoming blocked, and means bacteria are less likely to thrive. It also reduces the inflammation in the skin.
Isotretinoin can have serious side effects and its use must be supervised by a dermatologist. It is reserved for the treatment of severe acne (such as nodular or conglobate acne or acne at risk of permanent scarring) that has not improved with standard treatment involving oral antibiotics and topical medicines.
Your acne may worsen at the start of treatment, but this usually subsides within 7 to 10 days of continued treatment. In most cases, complete or near-complete clearing of acne is achieved with a 12 to 16 week course of treatment, and you are likely to remain free of acne for a long time. Repeat courses are not normally recommended, unless a definite relapse is seen after treatment is stopped. Repeat courses should not be started until at least eight weeks after stopping treatment, as your acne may still improve in this time.
What is it used for?
Severe acne that has not responded to standard treatment with oral antibiotics and topical medicines.
Warning!
Isotretinoin causes major birth defects (serious malformations of a developing foetus) if taken during pregnancy. For this reason your doctor will not prescribe the treatment to women who could get pregnant, unless the following criteria are met: At least one, but preferably two (for example the pill and condoms), effective methods of contraception must be used at all times to prevent pregnancy. Contraception must start at least four weeks before starting treatment, be used at all times during treatment and for at least four weeks after stopping treatment, even if you don't have a period. Your doctor cannot prescribe isotretinoin until you have been using effective contraception for at least a month and have had a negative pregnancy test. Your doctor is only allowed to prescribe 30 days supply of isotretinoin at a time. You will need to have a follow-up visit every month, at which you will have to have a negative pregnancy test before a new prescription can be issued. Five weeks after stopping treatment you should have a final pregnancy test to make sure you have not fallen pregnant. If you think there is a chance you could be pregnant, either during treatment, or in the first month after stopping treatment, you must consult your doctor immediately.
There is no evidence to suggest that children fathered by men who are taking isotretinoin will be affected by the medicine, but men should remember not to give this medicine to anyone, particularly females.
You should never give this medicine to another person and you should return any unused medicine to your pharmacist at the end of treatment.
People taking this medicine must not donate blood during treatment, and for at least four weeks after stopping treatment. This is due to the potential risk of the medicine to an unborn child if the blood transfusion was received by a pregnant woman.
This medicine may cause depression, anxiety, mood changes, psychotic symptoms and rarely suicide attempts. For this reason, if you start to feel depressed, or experience any other mood changes during treatment, it is important to talk to your doctor.
You should avoid exposing your skin to intense sunlight or UV light while taking this medicine. You should use a sunscreen of at least SPF 15 when necessary.
Isotretinoin is likely to make your skin and lips very dry, so it is recommended that you use a moisturiser and lip balm from the start of treatment.
You should avoid waxing any part of your body while taking isotretinoin, and for at least six months after stopping treatment, as this could cause stripping of the top layer of skin. Chemical dermabrasion and cutaneous laser treatment should also be avoided during treatment with isotretinoin and for five to six months after stopping treatment, as this could cause scarring.
Isotretinoin can make your eyes dry. This can be relieved with artificial tear drops. Ask your doctor or pharmacist for advice. If you wear contact lenses you may find that they become uncomfortable during treatment and you have to wear glasses instead. Decreased night vision may also occur during treatment and after treatment has been stopped, and can occur suddenly. For this reason you are advised to be cautious when driving or operating any vehicle at night. If you experience any visual difficulties, inform your doctor so that your vision can be monitored. It may sometimes be necessary to stop treatment.
You will need to have a blood test to monitor your liver function before you start treatment with this medicine, one month after starting and then at further three-monthly intervals.
The amount of lipids (fats such as cholesterol) in your blood should also be monitored before treatment, one month after starting treatment and at three-monthly intervals. If your blood level of triglycerides becomes too high, your isotretinoin dose may need to be reduced and you may have to go on a low fat diet. If your triglycerides cannot be controlled, you may have to stop treatment with isotretinoin.
This medicine may increase your blood sugar level. People with diabetes may need to monitor their blood sugar more frequently during treatment with this medicine. Ask your doctor for advice.
If you experience severe bloody diarrhoea during treatment with this medicine you should stop taking it and consult your doctor immediately.
This medicine is not recommended for children under 12 years of age.
Use with caution in
Women who could get pregnant
History of depression
Decreased kidney function
Alcoholism
Diabetes
Obesity
Lipid metabolism disorders
Not to be used in
Pregnancy
Breastfeeding
Woman who could get pregnant, unless the criteria described in warnings above are met
Acne that has developed before reaching puberty (prepubertal acne)
Decreased liver function
High levels of fats
A condition resulting from the excessive consumption of vitamin A (hypervitaminosis A)
People taking tetracycline-type antibiotics
Peanut or soya allergy (Roaccutane capsules contain arachis oil and soya oil)
Rare hereditary problems of fructose intolerance (Roaccutane capsules contain fructose)
This medicine should not be used if you are allergic to one or any of its ingredients. Please inform your doctor or pharmacist if you have previously experienced such an allergy. If you feel you have experienced an allergic reaction, stop using this medicine and inform your doctor or pharmacist immediately.
Pregnancy and Breastfeeding
Certain medicines should not be used during pregnancy or breastfeeding. However, other medicines may be safely used in pregnancy or breastfeeding providing the benefits to the mother outweigh the risks to the unborn baby. Always inform your doctor if you are pregnant or planning a pregnancy, before using any medicine.
Isotretinoin MUST NOT be used during pregnancy as it causes major birth defects and serious malformations of the foetus. Women who could get pregnant will only be prescribed this medicine if all the criteria listed in warnings above are met. At least one and preferably two effective methods of contraception must be used to prevent pregnancy for at least one month before starting treatment, during treatment and for at least one month after finishing treatment. If you think you could be pregnant at any point during treatment or in the month after stopping treatment you must consult your doctor immediately.
This medicine must not be used by breastfeeding mothers, as it passes into breast milk and could have adverse effects on the nursing infant. Seek medical advice from your doctor.
Label warnings
Follow the printed instructions you have been given with this medication.
Take this medication with or after food.
TempalginIndications:
Mild to moderate pain of variable origin: headache; migrene; toothache; neuralgia; neuritis; plexitis; lumbalgia; myalgia and myositis; trauma; postsurgery interventions and dental procedures; dysmenorrhoea; burning; premedication in the dental practice.
Dosage and administration:
In adults, Tempalgin is used orally in dose of 1 - 2 tablets 3 - 4 times daily. In children over 10 years, the drug is administered in dose of 1 tablet 2 - 3 times daily. The treatment course duration should not exceed 5 to 7 days.
Contraindications:
Hypersensitivity to tempidon, metamizole and other pyrazolone drugs; acute hepatic porphyria and inborn deficiency of glucose-6-phosphate dehydrogenase; aplastic anemia, leucopenia and agranulocytosis; severe kidney and liver diseases; pregnancy; children younger than of 10 years.
Special warnings and precautions:
The drug is used cautiously in patients suffering from liver or kidney diseases. After more prolonged treatment with Tempalgin regular checks of blood count are necessary. In patients suffering from bronchial asthma, pollinosis, Quincke's edema, chronic airway infections or showing hypersensitivity to analgesic and nonsteroidal anti-inflammatory agents, as well as to other drugs or foods, there is a risk of allergic reactions and asthmatic attacks. During lactation the drug should be avoided, because both active ingredients are eliminated in the breast milk. Tempidon decreases the attention concentration and slows the reflexes. Because of this it should be used cautiously in car drivers and in people working with machines.
Drug interactions:
Because of the inhibition of hepatic enzyme systems metabolising drugs, Metamizole effect is potentiated by tricyclic antidepressants (psychophorin, amitriptyline), oral contraceptive agents, and allopurinol. Due to this its biotransformation is slower, and the toxicity is greater. Barbiturates and phenylbutazone are liver enzyme inductors, and they decrease the strength and duration of the metamizole pharmacodynamic effect. Metamizole lowers the plasma cyclosporin levels. Chloramphenicol increases the myelotoxic action of metamizole (additive effect). Alcohol augments the action of both components. Tempidon potentiates the activity of the hypnotic agents, general anesthetics, and narcotic and nonnarcotic analgesics.
Adverse reactions:
Itching, skin rash, urticaria, Stevens-Johnson's syndrome, Layell's syndrome, angioedema, vasomotor disturbances; asthmatic attack, allergic shock; nausea, vomiting, abdominal pain and discomfort, ulcers and bleeding in rare cases. In susceptible patients, agranulocytosis, leucopenia, aplastic anemia, retention of water and electrolytes are possible.
AnalginAnalgin tablets are used for the treatment of pains of different origin and variable intensity: toothache, headache, arthralgia, neuralgia, myositis, mild to moderate visceral pain, high fever, not responding to other drugs.
Analgin is used with increased caution in patients with a history for hypersensitivity to foods and drugs (particularly to analgesic and nonsteroidal antiinflammatory agents) and also in patients suffering from bronchial asthma, Quincke's edema, chronic pulmonary infections. In patients with hypotension and unstable blood pressure, Analgin should not be used parentarally. If Analgin application is quite necessary, the blood pressure and the heart rate should be monitored. In cases of prolonged Analgin treatment, regular blood count checks are necessary (differential count of the white blood cells). The high Analgin doses can influence unfavourably the active attention. Because of this in these cases driving and working with machines are not advised.
Analgin potentiates the analgesic and antipyretic action of the nonsteroidal antiinflammatory drugs. The Analgin effects are potentiated by the tricyclic antidepressants, oral contraceptive agents, allopurinol, alcohol. Analgin decreases the activity of the coumarin anticoagulants and plasma levels of cyclosporin. The enzyme inductors (barbiturates, glutethimide, phenylbutazone) attenuate the Analgin effects. Analgin potentiates the effects of the drugs possessing CNS depressant activity. Concurrent administration with chlorpromazine is related with a risk of severe hypothermia. Analgin can be used in combination with buscolysin, atropin, codein.
StimolSTIMOL (citrulline malate) - oral solution in sachets
Composition of the medicine:
Active ingredient: one sachet contains 50 % citrulline malate solution 2,0 g;
Excipients: purified water, natural sangria orange flavor, NaOH (for pH adjustment).
Pharmaceutical form. Oral solution.
Pharmacotherapeutic group.
Metabolism corrector to treat asthenia. The product belongs to amino acids.
Stimol utilizes lactate, ammonium, stimulates energy release, brings the cell to another energetic level.
Indications:
Symptomatic treatment of functional asthenia :
physical asthenia;
mental asthenia;
post-infectious asthenia:
postoperative asthenia;
asthenia during pregnancy;
senile asthenia,
asthenia of endocrinology origin (diabetic);
sportsmen's asthenia (muscle pain relief after the intensive training);
asthenia and vegetative syndrome by vegetal and vascular dystonia hypotonic type;
alcohol withdrawal syndrome;
sexual asthenia.
Administrate in case of the following symptoms of asthenia: general weakness, emotional lability, chronic tiredness, low capacity for work, drowse. It is recommended to administrate Stimol in case of muscular pain and cramps, resulting from the accumulation of lactate after the heavy training. This product is
recommended for the period of convalescence.
Contra-indications:
Hypersensitivity to any of the component of the product. Stomach and duodenal ulcer.
Warnings:
One sachet contains about 30 mg (1,3 mmol) of sodium to make pH solution 3,3. It must be taken into the account for patients with a salt free diet.
Interactions with other drugs: Not observed.
Methods of administration and dosage:
Children over 6 years: 1 sachet 2 times per day.
Adult and elderly people: 1 sachet 3 times per day.
Recommended duration of treatment - 4 weeks.
Stimol should be taken during meals. The content of sachet should be diluted up to 100 ml by water or sweetened beverages.
Side effects:
Several cases of discomfort in epigastrium without cancellation of administration. Point out to your physician every undesirable effect.
Shelf-life: 3 years.
Do not administrate after expiry date indicated on the box.
Storage conditions: Store at room temperature ( + 15-25°C), keep away from reach of children.
Packing: 18 sachets in aluminum and polyethylene paper in carton box.
Delivery conditions: Without prescription.
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