masteron dosage

Posted on 08/24/2016  in Articles

Imide is antifungal broad-spectrum topical. Antifungal effect of the active active substance clotrimazole (imidazole derivative) is connected masteron dosage with the violation of the synthesis of ergosterol, a component of the cell membrane of fungi that alters the permeability of the membrane and causes a subsequent cell lysis. In low concentrations fungistatic effect and in large – fungicide, and not only on the cell profiling. The fungicidal concentrations interacts with mitochondrial and peroxidase enzymes, resulting in an increase in hydrogen peroxide concentration to toxic levels, which also contributes to the destruction of the fungal cells.It is effective against dermatophytes, yeast and molds, as well as the causative agent of multi-colored lichen masteron dosage Pityriasis versicolor (Malazessia furfur) and the pathogen erythrasma. Has antimicrobial activity against Gram-positive (staphylococci, streptococci) and Gram-negative bacteria (Bacteroides, Gardnerella vaginalis), as well as against Trichomonas vaginalis.


  • Genital infections caused by yeast fungi of the genus Candida and / or Trichomonas vaginalis (vulvovaginal candidiasis, trichomoniasis);
  • genital superinfection caused by microorganisms sensitive to clotrimazole;
  • reorganization of the birth canal before delivery.

: Hypersensitivity to clotrimazole or excipients, I trimester of pregnancy. Avoid the use of pills during menstruation

Be wary – lactation.

Use during pregnancy and lactation
In clinical and experimental studies, it was found that the use of the drug during pregnancy or during breast-feeding has a negative impact on the health of the woman or the fetus (child). However, the question of the advisability of the appointment of the drug should be decided individually after consulting a doctor.

Dosing and Administration
Only for intravaginal use.
Vaginal tablets of 100 mg administered in the evening in the vagina, as far as possible, in the supine position with slightly bent legs, for 6 days. Repeated treatment is possible after consulting a doctor.

Side effects
itching, burning and swelling of the vaginal mucosa, vaginal discharge, headache, gastralgia, frequent urination masteron dosage, intercurrent cystitis, burning sensation in the penis in sexual partner, pain during sexual intercourse.

Use of the drug in high doses does not cause any reactions and conditions, life-threatening.

In the event of an unintended use of the drug (oral), the following symptoms: anorexia, nausea, vomiting, gastralgia, abnormal liver function; rarely – drowsiness, hallucinations, pollakiuria, skin allergic reactions.

No specific antidote. It should be given by mouth activated charcoal. If necessary – symptomatic treatment.

Interaction with other drugs
When clotrimazole vaginal administration reduces the activity of amphotericin B, and other polyene antibiotics. While the use of nystatin, clotrimazole activity may decrease.

must be simultaneous treatment of sexual partners to prevent urogenital reinfection. Trichomoniasis for a successful treatment in conjunction with other IMIDILom be applied drugs having systemic effect (e.g., metronidazole orally). When simultaneous infection of the labia and the surrounding areas (candida vulvitis) should be further carried out by local drug treatment imide cream.

During pregnancy, vaginal tablets treatment should be carried out without an applicator. Patients with hepatic insufficiency should periodically monitor liver function. When you see signs of hypersensitivity or irritation of the treatment is stopped. If there is no effect for 4 weeks should confirm the diagnosis.

Form release
On 6 tablets in aluminum strip. A strip with a tool for intravaginal use (applicator) and instructions for use in a cardboard box.

Shelf life
4 years.
Do not use after the expiration date.

Storage conditions:
The temperature is not above 25 ° C, protected masteron dosage from light and out of reach of children.

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oral masteron

Posted on 08/24/2016  in Articles


After oral administration, sumatriptan is rapidly absorbed,  of the maximum plasma concentration is reached after 45 minutes. After receiving 100 mg of the maximum concentration in plasma is on average. Bioavailability is as a result oral masteron of first-pass metabolism and incomplete absorption. Relationship to plasma proteins is low . Sumatriptan is metabolized by the action of monoamine oxidase A main metabolite – indoleacetic analog output of sumatriptan, preferably in the urine in the form of free acid and glucuronide conjugate. This metabolite has no activity against  -serotoninovym receptors.Migraine attacks, apparently no significant effect on the pharmacokinetics of sumatriptan ingestable.


  • Hypersensitivity to any component of the formulation.
  • Hemiplegic, basilar migraine and oftalmoplegicheskaya form.
  • Coronary heart disease (CHD) (including myocardial infarction, myocardial infarction, angina, Prinzmetal), as well as the presence of symptoms to suggest the presence of coronary artery disease.
  • Occlusive peripheral vascular disease
  • Stroke or transient ischemic attack (in Vol. H. In history)
  • Uncontrolled hypertension.
  • Receiving simultaneously with ergotamine or derivatives thereof (including methysergide).
  • The use in patients receiving monoamine oxidase inhibitors or earlier than 2 weeks after the cancellation of these drugs.
  • Severe liver and / or kidneys.
  • Age 18 years and older than 65 years (the safety and effectiveness of Imigran is not installed).
  • Pregnancy and lactation.

Precautions :

  • controlled hypertension.
  • diseases that may change the absorption, metabolism or excretion of the drug (eg, renal or hepatic function).
  • epilepsy (including any condition with a reduction in seizure threshold)
  • in patients with hypersensitivity to sulfonamides (administration sumatriptan can cause allergic reactions, the severity of which varies from cutaneous manifestations of anaphylaxis. Data on the cross-sensitivity is limited, however, caution should be exercised in the appointment of sumatriptan in these patients).

Inside, swallowing the tablet whole and with water.
The recommended dose is one tablet of 50 mg. Some patients may need a higher dose – 100 mg. If migraine symptoms do not disappear or diminish after the first dose of Imigran. something for the relief of the same re-taking the drug should not attack. However Imigran can be used for relief of subsequent migraine attacks.
If the patient has felt improvement after the first dose, and then resumed symptoms can take a second dose for the next 24 hours. Imigran maximum dose should not exceed 300 mg over a 24-hour period.

Adverse reactions are listed below, depending on the anatomical and physiological classification and occurrence frequency.
The frequency is defined as follows: very common (> 1/10); often (> 1/100 and <1/10); sometimes (> 1/1000 and <1/100); rare (> 1/10 000 and <1/1000); very rare (<1/10000), including isolated cases.Evaluated data from clinical trials, it must be remembered that the frequency of adverse reactions in patients receiving comparator drugs are not taken into account. Also taken into account post-marketing data. Clinical Studies : From the nervous system : often – dizziness, drowsiness, sensory disturbances including paresthesia and decrease in sensitivity. Since the cardiovascular system : often – a transient increase in blood pressure (shortly after administration), flushing. The respiratory system and the thoracic organs : often – shortness of breath; mild, transient irritation or burning sensation in the nose or throat, nose bleeding. On the part of the gastrointestinal tract : often – nausea, vomiting (cause-and-effect relationship has not been proved). On the part of the musculoskeletal system and connective tissue disorders : often – a feeling of heaviness (usually transient, may be intense and occur in any part of the body including the chest and throat). General and local reactions : often – pain, feeling cold or hot, a feeling of pressure or constriction (usually transient, may be intense and occur in any part of the body including the chest and throat). Often, weakness, fatigue (usually slightly or moderately expressed, transitory). Laboratory findings : very rarely -neznachitelnye deviation indicators liver function tests. Post-marketing surveillance Immune system : very rarely – hypersensitivity reactions, including skin manifestations and anaphylaxis Nervous system : very rarely – seizures (in some cases observed in patients with a seizure history or concomitant conditions predisposing to seizures, in some of the risk factors of patients have been identified), tremor, dystonia, nystagmus, scotoma. from a sight organ : very rare -melkanie, diplopia, blurred vision. Blindness (usually transient). However, visual disorders may be caused by a migraine attack itself. Since the cardiovascular system : very rarely – bradycardia, tachycardia, fibrillation, arrhythmias, transient ECG changes, coronary vasospasm, angina , myocardial infarction. Very rarely – hypotension, Raynaud’s syndrome. On the part of the gastrointestinal tract : rarely – ischemic colitis, dysphagia, abdominal discomfort.

Reception Imigran oral dose of 400 mg oral masteron did not cause any side effects other than those listed above.
In case of overdose Imigran should monitor the patient’s condition is not less than 10 hours and spend symptomatic therapy if necessary. No data on the effect of hemodialysis or peritoneal dialysis on plasma concentrations of sumatriptan.

Imigran should be used only if the diagnosis of migraine is not in doubt.
Imigran Tablets should not be used prophylactically.
In patients with previously diagnosed with migraine or patients with atypical migraine is necessary to exclude other neurological disorders. It should be noted that patients with migraine are at increased risk of certain cerebrovascular disorders (eg stroke, or transient ischemic attack).
After receiving sumatriptan may experience transient pain and tightness in the chest, extending to the neck. If there is reason to believe that these symptoms are a manifestation of coronary heart disease, it is necessary to conduct appropriate diagnostic testing.
Sumatriptan should not be administered to patients with the risk of cardiovascular disease without prior examination with a view to its elimination (in postmenopausal women, men over the age of 40 years and patients with risk factors for coronary heart disease). The survey is not always possible to identify heart disease in some patients. In very rare cases, patients may experience serious side effects to the cardiovascular system, a history that has not been observed for cardiovascular disease.
It should be administered with caution to patients with controlled hypertension, since in some cases there was a transient increase in blood pressure and peripheral vascular resistance; in patients suffering from such diseases that can significantly change the absorption, metabolism or excretion of the drug (eg, renal or hepatic function).
There are very rare reports resulting from post-marketing surveillance, the development of serotonin syndrome (including mental disorder, autonomic lability and neuromuscular disorders) resulting from concomitant use of selective serotonin reuptake inhibitors (SSRI) and sumatriptan. It was also reported on the development of serotonin syndrome on the background of co-administration of triptans with selective serotonin reuptake inhibitors and norepinephrine (SNRI). In the case of co-administration with drugs of the SSRI / SNRIs should be closely monitored condition of the patient.
Imigran should be used with caution in patients with epilepsy or organic brain damage in history with a reduction in seizure threshold.
The concomitant use of other triptans / 5-HT 1 agonists sumatriptan is not recommended.
in patients with hypersensitivity to sulfonamides receive Imigran may cause allergic reactions that range from skin manifestations of anaphylaxis. Data on cross-sensitivity is limited, however, caution should be exercised in the appointment of Imigran such patients.
The abuse of drugs intended for the relief of migraine attacks, associated with increasing headaches in susceptible patients (headache associated with the abuse of drugs). It should consider discontinuation of the drug.
Do not exceed the recommended dose of Imigran.

There was no interaction between sumatriptan with propranolol, flunarizine, pizotifenom and ethyl alcohol.
When concomitantly with ergotamine celebrated long spasm of blood vessels.
Sumatriptan can not assign earlier than 24 hours after taking the drugs containing ergotamine; Conversely, drugs oral masteron containing ergotamine, you can assign no sooner than 6 hours after administration of sumatriptan.
Perhaps the interaction between sumatriptan and MAOIs and their concurrent use is contraindicated.
There are very rare reports resulting from post-marketing surveillance, the development of serotonin syndrome ( including mental disorders, vegetative lability and neuromuscular disorders) resulting from concomitant use of selective serotonin reuptake inhibitors (SSRI) and sumatriptan. It was also reported on the development of serotonin syndrome on the background of co-administration of triptans with selective serotonin reuptake inhibitors and norepinephrine (SNRI).

Effects on ability to drive and / or other mechanisms
in patients with migraine may occur drowsiness, associated, with both the disease itself and the reception Imigran, so they need to be especially careful while driving and working with moving machinery.

coated tablets 50 mg and 100 mg. 2 tablets in A1 / A1 blister. 1 blister with instructions for use in a cardboard box.

Storage conditions
List B.
The temperature is not above 30 ° C. Keep out of the reach of children.

3 years. Do not use the drug after the expiry date printed on the package

Conditions of supply of pharmacies
by prescription.

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masteron 100

Posted on 08/24/2016  in Articles

Generation antibiotic for oral masteron 100 administration. Effective bactericidal (violates the synthesis of cell walls of microorganisms). It has a broad spectrum antimicrobial activity that includes various aerobic and anaerobic gram-positive and gram-negative microorganisms including.upper and lower respiratory tract infections (pharyngitis, tonsillitis, sinusitis, acute bronchitis, exacerbation of chronic bronchitis)otitis media,Urinary tract  masteron 100 infections (uncomplicated)uncomplicated gonorrhea of the urethra and cervix.

Advanced age, renal failure, colitis (in history).

Pregnancy and lactation
In pregnancy, the use of the drug is possible only., When the intended benefits to the mother outweighs the potential risk to the fetus. If necessary, use during lactation should stop breastfeeding.

. Inside For children over 12 years weighing more than 50 kg and adults, the average daily dose is 400 mg once daily (or 200 mg 2 times a day). In uncomplicated gonorrhea of the urethra and cervix – 400 mg . once children under the age of 12 years is prescribed at a dose of 8 mg / kg, 1 time per day or 4 mg / kg, 2 times a day (every 12 hours). For children aged 5-11 years, the daily dose of a suspension – 6-10 ml, aged 2-4 years – 5 ml, aged b months to 1 year – 2.5-4 mL. The average duration of the treatment – 10.7 days. In diseases caused of Streptococcus pyogenes , treatment should not be less than 10 days.If the kidney function the dose adjusted according to creatinine clearance (CC) in the blood serum: with CC 21-60 ml / min or in patients on hemodialysis , the daily dose should be reduced by 25%; QC at 20 ml / min or less and in patients undergoing peritoneal dialysis, the daily dose should be reduced by 2 times. A method for preparing the suspension . Turn the bottle and shake powder. The vial was added about half (17 ml), the required volume (34 ml), cooled to room temperature boiled water, capped, shaken thoroughly until a homogeneous suspension. Then add the cooled boiled water to the mark (arrow) on the label, close lid, carefully shaken until a homogeneous suspension. Allow to stand for 5 minutes before use prepared suspension stirred well. Use within 14 days after preparation.

Side effect Allergic reactions : rash, skin redness, itching, fever, erythema multiforme exudative (including Stevens-Johnson syndrome), toxic epidermal necrolysis (Lyell’s syndrome). From the digestive system : diarrhea, nausea, vomiting, stomatitis , constipation, abdominal pain, pseudomembranous enterocolitis, dysbiosis, cholestasis, cholestatic jaundice. From the nervous system : headache, dizziness, ringing in the ears. From the urogenital system : vaginitis, candidiasis, itching in the genital area. From the urinary system : renal failure masteron 100, interstitial nephritis. From the side of hematopoiesis : pancytopenia, leukopenia, neutropenia, thrombocytopenia, agranulocytosis, aplastic anemia, hemolytic anemia, bleeding. From the laboratory parameters : eosinophilia, increased activity of “liver” transaminases and alkaline phosphatase, hyperbilirubinemia, increase of urea nitrogen, hypercreatininemia, increased prothrombin time. Other : In the development of hypovitaminosis, shortness of breath.


Overdose Symptoms : increased risk of adverse reactions. Treatment : t. To specific antidote does not exist, it is shown gastric lavage, symptomatic and supportive therapy, including the use of corticosteroids, fluid resuscitation, mechanical ventilation.. The procedure of peritoneal dialysis and has no substantial effect on the concentration in the blood plasma of cefixime respectively hemo or peritoneal masteron 100 dialysis is not efficient.

Cefixime reduces prothrombin index, increases the effects of anticoagulants. Increases in serum carbamazepine. Blockers tubular secretion (including allopurinol, diuretics) cefixime delayed excretion by the kidneys, which can lead to increased toxicity. Antacids containing aluminum or magnesium hydroxide, slow absorption of the drug.

Patients who had a history of allergic reaction to penicillin, may be sensitive to cephalosporin antibiotics.
During treatment, the possibility of false-positive direct Coombs’ test and false-positive reaction of urine for glucose and ketone bodies. False-positive reaction of urine for ketones can be observed when using the test with nitroprusside, but not when using masteron 100 tests nitroferritsianidom. False-positive urine glucose rёaktsiya during the treatment may occur with the use of solutions or Benedict Fehlinga. It is preferable to conduct tests based on the enzyme reaction with glucose oxidase.

Product form
Powder for oral suspension 100 mg / 5 ml. 25 g of powder for the preparation of 50 ml of suspension was placed in a bottle of high-density polyethylene with a polypropylene cap with safety lock from children and gasket of laminated aluminum foil «LUPIN» inscription. On the cover indicate in English: «CLOSE TIGHTLY» (ie, close tightly), “TO OPEN» (ie open), «PUSH DOWN AND UNSCREW» ( ie tap and unscrew). On the bottle label is glued with an arrow indicating the level of added water. One vial is placed in a cardboard box with instructions for use.

Shelf Life
2 years (powder).
14 days (for the ready slurry).
Do not use after the expiration date printed on the package.

Storage conditions
In a dry place at temperatures no higher than 25 ° C.
Keep out of reach of children.

Conditions of supply of pharmacies
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Posted on 08/24/2016  in Articles


Active forms of vitamin A, which masteron has a regulatory effect on the growth of epithelial cells and their differentiation. It inhibits terminal differentiation of sebocytes and hyperproliferation of epithelium of the excretory ducts of the sebaceous glands, normalizes the composition of their secretion and facilitates its evacuation. This reduces the production of sebum and reduces the inflammatory reaction around the glands. Isotretinoin influences komedonogenez, inhibits follicular keratinization, suppresses acne caused Propionebacterium. Isotretinoin has anti-seborrhoeic, anti-inflammatory, keratolytic action.Erythromycin is a macrolide antibiotic of the group have an inhibitory effect on protein synthesis in bacteria by reversibly binding ribosomal subgroups. In the treatment of acne erythromycin efficiency manifested in the reduction of the population Propionebacterium acne.Isotretinoin is a component effective in comedonal acne izotreksina phase of the disease, whereas erythromycin is effective in treating acne inflammation or mild to moderate severity.

Percutaneous absorption of isotretinoin and erythromycin insignificant. During the study of the local absorption izotreksina two components in the treatment of patients suffering from acne, it noted only a slight increase of isotretinoin levels compared to baseline levels (isotretinoin is usually determined in the blood plasma). Performance remained below 5 ng / ml and did not grow in the presence of erythromycin. The levels of erythromycin were not detected in the blood plasma. |


Pregnancy and lactation

Application izotreksina when planned and established pregnancy is contraindicated. Percutaneous absorption of isotretinoin is negligible. However, due to the fact that it is unknown whether izotreksin stands out with mother’s milk, izotreksin should not be used during breastfeeding.

Dosing and Administration

The drug is applied thinly to the masteron affected area 2 times a day (in the morning before applying makeup and evening after washing).

The patient should be informed that in some cases to achieve a complete therapeutic effect may need six to eight weeks of treatment.

Side effect

Izotreksin may cause a slight tingling sensation, burning sensation and irritation, as well as erythema and desquamation of the skin at the site of application of the drug. Photosensitivity.


Accidental overdose izotreksina masteron unlikely due to the nature of the local application of the drug.

Interaction with other drugs

Not recommended simultaneous use of other drugs with keratolytic or exfoliative properties, including the group of retinoids. The drug is reduced with concomitant administration of tetracyclines, as well as local application of glucocorticoids.

Special conditions

Avoid contact with mucous membranes of the mouth, nose and eyes, as well as damaged or ulcerated skin surfaces. Application of medication to sensitive areas of the skin (around the eyes and neck) should be performed with caution. Due to the fact that izotreksin may cause increased sensitivity to sunlight, deliberate masteron or prolonged exposure to the sun should be kept to a minimum.

When side effects which typically occur at 1-2 weeks of treatment should be interrupted for a few days of treatment and resume the drug after irritation symptoms disappear. If side effects persist, treatment should be discontinued.

release Form

Gel for topical application.
For 6 g, 25 g, 30 g, 40 g, 50 g aluminum tubes. Each tube together with instructions for use in a stack of cardboard.

Storage conditions.

Store at temperatures not above 25 ° C. Keep out of the reach of children.

Shelf life

2 years.
Do not use after the expiration date printed on the package.

Conditions of supply of pharmacies

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masteron steroids

Posted on 08/24/2016  in Articles

Quickly metabolized and excreted through the kidneys. It is metabolized similar to endogenous purine nucleotides with the formation of uric acid. NN-dimethylamino-2-propranolon metabolized to N-oxide and the steam-to-atsetamidobenzoat atsilglyukuronida -up. Not detected drug accumulation in the body. The half-life is 3.5 hours for the NN-dimethylamino-2-propranolona masteron steroids and 50 minutes-for para-atsetamidobenzoata. The elimination of the drug and its metabolites are excreted occurs within 24-48 hours.

Treatment of influenza and other acute respiratory viral infections,
– infections caused by Herpes simplex virus 1 st, 2 nd, 3 rd and 4 th type: genital and labial herpes, herpetic keratitis, herpes zoster, chickenpox, infectious mononucleosis caused by a virus Epstein-Barr virus;
– cytomegalovirus infection;
– heavy current measles;
– human papillomavirus infection: laryngeal papilloma / vocal cords (the fibrous type), genital HPV infection in men and women, warts
– molluscum contagiosum.


– Hypersensitivity to the drug;
– gout,
– urolithiasis;
– arrhythmia;
– chronic renal failure;
– children up to 3 years (weight 15-20 kg).

Use of the drug during pregnancy and lactation

Do not use the drug during pregnancy and lactation, as safety of use has not been studied.

Dosing and Administration

The tablets are taken orally after meal with a little water.

The recommended dose for adults and children from 3 years old (body weight of 15-20 kg) is 50 mg / kg per day, divided into 3-4 receptions. Adults – 6.8 tablets per day, children – 2.1 tablets per 5 kg / body weight per day. In severe infections the dose may be increased individually to 100 mg / kg of body weight per day, divided into 4-6 doses. The maximum daily dose for adults 3-4 g / day, for children – 50 mg / kg / day.

Duration of treatment:

Acute disease: the duration of treatment in adults and children is usually 5 to 14 days. The treatment should continue until the disappearance of clinical symptoms and for a further 2 days, even at the absence of symptoms. If necessary, the duration of treatment can be increased individually supervised by a doctor.

In chronic recurrent diseases in adults and children, treatment should continue for several courses of 5-10 days with a break in reception in 8 days.

For maintenance therapy dose can be reduced to 500-1000 mg per day (1-2 tablets) for 30 days.

When herpes infection masteron steroids in adults and children is prescribed for 5-10 days before the disappearance of disease symptoms, asymptomatic period – 1 tablet 2 times a day for 30 days to reduce the number of relapses.

When infection papilomavirusnoy adult drug administered 2 tablets 3 times a day for children – 1/2 . Tablets of 5 kg / body weight per day in 3-4 divided doses for 14-28 days as monotherapy.

With recurrent genital warts adult drug administered 2 tablets 3 times children – 1.2 tablets per 5 kg / body weight per day in 3-4 divided doses a day or as monotherapy or in combination with surgery for 14-28 days, followed by a triple repetition of this course at intervals of 1 month. When cervical dysplasia, associated with human papilloma virus, administered 2 tablets 3 times a day for 10 days, then spend 2-3 similar course with an interval of 10-14 days.

Side effect

The incidence of side effects after the drug is classified according to WHO recommendations.

Often:> = 1% and <10%.

Sometimes:> = 0.1% and <1%.

From the gastrointestinal tract: often – nausea, vomiting, epigastric pain, sometimes – diarrhea, constipation.

Of the liver and biliary tract: often masteron steroids – a temporary increase in transaminases and alkaline phosphatase activity in plasma, increasing the concentration of urea in plasma.

Skin and subcutaneous tissue: often – itching.

From the nervous system: often – headache, dizziness, weakness; sometimes, drowsiness, insomnia.

From the mochevydelitelnoy system: sometimes – polyuria.

On the part of the musculoskeletal system and connective tissue disorders: often – joint pain, worsening of gout.


Cases of overdose have not been described.

Interaction with other drugs

Immunosuppressive drugs may reduce the effectiveness of the drug. Xanthine oxidase inhibitors and uricosuric drugs (including diuretics) may contribute to the risk of high levels of uric acid in the blood serum of patients taking Isoprinosine.

special instructions

After 2 weeks of use izoprinozin should be undertaken to control the concentration of uric acid in the serum and urine.

Chronic administration after 4 weeks of application it is advisable to carry out monthly monitoring of liver and kidney function (transaminase activity in blood plasma, creatinine, uric acid).

It is necessary to control the level of uric acid in blood serum when assigning Isoprinosine in combination with drugs that increase the levels of uric acid ilipreparatami violating kidney function.

Effects on ability to drive vehicles and other mechanisms

No specific contraindications.

release Form

Tablets mg.10 500 tablets per blister PVC / PVDC and aluminum foil.
2, 3, or 5 in blister pack carton along with instructions for use.

Shelf life
5 years.
Do not use after the date printed on the packaging.

Storage conditions

List B. Store at temperatures above +25 ° C in a dry, dark place. Keep out of the reach of children.

Conditions of supply

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