define equipoise

Immunoglobulin human is an immunologically active protein fraction separated from human plasma or define equipoise donor sera tested for the absence of antibodies to human immunodeficiency virus , hepatitis C virus and hepatitis B surface antigen . The active ingredient of the drug is the immunoglobulin G, containing incomplete define equipoise. It is used to prevent isoimmunization Rh-negative mother having been exposed to Rh-positive blood of the fetus at birth Rh-positive baby, abortion (both spontaneous and artificial), in the case of amniocentesis or receiving abdominal trauma during pregnancy. It reduces the frequency of Rh isoimmunization of mother at the introduction of the drug within 72 hours of birth at term Rh-positive baby Rh-negative mother.
The maximum concentration of antibody in the blood after 24 hours after intramuscular injection of the human immunoglobulin antirezus Rho (D). Period half-life of a human define equipoise immunoglobulin antirezus Rho (D) from the body – 4-5 weeks.

 

  • first pregnancy and the birth of a Rhesus positive baby;
  • artificial or spontaneous abortion;
  • when interrupted ectopic pregnancy;
  • under the threat of termination of pregnancy;
  • during amniocentesis and other procedures associated with the risk of fetal blood entering the mother’s bloodstream;
  • Rh-positive blood affiliation of her husband;
  • Receive abdominal trauma;
    2.Treatment of Rh-negative patients in the case of transfusion of Rh-positive blood, or products containing red blood cells.Contraindications
  • hypersensitivity;
  • Rh-negative puerperal sensitized  define equipoise antigen Rho (D), in which the serum antibody found Rh;
  • newborns;
  • Rh-positive patients.Dosing and Administration
    The drug is administered by intramuscular injection.
    Prior to administration of the drug vial is maintained for 2 hours at room temperature (18-22 ° C). To avoid the formation of foam formulation in a syringe needle with a wide clearance. The preparation of opening the bottle must not be stored. The drug is administered only intramuscularly once: postpartum women – within the first 48-72 hours after birth, when the artificial termination of pregnancy – immediately after the operation is completed. One dose – 300 mg at a titer of 1: 2000 or with 600 ug titer of 1: 1000. You can not be administered intravenously. Human Immunoglobulin antirezus Rho (D) are administered a single dose of 300 micrograms (1500 ME), sometimes two doses of 600 micrograms (3000 ME) intramuscularly once: puerperas – within 72 hours after birth; when abortion -neposredstvenno after surgery.You must meet the following criteria:
    1. The mother must be Rh-negative and should not already be sensitized to the Rho factor (D).
    2. Her child must be Rh positive.
    If the drug is administered before delivery, it is essential that the mother received another dose of the drug after the birth of a Rhesus positive baby within 72 hours after birth. If it is determined that the father Rh-negative, there is no need to inject the drug.Pregnancy and other conditions associated with pregnancy and childbirth:
    1. For the prevention of post-partum should introduce a single dose of 300 micrograms (1500 ME) product KamROU preferably within 72 hours after birth. The need for a given dose in the case of passing the full term of pregnancy can be different depending on the volume of fetal blood trapped in maternal circulation. In a dose of 300 micrograms (1500 ME) contains a sufficient amount of antibody to prevent sensitization to the Rhesus factor, if the amount of fetal erythrocytes caught in maternal blood flow does not exceed 15 ml. In those cases when it is assumed from entering the bloodstream larger volume of fetal erythrocytes mother (over 30 ml of whole blood or in excess of 15 ml erythrocytes), carry count of fetal erythrocytes by using an approved laboratory techniques (for example, a modified method of acid washing-staining Klyayhaueru and Bethke ) to set the required dose of immunoglobulin. The calculated amount of fetal red blood cells caught in the mother’s bloodstream, divided into 15 ml and get the number of doses of the drug KamROU to be entered. If the calculated dose is obtained fraction rounded number of doses up to the next whole number upwards (for example, when receiving the result of 1,4 type 2 doses of 600 mcg (3000 ME product)).
    2. For the prevention of prenatal about the 28th week of pregnancy, the drug is administered one dose of 300 micrograms (1500 ME). This was sure to introduce another dose of 300 micrograms (1500 ME), preferably within 48-72 hours after birth, if the child would be born Rh positive.
    3. In the case of continuing pregnancy after an abortion threat at any stage of pregnancy is recommended that a single dose of 300 micrograms (1500 ME). If the mother is suspected entering the bloodstream over a 15 ml fetal erythrocytes need to change the dose, as described in the above paragraph 1.
    4. After a miscarriage, abortion or ectopic pregnancy interruption of pregnancy over 13 weeks, it is recommended to introduce a dose of 300 micrograms (1500 ME). If suspected of entering the bloodstream mother more than 15 ml of fetal red blood cells, it is necessary to change the dose, as described in paragraph 1. If pregnancy is interrupted for a period of less than 13 weeks, possibly single use mini-dose KamROU (approximately 50 micrograms (250 ME)).
    5. After amniocentesis or at 15-18 weeks of gestation, or during the third trimester of pregnancy, or in the preparation of injury in the abdominal cavity during the second and / or third trimester recommended to introduce a dose of 300 micrograms (1500 ME). If suspected of entering the bloodstream mother more than 15 mL of red blood cells, it is necessary to change the dose, as described in paragraph 1. If the injury of the abdominal cavity, amniocentesis, or other adverse circumstance requires the introduction of the drug in the period 13-18 weeks of pregnancy, you must enter another dose of the drug 300 g (1500 ME) in the period 26-28 weeks. To maintain protection throughout pregnancy should not be allowed concentration level of falling passively derived antibodies to Rho (D) below the level required to prevent the immune response to Rh-positive red blood cells of the fetus. The half-life period of human immunoglobulin antirezus Rho (D) is 28-35 days. In any case, the dose should be administered 48-72 hours after birth – if the baby is Rh-positive. If the birth occurs within 3 weeks after the last dose, postpartum dose may be canceled (except when hit more than 15 mL of red blood cells of the fetus in the mother’s blood stream).

    Side effects Skin reactions: discomfort, swelling and redness at the injection site, hyperthermia up to 37.5 ° C (during the first day after administration). On the part of the digestive system: dyspepsia.Allergic reactions: seldom – (in case of hypersensitivity, including at failure IgA) – allergic reactions (up to anaphylactic shock).

     

    Overdose
    overdose cases in Rh-negative women are not described.

    The interaction with other drugs
    Therapy immunoglobulin may be combined with other drugs, including with antibiotics. Immunization of women with live vaccines should be carried out not earlier than 3 months after the introduction of immunoglobin antirezus.

    Cautions
    Children born to women who received human immunoglobulin antirezus Rho (D) before birth, at birth is possible to obtain a weakly positive results of tests for the presence of direct antiglobulin. The maternal serum antibodies can be detected to Rho (D), produced by a passive, if screening tests for antibodies produced after prenatal or postnatal administration to the human immunoglobulin Rho (D). Not suitable for the use of drugs in vials and syringes with a violation of the integrity or marking a change of physical properties (color change, turbidity of the solution, the presence of non-separating flakes), with an expired shelf life, if not properly stored.
    If it is determined that the Rho (D) father – negative administered drug is not necessary. After administration, patients should be monitored for 30 minutes. Medical offices must have a means of anti-shock therapy.

    Product form
    solution for intramuscular injection of 150 mcg / ml (750 IU / ml).
    In 2 ml solution for intramuscular injection in vials colorless hydrolytic glass (the USP) Type I, sealed with rubber rubber stoppers and crimped aluminum caps with plastic cover (flip-off ). 1 bottle with instruction on use and needle filter (in sterile packaging made ??of paper and PVC) is placed in a cardboard box.

    Storage:
    In the dark place at a temperature between 2 and 8 ° C. Do not freeze.
    Keep out of the reach of children.

    Shelf life
    2 years.
    Do not use beyond the expiration date.

    Conditions of supply of pharmacies
    by prescription.

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equipoise for sale

Combined medication. Lidocaine has a local anesthetic effect, which contributes to the rapid and lasting pain reduction in inflammation and damage to the mucous membrane equipoise for sale of the mouth and gums. Chamomile extract has anti-inflammatory, antiseptic and regenerating properties.
Pain syndrome with inflammation of the mucous membranes of the mouth and lips (with stomatitis, cheilitis, glacier erythema of the lips), gingivitis (inflammation of the gums), irritation of the oral mucosa when wearing dentures and braces, teething “wisdom”, dental procedures after orthopedic surgery in maxillofacial surgery.

 

Dosing and Administration
Locally. A strip of 0.5 cm length equipoise for sale of the drug is applied to the painful or inflamed areas of the oral mucosa and lips 3 times a day, rubbing gentle massage.
For the period of getting used to dentures in place of compression to rub the gel strip length of 0.5 cm.
The course of treatment depends on severity of the disease.

Side effects:
Allergic reactions are possible. If, during the application Kamistada® showing signs of allergies, medication should be discontinued and seek medical advice.

Overdose
Cases of overdose have been reported.

The interaction with other drugs
cases interaction or incompatibility with other drugs have not been described.

Cautions
Do not allow the drug to the eye.  Before equipoise for sale and after applying the gel is recommended to wash your hands.
Kamistad® contains sweetener sodium saccharin.

Form release
gel for topical use. 10 g of the aluminum tube with a polyethylene screw cap. Each tube with instruction on the medical use of the drug is placed in the pack.

Storage conditions
Store at a temperature not exceeding 30 ° C.
Keep out of reach of children.

Shelf life
5 years. Do not use the drug after the equipoise for sale expiry date stated on the package.
Once opened, use gel tubes for 12 months.

Conditions of supply of pharmacies
without a prescription. anabolic steroids

equipoise cycle

By reducing doxazosin vascular muscle tone decreases total peripheral vascular resistance which leads to lower blood pressure (BP). After a single ingestion maximum hypotensive effect observed in the period from 2 to six hours, but in general equipoise cycle hypotensive effect is maintained for 24 hours. During treatment with doxazosin in hypertensive patients with no differences quantities of BP in the standing and lying down. It is effective in hypertension, including, accompanied by metabolic disorders (obesity, impaired glucose tolerance). Reduces the risk of developing coronary heart disease. The drug in people with normal blood pressure (BP) is not accompanied by a decrease in blood pressure. With prolonged use of doxazosin in patients with no observed change in tolerance to the therapeutic antihypertensive effect. During treatment with doxazosin a decrease in the level of concentration in the blood plasma triglycerides, total cholesterol. At the same time there is some (4 – 13%) increase in HDL / total ratio equipoise cycle cholesterol. Prolonged treatment doxazosin observed left ventricular hypertrophy regression, inhibition of platelet aggregation and improvement in their tissues active plasminogen. Due to the fact that doxazosin blocks alpha1-adrenergic receptors, located in the stroma and prostatic capsule and bladder neck, there is a decrease of resistance and pressure in the urethra, internal sphincter resistance decrease.

 

Pregnancy and lactation
Pregnant women can be given the drug only for health reasons, when benefit to the mother outweighs the potential risk to the fetus / baby. Safety of the drug in infants has not been established, therefore, nursing mothers should stop feeding during treatment with doxazosin.

Dosing and Administration
Inside, 1 time a day (morning or evening), regardless of the meal, not chewing and drinking plenty of water.
The dose should be adjusted depending on the efficacy or potential side effects in certain patients. Patients with hepatic impairment require lower doses of the drug due to slow metabolism.
If the patient has forgotten to take the drug at the usual time, it should be as soon as possible to take the proper dose. If it is time for the next dose, you should only accept it (not doubling the dose). It is important to take the drug regularly. If the patient did not take the drug for a few days, the new course of therapy should be started with the lowest dose. Hypertension: The equipoise cycle CL is 1 tablet (4 mg) per day. Its effect can be observed on the first day, the therapeutic effect occurs within 4 weeks after starting treatment. After 4 weeks, in case of good tolerability and if the doctor considers the effect of higher doses may be administered insufficient. The maximum recommended daily dose of Camiri ® CL is 2 tablets (8 mg) in one go. If the therapeutic effect is not sufficient, patients may simultaneously receive other antihypertensive agents: beta-blockers, diuretics, blockers “slow” calcium channel blockers and ACE inhibitors. After reaching a stable the therapeutic effect of the dose is usually somewhat lower (average therapeutic dose for maintenance therapy is usually 2-4 mg per day), you can go to the reception Camiri, tablets of 2 or 4 mg. Benign prostatic hyperplasia in patients with normal blood pressure: the usual dose is 1 tablet (4mg) Camiri ® CL per day. The patient should take the first dose in the evening before bedtime. Depending on the drug, the dose can be gradually increased at intervals of 1-2 weeks up to 8 mg once daily. Typically, the average daily dose range from 2 mg to 4 mg, can go to the reception Camiri tablets  equipoise cycleat 2 or 4 mg maximum daily dose of 8 mg. Benign prostatic hyperplasia in hypertensive patients: dose are the same as in case of hypertension without benign prostatic hyperplasia (see. dose in hypertension). The drug is used for a long time. Duration of treatment is determined by the attending physician.

 

Side effects Hypertension frequently observed in clinical trials, especially in the beginning of treatment, orthostatic hypotension, which in rare cases may cause fainting. Common reactions: asthenia, fatigue, malaise. Cardio-vascular system: . Swelling, fainting eliminating alpha -adrenostimuliruyuschie effects of epinephrine may cause tachycardia and hypotension.

 

Cautions
Particular caution should be exercised in the appointment of the drug to patients with impaired liver function, especially in those cases where both are used drugs that can affect the liver. In case of deterioration of the functional state of the liver drug overturned immediately.
In order to prevent orthostatic reactions, patients should avoid unexpected and sudden shifts in body position (transition from the “lying” to “standing”).
Drinking alcohol can increase adverse reactions.
Safety and efficacy of doxazosin in children has not been established, so it is not recommended to prescribe a drug for children.
The effect of the “first” of the drug is especially pronounced against the background of previous diuretic therapy and dietary sodium restriction.
Before therapy is necessary to exclude malignant degeneration of the prostate. prostate
due to the fact that doxazosin is capable cause orthostatic reactions at the beginning of treatment or during the period of increasing dosages to patients it is advisable to refrain from any potentially dangerous activities, in particular from road transport management and other vehicles and machinery.

Product form
tablets with modified release of 4 mg. 10 tablets in a blister pack. 1, 3 or 9 blisters in a carton box together with instructions for use.

Storage conditions
Store at a temperature not exceeding 25 ° C.
Keep out of reach of children.

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

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equipoise for horses

By reducing doxazosin vascular muscle tone decreases total peripheral vascular resistance equipoise for horses which leads to lower blood pressure (BP). After a single ingestion maximum hypotensive effect observed in the period from 2 to 6 hours, and in general hypotensive effect is maintained for 24 hours. During treatment with doxazosin in hypertensive patients with no differences quantities of BP in the standing and lying down. It is effective in hypertension, including, accompanied by metabolic disorders (obesity, impaired glucose tolerance). Reduces the risk of developing coronary heart disease. The drug in ” normotensive “is not accompanied by a decrease in blood pressure. With prolonged use of doxazosin in patients with no observed change in tolerance to the therapeutic antihypertensive effect. During treatment with doxazosin a decrease in the level of concentration in the blood plasma triglycerides, total cholesterol. At the same time there is some  total ratio cholesterol. Prolonged treatment doxazosin observed left ventricular hypertrophy regression, inhibition of platelet aggregation and improvement in their tissues active plasminogen. Due to the fact that doxazosin blocks alpha1-adrenergic receptors, located in the stroma and prostatic capsule and bladder neck, there is a decrease of resistance and pressure in the urethra, internal sphincter resistance decrease. Therefore, the appointment of doxazosin to patients with symptomatic equipoise for horses benign prostatic giterplazii leads to a significant improvement in urodynamics and reduce symptoms of the disease symptoms.

Pharmacokinetics
Following oral administration at therapeutic doses doxazosin well absorbed, absorption – 80-90% (together with food slows absorption at 1 hour), time to maximum concentration -3 hours in the evening reception -. Time to maximum concentration is prolonged to 5 hours.
bioavailability – 60-70% (first pass metabolism). Contact with blood plasma proteins – about 98%. Elimination from plasma takes place in 2 phases, with a terminal half-life -. 19-22 hours, allowing you to assign the drug 1 time per day.
Intensively metabolized in the liver by on-demethylation and hydroxylation. In patients with impaired liver function, as well as when taking drugs that may alter hepatic metabolism, the process can break down the drug biotransformation. The main excretion through the intestine, mainly in the form of metabolites, only 5% excreted in the urine in unchanged form. The kidneys remove 10%. Pharmacokinetic studies with doxazosin in the elderly and patients with kidney disease showed no significant pharmacokinetic differences.

 

Contraindications
Camiri should not be administered to patients with hypersensitivity to doxazosin and other derivatives equipoise for horses of quinazoline (prazosin, terazosin), or to other components of the drug, at the age of 18 years (effectiveness and safety have not been established).
Precautions: aortic or mitral stenosis, abnormal liver function , orthostatic hypotension.

Pregnancy and lactation
Pregnant women can be given the drug only for health reasons, when benefit to the mother outweighs the potential risk to the fetus / baby. Safety of the drug in infants has not been established, therefore, nursing mothers should stop feeding during treatment with doxazosin.

Dosing and Administration
Inside, 1 time a day (morning or evening), regardless of the meal, not chewing and drinking plenty of water.
The dose should be adjusted depending on the efficacy or potential side effects in certain patients. Patients with hepatic impairment require lower doses of the drug due to slow metabolism.
If the patient has forgotten to take the drug at the usual time, it should be as soon as possible to take the proper dose. If it is time for the next dose, you should only accept it (not doubling the dose). It is important to take the drug regularly. If the patient did not take the drug for a few days, the new course of therapy should be started with the lowest dose. Hypertension: Initial dose Camiri ® is 1 mg per day.The first dose should be taken at night before bedtime. After the first dose the patient must stay in bed for 6-8 hours. This is required because of the possibility of “first dose phenomenon”, especially expressed on the background of prior diuretics. Depending on the therapeutic action of the drug, the dose can be gradually increased at intervals of 1-2 weeks to 2 mg, 4 mg and 8 mg 1 time in a day. As a rule, the usual daily doses range from 2 mg to 8 mg. The maximum daily dose is 16 mg. If the therapeutic effect is not sufficient, patients may receive other antihypertensive agents at the same time:. Beta-blockers, diuretics, blockers “slow” calcium channel blockers and ACE inhibitors After achieving lasting therapeutic effect of the dose is usually somewhat lower (average therapeutic dose of maintenance therapy is usually 2-4 mg per day). Benign prostatic hyperplasia in patients with normal blood pressure: initial dose of 1 mg Camiri ® per day. The patient should take the first dose in the evening before bedtime. Depending on the drug, the dose can be gradually increased at intervals of 1-2 weeks to 2 mg, 4 mg, and 8 mg once daily. Typically, the average daily dose range from 2 mg to 4 mg. The maximum daily dose is 8 mg. Benign prostatic hyperplasia in patients with hypertension: . Dose are the same as in the case of hypertension without benign prostatic hyperplasia (. Cm dose in hypertension) drug is used for a long time. Duration of treatment is determined by the attending equipoise for horses physician.

Side effects Hypertension frequently observed in clinical trials, especially in the beginning of treatment, orthostatic hypotension, which in rare cases may cause fainting. Common reactions: asthenia, fatigue, malaise. Cardio-vascular system: edema, fainting. From the central and peripheral nervous system: dizziness, headache, somnolence. On the part of the gastrointestinal tract: nausea. The respiratory system: rhinitis.

Benign prostatic hyperplasia (BPH)
in patients with BPH found the same side effects as the patients with arterial hypertension, as well as: Systemic reactions: allergic reactions, skin rash, urticaria, back pain, feeling of heat ( “tides” of blood to the skin persons). on the part of the cardiovascular system: decrease in blood pressure, orthostatic hypotension. on the part of the central and peripheral nervous system: dry mouth, priapism, gipostezii, paresthesias, tremor, impotence, insomnia, irritability. From the endocrine: gynecomastia. From the gastrointestinal tract: abdominal pain, constipation, diarrhea, dyspepsia, flatulence, nausea, loss of appetite. From the side of hematopoiesis: leukopenia, purpura, thrombocytopenia. From the hepatobiliary system: increased activity of “liver” enzymes, cholestasis, hepatitis , jaundice. From the musculoskeletal system equipoise for horses: arthralgia, muscle cramps, muscle weakness, myalgia. The respiratory system: bronchospasm, cough, shortness of breath, nasal bleeding. With the skin: alopecia. From the senses: blurred vision , ringing in the ears. from the mochevydelitelnoy system: . dysuria, hematuria, violation of urination, nocturia, polyuria, urinary incontinence and notes the following adverse reactions in patients with arterial gipertepziey (cause-and-effect relationship has not been established): bradycardia, tachycardia, palpitations, pain chest, angina, myocardial infarction, cerebrovascular disease and arrhythmias.

 

Overdose Symptoms: marked reduction of blood pressure, sometimes accompanied by fainting. Treatment: The patient should be put immediately into a horizontal position with his head down, lift the leg.Symptomatic therapy. Dialysis is ineffective.

Interaction with other drugs
Doxazosin increases the hypotensive effect of antihypertensive drugs.
There were no adverse interaction with the simultaneous use of doxazosin and tiazidngh diuretics, furosemide, b – blockers, blockers “slow” calcium channel blockers, ACE inhibitors, antibiotics, oral hypoglycaemic agents, anticoagulants and urikozuricheskih . means
the simultaneous use of inducers equipoise for horses of microsomal oxidation in the liver may increase the effectiveness of doxazosin with inhibitors – reducing. Nonsteroidal anti-inflammatory drugs (especially indomethacin), estrogen (fluid retention) and sympathomimetic agents may reduce the antihypertensive effect of doxazosin. Eliminating alpha adrenostimuliruyuschee effects of epinephrine may cause tachycardia and hypotension.

Cautions
Particular caution should be exercised in the appointment of the drug to patients with impaired liver function, especially in those cases where both are used drugs that can affect the liver. In case of deterioration of the functional state of the liver drug overturned immediately.
In order to prevent orthostatic reactions, patients should avoid unexpected and sudden shifts in body position (transition from the “lying” to “standing”).
In connection with the fact that doxazosin can cause orthostatic reactions at the beginning of treatment or during the period of increasing dosages to patients it is advisable to refrain from any potentially dangerous activities, in particular from road transport management and other vehicles and machinery.
drinking alcohol can increase adverse reactions.
Safety and efficacy of doxazosin in children has not been established, therefore, not appoint a drug to children.
The effect of the “first” of the drug is especially pronounced against the background of previous diuretic therapy and dietary sodium restriction.
Before therapy is necessary to exclude malignant degeneration of the prostate gland.

Composition
Tablets 1, 2 and 4 mg. 10 tablets in blister PVC / PVDC-aluminum foil. 2 or 3 blisters in a carton box together with instructions for use.

Storage conditions
Store at a temperature not exceeding 30 ° C.
Keep out of reach of children.

Shelf life
5 years.
Do not use after the expiration date printed on the package. omni diet plan hcg shots for weight loss and testosterone

equipoise definition

Chlorobutanol has a moderate equipoise definition local anesthetic, anti-inflammatory and antiseptic effect. Camphor is irritating and somewhat antiseptic effect, increases blood flow to the site of application. Levomenthol has local irritating effect, accompanied by a sensation of cold. Irritant (distracting) effect helps to eliminate pain. It has also weak antiseptic properties. Eucalyptus oil has a stimulating effect on the receptors of the mucous membranes has also equipoise definition a weak local anti-inflammatory and antiseptic activity. The combination of these pharmacological properties, provides a comprehensive pathogenetic therapy of inflammatory diseases of the upper respiratory tract.  In view of the low systemic absorption data on the pharmacokinetics of the drug available.

 

Application of pregnancy and lactation
have sufficient experience of use of the drug during pregnancy and lactation is not. If necessary, use during pregnancy should evaluate the potential benefits for the mother and the potential risk to the fetus. Due to the low systemic absorption of equipoise definition the components that make up the drug, it may be used in breast-feeding period.

Dosing and Administration
The drug is used topically. Before applying a spray gun remove the cap, using a bottle should be kept upright so that the sprayer is at the top; You can not use the bottle upside down. After application of the drug on the sprayer should be put on the protective cap.
Pre-clean the nose of mucus, and then enter a nebulizer to a depth of 0.5 cm. The spraying Kameton aerosol formulation, it should be carried out on the “inspiration” phase for the treatment of rhinitis by clicking on the large base of the spray gun and index finger from the top down until it stops. For one application in adults is carried out in 2-3 spray in each nostril, in children aged 5 to 12 years – 1 spray in children 12 to 15 years – 1-2 spraying. The frequency of application – 3-4 times per day. The course of treatment – 7-10 days. In the treatment of inflammatory diseases of the pharynx and larynx (tonsillitis, pharyngitis, laryngitis) a spray nozzle introduced into the oral cavity. The drug should be used after meals, pre-rinse your mouth with warm boiled water. Spray the drug in this case is carried out regardless of the phase of “inhalation” and “exhalation”. For one application in adults is carried equipoise definition out in 2-4 spraying left and right, in children aged 5 to 12 years – 1 spray in children between the ages of 12 to 15 years – 1-2 spraying. The frequency of application – 3-4 times per day. The course of treatment – 7-10 days.

Side effects:
The individual intolerance, allergic reactions such as skin rashes, which are independently after discontinuation of the drug. In applying the drug may be feeling light burning and tingling.

Interaction with other drugs
Systemic effects when using the drug as directed virtually eliminated, allowing you to simultaneously use other drugs without the risk of their interaction with the components of the preparation.

Cautions
When sprayed in the nasal cavity do not throw back his head and did not turn the can upside down. It is not equipoise definition recommended to use the same balloon to several persons in order to avoid the spread of infection.During spraying of the drug should be avoided eye contact.
The cylinder is under pressure, so containers should be protected from shocks and direct sunlight, they can not heat, crush, puncture or incinerate, even when they are empty.

Form release
spray for topical use. 30 g in aluminum monobloc aerosol cans with a self-protection, sealed with a metering valve and fitted with a spray with a protective cap. Each cylinder with the spray protection cap and instructions for use placed in a pile of cardboard.

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

Storage conditions
Store at a temperature of from 3 equipoise definition to 25 ° C. Protect against drops, shocks, exposure to direct sunlight. Keep out of the reach of children. Running low dose t3 clen cycle trying to lose bodyfat isn’t a real hot idea imo.