anavar half life

The drug is taken orally once or twice daily.  The tablets do not chew and drink plenty of fluids (0.5 to 1 cup), can be taken before meals or between meals. Doses oxandrolone anavar half life are determined by the nature and severity of the infection and the sensitivity of the alleged pathogen.

Patients with normal or moderately decreased kidney function, the recommended dose regimen of the drug:

Sinusitis (inflammation of the sinuses): 500 mg 1 time per day – 10 -14 days.

Exacerbation of chronic bronchitis: 250 mg or 500 mg 1 time per day -7-10 days.

Vnebolnichnaya pneumonia: 500 mg 1-2 times a day – 7-14 days.

Uncomplicated urinary tract infections: 250 mg 1 time per day – 3 days.

Prostatitis: 500 mg – 1 per day – 28 days.

Complicated urinary tract infections, including pyelonephritis: 250 mg 1 time per day – 7-10 days.

Infections of skin and soft tissues: 250 mg 1 time per day or 500 mg 1-2 times a day – 7-14 days.

Septicemia / bacteremia: 250 mg or 500 mg 1-2 times a day – 10-14 days.

Intra-abdominal infections: 250 mg or 500 mg 1 time per day – 7-14 days (in combination with antibacterial drugs acting on the anaerobic flora).

Skin reactions and general hypersensitivity reactions
sometimes itching and redness of the skin. Rare: general reactions of hypersensitivity (anaphylactic and anaphylactoid reaction) with symptoms such as urticaria, bronchoconstriction and possibly – heavy gasps. In very rare cases, – swelling of the skin and mucous membranes ( for example in the areas of the face and throat), sudden drop in blood pressure and shock; increased sensitivity to sunlight and ultraviolet radiation (see “Cautions.”); hypersensitivity pneumonitis; vasculitis. In some cases: severe rash with blistering, such as Stevens-Johnson syndrome, toxic epidermal necrolysis anavar half life and exudative erythema multiforme. General hypersensitivity reactions may sometimes be preceded by lighter skin reactions. The above-mentioned reaction may develop after the first dose in a few minutes or hours after administration.


Action on the gastrointestinal tract and metabolism Common: nausea, diarrhea. Sometimes: loss of appetite, vomiting, abdominal pain, dyspepsia. Rare: bloody diarrhea which in very rare cases, it may be a sign of bowel inflammation and even pseudomembranous colitis (see .. “Cautions”) Very rare: drop in blood sugar levels (hypoglycemia), which has particular buy anabolic uk importance for patients with diabetes; Possible symptoms of hypoglycemia: “wolf” appetite, nervousness, sweating, trembling. Experience with other quinolones suggests that they are capable of causing an exacerbation of porphyria (a very rare metabolic disease) in patients who are already suffering from the disease. Such an effect is not excluded when using levofloxacin formulation.

Nervous system Occasionally: headache, dizziness, and / or numbness, drowsiness, and sleep disorders. Rare: depression, anxiety, psychotic reactions (eg, hallucinations), discomfort (eg, paresthesias in the hands), tremor, psychotic reactions such as hallucinations and depression, restlessness, seizures, and mental confusion. Very rare: visual and hearing impairment, disturbances of taste and smell sensitivity, reduction of tactile sensitivity.


The action on the cardiovascular system Rare: increased heart rate, decreased blood pressure. Very rare: (shock-like) vascular collapse. In some cases: lengthening  interval.


Action on myshiy, tendons and bones Rare: defeat tendons (including tendonitis), joint and muscle pain. Very rare: tendon rupture (eg Achilles tendon); this side effect may occur within 48 hours after the start of treatment and may be bilateral in nature (see “Cautions.”); muscle weakness, which is of particular importance for patients with bulbar syndrome. In some cases: muscle damage (rhabdomyolysis).


Action on the liver and kidney Common: increase in anavar half life liver enzymes (eg, alanine aminotransferase and aspartate aminotransferase). Rare: increased levels of bilirubin and serum creatinine (sign of limitation of the liver or kidney). Very rare: hepatic reactions (eg, inflammation of the liver); deterioration of renal function until the acute renal failure, for example, due to allergic reactions (interstitial nephritis).



anavar oxandrolone

A synthetic antibacterial agent of a broad spectrum fluoroquinolone, containing as active substance levofloxacin – laevorotatory isomer of ofloxacin.Levofloxacin blocking gyrase, and crosslinking gives supercoiling breaks, inhibit anavar oxandrolone synthesis, causes profound morphological change in the cytoplasm, the cell wall and membranes. Levofloxacin is active against most strains where to buy aromasin bodybuilding of microorganisms in conditions in vitro and in vivo.

Levofloxacin is rapidly and almost completely absorbed after oral administration. Food intake has little effect on the speed and completeness of removals. Bioavailability of 500 mg oral levofloxacin after is nearly 100%. After administration of a single 500 mg dose of levofloxacin is the maximum concentration of 5.2-6.9 g / ml, time to maximum concentration -. 1,3ch half-life – 8.6 hours.

Relationship to plasma proteins – 30-40%. It penetrates the tissues and organs: lungs, bronchial mucosa, sputum, organs of the urogenital system dynabolon, bone tissue, cerebrospinal fluid, the prostate gland, polymorphonuclear leukocytes, alveolar macrophages.

In the liver, a small part of the oxidized and / or deacetylated. Report from the body mainly by the kidneys by glomerular filtration and tubular secretion. Following anavar oxandrolone oral administration, approximately 87% of the dose is excreted in the urine unchanged within 48 hours, less than 4% in the faeces within 72 hours.

Indications for use:

Infectious-inflammatory diseases, caused by susceptible microorganisms: acute sinusitis, acute exacerbations of chronic bronchitis, community-acquired pneumonia, complicated urinary tract infections (including pyelonephritis), uncomplicated urinary tract infections, prostatitis, infections of skin and soft tissues, septicemia / bacteremia associated sustanon 250 gains with the above readings, intra-abdominal infection.


  • hypersensitivity to levofloxacin or other quinolones;
  • epilepsy;
  • tendon injury during the earlier treatment of quinolones;
  • childhood and adolescence (18 years);
  • pregnancy and lactation.


The drug should be used with caution in the elderly, due to the high probability of the presence of a concomitant decrease in renal function british dragon reviews, with a deficit of anavar oxandrolone dehydrogenase.


anavar pills

For topical administration the therapeutic concentration of drug achieved in the eye tissues. Infectious-inflammatory diseases of the anterior eye, caused anavar pills by susceptible microorganisms to ofloxacin, blepharitis, barley, conjunctivitis, dacryocystitis, keratitis, corneal ulcer, chlamydial eye infection, prevention and treatment of bacterial infection primobolan side effects after eye injuries and surgeries.

Contraindications :

Hypersensitivity to the drug, pregnancy, lactation.

Dosage and administration :

Drops drug instilled 1 drop in the conjunctival sac of the patient’s eyes 2-4 times a day, is not recommended to use the drug for more than 2 weeks. With the simultaneous use of more than one drug is necessary to observe a minimum of 5-minute interval between installations. Ointment 1.5 cm strip of ointment is pawned for the lower eyelid of the patient’s eyes 2-3 times a day, in the case of Chlamydia infection – 5 times a day, is not recommended to use the drug clen for more than 2 weeks. Perhaps a combination of eye anavar pills drops and ointments Floksal.With simultaneous use of more than one drug ointment should be used last.

Use during pregnancy and lactation :

No information about the harmful effects of ofloxacin on the fetus, but not rekomendetsya use the drug during pregnancy and lactation.

Side effects :

Allergic reactions; transient conjunctival hyperemia, burning sensation; discomfort in the eyes, itching and dryness of the conjunctiva, photophobia, lacrimation, rarely – dizziness.

Interaction with other drugs :

Drug interactions of the drug has not been described.

Special instructions :

Do not wear contact lenses while using the drug. Wear sunglasses (because of the possible development of photophobia) and avoid prolonged exposure to bright light. After applying the ointment temporarily reduced visual acuity, it is necessary to take into account when driving or operating machinery.

Product form :

0.3% eye drops in bottles winstrol of 5 ml; 0.3% eye ointment in tubes, 3 g in a carton box with instruction on the medical application.

Storage conditions :

In the dark, at a temperature no higher anavar pills than 25 ° C and out of reach of children.



Phlogenzym is a combination of two complementary enzymes and trypsin bromelain in combination with Rutoside. Enzymes are absorbed through the intestine intact molecules claim resorption. Contacting blood transport proteins into the bloodstream. Subsequently, migrating but bloodstream, accumulate in the area of the pathological process, irrespective of localization in the body. Trypsin, bromelain and promote rapid cell splitting “fragments” n metabolic products of the inflammatory process, and restores rutin permeability of vascular walls, resulting in a reduction of edema and hematoma. . At the same enzymes that are part of the drug, and implement their activity by the anti-inflammatory, immunomodulatory, fibrinolytic, antiagregatnogo, decongestant action, acting on a complex pathophysiological processes .
Phlogenzym improves the oxandrolone functional state of the blood cells and the vascular wall; reduces the viscosity of the blood and the risk of blood clots in blood vessels, helps dissolve clots already formed. It improves the microcirculation, resulting in faster dissolve swelling and bruising. decreases pain.
Phlogenzym improves microcirculation in the foci of chronic inflammation, increases the delivery of oxygen and nutrients (blood supply), thus stimulating repair processes in chronic diseases and in the postoperative period.
Phlogenzym improves blood circulation of the bronchi and lung tissue in chronic respiratory diseases, including those caused by smoking; liquefies phlegm, improves the function of the ciliated epithelium of the bronchi drainage and restores function.
Phlogenzym increases the effectiveness of antibiotic therapy.

Surgery: in the treatment of post-operative complications, dentistry and plastic surgery (abscess, thrombosis, adhesion); in order to prevent disease, lymph edema and microcirculation disorders, burns.
Traumatology: in the treatment of damaged tendons and ligaments, sports injuries.
Angiology: in the treatment of acute deep vein thrombosis, thrombophlebitis of superficial veins, postthrombophlebitic disease, obliterating atherosclerosis of lower limb arteries and . other chronic arteriopathies
. Urology: in the treatment of acute and chronic inflammation of the urogenital tract: cystitis, urethritis, cystopyelitis, prostatitis
Gynecology: in the treatment of acute and chronic inflammatory diseases of the pelvic organs (adnexitis, salpingo); vascular complications of menopause. To reduce the frequency and severity of complications of hormone replacement therapy.
Cardiology: in the treatment of coronary heart disease, prevention of angina attacks.
Gastroenterology: in the treatment of hepatitis.
Rheumatology: in the treatment of rheumatoid arthritis, ankylosing spondylitis, reactive arthritis, rheumatic soft tissue.

Individual intolerance. Congenital oxandrolone or acquired bleeding disorders (eg, hemophilia). The experience of childhood is absent.

The caution (only after consultation with your doctor)
Pregnancy, lactation. Hemodialysis.

Dosing and Administration
Inside, at least 30 minutes. before eating, not chewing, washing down with water (200 ml). Adults:
With the purpose of treatment Phlogenzym take 3 tablets 3 times a day for 2 weeks if the doctor has not been appointed for a longer period of treatment for prevention Phlogenzym recommended at a dose of 2 tablets 3 times a day for 2 weeks.
Changing the receiving rate and the dosage of the drug is possible only after consultation with your doctor.

Side effects
Phlogenzym well tolerated by patients. In some cases, there may be more frequent stools, change in stool consistency and smell, which quickly cease with temporary reduction of dosage of the drug.Occasionally allergic reactions may occur (skin rash, itching), which disappears after discontinuation of treatment. When using the drug were observed: nausea, flatulence, abdominal pain, headache, dizziness, rash, general weakness. You may receive a temporary feeling of overcrowding in the intestine. This can be prevented by dividing the daily dose into more single doses.

No cases of overdose is unknown.

The interaction with other drugs
cases of incompatibility with other drugs was observed. Application Flogenzima conjunction with antibiotics increases the effectiveness of antibiotic therapy.

Specific guidance
in the case of infectious processes Phlogenzym not a substitute for antibiotics.
In the case of aggravation of the disease while recommended temporary dose reduction and should see a doctor.
The drug is not doping, and has no negative effect on driving and performance of work requiring a high rate of mental and physical reactions.
Patients suffering from diabetes, it should oxandrolone be noted that each tablet contains 0.015 bread units.

Product form
The tablets are packaged in blisters to 20 pcs. and placed in cartons of 2, 5 and 10 blisters with enclosed instructions for use. Package 800 includes tablets tablets are not packed in blisters placed  with embedded instructions.



No data on acute or chronic overdose . In healthy volunteers, intranasal administration of 2 mg fluticasone propionate twice daily for 7 days had no effect on the function of the hypothalamic-pituitary-adrenal system (doses 20 times higher than therapeutic). Use of the drug in doses higher than those recommended for a long period of time can lead to temporary suppression of adrenal function.
In such patients, treatment of fluticasone propionate should be continued at the doses needed to control symptoms; restore adrenal function takes a few days, its monitoring is carried out by measuring the cortisol level in the plasma.

The interaction with other drugs
Because of the very low concentrations of fluticasone propionate in plasma after administration of oxandralone andralone clinically significant interactions are very unlikely.
Ritonavir  is able to much increase, the plasma concentration of fluticasone propionate, whereby dramatically reduced levels of cortisol in human serum, there systemic side effects including Cushing’s syndrome and adrenal suppression. Inhibitors  enzyme system cytochrome  produce negligible (erythromycin) and minor (ketoconazole) increase fluticasone propionate plasma concentrations, which do not entail any significant reduction in serum cortisol concentrations. However, caution should be exercised with the concomitant use  inhibitors of cytochrome  enzyme system (eg, ketoconazole) and fluticasone propionate in view of a possible rise in the plasma concentration of the latter.

Special instructions and precautions for the use of
drug is indicated only for intranasal use.
Without medical supervision  should not be constantly used for more than 6 months.
In the long-term use requires regular monitoring of adrenocortical function.
There are reports of the manifestation of systemic effects when using nasal glucocorticosteroids very high doses for a prolonged time. These effects are much less likely than with oral dosage forms of corticosteroids, and may vary among individual patients and also between different glucocorticosteroids.
Full effect fluticasone propionate nasal spray can occur only after several days of treatment. To achieve maximum therapeutic effect is necessary to adhere to a regular patterns of use.
Care should be taken when transferring patients from systemic glucocorticosteroid therapy for the treatment of nasal spray fluticasone propionate, if there is reason to believe a violation of adrenal function. In most patients, nasal spray fluticasone propionate eliminates the symptoms of seasonal allergic rhinitis, but in some cases, at very high concentrations in the air of allergens, may need additional treatment.
Additional treatment may be required for the relief of ocular manifestations against the background of a successful treatment of seasonal allergic rhinitis.
In the post-registration monitoring reported oxandralone cases the occurrence of systemic effects of corticosteroids, such as Cushing’s syndrome and adrenal suppression, with concomitant use of fluticasone propionate and ritonavir.
Therefore, the simultaneous use of ritonavir and fluticasone propionate should be avoided unless the potential benefit to the patient exceeds the possible risk of systemic corticosteroid side effects.

Effects on ability to drive vehicles, mechanisms
In clinical studies, no data on the effect of the drug on the ability to drive vehicles and other mechanisms, but consider the side effects, which can cause the drug.

Product Form
Spray nasal dosage 50 .mu.g / dose.
Each vial is provided with a metering device. Per vial and a metering device worn adapter for intranasal administration. The vial is further provided with a cap to protect the adapter from dust.
Each vial with oxandralone a metering device, an adapter and a protective cap (mounted) and instructions for medical use is placed in a cardboard box.