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omnadren cycle

Taurine is a sulfur-containing amino acid produced by the body in the process of converting a cysteine. It stimulates the repair and regeneration processes at dystrophic diseases and diseases accompanied by a sharp violation of the eye tissue metabolism.

It promotes normalization of functions of cell membranes, activation energy and metabolism, preservation of the electrolyte composition of the cytoplasm due to the accumulati onomnadren cycle, improve the conditions of the nervous impulse.

When applied topically, systemic absorption is low.


Indications for use:

The drug is prescribed for adults with:


-Distrofiyah Cornea
– senile, traumatic, radiation and other types of cataracts,
corneal -Travmah (as a stimulator of reparative processes);
-Pervichnoy open-angle glaucoma in combination with a (3-blockers (to improve the outflow of aqueous humor).

For all indications a drug used as part of combination therapy.



Individual  omnadren cycle hypersensitivity to taurine, children up to 18 years.


Pregnancy and lactation: Sufficient experience with the use of the drug during pregnancy, breast-feeding is not. Perhaps the use of taufon for the treatment of pregnant and lactating mothers prescribed by a doctor, if the expected therapeutic effect is greater than the risk of possible side effects.


Dosage and administration:


When cataracts Taufon administered in the form of instillation to 1 to 2 drops 2-4 times a day for three months. The course is repeated at monthly intervals. For injuries and degenerative diseases of the cornea is used in the same doses in one month.

In open-angle glaucoma (in combination with butilaminogidroksipropoksifenok-simeto metiloksadiazolom and combined forms or timolol) -by 1 to 2 drops 2 times a day, 15-20 minutes prior to the appointment of one of the antihypertensive agents, for 6 weeks and then cancel 2 weeks.


Side effect:

allergic reactions.


If these instructions are compounded by the side effects, or if you notice any other side effects not mentioned in the instructions, inform the doctor.



Data on overdose are not available.



Interaction with other drugs:


In patients with glaucoma (open-) showed a significant increase in the hypotensive effect of b-blockers (timolol and butilaminogidroksi-propoksifenoksimetil metiloksadiazola) in the case of a joint application with taufon.

Strengthening effect is achieved by increasing the ratio of lightness outflow and reducing aqueous humor omnadren cycle production.


Product form:


4% eye drops. 10 ml tube-droppers with the instructions for use of the drug, and instructions on the use of tube-dropper in a pile of cardboard partitions or without partitions.


testosterone blend

Other anti means, it has a metabolic effect. Taurine is a sulfur-containing amino acid produced by the body in the process of converting a cysteine. Stimulates the repair and regeneration processes at dystrophic diseases and diseases accompanied by a sharp violation of the eye tissue metabolism. Promotes normalization of cell membrane functions, activation energy and metabolism, preservation of the electrolyte composition of the cytoplasm due to accumulation of the testosterone blend improve the conditions of the nervous impulse. When applied topically, systemic absorption is low.


Corneal Dystrophy; cataract (senile, diabetic, traumatic, radiation); corneal injury (as a stimulator of reparative processes).

Individual hypersensitivity to the drug, testosterone blend children under 18 years.

Use during pregnancy and breastfeeding
have sufficient experience of use of the drug during pregnancy, breast-feeding is not. Taurine is possible to use for the treatment of pregnant and lactating mothers prescribed by a doctor, if the expected benefits exceed the risk of possible side effects.

Dosage and administration
At cataract Taurine administered in the form of installations, 1-2 drops 2-4 times a day for 3 months. The course is repeated at monthly intervals.
For injuries and degenerative testosterone blend diseases of the cornea Taurine is used in the same doses for 1 month.

omnadren 250

Once inside quickly and almost completely absorbed. Bioavailability is 96% -100%. Linking plasma protein – 6-10%. Maximum plasma concentrations after a single oral administration of 200 mg is achieved in omnadren 250. Well into the various tissues and body fluids: the skin, soft tissues, bone, and organs of the abdomen and pelvis, respiratory system, urine, saliva, bile secretion of the prostate, breast milk. It penetrates through the BBB and placental barrier. It is metabolized in the liver for about 5% of the formulation. Report the news mostly unchanged – up to 90%. The half-life – 6-7 hours.


Infectious-inflammatory diseases caused by susceptible to malaria infections:

  • respiratory tract infection (except pneumococcal infection);
  • ear infections, nose and throat (except acute tonsillitis);
  • infections of the abdominal cavity and biliary tract;
  • urogenital tract infections (including gonococcal breed);
  • infections of bones and joints;
  • skin and soft tissue infections


Inside, on an empty stomach or after omnadren 250 eating, drinking plenty of water. Dose and duration of therapy assignment depend on the severity of infection, renal function, the patient’s condition and body weight. Adults – 200 mg 2 times a day at intervals of 12 hours (daily dose – 400 mg) or 400-800 mg 1 time per day. In patients with impaired renal function the dose depends on creatinine clearance: with creatinine clearance 20-50 ml / min – an initial dose of 200 mg, then – 100 mg every 24 hours; less than 20 ml / min – 200 mg, and then – 100 mg every 48 hours; hemodialysis and peritoneal dialysis – 100 mg every 24 hours. Patients with liver failure, the maximum daily dose should not exceed 400 mg. The duration of therapy is determined by the sensitivity of the causative agent and the clinical picture of the disease. Treatment should continue for at least 3 days after the disappearance of symptoms and complete normalization of body temperature. The course of treatment in most cases of acute infectious and inflammatory diseases – not more than 7-10 days, while salmonellosis – 7-8 days in uncomplicated infections of the lower urinary tract – 3-5 days.

Side effect

Allergic reactions: seldom – skin rash, itching, angio-neurotic edema, bronchospasm, and in rare cases – erythema multiforme, Stevens-Johnson syndrome, toxic skin necrosis, and vascular purpura photosensitivity, anaphylactic shock.

Gastrointestinal tract: dry mouth, loss of appetite, nausea, vomiting, abdominal pain, diarrhea, rarely – pseudomembranous colitis.

Hematology: anemia, leukopenia, neutropenia, agranulocytosis rarely, eosinophilia, thrombocytopenia, and in rare cases – hemolytic anemia, pancytopenia.

Kidneys: renal failure (increased urea and creatinine), very rarely – interstitsionalny nephritis.

Liver: increased activity of “liver” transaminases, hyperbilirubinemia, cholestatic jaundice.

CNS: dizziness, headache, disturbance of taste and smell (including visual and auditory hallucinations), drowsiness, sleep omnadren 250 disturbances, anxiety, psychotic reactions, rarely – extrapyramidal disorders, and other disorders of muscular coordination..

Other: arthralgia, myalgia, sore tendons, hypoglycaemia in diabetic patients, an increase in temperature. Perhaps the emergence of resistant microorganisms to ofloxacin.


  • Hypersensitivity to ofloxacin and other quinolone drugs.;
  • epilepsy;
  • CNS, accompanied by a reduction in seizure threshold (after traumatic brain injury, stroke, and inflammatory processes in the CNS field);
  • pregnancy;
  • lactation (breastfeeding);
  • childhood and adolescence (until the completion of growth and formation of the skeleton)

special instructions

During treatment is not recommended to be exposed to sunlight, ultraviolet irradiation (mercury-quartz lamp, solarium), you must refrain from driving vehicles and moving machinery, women are advised not to use tampons “Tampax” due to the risk of thrush.

Drug interactions

Antacids (preparations containing aluminum hydroxide or magnesium), ferrous sulfate, saline laxatives, sucralfate, zinc, and reduce the absorption dedalon taritsina reduced activity (interval between reception of delivery has to be not less than 2 hours). Cimetidine, furosemide and methotrexate inhibit the excretion taritsina and may increase its toxicity. Taritsin increases the omnadren 250 concentration of glibenclamide. While the use of vitamin K antagonists should be carried out monitoring of the blood coagulation system. Decreases theophylline clearance by 25% (while the appointment with taritsinom necessary to decrease the dose of theophylline).

testosterone blend 250mg

The most important symptoms of overdose are the symptoms of the central nervous system: dizziness, confusion, lethargy, disorientation, drowsiness, as well as the response from the gastrointestinal tract.
In case of overdose, it is testosterone blend 250mg recommended to carry out gastric lavage (relates to tablets) and symptomatic therapy. There is no specific antidote.

The interaction with other drugs
Antacids containing aluminum hydroxide (including sucralfate) and magnesium, aluminum phosphate, zinc, iron reduces the absorption of ofloxacin. When receiving antacids and ofloxacin between their intake should be observed approximately a two-hour interval.
With the simultaneous use of vitamin K antagonists should be monitored for blood coagulation system.
Ofloxacin may slightly increase the plasma concentrations of glibenclamide, while using.
If you are using high doses of ofloxacin and other drugs that are excreted via renal tubular secretion, such as probenicid, cimetidine, furosemide, methotrexate, or may increase ofloxacin concentration in the serum.
in clinical studies revealed no pharmacokinetic interactions with theophylline ofloxacin. However, a significant lowering of the threshold for seizure activity could be observed in the appointment of quinolones in combination with theophylline, fenbufenom or other non-steroidal anti-inflammatory drugs, as well as other drugs, lowering the threshold for seizure activity.
In the appointment in conjunction with non-steroidal anti-inflammatory agents, derivatives of nitroimidazole and methylxanthines increases the risk of neurotoxic effects.
When concomitant administration with corticosteroids increases the risk of tendon rupture, particularly in elderly people.
When coadministered with drugs prolong the interval testosterone blend 250mg increases the risk  interval prolongation.
in the appointment of drugs , alkalizing urine (carbonic anhydrase inhibitors, citrate, sodium bicarbonate), increases the risk of crystalluria and nephrotoxic effects.

special instructions

  • Renal failure
    in connection with what is displayed ofloxacin mainly via the kidneys in patients with renal failure require dosage adjustment ofloxacin.
  • Prevention of photosensitivity
    during treatment with ofloxacin, due to the risk of photosensitivity, avoid exposure to bright sunlight and UV rays.
  • Secondary infection
    As with other antibiotics in the treatment, receiving ofloxacin, especially prolonged, can cause secondary infection associated with an increase in drug-resistant microorganisms. It needs re-evaluation of the patient’s condition. If a secondary infection occurs during therapy, appropriate measures should be taken.
  • Pseudomembranous colitis
    Occurrence of diarrhea, particularly in severe, persistent and / or mixed with blood, during or after treatment with ofloxacin may be a manifestation of pseudomembranous colitis. If you suspect that the development of pseudomembranous colitis treatment with ofloxacin must be discontinued immediately and appropriate specific antibiotic therapy (eg vancomycin inside, inside teicoplanin or metronidazole) should be instituted without delay. In this clinical situation are counter drugs that inhibit intestinal motility.
  • Patients predisposed to occurrence of epileptic seizures
    As with other quinolones, ofloxacin should be with great care given to patients predisposed to the development of epileptic seizures (patients with damage to the central nervous system in history, taking fenbufen and similar non-steroidal anti-inflammatory drugs, or drugs that lower the threshold for seizure activity, for example, theophylline).
  • Tendonitis
    Tendonitis, are very rare, can sometimes lead to tendon razrshu predominantly Achilles tendon, particularly in elderly patients. In the event of signs of tendonitis (tendon inflammation), should immediately stop treatment, immobilization of the Achilles tendon to produce and provide advice orthopedist.
  • QT prolongation
    is needed a certain caution when receiving fluoroquinolones, including ofloxacin, in patients with known risk factors for prolongation of the testosterone blend 250mg interval, such as:

    • elderly age;
    • uncorrectable electrolyte imbalance (eg, hypokalemia, hypo-magniemiya);
    • congenital prolongation of the interval ;
    • diseases of the cardiovascular system (heart failure, myocardial infarction, bradycardia)
    • concomitant use of drugs prolonging the interval (IA and class III anti-arrhythmic drugs, tricyclic antidepressants, macrolides).
  • Myasthenia gravis
    Ofloxacin can lead to a worsening of myasthenia gravis.
  • Porphyry
    Perhaps more frequent attacks of porphyria. During treatment with ofloxacin may cause false-positive results in the determination of opiates and porphyrin in the urine.
  • Other
    Ofloxacin inhibits release of Mycobacterium tuberculosis, leading to false negative results when bacteriological diagnosis of tuberculosis.Also during the period of treatment is not recommended to use ethanol.In applying the drug to women is not recommended to use tampons with an increased risk of developing thrush.Ofloxacin is not the drug of choice for pneumonia caused by pneumococcus.Not indicated in the treatment of acute testosterone blend 250mg tonsillitis.Driving or other mechanisms
    Some side reactions such as dizziness, somnolence, and visual disturbances can reduce response and the ability to concentrate, and therefore increase the risk of situations in which the presence of these capabilities is particularly important (such as when driving or other mechanisms) .


jelfa omnadren

Following oral administration of ofloxacin is rapidly and almost completely absorbed from the gastrointestinal tract. Bioavailable is almost 100%. The maximum concentration of ofloxacin in the blood plasma after administration  achieved after a protein binding is 25%.. Metabolized jelfa omnadren of ofloxacin. The half-life of 6-7 hours. The volume of distribution of approximately 120 liters. Up to 90% of ofloxacin excreted by the kidneys in an unmodified form, about 4% in the bile.

Treatment of infectious and inflammatory diseases caused by microorganisms sensitive to ofloxacin:


  • respiratory tract infections (except in cases of pneumococcal infection);
  • ear infections, nose and throat (except in cases of acute tonsillitis);
  • abdominal infections and biliary tract;
  • kidney infection, urinary tract, prostate, urethra (including gonococcal origin);
  • pelvic infection;
  • infections of bones and joints;
  • skin and soft tissue infections.
  • prevention of infections in patients with impaired immune status (including neutropenia).Contraindications
  • Hypersensitivity to ofloxacin, other quinolones or components of the drug;
  • epilepsy;
  • damage to the central nervous system with a reduced seizure threshold (after traumatic brain injury, stroke, inflammatory processes in the central nervous system (CNS);
  • tendon injury during jelfa omnadren the earlier treatment of quinolones;
  • age of 18 years;
  • pregnancy and lactation;Precautions: patients with cerebral atherosclerosis, blood circulation (in history), chronic renal insufficiency, organic  lesions, with prolongation of the interval.

    Dosage and administration
    . Inside
    dose of ofloxacin and the duration of jelfa omnadren treatment depend on the severity and type of infection, the patient’s general condition and renal function.
    The average daily dose for adults – from 200 mg to 600 mg. Treatment duration -7-10 days.
    The dose to 400 mg / day may be administered in 1 intake, preferably in the morning. Doses in excess of 400 mg / day should be divided into 2 doses with regular intervals. Tablets should be taken whole with a glass of water both before and during the meal. It is necessary to avoid the simultaneous reception with antacids. In severe infections, or in patients who are overweight daily dose may be increased to 800 mg.