RUTASKORBIN table

INGREDIENTS:

Active substances in one tablet: Rutosid-20 mg, Ascorbic acid-100 mg.

Other ingredients: hydroxypropyl cellulose, copovidone, crospovidone, talc, magnesium stearate, microcrystalline cellulose, colloidal anhydrous silica, disodium edetat.filmovo coverage: eudrazhit, talc, titanium dioxide, macrogol, polysorbate, E110.

PHARMACEUTICAL FORM AND CONTENTS:

tablets 5 mg, 50 pcs. in dark glass bottles in a carton.

ACTION:

Rutoside involved in cellular redox processes and stabilize the cell membrane and capillary wall. Prevents bleeding, has anti-inflammatory and antiallergic effects. Ascorbic acid plays an important role in the life processes of the organism as a universal activator of cellular metabolism.

INDICATIONS

Symptomatic treatment complex therapy:

 diseases associated with increased permeability and capillary fragility, bleeding into the skin, mucous membranes, and retina, parenchymal hemorrhage, cerebral hemorrhage, affecting the retina from diabetes, glaucoma (increased eye pressure), hematuria (blood in urine), and allergic inflammatory responses, atherosclerosis, high blood pressure;

 Treatment and prevention of interference of capillaries (small blood vessels) of medication (aspirin, indomethacin, phenylbutazone, anticoagulants, anticoagulation agents, arsenic compounds, gold salts, etc..) Reduces capillary resistance.

INFORMATION REQUIRED BEFORE USE

CONTRAINDICATIONS:

Hypersensitivity to the active and / or any of the excipients. The product should not be administered to patients with abnormal blood clotting, severe liver or renal function, patients with artificial heart valves, glucose-6-fosfatdehidrogenaza.

SPECIAL PRECAUTIONS FOR USE:

No.

DRUG INTERACTIONS AND OTHER:

Rutaskorbin can be used in conjunction with other means strengthening capillaries and veins, with anti-inflammatory products and reduce mastite.Rutaskorbin can reduce the radiation from the body of barbiturates and increase the sedative effect. Ascorbic acid can destroy vitamin B12 in the digestive tract, which must be taken at least 2 hours before or after meals. You can reduce the toxic effects of disulfiram.

WARNINGS in special patient groups:

Use with caution in patients with bladder stones, and of an increase in oxalates in the urine, some blood-system diseases, thrombosis, thrombophilic; diabetes.

Use in pregnant and breast-feeding:

Due to lack of data on safety in pregnancy and lactation, its use is not recommended.

EFFECTS ON ABILITY TO DRIVE AND USE MACHINES:

No evidence of impairment of alertness, reflexes and motor activity.

DATA excipients

The product contains colorant E 110, which may cause allergic-type reactions including. asthma attack. The risk of allergies is higher in patients allergic to aspirin.

INFORMATION FOR PROPER USE

DOSAGE AND ADMINISTRATION:

Accepted from 1 to 3 tablets three times daily by mouth before or after meals. The duration of treatment is usually 5-6 weeks, in some cases up to 3-6 months.

OVERDOSE In:

Taking a higher dose can cause increased clotting blood clotting tendency, anxiety, insomnia, headaches, high blood pressure, diarrhea, urine sugar. Treatment is symptomatic and is conducted by a physician precautions to reduce the absorption of the product, gastric lavage, activated charcoal.

SIDE EFFECTS:

During treatment with this product may experience mild gastrointestinal complaints, most commonly nausea, you need to take after eating. Very rarely can be observed reactions of skin rashes and itching.

PHARMACEUTICAL FORM AND CONTENTS:

Film-coated tablets of 50 pieces in glass bottles packed in a cardboard box.

STORAGE:

In a dry and dark place at a temperature below 25 ° C. Keep out of reach of children.

SHELF LIFE

4 (four) years from date of manufacture