BRAUNOVIDON 100 g

BRAUNOVIDON 100 g
€ 12.00
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Skin burns dry heat and hot liquids, treatment of wounds, decubitus with bacterially infected ulcerative changes (decubitus ulcers).
Difficult healing skin lesions with inflammatory or ulcerative changes.

BRAUNOVIDON 100 g

 
 
povidone iodine
100 g of ointment contains:
Active ingredient: 10 g of povidone iodine (povidone iodine) with a content of 10% available iodine.
Excipients: macrogol 400, macrogol 4000, Purified water Sodium hydrogen carbonate.
 
 
Pharmaceutical form and content
Ointment 20 g, 100 g, 250 g tubes 
 
 
indications
Skin burns dry heat and hot liquids, treatment of wounds, decubitus with bacterially infected ulcerative changes (decubitus ulcers).
Difficult healing skin lesions with inflammatory or ulcerative changes.
Purulent skin eruptions (pyoderma).
Skin diseases caused by bacteria or fungi, or secondary infection by the same pathogen.
 
 
Contraindications
Sensitivity to iodine or other ingredients.
Acute or recent thyroid disease affecting of iodine.
Patients with goitre or autonomous functional adenoma (mainly elderly).
Before and after treatment with radioactive iodine (to complete recovery). Syndrome dermatitis herpetiformis. Neonates and infants up to 6 months.
 
 
Precautions for use
Due to the oxidative effect of povidone-iodine, some laboratory studies to have a false-positive results (e.g.,. O-toluidine acid or lignum resin for determining hemoglobin or glucose).
Povidone-iodine can reduce imports of iodine the thyroid gland. This may compromise the studies of thyroid (scintigraphy, determination of protein bound iodine, radioiodine) and thus make it impossible to treatment with radioactive iodine. Within 1-2 weeks after treatment with Braunovidon ointment should be made scintigraphy.
 
 
Interaction with other medicinal products and other forms of interaction
Iodine reacts with mercury compounds are highly corrosive mercuric iodide. Povidone-iodine act at pH values between 2 and 7 is to be expected that the povidone-iodine will react with the proteins and other organic compounds which reduces its efektivnost.Da not combine povidone-iodine with enzyme preparations for treatment of wounds of taurolidine, or with hydrogen peroxide.
 
Note:
Care must be taken on chemical incompatibilities with other substances.
 
 
special warnings
 
Use in pregnancy and lactation
Caution should be exercised in pregnant women in the third month. After the third month of pregnancy and during breastfeeding to six months of age must be weighed against the benefit of treatment the possibility of influencing the thyroid gland of the fetus or newborn.
 
 
Dosage and method of administration
Braunovidon ointment is applied to the wound a few times a day according to the size of the area in need of treatment. The wound should be completely covered. In the case of highly inflamed or eksudirashti wounds Renew ointment every 4-6 hours for optimal antimicrobial effect.
The cavities of the abscess may be swabbed using Braunovidon ointment.
The ointment can be left on the wound for longer periods of time and must be replaced when they become discolored.
The application of the ointment Braunovidon should continue until there are signs of infection or risk of infection.
 
 
Note
Brown color of the ointment is an intrinsic characteristic of the preparation. It demonstrates the existence of free iodine and is therefore an indicator of performance.
When the brown color fall, it is a re-administration. Surface in need of treatment should be fully covered as an antimicrobial effect Braunovidon ointment is extremely local.
Due to the fact that povidone-iodine is soluble, stains on fabrics can be removed with soap and water. Stubborn stains can be easily removed using a solution of ammonia and thiosulfate.
 
 
side effects
Allergic reactions are very rare, even in patients sensitive to iodine.
In susceptible patients in isolated cases may occur feelings of pain, parenei warming.
After long periods of use or in the treatment of large burns have been reported instances of interference in serum electrolytes and osmolarity, metabolic acidosis and renal failure.
If administered Braunovidon ointment for a long period of time or over a large surface, in particular burns, or is administered in patients with thyroid disease, or infants, it is advisable during treatment to check the function of the thyroid cancer patient.
 
 
Special precautions for storage
Do not store above 25 ° C.
 
Shelf life
Do not use after the expiry date stated on the label.
Braunovidon ointment in practical 20 g tube with a tip
Ideal for precision or prolonged treatment healing in cases of wounds, burns and skin diseases.
Does not retain fat washed.
a) if necessary shorten the tip to the desired diameter
b) facilitating the application of the desired quantity of ointment in a smaller or a larger opening. After use, close with the screw cap.
 
 
€ 12.00
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