BRAUNOL mucous membrane tip, 10x1000 ml

Instructions for use for BRAUNOL mucous membrane tip, 10x1000 ml

Detailed instructions for BRAUNOL mucous membrane tip, 10x1000 ml

Field of use

• The medicine is an antiseptic (germicidal agent) for application to skin, mucous membrane and wounds.
• For a one -time application:
  • Disinfection of the intact external skin or antiseptic of the mucous membrane such. B. before operations, biopsies, injections, punctures, blood samples and bladder catheterization.
• For repeated, limited use:
  • Antiseptic wound treatment (e.g. pressure ulcers, lower leg ulcers), burns, infected and super -infected skin diseases.
• Hygienic and surgical hand disinfection.

Active ingredients / ingredients / ingredients

75 mg povidon iod
7.5 mg iodine
Natrium dihydrogen phosphate 2-water auxiliary material (+)
Sodium hydroxide auxiliary substance (+)
Sodium iodate auxiliary substance (+)
Polidocanol 600 auxiliary material (+)
Water, cleaned auxiliary material (+)

Contradictions

• The medicine must not be used,
  • if you are sensitive to povidon iodine or one of the other components.
  • if you suffer from an overactive thyroid (hyperthyroidism) or another existing (manifest) thyroid disease,
  • if you are ill from the very rare chronic dermatitis dermatitis herpetiformis duhring,
  • if you have a radiation therapy of the thyroid with iodine (radioiodine therapy) planned or carried out (until the treatment).
  • in very small premature babies (birth weight below 1500 g)

dosage

• Always apply the preparation exactly according to the instruction. Please ask your doctor or pharmacist if you are not quite sure.
• For skin disinfection or antiseptic of the mucous membrane, e.g. B. before surgical interventions, biopsies, injections, punctures, blood samples, bladder catheterization, the preparation is undiluted.
• For the skin disinfection of low -sebum glands, the exposure time is at least 15 seconds, and at least 10 minutes for the skin -rich skin. The skin must be kept damp through the undiluted preparation during the entire period of exposure.
• In the case of preoperative skin disinfection, "puddle formation" must be avoided among the patient due to possible skin irritation.
• The medicine is undiluted for hand disinfection.
• 3 Ml are rubbed into the hands for hygienic hand disinfection. Wash hands after an exposure time of 1 minute.
• For surgical hand disinfection, 2 x 5 ml are rubbed into the hands over an exposure time of 5 minutes. The hands must be kept damp through the undiluted preparation during the entire period of exposure.
• For an antiseptic treatment of superficial wounds, the medicine is applied undiluted to the areas to be treated.
• The solution can be diluted for antiseptic rinsing, washes and bathrooms.
  • The following dilutions are recommended as guidelines:
    • Rinses in the context of wound treatment (e.g. decubitus, ulcus cruris, gangrene) and perioperative infection prophylaxis 1: 2 to 1:20
    • Antiseptic washes 1: 2 to 1:25
    • Antiseptic sub -baths approx. 1:25
    • Antiseptic full baths approx. 1: 100

• Frequency and duration of the application
  • At a repeatthe frequency and duration of the application is based on the present indication.
  • The medicine can be applied one to several times a day.
  • Wound treatment should be continued as long as there are signs of infection or a significant risk of infection of the wound conditions. If, after a multi -day (2 to 5 days) regular application, your symptoms have not improved or if symptoms occur again after the treatment has been completed, please see your doctor.

• If you have any further questions about the application of the drug, ask your doctor or pharmacist.

Taking

• The medicine is undiluted and intended for external use in dilutions.
• The medicine must be applied to the area to be treated until full wetting. The film, which is forming when drying, can be easily washed off with water.
• Normal tap water is suitable for dilution. If approximate isotony is desired, physiological saline solution or wrestling solution can be used. The dilution must always be made fresh and consumed soon.
• For the production of antiseptic full baths, water should first be left into the tub and then the required amount of medicines should be avoided in order to avoid discoloration of the tub by developing iodine -containing vapors.
• The brown color of the drug is a property of the preparation and indicates its effectiveness. A extensive decolorization indicates the exhaustion of the effectiveness of the preparation.

Patient information

• Particular caution when using the drug is required:
  • After thyroid diseases or in the event of a goiter, you should only apply over a longer period of time and large (e.g. over 10% of the body surface and longer than 14 days) only on the express instruction of the doctor. Even after the termination of the therapy (up to 3 months), early symptoms of a possible overactive thyroid must be observed and, if necessary, monitoring the thyroid function.
  • With simultaneous lithium therapy, a regular application of the drug must be avoided
  • Due to the oxidizing effect of the active ingredient povidon iodine, various diagnostics can provide false positive results under treatment with the medicine (including toluidine and guajakharz to hemoglobinoder
    Glucose determination in the chair or urine).
  • Povidon iodine can influence the iodine recording of the thyroid gland; This can lead to disorders of diagnostic examinations of the thyroid gland (thyroid scintigraphy, PBI determination, radioiod diagnostics) under the treatment with the medicine and make planned radioiod therapy impossible. Until the absorption of a new scintigram, a distance of at least 1 - 2 weeks after discontinuation of the treatment with the medicine should be observed
  • Children:
    • Avoid repeated application for newborns. After using the preparation, checking the thyroid function is necessary.
    • The random recording by the infant with the mouth must be avoided.
  • Older people:
    • In older people, the risk of an overactive thyroid triggered by iodine is increased. You should therefore only use the medicine after consultation with your doctor. In older patients with a goiter or special predisposition to thyroid dysfunction, a large -scale and long -term application of the drug should only be carried out on the express instruction of the doctor. If necessary, the thyroid function must be monitored.

Pregnancy

• Pregnancy
  • During pregnancy and breastfeeding, the medicine is only to be applied to the express instruction of the doctor and extremely limited. In this case, the child's thyroid function is required.
• Breastfeeding
  • The random absorption of the drug by the infant with his mouth on the breast of the breastfeeding mother must be avoided.

Hints

Miscellaneous

- Dilutions are always freshly produced and soon consumed.
- The brown color of Povidon iod is a property of the drug and indicates its effectiveness. A extensive decolorization indicates the exhaustion of the effectiveness of the drug.

Therapy monitoring/control measures:
- After using the drug, the thyroid function is indicated in infants and small children. In the case of an underactive thyroid gland, early treatment with thyroid hormones must be carried out until the normalization of the thyroid fabric.

Influence of laboratory parameters.
- Due to the oxidizing effect of the active ingredient, various examinations can provide false-positive results under the treatment with the medicine (including toluidine and guajak resin for hemoglobin or glucose determination in stool or urine).
- Under the application of the drug, the iodine recording of the thyroid gland can be reduced. This can lead to disorders of thyroid scintigraphy, the PBI (protein-bound iodine) determination and radio iodine diagnostics and make planned radio iodine treatment impossible.

Incompatibilities:
- The active ingredient is not compatible with reducing substances, alkaloid salts, tannic acid, salicylic acid, silver, mercury and whisperal salts, taurolidine, hydrogen peroxide.