What is Braunol 7,5%, roztwór na skórę used for?

Minims Povidone Iodine 5% w/v eye drops, solution is indicated for cutaneous peri-ocular and conjunctival antisepsis prior to ocular surgery and/or intravitreal injection to support post-procedural infection control.

What is the active ingredient in Braunol 7,5%, roztwór na skórę?

Povidonum iodinatum (Polyvidonum iodinatum)

What pharmaceutical form is Braunol 7,5%, roztwór na skórę available in?

Braunol 7,5%, roztwór na skórę: Roztwór na skórę 75 mg/ml (na skórę, na błony śluzowe)

Is Braunol 7,5%, roztwór na skórę OTC or prescription only?

Braunol 7,5%, roztwór na skórę is available over-the-counter (OTC) — no prescription required.

What are the side effects of Braunol 7,5%, roztwór na skórę?

The most serious adverse reaction that occur with Minims Povidone Iodine 5% w/v eye drops, solution is hypersensitivity reaction. Adverse events are categorized by frequency as follows: - Very common (≥ 1/10) - Common (≥ 1/100 to < 1/10) - Uncommon (≥ 1/1,000 to < 1/100) - Rare (≥ 1/10,000 to < 1/1,000) - Very rare (< 1/10,000) - Not known (cannot be estimated from the available data) Immune System Disorders: Not known: hypersensitivity, anaphylactic reactions (urticaria, Quincke's oedema, anaph

Who should NOT take Braunol 7,5%, roztwór na skórę?

This medicinal product must not be used in the following situations: - Hypersensitivity to iodinated povidone, to iodine or to any of the excipients listed in section 6.1. - In pre-term infants. - Minims Povidone Iodine 5% w/v eye drops, solution is contraindicated for intra-ocular or peri-ocular injection.

Does Braunol 7,5%, roztwór na skórę interact with other medications?

Concomitant or subsequent use with other antiseptic agents should be avoided, because of the potential for interference (antagonism, inactivation). Special caution is needed in relation to iodine incompatibilities. In particular, do not use at the same time a mercury-based derivative: the combination iodine/mercury-based preservatives must be avoided, due to the risk of caustic compounds formation. Particularly, special care must be taken in relation to the mercurial preservatives used in many o

Can Braunol 7,5%, roztwór na skórę be used during pregnancy?

Pregnancy Animal studies have not shown teratogenic effects. Given the absence of teratogenic effects in animals, malformation effects are not expected in humans (see section 5.3). Currently, relevant clinical data is not sufficiently available to assess the potential malformation impact of povidone iodine when it is administered within the first trimester of pregnancy. The foetal thyroid begins to accumulate iodine around the 14 th week of amenorrhoea. No effects during pregnancy are anticipate

What precautions should be taken with Braunol 7,5%, roztwór na skórę?

For single use only. Discard immediately after first use. Any unused product or waste material should be disposed of in accordance with local requirements.

What ATC class does Braunol 7,5%, roztwór na skórę belong to?

Braunol 7,5%, roztwór na skórę: ATC D08AG02. ATC is the WHO Anatomical Therapeutic Chemical classification — it groups drugs by organ system and pharmacological mechanism.

Braunol 7,5%, roztwór na skórę

This information is for educational purposes only. It is not intended as medical advice. Always consult a qualified healthcare professional.

Braunol 7,5%, roztwór na skórę — Description, Dosage, Side Effects | PillsCard

Pharmacotherapeutic group: Ophthalmologicals; anti-infectives ATC code: S01AX18 Broad-spectrum antiseptic, bactericidal, virucidal and fungicide. Antiseptic group: Halogen oxidant (iodophore). Mechanism of action Povidone iodine is an iodophore that has an established use as a broad-spectrum antiseptic, mainly for the treatment of contaminated wounds and for the preoperative preparation of the skin, mucous membranes and the ocular surface. The organic complex contains approximately 10% of active available iodine. Its spectrum of activity is iodine which gradually and slowly released exerts: - bactericidal effect in less than 5 minutes in vitro, for all bacteria, - fungicide effect for yeasts and filamentous fungi. Solutions of povidone iodine gradually release iodine to exert an antimicrobial effect against bacteria, fungi, viruses, and spores. Although povidone iodine is less potent than preparations containing free iodine, it is also less toxic. Organic materials (proteins, serum and blood) reduce the activity of free iodine, the active form of the medicinal product. Iodophor e s are unstable at alkaline pH. Pharmacodynamic effects Povidone iodine is a complex of the polymer polyvinylpyrrolidone (povidone) with iodine which, after application, continues to deliver iodine to the ocular surface over the short time that the solution is in contact with the eye. After application, exposure of the ocular surface to iodine arises from the presence of free iodine in solution, and iodine bound to the polymer, which serves as a reservoir. As the preparation comes in contact with the eye, more and more iodine dissociates from the polymer. Mechanisms of resistance There are no reports of bacterial cross-resistance to antibiotics arising from exposure to povidone iodine, or iodine, or of co-resistance due to any known genetic linkage of resistance determinants. There are limited reports of contamination of iodophores with Pseudomonas species, in nutrient restricted environments, such as hospital waste water, indicating that resistance to povidone-iodine can occur. However, this is of limited relevance to the use of povidone iodine in ocular antisepsis.

Braunol 7,5%, roztwór na skórę

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