Інструкція із застосування BROMEXINA PENSA
Зміст інструкції
BROMEXINA PENSA 4 mg/5 ml syrup
Bromexine hydrochloride
Generic medicine
Read this leaflet carefully before taking this medicine as it contains important
information for you.
- Take this medicine exactly as described in this leaflet or as your doctor or pharmacist has told you.
- Keep this leaflet. You may need to read it again.
- If you want more information or advice, ask your pharmacist.
- If any side effects occur, including those not listed in this leaflet, tell your doctor or pharmacist. See section 4.
- See a doctor if you do not feel better or if your symptoms worsen after a short period.
Contents of this leaflet:
- 1. What BROMEXINA PENSA is and what it is used for
- 2. What you need to know before you take BROMEXINA PENSA
- 3. How to take BROMEXINA PENSA
- 4. Possible side effects
- 5. How to store BROMEXINA PENSA
- 6. Contents of the pack and other information
1. What is BROMEXINA PENSA and what is it used for
BROMEXINA PENSA contains the active ingredient bromhexine, which belongs to a group of medicines
called mucolytics used to facilitate the elimination of mucus from the respiratory tract.
BROMEXINA PENSA is therefore indicated in the treatment of acute and chronic respiratory diseases (such as
bronchitis) in the presence of cough and phlegm. Consult your doctor if you do not notice any improvement or if you notice a
worsening of symptoms after a short period.
2. What you need to know before taking BROMEXINA PENSA
Do not take BROMEXINA PENSA
- if you are allergic to bromexine or any of the other ingredients of this medicine (listed in section 6);
- if you suffer from stomach or intestinal ulcers;
- if you are breastfeeding (see section “Pregnancy and breastfeeding”);
- if the person who is going to take the medicine is a child under 2 years of age (see section “Children”).
Warnings and precautions
Consult your doctor or pharmacist before taking BROMEXINA PENSA.
Avoid taking this medicine for prolonged periods. After a short period of treatment without
noticeable results, consult your doctor.
Cases of severe skin reactions associated with the administration of bromexine have been reported. If
you develop a skin rash (including lesions of mucous membranes such as mouth, throat, nose, eyes,
genitals), stop taking BROMEXINA PENSA and consult your doctor immediately.
Treatment with BROMEXINA PENSA involves an increase in bronchial secretion
favoring its elimination.
Children
BROMEXINA PENSA is contraindicated in children under 2 years of age because it can cause
bronchial obstruction.
Othermedicinesand BROMEXINA PENSA
Tell your doctor or pharmacist if you are taking, have recently taken or might take any
other medicines.
There is no information on interactions between BROMEXINA PENSA and other medicines.
Pregnancy and breastfeeding
If you are pregnant, suspect you may be pregnant, are planning to become pregnant, or are breastfeeding with breast
milk, ask your doctor or pharmacist for advice before taking this medicine.
Pregnancy
If you are pregnant, take this medicine only after consulting your doctor and only if absolutely
necessary. Use caution especially during the first trimester of pregnancy.
Breastfeeding
Do not take BROMEXINA PENSA while breastfeeding as bromexine passes into breast
milk.
Driving and using machines
BROMEXINA PENSA does not affect the ability to drive vehicles and operate machines.
BROMEXINA PENSA contains sorbitol, ethanol (alcohol), benzoic acid and sodium
This medicine contains 571.4 mg of sorbitolper ml. Sorbitol is a source of fructose. If your doctor has
diagnosed you with intolerance to certain sugars or if you have a diagnosis of hereditary fructose intolerance,
a rare genetic disease in which patients cannot metabolize fructose, contact them before
taking this medicine. It may cause gastrointestinal problems and have a mild laxative effect. Calorie
value 2.6 kcal/g of sorbitol.
This medicine contains 30 mg of ethanolper ml, which is equivalent to 3.7 vol % of ethanol. A dose of
10 ml may contain up to 0.3 g of ethanol per dose equivalent to 7.4 ml of beer and 3 ml of wine per dose. The
amount of alcohol in this medicine does not appear to have an effect on adults and adolescents and its effects in
children are not evident. Some effects may occur in small children, for example feeling
sleepy.
The alcohol in this medicine may alter the effects of other medicines. Talk to your doctor or pharmacist if
you are taking other medicines. If you are pregnant, talk to your doctor or pharmacist before taking this
medicine. If you have an alcohol dependence, talk to your doctor before taking this medicine.
This medicine contains 2 mg of benzoic acid per ml.
This medicine contains 0.46 mg of sodium per ml, less than 1 mmol (23 mg) of sodium per 10 ml dose,
i.e. essentially ‘sodium-free’.
3. How to take BROMEXINA PENSA
Take this medicine following exactly the instructions in this leaflet or as indicated by your doctor or pharmacist. If you have any doubts, consult your doctor or pharmacist.
Adults
The recommended dose is 5-10 ml 3 times a day. The doctor may decide to increase it to 48 mg
divided into three times the dose at the beginning of treatment.
Use in children over 2 years
The recommended dose in children over 2 years is 2.5-5 ml 3 times a day.
Avoid exceeding the recommended doses and taking this medicine for long periods.
Take this medicine after meals.
If you do not notice improvements or if you notice a worsening of symptoms after a short period of treatment, consult
your doctor.
This medicine can be taken by children over 2 years and by diabetics because it does not contain fructose and
sucrose, but contains sorbitol which may induce hyperglycemia and as such should be considered when making
any correction to the units of insulin to be administered (see paragraph “BROMEXINA PENSA
contains sorbitol, ethanol (alcohol), benzoic acid and sodium”).
If you take more BROMEXINA PENSA than you should
If you (or someone else) have ingested an excessive amount of syrup, or if you think a child has
ingested the medicine, consult a doctor immediately.
In case of accidental ingestion/taking of an excessive dose of BROMEXINA PENSA, immediately notify
your doctor or go to the Emergency Room of the nearest hospital.
If you forget to take BROMEXINA PENSA
If you forget to take a dose of the medicine, take it as soon as you remember, unless it is almost
time to take the next dose. Do not take a double dose to make up for a missed dose.
If you have any doubts about the use of this medicine, consult your doctor or pharmacist.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The side effects reported with the use of BROMEXINA PENSA are:
Rare(may affect up to 1 in 1,000 people)
- hypersensitivity reactions;
- rash, urticaria.
Not known(frequency cannot be estimated from available data)
- Anaphylactic reactions, including anaphylactic shock, angioedema (rapid swelling of the skin, subcutaneous tissues, mucous membranes and submucosal tissues) and pruritus;
- Severe cutaneous adverse reactions (including erythema multiforme, Stevens-Johnson syndrome/toxic epidermal necrolysis and acute generalized exanthematous pustulosis). Cases of diarrhea, nausea, vomiting, other mild gastrointestinal disorders, bronchospasm and bronchial obstruction have also been reported.
Reporting of side effects
If you get any side effects, even those not listed in this leaflet, tell your
doctor or pharmacist or nurse. You can also report side effects directly through
the national reporting system at https://ww.aifa.gov.it/content/segnalazioni-reazioni-avverse.
By reporting side effects you can help provide more information on the safety of
this medicine.
5. How to store BROMEXINA PENSA
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the packaging after “Scad.”. The expiry date
refers to the last day of that month.
After the first opening of the bottle, the medicine must be consumed within 9 months, if the medicine is
stored at a temperature below 25°C; after this period, any excess medicine must be
discarded.
Do not dispose of any medicine in wastewater or household waste. Ask your pharmacist how to dispose of
medicines you no longer use. This will help protect the environment.
6. Contents of the pack and other information
What BROMEXINA PENSA contains
- The active ingredient is bromhexine hydrochloride. 5 ml of syrup contains 4 mg of bromhexine hydrochloride (equivalent to 3.65 mg of bromhexine).
- The other ingredients are: tartaric acid, benzoic acid, sodium carboxymethylcellulose, glycerol, liquid sorbitol, ethanol (96%), all fruit flavour, sodium hydroxide, purified water.
Description of the appearance of BROMEXINA PENSA and contents of the pack
BROMEXINA PENSA is available in syrup form. The pack contains one bottle of 250
ml.
Marketing Authorisation Holder
Pensa Pharma S.p.A., Via Ippolito Rosellini 12, 20124, Milan.
Manufacturer
ABC Farmaceutici S.p.A., Canton Moretti 29, Località San Bernardo, 10090 Ivrea (TO)

- Країна реєстрації
- Лікарська формаSyrup, 4 MG/5 ML
- Код АТХR05CB02
- Діюча речовина
- Потрібен рецептНі
- Виробник
- Ця інформація надана лише для ознайомлення і не є медичною порадою. Рішення щодо лікування завжди приймає лікар.
- Альтернативи до BROMEXINA PENSAЛікарська форма: Oral solution, 2 MG/MLДіюча речовина: bromhexineВиробник: OPELLA HEALTHCARE ITALY S.R.L.Рецепт не потрібенЛікарська форма: Syrup, 4 MG/5 MLДіюча речовина: bromhexineВиробник: AESCULAPIUS FARMACEUTICI SRLРецепт не потрібенЛікарська форма: Syrup, 4 MG/5 MLДіюча речовина: bromhexineВиробник: COOPER CONSUMER HEALTH B.V.Рецепт не потрібен
Аналоги BROMEXINA PENSA в інших країнах
Препарати з тією самою діючою речовиною, доступні в інших країнах.
Аналог BROMEXINA PENSA у Іспанія
Аналог BROMEXINA PENSA у Польща
Аналог BROMEXINA PENSA у Україна
Лікарі онлайн щодо BROMEXINA PENSA
Застосування, безпека та можливість призначення рецепта — за результатами медичної оцінки.
Отримайте рецепт на BROMEXINA PENSA онлайн
Заповніть форму за 2 хвилини
Розкажіть про симптоми, історію хвороби та потрібний препарат.
Оберіть лікаря або ми призначимо
Оберіть спеціаліста або ми підберемо найближчого доступного лікаря.
Лікар розглядає ваш випадок
Зазвичай протягом 30 хвилин. Може ставити уточнювальні запитання в чаті.
Отримайте в будь-якій аптеці
Електронний рецепт надсилається на вашу пошту — дійсний по всій Польщі.
Часті запитання
BROMEXINA PENSA не потребує рецепта в Італія. Ви можете обговорити з лікарем онлайн, чи підходить цей лікарський засіб для вашої ситуації.
Діюча речовина у BROMEXINA PENSA — bromhexine. Це допомагає визначити препарати з тим самим складом, але під іншими торговими назвами.
BROMEXINA PENSA виробляється компанією TOWA PHARMACEUTICAL S.P.A.. Назва бренду та упаковка можуть відрізнятися залежно від дистрибʼютора.
Лікарі, зокрема Сімейні лікарі, Психіатри, Дерматологи, Кардіологи, Ендокринологи, Гастроентерологи, Пульмонологи, Нефрологи, Ревматологи, Гематологи, Інфекціоністи, Алергологи, Геріатри, Педіатри, Онкологи, можуть оцінити доцільність застосування BROMEXINA PENSA з урахуванням вашого стану та місцевих правил. Ви можете записатися на онлайн-консультацію, щоб обговорити симптоми та можливі подальші кроки.
Польща має добре розвинену систему охорони здоров'я у великих містах, таких як Варшава, Краків, Вроцлав і Гданськ. Аптеки широко доступні та працюють відповідно до чинного законодавства, забезпечуючи доступ до рецептурних препаратів.
Ви можете придбати BROMEXINA PENSA у Варшаві, Кракові, Вроцлаві або Гданську в будь-якій аптеці за наявності дійсного рецепта.
Щоб отримати рецепт, ви можете скористатися Oladoctor:
Інші препарати з тією самою діючою речовиною (bromhexine) включають BISOLVON, FLUTOXIL, FROBEN TOSSE GRASSA. Вони можуть відрізнятися торговою назвою або формою випуску, але містять той самий терапевтичний компонент. Перед зміною або початком прийому нового препарату варто проконсультуватися з лікарем.
















