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BROMHEXIN SOPHARMA TBL 8MG N20

Attention: Information on this site is provided for informational purposes and is not meant to substitute for the advice provided by your own physician or other medical professional. You should not use the information contained herein for treating a health problem or disease, or prescribing any medication. iDrugs24.com is not responsible for any damage to your health as the result of self treatment.

# On 2024-Mar-29
BROMHEXIN-drug/medicine -tablets aproximate price on "BROMHEXIN SOPHARMA TBL 8MG N20" in Riga city, Latvia is:
  • 0.70€  0.76$  0.6£  81Rub  8.1SEK  3PLN  2.79₪ 


Maximum allowed state defined price ( from ZVA webpage) Euro:State defined maximum allowed price indicated on the picture on drug/medicine -tablets  BROMHEXIN SOPHARMA TBL 8MG N20     Recheck

ATC codeR05CB02 

Active substances: Bromhexinum

 


Vendor, principal: Sopharma Ad
No prescription needed/Patient care products, dressings, gloves, medical devices,...

Similar or the same name medicines, products list *
Medicament / Item title  Prices Pharmacies chain
BROMHEXIN SOPHARMA TBL 8MG N20
3.12€ , Mar.2024 Internet pharmacy Latvija Maija Aptieka, Skrunda, Alsunga Phone: +37163350065Buy
* This table was compiled fully automatically, independently from any advertisers, transparently and without any modification relaying the open offers available on the mentioned dates.
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BROMHEXINE-GRINDEKS 0.8MG/1ML 100ML

Package leaflet: Information for the user

BROMHEXINE-GRINDEKS, 4 mg/5 ml syrup

Bromium hexidine hydrogen chloride

Read all of this leaflet carefully before you start using this medicine because it contains important information for you.

Always use this medicine exactly as described in this leaflet or as a your doctor or pharmacist has told you.
-   Keep this leaflet. You may need to read it again.
-   Ask your pharmacist if you need more information or advice.
-   If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.
-   You must talk to a doctor if you do not feel better or if you feel worse after 5 days. .

What is in this leaflet

1.   What Bromhexine-Grindeks is and what it is used for
2.   What you need to know before you use Bromhexine-Grindeks
3.   How to take Bromhexine-Grindeks
4.   Possible side effects
5.   How to store Bromhexine-Grindeks
6.   Contents of the pack and other information

1. What Bromhexine-Grindeks is and what it is used for

Bromhexine-Grindeks is an expectorant that liquefies the sputum and makes it easier to cough it out.

2. What you need to know before you use Bromhexine-Grindeks

Do not use Bromhexine-Grindeks:

-   if you are allergic to bromium hexidine or any of the other ingredients of this medicine (listed in section 6) .
-   if you have gastric or duodenal ulcers,
-   along with cough medicines that inhibit the cough reflex (e.g. codeine), especially before going to sleep; this combination inhibits coughing out sputum.

Warnings and precautions

Talk to your doctor or pharmacist for advice before taking any Bromhexine-Grindeks:
-   If you have a weakened body;
-   If you have bronchial asthma or mechanical narrowing of bronchial lumen (inhibited excretion of secretions from the bronchi);
-   If you have a history of gastric or duodenal ulcer; bromium hexidine irritates the gastrointestinal mucosa; therefore, this medicine should be used with caution.
It should be taken into account that patients with severe liver or kidney failure have a decreased
excretion of bromium hexidine and its metabolites from the body.
Severe skin reactions have been reported in connection with bromhexin administration. If you develop blemishes (including ulcers on mucous membranes, such as your mouth, throat, nose, eyes, genitals), stop using Bromhexine-Grindex and contact your doctor immediately.

Children and adolescents

This medicine is not suitable for children under 1 year.

Other medicines and Bromhexine-Grindeks

Tell your pharmacist if you are taking, have recently taken or might take any other medicines. Bromhexine-Grindeks enhances the adsorption of antibiotics (erythromycin, cefalexine) into the lung parenchyma if used concomitantly.
Bromhexine-Grindeks may be used along with bronchial dilators and cardiac medicines. Concomitant use of various anti-inflammatory and anti-rheumatic medicines (e.g. salicylates, phenylbuthazone and oxyphenylbuthazone) may increase its irritation effect on the gastric mucosa. The syrup contains ethanol that may change the effect of other medicines.

Pregnancy and breast-feeding

Ask your doctor or pharmacist for advice before taking this medicine.
The safety of using bromium hexidine in pregnant women has not been established, therefore the use of Bromhexine-Grindeks during pregnancy is contraindicated.
Bromium hexidine is excreted into breast milk in small quantities; therefore the use of the medicine must be stopped during breastfeeding.
Pregnant and breast-feeding women must consider that the medicine contains ethanol (see below).

Driving and using machines

Bromhexine-Grindeks does not affect the ability to drive or use machines.
However, it must be considered that the medicine contains ethanol that may affect your ability to drive transport vehicles or use machines.

Bromhexine-Grindeks contains ethanol, sorbitol (E 420) and methyl parahydroxybenzoate (E 420).

One measuring spoon (5 mL) of syrup contains:
•   0.625 ml of 96% ethanol, which is detrimental in alcoholism. It must be considered also in pregnant or breast-feeding women, children and risk groups, such as patients with liver function disorders or epilepsy.
•   2 g of sorbitol (E 420) If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.
•   5 mg of methyl parahydroxybenzoate (E 218) may cause allergic reactions (also delayed-type).

3. How to take Bromhexine-Grindeks

Always take this medicine exactly as described in this leaflet or as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.
This medicine is taken orally 3 times daily, independent of eating.
1 measurement spoon or 5 mL of the syrup contains 4 mg of bromium hexidine hydrogen chloride. The one-time dose of the syrup according to the age of the patient:
Age of patient
Dose (in full measurement spoons)
Children 1-2 years of age
'/2
2-6 years
/...1
6-14 years
1...2
Adults and adolescents from the age of 14:
2...3
The treatment effect is evident usually on the 2nd to 5th day of administration. If the symptoms are not better or are worse, the patient should consult with his/her doctor, who will determine the further treatment.
This medicine is not suitable for children under 1 year.
If you feel that the effect of the medicine is too strong or too weak, talk to your doctor.

If you take more Bromhexine-Grindeks than you should

No cases of overdose with bromium hexidine have been described to date. Turn to the doctor immediately if you suspect overdose.

If you forget to take Bromhexine-Grindeks

Do not take a double dose to make up for a forgotten dose.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.
Bromhexine-Grindeks is usually well tolerated.
Stop using this medicine and turn to a doctor immediately, if you experience any of the
following symptoms:
•   Breathing difficulties; swelling of lips, tongue or larynx, increased heart rate, low blood pressure, itching or swelling of skin, rash. These may be a sign of a severe allergic reaction -anaphylactic shock.
Uncommon (can influence up to 1 person in 1,000):
•   Hypersensitivity reactions (skin and mucous membrane rash, swelling of the face, difficulty in breathing, fever).
•   Rash, urticaria.
Unknown (frequency cannot be estimated from the available data):
•   Anaphylactic reactions including anaphylactic shock, angioedema (rapid onset of swelling of the skin, subcutaneous tissue, mucous membranes or mucous membranes) and itching.
•   Severe skin reactions (including erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis and acute generalized exanthematosus pustulosis).
•   Headache, vertigo, sweating (usually disappear after the discontinuation of the medicine).
•   Loss of appetite, nausea, abdominal pain and discomfort.
•   Brief elevation of serum aminotransferases.
Sensitive patients may experience a transient cough or bronchial spasm due to inhalation of bromium hexidine.

Reporting of side effects

If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via www.ravimiamet.ee. By reporting side effects, you can help provide more information on the safety of this medicine.

5. How to store Bromhexine-Grindeks

Store below 25 °°C.
Use within 1 year after first opening.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date that is stated on the label and carton.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

6. Contents of the pack and other information What Bromhexine-Grindeks contains

-   The active ingredient is bromium hexidine (Bromhexini hydrochloridum).
5 mL of syrup (1 measurement spoon) contains 4 mg of bromium hexidine hydrogen chloride.
-   The other ingredients are methyl parahydroxybenzoate (E 218), sorbitol (E 420), ethanol 96%. levomenthol, anise oil, peppermint oil, kemen oil, purified water.

What Bromhexine-Grindeks looks like and contents of the pack

Clear colourless or mild-toned fluid with characteristic smell.
100 mL of syrup in a glass bottle. The bottle with patient’s information leaflet is packed into a carton box. Every pack contains a measurement spoon.

Marketing Authorisation Holder and Manufacturer AS GRINDEKS.

Krustpils iela 53, Riga, LV-1057, Latvia Tel.: +371 67083205 Fax +371 67 083 505 E-mail: [email protected]
For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder.
AS GRINDEKS Estonian branch Tondi 33, 11316, Tallinn, Estonia
Phone: 6120224 Fax: 6120331
This leaflet was last revised in August 2018.





  Instruction, annotation source for medicine: State Agency of Medicines, Estonia




[*1]

DDD. Information source: WHO Collaborating Centre for Drug Statistics Methodology. Norwegian Institute of Public Health


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