Leaflet: Information for the User
BRONCOMEDICAL with Guaifenesina10 mg/100 mg Oral Solution
Dextromethorphan, hydrobromide/Guaifenesina
Read the entire leaflet carefully because it contains important information for you.
This medication can be purchased without a prescription. Nevertheless, to obtain the best results, it should be used properly.
Contents of the Leaflet:
It is a medication that contains dextromethorphan hydrobromide, which is a cough suppressant, and guaifenesina, which is an expectorant.
It is indicated for the relief of cough and to facilitate the expulsion of excess mucus and phlegm in colds and flu.
This medication can cause dependence. Therefore, treatment should be short-term.
Do not takeBRONCOMEDICAL with Guaifenesina
Be careful withBRONCOMEDICAL with Guaifenesina
Patients with the following conditions should consult their doctor before using this medication:
Patients with persistent or chronic cough, such as those due to smoking or who are sedated, debilitated, or bedridden, should not take this medication.
There have been cases of abuse with medications containing dextromethorphan by adolescents.
This can cause serious adverse effects (see section on If you take more BRONCOMEDICAL with Guaifenesina than you should).
Interference with analytical tests
If you are going to undergo any diagnostic test (including blood tests, urine tests, skin tests that use allergens, etc.), inform your doctor that you are taking this medication, as it may alter the results.
Use of other medications
Inform your doctor or pharmacist if you are using or have recently used any other medication, including those purchased without a prescription.
Note that these instructions may also apply to medications that have been used before or may be used after.
Do not take this medication during treatment or in the 2 weeks following treatment with the following medications, as it may cause excitement, high blood pressure, and fever above 40°C (hyperpyrexia):
selective serotonin reuptake inhibitors (paroxetine, fluoxetine)
If you are using any of the following medications, it may be necessary to modify the dose of one of them or interrupt treatment:
Expectorants and mucolytics (used to eliminate mucus and phlegm)
TakingBRONCOMEDICAL with Guaifenesinawith food and drinks
Alcoholic beverages should not be consumed during treatment, as they may cause adverse reactions.
Do not take with grapefruit or bitter orange juice, as they may increase the adverse effects of this medication.
Pregnancy and breastfeeding
Consult your doctor or pharmacist before using any medication.
Important for women
If you are pregnant or think you may be pregnant, consult your doctor before taking this medication. The use of medications during pregnancy can be hazardous to the embryo or fetus and should be monitored by your doctor.
Pregnant and breastfeeding women should not take this medication without consulting their doctor.
Driving and using machines
Rarely, during treatment, a decrease in reaction capacity or drowsiness and mild dizziness may occur, so if you notice these symptoms, you should not drive vehicles or operate machines.
Important information about some of the components ofBRONCOMEDICAL with Guaifenesina
This medication may be harmful to people with phenylketonuria because it contains aspartame (E-951), which is a source of phenylalanine.
This medication contains sorbitol (E-420). If your doctor has told you that you have an intolerance to certain sugars (such as fructose), consult with them before taking this medication.
Follow these instructions unless your doctor has given you different ones. Consult your doctor or pharmacist if you have doubts.
The normal dose is:
Adults: Take 1 sachet every 6 hours. If necessary, it can be taken every 4 hours. If it is not enough, 2 sachets can be taken every 4-6 hours as needed. In any case, the maximum amount of medication that can be taken in 24 hours is 12 sachets, divided into at least 6 doses.
Use in children:
Children between 6 and 12 years old: Take 1 sachet every 6 hours. If necessary, it can be taken every 4 hours.
The maximum amount of medication that can be taken in 24 hours is 6 sachets, divided into at least 6 doses.
Children under 6 years old: This medication is contraindicated in children under 6 years old.
Severe adverse effects can occur in children in case of overdose, including neurological disorders. Caregivers should not exceed the recommended dose.
How to take:
This medication is taken orally.
The oral solution can be taken directly from the sachet.
It is recommended to drink a glass of water after each dose and plenty of liquid throughout the day.
It can be taken with or without food.
Do not take with grapefruit or bitter orange juice or with alcoholic beverages (see section on Taking BRONCOMEDICAL with Guaifenesina with food or drinks).
If the symptoms worsen, if they persist for more than 7 days, or if during treatment you notice skin rashes, high fever, or persistent headache, you should stop treatment and consult a doctor.
If you take moreBRONCOMEDICAL with Guaifenesinathan you should
If you take more BRONCOMEDICAL with Guaifenesina than indicated, you may experience the following symptoms: nausea and vomiting, involuntary muscle contractions, agitation, confusion, drowsiness, disorders of consciousness, rapid and involuntary eye movements, cardiac disorders (accelerated heart rate), coordination disorders, psychosis with visual hallucinations, and hyperexcitability.
Other symptoms in case of massive overdose may be: coma, severe respiratory problems, and convulsions.
Contact your doctor or hospital immediately if you experience any of the mentioned symptoms.
Taking very high doses of this medication can cause children to become drowsy, nervous, nauseous, vomit, or have gait disturbances.
There have been cases of abuse with medications containing dextromethorphan, which can cause serious adverse effects, such as anxiety, panic, memory loss, tachycardia (accelerated heart rate), lethargy, hypertension or hypotension (high or low blood pressure), mydriasis (pupil dilation), agitation, vertigo, gastrointestinal discomfort, slurred speech, nystagmus (involuntary and uncontrolled eye movement), fever, tachypnea (rapid and shallow breathing), brain damage, ataxia (uncoordinated movements), convulsions, respiratory depression, loss of consciousness, arrhythmias (irregular heartbeats), and death.
In case of overdose or accidental ingestion, consult your doctor or call the Toxicology Information Service (phone: 91.5620420), indicating the medication and the amount ingested.
If you forget to takeBRONCOMEDICAL with Guaifenesina
If you forget to take BRONCOMEDICAL with Guaifenesina and the symptoms continue, do not take a double dose to make up for the forgotten dose. If necessary, take the medication again as indicated in section 3. HOW TO TAKE BRONCOMEDICAL with Guaifenesina.
Like all medications, BRONCOMEDICAL with Guaifenesina can have side effects, although not everyone experiences them.
During the use of dextromethorphan and guaifenesina, the following side effects have been observed, whose frequency has not been established with precision:
In some cases, the following have occurred: drowsiness, dizziness, vertigo, constipation, gastrointestinal discomfort, nausea, vomiting, headache, and skin itching (urticaria).
In rarer cases: mental confusion.
If you consider that any of the side effects you are experiencing is serious, or if you notice any side effect not mentioned in this leaflet, inform your doctor or pharmacist.
Keep out of the reach and sight of children.
Do not use this medication after the expiration date shown on the packaging after CAD.
The expiration date is the last day of the month indicated.
No special storage conditions are required
Medications should not be thrown away through the sewage system or in the trash. Deposit the packaging and medications you no longer need in the SIGRE point of your usual pharmacy. Ask your pharmacist how to dispose of the packaging and medications you no longer need. This way, you will help protect the environment.
Composition ofBRONCOMEDICALwith Guaifenesina
Each sachet (5 ml of oral solution) contains:
Appearance of the product and packaging content
Packaging with 20 sachets of clear yellow oral solution with a strawberry flavor.
Marketing authorization holder and manufacturer
Marketing authorization holder
Medical, S.A.
Pol. Ind. Las Quemadas, Parcela 87 14014 - Córdoba.
SPAIN
Manufacturer
Laboratorios Alcalá Farma, S.L.
Avenida de Madrid, 82
28802 Alcalá de Henares (Madrid).
SPAIN
This leaflet was approved in June 2023
"Detailed and updated information about this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/"