


Ask a doctor about a prescription for NOTUS ANTITUSSIVE 2 mg/ml ORAL SOLUTION
Leaflet: information for the user
Notus Antitusivo 2 mg/ml oral solution
Dextromethorphan hydrobromide
Read the entire leaflet carefully before starting to take this medicine, as it contains important information for you.
Follow the administration instructions for the medicine contained in this leaflet or as indicated by your doctor or pharmacist.
You should consult a doctor if it worsens, or if you also have a high fever, skin rash, or persistent headache, or if it does not improve after 7 days of treatment.
Contents of the leaflet
Dextromethorphan, the active ingredient of this medicine, is a cough suppressant that inhibits the cough reflex.
It is indicated for the symptomatic treatment of cough that is not accompanied by expectoration (irritative cough, nervous cough) in adults and children over 2 years of age.
You should consult a doctor if it worsens or if it does not improve after 7 days of treatment.
Do not take Notus Antitusivo:
Children under 2 years of age should not take this medicine
Warnings and precautions
This medicine can cause dependence. Therefore, treatment should be short-term.
Consult your doctor or pharmacist before starting to take Notus Antitusivo:
Consult your doctor or pharmacist before starting to take Notus Antitusivo if you are a patient:
with liver disease
who is sedated, weakened, or bedridden.
There have been cases of abuse with medicines containing dextromethorphan by adolescents; therefore, this possibility should be taken into account, as serious side effects can occur (see section: If you take more Notus Antitusivo than you should).
Taking Notus Antitusivo with other medicines
Tell your doctor or pharmacist if you are taking, have recently taken, or may take any other medicine.
Do not take this medicine during treatment or in the 2 weeks following treatment with the following medicines, as excitement, high blood pressure, and fever above 40°C (hyperpyrexia) may occur:
Serotonin reuptake inhibitors (paroxetine, fluoxetine)
Before starting to take this medicine, consult your doctor if you are using any of the following medicines, as it may be necessary to modify the dose of one of them or interrupt treatment:
Expectorants and mucolytics (used to eliminate phlegm and mucus).
Taking Notus Antitusivo with food, drinks, and alcohol
Alcoholic beverages should not be consumed during treatment, as they may cause side effects.
Do not take with grapefruit or bitter orange juice, as they may increase the side effects of this medicine.
The rest of the food and drinks do not affect the efficacy of the medicine.
Pregnancy, breastfeeding
If you are pregnant or breastfeeding, or think you may be pregnant or plan to become pregnant, consult your doctor or pharmacist before using this medicine.
Pregnant or breastfeeding women should not take this medicine without consulting their doctor.
Driving and using machines
Rarely, during treatment, drowsiness and dizziness may occur; therefore, if you experience these symptoms, you should not drive vehicles or operate hazardous machinery.
This medicine contains maltitol (E-965)
If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medicine.
This medicine contains propylene glycol
This medicine contains 25.9 mg of propylene glycol per milliliter.
If the child is under 5 years of age, consult your doctor or pharmacist, especially if they have been given other medicines that contain propylene glycol or alcohol.
If you are pregnant or breastfeeding, do not take this medicine unless it is recommended by your doctor. Your doctor may perform additional checks while you are taking this medicine.
If you have liver or kidney failure, do not take this medicine unless it is recommended by your doctor. Your doctor may perform additional checks while you are taking this medicine.
This medicine contains sodium
This medicine contains less than 1 mmol of sodium (23 mg) per milliliter; that is, it is essentially "sodium-free".
This medicine contains sodium benzoate
This medicine contains 1 mg of sodium benzoate (E211) per milliliter.
Follow the administration instructions for the medicine contained in this leaflet or as indicated by your doctor or pharmacist. In case of doubt, ask your doctor or pharmacist.
The recommended dose is:
Adults and adolescents from 12 years of age: take 5-10 ml, depending on the intensity of the cough, every 4 hours if necessary. Do not exceed 6 doses in 24 hours.
It can also be taken 15 ml every 6 or 8 hours if necessary.
The maximum amount that can be taken in 24 hours is 120 mg divided into several doses.
Always use the lowest effective dose.
Use in children and adolescents
Pediatric population
Severe side effects can occur in children in case of overdose, including neurological disorders. Caregivers should not exceed the recommended dose.
Children between 6-11 years: take 2.5-5 ml, depending on the intensity of the cough, every 4 hours if necessary. Do not exceed 6 doses in 24 hours
It can also be taken 7.5 ml every 6 or 8 hours if necessary.
The maximum amount that can be taken in 24 hours is 60 mg divided into several doses.
Children between 2-5 years: under medical supervision, take 1.25-2.5 ml, depending on the intensity of the cough, every 4 hours if necessary. Do not exceed 6 doses in 24 hours. It can also be taken 3.75 ml every 6-8 hours if necessary.
The maximum amount that can be taken in 24 hours is 30 mg divided into several doses.
Children under 2 years:
This medicine is contraindicated in children under 2 years of age.
How to take
The medicine is taken orally.
Measure the amount of medicine to be taken with the measuring spoon included in the package. For correct dosing, a measuring spoon of 1.25, 2.5, and 5 ml is included.
Wash the spoon after each use.
Do not take with grapefruit or bitter orange juice or with alcoholic beverages.
Concomitant intake of this medicine with other foods or drinks does not affect its efficacy.
If it worsens, or if the cough persists for more than 7 days, or if it is accompanied by high fever, skin rash, or persistent headache, you should consult a doctor.
If you take more Notus Antitusivo than you should
If you take more Notus Antitusivo than indicated, you may experience the following symptoms: nausea and vomiting, involuntary muscle contractions, agitation, confusion, drowsiness, disorders of consciousness, rapid 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.
In case of overdose or accidental ingestion, consult your doctor or call the Toxicology Information Service (telephone: 91.5620420), indicating the medicine and the amount ingested.
Like all medicines, this medicine can have side effects, although not everyone gets them.
During the use of dextromethorphan, the following side effects have been observed, whose frequency has not been established with certainty:
? In some cases: drowsiness, dizziness, vertigo, constipation, gastrointestinal discomfort, nausea, vomiting
? In rarer cases: mental confusion and headache.
Reporting side effects:
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that is not listed in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines: https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Store in the original package. Do not freeze. Protect from light.
Do not use this medicine after the expiration date that appears on the package after CAD. The expiration date is the last day of the month indicated.
Medicines should not be thrown down the drain or into the trash. Deposit the packages and medicines you no longer need in the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of packages and medicines you no longer need. This way, you will help protect the environment.
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Composition of Notus Antitusivo
The other components (excipients) are sodium benzoate (E-211), anhydrous citric acid, maltitol (E-965), sodium saccharin, propylene glycol, strawberry and orange flavors, purified water, q.s.
Appearance of the product and package contents
Topaz-colored PET bottle closed with a high-density polyethylene cap containing 125 ml or 200 ml of solution.
Includes a measuring spoon of 1.25, 2.5, and 5 ml.
Only some package sizes may be marketed.
Marketing authorization holder and manufacturer:
Marketing authorization holder:
Teva Pharma S.L.U.
Anabel Segura 11, Edificio Albatros B 1st floor
28108 Alcobendas, Madrid (Spain)
Manufacturer:
Teva Pharma S.L.U
C/C, n 4 Polígono Industrial Malpica
50016 Zaragoza (Spain)
or
FARMASIERRA MANUFACTURING S.L.
Irún road, km 26,200.
28700 San Sebastián de los Reyes (Madrid), Spain
Or
Edefarm, S.L.
Enchilagar del Rullo industrial estate, 117
4691 Villamarchante, Valencia, Spain
Or
Farmalider, S.A.
Aragoneses 2, 28108 Alcobendas, Madrid, Spain
Date of the last revision of this text:January 2022
Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.es/
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