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Leaflet: Information for the Patient
Novag Antigripal Granules for Oral Solution
Paracetamol / Phenylephrine Bitartrate / Chlorphenamine Maleate
Read the entire leaflet carefully before starting to take this medication, as it contains important information for you.
Follow the administration instructions for the medication contained in this leaflet or as indicated by your doctor or pharmacist exactly.
Contents of the Leaflet
This medication is an association of paracetamol, chlorphenamine, and phenylephrine.
Paracetamol is an analgesic that reduces pain and fever.
Chlorphenamine is an antihistamine that relieves nasal secretion
Phenylephrine is a sympathomimetic that reduces nasal congestion.
It is indicated in adults and adolescents over 15 years old for the relief of symptoms of colds and flu that occur with fever or mild to moderate pain, congestion, and nasal secretion.
You should consult a doctor if your symptoms worsen or do not improve, or if the fever persists for more than 3 days or the pain or other symptoms persist for more than 5 days.
Do not take Novag Antigripal
Warnings and precautions
Consult your doctor or pharmacist before starting to take Novag Antigripal.
Do not take more medication than recommended in section 3. How to take Novag Antigripal
Avoid simultaneous use of this medication with other medications that contain paracetamol, as high doses can lead to liver damage. Do not use more than one medication that contains paracetamol without consulting your doctor.
Chronic alcoholics should be cautious not to take more than 2 grams of paracetamol (equivalent to 3 sachets of Novag Antigripal) in 24 hours.
While taking this medication, you cannot take other medications that contain paracetamol because a paracetamol overdose can occur, which could damage the liver.
Consult your doctor or pharmacist before starting to take this medication in the following cases:
Children and adolescents
This medication should not be administered to children under 15 years old due to the paracetamol dose (650 mg).
Interference with analytical tests
If you are going to have any diagnostic tests (including blood tests, urine tests, skin tests using allergens, etc.), inform your doctor that you are taking this medication, as it may alter the results.
Other medications and Novag Antigripal
Inform your doctor or pharmacist if you are taking or have recently taken or may need to take any other medication.
In particular, if you are using any of the following medications, it may be necessary to modify the dose of some of them or interrupt treatment:
Flucloxacillin (antibiotic), due to a serious risk of alteration of blood and fluids (metabolic acidosis with high anion gap) that should be treated urgently and may occur especially in cases of severe renal insufficiency, sepsis (when bacteria and their toxins circulate in the blood, leading to organ damage), malnutrition, chronic alcoholism, and if the maximum daily doses of paracetamol are used.
Interference with analytical tests
If you are going to have any analytical tests (including blood tests, urine tests, etc.), inform your doctor that you are taking this medication, as it may alter the results.
Taking Novag Antigripal with food, drinks, and alcohol
While taking this medication, you should not consume alcoholic beverages, as it may enhance the appearance of side effects of this medication.
Additionally, the use of medications containing paracetamol by patients who habitually consume alcohol (3 or more alcoholic beverages: beer, wine, liquor, etc. per day) can cause liver damage.
The medication can be taken with or without food.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before taking this medication.
This medication should not be taken during pregnancy unless your doctor considers it strictly necessary.
This medication cannot be taken during breastfeeding, as it may cause side effects in the baby.
Driving and using machines
This medication may cause drowsiness. If you experience drowsiness during treatment with this medication, avoid driving vehicles or using machines.
Novag Antigripal contains mannitol (E-421)
This medication may have a mild laxative effect because it contains mannitol.
Follow the administration instructions for the medication contained in this leaflet or as indicated by your doctor or pharmacist exactly. In case of doubts, ask your doctor or pharmacist.
Taking this medication is subject to the appearance of symptoms. As they disappear, you should suspend this medication.
The recommended dose is:
Adults and adolescents over 15 years old: 1 sachet every 6-8 hours (3 or 4 sachets per day) as needed. Do not take more than 4 sachets (equivalent to 2.6 grams of paracetamol) every 24 hours.
Do not take more than 3 grams of paracetamol every 24 hours (see "Warnings and precautions" section).
Patient with kidney disease: Should consult a doctor. These patients cannot take this medication due to the paracetamol dose it contains.
Patient with liver disease: Should consult a doctor. They should not take more than 3 sachets (equivalent to 2 grams of paracetamol) in 24 hours, and the minimum interval between doses will be 8 hours.
Use in children
This medication should not be administered to children and adolescents under 15 years old.
Use in elderly patients
Elderly people should not use this medication without consulting a doctor.
How to take
Novag Antigripal is taken orally. Pour the entire contents of the sachet into approximately half a glass of water. Shake and drink immediately.
Always take the smallest effective dose.
Taking this medication is subject to the appearance of symptoms. As they disappear, you should suspend treatment.
If the fever persists for more than 3 days of treatment, the pain or other symptoms persist for more than 5 days, or worsen, or new symptoms appear, you should consult a doctor.
If you take more Novag Antigripal than you should
If you have ingested an overdose, you should go to a medical center immediately, even if you do not notice symptoms, as they often do not appear until 3 days after ingestion, even in cases of severe poisoning.
The symptoms of overdose may be: dizziness, vomiting, loss of appetite, yellowing of the skin and eyes (jaundice), and abdominal pain. Anxiety, fear, agitation, headache (can be a symptom of high blood pressure), convulsions, insomnia (or intense drowsiness), clumsiness, feeling of fainting, instability, confusion, irritability, tremors, anorexia; psychosis with hallucinations (especially in children). Dryness of the mouth, nose, or throat. You may also notice effects such as high blood pressure, arrhythmias (rapid or irregular heartbeats), palpitations, decreased urine output, metabolic acidosis (decrease in blood alkaline reserve). In case of prolonged use, a decrease in blood volume may occur.
Treatment of overdose is most effective if started within 4 hours after taking the overdose of the medication.
Patient being treated with barbiturics or chronic alcoholics may be more susceptible to the toxicity of a paracetamol overdose.
In case of overdose or accidental ingestion, go to a medical center immediately or call the Toxicological Information Service (Telephone 91 562 04 20), indicating the medication and the amount ingested.
Like all medications, this medication can cause side effects, although not everyone will experience them.
During the period of use of paracetamol, phenylephrine, and chlorphenamine, the following side effects have been reported, whose frequency has not been established with precision:
Excitement (generally with high doses, and more frequent in the elderly and children), which may include symptoms such as: restlessness, insomnia, nervousness, and even convulsions. Other side effects that may appear with low frequency are: chest tightness, lung noises, rapid or irregular heartbeats (generally with overdose), liver disorders (which may present with stomach pain or abdominal pain, dark urine, or other symptoms), allergic reaction, severe hypersensitivity reactions (cough, difficulty swallowing, rapid heartbeats, itching, swelling of the eyelids or around the eyes, face, tongue, difficulty breathing, etc.), photosensitivity (sensitivity to sunlight), cross-sensitivity (allergy) to medications related to chlorphenamine. Blood disorders (changes in the blood cell formula, such as agranulocytosis, leukopenia, aplastic anemia, thrombocytopenia) with symptoms such as unusual bleeding, sore throat, or fatigue; low or high blood pressure, edema (swelling), ear disorders, impotence, menstrual disorders.
Paracetamol may damage the liver when taken in high doses or in prolonged treatments.
Very rare cases of severe skin reactions have been reported.
Reporting of side effects
If you experience any type of side effect, consult your doctor or pharmacist or nurse, even if it is a possible side effect not listed in this leaflet. You can also report them directly through the Spanish Medication Surveillance System for Human Use: https://www.notificaRAM.es/. By reporting side effects, you can contribute to providing more information on the safety of this medication.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiration date that appears on the packaging, after CAD. The expiration date is the last day of the month indicated.
No special storage conditions are required.
Medicines should not be disposed of via wastewater or household waste. Deposit the packaging and any unused medicines at the SIGRE collection point in your pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and any unused medicines. This will help protect the environment.
Composition of Novag Antigripal
Each sachet contains:
Appearance of the Product and Package Contents
Novag Antigripal is a white or yellowish-white granulate for oral solution with an orange flavor, presented in sachets packaged in cardboard boxes containing 10 sachets.
Marketing Authorization Holder
Tarbis Farma S.L.
Gran Via Carlos III, 94
08028 Barcelona
Manufacturer
Laboratorios Alcalá Farma, S.L
Avenida de Madrid, 82
28802 Alcalá de Henares (Madrid)
Date of the Last Revision of this Leaflet: November 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.gob.es/
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