


Ask a doctor about a prescription for APOGRIP POWDER FOR ORAL SOLUTION
Package Leaflet: Information for the User
Apogrip Powder for Oral Solution
Paracetamol / Phenylephrine Hydrochloride / Chlorphenamine Maleate
Read all of this leaflet carefully before you start taking this medicine, because it contains important information for you.
Follow the instructions for administration of the medicine contained in this leaflet or as indicated by your doctor or pharmacist.
Contents of the Package Leaflet:
It 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 for the relief of symptoms of colds and flu that occur with fever or mild to moderate pain, congestion, and nasal secretion, in adults and adolescents from 12 years of age.
You should consult your doctor if your symptoms worsen or do not improve, or if the fever persists for more than 3 days or the pain for more than 5 days.
Do not take Apogrip
Warnings and precautions
Consult your doctor or pharmacist before starting to take this medicine.
Children and adolescents
Children under 12 years of age cannot take this medicine.
Other medicines and Apogrip
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
Interference with laboratory tests:
Taking Apogrip powder with food, drinks, and alcohol
While being treated with this medicine, you should not consume alcoholic beverages, as it may enhance the appearance of side effects of this medicine.
Additionally, the use of medicines containing paracetamol by patients who habitually consume alcohol (3 or more alcoholic beverages: beer, wine, liquor... per day) may cause liver damage.
The medicine 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 medicine.
This medicine should not be taken during pregnancy unless your doctor considers it strictly necessary.
If necessary, Apogrip can be used during pregnancy. You should use the lowest possible dose that reduces pain or fever and use it for the shortest possible time. Contact your doctor or midwife if the pain or fever does not decrease or if you need to take the medicine more frequently.
This medicine should not be taken by breastfeeding mothers, as it may cause side effects in the baby.
Driving and using machines
This medicine may cause drowsiness. If you experience drowsiness during treatment with this medicine, avoid driving vehicles or using machines.
Apogrip sachets contain sucrose
Apogrip contains 3.994 g of sucrose in each sachet, which should be taken into account by patients with hereditary fructose intolerance, glucose/galactose malabsorption, sucrose-isomaltase deficiency, and diabetic patients.
Follow these instructions for administration of the medicine contained in this leaflet or as indicated by your doctor or pharmacist. In case of doubts, ask your doctor or pharmacist.
The recommended dose is:
Adults and adolescents from 12 years of age: 1 sachet every 6-8 hours as needed (3 or 4 sachets per day). You should not take more than 3 grams of paracetamol per day (4 sachets) every 24 hours.
Patients with liver failure: these patients should not take more than 1 sachet every 8 hours. In no case should they take more than 3 sachets per day.
Patients with kidney failure: they should not take this medicine due to the paracetamol dose.
Use in children
This medicine is contraindicated in children under 12 years of age.
Use in the elderly
The elderly should not use this medicine without consulting their doctor, as some side effects of the medicine, such as slow heartbeats (bradycardia) or reduced cardiac output, may affect them especially due to the phenylephrine and chlorphenamine content. They are also more likely to experience side effects such as sedation, confusion, hypotension, or excitement and may be more sensitive to effects such as dry mouth and urinary retention.
How to take
Apogrip is taken orally.
Dissolve the contents of the sachet completely in a little liquid, preferably half a glass of water, and then drink.
Always take the lowest effective dose.
Treatment with this medicine is subject to the appearance of symptoms. As they disappear, you should stop treatment.
If the fever persists for more than 3 days of treatment, the pain or other symptoms for more than 5 days, or worsen, or new symptoms appear, you should consult your doctor.
If you take more Apogrip than you should
If you have ingested an overdose, you should go immediately to a medical center, even if you do not notice symptoms, as they often do not appear until 3 days after ingestion of the overdose, 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). Dry mouth, nose, or throat. Overdose can also cause: coagulation disorders (blood clots and bleeding).
Effects such as high blood pressure, arrhythmias (rapid or irregular heartbeats), palpitations, reduced urine production. Metabolic acidosis (decrease in blood alkalinity). With prolonged use, it can cause depletion of plasma volume (decrease in blood volume).
Treatment of an overdose is more effective if started within 4 hours after taking the overdose of the medicine.
Patients being treated with barbiturates or chronic alcoholics may be more susceptible to the toxicity of a paracetamol overdose.
In case of overdose or accidental ingestion, go immediately to a medical center or call the Toxicology Information Service (Telephone 91 562 04 20), indicating the medicine and the amount ingested.
Do not take a double dose to make up for forgotten doses.
Like all medicines, Apogrip can cause side effects, although not everyone gets 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 elderly patients 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 eyelids or around the eyes, face, tongue, difficulty breathing, etc.), photosensitivity (sensitivity to sunlight), cross-sensitivity (allergy) with medicines related to chlorphenamine. Blood disorders (changes in blood cell formula, such as agranulocytosis, leucopenia, 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 for prolonged treatments.
If you experience side effects, consult your doctor or pharmacist, even if they are side effects not listed in this leaflet.
Keep this medicine out of the sight and reach of children.
Do not use Apogrip powder 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 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 Apogrip sachets
Appearance of the product and package contents
Apogrip is a white, homogeneous powder, without lumps and with an orange flavor, presented in sachets packaged in cardboard boxes containing 10 sachets.
Marketing authorization holder and manufacturer
Aurovitas Spain S.A.U.
Avda. de Burgos, 16-D
28036 Madrid,
Spain
Manufacturer
Laboratorios Alcalá Farma, S.L.
Avenida de Madrid 82
28802 Alcalá de Henares (Madrid)
Date of the last revision of this prospectus:February 2025
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/.
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for APOGRIP POWDER FOR ORAL SOLUTION – subject to medical assessment and local rules.