Label: Information for the Patient
Vincigrip Forte Granulated for Oral Solution, Chocolate Flavor
Paracetamol/Pseudoephedrine Hydrochloride/Chlorphenamine Maleate
Read this entire label carefully before taking this medication, as it contains important information for you.
Follow exactly the administration instructions contained in this label or those provided by your doctor, or pharmacist.
It is an association of paracetamol, pseudoephedrine and chlorphenamine.
Paracetamol is an analgesic that reduces pain and fever.
Chlorphenamine is an antihistamine that relieves nasal secretion.
Pseudoephedrine is a sympathomimetic that reduces nasal congestion.
It is indicated for symptomatic relief of catarrhal and flu-like processes that occur with or without fever, mild to moderate pain, congestion and nasal secretion in adults and adolescents aged 14 years and over.
You should consult a doctor if it worsens or does not improve or if the fever persists for more than 3 days or the pain or other symptoms persist for more than 5 days.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Vincigrip Forte.
Inform your doctor immediately if you experience:
Severe diseases, such as severe kidney failure or sepsis (when bacteria and their toxins circulate in the blood, causing damage to organs), or if you have malnutrition, chronic alcoholism, or if you are also taking flucloxacillin (an antibiotic). A severe disease called metabolic acidosis (an anomaly in the blood and fluids) has been reported in patients in these situations when using paracetamol at regular doses for a prolonged period or when taking paracetamol with flucloxacillin. Symptoms of metabolic acidosis may include: severe respiratory distress with deep and rapid breathing, somnolence, feeling unwell (nausea) and vomiting.
Consult your doctor before taking this medication:
Children and adolescents
This medication is contraindicated in children and adolescents under 14 years old.
Interference with laboratory tests
Inform your doctor if you are taking this medication, as it may alter test results.
This medication may interfere with skin tests that use allergens. It is recommended to stop taking this medication at least 3 days before starting the tests and inform your doctor.
Athletes
Inform athletes that this medication contains a component that may establish a positive analytical result for doping control.
Other medications and Vincigrip Forte
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
Particularly, if you are using any of the following medications, as it may be necessary to change the dose or discontinue treatment:
Do not use with other medications indicated for nasal congestion relief.
Use of Vincigrip Forte with food, drinks, and alcohol
While taking this medication, do not consume alcoholic beverages, as it may potentiate the appearance of adverse effects of this medication.
Additionally, the use of medications containing paracetamol by patients who regularly consume alcohol (3 or more alcoholic beverages: beer, wine, liquor, etc. per day) may cause liver damage.
Limit the consumption of drinks containing caffeine (coffee, tea, chocolate, and cola drinks) while taking this medication.
Do not take with bitter orange juice, as it may cause a hypertensive crisis.
The consumption of this medication with food does not affect its efficacy.
Pregnancy and lactation
If you are pregnant or breastfeeding, or if you think you may be pregnant or plan to become pregnant, consult your doctor or pharmacist before using this medication.
This medication is contraindicated in the first trimester of pregnancy, as it may cause malformations in the intestines and face of the newborn. Additionally, it should not be taken during the rest of pregnancy unless your doctor considers it strictly necessary.
Women breastfeeding should not take this medication, as it passes into breast milk and may cause adverse effects in the baby.
Driving and operating machinery
This medication may cause drowsiness, affecting mental and/or physical ability. If you experience these effects, avoid driving vehicles or operating machinery.
Vincigrip Forte contains sodium and mannitol (E-421)
This medication contains 30.93 mg of sodium (main component of table salt/for cooking) in each packet. This is approximately 1.55% of the recommended daily maximum sodium intake for an adult.
It may cause a mild laxative effect due to mannitol.
Follow exactly the medication administration instructions contained in this leaflet or those indicated by your doctor or pharmacist. In case of doubt, ask your doctor or pharmacist.
The recommended dose is:
Adults and adolescents over 14 years old: 1 tablet (650 mg of paracetamol) every 6-8 hours (3 or 4 times a day) if necessary.
Do not take more than 3 grams of paracetamol per 24 hours (see section “Warnings and precautions”).
Patients with liver, kidney, or heart diseases:should consult their doctor. (See section 2)
How to take:
Vincigrip Forte is taken orally.
Empty the contents of the tablet into a half glass of water, stirring until it dissolves completely.
If the medication is taken at night, it should be taken a few hours before going to bed to reduce the possibility of insomnia in patients with difficulty sleeping.
The medication should be taken as long as symptoms appear. As soon as they disappear, this medication should be discontinued.
Use in children and adolescents
This medication is contraindicated in children and adolescents under 14 years old.
Use in patients over 65 years old
These patients cannot take this medication without consulting their doctor.
They are often more prone to the adverse effects of pseudoephedrine and chlorphenamine.
If you take more Vincigrip Forte than you should
If you have ingested an overdose, you should go quickly to a medical center even if you do not have symptoms, as they often do not manifest 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, yellowish discoloration of the skin and eyes (jaundice) and abdominal pain. Anxiety, fear, agitation, headache (may be a symptom of high blood pressure), convulsions, insomnia (or intense drowsiness), clumsiness, feeling of fainting, instability, confusion, irritability, tremors, anorexia; psychosis with hallucinations (this last especially in children). Dryness of the mouth, nose, or throat. Effects such as high blood pressure, arrhythmias (rapid or irregular heartbeats), palpitations, reduced urine production. Metabolic acidosis (decrease in blood alkalinity reserve). In prolonged use, it may cause depletion of plasma volume (decrease in blood volume).
In more severe cases, it may cause: decreased potassium in the blood (hypokalemia), mental disorder with altered perception of reality (psychosis), convulsions, coma, and hypertensive crisis.
The treatment of overdose is more effective if it is initiated within 4 hours after ingestion of the overdose of the medication.
Patients on barbiturate treatment or chronic alcoholics may be more susceptible to the toxicity of a paracetamol overdose.
In case of overdose or accidental ingestion, go immediately to the doctor or the Emergency Service of the nearest hospital or consult the Toxicological Information Service (phone: 91 562 04 20), indicating the medication and the amount ingested.
Like all medicines, this medicine may cause side effects, although not everyone will experience them.
During the period of use of the association of paracetamol, chlorphenamine, and pseudoephedrine, the following side effects have been reported, whose frequency has not been established with precision.
The side effects that may appear most frequently are:
Mild drowsiness, dizziness, and muscle weakness, which may disappear in some patients after 2-3 days of treatment. Difficulty moving the face, clumsiness, tremors, alterations in sensations, and paresthesia; blurred vision or double vision, dryness of the nose and throat, thickening of mucosities, dryness of the mouth, loss of appetite, alterations in taste or smell, gastrointestinal discomfort (which may decrease if the medicine is taken with food) such as nausea, vomiting, diarrhea, constipation, and stomach pain, urinary retention, and increased sweating.
The side effects that may appear less frequently are:
Nervous excitement (usually with high doses and more frequently in the elderly and children) that may include symptoms such as: restlessness, insomnia, nervousness, anxiety, headache, discoordination, tremors, and even convulsions.
Other side effects that may appear are: dilated pupils, cardiac alterations (usually due to overdose) such as rapid heartbeats (tachycardia), irregular heartbeats (palpitations), and alterations in heart rhythm (arrhythmias). Increased blood pressure (hypertension) mainly in hypertensive patients or decreased blood pressure (hypotension). Cases of intestinal diseases with presence of blood in stools have been reported a few days after starting treatment.
Alterations in the skin such as hardened lesions (erythema), itching, and dermatitis.
Difficulty or pain urinating. Blood disorders (changes in blood formula such as agranulocytosis, leukopenia, aplastic anemia, or thrombocytopenia) with symptoms such as unusual bleeding, sore throat, or fatigue; severe hypersensitivity reactions, anaphylactic reaction (cough, difficulty swallowing, rapid heartbeats, itching, swelling of eyelids or around the eyes, face, tongue, and difficulty breathing), photosensitivity (sensitivity to sunlight), cross-sensitivity (allergy) with related chlorphenamine medications. Auditory alterations, chest tightness, breathing sounds (sibilance), edema (swelling). Liver disorders that may present with stomach or abdominal pain and dark urine, impotence, and alterations in menstruation.
The side effects that may appear in rare occasions:
Discomfort, increased levels of transaminases in blood, hallucinations (more frequent with high doses), nightmares, screaming, and confusion in children, slow heartbeats or bradycardia (frequent with high doses).
The side effects that may appear in very rare occasions:
Kidney diseases, cloudy urine, urticaria, jaundice (yellowish discoloration of the skin), blood disorders (neutropenia, hemolytic anemia), hypoglycemia (low blood sugar), myocardial infarction, and severe skin reactions.
The side effects whose frequency of appearance is unknown (cannot be estimated from available data:
A severe disease that may make the blood more acidic (metabolic acidosis) in patients with severe disease using paracetamol (see section 2).
:
Heptatitis that may lead to acute liver failure, angioedema (generalized urticaria accompanied by inflammation of feet, hands, throat, lips, and respiratory pathways), severe skin reactions (such as Stevens-Johnson syndrome, toxic epidermal necrolysis, and acute generalized pustular psoriasis) and ischemic colitis due to insufficient blood irrigation. Decreased blood flow to the optic nerve (ischemic optic neuropathy).
Severe diseases affecting the cerebral blood vessels known as reversible posterior encephalopathy syndrome (REPS) and reversible cerebral vasoconstriction syndrome (RCVS)
Stop using Vincigrip Forte immediately and seek urgent medical assistance if you experience symptoms that may be signs of reversible posterior encephalopathy syndrome (REPS) and reversible cerebral vasoconstriction syndrome (RCVS). These include:
Reporting of side effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this prospectus.
You can also report them directly through the Spanish System of Pharmacovigilance of Medicines for Human Use http://www.notificaram.es.
By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medication out of the sight and reach of children.
Do not store at a temperature above 86°F (30°C).
Do not use this medication after the expiration date that appears on the packaging after CAD. The expiration date is the last day of the month indicated.
Medicines should not be disposed of through drains or in the trash. Dispose of the packaging and medications you no longer need at your pharmacy's SIGRE collection point. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition of Vincigrip Forte
The active principles are: paracetamol, pseudoephedrine hydrochloride, and chlorphenamine maleate. Each blister pack contains 650 mg of paracetamol, 30 mg of pseudoephedrine hydrochloride, and 4 mg of chlorphenamine maleate.
The other components (excipients) are:
butylhydroxyanisole (E-320), butylhydroxytoluene (E-321), sorbic acid, povidone, polysorbate 80, polyethylene glycol 6000, sodium carboxymethyl cellulose (from potato starch), sodium saccharin, sodium cyclamate, cocoa lecithin, chocolate aroma, mannitol (E-421).
Appearance of the product and content of the packaging
Vincigrip Forte is presented in blister packs containing oral granules with a chocolate flavor.
Each package contains 10 or 20 blister packs.
Holder of the marketing authorization
Laboratorios Salvat, S.A.
C/ Gall, 30-36 - 08950
Esplugues de Llobregat
Barcelona - Spain
Responsible for manufacturing
Laboratorios Salvat, S.A.
C/ Gall, 30-36 - 08950
Esplugues de Llobregat
Barcelona - Spain
or
PHARMALOOP, S.L.
C/Bolivia, 15 – Polig Industrial Azaque
28006 Alcalá de Henares, Madrid
Spain
Date of the last review of this prospectus:January 2025
The updated and detailed information on this medication is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es
Have questions about this medication or your symptoms? Connect with a licensed doctor for guidance and personalized care.