Consult a doctor
In cases of liver insufficiency or Gilbert’s syndrome, do not exceed 3 tablets/24 hours and the minimum interval between doses will be 8 hours.
Use in children
This medication is contraindicatedin children and adolescents under 15 years of age.
Use in elderly patients
Elderly patients cannot use this medication without consulting a doctor.
Because they may be especially affected by some medication side effects such as the appearance of slow heartbeats (bradycardia) or reduced cardiac output, due to the content of phenylephrine and chlorphenamine. They may also be 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
Couldina instant with paracetamolis taken orally. Dissolve the tablet completely in a little liquid, preferably half a glass of water and then drink.
Always take the smallest effective dose.
The use of this medication is subject to the appearance of symptoms. As they disappear, treatment should be discontinued.
If feverpersists for more than 3 days of treatment, pain or other symptoms persist for more than 5 days, or worsen or new ones appear, consult a doctor.
If you take more Couldina instant with paracetamol than you should
If you have ingested an overdose, you must go immediately to a medical center, even if you do not feel the symptoms, as they often do not appear until 3 days after ingestion of the overdose, even in cases of severe poisoning.
The symptoms of an overdose may be: dizziness, vomiting, loss of appetite, yellowing 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 one especially in children). Dry 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, depletion of plasma volume (decrease in blood volume) may occur.
The treatment of an overdose is more effective if it is initiated within 4 hours of taking the overdose of the medication.
Patients undergoing barbiturate treatment or chronic alcoholics may be more susceptible to the toxicity of a paracetamol overdose.The overdose may also cause: coagulation disorders (blood clots and hemorrhages).
In case of overdose or accidental ingestion, go immediately to a medical center or call the Toxicological Information Service (Telephone 91 562 04 20), indicating the medication and the amount ingested.
Like all medications, Couldina instant with paracetamol may cause side effects, although not everyone will experience them.
During the period of use of the association of paracetamol, phenylephrine, and chlorphenamine, 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, muscle weakness: these side effects may disappear after 2-3 days of treatment. Difficulty in facial movements, clumsiness, tremors, alterations in sensations and paresthesias, dry mouth, loss of appetite, alterations in taste or smell, gastrointestinal discomfort (which may decrease if the medication is taken with food), nausea, vomiting, diarrhea, constipation, stomach pain, urinary retention, dryness of the nose and throat, thickening of mucosities, sweating, blurred vision, or other visual disturbances.
-The side effects that may appear with low frequency (rare) are::
Unpleasantness, low blood pressure (hypotension), and increased levels of transaminases in the blood. Myocardial infarction, ventricular arrhythmia (irregular heartbeats), pulmonary edema (increase in lung volume) and cerebral hemorrhage (at high doses or in sensitive patients).
Nervous excitement (usually at 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 sounds, rapid or irregular heartbeats (usually with overdose), liver disorders (which may present with stomach 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 related chlorphenamine medications. Blood disorders (changes in the formula of blood cells, 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 alterations, impotence, menstrual disorders.
-The side effects that may appear with very low frequency (very rare) are:
Renal diseases, cloudy urine, allergic dermatitis (skin rash), jaundice (yellow discoloration of the skin), blood disorders (neutropenia, hemolytic anemia) and hypoglycemia (low blood sugar).
Paracetamol may damage the liver when taken in high doses or with prolonged treatment.
There have been very rare cases of severe skin reactions reported.
-The side effects whose frequency of appearance is unknown are::
Anxiety, irritability, weakness, high blood pressure (hypertension, usually at high doses and in sensitive patients), headache (at high doses and may be a symptom of hypertension), very slow heartbeats (bradycardia), reduction of peripheral blood vessel diameter (vasoconstriction), reduction of heart function that affects the elderly and patients with poor cerebral or coronary circulation, possible production or worsening of heart disease, urinary retention, pallor, goosebumps, high blood sugar (hyperglycemia), low potassium levels in the blood, metabolic acidosis (metabolic disorder), coldness in the extremities (legs or arms), flushing, sensation of fainting (hypotension). At high doses, vomiting, palpitations, psychotic states with hallucinations may occur; with prolonged use, a decrease in blood volume may occur.
A severe disease that may make the blood more acidic (denominated metabolic acidosis) in patients with severe disease using paracetamol (see section 2).
Reporting of side effects
If you experience any of the side effects, consult your doctor or pharmacist, even if they are side effects that do not appear in this leaflet. You can also report them directly through the Spanish System for the Pharmacovigilance of Medicinal Products for Human Use:www.notificaram.es.By reporting side effects, you can contribute to providing more information on the safety of this medication.
Keep out of sight and reach of children.
Do not use Couldina Instant with Paracetamol after the expiration date that appears on the packaging, after CAD or Expiration. The expiration date is the last day of the month indicated.
Keep the packaging perfectly closed. Store in the original packaging.
Do not store at a temperature above 30°C.
Medicines should not be disposed of through drains or in the trash. Dispose of packaging and medicines you no longer need at the SIGRE point of the pharmacy. If in doubt, ask your pharmacist how to dispose of packaging and medicines you no longer need. In this way, you will help protect the environment.
Each sachet contains:
-Active ingredients: Each sachet contains 650 mg of paracetamol, 4 mg of chlorphenamine maleate and 10 mg of phenylephrine hydrochloride.
-The other components (excipients) are: polyvinylpyrrolidone K30 (E-1201), sodium docusate, anhydrous citric acid (E-330), sodium hydrogen carbonate (E-500ii), anhydrous sodium carbonate (E-500i), sodium saccharin (E-954) and lemon aroma.
Appearance of the product and contents of the packaging
This medicine is packaged in single-dose, heat-sealed sachets made from a complex laminate composed of a paper layer, an adhesive layer, an aluminum film and a heat-sealable copolymer of ethylene and acrylic acid. Contents of the boxes: 10 and 20 sachets.
Holder of the marketing authorization and responsible manufacturer
Laboratorios Alter, S.A.
C/Mateo Inurria, 30
28036, Madrid
Spain
Last review date of this leaflet: February 2025
The detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.es/
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