(1000 mg + 50 mg + 12.2 mg)/sachet, powder for oral solution, in a sachet
Paracetamol + Caffeine + Phenylephrine hydrochloride
This medicine should always be taken exactly as described in this patient leaflet or as directed by a doctor or pharmacist.
APAP Cold MAX is a combination medicine. It contains three active substances: paracetamol, caffeine, and phenylephrine. Caffeine increases the effectiveness of paracetamol in treating pain and accelerates its onset of action.
The indication for using APAP Cold MAX is the short-term treatment of cold and flu symptoms, such as: nasal congestion and sinusitis, runny nose, and headache, sore throat, muscle aches, and fever, feeling unwell, fatigue.
If symptoms worsen or do not improve after 3 days, consult a doctor.
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Before taking the medicine, consult a doctor or pharmacist.
The medicine contains paracetamol. Due to the risk of overdose, check if other medicines being taken contain paracetamol.
Do not drink alcohol while taking the medicine. Taking the medicine by people with liver failure, alcohol abusers, or those who are fasting poses a risk of toxic liver damage.
During treatment with APAP Cold MAX, immediately inform your doctor if:
If the patient has severe diseases, including severe kidney or liver dysfunction, or sepsis (when bacteria and their toxins circulate in the blood, leading to organ damage) or malnutrition, chronic alcoholism, or if the patient is also taking flucloxacillin (an antibiotic). In these situations, patients have developed a severe condition called metabolic acidosis (a blood and body fluid disorder), which must be treated urgently (see section 2).
It is recommended to consult a doctor even if the above warnings refer to past situations.
Do not use in children under 12 years of age.
Tell your doctor or pharmacist about all medicines being taken currently or recently, as well as any medicines the patient plans to take.
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Particular caution should be exercised when taking APAP Cold MAX with the following medicines:
Smoking accelerates caffeine metabolism.
Caffeine increases the risk of dependence on substances with effects similar to ephedrine (contained in nasal decongestants).
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The medicine can be taken regardless of meals.
Do not drink alcohol while taking the medicine.
Excessive consumption of coffee or tea while taking the medicine may cause a feeling of tension and irritability.
Drinking alcohol during paracetamol treatment leads to the formation of a toxic metabolite that can cause liver cell necrosis, which can lead to liver failure.
Do not use during pregnancy.
Do not use during breastfeeding.
While taking APAP Cold MAX, be cautious when driving vehicles and operating machines.
Warnings regarding excipients
This should be taken into account in patients with diabetes. If the patient has previously been diagnosed with intolerance to some sugars, they should consult a doctor before taking the medicine.
Aspartame is a source of phenylalanine. It may be harmful to patients with phenylketonuria. This is a rare genetic disorder in which phenylalanine accumulates in the body due to its improper excretion.
The medicine contains 2.5 mg of sorbitol (an ingredient of sorbitol syrup) in one sachet, which corresponds to 10 mg/4 sachets (maximum daily dose).
The medicine contains 117.2 mg of sodium (the main ingredient of common salt) in one sachet. This corresponds to 5.9% of the maximum recommended daily dose of sodium in the diet for adults.
The medicine contains a colorant - orange yellow E110)
The medicine may cause allergic reactions.
The medicine may rarely cause severe hypersensitivity reactions and bronchospasm.
Benzyl alcohol may cause allergic reactions.
Pregnant or breastfeeding women and patients with liver or kidney disease should consult a doctor before taking the medicine, as a large amount of benzyl alcohol may accumulate in their body and cause adverse effects (so-called metabolic acidosis).
This medicine should always be taken exactly as described in the patient leaflet or as directed by a doctor or pharmacist. In case of doubt, consult a doctor or pharmacist.
The recommended dose is:
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adults and adolescents over 12 years of age: 1 sachet, if necessary, the dose can be repeated, but not more often than every 4-6 hours. Do not take more than 4 sachets in 24 hours. Do not take for more than 3 days without consulting a doctor.
The medicine is taken orally.
The contents of one sachet should be dissolved in a glass of hot, but not boiling, water. Stir until dissolved. Let it cool to a temperature that allows drinking. The liquid should be drunk when it is warm.
After dissolution, the liquid has the form of an opalescent solution with a yellow color, a characteristic mint-citrus flavor, and no sediment.
Do not use in children under 12 years of age.
Immediately consult a doctor or pharmacist. The medicine contains three active substances. Symptoms of overdose may result from the action of one or all of the active substances.
nausea, vomiting, excessive sweating, drowsiness, general weakness, anxiety, tremors, palpitations, high blood pressure, seizures, difficulty urinating, and shortness of breath. These symptoms may resolve the next day, despite the fact that liver damage is beginning to develop, which will then manifest as abdominal distension, return of nausea, and jaundice.
In case of overdose, immediately consult a doctor, even if the patient feels well, due to the risk of delayed, severe liver damage.
Do not take with other medicinal products with a similar composition.
Treatment should be carried out in a hospital. It involves accelerating the elimination of the medicine's components from the body and maintaining vital functions. In the case of paracetamol overdose, it may be necessary to administer an antidote: N-acetylcysteine and/or methionine.
Do not take a double dose to make up for a missed dose.
The frequency of side effects has been classified as follows:
Common - may affect 1-10 in 100 treated patients;
Rare - may affect 1-10 in 10,000 treated patients;
Very rare - may affect less than 1 in 10,000 patients;
Frequency not known - cannot be estimated from the available data.
Possible side effects of the medicine due to the presence of paracetamol:
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liver failure, liver necrosis, jaundice.
Single cases of toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema multiforme, laryngeal edema, anaphylactic shock, and dizziness have been observed.
Possible side effects of the medicine due to the presence of phenylephrine:
Nephrotoxic effects are rare and have not been reported to be related to therapeutic doses, except in cases of chronic use of the medicine.
After taking caffeine, the following have been reported: palpitations, sudden flushing, high blood pressure, tachycardia.
If any side effects occur, including any possible side effects not listed in this leaflet, tell your doctor or pharmacist. Side effects can be reported directly to the Department of Drug Safety Monitoring of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products, Al. Jerozolimskie 181 C, 02-222 Warsaw, tel.: +48 22 49 21 301, fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl/
Side effects can also be reported to the marketing authorization holder.
Reporting side effects will help gather more information on the safety of the medicine.
Store in a temperature below 25°C. The medicine should be stored in a place out of sight and reach of children.
Do not use this medicine after the expiry date stated on the packaging (month/year).
Medicines should not be disposed of via wastewater or household waste.
Ask your pharmacist how to dispose of medicines that are no longer needed.
This will help protect the environment.
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The active substances of the medicine are: paracetamol 1000 mg, caffeine 50 mg, and phenylephrine hydrochloride 12.2 mg.
Other ingredients are: sucrose, sodium citrate, citric acid, acesulfame potassium (E950), aspartame (E951), quinoline yellow (E104), citrus flavor 87A069 (including sulfites, citral, citronellol, geraniol, limonene, linalol, anhydrous corn glucose syrup), citrus flavor 875060 (including citral, citronellol, geraniol, limonene, linalol, anhydrous corn glucose syrup), citrus flavor 501.476 AP0504 (including limonene, citral, linalol, geraniol, citronellol, farnesol, corn maltodextrin (contains glucose)), mint flavor 550469 TP0300 (including limonene), peppermint flavor SC447995 (including limonene, linalol, citronellol, eugenol, geraniol, benzyl alcohol, corn maltodextrin (contains glucose), sorbitol syrup, sulfites), orange yellow FCF (E110).
APAP Cold MAX is a yellow, powdery powder with a characteristic mint-citrus flavor.
Packaging:5, 8, 12 sachets in a cardboard box.
US Pharmacia Sp. z o.o.
ul. Ziębicka 40,
50-507 Wrocław
To obtain more detailed information about this medicine, contact:
USP Zdrowie Sp. z o.o.
ul. Poleczki 35
02-822 Warszawa
tel.: +48 (22) 543 60 00
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