(650 mg + 50 mg +10 mg)/ sachet
powder for oral solution preparation
(Paracetamol + Ascorbic Acid + Phenylephrine Hydrochloride)
This medicine should always be taken as described in the patient leaflet or as directed by a doctor,
or pharmacist.
APAP cold, powder for oral solution, is a multi-component medicine,
containing paracetamol, ascorbic acid, and phenylephrine hydrochloride. It has antipyretic, analgesic, and decongestant effects.
It alleviates the symptoms of colds and flu.
The indication for use of the medicine is short-term relief of cold, flu, and flu-like infection symptoms, such as:
fever, headache, sore throat, muscle and joint pain, and symptoms of nasal congestion occurring in colds and flu.
If after 3 days there is no improvement or you feel worse, you should consult a doctor.
Before starting to take the medicine, consult a doctor or pharmacist if you have:
You should contact your doctor, even if the above warnings concern situations that occurred in the past.
During the use of APAP cold medicine, you should immediately inform your doctor if:
If you have severe diseases, including severe kidney dysfunction or sepsis (when bacteria and their toxins circulate in the blood, leading to organ damage) or malnutrition,
chronic alcoholism or when you are also taking flucloxacillin (an antibiotic). In these situations, patients have been reported to develop a severe disease called metabolic acidosis (abnormal blood and body fluid acidity), when they took paracetamol in regular doses for a longer period or when they took paracetamol with flucloxacillin. Symptoms of metabolic acidosis may include: severe breathing difficulties, including rapid deep breathing, drowsiness, feeling of nausea (nausea) and vomiting.
APAP cold medicine should not be given to children under 12 years of age.
The medicine should not be taken simultaneously with other medicines containing:
You should consult a doctor before taking the medicine with:
You should inform your doctor or pharmacist if you are taking flucloxacillin (an antibiotic) due to the serious risk of blood and body fluid disorders (called metabolic acidosis), which requires emergency treatment (see point 2).
The ascorbic acid contained in the medicine increases the absorption of:
Food does not reduce the absorption of the medicine.
You should not drink alcohol while taking the medicine, due to the risk of toxic liver damage.
In pregnancy and during breastfeeding, or if you suspect you are pregnant, or plan to become pregnant, you should consult a doctor or pharmacist before taking this medicine.
Do not use during pregnancy.
Do not use during breastfeeding.
While taking the medicine, you should be cautious when driving vehicles and operating machinery.
The medicine contains 20 mg of aspartame (E 951) per sachet. 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 1.981 g of sucrose per sachet and 11.886 g of sucrose in the maximum daily dose (6 sachets). This should be taken into account in patients with diabetes.
If you have previously been diagnosed with intolerance to some sugars, you should consult a doctor before taking the medicine.
The medicine contains 78.13 mg of sodium (the main component of table salt) per sachet.
This corresponds to 3.9% of the maximum recommended daily intake of sodium in the diet for adults.
The medicine may rarely cause severe hypersensitivity reactions and bronchospasm.
This medicine should always be taken as described in the patient leaflet or as directed by a doctor,
or pharmacist. In case of doubt, consult a doctor or pharmacist.
Adults and children over 12 years of age:
1 sachet every 4-6 hours (maximum 6 sachets per day).
The contents of the sachet should be dissolved in a glass of hot water.
If you feel that the effect of the medicine is too strong or too weak, you should consult a doctor.
In case of taking a higher dose of the medicine than recommended, you should stop taking the medicine and immediately contact a doctor or the nearest hospital emergency department.
You should take the leaflet and the medicine packaging with you.
Procedure after overdose:
Symptoms may occur, such as nausea, vomiting, excessive sweating, drowsiness, and general weakness. These symptoms may resolve on their own, but this does not rule out the development of liver damage. Symptoms such as tremors, anxiety, insomnia, increased blood pressure, significant acceleration of heart rate, pallor of the skin and mucous membranes, and urinary retention may also occur. Later, abdominal pain and jaundice may appear.
The medicine is intended for short-term relief of cold, flu, and flu-like infection symptoms.
If you miss a dose of the medicine and the symptoms persist, you should take the next dose of the medicine.
Do not take a double dose to make up for the missed dose.
In case of any further doubts about the use of this medicine, you should consult a doctor or pharmacist.
Like all medicines, APAP cold medicine can cause side effects, although not everybody gets them.
These include:
Frequency not known (cannot be estimated from available data)
In the case of short-term use of the medicine, side effects occur rarely.
If you experience any side effects, including any possible side effects not listed in this leaflet, you should tell your doctor or pharmacist. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181C,
02-222 Warsaw,
tel.: +48 (22) 492 13 01,
fax: +48 (22) 492 13 09
website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder.
By reporting side effects, you can help provide more information on the safety of the medicine.
Store the medicine at a temperature below 25°C.
The medicine should be stored in a place invisible and inaccessible to children.
Do not use the medicine after the expiry date stated on the packaging.
Medicines should not be disposed of via wastewater or household waste.
You should ask your pharmacist how to dispose of medicines that are no longer used. This will help protect the environment.
One sachet contains active substances: paracetamol 650 mg, ascorbic acid 50 mg, phenylephrine hydrochloride 10 mg.
Other components of the medicine in one sachet are: sucrose, citric acid, sodium citrate, lemon flavor 87A069*,
lemon flavor 875060**, acesulfame potassium (E 950), lemon flavor 501.476/AP0504***,
lemon flavor 875928****, aspartame (E 951), quinoline yellow (E 104).
*lemon flavor 87A069 contains, among others, lemon juice concentrate (contains sulfites), natural citral (contains: citral, citronellol, geraniol, limonene, linalol), anhydrous corn glucose syrup
**lemon flavor 875060 contains, among others, natural citral, natural linalol (contains: citral, citronellol, geraniol, limonene, linalol), anhydrous corn glucose syrup, butylhydroxyanisole (E 320)
***lemon flavor 501.476/AP0504 contains, among others, corn maltodextrin
****lemon flavor 875928 contains, among others, citral, geraniol, limonene, linalol, anhydrous corn glucose syrup
Sachet with powder for oral solution.
The medicine is available in packages: 5, 8, 10, or 12 sachets in a cardboard box with a leaflet.
US Pharmacia Sp. z o.o.
ul. Ziębicka 40
50-507 Wrocław
To obtain more detailed information about this medicine, you should contact:
USP Zdrowie Sp. z o.o.
ul. Poleczki 35
02-822 Warsaw
tel. +48 (22) 543 60 00
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