Paracetamol + Codeine phosphate hemihydrate
This medicine should always be taken exactly as described in the patient leaflet or as directed by a doctor or pharmacist.
Solpadeine FORTE Tabs may be used in patients over 12 years of age for the short-term relief of moderate pain that requires a stronger analgesic effect than observed with other painkillers, such as those containing paracetamol, ibuprofen, or acetylsalicylic acid alone.
It may be used to treat headache, migraine with or without aura, toothache (including pain after tooth extraction), painful menstruation, back pain, muscle pain, neuralgia, bone and joint pain associated with arthritis and rheumatism, pain associated with injuries due to overexertion and sprains, and sciatica.
The tablets contain two active ingredients: paracetamol and codeine. Codeine and paracetamol are painkillers. Codeine belongs to a group of medicines called opioid analgesics, which relieve pain. It can be used alone or in combination with other painkillers.
Thanks to the dual mechanism of action of the ingredients, it is possible to quickly relieve moderate pain.
Codeine is converted to morphine by a certain liver enzyme. Morphine is a substance that relieves pain. Some people have a changed enzyme and this can affect them in different ways. In some people, morphine is not produced or is produced in very small amounts, which does not provide adequate pain relief. Other people are more prone to severe side effects caused by the production of very large amounts of morphine. If the patient experiences any of the following side effects, they should stop taking the medicine and consult a doctor immediately: slow or shallow breathing, disorientation, drowsiness, small pupils, nausea or vomiting, constipation, loss of appetite.
Taking codeine (the active substance of this medicine) regularly and for a long time can lead to dependence and misuse, which can cause overdose and/or death. This medicine should not be taken for longer than necessary. It should not be given to other people.
Before using, you should consult a doctor if the patient has liver or kidney problems, is underweight (<50kg), is malnourished, or regularly drinks alcohol, as this may increase the risk of liver damage. It may be necessary to reduce the amount of paracetamol taken or completely avoid using this product.
If the patient experiences severe illnesses, including severe kidney problems or sepsis (when bacteria and their toxins are in the blood, leading to organ damage) or malnutrition, chronic alcoholism, or is taking flucloxacillin (an antibiotic), they should consult a doctor. In these situations, patients taking paracetamol regularly for a long time or taking paracetamol with flucloxacillin have reported a serious condition called metabolic acidosis (a blood and body fluid disorder), which must be treated urgently (see section 2). Symptoms of metabolic acidosis may include: severe breathing difficulties, including rapid deep breathing, drowsiness, feeling sick (nausea) and vomiting.
This medicine should not be given to children under 12 years of age.
Use in children and adolescents after surgical removal of tonsils:
Codeine should not be used to relieve pain in children and adolescents after tonsillectomy or adenoidectomy due to obstructive sleep apnea.
Use in children with breathing difficulties:
Codeine is not recommended for children with breathing difficulties, as symptoms of morphine toxicity may be exacerbated in these children.
You should talk to a doctor or pharmacist before taking these tablets if the patient is taking prescription medicines, especially the following: metoclopramide or domperidone (used to treat nausea and vomiting); cholestyramine (used to lower blood cholesterol levels); monoamine oxidase inhibitors (MAOIs) prescribed for depression within the last 2 weeks or medicines that cause drowsiness (e.g., sedatives, antidepressants, or alcohol).
If the patient is taking blood-thinning medicines (e.g., warfarin and coumarin derivatives) and needs to take a painkiller every day, they should talk to a doctor about the risk of bleeding, but may still take occasional doses of Solpadeine FORTE Tabs with blood-thinning medicines. If the patient is taking probenecid, they should talk to a doctor, as it may be necessary to reduce the dose of Solpadeine FORTE Tabs.
Paracetamol and other medicines
The patient should inform their doctor or pharmacist if they are taking:
Taking Solpadeine FORTE Tabs and sedative medicines (e.g., benzodiazepines or derivatives) at the same time increases the risk of drowsiness, breathing difficulties (respiratory depression), or coma, which can be life-threatening. Therefore, combined treatment should only be considered when other treatment options are not available.
If Solpadeine FORTE Tabs are taken with other sedative medicines, the doctor should limit the dose and duration of concurrent use.
The patient should tell their doctor about all sedative medicines they are taking and strictly follow the dose prescribed by the doctor. It may be helpful to inform a relative or close friend of the patient about the possibility of the above symptoms. If these symptoms occur, the patient should consult a doctor.
Unless otherwise directed by a doctor, Solpadeine FORTE Tabs should be avoided during pregnancy.
Solpadeine FORTE Tabs should not be taken during breastfeeding. Codeine and morphine pass into breast milk.
If the patient feels dizzy or excessively drowsy while taking Solpadeine FORTE Tabs, they should not drive or operate machinery.
If the patient has previously been diagnosed with intolerance to some sugars, they should consult a doctor before taking the medicine.
The medicine contains less than 1 mmol of sodium (23 mg) per tablet, which means the medicine is considered "sodium-free".
This medicine should always be taken exactly as described in the patient leaflet or as directed by a doctor or pharmacist. If in doubt, the patient should consult a doctor or pharmacist.
Adults:
2 tablets with water. The medicine should be taken every 4 to 6 hours, as needed.
Elderly:
In elderly, frail, or bedridden patients, the dose may need to be reduced.
Kidney problems:
When giving paracetamol to patients with kidney failure, the dose should be reduced and the minimum interval between each administration should be at least 6 hours.
Adults:
Liver problems:
In patients with liver problems or Gilbert's syndrome, the dose should be reduced or the interval between doses prolonged.
Adolescents 16-18 years:
2 tablets with water. The medicine should be taken every 6 hours, as needed.
Glomerular filtration rate (GFR) | Dose |
10-50 ml/min | 500 mg every 6 hours |
<10 ml min< td> | 500 mg every 8 hours |
Adolescents 12-15 years:
1 tablet with water and take every 6 hours, as needed.
24 hours unless otherwise directed by a doctor:
This medicine should not be used for longer than 3 days. If the pain does not decrease after 3 days, the patient should consult a doctor.
In case of doubt, the patient should consult a doctor.
Solpadeine FORTE Tabs is not recommended for patients under 12 years of age due to the risk of severe breathing difficulties.
This medicine contains codeine and may cause dependence if taken continuously for more than 3 days. After stopping the medicine, withdrawal symptoms may occur.
If the symptoms do not go away or the headache does not improve, the patient should consult a doctor.
The patient should immediately talk to a doctor if they have taken too much of this medicine, even if they feel well. This is because too much paracetamol can cause delayed and severe liver damage.
The patient should not take a double dose to make up for a missed dose.
If the patient has any further doubts about the use of this medicine, they should consult a doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The patient should stop taking the medicine and immediately inform their doctor if they experience any of the following symptoms:
Other side effects:
Very rare cases of severe skin reactions have been reported.
Frequency of occurrence: "frequency not known" (cannot be estimated from the available data)
A serious condition that can cause acidification of the blood (called metabolic acidosis), in patients with severe illness taking paracetamol (see section 2).
When taking the medicine as directed on the packaging, the risk of dependence on the medicine is very low. However, in the following situations, it is important to talk to a doctor:
If the patient experiences any side effects, they should consult a doctor or pharmacist. This applies to all possible side effects not listed in this leaflet.
Side effects can also be reported directly to the Department of Drug Safety, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: 22 49-21-301, fax: 22 49-21-309,
Website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder.
By reporting side effects, it is possible to gather more information on the safety of the medicine.
The medicine should be stored out of sight and reach of children.
Do not store above 25°C.
Store in the original packaging to protect from moisture.
Do not use this medicine after the expiry date stated on the blister and carton after EXP. The expiry date refers to the last day of the month stated.
Medicines should not be disposed of via wastewater or household waste. The patient should ask their pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Solpadeine FORTE Tabs are red, film-coated tablets in the shape of capsules, measuring 15.8 mm x 8.4 mm, packaged in a blister pack of PVC/Aluminum, in a cardboard box.
Package sizes: 6, 10, 12, 16 tablets
Not all package sizes may be marketed.
Perrigo Poland Sp. z o.o.
ul. Domaniewska 48
02-672 Warsaw
tel.: +48 (22) 852 55 51
Swiss Caps GmbH
Grassingerstrasse 9
83043 Bad Aibling (Bavaria)
Germany
Ireland | Solpa-Plus Tablets Paracetamol 500 mg Codeine Phosphate Hemihydrate 12.8 mg |
Poland | Solpadeine FORTE Tabs |
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