Diclofenac potassium
Cataflam 50 contains diclofenac potassium, which belongs to a group of non-steroidal anti-inflammatory drugs (NSAIDs), with anti-rheumatic, anti-inflammatory, analgesic, and antipyretic properties. The mechanism of action of Cataflam 50 involves the inhibition of prostaglandin biosynthesis, which plays a key role in the pathogenesis of inflammation, pain, and fever.
Cataflam 50 is used for the short-term treatment of the following acute conditions:
In the case of diagnosed heart disease or significant risk factors for heart disease, the attending physician will periodically assess the patient's need for symptomatic treatment and their response to the medicine, especially if the treatment lasts longer than 4 weeks.
During the treatment period, regular blood tests should be performed in the case of any liver function disorders, kidney function disorders, and blood count abnormalities.
Both liver function (transaminase levels), kidney function (creatinine levels), and blood count (white blood cell count, red blood cell count, and platelet count) should be monitored. The attending physician will take into account the results of the blood tests when deciding to discontinue treatment with Cataflam 50 or change the dose of the medicine.
Like other non-steroidal anti-inflammatory drugs (NSAIDs), Cataflam 50 should not be used in people who may experience an asthma attack, urticaria, or acute rhinitis after taking acetylsalicylic acid or other prostaglandin synthesis inhibitors.
The patient should inform their doctor about the presence of these diseases.
Before using Cataflam 50, the patient should discuss the following with their doctor:
patients allergic to other substances (e.g., those who experience skin reactions, itching, or urticaria). The medicine should be administered with caution (preferably under medical supervision);
Before taking diclofenac, the patient should inform their doctor:
The medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means it is considered "sodium-free".
The occurrence of side effects can be limited by using the medicine in the smallest effective dose and for no longer than necessary.
The smallest dose of Cataflam 50 that provides pain and/or swelling relief should be used, and it should be used for the shortest possible time to minimize the risk of side effects.
If the patient experiences any symptoms suggesting heart or blood vessel problems, such as chest pain, shortness of breath, weakness, or slurred speech, they should immediately contact their doctor or the hospital emergency department.
Taking diclofenac may temporarily inhibit platelet aggregation.
Before taking Cataflam 50, the patient should tell their doctor if they have recently undergone or are scheduled to undergo stomach or gastrointestinal surgery, as Cataflam 50 may sometimes cause delayed wound healing in the intestines after surgical procedures.
The medicine should not be used in children and adolescents under 14 years of age. Children and adolescents under 14 years of age are recommended to use diclofenac in the form of suppositories, at a dose of 25 mg per day. Cataflam 50 should not be used in children under 1 year of age.
Elderly patients may be more sensitive to the effects of the medicine than other adults. They should follow the recommendations in the leaflet, use the smallest effective doses as recommended by their doctor, and report any side effects that occur during treatment to their doctor.
The patient should tell their doctor about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take.
The tablets should be swallowed whole, with a glass of water, preferably before a meal.
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a child, they should consult their doctor before using this medicine.
During pregnancy, in the first two trimesters, Cataflam 50 should not be used unless it is absolutely necessary.
As with other anti-inflammatory drugs, using Cataflam 50 in patients in the last 3 months of pregnancy is contraindicated, as it may seriously harm the fetus or have an unfavorable effect on delivery.
Cataflam 50 should not be used in breastfeeding women, as it may have a harmful effect on the infant.
The doctor will discuss the potential risks of using Cataflam 50 during pregnancy and breastfeeding with the patient.
Taking Cataflam 50 may make it more difficult to become pregnant. If the patient plans to become pregnant or is having trouble becoming pregnant, they should inform their doctor.
The effect of Cataflam 50 on the ability to drive vehicles, operate machinery, or perform other activities that require special attention is unlikely.
Cataflam 50 in the form of effervescent tablets contains sucrose. If the patient has previously been diagnosed with intolerance to some sugars, they should consult their doctor before taking the medicine.
This medicine should always be used as directed by the doctor. In case of doubts, the patient should consult their doctor or pharmacist.
The recommended doses should not be exceeded. If Cataflam 50 is used for more than a few weeks, regular medical check-ups should be performed to rule out any unnoticed side effects.
The general recommendation is to adjust the dose individually and use the smallest effective dose for the shortest possible period.
If the patient feels that the effect of the medicine is too strong or too weak, they should consult their doctor.
The recommended initial dose is 100 mg per day to 150 mg per day.
In milder cases, a dose of 75 mg to 100 mg per day is considered sufficient.
The tablets are for oral administration. The total daily dose should be divided into 2 to 3 doses, if applicable.
The daily dose should not exceed 150 mg.
In patients with primary dysmenorrhea, the initial dose of the medicine is 50 mg and should be taken when the first symptoms appear, and then the treatment should be continued with a dose of 50 mg, taken up to three times a day, for several consecutive days, as needed. If a dose of 150 mg per day does not provide sufficient pain relief for two to three consecutive menstrual cycles, the attending physician may recommend an initial dose of 100 mg and administration of up to 200 mg per day, divided into 2 to 3 doses, during subsequent menstrual cycles. The dose should not exceed 200 mg per day.
In the treatment of migraine, the initial dose of the medicine is 50 mg and should be taken when the first symptoms of the disease appear. If within 2 hours of taking the first dose, the pain relief is not sufficient, a second dose of 50 mg can be taken. If necessary, additional doses of 50 mg can be taken at 4 to 6 hour intervals. The dose should not exceed 200 mg per day.
Due to the high dose, Cataflam 50 is not recommended for children and adolescents under 14 years of age.
Children and adolescents under 14 years of age are recommended to use diclofenac in the form of suppositories, at a dose of 25 mg per day.
In the case of adolescents over 14 years of age, a dose of 75 mg to 100 mg per day, divided into 2 to 3 doses, is usually sufficient. The maximum daily dose should not be exceeded, which is 150 mg.
Cataflam 50 should not be used in children and adolescents (under 18 years of age) for the treatment of migraine.
The medicine should be used with caution in elderly patients. In the case of elderly patients and those with a low body mass, the smallest effective dose is recommended.
The tablets should be swallowed whole, with a glass of water, preferably before a meal. The tablets should not be divided or chewed.
Cataflam 50 should always be used as directed by the doctor.
If the patient is taking Cataflam 50 for a long time, they should regularly consult their doctor to ensure that no side effects have occurred.
In case of doubts about how long to use the medicine, the patient should consult their doctor or pharmacist.
Overdosing on Cataflam 50 does not cause characteristic symptoms, but the following may occur: vomiting, gastrointestinal bleeding, diarrhea, dizziness, tinnitus, or seizures. In the case of significant poisoning, acute kidney failure and liver damage may occur.
In the event of accidental ingestion of a larger amount of tablets than recommended, the patient should immediately consult their doctor, pharmacist, or go to the hospital emergency department.
If a dose is missed, it should be taken as soon as the patient remembers. However, if more than half of the time has passed between two doses, the missed dose should not be taken, and the next dose should be taken according to the previous dosing schedule. A double dose should not be taken to make up for the missed dose.
Like all medicines, Cataflam 50 can cause side effects, although not everybody gets them.
The frequency of side effects is estimated as follows:
very common (≥1/10); common (≥1/100 to <1>The following side effects include those reported with Cataflam 50, as well as those observed with other forms of diclofenac, used for short or long periods.
Taking medicines like Cataflam 50 may be associated with a small increased risk of heart attack (myocardial infarction) or stroke.
In some people, while taking Cataflam 50, other side effects may occur.
If any of the side effects get worse or if any side effects not listed in the leaflet occur, the patient should tell their doctor or pharmacist.
chest pain, which may be a symptom of a potentially severe allergic reaction called Kounis syndrome.
These uncommon side effects may occur in 1-10 patients per 1000, especially when using high daily doses (150 mg) for a long time
If the patient is taking Cataflam 50 for more than a few weeks, they should regularly consult their doctor to ensure that no side effects have occurred.
If side effects occur, including any side effects not listed in the leaflet, the patient should tell their doctor, pharmacist, or nurse. 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.: 22 49 21 301, fax: 22 49 21 309, website: https://smz.ezdrowie.gov.pl
By reporting side effects, more information can be collected on the safety of the medicine.
The medicine should be stored out of sight and reach of children.
Store in a temperature below 30°C, protect from moisture.
Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the given month.
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.
One packaging contains 10 effervescent tablets.
For more detailed information, the patient should contact the marketing authorization holder or parallel importer.
Novartis Pharma NV
Medialaan 40
Novartis Pharma NV
Medialaan 40
Medezin Sp. z o.o.
ul. Zbąszyńska 3
91-342 Łódź
Medezin Sp. z o.o.
ul. Zbąszyńska 3
91-342 Łódź
CEFEA Sp. z o.o. Sp. komandytowa
ul. Działkowa 56
02-234 Warsaw
SHIRAZ PRODUCTIONS Sp. z o.o.
ul. Tymiankowa 24/28
95-054 Ksawerów
CANPOLAND SPÓŁKA AKCYJNA
ul. Beskidzka 190
91-610 Łódź
[Information about the trademark]
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