Diclofenac sodium
Olfen 50 contains diclofenac sodium, belonging to the group of non-steroidal anti-inflammatory drugs (NSAIDs), which have anti-rheumatic, anti-inflammatory, analgesic, and antipyretic effects. The mechanism of action of Olfen 50 involves the inhibition of prostaglandin biosynthesis, which plays a fundamental role in the pathogenesis of inflammation, pain, and fever.
In adults, Olfen 50 may be used to treat pain and inflammation in the following cases:
In case of doubts about the action or reasons for prescribing Olfen 50, consult a doctor.
In the case of diagnosed heart disease or significant risk factors for cardiovascular diseases, the doctor will periodically assess the patient's need for symptomatic treatment and their response to the medicine, especially if treatment lasts longer than 4 weeks.
During treatment, regular blood tests should be performed in 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 and red blood cell count and platelet count) should be monitored. The doctor will take into account the results of blood tests when deciding to discontinue treatment with Olfen 50 or change the dose.
Follow all instructions given by the doctor or pharmacist carefully, even if they differ from the general information contained in this leaflet.
When not to take Olfen 50:
Like other non-steroidal anti-inflammatory drugs (NSAIDs), Olfen 50 should not be taken by people who may experience an asthma attack, hives, or acute rhinitis after taking acetylsalicylic acid or other prostaglandin synthesis inhibitors.
If any of the above symptoms occur in the patient, they should inform their doctor and not take Olfen 50 until the doctor determines that the medicine is suitable for the patient.
Before starting treatment with Olfen 50, discuss it with a doctor, pharmacist, or nurse.
Tell your doctor if:
Before taking diclofenac, inform your doctor:
Before taking Olfen 50, tell your doctor if the patient has recently undergone or is scheduled to undergo stomach or gastrointestinal surgery, as Olfen 50 may sometimes cause delayed wound healing after surgical procedures.
The occurrence of side effects can be reduced by using the medicine in the smallest effective dose and for no longer than necessary.
Take the smallest dose of Olfen 50 that relieves pain and (or) swelling and use it for the shortest time necessary to minimize the risk of side effects.
If, at any time during treatment with Olfen 50, the patient experiences symptoms indicating heart or blood vessel problems, such as chest pain, shortness of breath, weakness, or slurred speech, they should immediately contact a doctor or hospital emergency department.
In very rare cases (especially at the beginning of treatment), Olfen 50, like other anti-inflammatory drugs, may cause severe allergic skin reactions (e.g., exfoliative dermatitis, Stevens-Johnson syndrome with widespread rash, high fever, and joint pain, and toxic epidermal necrolysis with skin and mucous membrane lesions, high fever, and severe general condition). After the first signs of rash, mucous membrane lesions, or other symptoms of an allergic reaction, the medicine should be discontinued and a doctor consulted.
In rare cases, Olfen 50, like other anti-inflammatory drugs, may cause allergic reactions, including anaphylactic and pseudo-anaphylactic reactions, even if the medicine has not been used before.
Olfen 50 may mask the symptoms of infection (e.g., headache, high temperature), making it more difficult to diagnose and treat the infection. If the patient feels unwell and needs to see a doctor, they should inform the doctor about taking Olfen 50.
If any of the above warnings apply to the patient, they should inform their doctor before taking Olfen 50.
Other special warnings
Concomitant use of Olfen 50 with other systemically acting non-steroidal anti-inflammatory drugs, including selective cyclooxygenase-2 inhibitors, should be avoided.
Before taking the medicine, inform the doctor or pharmacist about the presence of the above-mentioned diseases.
Taking medicines like Olfen 50 may be associated with a small increased risk of heart attack (myocardial infarction) or stroke. Any risk is more likely after taking high doses and long-term treatment. Do not exceed the recommended dose or treatment duration.
The medicine may temporarily inhibit platelet aggregation.
Before taking Olfen 50, tell your doctor if the patient has recently undergone or is scheduled to undergo stomach or gastrointestinal surgery, as Olfen 50 may sometimes cause delayed wound healing after surgical procedures.
In case of heart problems, stroke, or suspected risk of these disorders (e.g., high blood pressure, diabetes, elevated cholesterol levels, or smoking), discuss the treatment with a doctor or pharmacist.
Olfen 50 should not be taken by children and adolescents under 14 years of age.
Elderly patients may be more sensitive to the effects of Olfen 50.
Therefore, they should follow the instructions in the leaflet and the doctor's recommendations carefully and take the minimum dose of the medicine that ensures the disappearance of symptoms.
It is particularly important for patients to report any side effects to their doctor immediately.
Tell your doctor or pharmacist about all medicines the patient is currently taking or has recently taken, as well as any medicines the patient plans to take.
Swallow the tablets whole with water, preferably during a meal. Do not divide or chew the tablet.
If the patient is pregnant or breastfeeding, or thinks they may be pregnant or plans to have a child, they should consult a doctor or pharmacist before taking this medicine.
Do not take Olfen 50 if the patient is in the last three months of pregnancy, as it may harm the unborn child or cause complications during delivery. Olfen 50 may cause kidney and heart problems in the unborn child. It may also increase the risk of bleeding in the patient and child and prolong or delay labor. During the first six months of pregnancy, Olfen 50 should not be taken unless the doctor considers it absolutely necessary. If treatment is necessary during this period or when trying to conceive, the smallest possible dose should be used for the shortest possible time. From the 20th week of pregnancy, taking Olfen 50 may lead to kidney problems in the unborn child, and if taken for more than a few days, it may lead to low amniotic fluid levels (oligohydramnios) or narrowing of the arterial duct (ductus arteriosus) in the child's heart. If treatment is required for a longer period, the doctor may recommend additional monitoring.
Do not breastfeed if taking Olfen 50, as the medicine may harm the baby.
The doctor will discuss the potential risks of taking Olfen 50 during pregnancy and breastfeeding with the patient.
Diclofenac may make it more difficult to conceive. Inform the doctor if the patient plans to conceive or has problems conceiving.
Do not drive or operate any machines if side effects occur while taking Olfen 50, such as vision disturbances, dizziness, vertigo, drowsiness, or other central nervous system disorders.
The medicine contains less than 1 mmol (23 mg) of sodium per coated tablet, which means the medicine is considered "sodium-free".
Always take this medicine exactly as the doctor has told you. If you are not sure, ask your doctor or pharmacist.
The doctor will tell you exactly how to take Olfen 50. Depending on the individual patient's response to treatment, the doctor may recommend a higher or lower dose of the medicine. The general recommendation is for the doctor to adjust the dose individually for each patient and use the smallest effective dose for the shortest possible period. If you feel that the effect of the medicine is too strong or too weak, talk to your doctor.
Do not exceed the recommended dose. It is important to use the smallest effective dose for the shortest time necessary to control symptoms and not to take Olfen 50 for longer than necessary.
Adults
The recommended dose for adults is 1 to 3 tablets per day (50 to 150 mg of the active substance diclofenac sodium), unless the doctor recommends otherwise.
Children and adolescents
Olfen 50 in a dose of 50 mg in the form of coated tablets is not recommended for children and adolescents under 14 years of age.
Patients with diagnosed cardiovascular disease or significant risk factors for cardiovascular events should be treated with diclofenac only after careful consideration and with doses not exceeding 100 mg per day if treatment lasts longer than 4 weeks.
Olfen 50 is contraindicated in patients with kidney failure.
No special studies have been conducted in patients with kidney function disorders, so no specific dosage recommendations can be made. Caution is recommended when administering Olfen 50 to patients with mild to moderate kidney function disorders.
Olfen 50 is contraindicated in patients with liver failure.
No special studies have been conducted in patients with liver function disorders, so no specific dosage recommendations can be made. Caution is recommended when administering Olfen 50 to patients with mild to moderate liver function disorders.
Swallow the tablets whole with water, preferably during a meal. Do not divide or chew the tablet.
Strictly follow the doctor's recommendations. If you are taking Olfen 50 for a long time, regularly consult your doctor to ensure that no side effects have occurred. In case of doubts, consult a doctor or pharmacist.
Overdose of Olfen 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. If a higher dose of Olfen 50 than recommended is taken accidentally, inform a doctor or pharmacist or go to the hospital emergency department immediately. Medical attention may be necessary.
If a dose is missed, take one tablet as soon as possible. If it is almost time for the next dose, take the next tablet at the usual time. Do not take a double dose to make up for the missed dose.
In case of further doubts about taking this medicine, consult a doctor or pharmacist.
Like all medicines, Olfen 50 can cause side effects, although not everybody gets them.
The following side effects have occurred during treatment with Olfen 50:
If you experience any of the above symptoms, inform your doctor immediately.
Medicines like diclofenac may slightly increase the risk of heart attack (myocardial infarction) or stroke. The risk of this is more likely after taking high doses and long-term treatment. Do not exceed the recommended dose or treatment duration.
Inform your doctor if you experience any of the above side effects.
If you experience any side effects, including any not listed in this leaflet, consult your doctor, pharmacist, or nurse.
If Olfen 50 is taken for more than a few weeks, ensure regular medical check-ups to ensure that no unnoticed side effects have occurred.
If you experience any side effects, including any not listed in this leaflet, tell your doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Drug Safety Monitoring, 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.
Reporting side effects will help gather more information on the safety of the medicine.
Keep the medicine out of the sight and reach of children.
Do not use this medicine after the expiry date stated on the carton after EXP. The expiry date refers to the last day of that month.
The batch number is stated on the packaging after "Batch number" or "Lot".
Store below 25°C. Protect from moisture.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines no longer required. This will help protect the environment.
The active substance of the medicine is diclofenac sodium. Each tablet contains 50 mg of diclofenac sodium.
Excipients:
Tablet core: sodium carboxymethylcellulose (type A), microcrystalline cellulose, sodium stearyl fumarate, silicon dioxide, talc, hypromellose.
Coating (gastro-resistant): methacrylic acid and ethyl acrylate copolymer (1:1), dispersion 30%, talc, triethyl citrate.
Coating (colored): hypromellose, macrogol 6000, titanium dioxide (E 171), yellow iron oxide (E 172), quinoline yellow (E104), talc.
Yellow, biconvex, coated tablets with beveled edges, with the inscription "mp" on one side and "O 50" on the other.
Aluminum/PVC/PVDC blister pack in a carton box.
Package of 20 tablets.
Teva B.V.
Swensweg 5,
2031 GA Haarlem,
Netherlands
Merckle GmbH,
Ludwig-Merckle-Strasse 3
89143 Blaubeuren, Germany
Teva Operations Poland Sp. z o.o.,
ul. Mogilska 80,
31-546 Kraków, Poland
For more information, contact the marketing authorization holder's representative:
Teva Pharmaceuticals Polska Sp. z o.o., tel. +48 22 345 93 00
Date of last revision of the leaflet:
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