Cefuroxime
Bioracef is an antibiotic used in adults and children over 5 years of age. The medicine works by killing bacteria that cause infections. It belongs to a group of medicines called cephalosporins.
Bioracef may also be used:
If any of the above applies to you, do not take Bioracefwithout consulting your doctor.
Before taking Bioracef, discuss it with your doctor or pharmacist. The film-coated tablets should not be crushed and are therefore not suitable for patients who have difficulty swallowing tablets. During treatment with Bioracef, pay attention to whether you experience symptoms such as allergic reactions, fungal infections (e.g. thrush), and severe diarrhea (pseudomembranous colitis). This will reduce the risk of complications. See "Symptoms to watch out for" in section 4. Severe skin reactions, such as Stevens-Johnson syndrome, toxic epidermal necrolysis, and drug reaction with eosinophilia and systemic symptoms (DRESS) have been reported with cefuroxime treatment. If you notice any of the symptoms associated with severe skin reactions described in section 4, seek medical attention immediately.
Bioracef may affect the results of blood tests for sugar and the Coombs test. If you are going to have a blood test, tell the person taking the sample that you are taking Bioracef.
Tell your doctor or pharmacist about all medicines you are taking now or have recently taken, and about any medicines you plan to take. This includes medicines that are available without a prescription.
Bioracef should be taken after a meal.This will help increase the effectiveness of the treatment.
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine. Your doctor will assess whether the benefits to you of taking Bioracef during pregnancy and breastfeeding outweigh the risks to your baby.
Bioracef may cause dizzinessand other side effects that may impair your alertness. Do not drive or operate machineryif you do not feel well.
The medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means it is essentially "sodium-free".
Always take this medicine exactly as your doctor has told you.If you are unsure, ask your doctor or pharmacist. Dosage
The usual dose of Bioracef is 250 mg to 500 mg twice a day, depending on the severity and type of infection.
The usual dose of Bioracef is 10 mg/kg body weight (not more than 125 mg) to 15 mg/kg body weight (not more than 250 mg) twice a day, depending on the severity and type of infection. Depending on the disease and how the patient responds to treatment, the initial dose may be changed or more than one treatment cycle may be necessary.
If you have kidney problems, your doctor may change the dose of Bioracef. If this applies to you, tell your doctor. Administration
Bioracef tablets should be swallowed whole with water. Do not chew, crush, or divide the tablets- this may reduce the effectiveness of the treatment.
If you take more Bioracef than prescribed, you may experience neurological disorders, particularly an increased risk of seizures (epileptic fits). Contact your doctor or call emergency services immediately.If possible, show the Bioracef packaging.
Do not take a double dose to make up for a missed dose.Take the next dose at the usual time.
It is important not to shorten the prescribed treatment period with Bioracef.Do not stop treatment without your doctor's advice, even if you feel better. Shortening the recommended treatment period may lead to a recurrence of the disease. If you have any further questions about taking this medicine, ask your doctor or pharmacist.
Like all medicines, Bioracef can cause side effects, although not everybody gets them.
A small number of people taking Bioracef have reported an allergic reaction or potentially severe skin reaction. Their symptoms may include:
Common side effects(occurring in less than 1 in 10 patients):
Common side effects that may be seen in blood tests:
Uncommon side effects(occurring in less than 1 in 100 patients):
Uncommon side effects that may be seen in blood tests:
Other side effects occur in a very small number of patients, but the exact frequency is unknown (the frequency cannot be estimated from the available data):
Side effects that may be seen in blood tests:
If you experience any side effects, including any not listed in this leaflet, tell your doctor or pharmacist. Side effects can 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.: +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. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep the medicine out of the sight and reach of children. Store in the original packaging to protect from light and moisture. Do not store above 25°C. Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the month stated. The packaging is marked with "EXP" (expiry date) and "Lot/LOT" (batch number). Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
The tablets are white to cream-colored, elongated, biconvex, with a smooth surface. The pack contains 10 or 14 tablets.
Zakłady Farmaceutyczne POLPHARMA S.A., ul. Pelplińska 19, 83-200 Starogard Gdański, tel. 22 + 48 364 61 01
Zakłady Farmaceutyczne POLPHARMA S.A., Production Plant in Duchnice, ul. Ożarowska 28/30, 05-850 Ożarów Mazowiecki, Zakłady Farmaceutyczne POLPHARMA S.A., ul. Pelplińska 19, 83-200 Starogard Gdański
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