
Ask a doctor about a prescription for Bioracef
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 the patient, they should not take Bioracefwithout consulting a doctor.
Before starting treatment with Bioracef, the patient should discuss it with their 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, the patient should be aware of the following symptoms: 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 the patient notices any of the symptoms associated with severe skin reactions described in section 4, they should contact their doctor immediately.
Bioracef may affect the results of blood tests for sugar and the Coombs test. If the patient is to have a blood test, they should tell the person taking the blood samplethat they are taking Bioracef.
The patient should tell their doctor or pharmacist about all medicines they are taking, or have recently taken, and about any medicines they plan to take, including those obtained without a prescription.
Bioracef should be taken after a meal.This will help increase the effectiveness of the treatment.
If the patient is pregnant, breastfeeding, or thinks they may be pregnant, or are planning to have a baby, they should ask their doctor or pharmacist for advice before taking this medicine. The doctor will assess whether the benefits of taking Bioracef during pregnancy and breastfeeding outweigh the risks to the baby.
Bioracef may cause dizzinessand other side effects that may impair the patient's alertness. The patient should not drive or operate machineryif they do not feel well.
The medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means it is essentially "sodium-free".
This medicine should always be taken exactly as advised by the doctor. If the patient is unsure, they should ask their 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 the patient has kidney problems, the doctor may change the dose of Bioracef. If this applies to the patient, they should tell their doctor. Administration The Bioracef tablets should be swallowed whole with water. The tablets should not be chewed, crushed, or divided- this may reduce the effectiveness of the treatment.
If the patient takes more Bioracef than they should, they may experience neurological disorders, in particular, the risk of seizures (epileptic fits) increases. The patient should contact their doctor or call the emergency services immediately. If possible, they should show the Bioracef packaging.
The patient should not take a double dose to make up for a missed dose.They should take the next dose at the usual time.
It is important not to shorten the prescribed treatment period with Bioracef.The patient should not stop treatment without their doctor's advice, even if they feel better. Shortening the recommended treatment period may lead to a recurrence of the disease. If the patient has any further questions about taking this medicine, they should ask their 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 a potentially severe skin reaction. The symptoms may be:
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 the patient experiences any side effects, including any not listed in this leaflet, they should tell their doctor or pharmacist. Side effects can be reported directly to the Department of Drug Safety, Office for Registration of Medicinal Products, Medical Devices, and Biocides, 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, more information can be gathered on the safety of the medicine.
The medicine should be stored out of 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 notation on the packaging after the abbreviation EXP means the expiry date, and after the abbreviation Lot/LOT means the batch number. Medicines should not be disposed of via wastewater or household waste. The patient should ask their pharmacist how to dispose of medicines they no longer use. 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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Discuss dosage, side effects, interactions, contraindications, and prescription renewal for Bioracef – subject to medical assessment and local rules.