


Ask a doctor about a prescription for CEFUROXIME STADA 500 mg FILM-COATED TABLETS
Package Leaflet: Information for the User
Cefuroxima Stada 500 mg film-coated tablets EFG
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
Cefuroxima is an antibiotic used in both adults and children. It works by killing the bacteria that cause infections. It belongs to a group of medicines called cephalosporins.
Antibiotics are used to treat bacterial infections and are not effective against viral infections such as flu or the common cold. It is important that you follow the instructions regarding dose, administration, and duration of treatment indicated by your doctor. Do not store or reuse this medication. If you have any leftover antibiotic after finishing treatment, return it to the pharmacy for proper disposal. Do not throw medicines down the drain or into the trash.  | 
Cefuroxima is used to treat infections of:
Cefuroxima can also be used to:
Do not take Cefuroxima Stada:
Be careful with Cefuroxima Stada
Severe skin reactions, including Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), have been reported with cefuroxima treatment. Seek medical attention immediately if you notice any of the symptoms related to these severe skin reactions described in section 4.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Cefuroxima Stada.
Cefuroxima is not recommended for children under 3 months, as safety and efficacy for this age group are unknown.
You should be aware of certain symptoms such as allergic reactions, fungal infections (such as Candida), and severe diarrhea (pseudomembranous colitis) while taking cefuroxima.
This will reduce the risk of possible complications. See “Symptoms to be aware of”in section 4.
If you need a blood test
Cefuroxima may affect the results of blood sugar tests or the Coomb test. If you need a blood test:
Other medicines and Cefuroxima Stada
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
Medicines used to reduce stomach acidity(e.g., antacidsto treat heartburn) may affect the action of cefuroxima.
Probenecid
Oral anticoagulants
Contraceptive pill
Cefuroxima may reduce the effectiveness of the contraceptive pill. If you are taking the contraceptive pill while taking cefuroxima, you should also use barrier contraceptive methods(such as condoms). Consult your doctor.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medicine.
Your doctor will assess the benefit of being treated with cefuroxima against the risk to your child.
Driving and using machines
Cefuroxima may cause dizzinessand other side effects that may impair your ability to be alert.
Cefuroxima Stada contains sodium
This medicine contains less than 23 mg of sodium (1mmol) per tablet; this is, essentially “sodium-free”.
Follow exactly the administration instructions of this medicine indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
Take Cefuroxima Stada after meals.This will help the treatment be more effective.
Swallow the cefuroxima tablets whole with water.
Do not chew, crush, or divide the tablets— this may make the treatment less effective.
Usual dose
Adults
The recommended dose of cefuroxima is 250 mg to 500 mg twice a day, depending on the severity and type of infection.
Use in children and adolescents
The recommended dose of cefuroxima is 10 mg/kg of the child's weight (up to a maximum of 125 mg) to 15 mg/kg of the child's weight (up to a maximum of 250 mg) twice a day, depending on:
Cefuroxima is not recommended in children under 3 months, as safety and efficacy for this patient group are unknown.
Depending on the disease and how you or your child respond to treatment, the initial dose may be adjusted or it may be necessary to administer more than one treatment cycle.
Patients with kidney problems
If you have kidney problems, your doctor may change your dose.
If you take more Cefuroxima Stada than you should
If you take too much cefuroxima, you may experience neurological disorders, in particular, you may have a higher probability of having epileptic seizures (convulsions).
In case of overdose or accidental ingestion, consult the Toxicology Information Service, Tel. 91 562 04 20, indicating the medicine and the amount taken. It is recommended to bring the packaging and the leaflet of the medicine to the healthcare professional.
If you forget to take Cefuroxima Stada
Do not take a double dose to make up for forgotten doses. Simply continue with the next dose as usual.
Do not stop treatment with Cefuroxima Stada without prior advice.
It is important that you complete the entire treatment of cefuroxima.Do not stop it unless your doctor tells you to, even if you have started to feel better. If you do not complete the treatment cycle, the infection may recur.
If you have any other questions about the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Symptoms to be aware of
A small number of people who took cefuroxima presented with a severe allergic reaction or a potentially severe skin reaction. The symptoms of these reactions include:
Common side effects (may affect up to 1 in 10 people):
Common side effects that may appear in blood tests:
Uncommon side effects(may affect up to 1 in 100 people):
Uncommon side effects that may appear in blood tests:
Other side effects
Other side effects have occurred in a very small number of people, but their exact frequency is unknown:
Side effects that may appear in blood tests:
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist, even if it is not listed in this leaflet. You can also report side effects directly through the Spanish Pharmacovigilance System for Human Use Medicines: www.notificaRAM.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
No special storage conditions are required.
Do not use this medicine after the expiry date which is stated on the packaging after EXP. The expiry date is the last day of the month indicated.
Medicines should not be disposed of via wastewater or household waste. Dispose of the packaging and any unused medicine in the pharmacy's SIGRE collection point. Ask your pharmacist how to dispose of the packaging and any unused medicine. This will help protect the environment.
Composition of Cefuroxima Stada
Appearance and packaging of the product
Light blue film-coated tablets, biconvex, capsule-shaped.
Each blister pack contains 10, 15, or 20 film-coated tablets.
Not all pack sizes may be marketed.
Marketing authorization holder and manufacturer
Marketing authorization holder
Laboratorio STADA, S.L.
Frederic Mompou, 5
08960- Sant Just Desvern (Barcelona)
Spain
Manufacturer:
Farmalider S.A.
C/Aragoneses, 2
28108 Alcobendas (Madrid)
Spain
or
Toll Manufacturing Services, S.L.
C/ Aragoneses, 2
28108 – Alcobendas (Madrid)
Spain
or
Laboratorios Atral, S.A.
Rua da Estação, 1 e 1A
2600 726 Castanheira do Ribatejo
Portugal
Date of last revision of this leaflet:February 2023
Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es
The average price of CEFUROXIME STADA 500 mg FILM-COATED TABLETS in November, 2025 is around 9.68 EUR. Prices may vary depending on the region, pharmacy, and whether a prescription is required. Always check with a local pharmacy or online source for the most accurate information.
The best alternatives with the same active ingredient and therapeutic effect.
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for CEFUROXIME STADA 500 mg FILM-COATED TABLETS – subject to medical assessment and local rules.