
Ask a doctor about a prescription for Zinnat
Cefuroxime
Zinnat and Zinadol are different trade names for the same medicine.
Zinnat is an antibiotic used in adults and children. The medicine works by killing bacteria that cause infections. It belongs to a group of medicines called cephalosporins.
Zinnat may also be used:
Your doctor may check what type of bacteria caused your infection and check if the bacteria are sensitive to Zinnat during treatment.
Severe skin side effects have been reported with cefuroxime, such as:
Stevens-Johnson syndrome, toxic epidermal necrolysis, and drug reaction with eosinophilia and systemic symptoms (DRESS). If you notice any of the symptoms related to severe skin reactions described in section 4, you should seek medical advice immediately.
Before taking Zinnat, you should discuss it with your doctor or pharmacist.
Zinnat is not recommended for use in children under 3 months of age, as the safety and efficacy of the medicine in this age group are not known.
During treatment with Zinnat, you should be aware of the possibility of side effects such as allergic reactions, fungal infections (e.g., thrush), and severe diarrhea (pseudomembranous colitis). This will reduce the risk of complications. See "Side effects to look out for" in section 4.
Zinnat may affect the results of blood tests for sugar in the blood and a blood test called the Coombs test. If you are going to have a blood test, you should:
You should tell your doctor or pharmacist about all the medicines you are taking now or have taken recently, as well as any medicines you plan to take.
If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a baby, you should consult your doctor or pharmacist before taking this medicine.
Zinnat may cause dizzinessand other side effects that may impair your alertness.
Zinnat contains methyl parahydroxybenzoate (E 218) and propyl parahydroxybenzoate (E 216)
Zinnat contains 0.00506 mg of sodium benzoate in each tablet.
The medicine contains less than 1 mmol (23 mg) of sodium in each tablet, which means the medicine is considered "sodium-free".
This medicine should always be taken exactly as advised by your doctor or pharmacist. If you are unsure, you should consult your doctor or pharmacist again.
Zinnat is available in the following strengths: 125 mg, 250 mg, 500 mg.
Zinnat should be taken after a meal. This will help increase the effectiveness of the treatment.
Zinnat tablets should be swallowed whole with water.
Tablets should not be chewed, crushed, or divided- this may reduce the effectiveness of the treatment.
The recommended dose of Zinnat is 250 mg to 500 mg twice daily, depending on the severity and type of infection.
Children under 40 kg should be treated with Zinnat oral suspension.
The recommended dose of Zinnat is 10 mg/kg body weight (not more than 250 mg) to 15 mg/kg body weight (not more than 250 mg) twice daily, depending on:
Zinnat is not recommended for use in children under 3 months of age, as the safety and efficacy of the medicine in this age group are not known.
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 Zinnat.
If you take more Zinnat than prescribed, you may experience neurological disorders, in particular, the risk of seizures (epileptic fits) increases.
You should not take a double dose to make up for a missed dose. You should take the next dose at the usual time.
It is important not to shorten the prescribed treatment period with Zinnat. You should 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 doubts about taking this medicine, you should consult your doctor or pharmacist.
Like all medicines, Zinnat can cause side effects, although not everybody gets them.
A small number of people taking Zinnat have reported an allergic reaction or a potentially severe skin reaction. The symptoms may be:
Widespread skin changes with blisters and peeling skin(may be a sign of Stevens-Johnson syndrome or toxic epidermal necrolysis - Lyell's disease).
May affect up to 1 in 10 people:
Common side effects that may be seen in blood tests:
May affect up to 1 in 100 people:
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:
Side effects that may be seen in blood tests:
If you experience any side effects, including any side effects not listed in this leaflet, you should tell your doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Pharmacovigilance of the 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
By reporting side effects, you can help provide more information on the safety of this medicine.
The medicine should be stored out of sight and reach of children.
Do not store above 30°C.
Do not use if the tablets are crushed or damaged in any way.
Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the month.
Medicines should not be disposed of via wastewater or household waste. You should ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
The active substance of Zinnat is cefuroxime: each film-coated tablet contains 500 mg of cefuroxime in the form of cefuroxime axetil.
The other ingredients of Zinnat are: microcrystalline cellulose, sodium croscarmellose (type A), sodium lauryl sulfate, hydrogenated vegetable oil, anhydrous colloidal silica; coating: hypromellose, propylene glycol, methyl parahydroxybenzoate (E 218), propyl parahydroxybenzoate (E
The tablets are white, oblong, biconvex, smooth on one side, and with the inscription "GXEG2" on the other. The tablets are packaged in Al/Al blisters, in a cardboard box. The pack contains 14 tablets.
For more detailed information, you should contact the marketing authorization holder or the parallel importer.
GlaxoSmithKline Monoprosopi A.E.B.E.
Leof. Kifisias 266
152 32 Chalandri
Athens, Greece
GlaxoSmithKline Trading Services Limited, 12 Riverwalk, Citywest Business Campus, D24 YK11
Dublin, Ireland
Delfarma Sp. z o.o.
ul. Św. Teresy od Dzieciątka Jezus 111
91-222 Łódź
Delfarma Sp. z o.o.
ul. Św. Teresy od Dzieciątka Jezus 111
91-222 Łódź
Marketing authorization number in Greece, the country of export: 41698/5-11-2009
Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, France, Hungary, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Poland, Romania, Slovakia, Slovenia, Spain, United Kingdom (Northern Ireland) - Zinnat
Germany - Elobact
Greece - Zinadol
Italy - Oraxim
Portugal - Zipos
Portugal - Zoref
Date of revision of the leaflet:24.10.2024
[Information about the trademark]
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Discuss dosage, side effects, interactions, contraindications, and prescription renewal for Zinnat – subject to medical assessment and local rules.