Prospect: information for the user
Zinnat 500 mg granulated for oral suspension
cefuroxima
Read this prospect carefully before starting to take this medicine,because it contains important information for you.
1.What is Zinnat and for what it is used
2.What you need to know before starting to take Zinnat
3.How to take Zinnat
4.Possible adverse effects
5.Storage of Zinnat
6.Contents of the package and additional information
Zinnat is an antibiotic used in both adults and children. It works by eliminating the bacteria that cause infections. It belongs to a group of medications calledcephalosporins.
Antibiotics are used to treat bacterial infections and do not work for viral infections such as the flu or a cold. It is essential to follow the instructions regarding dosage, administration, and treatment duration as indicated by your doctor. Do not store or reuse this medication. If you have leftover antibiotic after treatment, return it to the pharmacy for proper disposal. Do not dispose of medications through the drain or trash. |
Zinnat is used to treat infections of:
Zinnat can also be used to:
Your doctor may analyze the type of bacteria causing your infection and monitor whether the bacteria are sensitive to Zinnat during treatment.
Be especially careful with Zinnat:
Severe skin reactions, including Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), have been reported with cefuroxime 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 Zinnat.
Children
Zinnat is not recommended for children under 3 months,as the safety and efficacy for this age group are unknown.
You should be aware of certain symptoms such as allergic reactions, fungal infections (such asCandida), and severe diarrhea (pseudomembranous colitis) while taking Zinnat. This will reduce the risk of possible complications. See “Symptoms to be aware of” in section 4.
If you need a blood test
Zinnat may affect the results of blood sugar levels in blood tests, or theCoombs test. If you need a blood test:
Other medicines and Zinnat
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medicine.
Medicines used toreduce stomach acid(e.g.,antacidsfor treatingheartburn) may affect the mechanism of action of Zinnat.
Probenecid
Oral anticoagulants
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.
Driving and operating machinery
Zinnatmay cause dizzinessand other adverse effects that may impair your ability to be alert.
Zinnat 500 mg granulated for oral suspension contains aspartame (E951), sucrose, propylene glycol (E1520), and benzyl alcohol (E1519).
This medicine contains 12.2 g of sucrose in each sachet, which should be taken into account in patients with diabetes mellitus. If your doctor has told you that you have a certain sugar intolerance, consult with them before taking this medicine.
Patients with hereditary fructose intolerance, glucose absorption problems, or saccharase-isomaltase deficiency should not take this medicine.
This medicine contains 0.084 g ofaspartame(E951) in each sachet. Aspartame contains a source of phenylalanine that may be harmful in cases of phenylketonuria (PKU), a rare genetic disorder in which phenylalanine accumulates because the body is unable to eliminate it correctly.
This medicine contains 18 mg of benzyl alcohol (E1519) in each sachet.
Benzyl alcohol may cause allergic reactions.
Consult your doctor or pharmacist if you have liver or kidney disease, are pregnant or breastfeeding. This is because large amounts of benzyl alcohol may accumulate in the body and cause adverse effects (metabolic acidosis).
This product should not be used for more than one weekin children under 3 years of age unless advised by your doctor or pharmacist.
This medicine contains 24 mg of propylene glycol (E1520) in each sachet.
?Check with your doctorthatZinnat is suitable for you.
Take Zinnat after meals.This will help make the treatment more effective.
To prepare Zinnat sachets, follow the step-by-step instructions inInstructions for reconstitution,at the end of this leaflet.
The recommended dose is
Adultsand children with a weight of 40 kg or more
The recommended dose of Zinnat is 250 mg to 500 mg twice a day, depending on the severity and type of infection.
Children weighing less than 40 kg
Children weighing less than 40 kg should preferably be treated with Zinnat granulated suspension for oral use in a bottle orin sachets.
The recommended dose of Zinnat is 10 mg/kg of the child's weight (up to a maximum of 250 mg) to 15 mg/kg of the child's weight (up to a maximum of 250 mg) twice a day, depending on:
Zinnat is not recommended for children under 3 months,since the safety and efficacy for this group of patients is unknown.
Depending on the disease and how you or your child responds 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 Zinnat than you should
If you take too much Zinnat, you may experience neurological disturbances, particularly you may have a higher probability of havingseizures (convulsions).
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological Information Service, phone: 91 562 04 20, indicating the medication and the amount ingested.
If you forget to take Zinnat
Do not take a double dose to compensate for the missed doses.Simply continue with the next dose as usual.
If you interrupt treatment with Zinnat
Do not interrupt treatment with Zinnat without prior advice.
It is essential that you complete the entire Zinnat treatment.Do not interrupt 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 doubts about the use of this medication, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everyone will experience them.
Symptoms to be aware of
A small number of people who took Zinnat experienced a severe allergic reaction or a potentially serious skin reaction. The symptoms of these reactions include:
Other symptoms to be aware of while taking Zinnat:
Frequent side effects
May affectup to 1 in 10people:
Frequent side effects that may appear in blood tests:
Rare side effects
May affectup to 1 in 100people:
Rare 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 side effects
If you experience any type of side effect, consult your doctor or pharmacist even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through theSpanish System for the Pharmacovigilance of Medicines for Human Use:https://www.notificaram.es.By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medication out of the sight and reach of children.
Store in the original packaging. Do not store at a temperature above 30°C.
The reconstituted suspension should be taken immediately.
Do not take Zinnat if it shows any visible sign of deterioration.
Do not use this medication after the expiration date that appears on the packaging after the letters CAD/EXP. The expiration date is the last day of the month indicated.
Medications should not be disposed of through drains or in the trash. Dispose of the packaging and medications you no longer need at the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. By doing so, you will help protect the environment.
- The active ingredient is 500 mg of cefuroxime (as cefuroxime axetil) per dose.
-The other components are: aspartame (E951), xanthan gum, potassium acesulfame (E950), povidone K30, stearic acid, sucrose, tutti-frutti flavoring (contains propylene glycol (E1520)and benzyl alcohol (E1519)), and purified water.
See section 2 for important information about some of the components of Zinnat.
Appearance of the product and contents of the package
Zinnat 500 mg granulated for oral suspension is supplied in sachets.The sachets are inside a cardboard package.
Only some package sizes may be marketed.
Marketing authorization holder and manufacturer
Marketing authorization holder
BEXAL FARMACÉUTICA, S.A.
Centro Empresarial Parque Norte
Edificio Roble
C/ Serrano Galvache, 56
28033 Madrid
Spain
Manufacturer
GlaxoSmithKline Trading Services Limited
12 Riverwalk
Citywest Business Campus
Dublín 24
D24 YK11
Ireland
or
Lek Pharmaceuticals d. d.
Verovškova ulica 57
Ljubljana, 1526
Slovenia
Last review date of this leaflet:September 2023.
The detailed information about this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) http://www.aemps.gob.es
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Instructions for reconstitution
Instructions for preparing the suspension from the sachets
1.Empty the granulated contentfrom the sachet into aglass.
2.Adda small amount of cold water.
3.Shake wellanddrink immediately.
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