


Ask a doctor about a prescription for CEFAZOLINE SALA 1 g POWDER AND SOLVENT FOR INJECTABLE SOLUTION
Leaflet: Information for the user
Cefazoline Sala 1 g powder and solvent for injectable solution EFG
Cefazoline
Read the entire leaflet carefully before starting to use this medicine, as it contains important information for you
Contents of the leaflet:
Cefazoline is an antibiotic belonging to the group of cephalosporins.
Antibiotics are used to treat bacterial infections and are not effective against viral infections such as the flu or the common cold.
It is essential to follow the instructions regarding dosage, administration interval, and treatment duration as indicated by your doctor.
Do not store or reuse this medicine. If you have any leftover antibiotic after completing the treatment, return it to the pharmacy for proper disposal. Do not throw away medicines down the drain or in the trash.
This medicine is used to treat the following bacterial infections caused by sensitive pathogens located in:
Do not use Cefazoline Sala:
Warnings and precautions
Be particularly careful with Cefazoline Sala
On rare occasions, blood coagulation disorders may occur during treatment with cefazoline. Additionally, changes in blood coagulation may occur in patients with diseases that can cause or worsen bleeding, such as hemophilia or stomach or intestinal ulcers. In these cases, your blood coagulation will be monitored.
Other medicines and Cefazoline Sala
Inform your doctor or pharmacist if you are using or have recently used any other medicine, including those purchased without a prescription.
Cefazoline should not be administered with:
Pregnancy and breastfeeding
In case of pregnancy or breastfeeding, your doctor will decide whether to use this medicine. Consult your doctor or pharmacist before taking any medicine.
Driving and using machines
Cefazoline generally does not alter the ability to drive vehicles or operate machinery.
Cefazoline Sala contains sodium
Patients on low-sodium diets should note that this medicine contains 51 mg (2.2 mmol) of sodium per gram of cefazoline.
Cefazoline Sala contains lidocaine hydrochloride
This specialty contains lidocaine hydrochloride to increase local tolerance in intramuscular administration. Consequently, it should not be used intravenously or in patients with a history of hypersensitivity to lidocaine.
Lidocaine hydrochloride may produce a positive result in doping tests.
Follow your doctor's instructions for administering this medicine exactly. If in doubt, consult your doctor or pharmacist again.
Your doctor will indicate the appropriate dose and determine the duration of your treatment; do not stop it before completing it or prolong it.
Recommended dose
Adults and children over 12 years old: in the case of mild infections, 500 mg every 8 hours; in moderate to severe infections, 500 mg to 1 g every 6 or 8 hours; in more severe infections, 1 g to 1.5 g every 6 hours.
Children (under 12 years old and over 1 year old): a total daily dose of 25 to 50 mg per kg of body weight, divided into three or four equal doses, is effective in most mild to moderate infections. The total daily dose should not exceed 100 mg/kg, even in severe infections.
Prophylactic treatment
Patients with renal and/or hepatic insufficiency
A dose reduction may be necessary if you have any renal or hepatic impairment. In such cases, inform your doctor so that they can adjust the dose accordingly.
If you use more Cefazoline Sala than you should
In case of accidental overdose, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone: 91 562 04 20, indicating the medicine and the amount taken. Bring the leaflet with you.
If you forget to use Cefazoline Sala
Do not take a double dose to make up for forgotten doses.
If you interrupt treatment with Cefazoline Sala
Do not stop treatment before completing it, as the desired effect will not be achieved. It is very important to treat infections for the recommended time; otherwise, they may worsen.
If you have any other doubts about using this product, ask your doctor or pharmacist.
Like other medicines, this medicine can cause the following side effects, although not all people will experience them.
The incidence of adverse reactions associated with Cefazoline Sala treatment is classified as follows:
Severe allergic reactions(very rare, may affect up to 1 in 10,000 people).
If you have a severe allergic reaction, inform your doctor immediately.
Possible symptoms include:
Other possible side effects
Frequent(may affect up to 1 in 10 people):
Uncommon(may affect up to 1 in 100 people):
Rare(may affect up to 1 in 1,000 people):
Very rare(may affect up to 1 in 10,000 people):
Reporting side effects
If you experience any side effects, consult your doctor or pharmacist, even if they are not listed in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines (https://www.notificaram.es). By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiration date stated on the packaging. The expiration date is the last day of the month indicated.
Store in the outer packaging to protect it from light.
The reconstituted solution with the solvent is stable for 8 hours at a temperature not exceeding 25°C and for 24 hours if stored in the refrigerator (2-8°C).
Do not use this medicine if you notice visible signs of deterioration.
Medicines should not be thrown away down the drain or in the trash. Deposit the packaging and unused medicines in a SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and unused medicines. This will help protect the environment.
Composition of Cefazoline Sala 1 g powder and solvent for injectable solution EFG
The active ingredient is cefazoline. Each vial contains 1 g of cefazoline (DOE) (as cefazoline sodium).
Each ampoule of solvent includes 4 ml of lidocaine hydrochloride solution at 0.5% (20 mg)
Appearance of the product and package contents
Cefazoline Sala 1 g powder and solvent for injectable solution EFG is presented in a glass vial accompanied by a glass ampoule with the solvent.
Each package contains 1 vial with 1 ampoule, and the clinical package contains 100 vials and 100 ampoules.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Laboratorio Reig Jofre S.A.
Gran Capitán, 10 - 08970
Sant Joan Despí (Barcelona)
Spain
Manufacturer:
Laboratorio Reig Jofre, S.A.
C/Jarama 11, Polígono industrial-45007
Toledo-Spain
This leaflet was approved in:December 2024
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/
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This information is intended only for healthcare professionals

Intramuscular administration:reconstitute with the solvent from the ampoule. Shake well until dissolved. Cefazoline should be injected into a area of large muscle mass. It is infrequent to experience pain at the injection site, as the solvent ampoule contains lidocaine.
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