Zolecin 1000 mg Powder for solution for injection/infusion is indicated for the treatment of the following infections caused by cefazolin-susceptible micro-organisms:

•     Skin and soft tissue infections
•     Bone and joint infections.

Perioperative prophylaxis. For surgical operations with increased risk of infections with anaerobic pathogens, e.g. colorectal surgery, a combination with an appropriate drug with activity against anaerobes is recommended.

The use of cefazolin should be limited to cases where parenteral treatment is needed.

Susceptibility of causative organism to the treatment should be tested (if possible), although therapy may be initiated before the results are available.

Consideration should be given to official guidance on the appropriate use of antibacterial agents.

The dosage as well as the method of administration are dependent on the location and severity of the infection and on the clinical and bacteriological progress. Local therapeutic guidance should be taken into consideration.

Adults and adolescents (above 12 years of age and ≥ 40 kg bodyweight)

•     Infections caused by sensitive micro-organisms: 1000 mg - 2000 mg cefazolin per day divided into 2-3 equal doses.
•     Infections caused by moderately sensitive micro-organisms: 3000 mg - 4000 mg cefazolin per day divided into 3-4 equal doses.

In severe infections, doses of up to 6000 mg per day can be administered in three or four equal doses (one dose every 6 or 8 hours).

Special dosage recommendations

Peri-operative prophylaxis

•     To prevent postoperative infection in contaminated or potentially contaminated surgery, recommended doses are: 1000 mg cefazolin 30 – 60 minutes before surgery.
•     In case of long surgical interventions (2 hours or more) additional 500 – 1000 mg cefazolin during the intervention.
•     Prolonged continuation of administration beyond the surgical intervention should be supported by national official guidance.

It is important that (1) the preoperative dose be given just (30 min to 1 hour) prior to the start of surgery so that adequate antibiotic levels are present in the serum and tissues at the time of initial surgical incision; and (2) cefazolin be administered, if necessary, at appropriate intervals during surgery to provide sufficient levels of the antibiotic at the anticipated moments of greatest exposure to infective organisms.

Adult patients with renal impairment

Adults with renal impairment may need a lower dose to avoid overlapping.

This lower dose may be guided by determining blood levels. If not possible, the dosage can be established based on creatinine clearance.

 

Zolecin maintenance therapy in patients with renal impairment

Creatinine clearance (ml/min)	Serum creatinine (mg/dl)	Dosage
≥ 55	≤ 1.5	Normal dose and normal dosage interval
35-54	1.6-3.0	Normal dose, every 8 hours
11-34	3.1-4.5	Half of the normal dose every 12 hours
≤ 10	≥ 4.6	Half of the normal dose every 18 – 24 hours

In haemodialysis patients, the treatment schedule depends on the dialysis conditions.

 

Guidelines for adult dosage

Reconstitution table for intravenous injection

Content per vial	Minimum amount of diluent to be added	Approximate concentration
1000 mg	4 ml	220 mg/ml

 

Paediatric population:

Infections caused by sensitive microorganisms

A dose of 25-50 mg / kg body weight divided into two to four equal doses per day is recommended (one dose every 6, 8 or 12 hours).

Infections caused by moderately sensitive microorganisms

A dose of up to 100 mg / kg body weight divided in three or four equal doses is recommended (one dose every 6 or 8 hours).

Prematures and infants below the age of 1 month

Since safety of use in prematures and infants below the age of one month has not been determined, the use of Zolecin 1000 mg Powder for solution for injection/infusion in these patients is not recommended. See also section 4.4.

Guidelines for paediatric dosage

Intravenous injection

1000 mg vial: The content of 1 vial (1000 mg cefazolin) is dissolved in 4 ml of a compatible solvent (i.e. concentration approx. 220 mg/ml). The respective volume of this solution to be used is indicated in Table 1 in addition to the dose in mg.

Intravenous administration of lidocaine solutions must be strictly avoided.

 

Table 1: Appropriate volumes for intravenous for paediatric patients for Zolecin 1000 mg powder for solution for injection/infusion.

Body weight	Strength	5 kg	10 kg	15 kg	20 kg	25 kg
Divided dose every 12 hours at 25 mg/kg body weight/day	1000 mg vial	63 mg;	125 mg;	188 mg;	250 mg;	313 mg;
		0.29 ml	0.57 ml	0.85 ml	1.14 ml	1.42 ml
Divided dose every 8 hours at 25 mg/kg body weight/day	1000 mg vial	42 mg ;	85 mg;	125 mg;	167 mg;	208 mg;
		0.19 ml	0.439 ml	0.57 ml	0.76 ml	0.94 ml
Divided dose every 6 hours at 25 mg/kg body weight/ day	1000 mg vial	31 mg;	62 mg;	94 mg;	125 mg;	156 mg;
		0.14 ml	0.28 ml	0.43 ml	0.57 ml	0.71 ml
Divided dose every 12 hours at 50 mg/kg body weight/day	1000 mg vial	125 mg;	250 mg;	375 mg;	500 mg;	625 mg;
		0.57 ml	1.14 ml	1.7 ml	2.27 ml	2.84 ml
Divided dose every 8 hours at 50 mg/kg body weight/day	1000 mg vial	83 mg;	166 mg;	250 mg;	333 mg;	417 mg;
		0.438 ml	0.75 ml	1.14 ml	1.51 ml	1.89 ml
Divided dose every 6 hours at 50 mg/kg body weight/day	1000 mg vial	63 mg;	125 mg;	188 mg;	250 mg;	313 mg;
		0.29 ml	0.57 ml	0.85 ml	1.14 ml	1.42 ml
Divided dose every 8 hours at 100 mg/kg body weight/day	1000 mg vial	167 mg;	333 mg;	500 mg;	667 mg;	833 mg;
		0.76 ml	1.51 ml	2.27 ml	3.03 ml	3.79 ml
Divided dose every 6 hours at 100 mg/kg body weight/day	1-g vial	125 mg;	250 mg;	375 mg;	500 mg;	625 mg;
		0.57 ml	1.14 ml	1.7 ml	2.27 ml	2.84 ml

For volumes inferior of 1 ml, please use a 0.5 ml syringe for better accuracy of dosing.

Intravenous infusion

The dosage can be given as intravenous infusion, using the reconstituted and further diluted solution (10 mg/ml) described in section 6.6.

Paediatric patients with renal impairment

Children with renal impairment (like adults) may need a lower dose to avoid overlapping.

This lower dose may be guided by determining blood levels. If not possible, the dosage may be determined based on creatinine clearance, according to the following guidelines.

In children with moderate impairment (creatinine clearance 40 – 20 ml/min), 25% of the normal daily dose, divided into doses every 12 hours are sufficient.

In children with severe impairment (creatinine 20 – 5 ml/min) will be 10% of normal daily dose, given every 24 hours are sufficient.

All these guidelines are valid after an initial starting dose. See also section 4.4.

Elderly patients:

In elderly patients with normal renal function no dosage adjustment is necessary.

Method of administration

Zolecin 1000 mg Powder for solution for injection/infusion may be administered by slow intravenous injection or intravenous infusion after dilution.

The volume and type of diluent to be used for the reconstitution is dependent upon the method of administration.

For instructions on the reconstitution of the medicinal product before administration, please see section 6.6.

If lidocaine is used as a solvent, the resulting solution should never be administered intravenously (see section 4.3).

Duration of treatment

The duration of the treatment depends on the severity of the infection as well as on the clinical and bacteriological progress.

Hypersensitivity to cefazolin sodium. Patients with known hypersensitivity to cephalosporin antibiotics. History of severe hypersensitivity (e.g. anaphylactic reaction) to any other type of beta-lactam antibacterial agent (penicillins, monobactams and carbapenems).

Warnings

In case of any known hypersensitivity to penicillins or other beta-lactam antibiotics, attention is to be paid to a possible cross-sensitivity (see section 4.3).

As with all beta-lactam antibacterial agents, serious and occasionally fatal hypersensitivity reactions have been reported. In case of severe hypersensitivity reactions, treatment with cefazolin must be discontinued immediately and adequate emergency measures must be initiated.

Before beginning treatment, it should be established whether the patient has a history of severe hypersensitivity reactions to cefazolin, to other cephalosporins or to any other type of beta-lactam agent. Caution should be used if cefazolin is given to patients with a history of non-severe hypersensitivity to other beta-lactam agents.

Cefazolin should be administered only with special caution to patients with allergic reactivity (e. g. allergic rhinitis or bronchial asthma) as the risk for a serious hypersensitivity reaction is increased.

Antibacterial agent-associated pseudomembranous colitis has been reported with use of cefazolin and may range in severity from mild to life threatening. This diagnosis should be considered in patients with diarrhoea during or subsequent to the administration of cefazolin (see section 4.8). Discontinuation of therapy with cefazolin and the administration of specific treatment for Clostridium difficile should be considered. Medicinal products that inhibit peristalsis should not be given.

Paediatric use: As there are no sufficient experiences available so far, Zolecin 1000 mg Powder for solution for injection/infusion must not be applied to new-borns and babies in the first month of life.

Precautions

In case of a renal insufficiency with a glomerular filtration rate under 55 ml/min, an accumulation of cefazolin must be taken into consideration. Therefore, the dosage has to be reduced accordingly or the dosage interval has to be prolonged (see section 4.2).

In patients with renal impairment the use of cefazolin may be associated with seizures.

Prolonged prothrombin time may occur in patients with renal or hepatic impairment or poor nutritional state, as well as in patients receiving a protracted course of antimicrobial therapy, and patients previously stabilised on anticoagulant therapy. In these patients the prolongation of prothrombin time has to be monitored under treatment with cefazolin since it can very rarely cause plasmatic blood coagulation diseases (see sections 4.5 and 4.8). Therefore, INR (International Normalised Ratio) has to be measured regularly in patients with diseases which can cause haemorrhages (e.g. gastro-intestinal ulcers) as well as in patients with coagulation defects (inherited: e.g. haemophilia; acquired: e.g. by parenteral feeding, malnutrition, disordered liver or renal function or thrombocytopenia; caused by drugs: e.g. by heparin or other oral anticoagulants). Vitamin K can be substituted (10 mg per week) if necessary.

Long-term and repeated administration can lead to overgrowth of resistant organisms.

If superinfection occurs during therapy, appropriate measures should be taken.

Effects on laboratory tests

In rare cases, the non-enzymatic urine sugar test and the Coombs test can show false positive results.

Zolecin contains sodium

Zolecin contains sodium. Each vial of Zolecin 1000 mg Powder for Solution for Injection/Infusion contains 50.6 mg sodium per vial, equivalent to 2.53% of the WHO recommended maximum daily intake of 2 g sodium for an adult.

Anticoagulants

Cephalosporins may very rarely cause bleeding disorders (see 4.4). During concomitant use with oral anticoagulants (for e.g. warfarin or heparin) in high doses, the coagulation parameters should be monitored.

Vitamin K1

Some cefalosporins such as cefamandol, cefazolin and cefotetan can cause interference in the metabolism of vitamin K1, especially in cases of vitamin K1 deficiency. This may require vitamin K1 supplementation.

Probenecid

Due to its inhibitory effect on the renal diuresis, the administration of probenecid induces a higher concentration and a longer retention time of cefazolin in the blood.

Nephrotoxic substances

It cannot be excluded that the nephrotoxic effect of antibiotics (e.g. aminoglycosides, colistin, polymyxin B), iodine-containing contrast agents, organoplatinum compounds, high-dose methotrexate, some antivirals (e.g. aciclovir, foscarnet), pentamidine, ciclosporin, tacrolimus and diuretics (e.g. furosemide) is increased.

When co-administered with cefazolin, kidney function tests must be carefully monitored.

Pregnancy

Cefazolin reaches the embryo/foetus via the placenta. Animal studies do not indicate direct or indirect harmful effects with respect to reproductive toxicity. There is not sufficient experience in the human use of cefazolin. As a precautionary measure, it is preferable to avoid the use of Zolecin 1000 mg Powder for solution for injection/infusion during pregnancy, if the use is not necessary.

Breast-feeding

Cefazolin passes into breast milk in very low concentrations, and therefore at therapeutic doses, no effects on the infant are expected. If diarrhoea or candidosis occurs in the infant during breastfeeding, the mother should stop breastfeeding or cefazolin should be withdrawn.

Fertility

Animal studies have shown no effects on fertility.

 

Cefazolin has no or negligible influence on the ability to drive and use machines.

Dependent on the dose and duration of the treatment, patients are expected to experience one or several of the adverse reactions mentioned below.

System Organ Class	Common (≥ 1/100 to <1/10)	Uncommon (≥ 1/1,000 to <1/100)	Rare (≥ 1/10,000 to < 1/1,000)	Very rare (< 1/10,000)	Not known (cannot be estimated from available data)*
Infections and infestations		Oral candidiasis (prolonged use).	Genital Candidiasis (monoliasis), vaginitis
Blood and lymphatic system disorder			Increase or decrease in blood glucose concentration (hyperglycaemia or hypoglycaemia). Leukopenia, Granulocytopenia, neutropenia, thrombocytopenia, leukocytosis, granulocytosis, monocytosis, lymphocytopenia, basophilia and eosinophilia were observed in blood counts. These effects are rare and reversible.	Coagulation (blood clotting) disorders and bleeding as a consequence. At risk for these side effects are patients with a deficiency of vitamin K or other blood clotting factors, or patients on artificial nutrition, inadequate diet, impaired liver and renal function, thrombocytopenia and patients with disorders or diseases that cause bleeding (e.g., haemophilia, stomach and duodenal ulcers). Also see sections 4.4 and 4.5. Decreased haemoglobin and/or hematocrit, anaemia, agranulocytosis, aplastic anaemia, pancytopenia and hemolytic anaemia.
Immune system disorders		Erythema, erythema multiforme, exanthema, urticaria, reversible local permeability of the blood vessels, joints, or mucous membranes (angioedema), drug-induced fever and interstitial pneumonia or pneumonitis	Toxic epidermal necrolysis (Lyell's syndrome), Stevens-Johnson syndrome.	Anaphylactic shock, swelling of the larynx with narrowing of the airways, increased heart rate, shortness of breath, falling blood pressure, swollen tongue, anal pruritus, genital pruritus, face edema.
Nervous system disorders		Seizures (in patients with renal dysfunction, with inappropriate high treated doses).	Dizziness, malaise, fatigue. Nightmares, vertigo, hyperactivity, nervousness or anxiety, insomnia, drowsiness, weakness, hot flushes, disturbed colour vision, confusion and epileptogenic activity.
Respiratory, thoracic and mediastinal disorders			Pleural effusion, chest pain, dyspnoea or respiratory distress, cough, rhinitis.
Gastrointestinal disorders	Loss of appetite, diarrhoea, nausea and vomiting. These symptoms are usually moderate and often disappear during or after treatment.			Pseudomembranous colitis (see section 4.4)
Hepatobiliary disorders			Temporary increase in serum concentrations of AST, ALT, gamma GT, bilirubin and/or LDH and alkaline phosphatase, transient hepatitis, transient cholestatic jaundice.
Renal and urinary disorders			Nephrotoxicity, interstitial nephritis, undefined nephropathy, proteinuria, temporary increase in blood urea nitrogen (BUN) usually in patients treated concomitantly with other potential nephrotoxic medicines.
General		Intravenous administration may cause thrombophlebitis.

 

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via:

•     Saudi Arabia

The National Pharmacovigilance Centre (NPC)

SFDA Call Center: 19999

E-mail: npc.drug@sfda.gov.sa

Website: https://ade.sfda.gov.sa

•     Other GCC States

Please contact the relevant competent authority.

Symptoms of an overdose are headache, vertigo, paraesthesia, central nervous states of agitation, myoclonia and convulsions.

In case of poisoning, elimination accelerating measures are indicated. A specific antidote does not exist. Cefazolin can be haemodialysed.

 

Pharmacotherapeutic group: Other beta-lactam antibacterials, first generation cephalosporins.

ATC code: J01DB04

Cefazolin is a bactericidal cephalosporin antibiotic of the first generation for parenteral administration.

Cephalosporins inhibit cell wall synthesis (in the growth stage) through blocking the penicillin-binding proteins (PBPs) like transpeptidases. The outcome is a bactericidal action.

PK/PD relationship

For cephalosporins, the most important pharmacokinetic-pharmacodynamic index correlating with in vivo efficacy has been shown to be the percentage of the dosing interval that the unbound concentration remains above the minimum inhibitory concentration (MIC) of cefazolin for individual target species (i.e. %T>MIC).

Mechanisms of resistance

Resistance to cefazolin can rest upon one of the following mechanisms:

• Inactivation by beta-lactamases: cefazolin has a high stability against penicillinases of gram-positive bacteria, but only a low stability against plasmid-coded betalactamases, e.g. extended-spectrum beta lactamases or chromosomal-coded betalactamases of AmpC-type.
• Reduced affinity of the PBPs to cefazolin: the acquired resistance of pneumococci and other streptococci is caused by modifications of the PBPs due to mutations. The resistance of methicillin (oxacillin)-resistant Staphylococci is due to the formation of an additional PBP with a lower affinity to cefazolin.
• Insufficient penetration of cefazolin through the outer cell wall of gram-negative bacteria can lead to an insufficient inhibition of the PBPs.
• Cefazolin can be transported outside the cell through efflux pumps.

There is a partial or total cross-resistance of cefazolin with other cephalosporins and penicillins.

Breakpoints

The following breakpoints have been established by the European Committee for Antimicrobial Susceptibility Testing (EUCAST) Clinical MIC Breakpoints (Version 8.1, valid from 2018-05-15).

Species	Susceptible (≤)	Resistant (>)
Staphylococcus spp.	Note A	Note A
Streptococcus groups A, B, C and G	Note B	Note B
Viridans group streptococci	0.5 mg/L	0.5 mg/L
PK/PD (Non-species related) breakpoints	1 mg/L	2mg /L

^A Susceptibility of staphylococci to cephalosporins is inferred from the cefoxitin susceptibility except for cefixime, ceftazidime, ceftazidime-avibactam, ceftibuten and ceftolozane-tazobactam, which do not have breakpoints and should not be used for staphylococcal infections. Some methicillin-resistant S. aureus are susceptible to ceftaroline and ceftobiprole.

^B The susceptibility of streptococcus groups A, B, C and G to cephalosporins is inferred from the benzylpenicillin susceptibility.

Microbiological susceptibility

The following table shows clinically relevant pathogens classified as sensitive or resistant on the basis of in vitro and in vivo data. Cefazolin is effective against some species in vitro, but not clinically, thus these species are classified here as resistant.

The prevalence of acquired resistance may vary geographically and with time for selected species and local information is desirable, particularly when treating severe infections. If necessary, expert advice should be sought when the local prevalence of resistance is such that the efficacy of cefazolin is questionable. Especially in case of severe infections or failure of therapy, a microbiological diagnosis including identification of the microorganism and its susceptibility to cefazolin should be conducted.

Commonly susceptible species

Aerobe Gram-positive

• Staphylococcus aureus (methicillin-sensitive)

 

Species for which acquired resistance may be a problem

Aerobe Gram-positive

• Group A, B, C and G beta-haemolytic streptococci
• Staphylococcus epidermidis (methicillin-sensitive)
• Streptococcus pneumoniae

 

Aerobe Gram-negative

• Haemophilus influenzae

Inherently resistant organisms

Aerobe Gram-positive

Staphylococcus aureus, methicillin-resistant

Aerobe Gram-negative

•     Citrobacter spp.
•     Enterobacter spp.
•     Klebsiella pneumoniae
•     Morganella morganii
•     Proteus mirabilis
•     Proteus stuartii
•     Proteus vulgaris
•     Pseudomonas aeruginosa
•     Serratia spp.

Absorption

Cefazolin is administered parenterally. After administration of 500 mg intramuscular injection, maximum serum levels obtained after approximately an hour were 20-40 micrograms/ml. After administration of 1000 mg maximum serum levels of 37-63 micrograms/ml were obtained. In one continuous intravenous infusion of cefazolin study in healthy adults at doses of 3.5 mg / kg for one hour (approx 250 mg) followed by 1.5 mg/kg for the next two hours (approx 100 mg) a stable serum concentration of approx. 28 micrograms/ml was demonstrated in the third hour. The following table shows the mean serum concentration of cefazolin after intravenous injection of a single dose of 1000 mg.

 

Serum concentration µg/ml after intravenous administration of 1000 mg
5 min	15 min	30 min	1 hr	2 hr	4 hr
188.4	135.8	106.8	73.7	45.6	16.5

 

Distribution

Cefazolin for 70% - 86% bound to plasma proteins. The volume of distribution is approximately 11 L/1.73 m². When cefazolin is administered to patients without obstruction of the bile ducts the antibiotic levels 90 – 120 minutes after administration were generally higher than antibiotic levels in the serum.

Conversely, where obstruction exists the concentrations of antibiotic in the bile were much lower than serum levels. After administration of therapeutic doses in patients with inflamed meninges, varying concentrations of cefazolin from 0 to 0.4 micrograms/ml were measured in cerebrospinal fluid. Cefazolin can easily pass through inflamed synovial membranes and the antibiotic concentration achieved in joints is similar to serum levels.

Biotransformation

Cefazolin is not metabolised.

Elimination

The serum half-life is about 1 hour 35 minutes. Cefazolin is excreted in a microbiologically active form in the urine. Approximately 56 – 89% of an intramuscular dose of 500 mg is excreted in the first six hours, 80% to almost 100% is excreted within 24 hours. After intramuscular administration of 500 mg and 1000 mg urine levels can reach 500 – 4000 µg/ml. Cefazolin is mainly removed from the serum by glomerular filtration, the renal clearance is 65 ml/min/1.73 m².

 

The acute toxicity of cefazolin is low.

Repeated administration of cefazolin in dogs and rats for 1 – 6 months by different routes of administration did not show any significant effect on hematological and biochemical parameters. Renal toxicity was observed after repeated doses in rabbits, but not in dogs or rats. Cefazolin showed no teratogenic or embryotoxic activity.

No studies are available on the mutagenicity and carcinogenicity of cefazolin.

 

None.

Cefazolin is incompatible with amikacin disulfate, amobarbital-sodium, ascorbic acid, bleomycin sulphate, calcium gluceptate, calcium gluconate, cimetidine hydrochloride, colistimethate-sodium, erythromycin gluceptate, kanamycin sulphate, oxytetracyclin hydrochloride, pentobarbital-sodium, polymyxin-B-sulphate and tetracycline hydrochloride.

This medicinal product must not be mixed with other medicinal products except those mentioned in section 6.6.

As packaged for sale: 36 months. After reconstitution and dilution: For storage conditions of the reconstituted/diluted product, see section 6.6. Chemical and physical stability has been demonstrated for 12 hours at 25°C and for up to 24 hours in a refrigerator (2–8°C). From a microbiological point of view, unless the method of opening/reconstitution/dilution precludes the risk of microbial contamination, the product should be used immediately. If not used immediately, in-use storage times and conditions prior to use are the responsibility of the user and would normally not be longer than the times stated above for the chemical and physical in-use stability.

Do not store above 30°C.

Store in the original package in order to protect from light.

 

Clear vials with orange flip-off aluminum caps.

Pack size: 1 and/or 10 Vials.

Preparation of the solution

See the table for addition volumes and solution concentrations, which may be useful when fractional doses are required.

Intravenous injection

Reconstitute Zolecin 1000 mg Powder for solution for injection/infusion with one of the following compatible diluents according to the dilution table that follows:

•     Water for injection
•     0.9% sodium chloride solution or
•     5% and 10% glucose solution

Reconstitution table for intravenous injection

Content per vial	Minimum amount of diluent to be added	Approximate concentration
1000 mg	4 ml	220 mg/ml

Cefazolin is to be injected slowly over three to five minutes. In no case should the solution be injected in less than 3 minutes. This should be done directly into the vein or into the tube from which the patient receives intravenous solution.

Single doses exceeding 1000 mg should be given as intravenous infusion over 30 to 60 minutes.

Guidelines for paediatric dosage:

1000 mg vial: The content of 1 vial (1000 mg cefazolin) is dissolved in 4 ml of a compatible solvent (i.e. concentration approx. 220 mg/ml). The respective volume of this solution to be used is indicated in table 1 in addition to the dose in mg.

For the amount of diluent to be added for paediatric population please refer to section 4.2 - Guidelines for paediatric dosage. For volumes inferior of 1 ml, please use a 0.5 ml syringe for better accuracy of dosing.

Intravenous infusion

Zolecin 1000 mg Powder for solution for injection/infusion should first be reconstituted with one of the diluents detailed as compatible for intravenous injection.

Further dilution should take place with one of the following compatible diluents according to the dilution table that follows:

•     0.9% sodium chloride solution
•     5% Glucose
•     Ringer’s solution
•     Lactated Ringer's solution
•     Water for injection

Dilution table for intravenous infusion

Content per vial	Reconstitution	Dilution	Approximate concentration
	Minimum amount of diluent to be added	Amount of diluent to be added
1000 mg	4 ml	50 ml - 100 ml	20 mg/ml – 10 mg/ml

Cefazolin 1000 mg Powder for solution for injection/infusion solutions containing lidocaine should never be administered intravenously.

As for all parenteral medicinal products, inspect the reconstituted solution visually for particulate matter and discoloration prior to administration. The solution should only be used if the solution is clear and practically free from particles.

The reconstituted product is for single use only.

Any unused medicinal product or waste material should be disposed of in accordance with local requirements.