Pharmacy Guide

Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.

Pharmacy Guide

Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.

← Back to all medicines

Ceftazidime 1g Powder for Solution for Injection or Infusion

⚠ This medicine appears to have been discontinued

The electronic medicines compendium (emc) no longer publishes a Summary of Product Characteristics for this product, which usually means it is no longer marketed in the UK. The patient leaflet below is kept for reference, but the product may not be available.

If you were prescribed this medicine, other products containing Ceftazidime pentahydrate may still be available. Do not stop your treatment — ask your pharmacist or GP what to use instead.

Active substance: Ceftazidime pentahydrate

Source: electronic medicines compendium (emc)
Official leaflet: Read the PIL on emc

What it is and what it is used for

for

Ceftazidime is an antibiotic used in adults and children (including newborn babies). It works by killing bacteria that cause infections. It belongs to a group of medicines called cephalosporins. Ceftazidime is used to treat severe bacterial infections of:

  • the lungs or chest
  • the urinary tract
  • the lungs and bronchi in patients suffering from cystic fibrosis
  • the skin and soft tissues
  • the brain (meningitis)
  • the abdomen and abdominal wall (peritonitis)
  • the ear
  • the bones and joints. Ceftazidime can also be used:
  • to prevent infections during prostate surgery in men
  • to treat patients with low white blood cell counts (neutropenia) who have a fever due to a bacterial infection.

What you need to know before you take it

ceftazidime

You must not be given ceftazidime:

  • if you are allergic to ceftazidime or any of the other ingredients of this medicine (listed in section 6)
  • if you have had a severe allergic reaction to any other antibiotic (penicillins, monobactams and carbapenems) as you may also be allergic to ceftazidime ➣ Tell your doctor before you start ceftazidime if you think that this applies to you; you must not be given ceftazidime. Warnings and precautions Serious skin reactions including Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP) have been reported in association with ceftazidime treatment. Seek medical attention immediately if you notice any of the symptoms related to these serious skin reactions described in section 4. Talk to your doctor, pharmacist or nurse before you start on ceftazidime Take special care with ceftazidime You must look out for certain symptoms such as allergic reactions, nervous system disorders and gastrointestinal disorders such as diarrhoea while you are being given ceftazidime. This will reduce the risk of possible problems. See ('Conditions you need to look out for') in section 4. If you have had an allergic reaction to other antibiotics you may also be allergic to ceftazidime. If you need a blood or urine test Ceftazidime can affect the results of urine tests for sugar and a blood test known as Coombs test. If you are having tests: ➣ Tell the person taking the sample that you have been given ceftazidime. Other medicines and ceftazidime Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. This includes medicines you can obtain without a prescription. You shouldn't be given ceftazidime without talking to your doctor if you are also taking:
  • An antibiotic called chloramphenicol
  • Water tablets called furosemide
  • A type of antibiotic called aminoglycosides e.g.gentamicin, tobramycin ➣ Tell your doctor if this applies to you Pregnancy, breast-feeding and fertility If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine. Your doctor will consider the benefit of treating you with ceftazidime against the risk to your baby. Driving and using machines Ceftazidime can cause side effects that affect your ability to drive, such as dizziness. Don't drive or use machines unless you are sure you're not affected. Important information about some of the ingredients of ceftazidime Ceftazidime contains sodium This medicine contains 52mg sodium (main component of cooking/table salt) in each 1g vial. This is equivalent to 2.6% of the recommended maximum daily dietary intake of sodium for an adult. This medicine contains 104mg sodium (main component of cooking/table salt) in each 2g vial. This is equivalent to 5.2% of the recommended maximum daily dietary intake of sodium for an adult.

How to take it

Information for Health Care Professionals Ceftazidime 1g powder for solution for injection or infusion and Ceftazidime 2g powder for solution for injection or infusion Dosage and Administration Information Only Please refer to the Summary of Product Characteristics for further information

  • Posology and method of administration Method of administration The dose depends on the severity, susceptibility, site and type of infection and on the age and renal function of the patient. Ceftazidime should be administered by intravenous injection or infusion, or by deep intramuscular injection. Recommended intramuscular injection sites are the upper outer quadrant of the gluteus maximus or lateral part of the thigh. Ceftazidime solutions may be given directly into the vein or introduced into the tubing of a giving set if the patient is receiving parenteral fluids. The standard recommended route of administration is by intravenous intermittent injection or intravenous continuous infusion. Intramuscular administration should only be considered when the intravenous route is not possible or less appropriate for the patient. Posology Adults and children ≥ 40kg Intermittent administration Infection Dose to be administered Broncho-pulmonary infections in cystic fibrosis 100 to 150 mg/kg/day every 8h, maximum 9g per day Febrile neutropenia Nosocomial pneumonia 2g every 8h Bacterial meningitis Bacteraemia* Bone and joint infections Complicated skin and soft tissue infections Complicated intra-abdominal infections Peritonitis associated with dialysis in patients on CAPD Complicated urinary tract infections Peri-operative prophylaxis for transuretheral resection of prostate (TURP) Chronic suppurative otitis media Malignant otitis externa Continuous Infusion Infection Febrile neutropenia Nosocomial pneumonia Broncho-pulmonary infections in cystic fibrosis Bacterial meningitis Bacteraemia* Bone and joint infections Complicated skin and soft tissue infections Complicated intra-abdominal infections Peritonitis associated with dialysis in patients on CAPD

In adults with normal renal function 9g/day has been used without adverse effects.

  • When associated with, or suspected to be associated with, any of the infections listed in section 4.1. 1

Children < 40kg Infants and toddlers >2 months and children < 40kg Intermittent Administration

Infection Complicated urinary tract infections Chronic suppurative otitis media Malignant otitis externa Neutropenic children Broncho-pulmonary infections in cystic fibrosis Bacterial meningitis Bacteraemia* Bone and joint infections Complicated skin and soft tissue infections Complicated intra-abdominal infections Peritonitis associated with dialysis in patients on CAPD

Usual dose 100-150mg/kg/day in three divided doses, maximum 6g/day 150mg/kg/day in three divided doses, maximum 6g/day

100-150mg/kg/day in three divided doses, maximum 6g/day

Continuous Infusion Febrile neutropenia Nosocomial pneumonia Broncho-pulmonary infections in cystic fibrosis Bacterial meningitis Bacteraemia* Bone and joint infections Complicated skin and soft tissue infections Complicated intra-abdominal infections Peritonitis associated with dialysis in patients with CAPD

1-2g every 8h 1-2g every 8h or 12h 1g at induction of anaesthesia, and a second dose at catheter removal 1g to 2g every 8h

✂

Ceftazidime is usually given by a doctor or nurse. It can be given as a drip (intravenous infusion) or as an injection directly into a vein or into a muscle. Ceftazidime is made up by the doctor, pharmacist or nurse using water for injections or a suitable infusion fluid. The recommended dose The correct dose of ceftazidime for you will be decided by your doctor and depends on: the severity and type of infection, whether you are on any other antibiotics; your weight and age, how well your kidneys are working. Newborn babies (0-2 months) For every 1kg the baby weighs, they'll be given 25 to 60mg ceftazidime per day divided in two doses. Babies (over 2 months) and children who weigh less than 40kg For every 1kg the baby or child weighs, they'll be given 100 to 150mg of ceftazidime per day divided in three doses. Maximum 6g per day. Adults and adolescents who weigh 40kg or more 1 to 2g of ceftazidime three times daily. Maximum of 9g per day. Patients over 65 The daily dose should not normally exceed 3g per day, especially if you are over 80 years of age. Patients with kidney problems You may be given a different dose to the usual dose. The doctor or nurse will decide how much ceftazidime you will need, depending on the severity of the kidney disease. Your doctor will check you closely and you may have more regular kidney function tests. If you are given more ceftazidime than you should If you accidentally use more than your prescribed dose, contact your doctor or nearest hospital straight away. If you forget to use ceftazidime If you miss an injection, you should have it as soon as possible. However, if it is almost time for your next injection, skip the missed injection. Do not take a double dose (two injections at the same time) to make up for a forgotten dose.

Neonates and infants ≤ 2 months

Infection

Loading dose of 60-100mg/kg followed by a continuous infusion 100-200mg/kg/day, maximum 6g/day

Usual dose

Intermittent Administration

Dose to be administered Loading dose of 2g followed by a continuous infusion of 4 to 6g every 24h1

25-60mg/kg/day in two divided Most infections doses1 In neonates and infants ≤ 2 months, the serum half life of ceftazidime can be three to four times that in adults.

  • Where associated with or suspected to be associated with any of the infections listed in section 4.1. 1

Loading dose of 2g followed by a continuous infusion of 4 to 6g every 24h1

106648/7

Customer

Wockhardt UK Limited

Description

Ceftazidime

Item Code

106648/7

Profile

n/a

PRINTING COLOURS Black

16 East Park Road | Leicester | LE5 4QA | UK

APPROVAL SIGNATURE

DATE

Warning! We cannot accept responsibility for any errors in this proof after approval. Whilst we take extreme care at all times to ensure accuracy to our client's brief, the final responsibility must be taken by our client. IF YOU SIGN THIS PROOF YOU ARE SIGNIFYING FULL APPROVAL OF DESIGN AND TEXT.

Size

170 x 320mm

Min.Point Size

Other

Market

UK

Language

English

FPO

Pharma Height

7mm Minimum

Barcode Proof By

CJE

Proof No.

1

Date

17.09.2024

Body Text Fonts: Helvetica Neue LT Pro

Actual Min Point Size 5.5 pt

TECHNICAL COLOURS Keyline (non-printing)

FPO If you stop taking ceftazidime Don't stop taking ceftazidime unless your doctor tells you to. If you have any questions on the use of this medicine, ask your doctor or nurse.

Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them. Conditions you need to look out for Seek medical attention immediately if you notice any of the following symptoms. The following serious side effects have occurred in a small number of people but their exact frequency is unknown:

  • Severe allergic reaction. Signs include raised and itchy rash, swelling, sometimes of the face or mouth causing difficulty in breathing.
  • Skin rash, which may blister, and looks like small targets (central dark spot surrounded by a paler area, with a dark ring around the edge).
  • Reddish patches on the trunk, the patches are target-like macules or circular, often with central blisters, skin peeling, ulcers of mouth, throat, nose, genitals and eyes. These serious skin rashes can be preceded by fever and flu-like symptoms (Stevens-Johnson syndrome, toxic epidermal necrolysis).
  • Widespread rash, high body temperature and enlarged lymph nodes (DRESS syndrome or drug hypersensitivity syndrome).
  • A red, scaly widespread rash with bumps under the skin and blisters accompanied by fever. The symptoms usually appear at the initiation of treatment (acute generalised exanthematous pustulosis)
  • Nervous system disorders: tremors, fits and, in some cases coma. These have occurred in people when the dose they are given is too high, particularly in people with kidney disease. ➣ Contact a doctor or nurse immediately if you get any of these symptoms. Common side effects These may affect up to 1 in 10 people:
  • diarrhoea
  • pain, burning, swelling or inflammation at the injection site. ➣ Tell your doctor if any of these are troubling you.
  • swelling and redness along a vein
  • red raised skin rash which may be itchiness Common side effects that may show up in blood tests:
  • an increase in a type of white blood cell (eosinophilia)
  • an increase in liver enzymes.
  • an increase in the number of cells that help the blood to clot Uncommon side effects These may affect up to 1 in 100 people:
  • inflammation of the gut which can cause pain or diarrhoea which may contain blood
  • stomach ache
  • thrush (fungal infections in the mouth or vagina)
  • feeling sick or being sick
  • headache
  • fever and chills.
  • dizziness ➣ Tell your doctor if you get any of these. Uncommon side effects that may show up in blood tests:
  • a decrease in the number of white blood cells
  • an increase in the level of urea, urea nitrogen or serum creatinine in the blood.
  • a decrease in the number of blood platelets (cells that help the blood to clot) Very rare side effects These may affect up to 1 in 10,000 people:
  • inflammation or failure of the kidneys. Other side effects Other side effects have occurred in a small number of people but their exact frequency is unknown:
  • inflammation or failure of the kidneys
  • unpleasant taste in the mouth
  • pins and needles
  • yellowing of the whites of the eyes or skin. Other side effects that may show up in blood tests:
  • red blood cells destroyed too quickly
  • severe decrease in the number of white blood cells.
  • an increase in a certain type of white blood cells Reporting of side effects If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects you can help provide more information on the safety of this medicine.

How to store it

ceftazidime

Keep this medicine out of the sight and reach of children

  • Do not use this medicine after the expiry date which is stated on the carton and vial. The expiry date refers to the last day of that month
  • The vials should not be stored above 25o C
  • Keep the vial in the outer carton in order to protect from light
  • Chemical and physical in-use stability has been demonstrated for eight hours at 25o C and 24 hours at 4o C. From a microbiological point of view, once opened, 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 24 hours at 2-8o C, unless reconstitution has taken place in controlled and validated aseptic conditions. For single use only. Once reconstituted, any unused portion of solution should be discarded
  • Do not use this medicine if you notice that the solution contains particles or is cloudy. Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

Contents of the pack and other information

What ceftazidime contains The active substance is ceftazidime as ceftazidime pentahydrate. Each vial contains the equivalent of 1g or 2g of ceftazidime. It also contains the ingredient, sodium carbonate. The sodium content per vial is approximately 52mg (2.26mmol) for the 1g vial and 104mg (4.52mmol) for the 2g vial. What ceftazidime looks like and contents of the pack Ceftazidime is a white to cream coloured powder, which must be made into a solution before injection or infusion. It is available in packs of 1, 5 or 10 vials. Not all pack sizes are marketed. X-PIL Information To listen to or request a copy of this leaflet in Braille, large print or audio please call, free of charge: 0800 198 5000 (UK Only) Please be ready to give the following information: Product Name Reference Number Ceftazidime 1g powder for solution for injection or infusion 29831/0031 Ceftazidime 2g powder for solution for injection or infusion 29831/0032 This is a service provided by the Royal National Institute of Blind People. Marketing Authorisation Holder and Manufacturer Marketing Authorisation Holder: Wockhardt UK Ltd, Ash Road North, Wrexham, LL13 9UF, UK Manufacturer: CP Pharmaceuticals Ltd, Ash Road North, Wrexham, LL13 9UF, UK This leaflet was last revised in 09/2024

PREPARATION OF SOLUTION INTRAMUSCULAR INJECTION Strength

Diluent

Amount of diluent to be added (ml)

1g

0.5% lidocaine 1% lidocaine

3ml 3ml

Approximate Approximate available concentration (mg/ml) volume (ml) 278 270

3.6ml 3.7ml

Approximate displacement volume (ml) 0.6ml 0.7ml

INTRAVENOUS BOLUS Strength

Diluent

1g 2g

Water for Injection Water for Injection

Amount of diluent to be Approximate Approximate available added (ml) concentration (mg/ml) volume (ml) 10ml 10ml

92 172

10.9ml 11.6ml

Customer

Wockhardt UK Limited

Description

Ceftazidime

Item Code

106648/7

Profile

n/a

Size

170 x 320mm

Min.Point Size

Other

Approximate displacement volume (ml) 0.9ml 1.6ml

INTRAVENOUS INFUSION Diluent (see full list of Amount of diluent to Strength compatible diluents be added (ml)# below table) Compatible diluent 1g 50ml list below 0.9% sodium chloride 50ml 2g 5% glucose 50ml

DATE

Warning! We cannot accept responsibility for any errors in this proof after approval. Whilst we take extreme care at all times to ensure accuracy to our client's brief, the final responsibility must be taken by our client. IF YOU SIGN THIS PROOF YOU ARE SIGNIFYING FULL APPROVAL OF DESIGN AND TEXT.

Market

UK

Language

English

FPO

Pharma Height

7mm Minimum

Barcode Proof By

CJE

Proof No.

1

Date

17.09.2024

Body Text Fonts: Helvetica Neue LT Pro

Approximate concentration (mg/ml)

Approximate available volume (ml)

Approximate displacement volume (ml)

20

—

—

39 39

51.5ml 51.9ml

1.5ml 1.9ml

Note: addition should be in two stages. See preparation for intravenous infusion instructions below. Compatible diluents for intravenous infusion Ceftazidime at concentrations between 1mg/ml and 40mg/ml is compatible with the following diluent solutions for intravenous infusion preparation:

  • Sodium Chloride 0.9%
  • Glucose 5% and Sodium Chloride 0.9%
  • Ringer Solution
  • Glucose 5% and Sodium Chloride 0.45%
  • Ringer Lactate Solution
  • Glucose 5% and Sodium Chloride 0.2%
  • Glucose 5%
  • Dextran 40%/10% and Sodium Chloride 0.9%
  • Glucose 10%
  • Dextran 70%/6% and Sodium Chloride 0.9% Solutions range from light yellow to amber depending on concentration, diluent and storage conditions used. All sizes of vials as supplied are under reduced pressure. As the product dissolves, carbon dioxide is released and a positive pressure develops. For ease of use, it is recommended that the following techniques of reconstitution are adopted. Preparation of solution for bolus injection: 1. Insert the syringe needle through the vial closure and inject 10ml of Water for Injection. The vacuum may assist entry of the diluent. Remove the syringe needle. 2. Shake to dissolve: carbon dioxide is released and a clear solution will be obtained in about 1 to 2 minutes. 3. Invert the vial. With the syringe plunger fully depressed, insert the needle through the vial closure and withdraw the total volume of solution into the syringe (the pressure in the vial may aid withdrawal). Ensure that the needle remains within the solution and does not enter the head space. The withdrawn solution may contain small bubbles of carbon dioxide; they may be disregarded. These solutions may be given directly into the vein or introduced into the tubing of a giving set if the patient is receiving parenteral fluids. Preparation of solution for intravenous infusion: Prepare using a total of 50ml of compatible diluent, added in TWO stages as follows: 1. Insert the syringe needle through the vial closure and inject 10ml of Water for Injection or one of the listed compatible diluent solutions for intravenous infusion preparation to reconstitute. The vacuum may assist entry of the diluent. Remove the syringe needle. 2. Shake to dissolve: carbon dioxide is released and a clear solution obtained in about 1 to 2 minutes. 3. Do not insert a gas relief needle until the product has dissolved. Insert a gas relief needle through the vial closure to relieve the internal pressure. 4. Transfer the reconstituted solution to the final delivery vehicle (e.g. mini-bag or burette-type set) and add 40ml of compatible diluent* to make up a total volume of approximately 50ml and administer by slow intravenous infusion over 20 to 30 minutes. *For the second stage of preparation, use Sodium Chloride 0.9%, Glucose 5% or one of the listed compatible diluent solutions for intravenous infusion preparation, as Water for Injection produces hypotonic solutions when used at higher concentrations. Ceftazidime at concentrations between 1mg/ml and 40mg/ml is compatible with the diluent solutions for intravenous infusion preparation listed above NOTE: To preserve product sterility, it is important that a gas relief needle is not inserted through the vial closure before the product has dissolved. This leaflet was last revised in 09/2024 106648/7

#

PRINTING COLOURS Black

16 East Park Road | Leicester | LE5 4QA | UK

APPROVAL SIGNATURE

✂

Paediatric population The safety and efficacy of ceftazidime administered as continuous infusion to neonates and infants ≤ 2 months has not been established. Elderly In view of age related reduced clearance of ceftazidime in elderly patients, the daily dose should not normally exceed 3g in those over 80 years of age. Hepatic impairment Available data do not indicate the need for dose adjustment in mild or moderate liver function impairment. There are no study data in patients with severe hepatic impairment (see also section 5.2). Close clinical monitoring for safety and efficacy is advised. Renal impairment Ceftazidime is excreted unchanged by the kidneys. Therefore, in patients with impaired renal function, the dosage should be reduced (see also section 4.4). An initial loading dose of 1g should be given. Maintenance doses should be based on creatinine clearance. For recommended maintenance doses of ceftazidime in renal impairment (including haemodialysis and peritoneal dialysis), follow the dosage recommendations in the SPC.

  • Overdose Overdose can lead to neurological sequelae including encephalopathy, convulsion and coma. Symptoms of overdose can occur if the dose is not reduced appropriately in patients with renal impairment. Serum levels of ceftazidime can be reduced by haemodialysis or peritoneal dialysis.
  • Incompatibilities In the absence of compatibility studies, this medicinal product must not be mixed with other medicinal products. Ceftazidime is less stable in Sodium Bicarbonate Injection than other intravenous fluids. It is not recommended as a diluent. Ceftazidime and aminoglycosides should not be mixed in the same giving set or syringe. Precipitation has been reported when vancomycin has been added to ceftazidime in solution. Therefore, it would be prudent to flush giving sets and intravenous lines between administration of these two agents. Ceftazidime is incompatible with aminophylline. There is a possible incompatibility with pentamide.
  • Instructions for use/handling For single use. Discard any unused contents. Instructions for reconstitution: See table for addition volumes and solution concentrations, which may be useful when fractional doses are required.

Actual Min Point Size 5.5 pt

TECHNICAL COLOURS Keyline (non-printing)

Frequently asked questions about Ceftazidime 1g Powder for Solution for Injection or Infusion

How do I take Ceftazidime 1g Powder for Solution for Injection or Infusion?

Ceftazidime 1g Powder for Solution for Injection or Infusion comes as injection containing 1g. Always follow the dose your doctor or pharmacist has given you, and read the leaflet that comes with the medicine.

What is the active substance in Ceftazidime 1g Powder for Solution for Injection or Infusion?

The active substance in Ceftazidime 1g Powder for Solution for Injection or Infusion is ceftazidime pentahydrate.

Are there equivalent medicines to Ceftazidime 1g Powder for Solution for Injection or Infusion?

Medicines with the same active substance, strength and form include: Ceftazidime Venus Pharma 1 g powder for solution for injection/infusion, Ceftazidime, 1 g, powder for solution for injection/infusion. They are interchangeable only if your prescriber or pharmacist says so.

Where does this information come from?

This leaflet reproduces the patient information leaflet approved for Ceftazidime 1g Powder for Solution for Injection or Infusion, as published on the electronic medicines compendium (emc). The version printed inside your medicine’s packaging is the one that applies to you.

Can I get Ceftazidime 1g Powder for Solution for Injection or Infusion without a prescription?

Whether a medicine is available over the counter or on prescription only depends on its licence. Check the leaflet, or ask your pharmacist — they can tell you straight away.

About this leaflet

The text above reproduces the patient information leaflet approved for this medicine, restructured for easier reading.

Medical disclaimer: This page is for information only and does not replace advice from your doctor or pharmacist. Always read the leaflet supplied with your medicine. If you are unwell, call NHS 111; in an emergency, call 999.

Medicines with the same active substance: Ceftazidime pentahydrate (8 medicines)
See every medicine containing this substance, or browse the full A–Z of active substances.
⚕For healthcare professionals — Summary of Product Characteristics (SmPC)Full SmPC: dosage, interactions, contraindications, warnings+
Technical information intended for healthcare professionals (doctors and pharmacists). The Summary of Product Characteristics (SmPC) is the official document approved by the MHRA/EMA. It does not replace the patient leaflet or a doctor’s advice.

4.1. Therapeutic indications

Ceftazidime is indicated for the treatment of the infections listed below in adults and children including neonates (from birth).

• Nosocomial pneumonia

• Broncho-pulmonary infections in cystic fibrosis

• Bacterial meningitis

• Chronic suppurative otitis media

• Malignant otitis externa

• Complicated urinary tract infections

• Complicated skin and soft tissue infections

• Complicated intra-abdominal infections

• Bone and joint infections

• Peritonitis associated with dialysis in patients on CAPD.

Treatment of patients with bacteraemia that occurs in association with, or is suspected to be associated with, any of the infections listed above.

Ceftazidime may be used in the management of neutropenic patients with fever that is suspected to be due to a bacterial infection.

Ceftazidime may be used in the peri-operative prophylaxis of urinary tract infections for patients undergoing trans-urethral resection of the prostate (TURP).

The selection of ceftazidime should take into account its antibacterial spectrum, which is mainly restricted to aerobic Gram negative bacteria (see sections 4.4 and 5.1).

Ceftazidime should be co-administered with other antibacterial agents whenever the possible range of causative bacteria would not fall within its spectrum of activity.

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

4.2. Posology and method of administration

Posology

Table 1: Adults and children ≥ 40 kg

Intermittent Administration

Infection

Dose to be administered

Broncho-pulmonary infections in cystic fibrosis

100 to 150 mg/kg/day every 8 h, maximum 9 g per day1

Febrile neutropenia

2 g every 8 h

Nosocomial pneumonia

Bacterial meningitis

Bacteraemia*

Bone and joint infections

1-2 g every 8 h

Complicated skin and soft tissue infections

Complicated intra-abdominal infections

Peritonitis associated with dialysis in patients on CAPD

Complicated urinary tract infections

1-2 g every 8 h or 12 h

Peri-operative prophylaxis for transuretheral resection of prostate (TURP)

1 g at induction of anaesthesia, and a second dose at catheter removal

Chronic suppurative otitis media

1 g to 2 g every 8h

Malignant otitis externa

Continuous Infusion

Infection

Dose to be administered

Febrile neutropenia

Loading dose of 2 g followed by a continuous infusion of 4 to 6 g every 24 h1

Nosocomial pneumonia

Broncho-pulmonary infections in cystic fibrosis

Bacterial meningitis

Bacteraemia*

Bone and joint infections

Complicated skin and soft tissue infections

Complicated intra-abdominal infections

Peritonitis associated with dialysis in patients on CAPD

1 In adults with normal renal function 9 g/day has been used without adverse effects.

* When associated with, or suspected to be associated with, any of the infections listed in section 4.1.

Table 2: Children < 40 kg

Infants and toddlers >2 months and children < 40 kg

Infection

Usual dose

Intermittent Administration

Complicated urinary tract infections

100-150 mg/kg/day in three divided doses, maximum 6 g/day

Chronic suppurative otitis media

Malignant otitis externa

Neutropenic children

150 mg/kg/day in three divided doses, maximum 6 g/day

Broncho-pulmonary infections in cystic fibrosis

Bacterial meningitis

Bacteraemia*

Bone and joint infections

100-150 mg/kg/day in three divided doses, maximum 6 g/day

Complicated skin and soft tissue infections

Complicated intra-abdominal infections

Peritonitis associated with dialysis in patients on CAPD

Continuous Infusion

Febrile neutropenia

Loading dose of 60-100 mg/kg followed by a continuous infusion 100-200 mg/kg/day, maximum 6 g/day

Nosocomial pneumonia

Broncho-pulmonary infections in cystic fibrosis

Bacterial meningitis

Bacteraemia*

Bone and joint infections

Complicated skin and soft tissue infections

Complicated intra-abdominal infections

Peritonitis associated with dialysis in patients on CAPD

Neonates and infants ≤ 2 months

Infection

Usual dose

Intermittent Administration

Most infections

25-60 mg/kg/day in two divided doses1

1 In neonates and infants ≤ 2 months, the serum half life of ceftazidime can be three to four times that in adults.

* Where associated with or suspected to be associated with any of the infections listed in section 4.1.

Paediatric population

The safety and efficacy of Ceftazidime administered as continuous infusion to neonates and infants ≤ 2 months has not been established.

Elderly

In view of age related reduced clearance of Ceftazidime in elderly patients, the daily dose should not normally exceed 3 g in those over 80 years of age.

Hepatic impairment

Available data do not indicate the need for dose adjustment in mild or moderate liver function impairment. There are no study data in patients with severe hepatic impairment (see also section 5.2). Close clinical monitoring for safety and efficacy is advised.

Renal impairment

Ceftazidime is excreted unchanged by the kidneys. Therefore, in patients with impaired renal function, the dosage should be reduced (see also section 4.4).

An initial loading dose of 1 g should be given. Maintenance doses should be based on creatinine clearance:

Table 3: Recommended maintenance doses of Ceftazidime in renal impairment – intermittent infusion

Adults and children ≥ 40 kg

Creatinine clearance

(ml/min)

Approx. serum creatinine

μmol/l (mg/dl)

Recommended unit dose of Ceftazidime (g)

Frequency of dosing (hourly)

50-31

150-200

(1.7-2.3)

1

12

30-16

200-350

(2.3-4.0)

1

24

15-6

350-500

(4.0-5.6)

0.5

24

<5

>500

(>5.6)

0.5

48

In patients with severe infections the unit dose should be increased by 50% or the dosing frequency increased.

In children the creatinine clearance should be adjusted for body surface area or lean body mass.

Children < 40 kg

Creatinine clearance

(ml/min)**

Approx. serum creatinine*

μmol/l (mg/dl)

Recommended individual dose mg/kg body weight

Frequency of dosing (hourly)

50-31

150-200

(1.7-2.3)

25

12

30-16

200-350

(2.3-4.0)

25

24

15-6

350-500

(4.0-5.6)

12.5

24

<5

>500

(>5.6)

12.5

48

* The serum creatinine values are guideline values that may not indicate exactly the same degree of reduction for all patients with reduced renal function.

** Estimated based on body surface area, or measured.

Close clinical monitoring for safety and efficacy is advised.

Table 4: Recommended maintenance doses of Ceftazidime in renal impairment – continuous infusion

Adults and children ≥ 40 kg

Creatinine clearance

(ml/min)

Approx. serum creatinine

μmol/l (mg/dl)

Frequency of dosing (hourly)

50-31

150-200

(1.7-2.3)

Loading dose of 2 g followed by 1 g to 3 g /24 hours

30-16

200-350

(2.3-4.0)

Loading dose of 2 g followed by 1 g/24 hours

≤15

>350

(>4.0)

Not evaluated

Caution is advised in dose selection. Close clinical monitoring for safety and efficacy is advised.

Children < 40 kg

The safety and effectiveness of Ceftazidime administered as continuous infusion in renally impaired children < 40 kg has not been established. Close clinical monitoring for safety and efficacy is advised.

If continuous infusion is used in children with renal impairment, the creatinine clearance should be adjusted for body surface area or lean body mass.

Haemodialysis

The serum half-life during haemodialysis ranges from 3 to 5 h.

Following each haemodialysis period, the maintenance dose of ceftazidime recommended in the below table should be repeated.

Peritoneal dialysis

Ceftazidime may be used in peritoneal dialysis and continuous ambulatory peritoneal dialysis (CAPD).

In addition to intravenous use, ceftazidime can be incorporated into the dialysis fluid (usually 125 to 250 mg for 2 litres of dialysis solution).

For patients in renal failure on continuous arterio-venous haemodialysis or high-flux haemofiltration in intensive therapy units: 1 g daily either as a single dose or in divided doses. For low-flux haemofiltration, follow the dose recommended under renal impairment.

For patients on veno-venous haemofiltration and veno-venous haemodialysis, follow the dosage recommendations in the tables 5 & 6 below.

Table 5: Continuous veno-venous haemofiltration dose guidelines

Residual renal function (creatinine clearance ml/min)

Maintenance dose (mg) for an ultrafiltration rate (ml/min) of 1:

5

16.7

33.3

50

0

250

250

500

500

5

250

250

500

500

10

250

500

500

750

15

250

500

500

750

20

500

500

500

750

1 Maintenance dose to be administered every 12 h.

Table 6: Continuous veno-venous haemodialysis dose guidelines

Residual renal function (creatinine clearance in ml/min)

Maintenance dose (mg) for a dialysate in flow rate of 1:

1.0 litre/h

2.0 litre/h

Ultrafiltration rate (litre/h)

Ultrafiltration rate (litres/h)

0.5

1.0

2.0

0.5

1.0

2.0

0

500

500

500

500

500

750

5

500

500

750

500

500

750

10

500

500

750

500

750

1000

15

500

750

750

750

750

1000

20

750

750

1000

750

750

1000

1 Maintenance dose to be administered every 12 h.

Method of administration

The dose depends on the severity, susceptibility, site and type of infection and on the age and renal function of the patient.

Ceftazidime should be administered by intravenous injection or infusion, or by deep intramuscular injection. Recommended intramuscular injection sites are the upper outer quadrant of the gluteus maximus or lateral part of the thigh. Ceftazidime solutions may be given directly into the vein or introduced into the tubing of a giving set if the patient is receiving parenteral fluids.

The standard recommended route of administration is by intravenous intermittent injection or intravenous continuous infusion. Intramuscular administration should only be considered when the intravenous route is not possible or less appropriate for the patient.

4.3. Contraindications

Hypersensitivity to the active substance, to any other cephalosporin or to any of the excipients listed in section 6.1.

History of severe hypersensitivity (e.g. anaphylactic reaction) to any other type of beta-lactam antibacterial agent (penicillins, monobactams and carbapenems).

4.4. Special warnings and precautions for use

Severe cutaneous adverse reactions (SCARs) including Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalized exanthematous pustulosis (AGEP), which can be life-threatening or fatal, have been reported with unknown frequency in association with ceftazidime treatment. Patients should be advised of the signs and symptoms and monitored closely for skin reactions. If signs and symptoms suggestive of these reactions appear, ceftazidime should be withdrawn immediately, and an alternative treatment considered. If the patient has developed a serious reaction such as SJS, TEN, DRESS or AGEP with the use of ceftazidime, treatment with ceftazidime must not be restarted in this patient at any time.

Hypersensitivity

As with all beta-lactam antibacterial agents, serious and occasionally fatal hypersensitivity reactions have been reported. In case of severe hypersensitivity reactions, treatment with ceftazidime 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 ceftazidime, to other cephalosporins or to any other type of beta-lactam agent. Caution should be used if ceftazidime is given to patients with a history of non-severe hypersensitivity to other beta-lactam agents.

Spectrum of activity

Ceftazidime has a limited spectrum of antibacterial activity. It is not suitable for use as a single agent for the treatment of some types of infections unless the pathogen is already documented and known to be susceptible or there is a very high suspicion that the most likely pathogen(s) would be suitable for treatment with ceftazidime. This particularly applies when considering the treatment of patients with bacteraemia and when treating bacterial meningitis, skin and soft tissue infections and bone and joint infections. In addition, ceftazidime is susceptible to hydrolysis by several of the extended spectrum beta lactamases (ESBLs). Therefore information on the prevalence of ESBL producing organisms should be taken into account when selecting ceftazidime for treatment.

Pseudomembranous colitis

Antibacterial agent-associated colitis and pseudo-membranous colitis have been reported with nearly all anti-bacterial agents, including ceftazidime, and may range in severity from mild to life-threatening. Therefore, it is important to consider this diagnosis in patients who present with diarrhoea during or subsequent to the administration of ceftazidime (see section 4.8). Discontinuation of therapy with ceftazidime and the administration of specific treatment for Clostridium difficile should be considered. Medicinal products that inhibit peristalsis should not be given.

Renal function

Concurrent treatment with high doses of cephalosporins and nephrotoxic medicinal products such as aminoglycosides or potent diuretics (e.g. furosemide) may adversely affect renal function.

Ceftazidime is eliminated via the kidneys, therefore the dose should be reduced according to the degree of renal impairment. Patients with renal impairment should be closely monitored for both safety and efficacy. Neurological sequelae have occasionally been reported when the dose has not been reduced in patients with renal impairment (see sections 4.2 and 4.8).

Overgrowth of non-susceptible organisms

Prolonged use may result in the overgrowth of non-susceptible organisms (e.g. Enterococci, fungi) which may require interruption of treatment or other appropriate measures. Repeated evaluation of the patient's condition is essential.

Test and assay interactions

Ceftazidime does not interfere with enzyme-based tests for glycosuria, but slight interference (false-positive) may occur with copper reduction methods (Benedict's, Fehling's, Clinitest).

Ceftazidime does not interfere in the alkaline picrate assay for creatinine.

The development of a positive Coombs' test associated with the use of ceftazidime in about 5% of patients may interfere with the cross-matching of blood.

Sodium content

This medicinal product contains 52mg sodium per 1g vial, equivalent to 2.6% of the WHO recommended maximum daily intake of 2g sodium for an adult.

4.5. Interaction with other medicinal products and other forms of interaction

Interaction studies have only been conducted with probenecid and furosemide.

Concurrent use of high doses with nephrotoxic medicinal products may adversely affect renal function (see section 4.4).

Chloramphenicol is antagonistic in vitro with Ceftazidime and other cephalosporins. The clinical relevance of this finding is unknown, but if concurrent administration of ceftazidime with chloramphenicol is proposed, the possibility of antagonism should be considered.

4.6. Fertility, pregnancy and lactation

Pregnancy

There are limited amounts of data from the use of ceftazidime in pregnant women. Animal studies do not indicate direct or indirect harmful effects with respect to pregnancy embryonal/foetal development, parturition or postnatal development (see section 5.3).

Ceftazidime should be prescribed to pregnant woman only if the benefit outweighs the risk.

Breast Feeding

Ceftazidime is excreted in human milk in small quantities but at therapeutic doses of ceftazidime no effects on the breast-fed infant are anticipated. Ceftazidime can be used during breast-feeding.

Fertility

No data are available.

4.7. Effects on ability to drive and use machines

No studies on the effects on the ability to drive and use machines have been performed. However, undesirable effects may occur (e.g. dizziness), which may influence the ability to drive and use machines (see section 4.8).

4.8. Undesirable effects

The most common adverse reactions are eosinophilia, thrombocytosis, phlebitis or thrombophlebitis with intravenous administration, diarrhoea, transient increases in hepatic enzymes, maculopapular or urticarcial rash, pain and/or inflammation following intramuscular injection and positive Coomb's test.

Data from sponsored and un-sponsored clinical trials have been used to determine the frequency of common and uncommon undesirable effects. The frequencies assigned to all other undesirable effects were mainly determined using post-marketing data and refer to a reporting rate rather than a true frequency. Within each frequency grouping, undesirable effects are presented in order of decreasing seriousness. The following convention has been used for the classification of frequency:

Very common (≥1/10)

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)

Unknown (cannot be estimated from the available data)

System Organ Class

Common

Uncommon

Very rare

Unknown

Infections and infestations

Candidiasis (including vaginitis and oral thrush)

Blood and lymphatic system disorders

Eosinophilia

Thrombocytosis

Neutropenia

Leucopenia

Thrombocytopenia

Agranulocytosis

Haemolytic anaemia

Lymphocytosis

Immune system disorders

Anaphylaxis (including bronchospasm and/or hypotension) (see section 4.4)

Nervous system disorders

Headache

Dizziness

Neurological sequelae1

Paraesthesia

Vascular disorders

Phlebitis or thrombophlebitis with intravenous administration

Gastrointestinal disorders

Diarrhoea

Antibacterial agent-associated diarrhoea and colitis2 (see section 4.4)

Abdominal pain

Nausea

Vomiting

Bad taste

Hepatobiliary disorders

Transient elevations in one or more hepatic enzymes3

Jaundice

Skin and subcutaneous tissue disorders

Maculopapular or urticarial rash

Pruritus

Toxic epidermal necrolysis

Stevens-johnson syndrome

Erythema multiforme

Angioedema

Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) 4

Acute generalized exanthematous pustulosis (AGEP)

Renal and urinary disorders

Transient elevations of blood urea, blood urea nitrogen and/or serum creatinine

Interstitial nephritis

Acute renal failure

General disorders and administration site conditions

Pain and/or inflammation after intramuscular injection

Fever

Investigations

Positive Coombs' test5

1There have been reports of neurological sequelae including tremor, myoclonia, convulsions, encephalopathy and coma in patients with renal impairment in whom the dose of Ceftazidime has not been appropriately reduced.

2 Diarrhoea and colitis may be associated with Clostridium difficile and may present as pseudomembranous colitis.

3 ALT (SGPT), AST (SOGT), LHD, GGT, alkaline phosphatase.

4 There have been rare reports where DRESS has been associated with ceftazidime.

5 A positive Coombs test develops in about 5% of patients and may interfere with blood cross matching.

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 the Yellow Card Scheme at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.

4.9. Overdose

Overdose can lead to neurological sequelae including encephalopathy, convulsion and coma.

Symptoms of overdose can occur if the dose is not reduced appropriately in patients with renal impairment (see sections 4.2 and 4.4).

Serum levels of ceftazidime can be reduced by haemodialysis or peritoneal dialysis.

💬 Ask about this leaflet

Ask anything about Ceftazidime 1g Powder for Solution for Injection or Infusion. The assistant answers only from this leaflet — if the leaflet does not cover it, it will say so. It does not give medical advice.

Answers come from the patient leaflet published on the electronic medicines compendium (emc). They are not medical advice. Ask a pharmacist or your GP if you are unsure. For urgent help call NHS 111, or 999 in an emergency.

Pharmacies in major towns and cities — see the list
Pharmacies by county and region — see the full list

Browse all 2,009 towns and cities →