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

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Piperacillin/Tazobactam 2 g/0.25 g powder for solution for 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 Piperacillin sodium, Tazobactam sodium may still be available. Do not stop your treatment — ask your pharmacist or GP what to use instead.

Active substance: Piperacillin sodium, Tazobactam sodium

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

What it is and what it is used for

for Piperacillin belongs to the group of medicines known as "broad‐spectrum penicillin antibiotics". It can kill many kinds of bacteria. Tazobactam can prevent some resistant bacteria from surviving the effects of piperacillin. This means that when piperacillin and tazobactam are given together, more types of bacteria are killed. Piperacillin/Tazobactam is used in adults and adolescents to treat bacterial infections, such as those affecting the lower respiratory tract (lungs), urinary tract (kidneys and bladder), abdomen, skin or blood. Piperacillin/Tazobactam may be used to treat bacterial infections in patients with low white blood cell counts (reduced resistance to infections). Piperacillin/Tazobactam is used in children aged 2-12 years to treat infections of the abdomen such as appendicitis, peritonitis (infection of the fluid and lining of the abdominal organs), and gallbladder (biliary) infections. Piperacillin/Tazobactam may be used to treat bacterial infections in patients with low white blood cell counts (reduced resistance to infections). In certain serious infections, your doctor may consider using Piperacillin/Tazobactam in combination with other antibiotics.

What you need to know before you take it

e Piperacillin/Tazobactam Do not use Piperacillin/Tazobactam

  • if you are allergic to piperacillin or tazobactam or any of the other ingredients of this medicine (listed in section 6).
  • if you are allergic to antibiotics known as penicillins, cephalosporins or other beta-lactamase inhibitors, as you may be allergic to Piperacillin/Tazobactam. Warnings and precautions Talk to your doctor, pharmacist or nurse before using Piperacillin/Tazobactam
  • if you have allergies. If you have several allergies, make sure you tell your doctor or other healthcare professional before receiving this product.
  • if you are suffering from diarrhoea before, or if you develop diarrhoea during or after your treatment. In this case, make sure you tell your doctor or other healthcare professional immediately. Do not take any medicine for the diarrhoea without first checking with your doctor.
  • if you have low levels of potassium in your blood. Your doctor may want to check your kidneys before you take this medicine and may perform regular blood tests during treatment.
  • if you have kidney or liver problems, or are receiving haemodialysis. Your doctor may want to check your kidneys before you take this medicine, and may perform regular blood tests during treatment.
  • if you are taking another antibiotic called vancomycin at the same time as Piperacillin/Tazobactam, this may increase the risk of kidney injury (see also Other medicines and Piperacillin/Tazobactam in this leaflet).
  • if you are taking certain medicines (called anticoagulants) to avoid an excess of blood clotting (see also Other medicines and Piperacillin/Tazobactam in this leaflet) or any unexpected bleeding occurs during the treatment. In this case, you should inform your doctor or other healthcare professional immediately.
  • if you develop convulsions during the treatment. In this case, you should inform your doctor or other healthcare professional.
  • if you think you developed a new or worsening infection. In this case, you should inform your doctor or other healthcare professional.

resulting in inflammation (haemophagocytic lymphohistiocytosis). This condition may be life-threatening if not diagnosed and treated early. If you experience multiple symptoms such as fever, swollen glands, feeling weak, feeling lightheaded, shortness of breath, bruising, or skin rash, contact your doctor immediately. Children Piperacillin/tazobactam is not recommended for use in children below the age of 2 years due to insufficient data on safety and effectiveness. Other medicines and Piperacillin/Tazobactam Tell your doctor or other healthcare professional if you are taking or have recently taken or might take any other medicines, including medicines obtained without a prescription. Some medicines may interact with piperacillin and tazobactam. These include:

  • medicine for gout (probenecid). This can increase the time it takes for piperacillin and tazobactam to leave your body.
  • medicines to thin your blood or to treat blood clots (e.g. heparin, warfarin or aspirin).
  • medicines used to relax your muscles during surgery. Tell your doctor if you are going to have a general anaesthetic.
  • methotrexate (medicine used to treat cancer, arthritis or psoriasis). Piperacillin and tazobactam can increase the time it takes for methotrexate to leave your body.
  • medicines that reduce the level of potassium in your blood (e.g. tablets enhancing urination or some medicines for cancer).
  • medicines containing the other antibiotics tobramycin, gentamicin or vancomycin. Tell your doctor if you have kidney problems. Taking Piperacillin/Tazobactam and vancomycin at the same time may increase the risk of kidney injury even if you have no kidney problems. Effect on laboratory tests Tell the doctor or laboratory staff that you are taking Piperacillin/Tazobactam if you have to provide a blood or urine sample. Pregnancy and breast-feeding If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or other healthcare professional for advice before receiving this medicine. Your doctor will decide if Piperacillin/Tazobactam is right for you. Piperacillin and tazobactam can pass to a baby in the womb or through breast milk. If you are breas-tfeeding, your doctor will decide if Piperacillin/Tazobactam is right for you. Driving and using machines The use of Piperacillin/Tazobactam is not expected to affect the ability to drive or use machines. Piperacillin/Tazobactam contains sodium Piperacillin/Tazobactam 2 g/0.25 g This medicine contains 108 mg sodium (main component of cooking/table salt) in each vial. This is equivalent to 5.4% of the recommended maximum daily dietary intake of sodium for an adult. Piperacillin/Tazobactam 4 g/0.5 g This medicine contains 216 mg sodium (main component of cooking/table salt) in each vial. This is equivalent to 10.8% of the recommended maximum daily dietary intake of sodium for an adult. This should be taken into consideration if you are on a controlled-sodium diet.

How to take it

Piperacillin/Tazobactam Your doctor or other healthcare professional will give you this medicine through an infusion (a drip for 30 minutes) into one of your veins. Dosage The dose of medicine given to you depends on what you are being treated for, your age, and whether or not you have kidney problems. Adults and adolescents above 12 years of age The usual dose is 4 g/0.5 g of piperacillin/tazobactam given every 6-8 hours, which is given into one of your veins (directly into the blood stream). Children aged 2 to 12 years The usual dose for children with abdominal infections is 100 mg/12.5 mg/kg of body weight of piperacillin/tazobactam given every 8 hours into one of your veins (directly into the blood stream). The usual dose for children with low white blood cell counts is 80 mg/10 mg/kg of body weight of piperacillin/tazobactam given every 6 hours into one of your veins (directly into the blood stream).

There have been reports about a disease in which the immune system makes too many of otherwise normal white blood cells called histiocytes and lymphocytes,

Your doctor will calculate the dose depending on your child's weight but each individual dose will not exceed 4 g/0.5 g of Piperacillin/Tazobactam.

The following information is intended for healthcare professionals only:

to administration. The solution should only be used if the solution is clear and free from particles.

Note: Use for bacteraemia due to extended-beta-lactamase (ESBL) producing E. coli and K. pneumoniae (ceftriaxone non-susceptible), is not recommended in adult patients.

Intravenous use Reconstitute each vial with the volume of solvent shown in the table below, using one of the compatible solvents for reconstitution. Swirl until dissolved. When swirled constantly, reconstitution generally occurs within 2 minutes (for details on handling, please see below).

How to store Piperacillin/Tazobactam Unopened vials: Do not store above 30 °C. Keep the vial in the outer carton in order to protect from light. Reconstituted solution in vial Chemical and physical in-use stability has been demonstrated for up to 12 hours at 25 °C and 48 hours when stored in a refrigerator at 2-8 °C, when reconstituted with one of the compatible solvents for reconstitution (see Instructions for use below). Diluted reconstituted solution, for infusion The diluted reconstituted solution when using one of the compatible solvents at the suggested dilution volume (see Instructions for use below), demonstrated chemical and physical in-use stability for up to 12 hours at 25 °C and 48 hours when stored in a refrigerator at 2-8 °C. From a microbiological point of view, the reconstituted and diluted solutions 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 12 hours at 2-8 °C. Instructions for use Piperacillin/Tazobactam will be given by intravenous infusion (a drip for 30 minutes). The reconstitution and dilution is to be made under aseptic conditions. The solution is to be inspected visually for particulate matter and discolouration prior

Content of vial 2 g/0.25 g (2 g piperacillin and 0.25 g tazobactam) 4 g/0.5 g (4 g piperacillin and 0.5 g tazobactam)

Volume of solvent* to be added to vial 10 ml 20 ml

  • Compatible solvents for reconstitution:
  • 9 mg/ml (0.9%) sodium chloride solution
  • 50 mg/ml (5%) glucose solution
  • 50 mg/ml (5%) glucose in 9 mg/ml (0.9%) sodium chloride solution
  • Sterile water for injections(1) (1) Maximum recommended volume of sterile water for injections per dose is 50 ml.

The reconstituted solutions should be withdrawn from the vial by syringe. When reconstituted as directed, the vial contents withdrawn by syringe will provide the labelled amount of piperacillin and tazobactam. The reconstituted solutions may be further diluted to the desired volume (e.g. 50 ml to 150 ml) with one of the following compatible solvents:

  • 9 mg/ml (0.9%) sodium chloride solution
  • 50 mg/ml (5%) glucose solution
  • 50 mg/ml (5%) glucose in 9 mg/ml (0.9%) sodium chloride solution
  • Ringer's acetate solution

Read all of this leaflet carefully before you start using this medicine because it contains important information for you.

  • Keep this leaflet. You may need to read it again.
  • If you have any further questions, ask your doctor, pharmacist or nurse.
  • This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
  • If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4.

You will be given Piperacillin/Tazobactam until the sign of infection has gone completely (5 to 14 days). Patients with kidney problems Your doctor may need to reduce the dose of Piperacillin/Tazobactam or how often you are given it. Your doctor may also want to test your blood to make sure that your treatment is at the right dose, especially if you have to take this medicine for a long time. If you receive more Piperacillin/Tazobactam than you should As you will receive Piperacillin/Tazobactam from a doctor or other healthcare professional, you are unlikely to be given the wrong dose. However, if you experience side effects, such as convulsions, or think you have been given too much, tell your doctor immediately. If you miss a dose of Piperacillin/Tazobactam If you think you have not been given a dose of Piperacillin/Tazobactam, tell your doctor or other healthcare professional immediately. If you have any further 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. See a doctor immediately if you experience any of these potentially serious side effects of Piperacillin/Tazobactam: The serious side effects (with frequency in brackets) of Piperacillin/Tazobactam are:

  • serious skin rashes [Stevens-Johnson syndrome, dermatitis bullous (Not known), dermatitis exfoliative (Not known), toxic epidermal necrolysis (Rare)] appearing initially as reddish target-like spots or circular patches often with central blisters on the trunk. Additional signs include ulcers in the mouth, throat, nose, extremities, genitals and conjunctivitis (red and swollen eyes). The rash may progress to widespread blistering or peeling of the skin and potentially may be life-threatening.
  • severe potentially fatal allergic condition (drug reaction with eosinophilia and systemic symptoms) that can involve the skin and most importantly other organs under the skin such as the kidney and the liver.
  • a skin condition (acute generalised exanthematous pustulosis) accompanied by fever, which consists of numerous tiny fluid filled blisters contained within large areas of swollen and reddened skin.
  • swelling of the face, lips, tongue or other parts of the body (Not known)
  • shortness of breath, wheezing or trouble breathing (Not known)
  • severe rash or hives (Uncommon), itching or rash on the skin (Common)
  • yellowing of the eyes or skin (Not known)
  • damage to blood cells [the signs include: being breathless when you do not expect it, red or brown urine (Not known), nosebleeds (Rare) and small spot bruising (Not known)], severe decrease in white blood cells (Rare)
  • severe or persistent diarrhoea accompanied by a fever or weakness (Rare) If any of the following side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or other healthcare professional. Very common side effects (may affect more than 1 in 10 people):
  • diarrhoea Common side effects (may affect up to 1 in 10 people):
  • yeast infection
  • decrease in platelets, decrease of red blood cells or blood pigment / haemoglobin, abnormal lab test (positive direct Coombs), prolonged blood clotting time (activated partial thromboplastin time prolonged)
  • decrease in blood protein
  • headache, sleeplessness
  • abdominal pain, vomiting, nausea, constipation, upset stomach
  • increase in blood liver enzymes
  • skin rash, itching
  • abnormal kidney blood tests
  • fever, injection site reaction Uncommon side effects (may affect up to 1 in 100 people):
  • decrease in white blood cells (leukopenia), prolonged blood clotting time (prothrombin time prolonged)
  • decreased blood potassium, decreased blood sugar
  • fits (convulsions), seen in patients on high doses or with kidney problems
  • low blood pressure, inflammation of the veins (felt as tenderness or redness in the affected area), reddening of skin
  • increase of a blood pigment breakdown product (bilirubin)
  • skin reactions with redness, formation of skin lesions, nettle rash
  • joint and muscle pain
  • chills

Rare side effects (may affect up to 1 in 1,000 people):

  • severe decrease in white blood cells (agranulocytosis), bleeding of the nose
  • serious infection of the colon, inflammation of the mucous lining of the mouth
  • detachment of the top layer of the skin all over the body (toxic epidermal necrolysis) Not known (cannot be estimated from the available data) side effects:
  • severe decrease of red blood cells, white blood cells and platelets (pancytopenia), decrease in white blood cells (neutropenia), decrease of red blood cells due to premature breakdown or degradation, small spot bruising, bleeding time prolonged, increase of platelets, increase of a specific type of white blood cells (eosinophilia)
  • allergic reaction and severe allergic reaction
  • inflammation of the liver, yellow staining of the skin or whites of the eyes
  • serious body wide allergic reaction with skin and mucous lining rashes, blistering and various skin eruptions (Stevens-Johnson Syndrome), severe allergic condition involving skin and other organs such as the kidney and the liver (drug reaction with eosinophilia and systemic symptoms), numerous tiny fluid filled blisters contained within large areas of swollen and reddened skin accompanied by fever (acute generalised exanthematous pustulosis), skin reactions with blistering (dermatitis bullous)
  • poor kidney functions and kidney problems
  • a form of lung disease where eosinophils (a form of white blood cell) appear in the lung in increased numbers
  • acute disorientation and confusion (delirium). Piperacillin therapy has been associated with an increased incidence of fever and rash in cystic fibrosis patients. Beta-lactam antibiotics, including piperacillin/tazobactam, may lead to signs of altered brain function (encephalopathy) and convulsions. 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 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

Piperacillin/Tazobactam 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 after "EXP". The expiry date refers to the last day of that month. Unopened vials: Do not store above 30 °C. Keep the vial in the outer carton in order to protect from light. For single use only. Discard any unused solution. 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 Piperacillin/Tazobactam contains

  • The active substances are piperacillin and tazobactam. Each vial contains 2 g piperacillin (as sodium salt) and 0.25 g tazobactam (as sodium salt). Each vial contains 4 g piperacillin (as sodium salt) and 0.5 g tazobactam (as sodium salt).
  • There are no other ingredients. What Piperacillin/Tazobactam looks like and contents of the pack Piperacillin/Tazobactam 2 g/0.25 g is a white to off-white powder supplied in a vial. Packs containing 1 or 10 vials. Piperacillin/Tazobactam 4 g/0.5 g is a white to off-white powder supplied in a vial. Packs containing 1 or 10 vials. Not all pack sizes may be marketed. Marketing Authorisation Holder and Manufacturer AS KALCEKS Krustpils iela 71E, Rīga, LV-1057, Latvia Tel.: +371 67083320 E-mail: [email protected] This leaflet was last revised in 06/2023

27.06.2023. MiGB/I/0/1-N1

Incompatibilities Aminoglycoside Piperacillin/ Piperacillin/ Aminoglycoside Acceptable Whenever Piperacillin/Tazobactam is used Tazobactam Tazobactam concentration diluents concurrently with another antibiotic Dose diluent volume range* (mg/ml) (e.g. aminoglycosides), the substances must (ml) be administered separately. The mixing of Amikacin 2 g/0.25 g 50, 100, 150 1.75 – 7.5 0.9% sodium beta-lactam antibiotics with 4 g/0.5 g chloride or aminoglycosides, in vitro, can result in 5% glucose substantial inactivation of the Gentamicin 2 g/0.25 g 0.7 – 3.32 0.9% sodium 50, 100, 150 aminoglycoside. However, amikacin and 4 g/0.5 g chloride or gentamicin were determined to be 5% glucose compatible with piperacillin/tazobactam in vitro in certain diluents at specific concentrations (see Co-administration of

  • The dose of aminoglycoside should be based on Piperacillin/Tazobactam with aminoglycosides below). patient weight, status of infection (serious or life-threatening) and renal function (creatinine Piperacillin/Tazobactam should not be mixed with clearance). other substances in a syringe or infusion bottle since compatibility has not been established. Compatibility of Piperacillin/Tazobactam with other aminoglycosides has not been established. Only the Because of chemical instability, Piperacillin/Tazobactam concentration and diluents for amikacin and should not be used with solutions containing only gentamicin with the dose of Piperacillin/Tazobactam sodium bicarbonate. listed in the above table have been established as compatible for co-administration via Y-site infusion. Piperacillin/Tazobactam should not be added to blood Simultaneous co-administration via Y-site in any products or albumin hydrolysates. manner other than listed above may result in inactivation of the aminoglycoside by Co-administration of Piperacillin/Tazobactam with Piperacillin/Tazobactam. aminoglycosides Due to the in vitro inactivation of the aminoglycoside by beta-lactam antibiotics, Piperacillin/Tazobactam and the aminoglycoside are recommended for separate administration. Piperacillin/Tazobactam and the aminoglycoside should be reconstituted and diluted separately when concomitant therapy with aminoglycosides is indicated. In circumstances where co-administration is recommended, Piperacillin/Tazobactam is compatible for simultaneous co-administration via Y-site infusion only with the following aminoglycosides under the following conditions:

Frequently asked questions about Piperacillin/Tazobactam 2 g/0.25 g powder for solution for infusion

How do I take Piperacillin/Tazobactam 2 g/0.25 g powder for solution for infusion?

Piperacillin/Tazobactam 2 g/0.25 g powder for solution for infusion comes as infusion containing 2g / 0.25g. 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 Piperacillin/Tazobactam 2 g/0.25 g powder for solution for infusion?

The active substance in Piperacillin/Tazobactam 2 g/0.25 g powder for solution for infusion is piperacillin sodium, tazobactam sodium.

Are there equivalent medicines to Piperacillin/Tazobactam 2 g/0.25 g powder for solution for infusion?

Medicines with the same active substance, strength and form include: Piperacillin/Tazobactam 2 g / 0.25 g powder for solution for infusion, Piperacillin/Tazobactam 2 g/0.25 g powder for solution for infusion, Piperacillin/Tazobactam 2g/0.25g Powder for Solution for Infusion. In total there are 4 equivalent products. 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 Piperacillin/Tazobactam 2 g/0.25 g powder for solution for 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 Piperacillin/Tazobactam 2 g/0.25 g powder for solution for 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: Piperacillin sodium, tazobactam sodium (11 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

Piperacillin/Tazobactam is indicated for the treatment of the following infections in adults and children over 2 years of age (see sections 4.2 and 5.1):

Adults and adolescents

– Severe pneumonia including hospital-acquired and ventilator-associated pneumonia

– Complicated urinary tract infections (including pyelonephritis)

– Complicated intra-abdominal infections

– Complicated skin and soft tissue infections (including diabetic foot infections)

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

Piperacillin/Tazobactam may be used in the management of neutropenic patients with fever suspected to be due to a bacterial infection.

Note: Use for bacteraemia due to extended-beta-lactamase (ESBL) producing E. coli and K. pneumoniae (ceftriaxone non-susceptible), is not recommended in adult patients, see section 5.1.

Children 2 to 12 years of age

– Complicated intra-abdominal infections

Piperacillin/Tazobactam may be used in the management of neutropenic children with fever suspected to be due to a bacterial infection.

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

4.2. Posology and method of administration

Posology

The dose and frequency of Piperacillin/Tazobactam depends on the severity and localisation of the infection and expected pathogens.

Adult and adolescent patients

Infections

The usual dose is 4 g piperacillin/0.5 g tazobactam given every 8 hours.

For nosocomial pneumonia and bacterial infections in neutropenic patients, the recommended dose is 4 g piperacillin/0.5 g tazobactam administered every 6 hours. This regimen may also be applicable to treat patients with other indicated infections when particularly severe.

The following table summarises the treatment frequency and the recommended dose for adult and adolescent patients by indication or condition:

Treatment frequency

Piperacillin/tazobactam 4 g/0.5 g

Every 6 hours

Severe pneumonia

Neutropenic adults with fever suspected to be due to a bacterial infection

Every 8 hours

Complicated urinary tract infections (including pyelonephritis)

Complicated intra-abdominal infections

Skin and soft tissue infections (including diabetic foot infections)

Patients with renal impairment

The intravenous dose should be adjusted to the degree of actual renal impairment as follows (each patient must be monitored closely for signs of substance toxicity; medicinal product dose and interval should be adjusted accordingly):

Creatinine clearance (ml/min)

Piperacillin/Tazobactam (recommended dose)

> 40

No dose adjustment necessary

20-40

Maximum dose suggested: 4 g/0.5 g every 8 hours

< 20

Maximum dose suggested: 4 g/0.5 g every 12 hours

For patients on haemodialysis, one additional dose of piperacillin/tazobactam 2 g/0.25 g should be administered following each dialysis period, because haemodialysis removes 30%-50% of piperacillin in 4 hours.

Patients with hepatic impairment

No dose adjustment is necessary (see section 5.2).

Elderly patients

No dose adjustment is required for the elderly with normal renal function or creatinine clearance values above 40 ml/min.

Paediatric population (2-12 years of age)

Infections

The following table summarises the treatment frequency and the dose per body weight for paediatric patients 2-12 years of age by indication or condition:

Dose per weight and treatment frequency

Indication/condition

80 mg Piperacillin/10 mg Tazobactam per kg body weight / every 6 hours

Neutropenic children with fever suspected to be due to bacterial infections*

100 mg Piperacillin/12.5 mg Tazobactam per kg body weight / every 8 hours

Complicated intra-abdominal infections*

* Not to exceed the maximum 4 g/0.5 g per dose over 30 minutes.

Patients with renal impairment

The intravenous dose should be adjusted to the degree of actual renal impairment as follows (each patient must be monitored closely for signs of substance toxicity; medicinal product dose and interval should be adjusted accordingly):

Creatinine clearance (ml/min)

Piperacillin/Tazobactam (recommended dose)

> 50

No dose adjustment needed.

≤ 50

70 mg piperacillin/8.75 mg tazobactam/kg every 8 hours.

For children on haemodialysis, one additional dose of 40 mg piperacillin/5 mg tazobactam/kg should be administered following each dialysis period.

Use in children aged below 2 years

The safety and efficacy of Piperacillin/Tazobactam in children 0-2 years of age has not been established.

No data from controlled clinical studies are available.

Treatment duration

The usual duration of treatment for most indications is in the range of 5-14 days. However, the duration of treatment should be guided by the severity of the infection, the pathogen(s) and the patient's clinical and bacteriological progress.

Method of administration

Piperacillin/Tazobactam 2 g/0.25 g is administered by intravenous infusion (over 30 minutes).

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

4.3. Contraindications

Hypersensitivity to the active substances, any other penicillin-antibacterial agent or to any of the excipients listed in section 6.1.

History of acute severe allergic reaction to any other beta-lactam active substances (e.g. cephalosporin, monobactam or carbapenem).

4.4. Special warnings and precautions for use

The selection of piperacillin/tazobactam to treat an individual patient should take into account the appropriateness of using a broad-spectrum semi-synthetic penicillin based on factors such as the severity of the infection and the prevalence of resistance to other suitable antibacterial agents.

Before initiating therapy with Piperacillin/Tazobactam, careful inquiry should be made concerning previous hypersensitivity reactions to penicillins, other beta-lactam agents (e.g. cephalosporin, monobactam or carbapenem) and other allergens. Serious and occasionally fatal hypersensitivity (anaphylactic/anaphylactoid [including shock]) reactions have been reported in patients receiving therapy with penicillins, including piperacillin/tazobactam. These reactions are more likely to occur in persons with a history of sensitivity to multiple allergens. Serious hypersensitivity reactions require the discontinuation of the antibiotic, and may require administration of epinephrine and other emergency measures.

Piperacillin/Tazobactam may cause severe cutaneous adverse reactions, such as Stevens-Johnson syndrome, toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms, and acute generalised exanthematous pustulosis (see section 4.8). If patients develop a skin rash they should be monitored closely and Piperacillin/Tazobactam discontinued if lesions progress.

Haemophagocytic lymphohistiocytosis (HLH): Cases of HLH have been reported in patients treated with piperacillin/tazobactam, often following treatment longer than 10 days. HLH is a life-threatening syndrome of pathologic immune activation characterised by clinical signs and symptoms of an excessive systemic inflammation (e.g., fever, hepatosplenomegaly, hypertriglyceridaemia, hypofibrinogenaemia, high serum ferritin, cytopenias and haemophagocytosis). Patients who develop early manifestations of pathologic immune activation should be evaluated immediately. If diagnosis of HLH is established piperacillin/tazobactam treatment should be discontinued.

Antibiotic-induced pseudomembranous colitis may be manifested by severe, persistent diarrhoea which may be life-threatening. The onset of pseudomembranous colitis symptoms may occur during or after antibacterial treatment. In these cases Piperacillin/Tazobactam, should be discontinued.

Therapy with Piperacillin/Tazobactam may result in the emergence of resistant organisms, which might cause super-infections.

Bleeding manifestations have occurred in some patients receiving beta-lactam antibiotics. These reactions sometimes have been associated with abnormalities of coagulation tests, such as clotting time, platelet aggregation and prothrombin time, and are more likely to occur in patients with renal failure. If bleeding manifestations occur, the antibiotic should be discontinued and appropriate therapy instituted.

Leukopenia and neutropenia may occur, especially during prolonged therapy; therefore, periodic assessment of haematopoietic function should be performed.

As with treatment with other penicillins, neurological complications in the form of convulsions (seizures) may occur when high doses are administered, especially in patients with impaired renal function (see section 4.8).

Piperacillin/Tazobactam 2 g/0.25 g

This medicinal product contains 108 mg sodium per vial, equivalent to 5.4% of the WHO recommended maximum daily intake of 2 g sodium for an adult.

This should be taken into consideration for patients who are on a controlled sodium diet.

Hypokalaemia may occur in patients with low potassium reserves or those receiving concomitant medicinal products that may lower potassium levels; periodic electrolyte determinations may be advisable in such patients.

Renal impairment

Due to its potential nephrotoxicity (see section 4.8), piperacillin/tazobactam should be used with care in patients with renal impairment or in hemodialysis patients. Intravenous dosages and administration intervals should be adjusted to the degree of renal function impairment (see section 4.2).

In a secondary analysis using data from a large multicenter, randomized-controlled trial when glomerular filtration rate (GFR) was examined after administration of frequently used antibiotics in critically ill patients, the use of piperacillin/tazobactam was associated with a lower rate of reversible GFR improvement compared with the other antibiotics. This secondary analysis concluded that piperacillin/tazobactam was a cause of delayed renal recovery in these patients.

Combined use of piperacillin/tazobactam and vancomycin may be associated with an increased incidence of acute kidney injury (see section 4.5).

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

Non-depolarising muscle relaxants

Piperacillin when used concomitantly with vecuronium has been implicated in the prolongation of the neuromuscular blockade of vecuronium. Due to their similar mechanisms of action, it is expected that the neuromuscular blockade produced by any of the non-depolarising muscle relaxants could be prolonged in the presence of piperacillin.

Anticoagulants

During simultaneous administration of heparin, oral anticoagulants and other substances that may affect the blood coagulation system including thrombocyte function, appropriate coagulation tests should be performed more frequently and monitored regularly.

Methotrexate

Piperacillin may reduce the excretion of methotrexate; therefore, serum levels of methotrexate should be monitored in patients to avoid substance toxicity.

Probenecid

As with other penicillins, concurrent administration of probenecid and piperacillin/tazobactam produces a longer half-life and lower renal clearance for both piperacillin and tazobactam; however, peak plasma concentrations of either substances are unaffected.

Aminoglycosides

Piperacillin, either alone or with tazobactam, did not significantly alter the pharmacokinetics of tobramycin in subjects with normal renal function and with mild or moderate renal impairment. The pharmacokinetics of piperacillin, tazobactam, and the M1 metabolite were also not significantly altered by tobramycin administration.

The inactivation of tobramycin and gentamicin by piperacillin has been demonstrated in patients with severe renal impairment.

For information related to the administration of piperacillin/tazobactam with aminoglycosides please refer to sections 6.2 and 6.6.

Vancomycin

Studies have detected an increased incidence of acute kidney injury in patients concomitantly administered piperacillin/tazobactam and vancomycin as compared to vancomycin alone (see section 4.4). Some of these studies have reported that the interaction is vancomycin dose-dependent.

No pharmacokinetic interactions have been noted between piperacillin/tazobactam and vancomycin.

Effects on laboratory tests

Non-enzymatic methods of measuring urinary glucose may lead to false-positive results, as with other penicillins. Therefore, enzymatic urinary glucose measurement is required under Piperacillin/Tazobactam therapy.

A number of chemical urine protein measurement methods may lead to false-positive results. Protein measurement with dip sticks is not affected.

The direct Coombs test may be positive.

Bio-Rad Laboratories Platelia Aspergillus EIA tests may lead to false-positive results for patients receiving Piperacillin/Tazobactam. Cross-reactions with non-Aspergillus polysaccharides and polyfuranoses with Bio-Rad Laboratories Platelia Aspergillus EIA test have been reported.

Positive test results for the assays listed above in patients receiving Piperacillin/Tazobactam should be confirmed by other diagnostic methods.

4.6. Fertility, pregnancy and lactation

Pregnancy

There are no or a limited amount of data from the use of Piperacillin/Tazobactam in pregnant women.

Studies in animals have shown developmental toxicity, but no evidence of teratogenicity, at doses that are maternally toxic (see section 5.3).

Piperacillin and tazobactam cross the placenta. Piperacillin/tazobactam should only be used during pregnancy if clearly indicated, i.e. only if the expected benefit outweighs the possible risks to the pregnant woman and foetus.

Breast-feeding

Piperacillin is excreted in low concentrations in human milk; tazobactam concentrations in human milk have not been studied. Women who are breast-feeding should be treated only if the expected benefit outweighs the possible risks to the woman and child.

Fertility

A fertility study in rats showed no effect on fertility and mating after intraperitoneal administration of tazobactam or the combination piperacillin/tazobactam (see section 5.3).

4.7. Effects on ability to drive and use machines

No studies on the effect on the ability to drive and use machines have been performed.

4.8. Undesirable effects

The most commonly reported adverse reaction is diarrhoea (occurring in 1 patient out of 10).

Among the most serious adverse reactions pseudo-membranous colitis and toxic epidermal necrolysis occur in 1 to 10 patients in 10,000. The frequencies for pancytopenia, anaphylactic shock and Stevens-Johnson syndrome cannot be estimated from the currently available data.

In the following table, adverse reactions are listed by system organ class and MedDRA-preferred term. Within each frequency grouping, undesirable effects are presented in order of decreasing seriousness.

System Organ Class

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)

Frequency not known

(cannot be estimated from available data)

Infections and infestations

candida infection*

pseudo-membranous colitis

Blood and lymphatic system disorders

thrombocytopenia, anaemia*

leukopenia

agranulocytosis

pancytopenia*, neutropenia, haemolytic anaemia*, thrombocytosis*, eosinophilia*

Immune system disorders

anaphylactoid shock*, anaphylactic shock*, anaphylactoid reaction*, anaphylactic reaction*, hypersensitivity*

Metabolism and nutrition disorders

hypokalaemia

Psychiatric disorders

insomnia

delirium*

Nervous system disorders

headache

seizure*

Vascular disorders

hypotension, phlebitis, thrombophlebitis, flushing

Respiratory, thoracic and mediastinal disorders

epistaxis

eosinophilic pneumonia

Gastrointestinal disorders

diarrhoea

abdominal pain, vomiting, constipation, nausea, dyspepsia

stomatitis

Hepatobiliary disorders

hepatitis*, jaundice

Skin and subcutaneous tissue disorders

rash, pruritus

erythema multiforme*, urticaria, rash maculo-papular*

toxic epidermal necrolysis*

Stevens-Johnson syndrome*, dermatitis exfoliative, drug reaction with eosinophilia and systemic symptoms (DRESS)*, acute generalised exanthematous pustulosis (AGEP)*, dermatitis bullous, purpura

Musculoskeletal and connective tissue disorders

arthralgia, myalgia

Renal and urinary disorders

renal failure, tubulointerstitial nephritis*

General disorders and administration site conditions

pyrexia, injection site reaction

chills

Investigations

alanine aminotransferase increased, aspartate aminotransferase increased, protein total decreased, blood albumin decreased, Coombs direct test positive, blood creatinine increased, blood alkaline phosphatase increased, blood urea increased, activated partial thromboplastin time prolonged

blood glucose decreased, blood bilirubin increased, prothrombin time prolonged

bleeding time prolonged, gamma-glutamyl transferase increased

*ADR identified post marketing

Piperacillin therapy has been associated with an increased incidence of fever and rash in cystic fibrosis patients.

Beta-lactam antibiotic class effects

Beta-lactam antibiotics, including piperacillin/tazobactam, may lead to manifestations of encephalopathy and convulsions (see section 4.4).

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

4.9. Overdose

Symptoms

There have been post-marketing reports of overdose with piperacillin/tazobactam. The majority of those events experienced, including nausea, vomiting, and diarrhoea, have also been reported with the usual recommended dose. Patients may experience neuromuscular excitability or convulsions if higher than recommended doses are given intravenously (particularly in the presence of renal failure).

Treatment

In the event of an overdose, piperacillin/tazobactam treatment should be discontinued. No specific antidote is known.

Treatment should be supportive and symptomatic according to the patient's clinical presentation.

Excessive serum concentrations of either piperacillin or tazobactam may be reduced by haemodialysis (see section 4.4).

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