Piperacillin/Tazobactam 2 G/0.25 G Powder For Solution For Infusion.
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Piperacillin/Tazobactam 2 g/0.25 g Powder for Solution for Infusion
Piperacillin/Tazobactam 4 g/0.5 g Powder for Solution for Infusion
Piperacillin (as Sodium) with Tazobactam (as Sodium) Please read all of this leaflet carefully before you start taking this medicine.
• Keep this leaflet. You may need to read it again
• This medicine is prescribed for you. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours
• If any of the side effects get serious, please tell your doctor. If you notice any side effects not listed in the leaflet please tell your doctor
• If you have any further questions, please ask your doctor. The name of your medicine is Piperacillin/Tazobactam 2 g/0.25 g and 4 g/0.5 g Powder for Solution for Infusion.
In the rest of this leaflet Piperacillin/Tazobactam 2 g/0.25 g and 4 g/0.5 g Powder for Solution for Infusion is called Piperacillin with Tazobactam.
In this leaflet:
1. What Piperacillin with Tazobactam is and what it is used for
2. Before you are given Piperacillin with Tazobactam
3. How Piperacillin with Tazobactam is given
4. Possible side effects
5. How to store Piperacillin with Tazobactam
6. Further information.
• if you develop convulsions during the treatment. In this case, you should inform your doctor or other healthcare professional.
• if you develop a skin rash you should inform your doctor. If your rash progresses your doctor will stop this medicine. This is because the rash might be a sign of Stevens-Johnson syndrome or toxic epidermal necrolysis which are serious skin diseases
• if you think you developed a new or worsening infection. In this case, you should inform your doctor or other healthcare professional.
Children below 2 years
Piperacillin with Tazobactam is not recommended for use in children below the age of 2 years due to insufficient data on safety and effectiveness.
Taking other medicines
Please tell your doctor or other healthcare professional if you are taking or have recently taken 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 tor 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 totobramycin or gentamycin. Tell your doctor if you have kidney problems.
Effect on laboratory tests
Tell the doctor or laboratory staff that you are taking Piperacillin with Tazobactam if you have to provide a blood or urine sample. Pregnancy and breast-feeding
If you are pregnant, think you may be pregnant or are trying to become pregnant, tell your doctor or other healthcare professional before receiving this product. Your doctor will decide if this medicine is right for you. Piperacillin and Tazobactam can pass to a baby in the womb or through breast milk. If you are breast-feeding, your doctor will decide whether this medicine is right for you.
Your doctor will advise you if you should have this medicine.
Driving and using machines
The use of Piperacillin with Tazobactam is not expected to affect the ability to drive or use machines.
Important information about some of the ingredients of this product Piperacillin/Tazobactam 2 g/0.25g contains 4.72 mmol (109 mg) of sodium per vial of powder for solution for infusion. Piperacillin/Tazobactam 4 g/0.5 g contains 9.44 mmol (217 mg) of sodium per vial of powder for solution for infusion.
To be taken into consideration by patients on a controlled sodium diet.
3. How Piperacillin with Tazobactam is given
Your doctor or other healthcare professional will give you this medicine through an infusion (a drip for 30 minutes) into one of your veins. 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.
This product must not be mixed or Co-administered with any aminoglycoside and must not be reconstituted or diluted with Lactated Ringer’s (Hartmann’s) solution. Adults and adolescents aged 12 years or older
The usual dose is 4 g/0.5 g piperacillin/tazobactam given every 6 to 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).
Your doctor will calculate the dose depending on your child's weight but the daily dose will not exceed 4 g/0.5 g.
You will be given Piperacillin with 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 with 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.
INFORMATION FOR HEALTHCARE PROFESSIONALS
Piperacillin/Tazobactam 2 g/0.25 g Powder for Solution for Infusion.
Piperacillin/Tazobactam 4 g/0.5 g Powder for Solution for Infusion.
Please refer to the Summary of Product Characteristics (SmPC) for further details on this product.
Qualitative and Quantitative Composition
Piperacillin/Tazobactam 2 g/0.25 g:
Each vial contains 2 g piperacillin (as sodium salt) and 0.25 g tazobactam (as sodium salt).
One vial of powder for solution for infusion contains 4.72 mmol (109 mg) of sodium.
Piperacillin/Tazobactam 4 g/0.5 g:
Each vial contains 4 g piperacillin (as sodium salt) and 0.5 g tazobactam (as sodium salt).
One vial of powder for solution for infusion contains 9.44 mmol (217 mg) of sodium.
For a full list of excipients see section 6.1.
Pharmaceutical Form
Powder for solution for infusion.
White to off white powder.
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.
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.
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 eight hours.
For nosocomial pneumonia and bacterial infections in neutropenic patients, the recommended dose is 4 g piperacillin / 0.5 g tazobactam administered every six 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 six hours |
Severe pneumonia |
|
Neutropenic adults with fever suspected to be due to a bacterial infection. | |
|
Every eight hours |
Complicated urinary tract infections (including pyelonephritis) |
|
Complicated intra-abdominal infections | |
|
Skin and soft tissue infections (including diabetic foot infections) |
Renal impairment
The intravenous dose should be adjusted to the degree of actual renal impairment (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 eight hours |
|
< 20 |
Maximum dose suggested: 4 g / 0.5 g every 12 hours |
For patients on haemodialysis, one additional dose of Piperacillin/Tazobactam 2g/0.25g should be administered following each dialysis period, because haemodialysis removes 30%-50% of piperacillin in four hours.
Hepatic Impairment
No dose adjustment is necessary (see section 5.2).
Dose in 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 six hours |
Neutropenic children with fever suspected to be due to bacterial infections1 2 |
|
100 mg Piperacillin / 12.5 mg Tazobactam per kg body weight / every eight hours |
Complicated intra-abdominal infections2 |
* Not to exceed the maximum 4 g / 0.5 g per dose over 30 minutes.
If you are given more Piperacillin with Tazobactam than you should
As you will be given Piperacillin with Tazobactam by 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 with Tazobactam
If you think you have not been given a dose of Piperacillin with Tazobactam, tell your doctor or other healthcare professional immediately.
If you have any further questions on the use of this product, ask your doctor or other health care professional.
4. Possible side effects
Like all medicines, Piperacillin with Tazobactam can cause side effects, although not everybody gets them.
See a doctor immediately if you experience any of these potentially serious side effects with this medicine:
The serious side effects of this medicine are:
• swelling of the face, lips, tongue or other parts of the body
• shortness of breath, wheezing or trouble breathing
• severe rash, itching or hives on the skin
• yellowing of the eyes or skin
• damage to blood cells (the signs include: being breathless when you do not expect it, red or brown urine, nosebleeds and bruising)
• severe or persistent diarrhoea accompanied by a fever or weakness
• unexpected bleeding, particularly if you are taking anticoagulants such as warfarin
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.
Common side effects (affecting less than 1 in 10 patients but more than 1 in 100) are:
• diarrhoea
• nausea and vomiting
• skin rashes.
Uncommon side effects (affecting less than 1 in 100 patients but more than 1 in 1,000) are:
• allergic reaction
• headache
• sleeplessness
• low blood pressure
• inflammation of the veins (felt as tenderness or redness in the affected area)
• constipation
• upset stomach, indigestion
• jaundice (yellowing of the skin or whites of the eyes)
• inflammation of the mucous lining of the mouth
• itching, nettle rash
• fever
• injection site reaction
• (abnormal) decrease in white blood cells (leukopenia, neutropenia) and platelets (thrombocytopenia).
• increase of certain enzymes in the blood (alanine aminotransferase increased, aspartate aminotransferase increased)
• increase of muscle metabolism product in the blood (blood creatinine increased)
• yeast infection (candidal superinfection)
• thrush
Rare side effects (effecting less than 1 in 1,000 patients but more than 1 In 10,000) are:
• (abnormal) decrease of red blood cells or blood pigment/ haemoglobin, (abnormal) decrease of red blood cells due to premature breakdown (degradation) (haemolytic anaemia), small spot bruising (purpura), bleeding of the nose (epistaxis) and bleeding time prolonged, (abnormal) increase of a specific type of white blood cells (eosinophilia)
• severe allergic reaction (anaphylactic/anaphylactoid reaction, including shock)
• flushed red skin
• a certain form of infection of the colon (pseudomembranous colitis), abdominal pain
• skin reactions with redness and formation of skin lesions (exanthema, erythema multiforme), skin reactions with blistering (bullous dermatitis)
• joint and muscle pain
• poor kidney functions and kidney problems
• inflammation of the liver (hepatitis), increase of a blood pigments breakdown product (bilirubin), increase of certain enzymes in the blood (blood alkaline phosphatase increased, gamma-glutamyltransferase increased)
• rigors chill/rigidity.
There have been very rare reports (in less than 1 in 10,000 patients) of:
• severe decrease of granular white blood cells (agranulocytosis), severe decrease of red blood cells, white blood cells and platelets (pancytopenia)
• prolonged time for blood clot formation (prolonged partial thromboplastin time, prothrombin time prolonged), abnormal lab test (positive direct Coombs), increase of platelets (thrombocythaemia)
• decrease of potassium in the blood (hypokalaemia), decrease of blood sugar (glucose), decrease of the blood protein albumin, decrease of blood total protein
• detachment of the top layer of the skin all over the body (toxic epidermal necrolysis), serious bodywide allergic reaction with skin and mucous lining rashes and various skin eruptions (Stevens-Johnson Syndrome)
• blood urea nitrogen increased.
Piperacillin therapy has been associated with an increased incidence of fever and rash in cystic fibrosis patients. 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 national reporting systems listed below:
United Kingdom:
Yellow Card Scheme
Website: http://www.mhra.gov.uk/yellowcard Ireland:
HPRA Pharmacovigilance, Earlsfort Terrace, IRL - Dublin 2; Tel: +353 1 6764971; Fax: +353 1 6762517; Website: www.hpra.ie; e-mail: medsafety@hpra.ie
5. How to store Piperacillin with Tazobactam
Keep your medicine out of the reach and sight of children.
Do not use your medicine after the expiry date given on the carton and the label on the small glass container (vial). The expiry date is the last day of the month written on the packaging.
Do not store above 25°C.
Made-up solutions may be stored for up to 24 hours in a refrigerator (2°C - 8°C). For single use only. Discard any unused solution.
Give any leftover medicine to your doctor, nurse or pharmacist. If you do this, it will help protect the environment. Do not put it down the drain or in the dustbin.
6. Further Information
What Piperacillin with Tazobactam contains
The active substances are piperacillin as the sodium salt and tazobactam as the sodium salt. There are no other ingredients. Piperacillin with Tazobactam 2 g/0.25 g contains 2 g of piperacillin (as sodium salt) and 0.25 g of tazobactam (as sodium salt).
Piperacillin with Tazobactam 4 g/0.5 g contains 4 g of piperacillin (as sodium salt) and 0.5 g of tazobactam (as sodium salt).
What Piperacillin with Tazobactam looks like
Piperacillin with Tazobactam is a powder for solution for intravenous infusion.
Contents of the pack
The powder comes in a glass vial with a rubber cap and metal/ plastic seal. 1, 2, 5, or 10 vials come in a box. Not all pack sizes may be available.
Other formats:
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 |
|
Piperacillin/Tazobactam 2 g/0.25 g Powder for Solution for Infusion. |
29831/0329 |
|
Piperacillin/Tazobactam 4 g/0.5 g Powder for Solution for Infusion. |
29831/0341 |
This is a service provided by the Royal National Institute of Blind People.
Marketing Authorisation Holder and Manufacturer Marketing Authorisation Holder: Wockhardt UK Limited, Ash Road North, Wrexham, LL13 9UF, UK.
Manufacturer: Laboratory Reig Jofre S.A., C/Jarama s/n Pol Ind, 45007, Toledo, Spain.
This leaflet was approved in 10/2014
103276-4 fwOCKHARDT
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. |
|
O LO VI |
70 mg piperacillin / 8.75 mg tazobactam / kg every eight 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.
Route of administration
Piperacillin/Tazobactam 2 g / 0.25 g is administered by intravenous infusion (over 30 minutes). Piperacillin/Tazobactam 4 g / 0.5 g is administered by intravenous infusion (over 30 minutes).
For reconstitution instructions, see section 6.6. Pharmaceutical Particulars List of excipients None
Incompatibilities
This medicinal product must not be mixed with other medicinal products except those mentioned in section 6.6.
Whenever Piperacillin/Tazobactam is used concurrently with another antibiotic (e.g. aminoglycosides), the substances must be administered separately. The mixing of Piperacillin/ Tazobactam with an aminoglycoside in vitro can result in substantial inactivation of the aminoglycoside. Piperacillin/ Tazobactam should not be mixed with other substances in a syringe or infusion bottle since compatibility has not been established.
Because of chemical instability, Piperacillin/Tazobactam should not be used with solutions containing only sodium bicarbonate.
Lactated Ringer's solution is not compatible with Piperacillin/ Tazobactam.
Piperacillin/Tazobactam should not be added to blood products or albumin hydrolysates.
Shelf life
Unopened - 3 years
When reconstituted with water for injections or saline, reconstituted solutions will remain stable for 24 hours at 25°C and for 48 hours at 4°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 2-8°C, unless reconstitution has taken place in controlled and validated aseptic conditions.
Special precautions for storage Unopened: Do not store above 25°C.
After reconstitution: Store at 2-8°C (see 6.3 Shelf Life).
Nature and contents of container
Packs of one two, five and ten* Type II glass vial with butyl
rubber stopper and aluminium/plastic seal
*Not all pack sizes may be marketed.
Special precautions for disposal and other handling Intravenous use
Each vial of Piperacillin/Tazobactam 2 g/0.25 g Powder for Solution for Infusion should be reconstituted with 10ml of one of the diluents detailed below.
Each vial of Piperacillin/Tazobactam 4 g/0.5 g Powder for Solution for Infusion should be reconstituted with 20ml of one of the following diluents:
• Sterile water for injections
• 0.9% sodium chloride for injection
To achieve effective reconstitution, invert and shake the vial thoroughly to detach any powder adhering to the walls prior to addition of the diluent. Add the solvent and shake until complete dissolution is achieved.
The reconstituted solution should be further diluted to at least 50ml with one of the reconstitution diluents, or with Dextrose 5% in Water.
Displacement Volume
Each gram of Piperacillin/Tazobactam Powder for Solution for Infusion has a displacement volume of 0.7ml. Piperacillin/Tazobactam 2 g/0.25 g Powder for Solution for Infusion will displace 1.58ml.
Piperacillin/Tazobactam 4 g/0.5 g Powder for Solution for Infusion will displace 3.15ml.
The reconstitution/dilution is to be made under aseptic conditions. The solution is to be inspected visually for particulate matter and discoloration prior to administration. The solution should only be used if the solution is clear and free from particles.
Any unused product or waste material should be disposed of in accordance with local requirements.
Marketing Authorisation Holder
Wockhardt UK Limited, Ash Road North, Wrexham LL13 9UF
Marketing Authorisation Number
PL 29831/0329, PA 1339/1/1 (Piperacillin/Tazobactam 2 g/0.25 g
Powder for Solution for Infusion)
PL 29831/0341, PA 1339/1/2 (Piperacillin/Tazobactam 4 g/0.5 g Powder for Solution for Infusion)
Date of First Authorisation/Renewal of Authorisation UK: 17 April 2009. Ireland: 19 June 2009 Date of Revision of Text October 2012
103276-4 PwOCKHARDT
1. What Piperacillin with Tazobactam is and what it is used for
Piperacillin belongs to the group of medicines called 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 with 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 with Tazobactam may be used to treat bacterial infections in patients with low white blood cell counts (reduced resistance to infections).
Piperacillin with 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 with 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 with Tazobactam in combination with other antibiotics.
2. Before you are given Piperacillin with Tazobactam
Do not use Piperacillin with Tazobactam:
• if you are allergic (hypersensitive) to piperacillin or tazobactam or any of the other ingredients of this medicine
• if you are allergic (hypersensitive) to antibiotics known as penicillins, cephalosporins or other beta-lactamase inhibitors, as you may be allergic to Piperacillin with Tazobactam.
Take special care with Piperacillin with 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 liver or kidney 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 certain medicines (called anticoagulants) to avoid an excess of blood clotting (see also Using other medicines in this leaflet) or any unexpected bleeding occurs during the treatment.
In this case, you should inform your doctor or other healthcare
professional immediately.