Package Leaflet: Information for the User
Piperacillin/Tazobactam Aurovitas 4 g/0.5 g powder for solution for infusion EFG
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
Piperacillin belongs to a group of medicines called “broad-spectrum penicillin antibiotics” and can kill many types of bacteria. Tazobactam can prevent some resistant bacteria from surviving the effects of piperacillin. In this way, when piperacillin and tazobactam are administered together, more types of bacteria are killed.
Antibiotics are used to treat bacterial infections and do not work for viral infections such as the flu or the common cold.
It is essential that you follow the instructions regarding dosage, administration interval, and treatment duration indicated by your doctor.
Do not store or reuse this medicine. If you have any leftover antibiotic after finishing treatment, return it to the pharmacy for proper disposal. Do not throw away medicines via wastewater or household waste.
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 can be used to treat bacterial infections in patients with low white blood cell counts (lower resistance to infections).
Piperacillin/tazobactam is used in children between 2 and 12 years old to treat infections in the abdomen, such as appendicitis, peritonitis (infection of the fluid and lining of the abdominal organs), and infections of the gallbladder. Piperacillin/tazobactam can be used to treat bacterial infections in patients with low white blood cell counts (lower resistance to infections).
In certain severe infections, your doctor may consider using piperacillin/tazobactam in combination with other antibiotics.
Do not use Piperacillin/Tazobactam Aurovitas
Warnings and precautions
Consult your doctor, pharmacist, or nurse before starting to use Piperacillin/Tazobactam Aurovitas:
Hemophagocytic lymphohistiocytosis
Cases of a disease in which the immune system produces too many white blood cells, called histiocytes and lymphocytes, have been reported, causing inflammation (hemophagocytic lymphohistiocytosis). This disease can be potentially fatal if not diagnosed and treated early. If you experience multiple symptoms such as fever, swelling of the lymph nodes, weakness, dizziness, difficulty breathing, bruising, or skin rash, contact your doctor immediately.
Children under 2 years
Piperacillin/tazobactam is not recommended for use in children under 2 years due to the lack of data on safety and efficacy.
Other medicines and Piperacillin/Tazobactam Aurovitas
Tell your doctor or pharmacist if you are using, have recently used, or might use any other medicines, including those obtained without a prescription.
Some medicines may interact with piperacillin or tazobactam. These include:
Effects on laboratory tests
If you need to provide a blood or urine sample, tell your doctor or laboratory staff that you are using piperacillin/tazobactam.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before using this medicine. Your doctor will decide whether piperacillin/tazobactam is suitable for you.
Piperacillin and tazobactam may pass to the fetus in the womb or through breast milk. If you are breastfeeding, your doctor will decide whether piperacillin/tazobactam is suitable for you.
Driving and using machines
Piperacillin/tazobactam is not expected to affect your ability to drive or use machines.
Piperacillin/Tazobactam Aurovitas contains sodium
This medicine contains 216 mg of sodium (the main component of table salt/cooking salt) in each vial. This is equivalent to 10.8% of the maximum recommended daily intake of sodium for an adult. This should be taken into consideration in patients on a low-sodium diet.
Your doctor or another healthcare professional will administer this medicine to you by intravenous infusion (into a vein with a drip over 30 minutes).
Dosage
The dose of medicine that you will be given depends on what you are being treated for, your age, and whether you have kidney problems.
Adults and adolescents 12 years and older
The normal dose is 4 g/0.5 g of piperacillin/tazobactam administered every 6-8 hours through a vein (directly into the bloodstream).
Children 2 to 12 years old
The normal dose for children with abdominal infections is 100 mg/12.5 mg/kg of body weight of piperacillin/tazobactam administered every 8 hours through a vein (directly into the bloodstream). The usual dose for children with low white blood cell counts is 80 mg/10 mg/kg of body weight of piperacillin/tazobactam administered every 6 hours through a vein (directly into the bloodstream).
Your doctor will calculate the dose based on the child's weight, but each individual dose will not exceed 4 g/0.5 g of piperacillin/tazobactam.
You will be given piperacillin/tazobactam until the signs of infection have completely disappeared (from 5 to 14 days).
Patients with kidney problems
Your doctor may need to reduce the dose of piperacillin/tazobactam or the frequency of administration. Your doctor may also want to perform blood tests to ensure you are receiving the correct dose of treatment, especially if you need to use this medicine for a long time.
If you use more Piperacillin/Tazobactam Aurovitas than you should
Because a doctor or another healthcare professional will administer piperacillin/tazobactam to you, it is unlikely that you will receive an incorrect dose. However, if you experience side effects such as seizures or think you have been given too much medicine, tell your doctor immediately.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone 91 562 04 20, indicating the medicine and the amount administered.
If you miss a dose of Piperacillin/Tazobactam Aurovitas
If you think you have missed a dose of piperacillin/tazobactam, tell your doctor or another healthcare professional immediately.
If you have any other questions about the use of this medicine, ask your doctor or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Consult your doctor immediatelyif you experience any of these potentially serious side effects of piperacillin/tazobactam.
The serious side effects (with frequency in parentheses) of piperacillin/tazobactam are:
If any of the followingside effects is severe or if you experience any side effect not mentioned in this leaflet, inform your doctor or another healthcare professional.
Very common side effects(may affect more than 1 in 10 people)
Common side effects(may affect up to 1 in 10 people)
Uncommon side effects(may affect up to 1 in 100 people)
Rare side effects(may affect up to 1 in 1,000 people)
Side effects with frequency not known(cannot be estimated from the available data)
In patients with cystic fibrosis, treatment with piperacillin has been associated with an increased incidence of fever and skin rashes.
Beta-lactam antibiotics, including piperacillin/tazobactam, may cause signs of brain function impairment (encephalopathy) and seizures.
Reporting of side effects
If you experience any side effects, talk to your doctor, pharmacist, or nurse, even if it is possible that the side effects are not listed in this leaflet. You can also report side effects directly through the Spanish Medicines Monitoring System: www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the carton and on the label of the vial after EXP. The expiry date refers to the last day of the month stated.
Powder:
Unopened vials: Store below 25°C.
For single use only. Discard unused solution.
The reconstituted/diluted solutions of the medicinal product are physically compatible and chemically stable for 24 hours at controlled room temperature (25°C) and 48 hours at 2-8°C.
From a microbiological point of view, the reconstituted and diluted solutions should be used immediately. If not used immediately, the storage times and conditions before use are the responsibility of the user and normally should not exceed 24 hours at 2-8°C, unless the reconstitution and dilution have taken place in controlled and validated aseptic conditions.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help to protect the environment.
Composition of Piperacillin/Tazobactam Aurovitas
Appearance and Package Contents of the Product
White to off-white powder for solution for infusion.
Piperacillin/Tazobactam Aurovitas is available in packs of 1, 10 or 12 vials packaged in cardboard boxes with a leaflet.
Not all pack sizes may be marketed.
Marketing Authorisation Holder and Manufacturer
Marketing Authorisation Holder:
Eugia Pharma (Malta) Limited
Vault 14, Level 2, Valletta Waterfront
Floriana, FRN 1914
Malta
Manufacturer:
APL Swift Services (Malta) Limited
HF26, Hal Far Industrial Estate, Hal Far
Birzebbugia, BBG 3000
Malta
For further information on this medicinal product, please contact the local representative of the Marketing Authorisation Holder:
Aurovitas Spain, S.A.U.
Avda. de Burgos, 16-D
28036 Madrid
Spain
Date of Last Revision of this Leaflet:December 2022
Detailed information on this medicinal product is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es).
This information is intended for healthcare professionals only:
Note: Use is not recommended for bacteremia due to E. coliand K. pneumoniae(non-susceptible to ceftriaxone) producing extended-spectrum beta-lactamase (ESBL) in adult patients.
Piperacillin/Tazobactam Aurovitas 4 g/0.5 g powder for solution for infusion EFG
The following text is an excerpt from the Summary of Product Characteristics that serves as a guide for the administration of Piperacillin/Tazobactam Aurovitas. When determining the suitability of use in a specific patient, the prescribing physician should be familiar with the Summary of Product Characteristics.
For slow intravenous infusion.
Incompatibilities with Diluents and Other Medicinal Products
Instructions for Use, Handling, and Disposal
Reconstitution and dilution should be carried out under aseptic conditions. Before administration, the solution should be visually inspected for particles and color change. The solution should only be used if it is clear and free of particles.
Instructions for inserting the needle into the rubber stopper
To avoid the rubber stopper being dislodged when inserting the needle into the rubber stopper, it is recommended to use a needle with an outer diameter of 0.8 mm or less for reconstitution of the medicinal product.
The needle should be inserted only into the center of the rubber stopper, vertically.
For single use only. Discard unused solution.
Disposal of unused medicinal products and all materials that have come into contact with them should be carried out in accordance with local regulations.
Sterile diluents for preparing the reconstituted solution
Instructions for dilution (for intravenous infusion)
Each vial of piperacillin/tazobactam 4 g/0.5 g should be reconstituted with 20 ml of the above diluents.
Shake until completely dissolved.
The reconstituted solutions can be further diluted to a concentration range of 13.33/1.67 mg/ml to 80/10 mg/ml with the following diluents:
Special Precautions for Storage
Unopened vials: Store below 25°C.
The reconstituted/diluted solutions of the medicinal product are physically compatible and chemically stable for 24 hours at controlled room temperature (25°C) and 48 hours at 2-8°C.
From a microbiological point of view, the reconstituted and diluted solutions should be used immediately. If not used immediately, the storage times and conditions before use are the responsibility of the user and normally should not exceed 24 hours at 2-8°C, unless the reconstitution and dilution have taken place in controlled and validated aseptic conditions.