


Ask a doctor about a prescription for AMOXICILLIN/CLAVULANIC ACID SANDOZ 1000 mg/200 mg POWDER FOR INJECTION AND INFUSION SOLUTION
Package Leaflet: Information for the User
Amoxicillin/Clavulanic Acid Sandoz 1000 mg/200 mg Powder for Solution for Injection and Infusion EFG
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
Contents of the Package Leaflet
Amoxicillin/clavulanic acid is an antibiotic that eliminates the bacteria that cause infections. It contains two different medicines called amoxicillin and clavulanic acid. Amoxicillin belongs to a group of medicines known as "penicillins" which can sometimes lose their effectiveness (become inactivated). The other component (clavulanic acid) prevents this from happening.
Antibiotics are used to treat bacterial infections and are not effective against viral infections such as the flu or the common cold.
It is important that you follow the instructions regarding dosage, administration, and duration of treatment as indicated by your doctor.
Do not store or reuse this medicine. If you have any leftover antibiotic after completing your treatment, return it to the pharmacy for proper disposal. Do not throw medicines down the drain or in the trash.
Amoxicillin/clavulanic acid is used in adults and children to treat the following infections:
Amoxicillin/clavulanic acid is used in adults to prevent infections associated with major surgical procedures.
Do not use Amoxicillin/Clavulanic Acid Sandoz:
Do not receive Amoxicillin/Clavulanic Acid Sandoz if any of the above applies to you.If you are not sure, consult your doctor, pharmacist, or nurse.
Warnings and Precautions
Consult your doctor, pharmacist, or nurse before starting to use amoxicillin/clavulanic acid if:
If you are not sure if any of the above symptoms affect you, inform your doctor, pharmacist, or nurse before receiving amoxicillin/clavulanic acid.
In some cases, your doctor may investigate the type of bacteria causing your infection. Depending on the results, you may be prescribed a different formulation of amoxicillin/clavulanic acid or another medicine.
Symptoms to be aware of
Amoxicillin/clavulanic acid can worsen certain existing conditions or cause serious side effects. These include allergic reactions, seizures, and inflammation of the large intestine. You should be aware of certain symptoms while being administered amoxicillin/clavulanic acid to reduce the risk of problems. See "Symptoms to be aware of" in section4.
Blood and urine tests
If you are having blood tests (such as red blood cell status or liver function studies) or urine tests (to check glucose levels), inform your doctor or nurse that you are being administered amoxicillin/clavulanic acid. This is because amoxicillin/clavulanic acid can alter the results of these types of tests.
Using Amoxicillin/Clavulanic Acid Sandoz with other medicines
Tell your doctor or pharmacist if you are using or have recently used or might use any other medicines, including those obtained without a prescription and herbal medicines.
If you are taking allopurinol (used for gout) with amoxicillin/clavulanic acid, you may be more likely to have a skin allergic reaction.
Probenecid (used to treat gout), concomitant use of probenecid may reduce the excretion of amoxicillin and is not recommended.
If you are taking anticoagulants (such as warfarin) with amoxicillin/clavulanic acid, more blood tests will be needed.
Methotrexate (a medicine used to treat cancer and severe psoriasis), penicillins may reduce the excretion of methotrexate and cause a potential increase in side effects.
Amoxicillin/clavulanic acid may affect how mycophenolate mofetil (a medicine used to prevent organ rejection in transplant patients) works.
Pregnancy and Breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor, pharmacist, or nurse before using this medicine.
Amoxicillin/Clavulanic Acid Sandoz contains sodium and potassium
This medicine contains 59.3 mg of sodium per vial, equivalent to 2.9% of the maximum daily intake of 2 g of sodium recommended by the WHO for an adult.
This medicine contains less than 39 mg (1 mmol) of potassium per vial, and is therefore considered "essentially potassium-free".
You will never administer this medicine to yourself. A qualified person, such as a doctor or nurse, will administer it to you.
The usual doses are:
Adults and children weighing 40 kg or more
Standard dose | 1000 mg/200 mg every 8 hours. |
To prevent infections during and after surgery. | 1000 mg/200 mg before surgery when you are given your anesthetic. The dose may vary depending on the type of surgery you are having. Your doctor may repeat the dose if the surgery lasts more than one hour. |
Children weighing less than 40 kg
Children 3 months or older: | 25 mg/5 mg per kilogram of body weight every 8 hours. |
Children under 3 months and weighing less than 4 kg | 25 mg/5 mg per kilogram of body weight every 12 hours. |
Patients with kidney and liver problems
How Amoxicillin/Clavulanic Acid Sandoz will be administered to you
If you use more Amoxicillin/Clavulanic Acid Sandoz than you should
It is very unlikely that you will be given too much amoxicillin/clavulanic acid, but if you think you have been given too much, tell your doctor, pharmacist, or nurse immediately. The symptoms may be stomach upset (nausea, vomiting, or diarrhea) or seizures.
If you have any further questions on how this product is administered, ask your doctor, pharmacist, or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The following side effects may occur with this medicine.
Symptoms to be aware of
Allergic reactions:
Contact your doctor immediatelyif you experience any of these symptoms. Stop using Amoxicillin/Clavulanic Acid Sandoz.
Inflammation of the large intestine
Inflammation of the large intestine, which causes watery diarrhea normally with blood and mucus, stomach pain, and/or fever.
Contact your doctor as soon as possiblefor advice if you have these symptoms.
Common side effects (may affect up to 1 in 10 people)
Uncommon side effects (may affect up to 1 in 100 people)
Uncommon side effects that may appear in your blood tests:
Rare side effects (may affect up to 1 in 1,000 people)
Rare side effects that may appear in your blood tests:
Other side effects
Other side effects that have occurred in a very small number of patients and whose exact frequency is unknown:
Side effects that may appear in your blood or urine tests:
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly through the Spanish Pharmacovigilance System for Human Use Medicines: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
The expiration date and storage instructions on the label are for the information of the doctor or nurse. The doctor, pharmacist, or nurse will reconstitute your medicine, which must be used within 15 minutes of reconstitution.
Do not store above 25°C.
Keep this medicine out of the sight and reach of children.
Do not use Amoxicillin/Clavulanic Acid Sandoz after the expiration date stated on the pack. The expiration date is the last day of the month indicated.
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 protect the environment.
Composition of Amoxicillin/Clavulanic Acid Sandoz
Each vial contains as active ingredients 1,000 mg of amoxicillin (as amoxicillin sodium) and 200 mg of clavulanic acid (as potassium clavulanate).
It does not contain excipients.
Product Appearance and Container Content
Vials containing a sterile white to off-white powder.
Packaging of 1 vial, 10 vials, or 100 vials of 20 ml.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Sandoz Pharmaceutical, S.A.
Business Center Parque Norte
Edificio Roble
C/ Serrano Galvache, 56
28033 Madrid
Spain
Manufacturer
Sandoz GmbH
Biochemiestrasse, 10
A-6250 Kundl
Austria
Date of the Last Revision of this Prospectus:July 2020
Detailed and updated information about this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/
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This information is intended only for doctors or healthcare professionals:
Please see the Technical Sheet for additional information
Administration
Amoxicillin/Clavulanic Acid Sandoz can be administered by slow intravenous injection over a period of 3 to 4 minutes directly into a vein or by a drip infusion over 30-40 minutes. Amoxicillin/Clavulanic Acid Sandoz is not suitable for intramuscular administration.
Reconstitution
For single use. Any unused solution must be discarded.
Reconstitution/dilution must be performed under aseptic conditions. The solution must be visually inspected before administration to detect any foreign particles and discoloration. The solution should only be used if it is clear and free of particles. Reconstitution of the solution for intravenous injection or reconstitution and dilution of the solution for infusion must be performed at the time of administration.
Preparation of Solutions for Intravenous Injection
The usual solvent is water for injectable preparations. Amoxicillin/Clavulanic Acid Sandoz 1,000 mg/200 mg must be dissolved in 20 ml of solvent. This results in approximately 20.9 ml of solution for single-dose use. A pale pink coloration may be observed during reconstitution. Reconstituted solutions are normally colorless or pale straw-colored.
Amoxicillin/Clavulanic Acid Sandoz must be administered within 15 minutes after reconstitution.
Preparation of Solutions for Intravenous Infusion
Amoxicillin/Clavulanic Acid Sandoz must be reconstituted as described above for injection.
Immediately, the reconstituted solution must be added to 100 ml of infusion fluid using a minibag or in-line burette.
Glucose (dextrose) injectable solutions, sodium bicarbonate, or dextran must not be used as solvents.
In general, it is recommended not to mix it with any other product in the same syringe or infusion bottle. The combination of amoxicillin and clavulanic acid is incompatible with: blood and plasma, hydrocortisone succinate, amino acid solutions, protein hydrolysates, lipid emulsions, phenylephrine HCl, mannitol solutions.
Amoxicillin/Clavulanic Acid Sandoz must not be mixed in the same syringe with aminoglycoside antibiotics, as this may result in a loss of aminoglycoside activity under these conditions.
The vials of Amoxicillin/Clavulanic Acid Sandoz are not suitable for multiple-dose use.
Stability of Prepared Solutions
Reconstituted Vials (for Intravenous Injection or before Dilution for Infusion)
The solution obtained after reconstitution of the vial (1 vial with 20 ml of water for injectables Ph. Eur.) has been shown to be stable from a chemical and physical point of view for 15 minutes at 25 °C ± 2°C/ 60% ±5% HR.
Reconstituted and Diluted Vials for Infusion
The solution obtained by diluting immediatelythe reconstituted vial with 100 ml of water for injectables Ph. Eur. or NaCl 0.9% or sodium lactate 1/6M or Ringer's solution or Hartmann's solution has been shown to be stable from a chemical and physical point of view for 60 minutes at 25°C ± 2°C/ 60% ±5% HR.
Any unused antibiotic solution must be discarded.
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