Package Leaflet: Information for the User
Meropenem Kalceks 500mg powder for solution for injection and infusion EFG
Meropenem Kalceks 1g 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 pack
Meropenem Kalceks contains the active substance meropenem. It belongs to a group of medicines called carbapenem antibiotics. It works by killing bacteria that can cause serious infections.
Antibiotics are used to treat bacterial infections and do not work for viral infections such as flu or common cold.
It is important that you follow the instructions regarding dose, administration interval, and treatment duration indicated by your doctor.
Do not store or reuse this medicine. If you have any leftover antibiotic after finishing the treatment, return it to the pharmacy for proper disposal. Do not throw away medicines via wastewater or household waste.
This medicine is used to treat the following infections in adults and children from 3 months of age:
This medicine can be used to treat patients with low levels of a type of white blood cell called neutrophils with fever whose origin is suspected to be due to a bacterial infection.
This medicine can be used to treat bacterial infections of the blood that may be associated with one of the aforementioned infections.
Do not use Meropenem Kalceks
Warnings and precautions
Consult your doctor or nurse before starting to use this medicine if:
You may test positive in a test called Coombs test, which indicates the presence of antibodies that can destroy red blood cells. Your doctor will discuss this with you.
You may experience signs and symptoms of severe skin reactions (see section 4). If this happens, inform your doctor or nurse immediately so that they can treat the symptoms.
If you are not sure if you are in any of these situations, consult your doctor or nurse before using this medicine.
Other medicines and Meropenem Kalceks
Tell your doctor if you are using, have recently used, or might use any other medicines.
This is because meropenem may affect how some medicines work, and some of these may have an effect on meropenem.
In particular, tell your doctor or nurse if you are taking any of the following medicines:
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 for advice before taking this medicine.
Pregnancy
It is preferable to avoid the use of meropenem during pregnancy. Your doctor will decide if you should use it.
Breastfeeding
It is very important that, before receiving treatment with meropenem, you inform your doctor if you are breastfeeding or plan to breastfeed. A small amount of this medicine may pass into breast milk. Therefore, your doctor will decide if you should use meropenem during breastfeeding.
Driving and using machines
No studies on the effects on the ability to drive and use machines have been performed. However, meropenem has been associated with headache, tingling, or numbness of the skin (paresthesia). Any of these side effects could affect your ability to drive or use machines. This medicine can cause involuntary muscle movements, which can cause the person's body to shake rapidly and uncontrollably (convulsions). This is usually accompanied by a loss of consciousness. Do not drive or use machines if you experience this side effect.
Meropenem Kalceks contains sodium
Meropenem Kalceks 500 mg: This medicine contains 45 mg of sodium (main component of table/cooking salt) per vial. This is equivalent to 2.25% of the maximum recommended daily sodium intake for an adult.
Meropenem Kalceks 1 g: This medicine contains 90 mg of sodium (main component of table/cooking salt) per vial. This is equivalent to 4.5% of the maximum recommended daily sodium intake for an adult.
Follow exactly the administration instructions of this medicine indicated by your doctor or nurse. If in doubt, consult your doctor or nurse again.
Use in adults
Use in children and adolescents
How to use Meropenem Kalceks
If you use more Meropenem Kalceks than you should
If you accidentally use more doses than prescribed, contact your doctor or go to the nearest hospital 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 ingested.
If you forget to use Meropenem Kalceks
If you forget an injection, you should receive it as soon as possible. However, if it is almost time for your next injection, do not receive the missed one. Do not use a double dose (two injections at the same time) to make up for missed doses.
If you stop using Meropenem Kalceks
Do not stop this medicine until your doctor tells you to.
If you have any further questions on the use of this medicine, ask your doctor or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Severe allergic reactions(uncommon)
If you experience a severe allergic reaction, stop using this medicine and go to a doctor immediately. You may need urgent medical treatment. The signs and symptoms can include a sudden onset of any of the following:
Severe skin reactionssuch as:
Damage to red blood cells(uncommon). The signs include:
If you notice any of the above, go to a doctor immediately.
Other possible side effects:
Common(may affect up to 1 in 10 people)
Uncommon(may affect up to 1 in 100 people)
Rare(may affect up to 1 in 1,000 people)
Reporting of side effects
If you experience any side effects, talk to your doctor or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly through the Spanish Medicines Information System: https://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.
This medicine does not require special storage conditions.
Injection
The reconstituted solutions for intravenous injection should be used immediately. The time interval between the start of reconstitution and the end of intravenous injection should not exceed one hour.
Infusion
The reconstituted solution should be diluted immediately after reconstitution. The time interval between the start of reconstitution and the end of intravenous infusion should not exceed one hour.
Do not freeze the reconstituted solution.
Do not use this medicine after the expiry date which is stated on the carton and vial after EXP. The expiry date is the last day of the month stated.
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 Meropenem Kalceks
The active ingredient is meropenem.
Meropenem Kalceks 500 mg
Each vial contains meropenem trihydrate equivalent to 500 mg of meropenem.
Meropenem Kalceks 1 g
Each vial contains meropenem trihydrate equivalent to 1 g of meropenem.
The other component is sodium carbonate.
Appearance of Meropenem Kalceks and Container Contents
Meropenem is a white to light yellow powder, packaged in glass vials. The vials are placed in cardboard boxes.
Presentation: 1 or 10 (clinical packaging) vials
Only some package sizes may be marketed.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
AS KALCEKS
Krustpils iela 71E,
Riga, LV-1057,
Latvia
Tel.: +371 67083320
E-mail: kalceks@kalceks.lv
Manufacturer
ACS Dobfar S.p.A.
Nucleo Industriale S. Atto (loc. San Nicolò a Tordino)
64100 Teramo (TE), Italy
You can request more information about this medication by contacting the local representative of the marketing authorization holder
Grindeks Kalceks España, S.L.
c/ José Abascal, 58 2º dcha
28003 Madrid
Spain
This medication is authorized in the member states of the European Economic Area under the following names:
Denmark Meropenem Kalceks
Austria, Germany Meropenem Kalceks 500 mg Pulver zur Herstellung einer Injektions-/Infusionslösung
Meropenem Kalceks 1 g Pulver zur Herstellung einer Injektions-/Infusionslösung
Italy, Norway, Sweden Meropenem Kalceks
Belgium Meropenem Kalceks 500 mg, 1 g poeder voor oplossing voor injectie/infusie
Meropenem Kalceks 500 mg, 1 g poudre pour solution injectable/pour perfusion
Meropenem Kalceks 500 mg, 1 g Pulver zur Herstellung einer Injektions-/Infusionslösung
Croatia Meropenem Kalceks 500 mg, 1000 mg prašak za otopinu za injekciju/infuziju
Finland Meropenem Kalceks 500 mg, 1 g injektio-/infuusiokuiva-aine liuosta varten
France MEROPENEM KALCEKS 500 mg poudre pour solution injectable/pour perfusion
MEROPENEM KALCEKS 1 g poudre pour solution injectable/pour perfusion
Hungary Meropenem Kalceks 500 mg, 1 g por oldatos injekcióhoz vagy infúzióhoz
Ireland Meropenem 500 mg, 1 g powder for solution for injection/infusion
Latvia Meropenem Kalceks 500 mg, 1 g pulveris injekciju/infuziju šķiduma pagatavošanai
Lithuania Meropenem Kalceks 500 mg, 1 g milteliai injekciniam ar infuziniam tirpalui
Netherlands Meropenem Kalceks 500 mg, 1 g poeder voor oplossing voor injectie/infusie
Romania Meropenem Kalceks 500 mg, 1 g pulbere pentru solutie injectabila/perfuzabila
Slovenia Meropenem Kalceks 500 mg, 1000 mg prašek za raztopino za injiciranje/infundiranje
Slovakia Meropenem Kalceks 500 mg, 1 g prášok na injekčný/infúzny roztok
Spain Meropenem Kalceks 500 mg, 1 g polvo para solución inyectable y para perfusión EFG
Date of the last revision of this prospectus:December 2022
Detailed 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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Health Advice/Education
Antibiotics are used to treat infections caused by bacteria. They have no effect against infections caused by viruses.
Sometimes a bacterial infection does not respond to treatment with an antibiotic. One of the most common reasons for this is that the bacteria causing the infection are resistant to the antibiotic being taken. This means they can survive and even multiply despite the antibiotic.
Bacteria can become resistant to antibiotics for many reasons. Using antibiotics with caution can help reduce the likelihood of bacteria becoming resistant to them.
When your doctor prescribes antibiotic treatment, it is to treat only your current illness. Paying attention to the following tips will help prevent the emergence of resistant bacteria that could stop the antibiotic from working.
Instructions for Administering Meropenem Kalceks to Yourself or Others at Home
Some patients, parents, and caregivers are trained to administer Meropenem Kalceks at home.
Warning: This medication should only be administered to yourself or another person at home after a doctor or nurse has trained you.
Injection
To administer meropenem by intravenous bolus injection, prepare the medication by reconstituting it in 'sterile water for injections' to a final concentration of 50 mg/ml.
The reconstitution time should not exceed 2 minutes.
Infusion
The vials of meropenem for intravenous infusion can be reconstituted directly with 9 mg/ml (0.9%) sodium chloride solution or 50 mg/ml (5%) glucose solution, and diluted with the same solvent to a final concentration of 1 to 20 mg/ml.
How to Prepare this Medication
Dose of Meropenem Kalceks | Recommended amount of 'Water for injections' needed for dilution |
500 mg (milligrams) | 10 ml (milliliters) |
1 g (grams) | 20 ml |
1.5 g | 30 ml |
2 g | 40 ml |
Notes:If the amount of this medication prescribed for you is more than 1 g, you will need to use more than one Meropenem Kalceks vial. You can then draw up the liquid (solvent) from the vials into a syringe.
Administration of the Injection
You can administer this medication through a short intravenous catheter, an intravenous line, or through a central port or line.
Administration of Meropenem Kalceks through a Short Intravenous Catheter or Intravenous Line
Administration of Meropenem Kalceks through a Central Port or Line
The disposal of unused medication or all materials that have come into contact with it will be carried out in accordance with local regulations.