Package Leaflet: Information for the User
Meropenem Qilu 1 g 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
Meropenem Qilu contains the active substance meropenem and belongs to a group of medicines called carbapenem antibiotics. It works by killing bacteria that can cause serious infections.
Meropenem Qilu 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 weakened immune systems (neutropenic patients) who have a fever that is suspected to be due to a bacterial infection.
Meropenem Qilu can be used to treat bacterial infection of the blood that may be associated with one of the aforementioned types of infection.
Do not use Meropenem Qilu
Warnings and precautions
Talk to your doctor or pharmacist before starting Meropenem Qilu
Blood tests
You may develop a positive response to a test (Coombs test) that indicates the presence of antibodies that can destroy red blood cells.
Your doctor will discuss this with you.
Skin reactions
You may develop 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 in any of these situations, or if you have doubts, consult your doctor before using this medicine.
Other medicines and Meropenem Qilu
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines. This is because Meropenem Qilu may affect the way some medicines work, and some of these may affect Meropenem Qilu.
In particular, tell your doctor or nurse if you are taking any of the following medicines:
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medicine.
It is preferable to avoid the use of meropenem during pregnancy.
Your doctor will decide whether you should use Meropenem Qilu.
It is important that you inform your doctor if you are breastfeeding or plan to breastfeed before receiving Meropenem Qilu. Small amounts of this medicine pass into breast milk. Therefore, your doctor will decide whether you should use meropenem during breastfeeding.
Driving and using machines
No studies have been conducted on the effects on the ability to drive and use machines.
However, meropenem has been associated with headache and tingling or numbness in the skin (paresthesia). Either of these effects could affect your ability to drive or use machines.
This medicine may cause involuntary muscle movements, leading to rapid and uncontrolled body movements (convulsions), which are usually accompanied by loss of consciousness. Do not drive or use machines if you experience this side effect.
Meropenem Qilu contains sodium
This medicine contains 90 mg of sodium (a major component of cooking/table salt) per 1 g dose. This is equivalent to 4.5% of the maximum recommended daily intake of sodium for an adult.
If you have a condition that requires you to control your sodium intake, inform your doctor, pharmacist, or nurse.
Follow exactly the instructions for administration of this medicine given by your doctor or pharmacist. In case of doubt, ask your doctor, pharmacist, or nurse.
Use in adults
Use in children and adolescents
The dose for children over 3 months and up to 12 years is decided using the child's age and weight. The normal dose is between 10 mg and 40 mg of meropenem per kilogram (kg) of the child's weight. You will usually be given a dose every 8 hours. Children who weigh more than 50 kg will be given an adult dose.
How to use Meropenem Qilu
If you use more Meropenem Qilu than you should
If you accidentally use more than the prescribed dose, 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, telephone 91 562 04 20, indicating the medicine and the amount ingested.
If you forget to use Meropenem Qilu
If you miss a dose, you should receive it as soon as possible. However, if it is almost time for your next dose, do not receive the missed dose. Do not use a double dose (two injections at the same time) to make up for a missed dose.
If you stop using Meropenem Qilu
Do not stop using Meropenem Qilu until your doctor tells you to.
If you have any further questions on the use of this medicine, ask your doctor, pharmacist, or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Severe allergic reactions
If you experience any of these symptoms, inform your doctor or nurse immediately. You may need urgent medical treatment. The symptoms can include a sudden onset of:
Damaged red blood cells
The symptoms include:
If you notice any of the above, go to a doctor immediately.
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, pharmacist, or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly through the Spanish Medicines Agency's website: 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 vial label after EXP. The expiry date refers to the last day of the month shown.
This medicine does not require any special storage conditions.
After reconstitution/dilution:
Administration of intravenous bolus injection
An injection solution is prepared by dissolving the medicine in water for injection, to a final concentration of 50 mg/ml.
The reconstituted solution of the medicinal product in water for injection must be used immediately.
Administration by intravenous infusion
An infusion solution is prepared by dissolving the medicine in a 9 mg/ml sodium chloride (0.9%) infusion solution or in a 50 mg/ml dextrose (5%) infusion solution, to a final concentration of 1 to 20 mg/ml.
The reconstituted solution of the medicinal product in 9 mg/ml sodium chloride (0.9%) infusion solution must be used immediately. The maximum time that should elapse between the start of reconstitution and the end of infusion should not exceed one hour.
The reconstituted solution of the medicinal product in 50 mg/ml dextrose (5%) infusion solution must be used immediately.
Do not freeze the reconstituted solution.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
Composition of Meropenem Qilu
The active substance is meropenem.
Each vial contains 1 g of meropenem (as meropenem trihydrate).
The other ingredient is sodium carbonate.
Appearance of Meropenem Qilu and pack contents
Meropenem Qilu is presented in vials containing a white or slightly yellow powder for solution for injection or infusion.
Pack sizes of 1 or 10 vials (clinical pack).
Not all pack sizes may be marketed.
Marketing authorization holder and manufacturer
Marketing authorization holder
QILU PHARMA SPAIN S.L.
Paseo de la Castellana 40, 8th floor,
28046 Madrid,
Spain
Manufacturer
KYMOS, S.L.
Ronda de Can Fatjó,
7B (Parque Tecnológico del Vallès),
Cerdanyola del Vallès,
08290 Barcelona,
Spain
Eurofins Analytical Services Hungary Kft.
Anonymus utca 6, Budapest
H-1045,
Hungary
LLC “UNIFARMA”
Vangazu street 23,
Riga, LV-1024,
Latvia
Local representative:
Sun Pharma Laboratorios, S.L.
Rambla de Catalunya, 53-55
08007 – Barcelona
Spain
Tel.: +34 93 342 7890
This medicine is authorized in the Member States of the European Economic Area under the following names:
Member State | Medicine name |
Germany | Meropenem Qilu 1 g Powder for solution for injection/infusion |
Bulgaria | Meropenem Qilu 1 g ????? ?? ???????????/?????????? ??????? |
Croatia | Meropenem Qilu 1000 mg powder for solution for injection/infusion |
Denmark | Meropenem Qilu |
Estonia | Meropenem Qilu |
Finland | Meropenem Qilu 1 g injektio-/infuusiokuiva-aine liuosta varten |
France | MEROPENEM QILU 1g, powder for solution for injection/infusion |
Hungary | Meropenem Qilu 1 g por oldatos injekcióhoz/infúzióhoz |
Italy | Meropenem Qilu |
Lithuania | Meropenem Qilu 1 g milteliai injekciniam ar infuziniam tirpalui |
Latvia | Meropenem Qilu 1 g pulveris injekciju/infuziju škiduma pagatavošanai |
Norway | Meropenem Qilu |
Spain | Meropenem Qilu 1 g polvo para solución inyectable y para perfusión EFG |
Sweden | Meropenem Qilu 1 g pulver till injektions-/infusionsvätska, lösning |
Slovenia | Meropenem Qilu 1000 mg prašek za raztopino za injiciranje/infundiranje |
Date of last revision of this leaflet: 12/2023
Other sources of information:
Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/