


Ask a doctor about a prescription for CEFTRIAXONE QILU 2 g POWDER FOR INJECTION AND INFUSION SOLUTION
Package Leaflet: Information for the Patient
Ceftriaxone Qilu 2 g Powder for Solution for Injection and Infusion EFG
ceftriaxone (as ceftriaxone sodium)
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
Contents of the pack
Ceftriaxone is an antibiotic for adults and children (including newborn babies). It works by killing the bacteria that cause infections. It belongs to a group of medicines called cephalosporins.
Antibiotics are used to treat bacterial infections and do not work for viral infections such as flu or the common cold.
It is important to follow the instructions regarding dose, administration interval, and treatment duration as 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 medicines down the drain or in the trash.
Ceftriaxone is used to treat infections of:
Ceftriaxone can be used:
You should consult a doctor if you get worse or do not improve
Do not use Ceftriaxone Qilu:
Ceftriaxone Qilu must not be administered to babies if:
Warnings and precautions
Talk to your doctor, pharmacist, or nurse before taking Ceftriaxone:
If you need a blood or urine test
If you are going to receive ceftriaxone for a long time, you may need to have regular blood tests. Ceftriaxone can affect the results of a urine test for sugar (glucosuria) and a blood test called the Coombs test. If you are having tests:
If you are diabetic or need to control your blood sugar levels, you should not use certain blood sugar control systems that may give incorrect glucose estimates while you are being treated with ceftriaxone. If you use such a system, consult the instructions for use and talk to your doctor, pharmacist, or nurse. If necessary, alternative test methods should be used.
Children
Before your child receives ceftriaxone, talk to your doctor, pharmacist, or nurse if:
Using Ceftriaxone Qilu with other medicines
Tell your doctor or pharmacist if you are using, have recently used, or might use any other medicines.
Particularly, tell your doctor or pharmacist 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.
Your doctor will assess the expected benefits of treatment with ceftriaxone against the risks for your baby.
Driving and using machines
Ceftriaxone may cause dizziness. If you feel dizzy, do not drive or use tools or machines. Talk to your doctor if you have this symptom.
Ceftriaxone Qilu contains sodium
Vial of 2 g: this medicine contains 165.6 mg of sodium (the main component of cooking salt) per vial. This is equivalent to 8.28% of the maximum recommended daily intake of sodium in the adult diet, which should be taken into account in patients on low-sodium diets.
Ceftriaxone is usually given by a doctor or nurse. It can be given:
Ceftriaxone is prepared for administration by a doctor, pharmacist, or nurse. It must not be mixed or given at the same time as other injected products containing calcium.
Recommended dose
Your doctor will decide the correct dose of ceftriaxone for you. The dose will depend on the type and severity of the infection, whether you are already receiving other antibiotics, your weight and age, as well as the condition of your liver and kidneys. The number of days or weeks you will receive ceftriaxone will depend on the type of infection.
Adults, elderly patients, and children from 12 years of age with a weight of 50 kg or more:
Newborns, infants, and children from 15 days to 12 years of age with a weight below 50 kg:
Newborns (0-14 days)
Patients with liver or kidney problems
If you have impaired kidney or liver function, you may receive a different dose than recommended. Your doctor will decide how much ceftriaxone you need and will examine you thoroughly according to the severity of the kidney or liver disease.
If you use more Ceftriaxone Qilu than you should
If you receive a higher dose than prescribed by mistake, contact your doctor or go to the nearest hospital as soon as possible.
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 taken.
If you forget to use Ceftriaxone Qilu
If you miss a dose of this medicine, you should receive it as soon as possible. However, if it is almost time for the next injection, skip the missed injection. You should not receive a double dose (two injections at the same time) to make up for a missed dose.
If you stop using Ceftriaxone Qilu
Do not stop receiving Ceftriaxone unless 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.
Serious side effects
Severe allergic reactions (frequency not known, cannot be estimated from the available data)
If you have a severe allergic reaction, tell your doctor immediately.
The signs may be:
Severe skin reactions (frequency not known, cannot be estimated from the available data)
If you have a severe skin rash, inform a doctor immediately.
The symptoms may include:
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)
Frequency not known (cannot be estimated from the available data)
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 Monitoring System: www.notificaRAM.es.
By reporting side effects, you can help provide more information on the safety of this medicine.
Physical and chemical stability has been demonstrated for 6 hours at 25°C and for 24 hours at 2-8°C.
From a microbiological point of view, unless the opening method allows the risk of microbial contamination to be ruled out, the product should be used immediately. If not used immediately, the in-use storage times and conditions are the responsibility of the user.
Medicines should not be disposed of via wastewater or household waste. Return any unused medicine to the pharmacy. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Composition of Ceftriaxone Qilu
The active ingredient of Ceftriaxone powder for injection and infusion is ceftriaxone.
2 g: each vial contains ceftriaxone sodium equivalent to 2 g of ceftriaxone.
Each gram of ceftriaxone sodium contains approximately 3.6 mmol (82.8 mg) of sodium.
Ceftriaxone does not include other components.
Product Appearance and Container Content
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
QILU PHARMA SPAIN S.L.
Paseo de la Castellana 40,
floor 8, 28046 - Madrid,
Spain
Manufacturer
KYMOS, S.L.
Ronda de Can Fatjó,
7B (Parque Tecnológico del Vallès),
Cerdanyola del Vallès, 08290
Barcelona, Spain
MIAS Pharma Limited
Suite 2, Stafford House, Strand Road,
Portmarnock, Co. Dublin,
Ireland
Tillomed Malta Ltd.
Malta Life Sciences Park, LS2.01.06 Industrial Estate,
San Gwann, SGN 3000,
Malta
Local Representative
Sun Pharma Laboratorios, S.L.
Rambla de Catalunya, 53-55
08007 – Barcelona
Spain
Tel.: + 34 93 342 78 90
This medicinal product is authorized in the Member States of the European Economic Area under the following names:
United Kingdom | : | Ceftriaxone 2 g powder for solution for injection/infusion |
Germany | : | Ceftriaxon Qilu 2 g Pulver zur Herstellung einer Injektions-/Infusionslösung |
Spain | : | Ceftriaxona Qilu 2 g polvo para solución inyectable y para perfusión EFG |
France | : | Ceftriaxone Qilu 2 g, poudre pour solution injectable/pour perfusion |
Italy | : | Ceftriaxone Qilu |
Croatia | : | Ceftriakson Qilu 2 g prašak za otopinu za injekciju/infuziju |
Hungary | : | Ceftriaxone Qilu 2 g por oldatos injekcióhoz vagy infúzióhoz |
Slovenia | : | Ceftriakson Qilu 2 g prašek za raztopino za injiciranje/infundiranje |
Date of the last revision of this leaflet:May 2024
Detailed and updated information on this medicinal product is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.es/
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This information is intended only for healthcare professionals:
INFORMATION FOR HEALTHCARE PROFESSIONALS
Ceftriaxone Qilu 2 g powder for solution for injection and infusion EFG
ceftriaxone (as ceftriaxone sodium)
Consult the complete prescribing information in the Summary of Product Characteristics or the Package Leaflet.
Intramuscular administration
Ceftriaxone can be administered by deep intramuscular injection. In intramuscular injections, a relatively large muscle mass should be chosen for the injection, and no more than 1 g should be injected at the same site.
Since the solvent used is lidocaine, the resulting solution should never be administered intravenously. The information collected in the Summary of Product Characteristics or the Package Leaflet of lidocaine should be taken into account.
Intravenous administration
Ceftriaxone can be administered by intravenous infusion over at least 30 minutes (preferred route) or by slow intravenous injection over 5 minutes. Intermittent intravenous injections should be administered over 5 minutes, preferably in large veins. Intravenous doses of 50 mg/kg or more in infants and children up to 12 years of age should be administered by infusion. In neonates, intravenous doses should be administered over approximately 60 minutes to reduce the risk of bilirubin encephalopathy. Intramuscular administration should be considered when the intravenous route is not possible or is less suitable for the patient. For doses greater than 2 g, intravenous administration should be used.
Ceftriaxone is contraindicated in neonates (≤ 28 days) if they require (or are expected to require) treatment with intravenous solutions containing calcium, including continuous infusions containing calcium, such as parenteral nutrition, due to the risk of precipitation of ceftriaxone calcium.
Diluents containing calcium (e.g., Ringer's solution or Hartmann's solution) should not be used to reconstitute ceftriaxone vials or for subsequent dilution of a reconstituted vial for intravenous administration, as a precipitate may form. Precipitation of ceftriaxone calcium can also occur if ceftriaxone is mixed with solutions containing calcium in the same intravenous administration line. Therefore, ceftriaxone and solutions containing calcium should not be mixed or administered simultaneously.
For preoperative prophylaxis of surgical site infections, ceftriaxone should be administered 30-90 minutes before surgery.
Instructions for Use
Physical and chemical stability has been demonstrated for 6 hours at 25 °C and for 24 hours at 2-8 °C.
From a microbiological point of view, unless the opening method allows the risk of microbial contamination to be ruled out, the product should be used immediately. If not used immediately, the period and conditions of storage are the responsibility of the user.
Ceftriaxone should not be mixed in the same syringe with any drug other than a 1.06% lidocaine hydrochloride solution (for intramuscular injection only).
Intramuscular injection: 1 g of ceftriaxone should be dissolved in 3.5 ml of 1.06% lidocaine hydrochloride solution. The solution should be administered by deep intramuscular injection. Doses greater than 1 g should be divided and injected into more than one site.
Lidocaine solutions should not be administered intravenously.
Intravenous injection: 1 g of ceftriaxone should be dissolved in 10 ml of water for injections. The injection should be administered over 5 minutes, directly into a vein or through an intravenous infusion catheter.
Intravenous infusion: 2 g of ceftriaxone should be dissolved in 40 ml of one of the following calcium-free solutions: 5% or 10% dextrose for injection, sodium chloride for injection, sodium chloride and dextrose for injection (0.45% sodium chloride and 2.5% dextrose), 6% dextran in 5% dextrose for injection, or 6-10% hydroxyethyl starch for infusion. The infusion should be administered over at least 30 minutes.
Consult the sections Dosageand Administrationfor more information.
The displacement value of 1 g of ceftriaxone is 0.6 ml when reconstituted with 10 ml of water for injections.
The displacement value of 1 g of ceftriaxone is 0.68 ml when reconstituted with 3.5 ml of 1.06% lidocaine hydrochloride solution.
Incompatibilities
According to specialized literature, ceftriaxone is incompatible with amsacrine, vancomycin, fluconazole, aminoglycosides, and labetalol.
Solutions containing ceftriaxone should not be mixed or added to other compounds, except those mentioned in the Instructions for Usesection. In particular, diluents containing calcium (e.g., Ringer's solution or Hartmann's solution) should not be used to reconstitute ceftriaxone vials or for subsequent dilution of a reconstituted vial for intravenous administration, as a precipitate may form. Ceftriaxone and solutions containing calcium should not be mixed or administered simultaneously, including those for total parenteral nutrition.
If combination treatment with ceftriaxone and another antibiotic is planned, administration should not be performed with the same syringe or in the same infusion solution.
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