
Ask a doctor about a prescription for CEFTRIAXONE Fresenius Kabi 2 g POWDER FOR SOLUTION FOR INFUSION
Package Leaflet: Information for the User
Ceftriaxone Fresenius Kabi 2 g powder for solution for infusion EFG
ceftriaxone
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
Contents of the pack
Ceftriaxone Fresenius Kabi is an antibiotic used in adults and children (including newborns). It works by killing the bacteria that cause infections. It belongs to a group of antibiotics called cephalosporins.
Antibiotics are used to treat bacterial infections and will not work for viral infections such as the common cold or flu.
It is important that you follow the instructions regarding dose, administration and duration of treatment given by your doctor.
Do not store or reuse this medicine. If you have any leftover antibiotic after you finish treatment, return it to the pharmacy for proper disposal. Do not throw away medicines via wastewater or household waste.
Ceftriaxone Fresenius Kabi is indicated for the treatment of infections related to:
It can be used in the following cases:
Do not use Ceftriaxone Fresenius Kabi:
Ceftriaxone Fresenius Kabi must not be used in babies if:
.
Warnings and precautions
Consult your doctor, pharmacist or nurse before starting treatment with Ceftriaxone Fresenius Kabi if:
If you are to have a blood or urine test
If you have been prescribed Ceftriaxone Fresenius Kabi for a long period, you will need to have regular blood tests.
Ceftriaxone Fresenius Kabi may affect the results of urine tests for glucose detection and blood tests for 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 incorrectly measure your blood sugar levels while you are using ceftriaxone. If you use such systems, you should review the instructions for use and consult your doctor, pharmacist or nurse. Alternative methods should be used if necessary.
Children
Consult your doctor or pharmacist or nurse before Ceftriaxone Fresenius Kabi is administered to your child if:
Other medicines and Ceftriaxone Fresenius Kabi
Tell your doctor or pharmacist if you are using, have recently used or might use any other medicines.
In particular, consult your doctor or pharmacist if you are using any of the following medicines:
Pregnancy, breast-feeding and fertility
If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine.
Your doctor will decide whether to treat you with Ceftriaxone Fresenius Kabi and the risk it may pose to your baby.
Driving and using machines
Ceftriaxone Fresenius Kabi may cause dizziness. If you feel dizzy, do not drive or use any tools or machines. Consult your doctor if you experience these symptoms.
Ceftriaxone Fresenius Kabi contains sodium
This medicine contains 82.3 mg of sodium (main component of cooking/table salt) per vial. This is equivalent to 4.1% of the maximum recommended daily intake of sodium for an adult.
Ceftriaxone Fresenius Kabi is usually given by a doctor or nurse. It can be given through a drip (intravenous infusion) or by intravenous or intramuscular injection. Ceftriaxone Fresenius Kabi is prepared by a doctor, pharmacist or nurse and must not be mixed or given with other injections that contain calcium.
Usual dose
Your doctor will decide the right dose of Ceftriaxone Fresenius Kabi for you. The dose will depend on the severity and type of infection; whether you are taking other antibiotics; your weight and age; how well your kidneys and liver are working. The number of days or weeks you will be treated with Ceftriaxone Fresenius Kabi will depend on the type of infection you have.
Adults, elderly, children over 12 years and ≥ 50 kg:
Newborns, infants and children from 15 days to 12 years with < 50 kg:
Newborns (0-14 days)
Patients with liver or kidney problems
You will be given a different dose than usual. Your doctor will decide the dose you need of Ceftriaxone Kabi and will closely monitor you depending on the severity of liver and kidney disease.
If you use more Ceftriaxone Fresenius Kabi than you should
If you accidentally receive more doses than prescribed, inform your doctor or go to the nearest hospital.
If you forget to use Ceftriaxone Fresenius Kabi
If you miss an injection, it should be given as soon as possible. However, if it is almost time for your next injection, skip the missed injection. Do not take a double dose (two injections at the same time) to make up for missed doses.
If you stop treatment with Ceftriaxone Fresenius Kabi
Do not stop Ceftriaxone Fresenius Kabi unless your doctor tells you to.
If you have any further questions on the use of this product, ask your doctor 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:
Severe allergic reactions (frequency not known, cannot be estimated from the available data)
If you have a severe allergic reaction, tell your doctor immediately.
Symptoms may include:
Severe skin reactions (frequency not known, cannot be estimated from the available data)
If you have a severe skin reaction, tell your doctor immediately.
Symptoms may include:
Other possible symptoms:
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 1000 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, even if it is possible side effects not listed in this leaflet. You can also report side effects directly through the Spanish Medicines Monitoring System for Human Use (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 after EXP. The expiry date is the last day of the month shown.
Do not store above 25°C.
Store the vial in the outer packaging to protect it from light.
The reconstituted solution is stable for 8 hours at 25 °C and 24 hours in the refrigerator (2 - 8 °C).
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 Ceftriaxone Fresenius Kabi
The active ingredient is ceftriaxone sodium equivalent to 2.0 g of ceftriaxone.
Appearance of the Product and Container Content
The solutions may vary from colorless to pale yellow.
Ceftriaxone Fresenius Kabi powder for infusion is presented in containers containing 1, 10, or 100 glass vials of powder, closed with a rubber stopper and an aluminum cap. Not all package sizes may be marketed.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Fresenius Kabi España, S.A.U.
Torre Mapfre-Vila Olímpica
Marina 16-18, 08005 – Barcelona
Spain
Manufacturer
LABESFAL – Laboratórios Almiro S.A.
Lagedo, 3465-157 Santiago de Besteiros, Portugal
This medicinal product is authorized in the Member States of the European Economic Area under the following names:
Austria | Ceftriaxone Kabi 2 g Powder for Solution for Infusion |
Belgium | Ceftriaxone Fresenius Kabi 2g Powder for Solution for Infusion |
Czech Republic | Ceftriaxone Kabi 2g, Powder for Solution for Infusion |
Denmark | Ceftriaxone Fresenius Kabi |
Estonia | Ceftriaxone Kabi 2 g |
Finland | Ceftriaxone Fresenius Kabi 2 g Powder for Solution for Infusion |
Germany | Ceftriaxone Kabi 2 g Powder for Solution for Infusion |
Greece | Ceftriaxone Kabi 2g, Powder for Solution for Infusion |
Hungary | Ceftriaxone Kabi 2 g Powder for Solution for Infusion |
Italy | Ceftriaxone FKI |
Luxembourg | Ceftriaxone Kabi 2 g Powder for Solution for Infusion |
Lithuania | Ceftriaxone Kabi 2 g Powder for Solution for Infusion |
Latvia | Ceftriaxone Kabi 2 g Powder for Solution for Infusion |
Netherlands | Ceftriaxone Fresenius Kabi 2g Powder for Solution for Infusion |
Norway | Ceftriaxone Fresenius Kabi 2 g Powder for Solution for Infusion |
Poland | Ceftriaxone Kabi |
Portugal | CEFTRIAXONA FRESENIUS KABI |
Slovakia | Ceftriaxone Kabi 2 g |
Sweden | Ceftriaxone Fresenius Kabi 2 g Powder for Solution for Infusion |
Date of Last Revision of this Leaflet: July 2022.
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.gob.es/
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This information is intended solely for healthcare professionals:
Solutions containing ceftriaxone should not be mixed or added with other agents. In particular, diluents containing calcium (e.g., Ringer's solution, Hartmann's solution) should not be used to reconstitute ceftriaxone vials or to dilute reconstituted vials when administered intravenously, as they may form precipitates.
Ceftriaxone should not be mixed or administered simultaneously with solutions containing calcium (see sections 4.2, 4.3, 4.4, and 4.8 of the summary of product characteristics and section 6 of the package leaflet).
Infusion should be administered over at least 30 minutes.
For this infusion, the vial of Ceftriaxone Fresenius Kabi 2 g should be dissolved in 40 ml of one of the following calcium-free infusion solutions: 0.9% sodium chloride, 0.45% sodium chloride + 2.5% dextrose, 5% dextrose, 10% dextrose, 6% hydroxyethyl starch in 5% dextrose, or sterile water for injection.
The dose and administration schedule used depend on the patient's age and weight, as well as the severity of the infection.
Adults and Children Over 12 Years: The usual dose is 1-2 g of ceftriaxone administered once daily (every 24 hours). In severe cases or infections caused by moderately sensitive microorganisms, the dose may be increased up to a maximum of 4 g once daily.
Stages II and III of Lyme Disease
A dose of 50 mg/kg body weight, up to a maximum of 2 grams daily, is recommended, administered once daily for 14 days.
Perioperative Prophylaxis
A single dose of 1-2 g, 30-90 minutes before surgery. In colorectal surgery, another antibiotic with adequate spectrum against anaerobes should be associated.
Combination Therapy:
In infections caused by gram-negative microorganisms, combination with aminoglycosides may be necessary, especially in severe or life-threatening infections.
Newborns and Children Under 12 Years
Newborns (up to 14 days): 20 to 50 mg/kg body weight, administered in a single dose, with no differences between term and preterm infants. The dose should not exceed 50 mg/kg body weight.
Infants and Children (from 15 days to 12 years): single daily dose of 20-80 mg/kg body weight.
Children with a weight of >50 kg: the same dose as for adults will be used. The intravenous dose of 50 mg per kg body weight or more should be administered by infusion over at least 30 minutes.
Bacterial Meningitis in Infants and Children
Treatment will be initiated with a dose of 100 mg/kg (not exceeding 4 g) once daily. As soon as the causal microorganism is identified and its sensitivity determined, the dose may be adjusted accordingly.
Elderly: No modification of the recommended doses for adults is required, provided there is no impairment of renal and/or hepatic function.
Patients with Renal Impairment
In patients with impaired renal function, it is not necessary to reduce the dose, provided hepatic function remains normal. Only in cases of preterminal renal failure (creatinine clearance <10 ml min), the dose of ceftriaxone should not exceed 2 g daily.< p>
In cases of severe concomitant renal and hepatic dysfunction, the dose of ceftriaxone should not exceed 2 g daily, unless plasma concentrations are determined at regular intervals, adjusting the dose if necessary.
In dialyzed patients, it is not necessary to administer an additional supplementary dose after the dialysis session; in any case, the patient's clinical situation will be monitored to adjust the dose if necessary.
Patients with Hepatic Impairment
In cases of hepatic impairment, it is not necessary to reduce the dose if renal function is intact. In cases of severe concomitant renal and hepatic dysfunction, the dose of ceftriaxone should not exceed 2 g daily, unless plasma concentrations are determined at regular intervals, adjusting the dose if necessary.
Duration of Therapy
Varying with the severity of the disease. In general, administration of ceftriaxone will be maintained for at least 48 to 72 hours after improvement of the clinical condition or until microbiological eradication is achieved.
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