


Ask a doctor about a prescription for CEFEPIMA LDP- LABORATORIOS TORLAN 1 g POWDER FOR INJECTABLE SOLUTION AND FOR INFUSION
Package Leaflet: Information for the User
Cefepime LDP-Laboratorios TORLAN 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 package leaflet
Cefepime LDP-Laboratorios TORLAN is indicated for the treatment of infections caused by bacteria susceptible to cefepime, namely:
The official guidelines on the appropriate use of antibacterial agents should be considered.
Do not use Cefepime LDP-Laboratorios TORLAN:
Warnings and precautions
Consult your doctor or pharmacist before starting to use Cefepime LDP-Laboratorios TORLAN.
Special care should be taken when using Cefepime LDP-Laboratorios TORLAN:
Cefepime should be discontinued in the event of any type of hypersensitivity reaction and appropriate therapeutic measures should be initiated.
Using Cefepime with other medicines
Inform your doctor or pharmacist if you are using, have recently used, or may need to use any other medicine, including those obtained without a prescription.
Renal function should be carefully monitored when Cefepime LDP-Laboratorios TORLAN is combined with medicines that may affect the kidneys (such as aminoglycosides and potent diuretics).
Cephalosporins may enhance the effect of coumarin anticoagulants.
Interaction with diagnostic tests
Cefepime may produce a false positive reaction in some laboratory tests (Coombs test results and glucose in urine).
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.
Do not use this medicine during pregnancy, unless it is absolutely necessary and specifically indicated by your doctor. If you become pregnant during treatment with Cefepime LDP-Laboratorios TORLAN, consult your doctor.
Cefepime LDP-Laboratorios TORLAN may be transferred to breast milk, therefore, this medicine should be used during breastfeeding with great caution and only after consulting your doctor.
Driving and using machines
No studies have been conducted to determine the effects on the ability to drive and use machines.
However, you may experience altered state of consciousness, dizziness, confusion, or hallucinations, which may affect your ability to drive or use machines.
Follow exactly the administration instructions of this medicine as indicated by your doctor or pharmacist. In case of doubt, ask your doctor or pharmacist.
Cefepime LDP-Laboratorios TORLAN can be administered by intravenous or intramuscular route.
After reconstitution, the solution is yellow to yellow-brown in color.
The usual dose and route of administration vary according to the severity of the infection, renal function, and the patient's general condition.
The intravenous route is preferred in patients with severe infections or in a life-threatening situation, particularly if there is a risk of shock.
Recommended dosage for adults and children (> 12 years) with normal renal function:
Severity of infection | Dose and route of administration | Dosing interval |
Mild to moderate urinary tract infections (UTI) | 500 mg to 1 g IV or IM | every 12 hours |
Other mild to moderate infections (non-UTI) | 1 g IV or IM | every 12 hours |
Severe infections | 2 g IV | every 12 hours |
Life-threatening infections | 2 g IV | every 8 hours |
The usual duration of therapy is 7 to 10 days. However, more severe infections may require longer treatment. For the empirical treatment of febrile neutropenia, the usual duration of therapy is 7 days or until the resolution of neutropenia.
In patients with a weight ≤ 40 kg, the recommended dosage is indicated for children.
Use in children
In children with normal renal function:
The recommended dose is:
Experience in children under 2 months is limited. Administration of Cefepime LDP-Laboratorios TORLAN in children of this age should be carefully monitored.
In children weighing > 40 kg, the recommended dose is the same as for adults.
Do not exceed the maximum recommended dose for adults (2 g every 8 hours). Experience with intramuscular use in children is limited.
Elderly patients, patients with renal impairment, patients on dialysis, and children with renal impairment:
The doctor will determine the dose to be administered.
If you use more Cefepime LDP-Laboratorios TORLAN than you should:
Contact your doctor or other healthcare professional immediately, as you may experience more severe side effects in certain situations.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Cefepime LDP-Laboratorios TORLAN may cause one or more of the following side effects:
Very common(may affect more than 1 in 10 people):
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(frequency not known)
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 them 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.
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 stated.
This medicine does not require special temperature storage conditions. Store the container in the outer packaging. Do not use this medicine if you notice visible signs of deterioration.
Medicines should not be disposed of via wastewater or household waste.
If you are unsure, ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Composition of Cefepima LDP-Laboratorios TORLAN
Each vial of Cefepima LDP-Laboratorios TORLAN 1g powder for solution for injection and infusion contains 1g of cefepime (as dihydrochloride monohydrate).
Appearance of Cefepima LDP-Laboratorios TORLAN and Container Content
Cefepima LDP-Laboratorios TORLAN 1g is a white to pale yellow powder for solution for injection/infusion, packaged in a 20 ml glass vial closed with a flip-off cap. The vials are packaged in cardboard boxes.
Presentation: 1, 5, 10, 20, 25, 50, and 100 vials.
Only some package sizes may be marketed.
Marketing Authorization Holder
LDPLABORATORIOS TORLAN,S.A.
Ctra de Barcelona, 135-B
08290 Cerdanyola del Valles
Barcelona
Spain
Manufacturer
LDPLABORATORIOS TORLAN,S.A.
Ctra de Barcelona, 135-B
08290 Cerdanyola del Valles
Barcelona
Spain
Local Representative
LAPHYSAN, SAU
C/ Anabel Segura nº11. Edificio A, Planta 4, puerta D,
28108 Alcobendas
Madrid
Spain
This medicinal product is authorized in the Member States of the European Economic Area under the following names:
Portugal: Cefepima LDP Laboratorios TORLAN
Belgium: Cefepime LDP-Laboratorios TORLAN 1000 mg | 2000 mg, Powder for solution for injection/infusion
United Kingdom: Renapime 1g | 2g, Powder for solution for injection/infusion
Date of the last revision of this prospectus: November 2017
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 only for doctors or healthcare professionals:
The disposal of unused medicinal products and all materials that have come into contact with them must be carried out in accordance with local regulations.
Preparation and administration of the reconstituted solution:
Cefepima LDP-Laboratorios TORLAN, powder for solution for injection and infusion, must be dissolved in:
or in one of the solutions listed in section b) shown below for intravenous administration
sodium chloride 0.9% with 5% glucose solution
5% or 10% glucose solution
Ringer's Lactate solution
Ringer's Lactate solution with 5% glucose solution
1/6 M sodium lactate solution.
For intravenous injection,the volume of diluent to be added to each vial and the resulting concentration of cefepime are presented in the following table:
Amount of cefepime per vial | Volume of diluent to be added (ml) | Approximate final volume (ml) | Approximate concentration of cefepime (mg/ml) |
1 g IV | 10.0 | 11.4 | 90 |
2 g IV | 10.0 | 12.8 | 160 |
For intravenous infusion,the volume of infusion diluent (solution listed in section b)) to be used for reconstitution and the resulting concentration of cefepime are presented in the following table:
The volume of infusion diluent to be used for each vial and the resulting concentration of cefepime are presented in the following table:
Amount of cefepime per vial | Volume of diluent to be added (ml) | Approximate final volume (ml) | Approximate concentration of cefepime (mg/ml) |
1 g IV | 50.0 | 51.4 | 19 |
2 g IV | 50.0 | 52.8 | 38 |
The resulting solution should be administered over approximately 30 minutes.
For intramuscular administrationreconstitute the 1g vial with 3.0 ml of water for injectable preparations.
Note:
The reconstitutedsolutions, which are prepared correctly, may present a yellow to yellow-brown color. This does not mean that the efficacy of Cefepima LDP-Laboratorios TORLAN may be compromised.
The content of the vial is intended for single use. The remaining reconstituted solution must be discarded.
Inspect the vial before use. It can only be used if the solution does not present particles.
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