Daptomycin Dr. Reddys 500 mg powder for solution for injection and infusion EFG
daptomycin
Read the entire leaflet carefully before starting to use this medicine, as it contains important information for you.
Contents of the pack
The active substance of Daptomycin Dr. Reddys is daptomycin. Daptomycin is an antibacterial agent capable of stopping the growth of certain bacteria.
Antibiotics are used to treat bacterial infections and do not work for viral infections such as flu or cold.
It is essential that you follow the instructions regarding dosage, administration interval, and treatment duration as indicated by your doctor.
Do not store or reuse this medication. 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.
Daptomycin Dr. Reddys is used in adults and in children and adolescents (aged 1 to 17 years) to treat skin and underlying tissue infections. It is also used to treat blood infections when associated with a skin infection. Daptomycin Dr. Reddys is also used in adults to treat infections in the tissues that line the inside of the heart (including heart valves), caused by a type of bacteria called Staphylococcus aureus.It is also used to treat blood infections caused by the same type of bacteria when associated with heart infection.
Depending on the type of infection(s) you are suffering from, your doctor may also prescribe other antibacterial agents while you are receiving treatment with Daptomycin Dr. Reddys.
If this is the case, inform your doctor or nurse. If you think you may be allergic, consult your doctor or nurse.
Warnings and precautions
Consult your doctor or nurse before receiving Daptomycin Dr. Reddys:
If any of the above cases apply to you, inform your doctor or nurse before receiving Daptomycin Dr. Reddys.
Tell your doctor or nurse immediately if you develop any of the following symptoms:
Daptomycin may interfere with laboratory tests that measure the blood's ability to clot. The results may appear to suggest poor clotting, even though there is actually no problem. Therefore, it is essential that your doctor is aware that you are receiving daptomycin. Inform your doctor that you are being treated with daptomycin.
Your doctor will perform blood tests to monitor the health of your muscles before you start treatment and frequently during treatment with daptomycin.
Children and adolescents
Daptomycin must not be administered to children under one year of age. Animal studies have shown that this age group may experience severe side effects.
Use in elderly patients
Patients over 65 years of age may receive the same dose as other adults, provided their kidneys are functioning correctly.
Use of Daptomycin Dr. Reddys with other medicines
Tell your doctor or nurse if you are using, have recently used, or might use any other medicines.
It is particularly important that you mention the following:
Pregnancy and breastfeeding
Daptomycin is not normally administered to pregnant women. If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before receiving this medicine.
You must not breastfeed if you are receiving daptomycin, as it may pass into breast milk and affect the baby.
Driving and using machines
Daptomycin has no known effects on the ability to drive or use machines.
Daptomycin Dr. Reddys contains sodium hydroxide as an excipient
This medicine contains less than 23 mg (1 mmol) of sodium per vial, so it is considered essentially "sodium-free"
Daptomycin Dr. Reddys will be administered to you by your doctor or nurse.
Adults (18 years of age and older)
The dose will depend on your weight and the type of infection being treated. The usual dose for adults is 4 mg per kilogram of body weight once a day for skin infections or 6 mg per kilogram of body weight once a day for heart or blood infections associated with skin infections. In adult patients, this dose is administered directly into the bloodstream (into a vein), either as an infusion lasting approximately 30 minutes or as an injection lasting approximately 2 minutes. The same dose is recommended for people over 65 years of age, provided their kidneys are functioning correctly.
If your kidneys do not function properly, you may receive daptomycin less frequently, e.g., every other day. If you are undergoing dialysis and your next dose of daptomycin is due on a dialysis day, you will normally receive daptomycin after the dialysis session.
Children and adolescents (1 to 17 years of age)
The recommended doses in children and adolescents (1 to 17 years) being treated for skin infections depend on the patient's age and the type of infection being treated. This dose is administered directly into the bloodstream (into a vein), as an infusion lasting approximately 30-60 minutes.
A complete treatment for skin infections usually lasts between 1 and 2 weeks. Your doctor will decide the duration of your treatment for blood or heart infections and skin infections.
Detailed instructions for use and handling are provided at the end of the leaflet.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The following are described the most serious side effects:
Serious side effects with unknown frequency(frequency cannot be estimated from the available data)
Some cases of hypersensitivity reactions (severe allergic reactions including anaphylaxis, angioedema, drug rash with eosinophilia and systemic symptoms (DRESS)) have been reported during the administration of daptomycin. These severe allergic reactions require immediate medical attention. Inform your doctor or nurse immediately if you have any of the following symptoms:
Tell your doctor immediately if you experience unexplained muscle pain, tenderness, or weakness. Muscle problems can be severe, including muscle breakdown (rhabdomyolysis), which can cause kidney damage.
Other serious side effects that have been reported with the use of daptomycin are:
If you experience these symptoms, inform your doctor or nurse immediately. Your doctor will perform additional tests to make a diagnosis.
The following are described the most frequently reported side effects:
Common side effects(may affect up to 1 in 10 patients)
The following are described other side effects that may occur after treatment with daptomycin:
Uncommon side effects(may affect up to 1 in 100 patients)
Rare side effects(may affect up to 1 in 1,000 patients)
Frequency not known(cannot be estimated from the available data)
Antibiotic-associated colitis, including pseudomembranous colitis (severe or persistent diarrhea containing blood and/or mucus, associated with abdominal pain or fever), easy bruising, bleeding gums, or nosebleeds.
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: 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.
Store in a refrigerator (between 2°C and 8°C).
After reconstitution: The chemical and physical stability of the reconstituted solution in the vial has been demonstrated for 12 hours at 25°C and up to 48 hours at 2°C - 8°C. The chemical and physical stability of the diluted solution in infusion bags is 12 hours at 25°C or 24 hours between 2°C - 8°C.
For intravenous infusion over 30 minutes, the combined storage time (reconstituted solution in vial and diluted solution in infusion bag; see section 6.6) at 25°C must not exceed 12 hours (or 24 hours between 2°C -8°C).
For intravenous injection over 2 minutes, the storage time of the reconstituted solution in the vial (see section 6.6) at 25°C must not exceed 12 hours (or 48 hours between 2°C - 8°C).
However, from a microbiological point of view, the product should be used immediately. The product does not contain preservatives or bacteriostatic agents. If not used immediately, the storage time is the responsibility of the user and will normally not exceed 24 hours at 2°C - 8°C, unless reconstitution/dilution has taken place under controlled and validated aseptic conditions.
Do not use this medicine after the expiry date which is stated on the carton after EXP and on the label after EXP. The expiry date is the last day of the month indicated.
Do not use this medicine if you notice visible signs of deterioration.
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.
The active ingredient is daptomycin
The active ingredient is daptomycin. A vial of powder contains 500 mg of daptomycin.
One ml provides 50 mg of daptomycin after reconstitution with 10 ml of sodium chloride solution (0.9%).
The other component is sodium hydroxide.
Appearance of the product and packaging content
Daptomycin Dr. Reddys 500 mg powder for solution for injection/infusion EFG is presented in a glass vial as a pale yellow to light brown powder or cake. It is mixed with a solvent to form a solution before administration.
Daptomycin Dr. Reddys is presented in packs containing 1 vial.
Marketing authorization holder and manufacturer
Marketing authorization holder
Reddy Pharma Iberia, S.A.
Avenida Josep Tarradellas, nº 38
08029 Barcelona-Spain
Tel.: +34 93 355 49 16
Fax: +34 93 355 49 61
Manufacturer
Dr. Reddy´s Laboratories (UK) Ltd.
6, Riverview Road, Beverley,
East Yorkshire, HU17 0LD
United Kingdom
Fax: +44 1482872042
Tel: +44 1482860228
or
Betapharm Arzneimittel GmbH
Kobelweg 95,
86156 Augsburg, Germany
This medicinal product is authorized in the Member States of the European Economic Area and in the United Kingdom (Northern Ireland) under the following names:
Denmark: Daptomycin beta 500 mg Powder for solution for injection/infusion
Spain: Daptomicina Dr. Reddys 500 mg, powder for solution for injection and for infusion EFG
United Kingdom: Daptomycin Dr. Reddy's 500 mg Powder For Solution For Injection/Infusion
Italy: Daptomicina Dr. Reddy's 500 mg, Powder for solution for injection or infusion
France: Daptomycine Dr. Reddy's 500 mg, powder for solution for injection or infusion
Date of last revision of this leaflet: December 2021
This information is intended only for healthcare professionals:
Important: Please consult the Summary of Product Characteristics or Package Leaflet before prescribing.
Instructions for use and handling
In adults, daptomycin can be administered intravenously as an infusion over 30 or 60 minutes or as an injection over 2 minutes. Unlike adults, daptomycin should not be administered to pediatric patients as an injection over 2 minutes. Pediatric patients from 7 to 17 years of age should receive daptomycin as an infusion over 30 minutes. Pediatric patients under 7 years of age who receive doses of 9-12 mg/kg should be administered daptomycin as an infusion over 60 minutes. The preparation of the infusion solution requires an additional dilution phase, as described below.
Daptomycin Dr. Reddys administered as an intravenous infusion over 30 or 60 minutes
Reconstituting the lyophilized product with 10 ml of an injectable solution containing 9 mg/ml of sodium chloride (0.9%) yields a concentration of 50 mg/ml of Daptomycin Dr. Reddys for infusion.
The lyophilized product takes approximately 15 minutes to dissolve. The fully reconstituted product has a transparent appearance and may present some small bubbles or foam around the edge of the vial.
To prepare Daptomycin Dr. Reddys for intravenous infusion, follow these instructions:
To reconstitute or dilute Daptomycin Dr. Reddys lyophilized product, aseptic technique must be used throughout the process.
For Reconstitution:
For Dilution:
Daptomycin Dr. Reddys is not physically or chemically compatible with solutions containing glucose. The following drugs have been shown to be compatible when added to infusion solutions containing daptomycin: aztreonam, ceftazidime, ceftriaxone, gentamicin, fluconazole, levofloxacin, dopamine, heparin, and lidocaine.
The combined storage time (reconstituted solution in the vial and diluted solution in infusion bags) at 25°C should not exceed 12 hours (24 hours if refrigerated).
The stability of the diluted solution in infusion bags has been established for 12 hours at 25°C or 24 hours if refrigerated at 2°C - 8°C.
Daptomycin Dr. Reddys administered as an intravenous injection over 2 minutes (only for adult patients)
Water should not be used for the reconstitution of Daptomycin Dr. Reddys for intravenous injection. Daptomycin Dr. Reddys should be reconstituted only with 9 mg/ml of sodium chloride (0.9%).
Reconstituting the lyophilized product with 10 ml of an injectable solution containing 9 mg/ml of sodium chloride (0.9%) for injection yields a concentration of 50 mg/ml of Daptomycin Dr. Reddys for injectable solution.
The lyophilized product takes approximately 15 minutes to dissolve. The fully reconstituted product has a transparent appearance and may present some small bubbles or foam around the edge of the vial.
To prepare Daptomycin Dr. Reddys for intravenous injection, follow these instructions:
To reconstitute Daptomycin Dr. Reddys lyophilized product, aseptic technique must be used throughout the process.
The physical and chemical stability during use of the reconstituted solution in the vial has been demonstrated for 12 hours at 25°C and up to a maximum of 48 hours if refrigerated (2°C - 8°C).
However, from a microbiological point of view, the product should be used immediately. If not used immediately, the storage time during use is the responsibility of the user and normally should not exceed 24 hours at 2°C - 8°C, unless the reconstitution/dissolution has taken place in controlled and validated aseptic conditions.
This medicinal product should not be mixed with other medicinal products except those mentioned above.
The vials of Daptomycin Dr. Reddys are for single use only. Any unused remainder of the vial should be discarded.