Label: information for the user
Cancidas 50mg powder for concentrate for solution for infusion
Cancidas 70mg powder for concentrate for solution for infusion
caspofungina
Read this label carefully before you or your child start using this medicine, because it contains important information for you.
What is Cancidas
Cancidas contains a medication called caspofungin. This belongs to a group of medications known as antifungals.
What is Cancidas used for
Cancidas is used to treat the following fungal infections in children, adolescents, and adults:
People who may be susceptible to this type of infection include those who have recently undergone surgery or those with a weakened immune system. Fever and chills that do not respond to antibiotic treatment are the most common symptoms of this type of infection.
People who may be susceptible to this type of infection include those undergoing chemotherapy, those who have undergone a transplant, and those with a weakened immune system.
How Cancidas works
Cancidas makes fungal cells fragile and prevents the fungus from growing properly. This prevents the infection from spreading and gives the body's natural defenses the opportunity to completely eliminate the infection.
No use Cancidas
If you are unsure, consult your doctor, pharmacist, or nurse before starting to use your medication.
Warnings and Precautions
Consult your doctor, pharmacist, or nurse before starting to use Cancidas if:
If any of the above points apply to you (or you are unsure), consult your doctor, pharmacist, or nurse before starting to use Cancidas.
Cancidas may also cause severe skin reactions, such as Stevens-Johnson syndrome (SSJ) and toxic epidermal necrolysis (TEN).
Other Medications and Cancidas
Inform your doctor, pharmacist, or nurse if you are using, have used recently, or may need to use any other medication. This includes medications obtained without a prescription, including herbal remedies.This is because Cancidas may affect how other medications work. Also, other medications may affect how Cancidas works.
Inform your doctor, pharmacist, or nurse if you are taking any of the following medications:
If any of the above points apply to you (or you are unsure), consult your doctor, pharmacist, or nurse before starting to use Cancidas.
Pregnancy and Breastfeeding
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor before using this medication.
Driving and Operating Machinery
There is no information to suggest that Cancidas affects your ability to drive or operate machinery.
Cancidas contains sodium
This medication contains less than 1mmol of sodium (23mg) per vial; it is essentially “sodium-free”.
Cancidas will always be prepared and administered by a healthcare professional.
Cancidas will be administered to you:
Your doctor will determine the duration of treatment and the amount of Cancidas to be administered each day. Your doctor will monitor the effectiveness of the medication. If you weigh more than 80kg, you may need a different dose.
Use in children and adolescents
The dosage for children and adolescents may be different from that for adults.
If you use more Cancidas than you should
Your doctor will decide how much Cancidas you need and for how long each day. If you are concerned that you may have been given too much Cancidas, inform your doctor or nurse immediately.
If you have any other questions about the use of this medication, ask your doctor, pharmacist, or nurse.
Like all medicines, this medicine may cause side effects, although not everyone will experience them.
Consult your doctor or nurse immediately if you notice any of the following side effects – you may need urgent medical treatment:
As with any prescription medication, some side effects can be serious. Ask your doctor for more information.
Other side effects in adults include:
Frequent:can affect up to 1 in 10 people:
Rare:can affect up to 1 in 100 people:
Other side effects in children and adolescents
Very frequent:can affect more than 1 in 10 people:
Frequent:can affect up to 1 in 10 people:
Reporting of side effects
If you experience any type of side effect, consult your doctor, pharmacist, or nurse, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through thenational notification system included in theAppendixV.By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears onthe boxand on the vial (the first two numbers are the month; the next four numbers are the year). The expiration date is the last day of the month indicated.
Store in the refrigerator (between 2°C and 8°C).
Once Cancidas has been prepared, it should be used immediately. This is because it does not contain any component to prevent the growth of bacteria. Only a trained healthcare professional who has read the complete instructions should prepare the medication (see further on “Instructions for reconstituting and diluting Cancidas”).
Medicines should not be thrown down the drain or in the trash. Ask your pharmacist how to dispose of the containers and medications that you no longer need. In this way, you will help protect the environment.
Composition of Cancidas
Cancidas 50mg powder for concentrate for solution for infusion
Each vial of Cancidas contains 50mg of caspofungin.
Cancidas 70mg powder for concentrate for solution for infusion
Each vial of Cancidas contains 70mg of caspofungin.
Appearance of the product and contents of the container
Cancidas is a compact, sterile, white to off-white powder.
Each container contains a vial of powder.
Holder of the marketing authorization and responsible for manufacturing
Holder of the marketing authorization Merck Sharp & Dohme B.V. Waarderweg 39 2031 BN Haarlem Netherlands | Responsible for manufacturing Merck Sharp & Dohme B.V. Waarderweg 39, 2031 BN Haarlem Netherlands or FAREVA Mirabel Route de Marsat-Riom 63963 Clermont-Ferrand Cedex 9 France |
You can request more information about this medicine by contacting the local representative of the marketing authorization holder:
Belgique/België/Belgien MSD Belgium Tél/Tel: +32(0)27766211 | Lietuva UAB Merck Sharp & Dohme Tel.:+37052780247 |
Luxembourg/Luxemburg MSD Belgium Tél/Tel: +32(0)27766211 | |
Ceská republika Merck Sharp & Dohme s.r.o. Tel.:+420233010111 | Magyarország MSD Pharma Hungary Kft. Tel.:+3618885300 |
Danmark MSD Danmark ApS Tlf: +45 44 82 40 00 | Malta Merck Sharp& Dohme CyprusLimited Tel.:8007 4433 (+ 35699917558) |
Deutschland MSD Sharp & Dohme GmbH Tel: 0800 673 673 673 (+49 (0) 89 4561 0) | Nederland Merck Sharp & Dohme B.V. Tel:0800 9999000 (+31 23 5153153) |
Eesti Merck Sharp & Dohme OÜ Tel.: +3726144 200 | Norge MSD (Norge) AS Tlf: +47 32 20 73 00 |
Eλλ?δα MSD Α.Φ.Β.Ε.Ε Τηλ: + 30 210 98 97 300 | Österreich Merck Sharp & Dohme Ges.m.b.H. Tel: +43 (0) 1 26 044 dpoc_austria@merck.com |
España Merck Sharp & Dohme de España, S.A. Tel: +34 91 321 06 00 | Polska MSD Polska Sp.z o.o. Tel.:+48225495100 |
France MSD France Tél: + 33 (0) 1 80 46 40 40 | Portugal Merck Sharp & Dohme, Lda Tel: +351 214465700 |
Hrvatska Merck Sharp & Dohme d.o.o. Tel: + 385 1 6611 333 | România Merck Sharp & Dohme Romania S.R.L. Tel: + 4021 529 29 00 |
Ireland Merck Sharp & Dohme Ireland (Human Health) Limited Tel: +353 (0)1 2998700 | Slovenija Merck Sharp & Dohme, inovativna zdravilad.o.o. Tel:+38615204201 |
Ísland Vistor hf. Sími: +354 535 7000 | Slovenská republika Merck Sharp & Dohme, s. r. o. Tel.:+421258282010 |
Ιtalia MSD Italia S.r.l. Tel:800 23 99 89 (+39 06 361911) | Suomi/Finland MSD Finland Oy Puh/Tel: +358 (0) 9 804 650 |
Κ?προς Merck Sharp & Dohme Cyprus Limited Τηλ.:800 00 673 (+35722866700) cyprus_info@merck.com | Sverige Merck Sharp & Dohme (Sweden) AB Tel: +46 (0)77 5700488 |
Latvija SIA Merck Sharp & Dohme Latvija Tel:+37167364224 | United Kingdom (Northern Ireland) Merck Sharp & Dohme Ireland (Human Health) Limited Tel: +353 (0)1 2998700 |
Last update of this leaflet:
The detailed information on this medicine is available on the website of the European Medicines Agency:http://www.ema.europa.eu.
This information is intended solely for healthcare professionals:
Instructions for reconstituting and diluting CANCIDAS:
Reconstitution of CANCIDAS
DO NOT USE DILUENTS CONTAINING GLUCOSE, as CANCIDAS is not stable in glucose-containing diluents.DO NOT MIX OR INFUSE CANCIDAS CONCURRENTLY WITH ANY OTHER MEDICAMENT, as there are no data on the compatibility of CANCIDAS with other substances, additives or intravenous pharmaceutical specialties.The infusion solution must be visually inspected for particulate matter or a change in color.
CANCIDAS 50mg powder for concentrate for solution for infusion
Instructions for use in adult patients (vial of 50mg)
Paso 1 Reconstitution of the vials
To reconstitute the powder, bring the vial to room temperature and add asetically 10.5ml of water for injection. The concentration of the reconstituted vial will be 5.2mg/ml.
The compact, white to off-white lyophilized powder will completely dissolve. Gently mix until a transparent solution is obtained. The reconstituted solutions must be visually inspected for particulate matter or a change in color. The reconstituted solution can be stored for a maximum of 24hours at a temperature equal to or below 25°C.
Paso 2 Addition of reconstituted CANCIDAS to the patient's infusion solution
The diluents for the final infusion solution are: sodium chloride injection or Ringer lactate solution. The infusion solution is prepared by adding asetically the appropriate amount of the reconstituted concentrate (as shown in the following table) to a 250ml infusion bag or bottle. Infusions of reduced volume in 100ml may be used, if medically necessary, for daily doses of 50mg or 35mg. Do not use if the solution is turbid or has precipitated.
VIAL of 50mg: PREPARATION OF THE INFUSION SOLUTION IN ADULTS
DOSAGE* | Volume of reconstituted CANCIDAS to transfer to an intravenous bag or bottle | Standard preparation (reconstituted CANCIDAS added to 250ml) final concentration | Infusion of reduced volume (reconstituted CANCIDAS added to 100ml) final concentration |
50mg | 10ml | 0.20mg/ml | - |
50mg in reduced volume | 10ml | - | 0.47mg/ml |
35mg for moderate hepatic impairment (from a vial of 50mg) | 7ml | 0.14mg/ml | - |
35mg for moderate hepatic impairment (from a vial of 50mg) in reduced volume | 7ml | - | 0.34mg/ml |
*10.5ml must be used for the reconstitution of all vials.
Instructions for use in pediatric patients (vial of 50mg)
Calculation of body surface area (SC) for pediatric dosing
Before preparing the infusion, calculate the patient's body surface area (SC) using the following formula: (Mosteller formula[1])
Preparation of the 70mg/m2infusion solution for pediatric patients >3months (using a vial of 50mg)
1.Determine the actual loading dose to be used in the pediatric patient using the patient's SC (as calculated above) and the following equation:
SC(m2)X70mg/m2=loading dose
The maximum loading dose on day 1 should not exceed 70mg regardless of the dose calculated for the patient.
2.Wait for the refrigerated vial of CANCIDAS to reach room temperature.
3.Add asetically 10.5ml of water for injection.aThis reconstituted solution can be stored for up to 24hours at a temperature equal to or below 25°C.bThis will result in a final concentration of caspofungin in the vial of 5.2mg/ml.
4.Withdraw from the vial a volume of the medication equal to the calculated loading dose (Step1). Transfer asetically this volume (ml)cof reconstituted CANCIDAS to an IV bag or bottle that contains 250ml of sodium chloride injection or Ringer lactate solution. Alternatively, the volume (ml)cof reconstituted CANCIDAS can be added to a reduced volume of sodium chloride injection or Ringer lactate solution, without exceeding a final concentration of 0.5mg/ml. This infusion solution must be used within 24hours if stored at a temperature equal to or below 25°C or within 48hours if stored refrigerated between 2 and 8°C.
Preparation of the 50mg/m2infusion solution for pediatric patients >3months (using a vial of 70mg)
1.Determine the actual daily maintenance dose to be used in the pediatric patient using the patient's SC (as calculated above) and the following equation:
SC(m2)X50mg/m2=daily maintenance dose
The daily maintenance dose should not exceed 70mg regardless of the dose calculated for the patient.
2.Wait for the refrigerated vial of CANCIDAS to reach room temperature.
3.Add asetically 10.5ml of water for injection.aThis reconstituted solution can be stored for up to 24hours at a temperature equal to or below 25°C.bThis will result in a final concentration of caspofungin in the vial of 7.2mg/ml.
4.Withdraw from the vial a volume of the medication equal to the calculated daily maintenance dose (Step1). Transfer asetically this volume (ml)cof reconstituted CANCIDAS to an IV bag or bottle that contains 250ml of sodium chloride injection or Ringer lactate solution. Alternatively, the volume (ml)cof reconstituted CANCIDAS can be added to a reduced volume of sodium chloride injection or Ringer lactate solution, without exceeding a final concentration of 0.5mg/ml. This infusion solution must be used within 24hours if stored at a temperature equal to or below 25°C or within 48hours if stored refrigerated between 2 and 8°C.
Preparation notes:
a.The white to off-white powder will completely dissolve. Gently mix until a transparent solution is obtained.
b.Visually inspect the reconstituted solution for particulate matter or a change in color during reconstitution and before infusion. Do not use if the solution is turbid or has precipitated.
c.CANCIDAS is formulated to provide the full dose of the vial as stated in the product information (50mg) when 10ml is withdrawn from the vial.
CANCIDAS 70mg powder for concentrate for solution for infusion
Instructions for use in adult patients (vial of 70mg)
Paso 1 Reconstitution of the vials
To reconstitute the powder, bring the vial to room temperature and add asetically 10.5ml of water for injection. The concentration of the reconstituted vial will be 7.2mg/ml.
The compact, white to off-white lyophilized powder will completely dissolve. Gently mix until a transparent solution is obtained. The reconstituted solutions must be visually inspected for particulate matter or a change in color. The reconstituted solution can be stored for a maximum of 24hours at a temperature equal to or below 25°C.
Paso 2 Addition of reconstituted CANCIDAS to the patient's infusion solution
The diluents for the final infusion solution are: sodium chloride injection or Ringer lactate solution. The infusion solution is prepared by adding asetically the appropriate amount of the reconstituted concentrate (as shown in the following table) to a 250ml infusion bag or bottle. Infusions of reduced volume in 100ml may be used, if medically necessary, for daily doses of 50mg or 35mg. Do not use if the solution is turbid or has precipitated.
VIAL of 70mg: PREPARATION OF THE INFUSION SOLUTION IN ADULTS
DOSAGE* | Volume of reconstituted CANCIDAS to transfer to an intravenous bag or bottle | Standard preparation (reconstituted CANCIDAS added to 250ml) final concentration | Infusion of reduced volume (reconstituted CANCIDAS added to 100ml) final concentration |
70mg | 10ml | 0.28mg/ml | Not recommended |
70mg (from two vials of 50mg)** | 14ml | 0.28mg/ml | Not recommended |
35mg for moderate hepatic impairment (from a vial of 70mg) | 5ml | 0.14mg/ml | 0.34mg/ml |
*10.5ml must be used for the reconstitution of all vials
**If the vial of 70mg is not available, the dose of 70mg can be prepared from two vials of 50mg
Instructions for use in pediatric patients (vial of 70mg)
Cálculo de la superficie corporal (SC) para la dosificación pediátrica
Antes de preparar la perfusión, calcular la superficie corporal (SC) del paciente utilizando la siguiente fórmula: (Fórmula de Mosteller
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