Caspofungin Accord

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

caspofungin acetate

Available from:

Accord Healthcare S.L.U.

ATC code:

J02AX04

INN (International Name):

caspofungin

Therapeutic group:

Antimycotics for systemic use

Therapeutic area:

Candidiasis; Aspergillosis

Therapeutic indications:

Treatment of invasive candidiasis in adult or paediatric patients.Treatment of invasive aspergillosis in adult or paediatric patients who are refractory to or intolerant of amphotericin B, lipid formulations of amphotericin B and/or itraconazole. Refractoriness is defined as progression of infection or failure to improve after a minimum of 7 days of prior therapeutic doses of effective antifungal therapy.Empirical therapy for presumed fungal infections (such as Candida or Aspergillus) in febrile, neutropaenic adult or paediatric patients.

Product summary:

Revision: 6

Authorization status:

Withdrawn

Authorization date:

2016-02-11

Patient Information leaflet

                                30
B. PACKAGE LEAFLET
31
PACKAGE LEAFLET: INFORMATION FOR THE USER
CASPOFUNGIN ACCORD 50 MG POWDER FOR CONCENTRATE FOR SOLUTION FOR
INFUSION
CASPOFUNGIN ACCORD 70 MG POWDER FOR CONCENTRATE FOR SOLUTION FOR
INFUSION
caspofungin
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU OR YOUR CHILD ARE GIVEN
THIS MEDICINE BECAUSE IT
CONTAINS IMPORTANT INFORMATION FOR YOU.

Keep this leaflet. You may need to read it again.

If you have any further questions, ask your doctor, nurse or
pharmacist.

If you get any side effects, talk to your doctor, nurse or pharmacist.
This includes any possible
side effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Caspofungin Accord is and what it is used for
2.
What you need to know before you are given Caspofungin Accord
3.
How to use Caspofungin Accord
4.
Possible side effects
5.
How to store Caspofungin Accord
6.
Contents of the pack and other information
1.
WHAT CASPOFUNGIN ACCORD IS AND WHAT IT IS USED FOR
WHAT CASPOFUNGIN ACCORD IS
Caspofungin Accord contains a medicine called caspofungin. This
belongs to a group of medicines
called anti-fungals.
WHAT CASPOFUNGIN ACCORD IS USED FOR
Caspofungin Accord is used to treat the following infections in
children, adolescents and adults:

serious fungal infections in your tissues or organs (called
‘invasive candidiasis’). This infection
is caused by fungal (yeast) cells called Candida.
People who might get this type of infection include those who have
just had an operation or
those whose immune systems are weak. Fever and chills that do not
respond to an antibiotic are
the most common signs of this type of infection.

fungal infections in your nose, nasal sinuses or lungs (called
‘invasive aspergillosis’) if other
anti-fungal treatments have not worked or have caused side effects.
This infection is caused by a
mould called Aspergillus.
People who might get this type of infection include those having
chemotherapy, those who have
had a transplant and those whose immune systems are weak.

sus
                                
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Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Caspofungin Accord 50 mg powder for concentrate for solution for
infusion
Caspofungin Accord 70 mg powder for concentrate for solution for
infusion
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
_ _
Caspofungin Accord 50 mg powder for concentrate for solution for
infusion
Each vial contains 50 mg caspofungin (as acetate).
Caspofungin Accord 70 mg powder for concentrate for solution for
infusion
Each vial contains 70 mg caspofungin (as acetate).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Powder for concentrate for solution for infusion.
White to off-white, powder.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS

Treatment of invasive candidiasis in adult or paediatric patients.

Treatment of invasive aspergillosis in adult or paediatric patients
who are refractory to or
intolerant of amphotericin B, lipid formulations of amphotericin B
and/or itraconazole.
Refractoriness is defined as progression of infection or failure to
improve after a minimum of
7 days of prior therapeutic doses of effective antifungal therapy.

Empirical therapy for presumed fungal infections (such as Candida or
Aspergillus) in febrile,
neutropaenic adult or paediatric patients.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Caspofungin should be initiated by a physician experienced in the
management of invasive fungal
infections.
Posology
_Adult patients_
A single 70 mg loading dose should be administered on Day-1, followed
by 50 mg daily thereafter. In
patients weighing more than 80 kg, after the initial 70 mg loading
dose, caspofungin 70 mg daily is
recommended (see section 5.2). No dosage adjustment is necessary based
on gender or race (see
section 5.2).
_Paediatric patients (12 months to 17 years) _
In paediatric patients (12 months to 17 years of age), dosing should
be based on the patient’s body
surface area (see Instructions for Use in Paediatric Patients,
Mosteller
1
Formula). For all indications, a
single 70-mg/m
2
lo
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 05-03-2020
Summary of Product characteristics Summary of Product characteristics Bulgarian 05-03-2020
Public Assessment Report Public Assessment Report Bulgarian 21-03-2016
Patient Information leaflet Patient Information leaflet Spanish 05-03-2020
Public Assessment Report Public Assessment Report Spanish 21-03-2016
Patient Information leaflet Patient Information leaflet Czech 05-03-2020
Public Assessment Report Public Assessment Report Czech 21-03-2016
Patient Information leaflet Patient Information leaflet Danish 05-03-2020
Public Assessment Report Public Assessment Report Danish 21-03-2016
Patient Information leaflet Patient Information leaflet German 05-03-2020
Public Assessment Report Public Assessment Report German 21-03-2016
Patient Information leaflet Patient Information leaflet Estonian 05-03-2020
Public Assessment Report Public Assessment Report Estonian 21-03-2016
Patient Information leaflet Patient Information leaflet Greek 05-03-2020
Public Assessment Report Public Assessment Report Greek 21-03-2016
Patient Information leaflet Patient Information leaflet French 05-03-2020
Public Assessment Report Public Assessment Report French 21-03-2016
Patient Information leaflet Patient Information leaflet Italian 05-03-2020
Public Assessment Report Public Assessment Report Italian 21-03-2016
Patient Information leaflet Patient Information leaflet Latvian 05-03-2020
Public Assessment Report Public Assessment Report Latvian 21-03-2016
Patient Information leaflet Patient Information leaflet Lithuanian 05-03-2020
Summary of Product characteristics Summary of Product characteristics Lithuanian 05-03-2020
Public Assessment Report Public Assessment Report Lithuanian 21-03-2016
Patient Information leaflet Patient Information leaflet Hungarian 05-03-2020
Summary of Product characteristics Summary of Product characteristics Hungarian 05-03-2020
Public Assessment Report Public Assessment Report Hungarian 21-03-2016
Patient Information leaflet Patient Information leaflet Maltese 05-03-2020
Public Assessment Report Public Assessment Report Maltese 21-03-2016
Patient Information leaflet Patient Information leaflet Dutch 05-03-2020
Public Assessment Report Public Assessment Report Dutch 21-03-2016
Patient Information leaflet Patient Information leaflet Polish 05-03-2020
Public Assessment Report Public Assessment Report Polish 21-03-2016
Patient Information leaflet Patient Information leaflet Portuguese 05-03-2020
Summary of Product characteristics Summary of Product characteristics Portuguese 05-03-2020
Public Assessment Report Public Assessment Report Portuguese 21-03-2016
Patient Information leaflet Patient Information leaflet Romanian 05-03-2020
Public Assessment Report Public Assessment Report Romanian 21-03-2016
Patient Information leaflet Patient Information leaflet Slovak 05-03-2020
Public Assessment Report Public Assessment Report Slovak 21-03-2016
Patient Information leaflet Patient Information leaflet Slovenian 05-03-2020
Summary of Product characteristics Summary of Product characteristics Slovenian 05-03-2020
Public Assessment Report Public Assessment Report Slovenian 21-03-2016
Patient Information leaflet Patient Information leaflet Finnish 05-03-2020
Public Assessment Report Public Assessment Report Finnish 21-03-2016
Patient Information leaflet Patient Information leaflet Swedish 05-03-2020
Public Assessment Report Public Assessment Report Swedish 21-03-2016
Patient Information leaflet Patient Information leaflet Norwegian 05-03-2020
Summary of Product characteristics Summary of Product characteristics Norwegian 05-03-2020
Patient Information leaflet Patient Information leaflet Icelandic 05-03-2020
Summary of Product characteristics Summary of Product characteristics Icelandic 05-03-2020
Patient Information leaflet Patient Information leaflet Croatian 05-03-2020
Public Assessment Report Public Assessment Report Croatian 21-03-2016

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