Quinsair

Nazione: Unione Europea

Lingua: inglese

Fonte: EMA (European Medicines Agency)

Compra

Foglio illustrativo Foglio illustrativo (PIL)
22-12-2022
Scheda tecnica Scheda tecnica (SPC)
22-12-2022

Principio attivo:

levofloxacin

Commercializzato da:

Chiesi Farmaceutici S.p.A

Codice ATC:

J01MA12

INN (Nome Internazionale):

levofloxacin

Gruppo terapeutico:

Antibacterials for systemic use,

Area terapeutica:

Cystic Fibrosis; Respiratory Tract Infections

Indicazioni terapeutiche:

Quinsair is indicated for the management of chronic pulmonary infections due to Pseudomonas aeruginosa in adult patients with cystic fibrosis.Consideration should be given to official guidance on the appropriate use of antibacterial agents.

Dettagli prodotto:

Revision: 15

Stato dell'autorizzazione:

Authorised

Data dell'autorizzazione:

2015-03-25

Foglio illustrativo

                                31
B. PACKAGE LEAFLET
32
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
QUINSAIR 240 MG NEBULISER SOLUTION
levofloxacin
This medicine is subject to additional monitoring. This will allow
quick identification of new
safety information. You can help by reporting any side effects you may
get. See the end of section 4
for how to report side effects.
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START USING 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 or pharmacist.
-
This medicine has been prescribed for you only. Do not pass it on to
others. It may harm them,
even if their signs of illness are the same as yours.
-
If you get any side effects, talk to your doctor or pharmacist. This
includes any possible side
effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Quinsair is and what it is used for
2.
What you need to know before you use Quinsair
3.
How to use Quinsair
4.
Possible side effects
5.
How to store Quinsair
6.
Contents of the pack and other information
1.
WHAT QUINSAIR IS AND WHAT IT IS USED FOR
Quinsair contains an antibiotic medicine called levofloxacin. It
belongs to the group of antibiotics
called fluoroquinolones.
Quinsair is used to treat LUNG INFECTIONS caused by _Pseudomonas_
_aeruginosa _in adults with CYSTIC
FIBROSIS. It is an antibiotic medicine that is breathed (inhaled)
directly into the lungs where it kills the
bacteria causing the infection. This helps to improve breathing in
people with cystic fibrosis.
2.
WHAT YOU NEED TO KNOW BEFORE YOU USE QUINSAIR
DO NOT USE QUINSAIR:
-
if you are ALLERGIC to LEVOFLOXACIN, to any other QUINOLONE
ANTIBIOTICS, such as moxifloxacin,
ciprofloxacin or ofloxacin, or to any of the other ingredients of this
medicine (listed in
section 6)
-
if you have ever had a problem with your tendons (INFLAMMATION of a
TENDON or a RUPTURED
TENDON) during treatment with a QUINOLONE OR FLUOROQUINOLONE
ANTIBIOTIC
-
if you suffer
                                
                                Leggi il documento completo
                                
                            

Scheda tecnica

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
This medicinal product is subject to additional monitoring. This will
allow quick identification of
new safety information. Healthcare professionals are asked to report
any suspected adverse reactions.
See section 4.8 for how to report adverse reactions.
1.
NAME OF THE MEDICINAL PRODUCT
Quinsair 240 mg nebuliser solution
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each mL of nebuliser solution contains levofloxacin hemihydrate
equivalent to 100 mg of
levofloxacin. Each ampoule contains 240 mg of levofloxacin.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Nebuliser solution.
Clear, pale yellow solution.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Quinsair is indicated for the management of chronic pulmonary
infections due to _Pseudomonas _
_aeruginosa_ in adult patients with cystic fibrosis (CF, see section
5.1).
Consideration should be given to official guidance on the appropriate
use of antibacterial medicinal
products.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
The recommended dosage is 240 mg (one ampoule) administered by
inhalation twice daily (see
section 5.2). The doses should be inhaled as close as possible to 12
hours apart.
Quinsair is taken in alternating cycles of 28 days on treatment
followed by 28 days off treatment.
Cyclical therapy may be continued for as long as the physician
considers that the patient is obtaining
clinical benefit.
If a dose is missed, it should be taken as soon as the patient
remembers providing that at least an 8-
hour interval is allowed before inhaling the next dose. Patients
should not inhale the contents of more
than one ampoule to compensate for the missed dose.
If acute symptomatic bronchospasm occurs after receiving Quinsair,
patients may benefit from the use
of a short-acting inhaled bronchodilator at least 15 minutes to 4
hours prior to subsequent doses (see
sections 4.4 and 4.8).
_Elderly patients_
_(≥_
_ 65 years old)_
The safety and efficacy of Quinsair in elderly patients wi
                                
                                Leggi il documento completo
                                
                            

Documenti in altre lingue

Foglio illustrativo Foglio illustrativo bulgaro 22-12-2022
Scheda tecnica Scheda tecnica bulgaro 22-12-2022
Foglio illustrativo Foglio illustrativo spagnolo 22-12-2022
Scheda tecnica Scheda tecnica spagnolo 22-12-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione spagnolo 12-06-2015
Foglio illustrativo Foglio illustrativo ceco 22-12-2022
Scheda tecnica Scheda tecnica ceco 22-12-2022
Foglio illustrativo Foglio illustrativo danese 22-12-2022
Scheda tecnica Scheda tecnica danese 22-12-2022
Foglio illustrativo Foglio illustrativo tedesco 22-12-2022
Scheda tecnica Scheda tecnica tedesco 22-12-2022
Foglio illustrativo Foglio illustrativo estone 22-12-2022
Scheda tecnica Scheda tecnica estone 22-12-2022
Foglio illustrativo Foglio illustrativo greco 22-12-2022
Scheda tecnica Scheda tecnica greco 22-12-2022
Foglio illustrativo Foglio illustrativo francese 22-12-2022
Scheda tecnica Scheda tecnica francese 22-12-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione francese 12-06-2015
Foglio illustrativo Foglio illustrativo italiano 22-12-2022
Scheda tecnica Scheda tecnica italiano 22-12-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione italiano 12-06-2015
Foglio illustrativo Foglio illustrativo lettone 22-12-2022
Scheda tecnica Scheda tecnica lettone 22-12-2022
Foglio illustrativo Foglio illustrativo lituano 22-12-2022
Scheda tecnica Scheda tecnica lituano 22-12-2022
Foglio illustrativo Foglio illustrativo ungherese 22-12-2022
Scheda tecnica Scheda tecnica ungherese 22-12-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione ungherese 12-06-2015
Foglio illustrativo Foglio illustrativo maltese 22-12-2022
Scheda tecnica Scheda tecnica maltese 22-12-2022
Foglio illustrativo Foglio illustrativo olandese 22-12-2022
Scheda tecnica Scheda tecnica olandese 22-12-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione olandese 12-06-2015
Foglio illustrativo Foglio illustrativo polacco 22-12-2022
Scheda tecnica Scheda tecnica polacco 22-12-2022
Foglio illustrativo Foglio illustrativo portoghese 22-12-2022
Scheda tecnica Scheda tecnica portoghese 22-12-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione portoghese 12-06-2015
Foglio illustrativo Foglio illustrativo rumeno 22-12-2022
Scheda tecnica Scheda tecnica rumeno 22-12-2022
Foglio illustrativo Foglio illustrativo slovacco 22-12-2022
Scheda tecnica Scheda tecnica slovacco 22-12-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione slovacco 12-06-2015
Foglio illustrativo Foglio illustrativo sloveno 22-12-2022
Scheda tecnica Scheda tecnica sloveno 22-12-2022
Foglio illustrativo Foglio illustrativo finlandese 22-12-2022
Scheda tecnica Scheda tecnica finlandese 22-12-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione finlandese 12-06-2015
Foglio illustrativo Foglio illustrativo svedese 22-12-2022
Scheda tecnica Scheda tecnica svedese 22-12-2022
Foglio illustrativo Foglio illustrativo norvegese 22-12-2022
Scheda tecnica Scheda tecnica norvegese 22-12-2022
Foglio illustrativo Foglio illustrativo islandese 22-12-2022
Scheda tecnica Scheda tecnica islandese 22-12-2022
Foglio illustrativo Foglio illustrativo croato 22-12-2022
Scheda tecnica Scheda tecnica croato 22-12-2022

Cerca alert relativi a questo prodotto

Visualizza cronologia documenti