Riarify (previously CHF 5993 Chiesi Farmaceutici S.p.A.)

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

formoterol fumarate dihydrate, glycopyrronium, Beclometasone dipropionate

Available from:

Chiesi Farmaceutici S.p.A.

ATC code:

R03AL09

INN (International Name):

beclometasone, formoterol

Therapeutic group:

Drugs for obstructive airway diseases,

Therapeutic area:

Pulmonary Disease, Chronic Obstructive

Therapeutic indications:

Maintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (COPD) who are not adequately treated by a combination of an inhaled corticosteroid and a long-acting beta2-agonist (for effects on symptoms control and prevention of exacerbations see section 5.1).

Product summary:

Revision: 4

Authorization status:

Authorised

Authorization date:

2018-04-23

Patient Information leaflet

                                34
B. PACKAGE LEAFLET
35
PACKAGE LEAFLET: INFORMATION FOR THE USER
RIARIFY 87 MICROGRAMS/5 MICROGRAMS/9 MICROGRAMS PRESSURISED
INHALATION, SOLUTION
beclometasone dipropionate/formoterol fumarate
dihydrate/glycopyrronium
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 Riarify is and what it is used for
2.
What you need to know before you use Riarify
3.
How to use Riarify
4.
Possible side effects
5.
How to store Riarify
6.
Contents of the pack and other information
1.
WHAT RIARIFY IS AND WHAT IT IS USED FOR
Riarify is a medicine to help breathing that contains the three active
substances:
•
beclometasone dipropionate,
•
formoterol fumarate dihydrate and
•
glycopyrronium.
Beclometasone dipropionate belongs to a group of medicines called
corticosteroids which act to
reduce the swelling and irritation in your lungs.
Formoterol and glycopyrronium are medicines called long-acting
bronchodilators. They act in
different ways to relax the muscles in your airways, helping to open
the airways wider and allowing
you to breathe more easily.
Regular treatment with these three active substances helps to relieve
and prevent symptoms such as
shortness of breath, wheezing and cough in adult patients with chronic
obstructive pulmonary disease
(COPD). Riarify can reduce exacerbations (flare-ups) of COPD symptoms
.
COPD is a serious long-
term disease in which the airways become blocked and air sacs inside
the lungs become damaged,
leading to difficulty breathing.
2.
WHAT YOU NEED TO KNOW BEFORE YOU USE RIARIFY
D
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Riarify 87 micrograms/5 micrograms/9 micrograms pressurised
inhalation, solution
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each delivered dose (the dose leaving the mouthpiece) contains 87
micrograms of beclometasone
dipropionate, 5 micrograms of formoterol fumarate dihydrate and 9
micrograms of glycopyrronium (as
11 micrograms glycopyrronium bromide).
Each metered dose (the dose leaving the valve) contains 100 micrograms
of beclometasone
dipropionate, 6 micrograms of formoterol fumarate dihydrate and 10
micrograms of glycopyrronium
(as 12.5 micrograms glycopyrronium bromide).
Excipient with known effect
Riarify contains 8.856 mg ethanol per actuation.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Pressurised inhalation, solution (pressurised inhalation)
Colourless to yellowish liquid solution.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Maintenance treatment in adult patients with moderate to severe
chronic obstructive pulmonary
disease (COPD) who are not adequately treated by a combination of an
inhaled corticosteroid and a
long-acting beta2-agonist or a combination of a long-acting
beta2-agonist and a long-acting
muscarinic antagonist (for effects on symptoms control and prevention
of exacerbations see
section 5.1).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
The recommended dose is two inhalations twice daily.
The maximum dose is two inhalations twice daily.
Special populations
_ _
_Elderly _
No dosage adjustment is required in elderly patients (65 years of age
and older).
_ _
_Renal impairment _
Riarify can be used at the recommended dose in patients with mild
(glomerular filtration rate [GFR]
≥50 to <80 mL/min/1.73 m
2
) to moderate (GFR ≥30 to <50 mL/min/1.73 m
2
) renal impairment. Use in
patients with severe (GFR <30 mL/min/1.73 m
2
) renal impairment or end-stage renal (GFR
<15 mL/min/1.73 m
2
) disease requiring dialysis, especially if associated with
significant body weight
3
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 13-12-2022
Summary of Product characteristics Summary of Product characteristics Bulgarian 13-12-2022
Public Assessment Report Public Assessment Report Bulgarian 06-09-2019
Patient Information leaflet Patient Information leaflet Spanish 13-12-2022
Public Assessment Report Public Assessment Report Spanish 06-09-2019
Patient Information leaflet Patient Information leaflet Czech 13-12-2022
Public Assessment Report Public Assessment Report Czech 06-09-2019
Patient Information leaflet Patient Information leaflet Danish 13-12-2022
Public Assessment Report Public Assessment Report Danish 06-09-2019
Patient Information leaflet Patient Information leaflet German 13-12-2022
Public Assessment Report Public Assessment Report German 06-09-2019
Patient Information leaflet Patient Information leaflet Estonian 13-12-2022
Public Assessment Report Public Assessment Report Estonian 06-09-2019
Patient Information leaflet Patient Information leaflet Greek 13-12-2022
Public Assessment Report Public Assessment Report Greek 06-09-2019
Patient Information leaflet Patient Information leaflet French 13-12-2022
Public Assessment Report Public Assessment Report French 06-09-2019
Patient Information leaflet Patient Information leaflet Italian 13-12-2022
Public Assessment Report Public Assessment Report Italian 06-09-2019
Patient Information leaflet Patient Information leaflet Latvian 13-12-2022
Public Assessment Report Public Assessment Report Latvian 06-09-2019
Patient Information leaflet Patient Information leaflet Lithuanian 13-12-2022
Summary of Product characteristics Summary of Product characteristics Lithuanian 13-12-2022
Public Assessment Report Public Assessment Report Lithuanian 06-09-2019
Patient Information leaflet Patient Information leaflet Hungarian 13-12-2022
Summary of Product characteristics Summary of Product characteristics Hungarian 13-12-2022
Public Assessment Report Public Assessment Report Hungarian 06-09-2019
Patient Information leaflet Patient Information leaflet Maltese 13-12-2022
Public Assessment Report Public Assessment Report Maltese 06-09-2019
Patient Information leaflet Patient Information leaflet Dutch 13-12-2022
Public Assessment Report Public Assessment Report Dutch 06-09-2019
Patient Information leaflet Patient Information leaflet Polish 13-12-2022
Public Assessment Report Public Assessment Report Polish 06-09-2019
Patient Information leaflet Patient Information leaflet Portuguese 13-12-2022
Summary of Product characteristics Summary of Product characteristics Portuguese 13-12-2022
Public Assessment Report Public Assessment Report Portuguese 06-09-2019
Patient Information leaflet Patient Information leaflet Romanian 13-12-2022
Public Assessment Report Public Assessment Report Romanian 06-09-2019
Patient Information leaflet Patient Information leaflet Slovak 13-12-2022
Public Assessment Report Public Assessment Report Slovak 06-09-2019
Patient Information leaflet Patient Information leaflet Slovenian 13-12-2022
Summary of Product characteristics Summary of Product characteristics Slovenian 13-12-2022
Public Assessment Report Public Assessment Report Slovenian 06-09-2019
Patient Information leaflet Patient Information leaflet Finnish 13-12-2022
Public Assessment Report Public Assessment Report Finnish 06-09-2019
Patient Information leaflet Patient Information leaflet Swedish 13-12-2022
Public Assessment Report Public Assessment Report Swedish 06-09-2019
Patient Information leaflet Patient Information leaflet Norwegian 13-12-2022
Summary of Product characteristics Summary of Product characteristics Norwegian 13-12-2022
Patient Information leaflet Patient Information leaflet Icelandic 13-12-2022
Summary of Product characteristics Summary of Product characteristics Icelandic 13-12-2022
Patient Information leaflet Patient Information leaflet Croatian 13-12-2022
Public Assessment Report Public Assessment Report Croatian 06-09-2019