Revatio

Country: Եվրոպական Միություն

language: անգլերեն

source: EMA (European Medicines Agency)

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PIL PIL (PIL)
15-01-2024
SPC SPC (SPC)
15-01-2024
PAR PAR (PAR)
21-11-2016

active_ingredient:

sildenafil

MAH:

Upjohn EESV

ATC_code:

G04BE03

INN:

sildenafil

therapeutic_group:

Urologicals

therapeutic_area:

Hypertension, Pulmonary

therapeutic_indication:

Treatment of adult patients with pulmonary arterial hypertension classified as World Health Organization (WHO) functional class II and III, to improve exercise capacity. Efficacy has been shown in primary pulmonary hypertension and pulmonary hypertension associated with connective tissue disease.Paediatric populationTreatment of paediatric patients aged one year to 17 years old with pulmonary arterial hypertension. Efficacy in terms of improvement of exercise capacity or pulmonary haemodynamics has been shown in primary pulmonary hypertension and pulmonary hypertension associated with congenital heart disease.Revatio solution for injection is for the treatment of adult patients with pulmonary arterial hypertension who are currently prescribed oral Revatio and who are temporarily unable to take oral therapy, but are otherwise clinically and haemodynamically stable.Revatio (oral) is indicated for treatment of adult patients with pulmonary arterial hypertension classified as WHO functional class II and III, to improve exercise capacity. Efficacy has been shown in primary pulmonary hypertension and pulmonary hypertension associated with connective tissue disease.

leaflet_short:

Revision: 50

authorization_status:

Authorised

authorization_date:

2005-10-28

PIL

                                81
B. PACKAGE LEAFLET
82
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
REVATIO 20 MG FILM-COATED TABLETS
sildenafil
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING 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 Revatio is and what it is used for
2.
What you need to know before you take Revatio
3.
How to take Revatio
4.
Possible side effects
5
How to store Revatio
6.
Contents of the pack and other information
1.
WHAT REVATIO IS AND WHAT IT IS USED FOR
Revatio contains the active substance sildenafil which belongs to a
group of medicines called
phosphodiesterase type 5 (PDE5) inhibitors.
Revatio brings down blood pressure in the lungs by widening the blood
vessels in the lungs.
Revatio is used to treat adults and children and adolescents from 1 to
17 years old with high blood
pressure in the blood vessels in the lungs (pulmonary arterial
hypertension).
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE REVATIO
DO NOT TAKE REVATIO
-
if you are allergic to sildenafil or any of the other ingredients of
this medicine (listed in section
6).
-
if you are taking medicines containing nitrates, or nitric oxide
donors such as amyl nitrate
(“poppers”). These medicines are often given for relief of chest
pain (or “angina pectoris”).
Revatio can cause a serious increase in the effects of these
medicines. Tell your doctor if you are
taking any of these medicines. If you are not certain, ask your doctor
or pharmacist.
-
if you are taking riociguat. This drug is used to treat pulmonary
arterial hypertension (i.e., high
blood pressure in the lungs) and chronic th
                                
                                read_full_document
                                
                            

SPC

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Revatio 20 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains 20 mg of sildenafil (as citrate).
Excipient(s) with known effect
Each tablet also contains 0.7 mg of lactose.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet.
White, round, biconvex film-coated tablets marked “PFIZER” on one
side and “RVT 20”on the other.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Adults
Treatment of adult patients with pulmonary arterial hypertension
classified as WHO functional class II
and III, to improve exercise capacity. Efficacy has been shown in
primary pulmonary hypertension
and pulmonary hypertension associated with connective tissue disease.
Paediatric population
Treatment of paediatric patients aged 1 year to 17 years old with
pulmonary arterial hypertension.
Efficacy in terms of improvement of exercise capacity or pulmonary
haemodynamics has been shown
in primary pulmonary hypertension and pulmonary hypertension
associated with congenital heart
disease (see section 5.1).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Treatment should only be initiated and monitored by a physician
experienced in the treatment of
pulmonary arterial hypertension. In case of clinical deterioration in
spite of Revatio treatment,
alternative therapies should be considered.
Posology
_Adults _
The recommended dose is 20 mg three times a day (TID). Physicians
should advise patients who
forget to take Revatio to take a dose as soon as possible and then
continue with the normal dose.
Patients should not take a double dose to compensate for the missed
dose.
_Paediatric population (1 year to 17 years) _
For paediatric patients aged 1 year to 17 years old, the recommended
dose in patients
≤
20 kg is 10 mg
three times a day and for patients > 20 kg is 20 mg three times a day.
Higher than recommended doses
should not be used in paediatric patients with PAH (see also secti
                                
                                read_full_document
                                
                            

documents_in_other_languages

PIL PIL բուլղարերեն 15-01-2024
SPC SPC բուլղարերեն 15-01-2024
PAR PAR բուլղարերեն 21-11-2016
PIL PIL իսպաներեն 15-01-2024
SPC SPC իսպաներեն 15-01-2024
PAR PAR իսպաներեն 21-11-2016
PIL PIL չեխերեն 15-01-2024
SPC SPC չեխերեն 15-01-2024
PAR PAR չեխերեն 21-11-2016
PIL PIL դանիերեն 15-01-2024
SPC SPC դանիերեն 15-01-2024
PAR PAR դանիերեն 21-11-2016
PIL PIL գերմաներեն 15-01-2024
SPC SPC գերմաներեն 15-01-2024
PAR PAR գերմաներեն 21-11-2016
PIL PIL էստոներեն 15-01-2024
SPC SPC էստոներեն 15-01-2024
PAR PAR էստոներեն 21-11-2016
PIL PIL հունարեն 15-01-2024
SPC SPC հունարեն 15-01-2024
PAR PAR հունարեն 21-11-2016
PIL PIL ֆրանսերեն 15-01-2024
SPC SPC ֆրանսերեն 15-01-2024
PAR PAR ֆրանսերեն 21-11-2016
PIL PIL իտալերեն 15-01-2024
SPC SPC իտալերեն 15-01-2024
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SPC SPC լատվիերեն 15-01-2024
PAR PAR լատվիերեն 21-11-2016
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SPC SPC լիտվերեն 15-01-2024
PAR PAR լիտվերեն 21-11-2016
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PAR PAR հունգարերեն 21-11-2016
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SPC SPC հոլանդերեն 15-01-2024
PAR PAR հոլանդերեն 21-11-2016
PIL PIL լեհերեն 15-01-2024
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PIL PIL պորտուգալերեն 15-01-2024
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SPC SPC ռումիներեն 15-01-2024
PAR PAR ռումիներեն 21-11-2016
PIL PIL սլովակերեն 15-01-2024
SPC SPC սլովակերեն 15-01-2024
PAR PAR սլովակերեն 21-11-2016
PIL PIL սլովեներեն 15-01-2024
SPC SPC սլովեներեն 15-01-2024
PAR PAR սլովեներեն 21-11-2016
PIL PIL ֆիններեն 15-01-2024
SPC SPC ֆիններեն 15-01-2024
PAR PAR ֆիններեն 21-11-2016
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