Tadalafil Lilly

Country: Unjoni Ewropea

Lingwa: Ingliż

Sors: EMA (European Medicines Agency)

Ixtrih issa

Ingredjent attiv:

tadalafil

Disponibbli minn:

Eli Lilly Nederland B.V.

Kodiċi ATC:

G04BE08

INN (Isem Internazzjonali):

tadalafil

Grupp terapewtiku:

Urologicals

Żona terapewtika:

Erectile Dysfunction

Indikazzjonijiet terapewtiċi:

Treatment of erectile dysfunction in adult males.In order for tadalafil to be effective, sexual stimulation is required.Tadalafil Lilly is not indicated for use by women.Treatment of the signs and symptoms of benign prostatic hyperplasia in adult males.

Sommarju tal-prodott:

Revision: 6

L-istatus ta 'awtorizzazzjoni:

Authorised

Data ta 'l-awtorizzazzjoni:

2017-03-22

Fuljett ta 'informazzjoni

                                61
B. PACKAGE LEAFLET
62
PACKAGE LEAFLET: INFORMATION FOR THE USER
TADALAFIL LILLY 2.5 MG FILM-COATED TABLETS
tadalafil
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 Tadalafil Lilly is and what it is used for
2.
What you need to know before you take Tadalafil Lilly
3.
How to take Tadalafil Lilly
4.
Possible side effects
5
How to store Tadalafil Lilly
6.
Contents of the pack and other information
1.
WHAT TADALAFIL LILLY IS AND WHAT IT IS USED FOR
Tadalafil Lilly is a treatment for adult men with erectile
dysfunction. This is when a man cannot get,
or keep a hard, erect penis suitable for sexual activity. Tadalafil
Lilly has been shown to significantly
improve the ability of obtaining a hard erect penis suitable for
sexual activity.
Tadalafil Lilly contains the active substance tadalafil which belongs
to a group of medicines called
phosphodiesterase type 5 inhibitors. Following sexual stimulation
Tadalafil Lilly works by helping the
blood vessels in your penis to relax, allowing the flow of blood into
your penis. The result of this is
improved erectile function. Tadalafil Lilly will not help you if you
do not have erectile dysfunction.
It is important to note that Tadalafil Lilly does not work if there is
no sexual stimulation. You and your
partner will need to engage in foreplay, just as you would if you were
not taking a medicine for
erectile dysfunction.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE TADALAFIL LILLY
DO NOT TAKE TADALAFIL LILLY IF YOU:
-
are allergic to tadalafil or any of the othe
                                
                                Aqra d-dokument sħiħ
                                
                            

Karatteristiċi tal-prodott

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Tadalafil Lilly 2.5 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
_ _
Each tablet contains 2.5 mg tadalafil.
Excipient with known effect
Each coated tablet contains 87 mg of lactose (as monohydrate).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet (tablet).
Light orange-yellow and almond shaped tablets of 8.58 mm by 5.23 mm,
marked "C 2 ½" on one side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Treatment of erectile dysfunction in adult males.
In order for tadalafil to be effective, sexual stimulation is
required.
Tadalafil Lilly is not indicated for use by women.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
_Adult men _
In general, the recommended dose is 10 mg taken prior to anticipated
sexual activity and with or
without food.
In those patients in whom tadalafil 10 mg does not produce an adequate
effect, 20 mg might be tried. It
may be taken at least 30 minutes prior to sexual activity.
The maximum dose frequency is once per day.
Tadalafil 10 and 20 mg is intended for use prior to anticipated sexual
activity and it is not
recommended for continuous daily use.
In patients who anticipate a frequent use of Tadalafil Lilly (i.e., at
least twice weekly) a once daily
regimen with the lowest doses of Tadalafil Lilly might be considered
suitable, based on patient choice
and the physician’s judgement.
In these patients the recommended dose is 5 mg taken once a day at
approximately the same time of
day. The dose may be decreased to 2.5 mg once a day based on
individual tolerability.
The appropriateness of continued use of the daily regimen should be
reassessed periodically.
3
_Special populations _
_Elderly men _
Dose adjustments are not required in elderly patients.
_Men with renal impairment _
Dose adjustments are not required in patients with mild to moderate
renal impairment. For patients
with severe renal impairment 10 mg is the maximum recommended dose.

                                
                                Aqra d-dokument sħiħ
                                
                            

Dokumenti f'lingwi oħra

Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Bulgaru 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Bulgaru 21-09-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Spanjol 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Spanjol 21-09-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ċek 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ċek 21-09-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Daniż 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Daniż 21-09-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ġermaniż 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ġermaniż 21-09-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Ġermaniż 07-04-2017
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Estonjan 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Estonjan 21-09-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Estonjan 07-04-2017
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Grieg 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Grieg 21-09-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Franċiż 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Franċiż 21-09-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Franċiż 07-04-2017
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Taljan 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Taljan 21-09-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Latvjan 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Latvjan 21-09-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Litwanjan 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Litwanjan 21-09-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Litwanjan 07-04-2017
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ungeriż 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ungeriż 21-09-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Ungeriż 07-04-2017
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Malti 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Malti 21-09-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Olandiż 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Olandiż 21-09-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Olandiż 07-04-2017
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Pollakk 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Pollakk 21-09-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Portugiż 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Portugiż 21-09-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Portugiż 07-04-2017
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Rumen 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Rumen 21-09-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Slovakk 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Slovakk 21-09-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Sloven 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Sloven 21-09-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Finlandiż 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Finlandiż 21-09-2023
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Finlandiż 07-04-2017
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Svediż 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Svediż 21-09-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Norveġiż 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Norveġiż 21-09-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Iżlandiż 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Iżlandiż 21-09-2023
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Kroat 21-09-2023
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Kroat 21-09-2023

Fittex twissijiet relatati ma 'dan il-prodott

Ara l-istorja tad-dokumenti