Tadalafil Lilly

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

tadalafil

Available from:

Eli Lilly Nederland B.V.

ATC code:

G04BE08

INN (International Name):

tadalafil

Therapeutic group:

Urologicals

Therapeutic area:

Erectile Dysfunction

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.Treatment of the signs and symptoms of benign prostatic hyperplasia in adult males.

Product summary:

Revision: 6

Authorization status:

Authorised

Authorization date:

2017-03-22

Patient Information leaflet

                                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
                                
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Summary of Product characteristics

                                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.

                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 21-09-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 21-09-2023
Public Assessment Report Public Assessment Report Bulgarian 07-04-2017
Patient Information leaflet Patient Information leaflet Spanish 21-09-2023
Public Assessment Report Public Assessment Report Spanish 07-04-2017
Patient Information leaflet Patient Information leaflet Czech 21-09-2023
Public Assessment Report Public Assessment Report Czech 07-04-2017
Patient Information leaflet Patient Information leaflet Danish 21-09-2023
Public Assessment Report Public Assessment Report Danish 07-04-2017
Patient Information leaflet Patient Information leaflet German 21-09-2023
Public Assessment Report Public Assessment Report German 07-04-2017
Patient Information leaflet Patient Information leaflet Estonian 21-09-2023
Public Assessment Report Public Assessment Report Estonian 07-04-2017
Patient Information leaflet Patient Information leaflet Greek 21-09-2023
Public Assessment Report Public Assessment Report Greek 07-04-2017
Patient Information leaflet Patient Information leaflet French 21-09-2023
Public Assessment Report Public Assessment Report French 07-04-2017
Patient Information leaflet Patient Information leaflet Italian 21-09-2023
Public Assessment Report Public Assessment Report Italian 07-04-2017
Patient Information leaflet Patient Information leaflet Latvian 21-09-2023
Public Assessment Report Public Assessment Report Latvian 07-04-2017
Patient Information leaflet Patient Information leaflet Lithuanian 21-09-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 21-09-2023
Public Assessment Report Public Assessment Report Lithuanian 07-04-2017
Patient Information leaflet Patient Information leaflet Hungarian 21-09-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 21-09-2023
Public Assessment Report Public Assessment Report Hungarian 07-04-2017
Patient Information leaflet Patient Information leaflet Maltese 21-09-2023
Public Assessment Report Public Assessment Report Maltese 07-04-2017
Patient Information leaflet Patient Information leaflet Dutch 21-09-2023
Public Assessment Report Public Assessment Report Dutch 07-04-2017
Patient Information leaflet Patient Information leaflet Polish 21-09-2023
Public Assessment Report Public Assessment Report Polish 07-04-2017
Patient Information leaflet Patient Information leaflet Portuguese 21-09-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 21-09-2023
Public Assessment Report Public Assessment Report Portuguese 07-04-2017
Patient Information leaflet Patient Information leaflet Romanian 21-09-2023
Public Assessment Report Public Assessment Report Romanian 07-04-2017
Patient Information leaflet Patient Information leaflet Slovak 21-09-2023
Public Assessment Report Public Assessment Report Slovak 07-04-2017
Patient Information leaflet Patient Information leaflet Slovenian 21-09-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 21-09-2023
Public Assessment Report Public Assessment Report Slovenian 07-04-2017
Patient Information leaflet Patient Information leaflet Finnish 21-09-2023
Public Assessment Report Public Assessment Report Finnish 07-04-2017
Patient Information leaflet Patient Information leaflet Swedish 21-09-2023
Public Assessment Report Public Assessment Report Swedish 07-04-2017
Patient Information leaflet Patient Information leaflet Norwegian 21-09-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 21-09-2023
Patient Information leaflet Patient Information leaflet Icelandic 21-09-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 21-09-2023
Patient Information leaflet Patient Information leaflet Croatian 21-09-2023
Public Assessment Report Public Assessment Report Croatian 07-04-2017

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