Open menu Close menu Open Search Close search

AMERICAN DRUGS | ANATOMY | HEALTH TOPICS | HIV/AIDS GLOSSARY | DISEASES | HEALTH ARTICLES | GENOME | OCCUPATIONS

Ypozane


Spanish Simplified Chinese French German Russian Hindi Arabic Portuguese
















Summary for the public


What is Ypozane?

Ypozane are round, white tablets that contain osaterone acetate as the active substance. The medicine is available as 1.875 mg, 3.75 mg, 7.5 mg or 15 mg tablets, which can be used for dogs of different weights (small, medium sized, large or very large dogs).


What is Ypozane used for?

Ypozane is used in male dogs for the treatment of “benign prostatic hypertrophy”, which means an increase of the size of the prostate gland that is not related to cancer (benign). The prostate is a gland that produces a fluid that is part of the semen. When it is enlarged, it can lead to abdominal pain, constipation and difficulties in urinating in the dogs affected.

Ypozane is given daily for 7 days. Its effect can be seen within about 2 weeks, and lasts for 5 months.


How does Ypozane work?

Osaterone acetate is a hormone that is chemically related to progesterone, and as such it has anti-androgen and progestagen activity. In male dogs, it blocks the transport of the male hormone testosterone into the prostate. By inhibiting testosterone, Ypozane helps the prostate to shrink back to its normal size.


How has Ypozane been studied?

Data were provided on the pharmaceutical quality of the product, the tolerance of Ypozane in dogs and the safety of the tablets when handled by humans.

The effectiveness of osaterone acetate was investigated in a large study undertaken in a number of veterinary practices across Europe. Dogs with enlarged prostates from various breeds, age groups and weights, were either treated with Ypozane or with another product, which is already authorised in the EU for this indication. The dogs received once a day for 7 days, one Ypozane tablet appropriate for their size to correspond to a daily dose of 0.25 – 0.5 mg osaterone acetate per kilogram bodyweight.


What benefit has Ypozane shown during the studies?

Treatment with Ypozane was effective in the treatment of benign prostatic hypertrophy. A clinical response to treatment (reduction of prostate volume) was seen within 14 days, which lasted for at least 5 months. After this time, the dog should be re-examined by a veterinarian and treatment might be repeated. Ypozane has no adverse effects on semen quality.


What is the risk associated with Ypozane?

Ypozane should be used with caution in dogs which have had liver problems.

The most common side effects are a transient increase in appetite, and changes in the behaviour of the dog (changes in activity levels, more sociable behaviour). Some dogs might also show vomiting, diarrhoea or increased thirst, or might develop a “feminisation syndrome”. This is when male dogs suddenly become attractive to other male dogs or the size of their mammary glands increases. All these effects disappear after a while without specific treatment.


What are the precautions for the person who gives the medicine or comes into contact with the animal?

This veterinary medicine has been developed especially for dogs and is not for use in humans. If a person accidentally takes the medicine, seek medical advice immediately and show the package leaflet or the label to a doctor. Wash hands after administration.

In female laboratory animals, osaterone acetate caused serious adverse effects on reproductive functions. Therefore, women of child-bearing age should avoid contact with, or wear disposable gloves, when handling the tablets.


Why has Ypozane been approved?

The Committee for Medicinal Products for Veterinary Use (CVMP) concluded that the benefits of Ypozane exceed its risks for the treatment of benign prostatic hypertrophy (BPH) in male dogs and recommended that Ypozane be given a marketing authorisation. The benefitrisk balance may be found in module 6 of this EPAR.


Other information about Ypozane

The European Commission granted a marketing authorisation valid throughout the European Union, for Ypozane to Virbac S.A. on 11.01.2007. Information on the prescription status of this product may be found on the label/outer package.

Authorisation details
Name: Ypozane
EMEA Product number: EMEA/V/C/000112
Active substance: osaterone acetate
INN or common name: osaterone acetate
Species: Dogs
ATCvet Code: QG04CX90
Marketing Authorisation Holder: Virbac S.A.
Revision: 0
Date of issue of Market Authorisation valid throughout the European Union: 11/01/2007
Contact address:
Virbac S.A.
1ère Avenue 2065 M
06516 Carros
France




Product Characteristics

ANNEX I

SUMMARY OF PRODUCT CHARACTERISTICS


1.
NAME OF VETERINARY THE MEDICINAL PRODUCT
YPOZANE 1.875 mg tablets for dogs
YPOZANE 3.75 mg tablets for dogs
YPOZANE 7.5 mg tablets for dogs
YPOZANE 15 mg tablets for dogs
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Active substance:
Each tablet contains 1.875 mg, 3.75 mg, 7.5 mg or 15 mg osaterone acetate
Excipients:
For a full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Tablet
Round, white, biconvex tablet of 5.5 mm, 7 mm, 9 mm and 12 mm.
4.
CLINICAL PARTICULARS
4.1
Target species
Dogs (male)
4.2
Indications for use, specifying the target species
Treatment of benign prostatic hypertrophy (BPH) in male dogs.
4.3
Contraindications
None.
4.4
Special warnings
In dogs with BPH associated with prostatitis, the product can be administered concurrently with
antimicrobials.
4.5
Special precautions for use
Special precautions for use in animals
A transient reduction of plasma cortisol concentration may occur; this may continue for several weeks
after administration. Appropriate monitoring should be implemented in dogs under stress (e.g. post-
operative) or those with hypoadrenocorticism. The response to an ACTH stimulation test may also be
suppressed for several weeks after administration of osaterone.
Use with caution in dogs with a history of liver disease, as safety of use of the product in these dogs
has not been thoroughly investigated, and as treatment of some dogs with liver disease has resulted in
reversible elevation of ALT and ALP in clinical trials.
2/26
Special precautions to be taken by the person administering the veterinary medicinal product to
animals
Wash hands after administration.
In the case of accidental ingestion by a person, seek medical advice immediately and show the
package leaflet or the label to the physician.
A single oral dose of 40 mg osaterone acetate in human males was followed by a sporadic decrease in
FSH, LH and testosterone, reversible after 16 days. There was no clinical effect.
In female laboratory animals, osaterone acetate caused serious adverse effects on reproductive
functions. Therefore, women of child-bearing age should avoid contact with, or wear disposable
gloves, when administering the product.
4.6 Adverse reactions (frequency and seriousness)
A transient increase in appetite occurs very commonly.
Transient behavioural changes such as increased or decreased activity, or more sociable behaviour, are
common.
Other adverse reactions, including transient vomiting and/or diarrhoea, polyuria/polydipsia, lethargy
or feminisation syndrome including mammary gland hyperplasia occur uncommonly.
A transient reduction in plasma cortisol occurs in most treated animals.
In clinical trials, treatment with the veterinary medicinal product was not discontinued and all dogs
recovered without any specific therapy.
4.7 Use during pregnancy, lactation or lay
Not applicable.
4.8 Interaction with other medicinal products and other forms of interaction
None known.
4.9
Amounts to be administered and administration route
For oral use.
Administer 0.25 – 0.5 mg osaterone acetate per kilogram bodyweight, once a day, for 7 days as
follows:
Dog’s weight
YPOZANE tablets to be
administered
Number of tablets per
day
Treatment duration
3 to 7.5 kg*
1.875 mg tablet
7.5 to 15 kg
3.75 mg tablet
1 tablet
7 days
15 to 30 kg
7.5 mg tablet
30 to 60 kg
15 mg tablet
*No data are available for dogs less than 3 kg bodyweight
3/26
 
Tablets can be given either directly into the mouth or with food. The maximum dose should not be
exceeded.
The onset of clinical response to treatment is usually seen within 2 weeks. The clinical response
persists for at least 5 months after treatment.
Re-evaluation by the veterinarian should take place 5 months after treatment or earlier if clinical signs
recur. A decision to retreat at this or at a later time point should be based on veterinary examination
taking into account the risk benefit profile of the product. If clinical response to treatment is
considerably shorter than expected, a re-evaluation of the diagnosis is necessary.
4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary
An overdose study (up to 1.25 mg/kg bodyweight for 10 days, repeated one month later) did not show
undesirable effects except for a decrease of cortisol plasma concentration.
4.11 Withdrawalperiod(s)
Not applicable.
5.
PHARMACOLOGICAL PROPERTIES
Pharmacotherapeutic group: drugs used in benign prostatic hypertrophy.
ATC vet code : QG04C X
Osaterone is a steroid anti-androgen, which inhibits the effects of an excess production of male
hormone (testosterone).
5.1
Pharmacodynamic properties
-hydroxylated -
osaterone acetate) has anti-androgenic activity. Osaterone acetate inhibits the effects of an excess of
male hormone (testosterone) through various mechanisms. It competitively prevents the binding of
androgens to their prostatic receptors and blocks the transport of testosterone into the prostate.
β
No adverse effects on semen quality have been observed.
5.2
Pharmacokinetic particulars
After oral administration with food in dogs, osaterone acetate is rapidly absorbed (T max about 2 hours)
and undergoes a first-pass effect mainly in the liver. After a dose of 0.25 mg/kg/day, the mean
maximum concentration (C max ) in plasma is about 60 µg/l.
-hydroxylated metabolite, which is also
pharmacologically active. Osaterone acetate and its metabolite are bound to plasma proteins (around
90% and 80% respectively), mainly to albumin. This binding is reversible and not affected by other
substances known to specifically bind to albumin.
β
Osaterone is eliminated within 14 days, mainly in faeces via biliary excretion (60%) and to a lesser
extent (25%) in urine. Elimination is slow with a mean half-life (T½) of about 80 hours. After repeated
administration of osaterone acetate at 0.25 mg/kg/day for 7 days, the factor of accumulation is about 3-
4 without change in the rates of absorption or elimination. Fifteen days after the last administration,
the mean plasma concentration is about 6.5 µg/l.
4/26
Osaterone acetate is a steroid chemically related to progesterone, and as such it has potent progestagen
and potent anti-androgen activity. Also, the major metabolite of osaterone acetate (15
Osaterone acetate is converted to its main, 15
6.
PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Lactose monohydrate
Pregelatinised starch
Carmellose calcium
Maize starch
Talc
Magnesium stearate
6.2 Incompatibilities
Not applicable.
6.3 Shelf life
Shelf-life of the veterinary medicinal product as packaged for sale: 3 years.
6.4. Special precautions for storage
This veterinary medicinal product does not require any special storage conditions.
6.5 Nature and composition of immediate packaging
Carton box containing one aluminium/aluminium blister with 7 tablets.
6.6 Special precautions for the disposal of unused veterinary medicinal product or waste
materials derived from the use of such products
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal
products should be disposed of in accordance with local requirements.
7.
MARKETING AUTHORISATION HOLDER
VIRBAC S.A.
1 ère avenue – 2065 m – LID
06516 Carros
France
8. MARKETING AUTHORISATION NUMBER(S)
EU/2/06/068/001-004
9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
11.01.2007
5/26
10
DATE OF REVISION OF THE TEXT
11.01.2007
Detailed information on this veterinary medicinal product is available on the website of the European
Medicines Agency (EMEA) http://www.emea.europa.eu /
PROHIBITION OF SALE, SUPPLY AND/OR USE
Not applicable.
6/26
ANNEX II
A. MANUFACTURING AUTHORISATION HOLDER(S) RESPONSIBLE FOR
BATCH RELEASE
B. CONDITIONS OR RESTRICTIONS OF THE MARKETING AUTHORISATION
REGARDING SUPPLY OR USE
C. CONDITIONS OR RESTRICTIONS OF THE MARKETING AUTHORISATION
WITH REGARD TO SAFE AND EFFECTIVE USE
D. STATEMENT OF THE MRLs
7/26
A.
MANUFACTURING AUTHORISATION HOLDER(S) RESPONSIBLE FOR BATCH
RELEASE
Name and address of the manufacturer responsible for batch release
Virbac S.A.
1 ère avenue – 2065 m – LID
06516 Carros
France
B. CONDITIONS OR RESTRICTIONS OF THE MARKETING AUTHORISATION
REGARDING SUPPLY OR USE
To be supplied only on veterinary prescription
The holder of this marketing authorisation must inform the European Commission about the marketing
plans for the medicinal product authorised by this decision.
C. CONDITIONS OR RESTRICTIONS OF THE MARKETING AUTHORISATION WITH
REGARD TO SAFE AND EFFECTIVE USE
Not applicable
D. STATEMENT OF THE MRLs
Not applicable
8/26
ANNEX III
LABELLING AND PACKAGE LEAFLET
9/26
PARTICULARS TO APPEAR ON THE OUTER PACKAGE
BOX - 1.875 mg
1.
NAME OF VETERINARY THE MEDICINAL PRODUCT
Ypozane 1.875 mg tablets for dogs
Osaterone acetate
2.
STATEMENT OF ACTIVE AND OTHER SUBSTANCES
Each tablet contains 1.875 mg osaterone acetate.
3.
PHARMACEUTICAL FORM
Tablet.
4.
PACKAGE SIZE
7 tablets.
5.
TARGET SPECIES
Dogs.
6.
INDICATION(S)
Treatment of benign prostatic hypertrophy in male dogs.
7.
METHOD AND ROUTE(S) OF ADMINISTRATION
Oral use.
Read the package leaflet before use.
8.
WITHDRAWAL PERIOD
Not applicable
9.
SPECIAL WARNING(S), IF NECESSARY
Read the package leaflet before use.
10/26
 
10. EXPIRY DATE
EXP {month/year}
11. SPECIAL STORAGE CONDITIONS
Not applicable
12. SPECIAL PRECAUTIONS FOR THE DISPOSAL OF UNUSED PRODUCTS OR
WASTE MATERIALS, IF ANY
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal
products should be disposed of in accordance with local requirements.
13. THE WORDS “FOR ANIMAL TREATMENT ONLY” AND CONDITIONS OR
RESTRICTIONS REGARDING SUPPLY AND USE, if applicable
For animal treatment only - to be supplied only on veterinary prescription.
14. THE WORDS “KEEP OUT OF THE REACH AND SIGHT OF CHILDREN”
Keep out of the reach and sight of children.
15. NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER
Virbac S.A.
1 ère avenue – 2065 m – LID
06516 Carros
France
16. MARKETING AUTHORISATION NUMBER(S)
EU/2/06/068/001
17. MANUFACTURER’S BATCH NUMBER
Batch {number}
11/26
 
MINIMUM PARTICULARS TO APPEAR ON BLISTERS
BLISTER - 1.875 mg
1.
NAME OF VETERINARY THE MEDICINAL PRODUCT
Ypozane 1.875 mg tablets for dogs
Osaterone acetate
2.
NAME OF THE MARKETING AUTHORISATION HOLDER
VIRBAC S.A.
3.
EXPIRY DATE
EXP {month/year}
4.
BATCH NUMBER
Batch {number}
5.
THE WORDS “FOR ANIMAL TREATMENT ONLY”
For animal treatment only.
12/26
 
PARTICULARS TO APPEAR ON THE OUTER PACKAGE
BOX - 3.75 mg
1.
NAME OF VETERINARY THE MEDICINAL PRODUCT
Ypozane 3.75 mg tablets for dogs
Osaterone acetate
2.
STATEMENT OF ACTIVE AND OTHER SUBSTANCES
Each tablet contains 3.75 mg osaterone acetate
3.
PHARMACEUTICAL FORM
Tablet.
4.
PACKAGE SIZE
7 tablets.
5.
TARGET SPECIES
Dogs.
6.
INDICATION(S)
Treatment of benign prostatic hypertrophy in male dogs.
7.
METHOD AND ROUTE(S) OF ADMINISTRATION
Oral use.
Read the package leaflet before use.
8.
WITHDRAWAL PERIOD
Not applicable
9.
SPECIAL WARNING(S), IF NECESSARY
Read the package leaflet before use.
13/26
 
10. EXPIRY DATE
EXP {month/year}
11. SPECIAL STORAGE CONDITIONS
Not applicable
12. SPECIAL PRECAUTIONS FOR THE DISPOSAL OF UNUSED PRODUCTS OR
WASTE MATERIALS, IF ANY
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal
products should be disposed of in accordance with local requirements.
13. THE WORDS “FOR ANIMAL TREATMENT ONLY” AND CONDITIONS OR
RESTRICTIONS REGARDING SUPPLY AND USE, if applicable
For animal treatment only - to be supplied only on veterinary prescription.
14. THE WORDS “KEEP OUT OF THE REACH AND SIGHT OF CHILDREN”
Keep out of the reach and sight of children.
15. NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER
Virbac S.A.
1 ère avenue – 2065 m – LID
06516 Carros
France
16. MARKETING AUTHORISATION NUMBER(S)
EU/2/06/068/002
17. MANUFACTURER’S BATCH NUMBER
Batch {number}
14/26
 
MINIMUM PARTICULARS TO APPEAR ON BLISTERS
BLISTER - 3.75 mg
1.
NAME OF VETERINARY THE MEDICINAL PRODUCT
Ypozane 3.75 mg tablets for dogs
Osaterone acetate
2.
NAME OF THE MARKETING AUTHORISATION HOLDER
VIRBAC S.A.
3.
EXPIRY DATE
EXP {month/year}
4.
BATCH NUMBER
Batch {number}
5.
THE WORDS “FOR ANIMAL TREATMENT ONLY”
For animal treatment only.
15/26
 
PARTICULARS TO APPEAR ON THE OUTER PACKAGE
BOX - 7.5 mg
1.
NAME OF VETERINARY THE MEDICINAL PRODUCT
Ypozane 7.5 mg tablets for dogs
Osaterone acetate
2.
STATEMENT OF ACTIVE AND OTHER SUBSTANCES
Each tablet contains 7.5 mg osaterone acetate
3.
PHARMACEUTICAL FORM
Tablet.
4.
PACKAGE SIZE
7 tablets.
5.
TARGET SPECIES
Dogs.
6.
INDICATION(S)
Treatment of benign prostatic hypertrophy in male dogs.
7.
METHOD AND ROUTE(S) OF ADMINISTRATION
Oral use.
Read the package leaflet before use.
8.
WITHDRAWAL PERIOD
Not applicable
9.
SPECIAL WARNING(S), IF NECESSARY
Read the package leaflet before use.
16/26
 
10. EXPIRY DATE
EXP {month/year}
11. SPECIAL STORAGE CONDITIONS
Not applicable
12. SPECIAL PRECAUTIONS FOR THE DISPOSAL OF UNUSED PRODUCTS OR
WASTE MATERIALS, IF ANY
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal
products should be disposed of in accordance with local requirements.
13. THE WORDS “FOR ANIMAL TREATMENT ONLY” AND CONDITIONS OR
RESTRICTIONS REGARDING SUPPLY AND USE, if applicable
For animal treatment only - to be supplied only on veterinary prescription.
14. THE WORDS “KEEP OUT OF THE REACH AND SIGHT OF CHILDREN”
Keep out of the reach and sight of children.
15. NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER
Virbac S.A.
1 ère avenue – 2065 m – LID
06516 Carros
France
16. MARKETING AUTHORISATION NUMBER(S)
EU/2/06/068/003
17. MANUFACTURER’S BATCH NUMBER
Batch {number}
17/26
 
MINIMUM PARTICULARS TO APPEAR ON BLISTERS
BLISTER - 7.5 mg
1.
NAME OF VETERINARY THE MEDICINAL PRODUCT
Ypozane 7.5 mg tablets for dogs
Osaterone acetate
2.
NAME OF THE MARKETING AUTHORISATION HOLDER
VIRBAC S.A.
3.
EXPIRY DATE
EXP {month/year}
4.
BATCH NUMBER
Batch {number}
5.
THE WORDS “FOR ANIMAL TREATMENT ONLY”
For animal treatment only.
18/26
 
PARTICULARS TO APPEAR ON THE OUTER PACKAGE
BOX - 15 mg
1.
NAME OF VETERINARY THE MEDICINAL PRODUCT
Ypozane 15 mg tablets for dogs
Osaterone acetate
2.
STATEMENT OF ACTIVE AND OTHER SUBSTANCES
Each tablet contains 15 mg osaterone acetate
3.
PHARMACEUTICAL FORM
Tablet.
4.
PACKAGE SIZE
7 tablets.
5.
TARGET SPECIES
Dogs.
6.
INDICATION(S)
Treatment of benign prostatic hypertrophy in male dogs.
7.
METHOD AND ROUTE(S) OF ADMINISTRATION
Oral use.
Read the package leaflet before use.
8.
WITHDRAWAL PERIOD
Not applicable
9.
SPECIAL WARNING(S), IF NECESSARY
Read the package leaflet before use.
19/26
 
10. EXPIRY DATE
EXP {month/year}
11. SPECIAL STORAGE CONDITIONS
Not applicable
12. SPECIAL PRECAUTIONS FOR THE DISPOSAL OF UNUSED PRODUCTS OR
WASTE MATERIALS, IF ANY
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal
products should be disposed of in accordance with local requirements.
13. THE WORDS “FOR ANIMAL TREATMENT ONLY” AND CONDITIONS OR
RESTRICTIONS REGARDING SUPPLY AND USE, if applicable
For animal treatment only - to be supplied only on veterinary prescription.
14. THE WORDS “KEEP OUT OF THE REACH AND SIGHT OF CHILDREN”
Keep out of the reach and sight of children.
15. NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER
Virbac S.A.
1 ère avenue – 2065 m – LID
06516 Carros
France
16. MARKETING AUTHORISATION NUMBER(S)
EU/2/06/068/004
17. MANUFACTURER’S BATCH NUMBER
Batch {number}
20/26
 
MINIMUM PARTICULARS TO APPEAR ON BLISTERS
BLISTER - 15 mg
1.
NAME OF VETERINARY THE MEDICINAL PRODUCT
Ypozane 15 mg tablets for dogs
Osaterone acetate
2.
NAME OF THE MARKETING AUTHORISATION HOLDER
VIRBAC S.A.
3.
EXPIRY DATE
EXP {month/year}
4.
BATCH NUMBER
Batch {number}
5.
THE WORDS “FOR ANIMAL TREATMENT ONLY”
For animal treatment only.
21/26
 
B. PACKAGE LEAFLET
22/26
PACKAGE LEAFLET
YPOZANE
1.
NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER AND OF
THE MANUFACTURING AUTHORISATION HOLDER RESPONSIBLE FOR BATCH
RELEASE
Marketing authorisation holder and manufacturer:
VIRBAC S.A. –
1ère avenue
2065 m – LID–
06516 Carros –
France
2.
NAME OF VETERINARY THE MEDICINAL PRODUCT
YPOZANE 1.875 mg tablets for dogs
YPOZANE 3.75 mg tablets for dogs
YPOZANE 7.5 mg tablets for dogs
YPOZANE 15 mg tablets for dogs
Osaterone acetate
3.
STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENT(S)
Each tablet contains 1.875 mg, 3.75 mg, 7.5 mg or 15 mg osaterone acetate
4.
INDICATION(S)
Treatment of benign prostatic hypertrophy in male dogs.
5.
CONTRAINDICATIONS
None.
6.
ADVERSE REACTIONS
The most commonly reported adverse reaction is a mild and transient increased appetite. Behavioural
changes such as modification of dog’s activity or more social behaviour are common. Other adverse
reactions such as transient vomiting and/or diarrhoea, increased thirst, lethargy or enlarged mammary
glands occur less commonly. All these adverse reactions are reversible without any specific treatment.
If you notice any serious effects or other effects not mentioned in this leaflet, please inform your
veterinary surgeon.
7.
TARGET SPECIES
Dogs (male)
23/26
8.
DOSAGE FOR EACH SPECIES, ROUTE(S) AND METHOD OF ADMINISTRATION
For oral use.
Administer 0.25 – 0.5 mg osaterone acetate per kilogram bodyweight, once a day, for 7 days as
follows:
Dog’s weight
YPOZANE tablets to be
administered
Number of tablet per
day
Treatment duration
3 to 7.5 kg
1.875 mg tablet
7.5 to 15 kg
3.75 mg tablet
1 tablet
7 days
15 to 30 kg
7.5 mg tablet
30 – 60 kg
15 mg tablet
9.
ADVICE ON CORRECT ADMINISTRATION
Tablets can be given either directly into the mouth or with food. The onset of clinical response to
treatment is usually seen within 2 weeks and persists for at least 5 months after treatment.
Re-evaluation by the veterinarian should take place 5 months after treatment, or earlier if clinical signs
recur. A decision to retreat at this or at a later time point should be based on veterinary examination
taking into account the risk benefit profile of the medicine.
If clinical response to treatment is considerably shorter than expected, a re-evaluation of the diagnosis
is necessary.
The maximum dose should not be exceeded.
10. WITHDRAWAL PERIOD
Not applicable.
11. SPECIAL STORAGE PRECAUTIONS
Keep out of the reach and sight of children.
This veterinary medicinal product does not require any special storage conditions.
Do not use after the expiry date stated on the blister after “EXP”
12. SPECIAL WARNING(S)
Use with caution in dogs with a history of liver disease.
Wash hands after administration.
In the case of accidental ingestion by a person, seek medical advice immediately and show the
package leaflet or the label to the physician.
A single oral dose of 40 mg osaterone acetate in human males was followed by a sporadic decrease of
sexual hormones, reversible after 16 days. There was no clinical effect.
24/26
 
In female laboratory animals, osaterone acetate caused serious adverse effects on reproductive
functions. Therefore, women of child bearing age should avoid contact with, or wear disposable
gloves, when administering the product.
13. SPECIAL PRECAUTIONS FOR THE DISPOSAL OF UNUSED PRODUCT OR WASTE
MATERIALS, IF ANY
Ask your veterinary surgeon how to dispose of medicines no longer required. These measures should help
to protect the environment.
14. DATE ON WHICH THE PACKAGE LEAFLET WAS LAST APPROVED :
11.01.2007
Detailed information on this product is available on the website of the European Medicines Agency
(EMEA) http://www.emea.europa.eu/ .
15. OTHER INFORMATION
Benign prostatic hypertrophy (BPH) is a natural consequence of ageing. Over 80% of male dogs above
5 years of age are affected. BPH is a development and enlargement of the prostate due to the male
hormone testosterone. This might lead to multiple non-specific clinical signs such as abdominal pain,
difficulties in defaecation and urination, blood in urine and locomotive disorders.
België/Belgique/Belgien
VIRBAC BELGIUM S.A.
Rue de la station 17
B-1300 WAVRE
Tel: 32 (0) 10 47 06 35
Luxembourg/Luxemburg
VIRBAC BELGIUM S.A.
Rue de la station 17
B-1300 WAVRE
Tel: 32 (0) 10 47 06 35
Česká republika
VIRBAC S.A.
1 ère avenue 2065 m – L.I.D
F-06516 Carros
Tel: 33 (0) 4 92 08 73 00
Magyarország
VIRBAC S.A.
1 ère avenue 2065 m – L.I.D
F-06516 Carros
Tel: 33 (0) 4 92 08 73 00
Danmark
VIRBAC S.A.
1 ère avenue 2065 m – L.I.D
F-06516 Carros
Tel: 33 (0) 4 92 08 73 00
Malta
VIRBAC S.A.
1 ère avenue 2065 m – L.I.D
F-06516 Carros
Tel: 33 (0) 4 92 08 73 00
Eesti
OÜ ZOOVETVARU
Pärnasalu 31
ET - 76505 Saue/Harjumaa, ESTONIA
Tel: + 372 6 709 006
Nederland
VIRBAC NEDERLAND BV
Postbus 313
NL-3771 AH-Barneveld
Tel: 31 (0) 342 427 127
25/26
Deutschland
VIRBAC Tierarzneimittel GmbH
West Rögen 20
D-23843 Bad Oldesloe
Tel: 49 (4531) 805 555
Norge
VIRBAC S.A.
1 ère avenue 2065 m – L.I.D
F-06516 Carros
Tel: 33 (0) 4 92 08 73 00
Ελλάδα
VIRBAC HELLAS A.E.
23 rd Klm National Road Athens-Lamia
145 65 Agios Stefanos
Athens
GREECE
Österreich
VIRBAC Österreich GmbH
Hildebrandgasse 27
A-1180 Wien
Tel: 43 (0) 1 21 834 260
España
VIRBAC ESPAÑA, S.A.
C/Angel Guimera 179-181-
E-08950 - Esplugues de Llobregat (Barcelona)
Tel: + + 34 93 470 79 40
Polska
VIRBAC S.A.
1 ère avenue 2065 m – L.I.D
F-06516 Carros
Tel: 33 (0) 4 92 08 73 00
France
VIRBAC S.A.
1 ère avenue 2065 m – L.I.D
F-06516 Carros
Tel: 33 (0) 4 92 08 73 00
Portugal
VIRBAC DE Portugal
LABORATÓRIOS LDA
P-2080 Almeirim
Tel: (351) 243 570 500
Ireland
C&M Veterinary Distributors Limited
IE-Limerick
Tel: 353 61 314 933
Slovenija
VIRBAC S.A.
1 ère avenue 2065 m – L.I.D
F-06516 Carros
Tel: 33 (0) 4 92 08 73 00
Ísland
VIRBAC S.A.
1 ère avenue 2065 m – L.I.D
F-06516 Carros
Tel: 33 (0) 4 92 08 73 00
Slovenská republika
VIRBAC S.A.
1 ère avenue 2065 m – L.I.D
F-06516 Carros
Tel: 33 (0) 4 92 08 73 00
Italia
VIRBAC SRL
Via dei Gracchi 30
I-20146 Milano
Tel: 39 02 48 53 541
Suomi/Finland
VIRBAC S.A.
1 ère avenue 2065 m – L.I.D
F-06516 Carros
Tel: 33 (0) 4 92 08 73 00
Κύπρος
GEO. PAVLIDES & ARAOUZOS LTD
25-27 Dimostheni Severi, 1080
CY-1080 Nicosia - CYPRUS
Τηλ: + 357 22456117
Sverige
VIRBAC S.A.
1 ère avenue 2065 m – L.I.D
F-06516 Carros
Tel: 33 (0) 4 92 08 73 00
Latvija
OÜ ZOOVETVARU
Pärnasalu 31
ET - 76505 Saue/Harjumaa, ESTONIA
Tel: + 372 6 709 006
United Kingdom
VIRBAC Ltd
UK-Suffolk IP30 9 UP
Tel: 44 (0) 1359 243243
Lietuva
OÜ ZOOVETVARU
Pärnasalu 31
ET - 76505 Saue/Harjumaa, ESTONIA
Tel: + 372 6 709 006
Република България
VIRBAC S.A.
1 ère avenue 2065 m – L.I.D
F-06516 Carros
Tel: 33 (0) 4 92 08 73 00
România
VIRBAC S.A.
1 ère avenue 2065 m – L.I.D
F-06516 Carros
Tel: 33 (0) 4 92 08 73 00
26/26


Source: European Medicines Agency



- Please bookmark this page (add it to your favorites).
- If you wish to link to this page, you can do so by referring to the URL address below this line.



https://theodora.com/drugs/eu/ypozane_veterinary.html

Copyright © 1995-2021 ITA all rights reserved.