Procox

Țară: Uniunea Europeană

Limbă: engleză

Sursă: EMA (European Medicines Agency)

Cumpara asta acum

Prospect Prospect (PIL)
10-02-2021

Ingredient activ:

emodepside, toltrazuril

Disponibil de la:

Vetoquinol S.A.

Codul ATC:

QP52AX60

INN (nume internaţional):

emodepside, toltrazuril

Grupul Terapeutică:

Dogs

Zonă Terapeutică:

Antiparasitic products, insecticides and repellents

Indicații terapeutice:

For dogs, when mixed parasitic infections caused by roundworms and coccidia of the following species are suspected or demonstrated:Roundworms (nematodes)Toxocara canis (mature adult, immature adult, L4);Uncinaria stenocephala (mature adult);Ancylostoma caninum (mature adult).CoccidiaIsospora ohioensis complex;Isospora canis.Procox is effective against the replication of Isospora and also against the shedding of oocysts. Although treatment will reduce the spread of infection, it will not be effective against the clinical signs of infection in already infected animals.

Rezumat produs:

Revision: 15

Statutul autorizaţiei:

Authorised

Data de autorizare:

2011-04-20

Prospect

                                16
B. PACKAGE LEAFLET
17
PACKAGE LEAFLET:
PROCOX 0.9 MG/ML + 18 MG/ML ORAL SUSPENSION FOR DOGS
1.
NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER AND OF
THE MANUFACTURING AUTHORISATION HOLDER RESPONSIBLE FOR BATCH
RELEASE, IF DIFFERENT
Marketing authorisation holder:
Vetoquinol S.A.
Magny-Vernois
70200 Lure
France
Manufacturer responsible for batch release:
KVP Pharma + Veterinär Produkte GmbH
Projensdorfer Str. 324
24106 Kiel
Germany
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Procox 0.9 mg/ml + 18 mg/ml oral suspension for dogs
emodepside / toltrazuril
3.
STATEMENT OF THE ACTIVE SUBSTANCES AND OTHER INGREDIENTS
1 ml contains:
ACTIVE SUBSTANCES:
emodepside
0.9 mg
toltrazuril
18 mg
EXCIPIENTS:
butylhydroxytoluene (E321; as antioxidant)
0.9 mg
sorbic acid (E200; as preservative)
0.7 mg
4.
INDICATIONS
For dogs, when mixed parasitic infections caused by roundworms and
coccidia of the following
species are suspected or demonstrated:
Roundworms (Nematodes):
-
_Toxocara canis_ (mature adult, immature adult, L4)
-
_Uncinaria stenocephala _(mature adult)
-
_Ancylostoma caninum _(mature adult)
_ _
-
_Trichuris vulpis_ (mature adult)
Coccidia:
-
_Isospora ohioensis _complex
18
-
_Isospora canis _
_ _
Treatment will reduce the spread of _Isospora_ infection but will not
be effective against symptoms in
already infected animals.
5.
CONTRAINDICATIONS
Do not use in dogs/puppies which are under 2 weeks of age or weigh
less than 0.4 kg.
Do not use in cases of hypersensitivity to the active substances or to
any of the excipients.
6.
ADVERSE REACTIONS
Slight and transient digestive tract disorders (e.g., vomiting or
loose stools) may occur in very rare
cases.
The frequency of adverse reactions is defined using the following
convention:
- very common (more than 1 in 10 animals treated displaying adverse
reaction(s))
- common (more than 1 but less than 10 animals in 100 animals treated)
- uncommon (more than 1 but less than 10 animals in 1,000 animals
treated)
- rare (more than 1 but less than 10 animals in 10,000 animals
tr
                                
                                Citiți documentul complet
                                
                            

Caracteristicilor produsului

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Procox 0.9 mg/ml + 18 mg/ml oral suspension for dogs
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
1 ml contains:
ACTIVE SUBSTANCES:
emodepside
0.9 mg
toltrazuril
18 mg
EXCIPIENTS:
butylhydroxytoluene (E321; as antioxidant)
0.9 mg
sorbic acid (E200; as preservative)
0.7 mg
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Oral suspension.
White to yellowish suspension.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Dogs.
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For dogs, when mixed parasitic infections caused by roundworms and
coccidia of the following
species are suspected or demonstrated:
Roundworms (Nematodes):
-
_Toxocara canis_ (mature adult, immature adult, L4)
-
_Uncinaria stenocephala _(mature adult)
-
_Ancylostoma caninum _(mature adult)
-
_Trichuris vulpis_ (mature adult)
Coccidia:
-
_Isospora ohioensis _complex
-
_Isospora canis _
Procox is effective against the replication of _Isospora_ and also
against the shedding of oocysts.
Although treatment will reduce the spread of infection, it will not be
effective against the clinical
signs of infection in already infected animals.
4.3
CONTRAINDICATIONS
Do not use in dogs/puppies which are under 2 weeks of age or weigh
less than 0.4 kg.
3
Do not use in cases of hypersensitivity to the active substances or to
any of the excipients.
4.4
SPECIAL WARNINGS
Procox is effective against the replication of coccidia and against
the shedding of oocysts. Replication
of the parasite damages the dog’s intestinal mucosa, which may cause
enteritis. Therefore, treatment
with Procox does not resolve clinical symptoms arising from mucosal
damage (e.g. diarrhoea) that
have arisen before treatment. In such cases supportive treatment may
be necessary.
Treatment against _Isospora _should aim to minimize the shedding of
oocysts into the environment,
thereby reducing the risk for reinfection in groups/kennels with known
and recurring _Isospora_
infections.
A pr
                                
                                Citiți documentul complet
                                
                            

Documente în alte limbi

Prospect Prospect bulgară 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului bulgară 10-02-2021
Raport public de evaluare Raport public de evaluare bulgară 13-06-2013
Prospect Prospect spaniolă 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului spaniolă 10-02-2021
Raport public de evaluare Raport public de evaluare spaniolă 13-06-2013
Prospect Prospect cehă 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului cehă 10-02-2021
Raport public de evaluare Raport public de evaluare cehă 13-06-2013
Prospect Prospect daneză 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului daneză 10-02-2021
Raport public de evaluare Raport public de evaluare daneză 13-06-2013
Prospect Prospect germană 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului germană 10-02-2021
Raport public de evaluare Raport public de evaluare germană 13-06-2013
Prospect Prospect estoniană 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului estoniană 10-02-2021
Raport public de evaluare Raport public de evaluare estoniană 13-06-2013
Prospect Prospect greacă 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului greacă 10-02-2021
Raport public de evaluare Raport public de evaluare greacă 13-06-2013
Prospect Prospect franceză 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului franceză 10-02-2021
Raport public de evaluare Raport public de evaluare franceză 13-06-2013
Prospect Prospect italiană 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului italiană 10-02-2021
Raport public de evaluare Raport public de evaluare italiană 13-06-2013
Prospect Prospect letonă 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului letonă 10-02-2021
Raport public de evaluare Raport public de evaluare letonă 13-06-2013
Prospect Prospect lituaniană 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului lituaniană 10-02-2021
Raport public de evaluare Raport public de evaluare lituaniană 13-06-2013
Prospect Prospect maghiară 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului maghiară 10-02-2021
Raport public de evaluare Raport public de evaluare maghiară 13-06-2013
Prospect Prospect malteză 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului malteză 10-02-2021
Raport public de evaluare Raport public de evaluare malteză 13-06-2013
Prospect Prospect olandeză 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului olandeză 10-02-2021
Raport public de evaluare Raport public de evaluare olandeză 13-06-2013
Prospect Prospect poloneză 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului poloneză 10-02-2021
Raport public de evaluare Raport public de evaluare poloneză 13-06-2013
Prospect Prospect portugheză 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului portugheză 10-02-2021
Raport public de evaluare Raport public de evaluare portugheză 13-06-2013
Prospect Prospect română 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului română 10-02-2021
Raport public de evaluare Raport public de evaluare română 13-06-2013
Prospect Prospect slovacă 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului slovacă 10-02-2021
Raport public de evaluare Raport public de evaluare slovacă 13-06-2013
Prospect Prospect slovenă 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului slovenă 10-02-2021
Raport public de evaluare Raport public de evaluare slovenă 13-06-2013
Prospect Prospect finlandeză 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului finlandeză 10-02-2021
Raport public de evaluare Raport public de evaluare finlandeză 13-06-2013
Prospect Prospect suedeză 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului suedeză 10-02-2021
Raport public de evaluare Raport public de evaluare suedeză 13-06-2013
Prospect Prospect norvegiană 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului norvegiană 10-02-2021
Prospect Prospect islandeză 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului islandeză 10-02-2021
Prospect Prospect croată 10-02-2021
Caracteristicilor produsului Caracteristicilor produsului croată 10-02-2021

Căutați alerte legate de acest produs

Vizualizați istoricul documentelor