Certifect

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

fipronil, amitraz, (S)-methoprene

Available from:

Merial

ATC code:

QP53AX65

INN (International Name):

fipronil / amitraz / (S)-methoprene

Therapeutic group:

Dogs

Therapeutic area:

Ectoparasiticides for topical use, incl. insecticides

Therapeutic indications:

Treatment and prevention of infestations in dogs by ticks (Ixodes ricinus, Dermacentor reticulatus, Rhipicephalus sanguineus, Ixodes scapularis, Dermacentor variabilis, Haemaphysalis elliptica, Haemaphysalis longicornis, Amblyomma americanum and Amblyomma maculatum) and fleas (Ctenocephalides felis and Ctenocephalides canis). Treatment of infestations by chewing lice (Trichodectes canis). Prevention of environmental flea contamination by inhibiting the development of all flea immature stages. The product can be used as part of a treatment strategy for the control of flea-allergy dermatitis. Elimination of fleas and ticks within 24 hours. One treatment prevents further infestations for five weeks by ticks and for up to five weeks by fleas.The treatment indirectly reduces the risk of transmission of tick-borne diseases (canine babesiosis, monocytic ehrlichiosis, granulocytic anaplasmosis and borreliosis) from infected ticks for four weeks.

Product summary:

Revision: 5

Authorization status:

Withdrawn

Authorization date:

2011-05-06

Patient Information leaflet

                                Medicinal product no longer authorised
B. PACKAGE LEAFLET
21
Medicinal product no longer authorised
PACKAGE LEAFLET FOR
(Box of 3 pipettes)
CERTIFECT 67 MG/ 60.3 MG/ 80 MG SPOT-ON SOLUTION FOR DOGS 2-10 KG
CERTIFECT 134 MG/ 120.6 MG/ 160 MG SPOT-ON SOLUTION FOR DOGS 10-20 KG
CERTIFECT 268
MG/ 241.2 MG/ 320
MG SPOT-ON SOLUTION FOR DOGS 20-40 KG
CERTIFECT 402 MG/ 361.8 MG/ 480 MG SPOT-ON SOLUTION FOR DOGS 40-60 KG
1.
NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER AND OF
THE MANUFACTURING AUTHORISATION HOLDER RESPONSIBLE FOR BATCH
RELEASE, IF DIFFERENT
Marketing authorisation holder:
MERIAL
29, avenue Tony Garnier
FR-69007 Lyon
France.
Manufacturer responsible for the batch release:
MERIAL
4, Chemin du Calquet
FR-31000 Toulouse Cedex
France
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
CERTIFECT 67 mg/ 60.3 mg/ 80 mg spot-on solution for dogs 2-10 kg
CERTIFECT 134 mg/ 120.6 mg/ 160 mg spot-on solution for dogs 10-20 kg
CERTIFECT 268 mg/ 241.2 mg/ 320 mg spot-on solution for dogs 20-40 kg
CERTIFECT 402 mg/ 361.8 mg/ 480 mg spot-on solution for dogs 40-60 kg
3.
STATEMENT OF THE ACTIVE SUBSTANCES AND OTHER INGREDIENTS
Spot-on solution.
Clear amber to yellowish solution.
Each unit dose (dual cavity pipette) delivers:
CERTIFECT spot-on solution
Volume of unit
dose (ml)
Fipronil
(mg)
(S)-methoprene
(mg)
Amitraz
(mg)
dogs 2-10 kg
1.07
67.0
60.3
80.0
dogs 10-20 kg
2.14
134.0
120.6
160.0
dogs 20-40 kg
4.28
268.0
241.2
320.0
dogs 40-60 kg
6.42
402.0
361.8
480.0
Excipients essential for proper administration: butylhydroxyanisole
(0.02 %) and butylhydroxytoluene
(0.01 %).
22
Medicinal product no longer authorised
4.
INDICATIONS
Treatment and prevention of infestations in dogs by ticks (
_Ixodes ricinus, Dermacentor reticulatus, _
_Rhipicephalus sanguineus, Ixodes scapularis, Dermacentor variabilis,
Haemaphysalis elliptica, _
_Haemaphysalis longicornis, Amblyomma americanum _
and
_Amblyomma maculatum) _
and fleas
_(Ctenocephalides felis _
and
_Ctenocephalides canis)._
Treatment of infestations by chewing lice (
_Trichodect
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                Medicinal product no longer authorised
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
1
Medicinal product no longer authorised
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
CERTIFECT 67 mg/ 60.3 mg/ 80 mg spot-on solution for dogs 2-10 kg
CERTIFECT 134 mg/ 120.6 mg/ 160 mg spot-on solution for dogs 10-20 kg
CERTIFECT 268 mg/ 241.2 mg/ 320 mg spot-on solution for dogs 20-40 kg
CERTIFECT 402 mg/ 361.8 mg/ 480 mg spot-on solution for dogs 40-60 kg
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Active substances:
Each unit dose delivers:
CERTIFECT spot-on solution
Volume of unit
dose (ml)
Fipronil
(mg)
(S)-Methoprene
(mg)
Amitraz
(mg)
dogs 2-10 kg
1.07
67
60.3
80
dogs 10-20 kg
2.14
134
120.6
160
dogs 20-40 kg
4.28
268
241.2
320
dogs 40-60 kg
6.42
402
361.8
480
Excipients:
Butylhydroxyanisole (0.02 %)
Butylhydroxytoluene (0.01 %)
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Spot-on solution.
Clear amber to yellowish solution.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Dogs
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Treatment and prevention of infestations in dogs by ticks (
_Ixodes ricinus, Dermacentor reticulatus, _
_Rhipicephalus sanguineus, Ixodes scapularis, Dermacentor variabilis,
Haemaphysalis elliptica, _
_Haemaphysalis longicornis, Amblyomma americanum _
and
_Amblyomma maculatum) _
and fleas
_(Ctenocephalides felis _
and
_Ctenocephalides canis)._
Treatment of infestations by chewing lice (
_Trichodectes canis_
).
Prevention of environmental flea contamination by inhibiting the
development of all flea immature
stages. The product can be used as part of a treatment strategy for
the control of Flea Allergy
Dermatitis (FAD). Elimination of fleas and ticks within 24 hours. One
treatment prevents further
infestations for 5 weeks by ticks and for up to 5 weeks by fleas.
2
Medicinal product no longer authorised
The treatment indirectly reduces the risk of transmission of
tick-borne diseases (canine babesiosis,
monocytic ehrlichiosis, granulocytic anaplasmosis and borreliosis)
from infect
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 27-07-2018
Summary of Product characteristics Summary of Product characteristics Bulgarian 27-07-2018
Public Assessment Report Public Assessment Report Bulgarian 27-07-2018
Patient Information leaflet Patient Information leaflet Spanish 27-07-2018
Public Assessment Report Public Assessment Report Spanish 27-07-2018
Patient Information leaflet Patient Information leaflet Czech 27-07-2018
Public Assessment Report Public Assessment Report Czech 27-07-2018
Patient Information leaflet Patient Information leaflet Danish 27-07-2018
Public Assessment Report Public Assessment Report Danish 27-07-2018
Patient Information leaflet Patient Information leaflet German 27-07-2018
Public Assessment Report Public Assessment Report German 27-07-2018
Patient Information leaflet Patient Information leaflet Estonian 27-07-2018
Public Assessment Report Public Assessment Report Estonian 27-07-2018
Patient Information leaflet Patient Information leaflet Greek 27-07-2018
Public Assessment Report Public Assessment Report Greek 27-07-2018
Patient Information leaflet Patient Information leaflet French 27-07-2018
Public Assessment Report Public Assessment Report French 27-07-2018
Patient Information leaflet Patient Information leaflet Italian 27-07-2018
Public Assessment Report Public Assessment Report Italian 27-07-2018
Patient Information leaflet Patient Information leaflet Latvian 27-07-2018
Public Assessment Report Public Assessment Report Latvian 27-07-2018
Patient Information leaflet Patient Information leaflet Lithuanian 27-07-2018
Summary of Product characteristics Summary of Product characteristics Lithuanian 27-07-2018
Public Assessment Report Public Assessment Report Lithuanian 27-07-2018
Patient Information leaflet Patient Information leaflet Hungarian 27-07-2018
Summary of Product characteristics Summary of Product characteristics Hungarian 27-07-2018
Public Assessment Report Public Assessment Report Hungarian 27-07-2018
Patient Information leaflet Patient Information leaflet Maltese 27-07-2018
Public Assessment Report Public Assessment Report Maltese 27-07-2018
Patient Information leaflet Patient Information leaflet Dutch 27-07-2018
Public Assessment Report Public Assessment Report Dutch 27-07-2018
Patient Information leaflet Patient Information leaflet Polish 27-07-2018
Public Assessment Report Public Assessment Report Polish 27-07-2018
Patient Information leaflet Patient Information leaflet Portuguese 27-07-2018
Summary of Product characteristics Summary of Product characteristics Portuguese 27-07-2018
Public Assessment Report Public Assessment Report Portuguese 27-07-2018
Patient Information leaflet Patient Information leaflet Romanian 27-07-2018
Public Assessment Report Public Assessment Report Romanian 27-07-2018
Patient Information leaflet Patient Information leaflet Slovak 27-07-2018
Public Assessment Report Public Assessment Report Slovak 27-07-2018
Patient Information leaflet Patient Information leaflet Slovenian 27-07-2018
Summary of Product characteristics Summary of Product characteristics Slovenian 27-07-2018
Public Assessment Report Public Assessment Report Slovenian 27-07-2018
Patient Information leaflet Patient Information leaflet Finnish 27-07-2018
Public Assessment Report Public Assessment Report Finnish 27-07-2018
Patient Information leaflet Patient Information leaflet Swedish 27-07-2018
Public Assessment Report Public Assessment Report Swedish 27-07-2018
Patient Information leaflet Patient Information leaflet Norwegian 27-07-2018
Summary of Product characteristics Summary of Product characteristics Norwegian 27-07-2018
Patient Information leaflet Patient Information leaflet Icelandic 27-07-2018
Summary of Product characteristics Summary of Product characteristics Icelandic 27-07-2018
Patient Information leaflet Patient Information leaflet Croatian 27-07-2018
Public Assessment Report Public Assessment Report Croatian 27-07-2018

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