Clevor

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

ropinirole hydrochloride

Available from:

Orion Corporation

ATC code:

QN04BC04

INN (International Name):

ropinirole

Therapeutic group:

Dogs

Therapeutic area:

Dopaminergic agents, Dopamine agonists

Therapeutic indications:

Induction of vomiting in dogs.,

Product summary:

Revision: 1

Authorization status:

Authorised

Authorization date:

2018-04-13

Patient Information leaflet

                                17
B. PACKAGE LEAFLET
18
PACKAGE LEAFLET:
CLEVOR 30 MG/ML EYE DROPS, SOLUTION IN SINGLE-DOSE CONTAINER FOR DOGS
1.
NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER AND
OF THE MANUFACTURING AUTHORISATION HOLDER RESPONSIBLE FOR
BATCH RELEASE, IF DIFFERENT
Orion Corporation
Orionintie 1
FI-02200 Espoo
FINLAND
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Clevor 30 mg/ml eye drops, solution in single-dose container for dogs
Ropinirole (ropinirol)
3.
STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENT(S)
Clevor is a very slightly yellow to yellow clear solution containing
30 mg/ml ropinirole, equivalent to
34.2 mg/ml ropinirole hydrochloride.
4.
INDICATION(S)
For induction of vomiting in dogs.
5.
CONTRAINDICATIONS
Your dog must not be given this medicine if it:
-
has decreased consciousness, seizures or other similar neurologic
symptoms or difficulties in
breathing or swallowing that could make the dog inhale a part of the
vomit potentially causing
aspiration pneumonia
-
has ingested sharp foreign objects, acids or alkalis (e.g. drain or
toilet bowl cleaners, household
detergents, battery fluids), volatile substances (e.g. petroleum
products, essential oils, air
fresheners) or organic solvents (e.g. antifreeze, windshield wiper
fluids, nail polish remover)
-
is hypersensitive to ropinirole or to any of the excipients.
6.
ADVERSE REACTIONS
This veterinary medicinal product may cause the following adverse
reactions:
Very common reactions: temporary mild or moderate redness of the eye,
increased tear production,
increased visibility of the third eyelid and/or squinting; temporary
mild tiredness and/or increased heart
rate.
Common reactions: temporary, mild swelling of the mucous membranes of
the eyelids, itching of the
eyes, rapid breathing, shivering, diarrhoea and/or irregular or
uncoordinated bodily movements.
19
Extended vomiting (for more than 60 minutes) which should be evaluated
by the responsible
veterinarian as it might need appropriate treatment.
In dogs with protracted vomiting (more than 60 minutes)
                                
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Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Clevor 30 mg/ml eye drops, solution in single-dose container for dogs
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each ml of solution contains:
ACTIVE SUBSTANCE:
Ropinirole (ropinirol)
30 mg
(equivalent to 34.2 mg ropinirole hydrochloride)
EXCIPIENTS:
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Eye drops solution in single-dose container.
Very slightly yellow to yellow clear solution.
pH 3.8–4.5 and osmolality 300–400 mOsm/kg.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Dogs
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Induction of vomiting in dogs.
4.3
CONTRAINDICATIONS
Do not use in dogs with depression of the central nervous system,
seizures or other marked neurologic
impairments that could lead to aspiration pneumonia.
Do not use in dogs which are hypoxic, dyspnoeic or lacking pharyngeal
reflexes.
Do not use in cases of the ingestion of sharp foreign objects,
corrosive agents (acids or alkalis), volatile
substances or organic solvents.
Do not use in cases of hypersensitivity to the active substance or to
any of the excipients.
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
The efficacy of the veterinary medicinal product has not been
established in dogs weighing less than
1.8 kg, or in dogs under 4.5 months of age or in elderly dogs. Use
only according to the benefit-risk
assessment by the responsible veterinarian.
Based on the clinical trial results, most dogs are expected to respond
to a single dose of the veterinary
medicinal product; however, a small proportion of dogs will require a
second dose to induce vomiting.
A very small proportion of dogs may fail to respond to the treatment
despite administration of a second
dose. It is not recommended to administer further doses to these dogs.
Please refer to sections 4.9 and
5.1 for further information.
3
4.5
SPECIAL PRECAUTIONS FOR USE
Special precautions for use in animals
This veterinary medicinal product may cause a transient in
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 07-02-2019
Summary of Product characteristics Summary of Product characteristics Bulgarian 07-02-2019
Public Assessment Report Public Assessment Report Bulgarian 16-05-2018
Patient Information leaflet Patient Information leaflet Spanish 07-02-2019
Public Assessment Report Public Assessment Report Spanish 16-05-2018
Patient Information leaflet Patient Information leaflet Czech 07-02-2019
Public Assessment Report Public Assessment Report Czech 16-05-2018
Patient Information leaflet Patient Information leaflet Danish 07-02-2019
Public Assessment Report Public Assessment Report Danish 16-05-2018
Patient Information leaflet Patient Information leaflet German 07-02-2019
Public Assessment Report Public Assessment Report German 16-05-2018
Patient Information leaflet Patient Information leaflet Estonian 07-02-2019
Public Assessment Report Public Assessment Report Estonian 16-05-2018
Patient Information leaflet Patient Information leaflet Greek 07-02-2019
Public Assessment Report Public Assessment Report Greek 16-05-2018
Patient Information leaflet Patient Information leaflet French 07-02-2019
Public Assessment Report Public Assessment Report French 16-05-2018
Patient Information leaflet Patient Information leaflet Italian 07-02-2019
Public Assessment Report Public Assessment Report Italian 16-05-2018
Patient Information leaflet Patient Information leaflet Latvian 07-02-2019
Public Assessment Report Public Assessment Report Latvian 16-05-2018
Patient Information leaflet Patient Information leaflet Lithuanian 07-02-2019
Summary of Product characteristics Summary of Product characteristics Lithuanian 07-02-2019
Public Assessment Report Public Assessment Report Lithuanian 16-05-2018
Patient Information leaflet Patient Information leaflet Hungarian 07-02-2019
Summary of Product characteristics Summary of Product characteristics Hungarian 07-02-2019
Public Assessment Report Public Assessment Report Hungarian 16-05-2018
Patient Information leaflet Patient Information leaflet Maltese 07-02-2019
Public Assessment Report Public Assessment Report Maltese 16-05-2018
Patient Information leaflet Patient Information leaflet Dutch 07-02-2019
Public Assessment Report Public Assessment Report Dutch 16-05-2018
Patient Information leaflet Patient Information leaflet Polish 07-02-2019
Public Assessment Report Public Assessment Report Polish 16-05-2018
Patient Information leaflet Patient Information leaflet Portuguese 07-02-2019
Summary of Product characteristics Summary of Product characteristics Portuguese 07-02-2019
Public Assessment Report Public Assessment Report Portuguese 16-05-2018
Patient Information leaflet Patient Information leaflet Romanian 07-02-2019
Public Assessment Report Public Assessment Report Romanian 16-05-2018
Patient Information leaflet Patient Information leaflet Slovak 07-02-2019
Public Assessment Report Public Assessment Report Slovak 16-05-2018
Patient Information leaflet Patient Information leaflet Slovenian 07-02-2019
Summary of Product characteristics Summary of Product characteristics Slovenian 07-02-2019
Public Assessment Report Public Assessment Report Slovenian 16-05-2018
Patient Information leaflet Patient Information leaflet Finnish 07-02-2019
Public Assessment Report Public Assessment Report Finnish 16-05-2018
Patient Information leaflet Patient Information leaflet Swedish 07-02-2019
Public Assessment Report Public Assessment Report Swedish 16-05-2018
Patient Information leaflet Patient Information leaflet Norwegian 07-02-2019
Summary of Product characteristics Summary of Product characteristics Norwegian 07-02-2019
Patient Information leaflet Patient Information leaflet Icelandic 07-02-2019
Summary of Product characteristics Summary of Product characteristics Icelandic 07-02-2019
Patient Information leaflet Patient Information leaflet Croatian 07-02-2019
Public Assessment Report Public Assessment Report Croatian 16-05-2018

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