GENESTRAN 75 MICROGRAMS/ML SOLUTION FOR INJECTION FOR CATTLE, HORSES AND PIGS

Ország: Írország

Nyelv: angol

Forrás: HPRA (Health Products Regulatory Authority)

Vedd Meg Most

Termékjellemzők Termékjellemzők (SPC)
10-03-2017

Aktív összetevők:

(+)-CLOPROSTENOL (AS (+)-CLOPROSTENOL SODIUM)

Beszerezhető a:

aniMedica GmbH

ATC-kód:

QG02AD90

INN (nemzetközi neve):

(+)-CLOPROSTENOL (AS (+)-CLOPROSTENOL SODIUM)

Adagolás:

75 Microgram/ML

Gyógyszerészeti forma:

Solution for Injection

Recept típusa:

POM

Terápiás csoport:

Bovine, Equine - Food, Porcine

Terápiás terület:

Cloprostenol

Terápiás javallatok:

Hormone

Engedélyezési státusz:

Authorised

Engedély dátuma:

2009-10-09

Termékjellemzők

                                SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Genestran 75 micrograms/ml solution for injection for cattle, horses
and pigs
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
3 PHARMACEUTICAL FORM
Solution for Injection.
A clear and odourless solution.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Cattle, horses and pigs.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
CATTLE:
- induction of luteolysis allowing resumption of oestrus and ovulation
in cyclic females when used during dioestrus
- synchronisation of oestrus (within 2 to 5 days) in groups of cyclic
females treated simultaneously
- treatment of suboestrus and uterine disorders related to a
functioning or persistent corpus luteum (endometritis, pyometra)
- treatment of ovarian luteal cysts
- induction of abortion until day 150 of pregnancy
- expulsion of mummified foetuses
- induction of parturition (within the last two weeks of gestation).
HORSES:
- induction of luteolysis in mares with a functional corpus luteum.
PIGS:
- induction or synchronisation of farrowing (generally within 24 to 36
hours) from day 113 of pregnancy onwards (day 1
of pregnancy is the last day of natural or artificial insemination).
4.3 CONTRAINDICATIONS
Do not use in case of hypersensitivity to the active substance or to
any of the excipients.
Do not use in animals with spastic respiratory or gastro-intestinal
diseases.
Do not use in pregnant animals, for which induction of abortion or
parturition is not intended.
Do not use for intravenous administration.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
None.
Each ml contains:
ACTIVE SUBSTANCE:
micrograms
R(+)-cloprostenol {as R(+)-cloprostenol sodium} 75
EXCIPIENTS:
Chlorocresol (as preservative)
1000
For the full list of excipients, see section 6.1
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