CHRONOGEST PMSG 6000 I.U. VETERINARY

Pays: Israël

Langue: anglais

Source: Ministry of Health

Ingrédients actifs:

PREGNANT MARE SERUM GONADOTROPHIN

Disponible depuis:

INTERVET ( ISRAEL) LTD

forme pharmaceutique:

POWDER FOR SOLUTION FOR INJECTION

Composition:

PREGNANT MARE SERUM GONADOTROPHIN 6000 IU/VIAL

Mode d'administration:

I.M

Type d'ordonnance:

Required

Fabriqué par:

INTERVET INTERNATIONAL GmbH, GERMANY

indications thérapeutiques:

Induction and synchronization of oestrus and ovulation in ewes and goats.

Date de l'autorisation:

2017-08-14

Notice patient

CONSUMER PACKAGE INSERT FOR A VETERINARY MEDICINAL PRODUCT
THE MEDICINE IS DISPENSED WITH A VETERINARIAN’S PRESCRIPTION ONLY
FOR ANIMAL USE ONLY
1.
NAME OF THE VETERINARY MEDICINE, ITS FORM AND STRENGTH:
CHRONOGEST PMSG 6000 I.U. VETERINARY
Powder for preparation of a solution for intramuscular injection
2.
ACTIVE INGREDIENTS:
Each vial contains:
Pregnant mare serum gonadotrophin 6000 I.U.
A list of inactive ingredients is detailed in section 13 –
“Further Information”.
3.
WHAT IS THE MEDICINE INTENDED FOR:
Induction and synchronization of ovulation in sheep, ewes and goats.
THERAPEUTIC GROUP: Sex hormones and modulators of the reproductive
system.
MECHANISM OF ACTION:
When the progestogen sponge is in the vagina of the sheep or goat, it
induces
progestative activity in the animal, similar to the luteal phase in
the reproductive
cycle. This artificial progestative period ends as soon as the sponge
is removed.
At this stage (or, in goats, sometimes two days earlier), injection of
Chronogest
PMSG induces the commencement of the follicular stage. The follicles
that
develop lead to the start of the estrus and ovulation at the scheduled
time.
Chronogest PMSG 6000 I.U. is part of the treatment regimen of
Chronogest to
control reproduction in sheep and goats.
4.
CONTRAINDICATIONS:
Do not use in cases of hypersensitivity to the active ingredient or to
any of the
inactive ingredients.
5.
SIDE EFFECTS:
As with any preparation that contain proteins, anaphylactoid reactions
may occur
in rare cases (1-10 out of 10,000 treated animals). Treatment based on
adrenaline and glucocorticoids must be rapidly administered.
Side effects can be reported to the Ministry of Health by clicking on
the link
“Report Side Effects of Drug Treatment” found on the Ministry of
Health
homepage (www.health.gov.il), that directs you to the online form for
reporting
side effects, or by entering the link:
https://sideeffects.health.gov.il
6.
TARGET ANIMALS:
Sheep and goats.
7.
METHOD OF ADMINISTRATION AND DOSAGE:
Intramuscular administratio