Dechra Veterinary Products Limited (A business unit of Dechra Pharmaceuticals PLC) Sansaw Business Park Hadnall, Shrewsbury Shropshire SY4 4AS Tel: 01939 211200 VOMEND® 5 MG/ML SOLUTION FOR INJECTION
diately and show the package leaflet or the label to
FOR DOGS AND CATS Qualitative and quantitative composition
pyramidal effects (agitation, ataxia, abnormal posi-
Metoclopramide (as hydrochloride monohydrate)
tions and/or movements, prostration, tremors and
4.457 mg (equivalent to metoclopramide hydro-
aggression, vocalisation) have been observed after
treatment of dogs and cats. The observed effects are
transient and disappear when treatment is stopped.
For a full list of excipients, see Excipients.
In very rare cases, allergic reactions may occur. Pharmaceutical form Use during pregnancy and lactation: Laboratory
studies in laboratory animals have not produced anyevidence of a teratogenic or foetotoxic effects. How-
Clinical particulars
ever, studies on laboratory animals are limited and
Target species: Dogs and cats.
the safety of the active substance has not been
evaluated in the target species. The use of the product
iting and reduced gastrointestinal motility associated
during pregnancy and lactation must be made ac-
with gastritis, pyloric spasm, chronic nephritis and
cording to the benefit/risk assessment carried out by
digestive intolerance to some drugs.
testinal perforation or obstruction.
administration of anticholinergic drugs (atropine) asthey may counteract the effects of metoclopramide
Special precautions for use in animals: The dosage
must be adapted in animals with renal or hepatic
In cases of simultaneous diarrhoea, there is no
insufficiency (due to an increase in the risk of side
contraindication to the use of anticholinergic drugs.
Concurrent use of metoclopramide with neurolep-
Avoid administration to animals with epilepsy. The
tics derivated from phenothiazine (acepromazine) and
dosage should be carefully observed, especially in
butyrophenones increases the risk of extrapyramidal
effects (see Adverse reactions).
Metoclopramide can potentiate the action of central
should be given to fluid and electrolyte replacement
nervous system depressants. If used concurrently, it
is advised to use the lowest dosage of metoclopram-
Special precautions to be taken by the person admin-istering the veterinary medicinal product to ani-Amounts to be administered and administration
Intramuscular or subcutaneous use. 0.5 mg
metoclopramide hydrochloride per kg body weight, if
In case of accidental self-injection, seek medical
advice immediately and show the package leaflet orthe label to the physician.
Most of the clinical signs reported after
In case of accidental exposure by spillage onto the
an overdosage are well known extrapyramidal side
skin or eyes, wash immediately with abundant water.
effects (see Adverse reactions). In the absence of a
If adverse effects appear, seek medical advice imme-
specific antidote, it is recommended to offer a calm
environment to the animal until extrapyramidal side
Shelf life after first opening the immediate packag-
effects disappear. Metoclopramide being rapidly me-
tabolised and eliminated, side effects generally dis-
Do not use after the expiry date stated on the label
Pharmacological properties Pharmacotherapeutic
package. Keep out of the reach and sight of children. ATC Vet Code: QA03FA01Pharmacodynamic properties
Metoclopramide is an original orthopramide mole-
type I, filled with 5, 10, 20, 25, 30 and 50 ml.
cule. The anti-emetic action of metoclopramide is
Bromobutyl rubber stoppers type I (the stoppers are
mainly due to its antagonist activity at D2 receptors
secured with aluminium caps). 1 vial in a cardboard
in the central nervous system, preventing nausea and
box. Not all pack sizes may be marketed.
vomiting triggered by most stimuli. The prokineticeffect on the gastro-duodenal transit (increase in
intensity and rhythm of stomach contractions and
or waste materials derived from such veterinary
opening of the pylorus) is mediated by muscarinic
medicinal products should be disposed of in accor-
activity, D2 receptor antagonist activity and 5-HT
receptor agonist activity at the gastrointestinal level. Marketing authorisation holder (if different from
Metoclopramide is rapidly and completely ab-
distributor)
sorbed after parenteral administration. After subcu-
25, 5531 AE Bladel, The Netherlands.
taneous administration to dogs and cats, maximum
Marketing authorisation number Vm 16849/4020
concentrations are obtained after 15-30 minutes. Metoclopramide is rapidly distributed into most tis-
Date of first authorisation 20.12.2010
sues and fluids, crosses the blood-brain barrier andenters the central nervous system. Metoclopramide
Date of revision of the text December 2010
is metabolised by the liver. The elimination of meto-clopramide is rapid, 65% of the dose being eliminated
Any other information
within 24 hours in the dog, primarily by the urinary
To be supplied only on veterinary prescription. Manufacturing authorisation holder responsible forbatch release: Eurovet Animal Health BV, Handelsweg
Pharmaceutical particulars
25, 5531 AE Bladel, The Netherlands.
sodium hydroxide (for pH adjustment), hydrochloric
Legal category POM-V
acid (for pH adjustment), water for injections. GTIN (Global Trade Item No)
Vomend 5 mg/ml Solution for Injection for Dogs and
Vomend 5 mg/ml Solution for Injection for Dogs and
product as packaged for sale: 2 years. Requested by: [email protected] Approved datasheets found: 1 Creation date: 9/10/2013 14:56:59 (UK) Approved for book but not on website: 0 Datasheets marked as draft (ignored): 0
Vomend 5 mg/ml Solution for Injection for
Directory of participants Dechra Veterinary Products Limited (A business unit of Dechra Pharmaceuticals PLC) Sansaw Business Park Hadnall, Shrewsbury Shropshire SY4 4AS Tel: 01939 211200Fax: 01939 211201email: [email protected]
LIST OF PRODUCTS BY THERAPEUTIC INDICATION
List of Products by Therapeutic Indication PHARMACEUTICALS Enteric preparations
Vomend 5 mg/ml Solution for Injection for Dogs
List of Products by Species
Please note that a species in brackets after a product name may not necessarily be a part of that product namebut is intended to make the index easier to use.
Vomend 5 mg/ml Solution for Injection for Dogs and
Vomend 5 mg/ml Solution for Injection for Dogs and
List of Products by Active Ingredients
This index of non-proprietary names (active ingredients) is provided to enable users of the Compendium toidentify the brand names of relevant products when only the non-proprietary names are known.
It should be noted that although different products may contain the same active ingredient this does not implythat they are equivalent in regard to bioavailability or therapeutic activity.
Some products contain a number of ingredients and it has not been possible in every instance to identify suchproducts by a reference in this index to each ingredient.
Non-proprietary name in bold type. Proprietary name in ordinary type. Metoclopramide
Vomend 5 mg/ml Solution for Injection for Dogs
GRED IN E IV Alphabetical Index of Products
1990 1. Desola Ala J. [Methylprednisolone and the Trendelenburg position in the treatment of air embolic dysbarism]. [Spanish] Medicina Clinica. 95(18):717-8, 1990 Nov 24. 2. Desola Ala J. [Diving accidents (3). Treatment of dysbaric embolism disorders]. [Review] [108 refs] [Spanish] Medicina Clinica. 95(7):265-75, 1990 Sep 8. 3. Neuman TS. Bove AA. Combined arterial gas embolism and decompres
REFERENTIEL DES EXAMENS DE BIOLOGIE MEDICALE Version 3 - page 2/39 ANALYSE Tube SEC ou tube SEC+gel (1 ml minimum) Autres tubes possibles : EDTA, héparine, héparine+gel Conservation 24H à température ambiante Jeûne de 2H après repas pauvre en graisse Stabilité après analyse : 7J à 2-8°C sinon -20°C au delà (conservation en sérothèque pendant 1 an)