DEXADRESON INJECTION

Krajina: Austrália

Jazyk: angličtina

Zdroj: APVMA (Australian Pesticides and Veterinary Medicines Authority)

Kúpte ho teraz

Stiahnuť Príbalový leták (PIL)
20-06-2017

Aktívna zložka:

DEXAMETHASONE AS THE SODIUM PHOSPHATE

Dostupné z:

INTERVET AUSTRALIA PTY LIMITED

INN (Medzinárodný Name):

dexamethasone as sod.phosphate(2mg/mL)

Forma lieku:

PARENTERAL LIQUID/SOLUTION/SUSPENSION

Zloženie:

DEXAMETHASONE AS THE SODIUM PHOSPHATE STEROID-GLUCOCORTICOID Active 2.0 mg/ml

Počet v balení:

50mL

Trieda:

VM - Veterinary Medicine

Výrobca:

INTERVET AUSTRALIA

Terapeutické skupiny:

CAT | CATTLE | DOG | GOAT | HORSE | PIGS | SHEEP | BEEF | BILLY | BITCH | BOAR | BOS INDICUS | BOS TAURUS | BOVINE | BUCK | BUFF

Terapeutické oblasti:

ENDOCRINE SYSTEM

Terapeutické indikácie:

CORTICOSTEROID | ADVANCING PARTURITION | ALLERGIC REACTIONS | ANTIADRENAL SUPPRESSION | ANTI-INFLAMMATORY | ANTISHOCK | ARTHRITIS | BRONCHITIS | CATABOLIC COMPLICATIONS | CHRONIC BRONCHITIS | CORTICOSTEROIDS | CORTICOSTEROIDS AND RELATE | COUGHS | DERMATITIS | DERMATOLOGICAL DISORDERS | DERMATOSES | ECZEMA | GLUCOGENIC STEROID | JOINT DISEASE | KETOSIS | LOCOMOTIVE DISEASES | MUSCULO SKELETAL INFLAMMAT | ORTHOPAEDIC | PARTURIENT UDDER OEDEMA | PARTURITION | PRURITIS | RESPIRATORY TRACT DISEASES | RHEUMATIC DISEASES | STRESS | TOXAEMIA | WATER RETENTION

Prehľad produktov:

Poison schedule: 4; Withholding period: WHP: MEAT: DO NOT USE less than 14 days Cattle & Pigs and 28 days Horses Sheep & Goats before slaughter for human consumption. MILK: Milk collecte d from Cattle within 3 days and Sheep & amp; Goats within 7 days following trea tment MUST NOT BE USED for human consum ption or processing. This milk should n ot be fed to bobby calves. EXPORT SLAU GHTER INTERVAL (ESI): This product does not have an ESI established; Host/pest details: CAT: [CORTICOSTEROID]; CATTLE: [CORTICOSTEROID]; DOG: [CORTICOSTEROID]; GOAT: [CORTICOSTEROID]; HORSE: [CORTICOSTEROID]; PIGS: [CORTICOSTEROID]; SHEEP: [CORTICOSTEROID]; Poison schedule: 4; Withholding period: ; Host/pest details: CAT: [CORTICOSTEROID]; CATTLE: [CORTICOSTEROID]; DOG: [CORTICOSTEROID]; GOAT: [CORTICOSTEROID]; HORSE: [CORTICOSTEROID]; PIGS: [CORTICOSTEROID]; SHEEP: [CORTICOSTEROID]; Aqueous solution of dexamethasone for intravenous, intramuscular or intra- articular injection for use in horses, cattle, sheep, goats, pigs, dogs and cats.Contraindications: Diabetes mellitus, osteoporosis, cardiac and renal diseases

Stav Autorizácia:

Registered

Dátum Autorizácia:

2023-07-01

Príbalový leták

                                DEXADRESON
®
INJECTION
DEXADRESON
®
DEXADRESON
®
045765 CBU880
03
45x45x90
185C, black
189
Batch No.: / Expiry:
DISPOSAL:
Dispose of empty containers by
wrapping with paper and putting in
garbage.
STORAGE:
Store below 25°C (Air conditioning).
Protect from light.
APVMA Approval No.:
52298/50M/0410
INTERVET AUSTRALIA PTY LIMITED
91-105 Harpin Street,
BENDIGO EAST VIC 3550
Phone: (03) 5440 9888
WARRANTY
Intervet Australia Pty Ltd (IAPL)
warrants that this product is of
merchantable quality and fit for its
intended purpose. IAPL's liability for
any loss, including consequential
losses or injury caused by act or
omission, including negligent acts or
omissions, by IAPL or its agent, is
limited to replacing or repairing the
product at the option of IAPL. If
possible, a sample of any product
causing concern should be retained
or delivered to IAPL within 30 days
for a scientific examination.
READ THE ENCLOSED LEAFLET
BEFORE USING THIS PRODUCT.
DIRECTIONS FOR USE:
STORE UPRIGHT. USE ALL CONTENTS
WITHIN 4 WEEKS OF OPENING
All parenteral routes may be used in all
species at a rate of 3 mL/100 kg. Normal
aseptic technique should be observed.
WITHHOLDING PERIODS:
MEAT: DO NOT USE LESS THAN 14 DAYS
CATTLE & PIGS AND 28 DAYS HORSES,
SHEEP & GOATS BEFORE SLAUGHTER FOR
HUMAN CONSUMPTION.
MILK: MILK COLLECTED FROM CATTLE
WITHIN 3 DAYS AND SHEEP & GOATS
WITHIN 7 DAYS FOLLOWING TREATMENT
MUST NOT BE USED FOR HUMAN
CONSUMPTION OR PROCESSING. THIS
MILK SHOULD NOT BE FED TO BOBBY
CALVES.
TRADE ADVICE:
EXPORT SLAUGHTER INTERVAL (ESI): This
product does not have an ESI
established.For advice on the ESI, contact
the manufacturer on 1800 033461 before
using this product.
FIRST AID:
If poisoning occurs, contact a doctor or
Poisons Information Centre.
Phone Australia 13 11 26
PRESCRIPTION ANIMAL REMEDY
KEEP OUT OF REACH OF CHILDREN
FOR ANIMAL TREATMENT ONLY
DEXADRESON
®
INJECTION
DEXAMETHASONE
2 MG/ML
(AS SODIUM PHOSPHATE)
Aqueous solution of
dexamethasone for
intravenous,
intramuscular or
intra-articular injection
for use in Horses,
Cat
                                
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Súhrn charakteristických

                                PRODUCT NAME: DEXADRESON® INJECTION
MATERIAL SAFETY DATA SHEET
THIS REVISION ISSUED: JULY, 2009
PAGE: 1 OF 6
MATERIAL SAFETY DATA SHEET
Issued by: Intervet Australia Pty Limited Phone: 1 800 033 461
(Business Hours)
Poisons Information Centre: 13 11 26 from anywhere in Australia, (0800
764 766 in New Zealand)
SUBSTANCE:
Water solution of ingredients. Dexadreson sodium phosphate sterile
injection.
TRADE NAME:
DEXADRESON
® INJECTION
PRODUCT CODE:
21125
RECOMMENDED USE:
Anti- inflammatory injection for use in horses, cattle, sheep, pigs,
dogs and cats as
indicated on the product label..
APVMA NO:
52298
CREATION DATE:
November, 2006
THIS VERSION ISSUED:
July, 2009
and is valid for 5 years from this date.
STATEMENT OF HAZARDOUS NATURE:
THIS PRODUCT IS CLASSIFIED AS:
Not classified as hazardous according to the criteria of SWA.
Not a Dangerous Good according to the Australian Dangerous Goods (ADG)
Code.
RISK PHRASES:
Not Hazardous - No criteria found.
SAFETY PHRASES:
S25, S45. Avoid contact with eyes. In case of accident or if you feel
unwell, contact a doctor or
Poisons Information Centre immediately (show the label where
possible).
SUSDP CLASSIFICATION:
S4
ADG CLASSIFICATION:
None allocated. Not a Dangerous Good under the ADG Code.
UN NUMBER:
None allocated
PHYSICAL DESCRIPTION & COLOUR:
Clear, colourless liquid.
ODOUR:
Slight alcohol odour.
MAJOR HEALTH HAZARDS:
no significant risk factors have been found for this product.
THIS IS A PHARMACOLOGICALLY ACTIVE MATERIAL USED IN SOME PAIN
RELIEVING PREPARATIONS. DESPITE IT BEING RELATIVELY
NON-HAZARDOUS, YOU ARE ADVISED TO AVOID CONTACT WITH THIS MATERIAL AS
MUCH AS IS PRACTICAL.
If injected in large quantities, effects such as Cushing’s syndrome
(fat redistribution, bruising, acne and hirsuitism), water
retention, electrolyte imbalance (e.g., oedema, low potassium), high
blood pressure, hyperglycaemia (high blood glucose)
and suppression of adrenal gland secretions may occur.
INHALATION:
SHORT TERM EXPOSURE:
Available data indicates that this product is not harmful.
                                
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