País: Austràlia
Idioma: anglès
Font: APVMA (Australian Pesticides and Veterinary Medicines Authority)
PHENYLPROPANOLAMINE HYDROCHLORIDE
VETOQUINOL AUSTRALIA PTY LTD
phenylpropanolamine HCl(50mg/mL)
ORAL SOLUTION/SUSPENSION
PHENYLPROPANOLAMINE HYDROCHLORIDE AMMONIUM-QUATERNARY Active 50.0 mg/ml
100mL; 30mL
VM - Veterinary Medicine
DOG - FEMALE (BITCH) | BITCH | CASTRATE
GENITOURINARY SYSTEM
URINARY INCONTINENCE (SPAYED BITCH) | INCONTINENCE
Poison schedule: 4; Withholding period: WHP: N/A; Host/pest details: DOG - FEMALE (BITCH): [URINARY INCONTINENCE (SPAYED BITCH)]; Poison schedule: 4; Withholding period: ; Host/pest details: DOG - FEMALE (BITCH): [URINARY INCONTINENCE (SPAYED BITCH)]; For use in bitches in the control of urinary incontinence associated with urethral sphincter incompetence.DO NOT use in pregnant bitches. DO NOT use above recommended dose. Effects on lactation have not been reported.
Registered
2023-07-01
Product Name: APVMA Approval No: PROPALIN 53680/134717 Label Name: PROPALIN Signal Headings: PRESCRIPTION ANIMAL REMEDY KEEP OUT OF REACH OF CHILDREN FOR ANIMAL TREATMENT ONLY Constituent Statements: 50 mg/mL PHENYLPROPANOLAMINE HYDROCHLORIDE Claims: For use only by or under supervision of a registered veterinarian. For use in bitches as an aid in the control of urinary incontinence associated with urethral sphincter incompetence. Net Contents: 30 mL 100 mL Directions for Use: Restraints: DO NOT USE in pregnant animals. DO NOT USE in conjunction with other hypertensive drugs. Contraindications: Precautions: Use with caution as the effects of Phenylpropanolamine on lactation have not been reported. Side Effects: Sympathomimetics may produce a wide range of effects, most of which mimic the results of excessive stimulation of sympathetic nervous system. Headache, hypertension and dizziness have been reported in humans. Propalin contains sorbitol which has laxative properties. However, such activity is unlikely at the recommended dose. RLP APPROVED It is probable that over dosage of Phenylpropanolamine would produce symptoms of excessive stimulation of the sympathetic nervous system. Aggressiveness and restlessness have been noted in some animals following treatment. Lethargy and inappetence have been reported in a dog following an overdose (2.5 mg/kg 3 times daily). Treatment should be symptomatic. No specific antidote is available. Dosage and Administration: Use the contents within 3 months of first broaching the syringe. Discard the unused portion. IN BITCHES: 3 mg/kg daily in divided dose given with food i.e. 1.5 mg/kg twice daily or 1.0 mg/kg three times daily, e.g. for 25 kg dog give 0.75 mL twice daily or 0.5 mL three times daily for a total daily dose of 1.5 mL (75mg). General Directions: Withholding Periods: Trade Advice: Safety Directions: First Aid Instructions: If poisoning occurs, contact a doctor or Poisons Information Centre. Phone Australia 13 11 26. First Aid Warnings: Additional User Safety: Ingesti Llegiu el document complet
PRODUCT NAME: PROPALIN® SYRUP PAGE: 1 OF 5 THIS VERSION ISSUED: OCTOBER, 2015 SAFETY DATA SHEET Issued by: Vetoquinol Australia Pty Ltd Phone: 1800 032 355 (BUSINESS HOURS) POISONS INFORMATION CENTRE: 13 1126 FROM ANYWHERE IN AUSTRALIA, (0800 764 766 IN NEW ZEALAND) SECTION 1 - IDENTIFICATION OF THE MATERIAL AND SUPPLIER VETOQUINOL AUSTRALIA PTY LTD PHONE: 1800 032 355 (BUSINESS HOURS) UNIT 302/2, 6-12 BORONIA ROAD, DA VINCI BUSINESS PARK, FAX: 1800 648 460 BRISBANE AIRPORT, QLD 4008 CHEMICAL NATURE: Phenylpropanolamine acts as an alpha-adrenergic receptor and beta-adrenergic receptor agonist as well as a dopamine receptor D1 partial agonist. TRADE NAME: PROPALIN® SYRUP APVMA CODE: 53680 PRODUCT USE: Sympathomimetic (phenylpropanolamine) in oral solution against the urinary incontinence associated with urethral sphincter incompetence of female dogs. CREATION DATE: OCTOBER, 2015 THIS VERSION ISSUED: OCTOBER, 2015 and is valid for 5 years from this date. POISONS INFORMATION CENTRE: PHONE 13 1126 FROM ANYWHERE IN AUSTRALIA SECTION 2 - HAZARDS IDENTIFICATION 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 Australian Dangerous Goods (ADG) Code, IATA or IMDG/IMSBC criteria. RISK PHRASES: Not Hazardous - No criteria found. SAFETY PHRASES: S25, S36. Avoid contact with eyes. Wear suitable protective clothing. SUSMP CLASSIFICATION: S4 ADG CLASSIFICATION: None allocated. Not a Dangerous Good according to Australian Dangerous Goods (ADG) Code, IATA or IMDG/IMSBC criteria. UN NUMBER: None allocated GHS SIGNAL WORD: NONE. NOT HAZARDOUS. PREVENTION P102: Keep out of reach of children. P262: Do not get in eyes, on skin, or on clothing. P281: Use personal protective equipment as required. RESPONSE P353: Rinse skin or shower with water. P301+P330+P331: IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. P370+P378: Not combustible. Use extinguishing media suited to burning materials. STORAGE P411: Store at temperatures not Llegiu el document complet
_P_ _ROPALIN®_ _P_ _ROPALIN®_ _P_ _HENYLPROPANOLAMINE HYDROCHLORIDE 50MG/ML_ READ THE ENCLOSED LEAFLET BEFORE USING THIS PRODUCT DIRECTIONS FOR USE To be used by, or under direction of, a registered veterinarian. IN BITCHES: 3mg/kg daily in divided dose given with food i.e. 1.5mg/kg twice daily or 1.0mg/kg three times daily e.g. for 25 kg dog give 0.75 mL twice daily or 0.5 mL three times daily for a total daily dose of 1.5mL (75mg). CONTRAINDICATION AND PRECAUTIONS Contraindicated in pregnant bitches. Use above the recommended dose is contraindicated. The effects of Phenylpropanolamine on lactation have not been reported. HUMAN SAFETY INFORMATION Ingestion of this product by a child could cause harm. Therefore, always ensure the child-resistant closure is replaced securely after each administration. Please also refer to the pack and the leaflet. FIRST AID: If poisoning occurs, contact a doctor or Poisons Information Centre. Phone Australia 131126 _P_ _ROPALIN®_ FOR USE IN BITCHES IN THE CONTROL OF URINARY INCONTINEN- CE ASSOCIATED WITH URETHRAL SPHINCTER INCOMPETENCE Following withdrawal of the first dose, the product should be used within 3 months. Any unused product should be discarded. Manufactured by: VETOQUINOL S.A., MAGNY VERNOIS, 70200 Lure (France) Distributed by: VETOQUINOL AUSTRALIA PTY LTD Unit 302/2, 6-12 Boronia Road, DaVinci Business Park, Brisbane Airport, Qld, 4008 Phone: 1800 032 355 sales.australia@vetoquinol.com Store below 25˚C (Air conditioning) Dispose of empty containers by wrapping in paper and putting in garbage. APVMA Approval N° 53680/100mL/0604 441500 0615 C _PHENYLPROPANOLAMINE HYDROCHLORIDE 50MG/ML_ SIDE EFFECTS Sympathomimetics may produce a wide range of effects, most of which mimic the results of excessive stimulation of the sympathetic nervous system. Headaches, hypertension and dizziness have been reported in man. Sorbitol has laxative properties but such activity is unlikely at the recommended dosage. It is probable that overdosage of Phenylpropanolamine would produce sym Llegiu el document complet