Fentadon vet.
Active substance
ATC code
Species
Dogs.
Indications
For intra-operative analgesia during surgical procedures such as soft tissue and orthopaedic surgery.
For the control of post-operative pain associated with major orthopaedic and soft tissue surgery.
Dose to be administered and administration route
For intravenous use.
To ensure a correct dosage, body weight should be determined as accurately as possible. Onset of action is seen within 5 minutes. The duration of the analgesic effect is 20 (lowest recommended dose) to 40 minutes (highest recommended dose).
Fentanyl can be administered according to the following dosage regimen:
Analgesia by Continuous Rate Infusion (CRI)
• 5 – 10 µg/kg (0.1 - 0.2 ml/kg) IV as a bolus, followed by 12 – 24 µg/kg/hr (0.24 - 0.48 ml/kg/hr) IV for intra-operative analgesia as CRI.
• 6 – 10 µg/kg/hr (0.12 - 0.2 ml/kg/hr) IV for subsequent post-operative analgesia as CRI in sedated animals. During post-operative CRI administration of fentanyl, animals should be monitored carefully.
Chemical-physical compatibility has only been demonstrated for dilutions 1:5 with the following solutions for infusion: sodium chloride 0.9%, Ringer’s solution and glucose
5%.
The veterinary medicinal product has a narrow margin of safety and it is important to measure the dose accurately to avoid overdosing.
Adverse reactions
Dogs:
Very common (>1 animal / 10 animals treated): |
Hyperactivity, Irritability, Vocalisation Involuntary defecation, Tongue protrusion, Vomiting Tremor a, Sedation Urination Increased respiratory rate, Panting Scratching |
Common (1 to 10 animals / 100 animals treated): |
Respiratory depression b Bradycardia c, Hypotension d |
Uncommon (1 to 10 animals / 1,000 animals treated): |
Hypothermia |
Rare (1 to 10 animals / 10,000 animals treated): |
Lowered nociceptive thresholds e |
a Tremors of the body. b Can be of long duration and may exhibit a biphasic pattern. c Due to increased cardiac vagal stimulation.
d Transient. Following intravenous administration of fentanyl citrate even at doses of 2.5 – 5 μg/kg. e When the effects of the drug dissipate.
Reporting adverse events is important. It allows continuous safety monitoring of a veterinary medicinal product. Reports should be sent, preferably via a veterinarian, to either the marketing authorisation holder or its local representative or the national competent authority via the national reporting system. See the package leaflet for respective contact details.
Dispensing
POM-V - Prescription Only Medicine – Veterinarian
PRICE | Only for registered vets. Create a free profile to access all features.. Login |
---|---|
Art. Nr. | 16849/5014 |
EAN | 8714225154784 |