New incident report
Incident Report Number: 2009-4891
Registrant Reference Number: 4193617
Registrant Name (Full Legal Name no abbreviations): Sure-Gro Inc.
Address: 150 Savannah Oaks Dr.
City: Brantford
Prov / State: Ontario
Country: Canada
Postal Code: N3V 1E7
Domestic Animal
Country: CANADA
Prov / State: ONTARIO
PMRA Registration No. 28352 PMRA Submission No. EPA Registration No.
Product Name: Wilson Predator Rat and Mouse Killer
Unknown
Unknown
Animal's Owner
Dog / Chien
Yorkshire Terrier
1
Male
1.25
13
lbs
Oral
>15 min <=2 hrs / >15 min <=2 h
>2 hrs <=8 hrs / > 2 h < = 8 h
System
Unknown / Inconnu
Unknown
Unknown
Unknown/Inconnu
Accidental ingestion/Ingestion accident.
(eg. description of the frequency and severity of the symptoms
Caller stated that his Dog "Chewy" had access to the block from 12- 1:30 CT and ate mostly 1/2 of one block. He is currently asymptomatic. His owner gave him a meal after that (unspecified time) and a family member gave him half of a peach after that (also unspecified time). Caller was advised to try and induce vomiting to try and recover some of the bait. If not much is recovered, can start Vitamin K1 x 30 days. Gave owner detailed instructions on how to induce. Chewy just ate, no need to feed prior to peroxide. Owner will call back with emesis results. The owner called back, the dog hasn't vomited after 1 dose of peroxide. It is active. Repeat, call us back. Chewy has had 2 doses of active H2O2 and has not vomited. Per the Dr.s recommendation we would be concerned about this exposure. Owner should take Chewy into the DVM to start Vitamin K-1 on either. Owner called back. He reports that he noticed this am that the color of the dog's stool this am was similar to the rodenticide. He wondered if he still needed to take the dog to the DVM. Advised owner that the color of the bait that he was seeing is most likely just the dyes in the product. The active ingredient most likely has been absorbed. Recommend taking the dog to the DVM as originally recommended
Minor
The information contained in this report is based on self-reported statements provided to the registrant during telephone Interview(s). These self-reported descriptions of an incident have not been independently verified to be factually correct or complete descriptions of the incident. For that reason, information contained in this report does not and can not form the basis for a determination of whether the reported clinical effects are causally related to exposure to the product identified.