Incident Report
Subform I: General Information
1. Report Type.
New incident report
Incident Report Number: 2016-3094
2. Registrant Information.
Registrant Reference Number: ProPharma Group case #: 1-44137251
Registrant Name (Full Legal Name no abbreviations): Syngenta Canada Inc.
Address: 140 Research Lane, Research Park
City: Guelph
Prov / State: Ontario
Country: Canada
Postal Code: N1G4Z3
3. Select the appropriate subform(s) for the incident.
Human
4. Date registrant was first informed of the incident.
16-MAY-16
5. Location of incident.
Country: CANADA
Prov / State: ALBERTA
6. Date incident was first observed.
16-MAY-16
Product Description
7. a) Provide the active ingredient and, if available, the registration number and product name (include all tank mixes). If the product is not registered provide a submission number.
Active(s)
PMRA Registration No.
PMRA Submission No.
EPA Registration No. Unknown
Product Name: Apron xl ls fungicide
7. b) Type of formulation.
Application Information
8. Product was applied?
Unknown
9. Application Rate.
10. Site pesticide was applied to (select all that apply).
11. Provide any additional information regarding application (how it was applied, amount applied, the size of the area treated etc).
To be determined by Registrant
12. In your opinion, was the product used according to the label instructions?
Unknown
Subform II: Human Incident Report (A separate form for each person affected)
1. Source of Report.
Other
2. Demographic information of data subject
Sex: Male
Age: >19 <=64 yrs / >19 <=64 ans
3. List all symptoms, using the selections below.
System
4. How long did the symptoms last?
Unknown / Inconnu
5. Was medical treatment provided? Provide details in question 13.
Unknown
6. a) Was the person hospitalized?
Unknown
6. b) For how long?
7. Exposure scenario
Unknown
8. How did exposure occur? (Select all that apply)
9. If the exposure occured during application or re-entry, what protective clothing was worn? (select all that apply)
Unknown
10. Route(s) of exposure.
Skin
11. What was the length of exposure?
Unknown / Inconnu
12. Time between exposure and onset of symptoms.
Unknown / Inconnu
13. Provide any additional details about the incident (eg. description of the frequency and severity of the symptoms, type of medical treatment, results from medical tests, outcome of the incident, amount of pesticide exposed to, etc.)
1-44137251 - The reporter indicated that an operator was exposed to a product with a fungicide containing the active ingredient Metalaxyl-M (Mefenoxam). On the day of initial contact with the registrant, the reporter stated the adult male operator got some of the product dust on his exposed skin and his skin is now very red. The reporter was informed that the product was not manufactured by the registrant, but the fungicide portion of the product was and the registrant is only able to give information on the fungicide. The reporter was informed that the fungicide can be a dermal irritant. The reporter was advised to get medical attention for the operator. No follow-up was attempted. No additional information is available.
To be determined by Registrant
14. Severity classification.
Minor
15. Provide supplemental information here.