Incident Report
Subform I: General Information
1. Report Type.
New incident report
Incident Report Number: 2018-2577
2. Registrant Information.
Registrant Reference Number: 10062015
Registrant Name (Full Legal Name no abbreviations): Heidi Liakve Kuus
Address: 450 Tapscott Road
City: Toronto
Prov / State: Ontario
Country: Canada
Postal Code: M1B 1Y4
3. Select the appropriate subform(s) for the incident.
Human
4. Date registrant was first informed of the incident.
10-JUN-15
5. Location of incident.
Country: CANADA
Prov / State: ONTARIO
6. Date incident was first observed.
10-JUN-15
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. 31463
PMRA Submission No.
EPA Registration No.
Product Name: Mosquito Shield PiActive Insect Repellent
7. b) Type of formulation.
Application Information
8. Product was applied?
Yes
9. Application Rate.
Unknown
10. Site pesticide was applied to (select all that apply).
Site: Res. - In Home / Rés. - à l'int. maison
11. Provide any additional information regarding application (how it was applied, amount applied, the size of the area treated etc).
Applied last night, onto legs and arms and chest and this morning wake-up with red itchy skin. When she first applied it there was no reaction, applied around 8pm, when she went to bed it was OK, but, when she woke-up she said she woke up with red, itchy skin.
To be determined by Registrant
12. In your opinion, was the product used according to the label instructions?
Yes
Subform II: Human Incident Report (A separate form for each person affected)
1. Source of Report.
Other
2. Demographic information of data subject
Sex: Female
Age: Unknown / Inconnu
3. List all symptoms, using the selections below.
System
- Skin
- Symptom - Itchy skin
- Symptom - Red skin
4. How long did the symptoms last?
Unknown / Inconnu
5. Was medical treatment provided? Provide details in question 13.
No
6. a) Was the person hospitalized?
No
6. b) For how long?
7. Exposure scenario
Non-occupational
8. How did exposure occur? (Select all that apply)
Application
9. If the exposure occured during application or re-entry, what protective clothing was worn? (select all that apply)
None
10. Route(s) of exposure.
Skin
11. What was the length of exposure?
Unknown / Inconnu
12. Time between exposure and onset of symptoms.
>8 hrs <=24 hrs / > 8 h < = 24 h
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.)
Red and itchy on all areas she sprayed. She did not spray her face, only back and front of arms, legs and chest.
To be determined by Registrant
14. Severity classification.
Minor
15. Provide supplemental information here.
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 in the telephone interviews.