Incident Report

Subform I: General Information

1. Report Type.

New incident report

Incident Report Number: 2007-4390

2. Registrant Information.

Registrant Reference Number: CA2007-00182

Registrant Name (Full Legal Name no abbreviations): SCHERING-PLOUGH ANIMAL HEALTH

Address: 3535 TRANS-CANADA

City: POINTE-CLAIRE

Prov / State: QUEBEC

Country: CANADA

Postal Code: H9R-1B4

3. Select the appropriate subform(s) for the incident.

Human

4. Date registrant was first informed of the incident.

14-MAY-07

5. Location of incident.

Country: CANADA

Prov / State: ONTARIO

6. Date incident was first observed.

12-MAY-07

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. 10043      PMRA Submission No.       EPA Registration No.

Product Name: DRI-KIL DUST

• Active Ingredient(s)
  • ACT_537
  • ACT_571

---

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: >12 <=19 yrs / >12 <=19 ans

3. List all symptoms, using the selections below.

System

• Respiratory System
  • Symptom - Difficulty Breathing

• Cardiovascular System
  • Symptom - Chest pain

4. How long did the symptoms last?

>8 hrs <=24 hrs / > 8 h < = 24 h

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

Non-occupational

8. How did exposure occur? (Select all that apply)

Drift from the application site

9. If the exposure occured during application or re-entry, what protective clothing was worn? (select all that apply)

10. Route(s) of exposure.

Respiratory

11. What was the length of exposure?

Unknown / Inconnu

12. Time between exposure and onset of symptoms.

<=30 min / <=30 min

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.)

DRI-KIL product was used on horses, patient was in direction of the wind (unknown if up or down wind), and the product was being used 30-40 m away on horses. Cardiogram of patient was negative; following day patient was asymptomatic.

To be determined by Registrant

14. Severity classification.

Moderate

15. Provide supplemental information here.