Incident Report

Subform I: General Information

1. Report Type.

New incident report

Incident Report Number: 2014-0618

2. Registrant Information.

Registrant Reference Number: 1194587

Registrant Name (Full Legal Name no abbreviations): Bayer CropScience Inc.

Address: 295 Henderson Drive

City: Regina

Prov / State: SK

Country: Canada

Postal Code: S4N 6C2

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

Human

4. Date registrant was first informed of the incident.

27-JUN-13

5. Location of incident.

Country: CANADA

Prov / State: SASKATCHEWAN

6. Date incident was first observed.

26-JUN-13

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)

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PMRA Registration No. 22659      PMRA Submission No.       EPA Registration No.

Product Name: THUMPER HERBICIDE (Canada)

• Active Ingredient(s)
  • 2,4-D (PRESENT AS LOW VOLATILE ESTERS)
  • BROMOXYNIL

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PMRA Registration No. 19346      PMRA Submission No.       EPA Registration No. Unknown

Product Name: Tilt Fungicide Propiconazole 41.8% (Syngenta Crop Protection)

• Active Ingredient(s)
  • PROPICONAZOLE

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PMRA Registration No.       PMRA Submission No.       EPA Registration No. Unknown

Product Name: Enhance Concentrate (Non-Company)

• Active Ingredient(s)

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PMRA Registration No.       PMRA Submission No.       EPA Registration No. Unknown

Product Name: Signal (Non-Company)

• Active Ingredient(s)

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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: Unknown / Inconnu

11. Provide any additional information regarding application (how it was applied, amount applied, the size of the area treated etc).

Please refer to field 13 on Subform II or field 17 of subform III for a detailed description regarding application.

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: Male

Age: >64 yrs / > 64 ans

3. List all symptoms, using the selections below.

System

• Nervous and Muscular Systems
  • Symptom - Muscle cramps

• Skin
  • Symptom - Cyanosis

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?

Unknown

7. Exposure scenario

Non-occupational

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

Application

Amount of time between application and contact 0

What was the activity? Please refer to field 13 on Subform II or field 17 of subform III for a detailed description regarding the activity

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.

Unknown

11. What was the length of exposure?

<=15 min / <=15 min

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.)

6/27/2013 Caller is calling on behalf of a relative that used all 4 products 6 hours ago. He has been having severe leg cramps all night, and his lips are blue. He may have gotten products on his hands, but caller is unsure of the exposure details. 6/28/2013 Callback to the original caller for follow up information. The line was answered and disconnected, unable to leave a message. 7/1/2013 Callback attempted to the original caller. A message was left requesting follow up information.

To be determined by Registrant

14. Severity classification.

Minor

15. Provide supplemental information here.