New incident report
Incident Report Number: 2020-4697
Registrant Reference Number: 6273114
Registrant Name (Full Legal Name no abbreviations): Premier Tech Brighton Ltd
Address: 10 Loyalist Dr
City: Brighton
Prov / State: ON
Country: Canada
Postal Code: K0K 1H0
Human
Country: CANADA
Prov / State: PRINCE EDWARD ISLAND
PMRA Registration No. 13074 PMRA Submission No. EPA Registration No.
Product Name: Pro Ant and Roach Pyrodust
Yes
Unknown
Site: Res. - In Home / Rés. - à l'int. maison
Unknown
Data Subject
Sex: Female
Age: >19 <=64 yrs / >19 <=64 ans
System
Unknown / Inconnu
Yes
Unknown
Unknown
Unknown
Unknown
Unknown / Inconnu
Unknown / Inconnu
Caller reports that they have a bug problem and an agency came and put an insecticide all over house. This is the 2nd application. Applied one time in August. And then another one last Tuesday. She had a reaction the first time as well that was prolonged. Product applied Tuesday last week. And stayed away from home. Doctor had said with her sensitivity to stay away longer. She went home Sunday to clean up an ended up the the ER. In the ER this time she got EPI and Benadryl. She is to be on Benadryl for the next few days to avoid her Epi. She is on Prednisone. Her face off and on symptomatic - if coming due for her next meds it is flushed and warm and tingling face. Today not terrible. Addendum Late entry clarification: In call, (name)/patient reports two separate exposures. 1. Most recent exposure; applied one time in August. Date of application Tuesday August 18th. Returned to house on Sunday the 23rd of August. Experienced a reaction and went to emergency department and was treated and released. 2. Prior exposure; on or around November 25, 2019 product applied, exposure and hospitalization. Prolonged recovery period. Caller reports that the emergency room sent a picture of the product to her phone and the product is "Domestic" and the Reg. Number is 13074 PCP ACT (This PCP code matches the Pro Ant and Roach Pyrodust PCP code.) A: Clarification: Adverse reaction to Pyrethrin product PCP Reg Number 13074. Patient medically evaluated, treated, and released.
Moderate
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 th reported clinical effects are causally related to exposure to the product identified.