Adverse Event/Side effectProduct Complaint
Reporter contact information/Initials*
Reporter Phone*
Reporter e-mail address*
Province* Select ProvinceAlbertaBritish ColumbiaManitobaNew BrunswickNewfoundland and LabradorNova ScotiaNorthwest TerritoriesNunavutOntarioPrince Edward IslandQuebecSaskatchewanYukon
HCP (Other Health Care Professional)DoctorPharmacistConsumer/Relative/OtherNurse
USAMexicoCanadaOther
Other Country
YesNo
Product/Drug name*
Dosage/Route/Frequency
Therapy Start date
Lot#
Product Expiry date
Reason for use of B+L product*
Patient Initials*
Date of birth
Height/Weight of Patient
Please select from below option
Elderly (Adult 65+ or other age group)AdultAdolescentChildrenInfant
FemaleMaleNon-binaryPrefer not to say
White or CaucasianFirst Nation or NativeAsianLatino or HispanicOther
YesNoN/A
Please describe the Adverse reaction/Side effect/Product complaint*
Please describe Concomitant Medication (Include medications taken within 30 days before Adverse Reaction onset. Do not include medications taken as a treatment for the Adverse Reaction)
Please provide Relevant Tests/Laboratory Data (including dates) (yyyy-mm-dd)
Please provide Other Relevant History, Including Pre-existing Medical Conditions (e.g., allergies, pregnancy, smoking etc.)
Date signed *
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