Welcome to AstraZeneca Medical

You can use this site to report an adverse event or product quality complaint. You can also ask a medical information inquiry.

What can we help you with?

Select all that apply

Adverse events are sometimes known as side effects and are unwanted or unexpected events or reactions to a medicine or device.

Medical Information enquiries are medical or scientific questions relating to our medicines and devices.

Product quality complaints relate to a physical issue with a medicine or a device and/or its packaging.

Please select an option

Adverse Event Reporting

Adverse events are sometimes known as side effects and are unwanted or unexpected events or reactions to a medicine.

Medical Information Enquiry

Medical Information enquiries are medical or scientific questions relating to our medicines and devices.

Product Quality Complaint

Product quality complaints relate to a physical issue with a medicine or device and/or its packaging

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AstraZeneca Medical

Patient Information

Pharmaceutical companies are required to report certain adverse events occurring in Northern Ireland to the European Medicines Agency.

Required by the health authorities.

Contact Information

Demographics

If the exact date is unknown, please enter month and year, or year.

Height

Weight

Height

Weight

Last Menstrual Date
Due Date

Reporter Information

It looks like you are reaching out on behalf of an HCP. Please provide details about yourself.

Health Care Provider

Pharmaceutical companies are required to report certain adverse events occurring in Northern Ireland to the European Medicines Agency.

Required by the health authorities.

Contact Information

Caregiver Information

Pharmaceutical companies are required to report certain adverse events occurring in Northern Ireland to the European Medicines Agency.

Required by the health authorities.

Contact Information

Your Information

Which best describes your role in AstraZeneca?

I am a ...

AZ initial aware date*

Patient Information

Pharmaceutical companies are required to report certain adverse events occurring in Northern Ireland to the European Medicines Agency.

Required by the health authorities.

Contact Information

Demographics

If the exact date is unknown, please enter month and year, or year.

Height

Weight

Height

Weight

Last Menstrual Date
Due Date

Caregiver Information

Pharmaceutical companies are required to report certain adverse events occurring in Northern Ireland to the European Medicines Agency.

Required by the health authorities.

Contact Information

Reporter Information

It looks like you are reaching out on behalf of an HCP. Please provide details about yourself.

Health Care Provider

Pharmaceutical companies are required to report certain adverse events occurring in Northern Ireland to the European Medicines Agency.

Required by the health authorities.

Contact Information

Patient Information

Pharmaceutical companies are required to report certain adverse events occurring in Northern Ireland to the European Medicines Agency.

Required by the health authorities.

Contact Information

Demographics

If the exact date is unknown, please enter month and year, or year.

Height

Weight

Height

Weight

Last Menstrual Date
Due Date

Health Care Provider

Health Care Provider’s Details

Health Care Provider’s Contact Information

Please provide at least one contact method

Adverse Event Medication / Device

Please add each medication / device separately using the Add Medication / Device button.

Expiration Date

Medication dates

Start Date

If the exact date is unknown, please enter month and year, or year.

End Date

If the exact date is unknown, please enter month and year, or year.

Vaccination Details

Dose 1