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First vaccine-related thrombosis confirmed in Sask.

The province of Saskatchewan has confirmed the first case of vaccine-induced immune thrombotic thrombocytopenia (VITT). The patient is a female aged 60-69 who had received the AstraZeneca/COVISHIELD vaccine on April 11.
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The province of Saskatchewan has confirmed the first case of vaccine-induced immune thrombotic thrombocytopenia (VITT). The patient is a woman aged 60-69.

The province of Saskatchewan has confirmed the first case of vaccine-induced immune thrombotic thrombocytopenia (VITT). The patient is a female aged 60-69 who had received the AstraZeneca/COVISHIELD vaccine on April 11. She has received treatment and is recovering. 

At this time, public health is planning to offer the second dose of COVID-19 vaccine to match the brand of the first dose received. However, national reviews of the safety and efficacy of interchanging the second dose brand are ongoing. As more evidence comes forward suggesting mixing brands is safe and based on the brand allocations we receive in Saskatchewan, public health recommendations on second doses may be updated. 

According to the Public Health Agency of Canada (PHAC), there were 18 confirmed reports of VITT in Canada as of May 12. Saskatchewan's confirmed case has been reported to PHAC for inclusion in the national statistics.   

As of May 1, PHAC is reporting nearly 2,050,000 first doses of AstraZeneca and AstraZeneca/COVISHIELD have been administered in Canada. Saskatchewan has administered approximately 72,000 AstraZeneca first doses to date. Internationally, reported rates of similar adverse events relative to AstraZenca at this time range from one per 26,500 (Norway), one in 50,000 (Netherlands) to one per 100,000 (UK) and one in 127,300 (Australia).

Adverse events to any immunization can range from minor side effects (ie local pain, swelling at injection site) to more severe reactions. Minor side effects usually occur within a few hours of injection and resolve after short period of time. Immunizers know the signs of allergic reactions and are prepared to take immediate action. This is why all residents are asked to remain at the vaccination clinic for 10 to 15 minutes following their immunization. 

Individuals who experience a severe or unusual reaction after getting a COVID-19 vaccination can report it by calling 811. Anyone experiencing a severe reaction such as difficulty breathing should call 911.  Any adverse event that may be related to a vaccination is reported in order to continuously monitor the safety of vaccines.