Media Release: CARPHA Announces Campaign To Promote Reporting Of Vaccine Side Effects

Press Release:-  The Caribbean Regulatory System (CRS) of the Caribbean Public Health Agency (CARPHA), in collaboration with the Pan American Health Organization / World Health Organization (PAHO/WHO), launches a week-long social media campaign to promote the importance of reporting suspected side effects following vaccination to the CRS or to national reporting systems.

Taking place from 1–7 November 2021, the sixth annual #MedSafetyWeek social media campaign will focus on vaccines. Medicines agencies from 64 countries will be encouraging healthcare professionals, national immunisation programme staff, as well as patients, their carers and families, to report problems experienced with vaccines including COVID-19 shots.

Vaccines are among the most important advances in medicine saving millions of lives annually and have proven to be the best method to protect individuals against infectious diseases. However, as with all medicines, side effects can happen.

According to Mr. Dean Chambliss, PAHO Subregional Program Director, Caribbean, “This campaign comes at a critical moment when millions of people are vaccinated against COVID-19.

Vaccine safety begins with the timely detection and reporting of adverse events following immunization. It is important to report suspected adverse events of vaccines and by extension all medicines.

Each report counts but to have an impact, countries need to assess this information and share safety updates regularly with the international community.”

In August 2021, CARPHA launched its online reporting form for adverse events following
immunization (AEFI) which can be used for any vaccine, including the novel COVID-19 vaccines.

Dr. Joy St. John, CARPHA Executive Director stated: “The reporting of an adverse effect following vaccination does not mean the event has been caused by the vaccine, or that the person who gave the vaccine made an error, but it is an important part of helping the national authorities to identify events that may need to be investigated further. The information from investigations and data analyses will assist Member States in identifying the types of reactions that persons are experiencing, and any additional monitoring or regulatory actions that may be needed.”

Reporting of side effects that last longer than three days, and those that cause persons to see a doctor is an important part of checking and ensuring that approved vaccines remain safe when used in larger populations.

Health workers are encouraged to use the relevant vaccine product information
from trusted sources, in order to guide patients, parents and caregivers.

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