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Moderna vaccine side effect how to#
Moderna vaccine side effect update#

Which vaccines are approved for use in Singapore? Which of these vaccines are included in the national vaccination programme? Can the vaccines protect me against all strains of COVID-19?Ĭlick Ctrl+F (On Windows) or Cmd+F (On Mac) to look for word of interest, or find latest FAQs on top of each section.How effective is the vaccine? How long does the protection last?.What happens if I develop an allergic reaction to my first dose?.What are the side effects of COVID-19 Vaccination? What should I do if I suffer from any side effects?.Will the COVID-19 vaccine cause infertility?.Is COVID-19 vaccination safe for those with chronic illness such as hypertension, high cholesterol and diabetes?.How can I be sure that it is medically safe for me to get vaccinated?.

What is myocarditis and pericarditis? Can the vaccine lead to myocarditis and pericarditis?.

How can we be sure that scientific rigour has not been compromised?

Vaccines for COVID-19 have been approved for use in a shortened timeframe compared to other vaccines or drugs.

What is the difference between the Bivalent Moderna/Spikevax and the Bivalent Pfizer-BioNTech/Comirnaty COVID-19 vaccines? Which should I receive?.

bivalent Moderna/Spikevax or bivalent Pfizer-BioNTech/Comirnaty) and the original vaccines?

What are the differences between the bivalent vaccines (e.g.

Are mRNA vaccines a form of genetic modification?.

Which vaccines are approved for use in Singapore? Which of these vaccines are included in the national vaccination programme?.

Patients and healthcare professionals should report any suspected side effects after receiving a COVID-19 vaccine to their national competent authority.

Moderna vaccine side effect update#

If needed, EMA may decide to update the vaccine's product information to provide the right advice to healthcare professionals and patients, require the manufacturer to conduct additional studies, or restrict the use of the vaccine. The PRAC then conducts a robust assessment of all combined safety data before concluding on how the signal affects the vaccine's safety and its benefit-risk balance. They review other sources of evidence, such as clinical studies, epidemiology and pharmacoepidemiology studies, the medical literature and information from regulators outside the EU. When assessing a safety signal, the PRAC looks for any unusual or unexpected patterns, such as a medical event occurring in vaccinated people at a higher rate than in the general population. The EU safety monitoring plan for COVID-19 vaccines requires EMA to monitor suspected side effects reported by individuals and healthcare professionals in the EU.Īn EU database called EudraVigilance holds these reports. The European suspected adverse drug reactions database provides public access to these data in a number of ways, while taking account of EU data protection law.ĮMA’s PRAC and the national competent authorities continuously monitor EudraVigilance to identify any new safety issues that require investigation.

Moderna vaccine side effect how to#

Important information on how to interpret the data.

European suspected adverse drug reactions database (.

European Centre for Disease Prevention and Control (ECDC) vaccine tracker.

If the PRAC recommends important safety-related changes to the product information of COVID-19 vaccines, EMA will include these in the PRAC highlights. Therefore, regular monthly safety updates are no longer necessary. These data have established the safety profiles of these vaccines. The wide uptake of COVID-19 vaccines during the COVID-19 pandemic led to the rapid accumulation of extensive safety data from clinical trials, studies and spontaneous reporting on side effects. In total, EMA published more than 50 monthly COVID-19 vaccine safety updates, beginning in December 2020.īy December 2022, the majority of the EU population had received at least one COVID-19 vaccine. EMA published the final issue of its monthly safety update on COVID-19 vaccines in December 2022.ĮMA’s monthly safety updates provided information from the Pharmacovigilance Risk Assessment Committee ( PRAC)'s assessment of COVID-19 vaccines, along with data on the number of doses administered in the EU/EEA.