report adverse reaction to vaccine

the vaccine adverse event reporting system (vaers) is a national program which collects information about adverse events associated with vaccinations for the purpose of monitoring the safety of vaccines used in the united states. vaers provides a database management system for the collection and analysis of these reports. these agencies monitor vaers reports to determine if any vaccine or vaccine lot has a higher than expected rate of events and the types of events reported for each vaccine. the louisiana immunization program is not part of the reporting system and does not analyze or utilize any of the information submitted to vaers. reports are usually submitted by health care providers, vaccine manufacturers, and vaccine recipients (or their parents or guardians).




patients, parents, and guardians are encouraged to seek the help of the vaccine provider in reporting adverse events. vaccine providers are required to report any event listed in ncvia reportable event table and any event listed in the package insert as a contraindication to subsequent doses. a report is not documentation that a vaccine caused the event. if you are a vaccine manufacturer or a professional who administers vaccines, you are required by law to report certain adverse events found in the reportable event table (pdf) . note: a report submitted to vaers does not initiate a report or claim wiith the national vaccine compensation program vicp).

the vaccine adverse event reporting system (vaers) is a national program which collects information about adverse events associated with vaccinations to monitor the safety of vaccines used in the united states. vaers provides a database management system for the collection and analysis of these reports. these agencies monitor vaers reports to determine if any vaccine or vaccine lot has a higher than expected rate of events and the types of events reported for each vaccine. the texas department of state health services (dshs) is not part of the reporting system but is available to assist with questions about vaccine safety or adverse event reporting by email to imm.epi@dshs.texas.gov. anyone can report to vaers. patients, parents, and guardians are encouraged to seek the help of the vaccine provider in reporting adverse events.

vaccine providers are required to report any event listed by the vaccine manufacturer as a contraindication to further  doses of the vaccine, and certain events listed in the vaers table of reportable events following vaccination that happens within a specific time period after vaccination. healthcare providers are also encouraged to report vaccine administration errors through vaers. each report of an adverse event provides valuable information that is added to the vaers database. accurate, complete, and timely reporting of post-vaccination health issues provides important information for vaccine safety monitoring and research. please note that a report to vaers does not initiate a report to or file a claim with the national vaccine injury compensation program (vicp). to file a report with the nvicp, please visit the vicp website.

important: if you are experiencing a medical emergency, seek immediate assistance from a healthcare provider or call 9-1-1. cdc and fda do not provide vaers is an early warning system used to monitor adverse events that happen after vaccination. learn how vaers reports are submitted and reviewed. vaers is the national vaccine safety monitoring system that accepts reports of adverse events after vaccination. the system can quickly detect potential, .

if you experience an adverse event (not a side effect) from one of our drugs, tell your doctor and then report it to us. this helps us track the safety of vaers is a national vaccine safety surveillance program created as an outgrowth of the national childhood vaccine injury act of 1986 (ncvia) anyone can report a post-vaccination health issue to the vaccine adverse event reporting system—which anti-vaccination activists often, .

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