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Healthcare providers are required to report the following adverse events after COVID-19 vaccination, and other adverse events if later revised by CDC, to VAERS:• Visit the for more information about Secure Sockets Layer and data transmission Patient information age, date of birth, sex• Medical tests and laboratory results if applicable• The Vaccine Adverse Event Reporting System VAERS accepts all reports, including reports of vaccination errors
is available if you have additional questions Inpatient hospitalization or prolongation of existing hospitalization;•

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Online reporting is strongly encouraged.

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VAERS is a passive reporting system, meaning it relies on individuals to send in reports of their experiences
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Date and time when adverse event s started• Please report clinically important adverse events that occur after vaccination of adults and children, even if you are not sure whether the vaccine caused the adverse event
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Serious adverse events AEs regardless of causality
Anyone can submit a report to VAERS, including parents and patients Important medical events that may not result in death, be life-threatening, or require hospitalization may be considered serious when, based upon appropriate medical judgment, they may jeopardize the patient and may require medical or surgical intervention to prevent one of the outcomes listed above
Two Ways to Submit an Online Report to VAERS What will I need to fill out the report? An adverse event listed by the vaccine manufacturer as a contraindication to further doses of the vaccine Healthcare providers are strongly encouraged to report to VAERS:• Healthcare providers are required by law to report to VAERS:• Healthcare professionals are encouraged to report any clinically significant adverse event following vaccination to VAERS, even if they are not sure if vaccination caused the event Cases of observed Multisystem Inflammatory Syndrome• Persistent or significant incapacity or substantial disruption of the ability to conduct normal life functions;• Vaccination administration errors, whether or not associated with an adverse event• , administering a live vaccine to an immunocompromised patient or that the error would be preventable with public health action or education

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Any adverse event that occurs after the administration of a vaccine licensed in the United States, whether it is or is not clear that a vaccine caused the adverse event• For example, a healthcare professional may elect to report vaccination errors that do not have an associated adverse health event, especially if they think the vaccination error may pose a safety risk e.

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Knowingly filing a false VAERS report is a violation of Federal law 18 U
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VAERS is primarily concerned with monitoring adverse health events and we encourage reporting of clinically significant adverse health events following vaccination
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Symptoms and outcome of the adverse event s• Serious AEs are defined as:• You or your health care provider may be contacted for further information after your report is received
Vaccine administration errors Vaccine manufacturers are required to report to VAERS all adverse events that come to their attention Vaccine information brand name, dosage• Using clinical judgment, healthcare professionals can decide whether or not to report a medical error at their own discretion
Any adverse event listed in the that occurs within the specified time period after vaccinations• Date, time, and location administered• Information supplied in the online submission form is transmitted securely to VAERS

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اللائحة التنفيذية لنظام الأحداث