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Added additional references to sources of vaccine-related information
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Polyhat
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The VAERS guideline has this:

What are healthcare providers required to report to VAERS?

Healthcare providers are required by law to report to VAERS:

Healthcare providers are strongly encouraged to report:

  • Any adverse event that occurs after the administration of a vaccine licensed in the United States, whether or not it is clear that a vaccine caused the adverse event
  • Vaccine administration errors

Vaccine manufacturers are required to report to VAERS all adverse events that come to their attention.

The link to that table is:

https://vaers.hhs.gov/docs/VAERS_Table_of_Reportable_Events_Following_Vaccination.pdf

...and in that table, the days required are listed individually by vaccine. The default is seven (7) days, and in no case does the table indicate a reporting time greater than forty-two (42) days. Because the COVID vaccines are not expressly listed, one would assume that the legal reporting requirement was seven days, the default as listed for the final entry in the table.

Vaccine/Toxoid Event and interval** from vaccination
Any new vaccine recommended by the Centers for Disease Control and Prevention for routine administration to children A. Shoulder Injury Related to Vaccine Administration (7 days)
B. Vasovagal syncope (7 days)
C. Any acute complication or sequelae (including death) of above events (interval - not applicable)
D. Events described in manufacturer’s package insert

NOTE: VAERS reporting for the COVID-19 vaccine is NOT required in certain circumstances, as quoted below.

VAERS reporting is not required for the following situations:

  • If a mixed series is given intentionally (e.g., due to hypersensitivity to a vaccine ingredient)
  • Mixing and matching of booster doses (as of October 21, 2021, mixing and matching of booster doses is allowed)

Full details HERE.


More information regarding the vaccine guidelines can be found via the information packaged with it. This may be difficult to find online, but the following site seems to have some of it.

https://vaxopedia.org/2020/12/09/where-are-the-covid-19-package-inserts/

More information, on a per-vaccine/vaccine maker basis, can be found via the FDA information, such as the following:

Moderna https://www.fda.gov/media/144637/download

Janssen https://www.fda.gov/media/146304/download

Comirnaty and Pfizer-BioNTech (US formulation) https://www.fda.gov/media/153713/download

Comirnaty and Pfizer-BioNTech (alternative, non-US formulation) https://www.fda.gov/media/153715/download

The VAERS guideline has this:

What are healthcare providers required to report to VAERS?

Healthcare providers are required by law to report to VAERS:

Healthcare providers are strongly encouraged to report:

  • Any adverse event that occurs after the administration of a vaccine licensed in the United States, whether or not it is clear that a vaccine caused the adverse event
  • Vaccine administration errors

Vaccine manufacturers are required to report to VAERS all adverse events that come to their attention.

The link to that table is:

https://vaers.hhs.gov/docs/VAERS_Table_of_Reportable_Events_Following_Vaccination.pdf

...and in that table, the days required are listed individually by vaccine. The default is seven (7) days, and in no case does the table indicate a reporting time greater than forty-two (42) days. Because the COVID vaccines are not expressly listed, one would assume that the legal reporting requirement was seven days, the default as listed for the final entry in the table.

Vaccine/Toxoid Event and interval** from vaccination
Any new vaccine recommended by the Centers for Disease Control and Prevention for routine administration to children A. Shoulder Injury Related to Vaccine Administration (7 days)
B. Vasovagal syncope (7 days)
C. Any acute complication or sequelae (including death) of above events (interval - not applicable)
D. Events described in manufacturer’s package insert

NOTE: VAERS reporting for the COVID-19 vaccine is NOT required in certain circumstances, as quoted below.

VAERS reporting is not required for the following situations:

  • If a mixed series is given intentionally (e.g., due to hypersensitivity to a vaccine ingredient)
  • Mixing and matching of booster doses (as of October 21, 2021, mixing and matching of booster doses is allowed)

Full details HERE.

The VAERS guideline has this:

What are healthcare providers required to report to VAERS?

Healthcare providers are required by law to report to VAERS:

Healthcare providers are strongly encouraged to report:

  • Any adverse event that occurs after the administration of a vaccine licensed in the United States, whether or not it is clear that a vaccine caused the adverse event
  • Vaccine administration errors

Vaccine manufacturers are required to report to VAERS all adverse events that come to their attention.

The link to that table is:

https://vaers.hhs.gov/docs/VAERS_Table_of_Reportable_Events_Following_Vaccination.pdf

...and in that table, the days required are listed individually by vaccine. The default is seven (7) days, and in no case does the table indicate a reporting time greater than forty-two (42) days. Because the COVID vaccines are not expressly listed, one would assume that the legal reporting requirement was seven days, the default as listed for the final entry in the table.

Vaccine/Toxoid Event and interval** from vaccination
Any new vaccine recommended by the Centers for Disease Control and Prevention for routine administration to children A. Shoulder Injury Related to Vaccine Administration (7 days)
B. Vasovagal syncope (7 days)
C. Any acute complication or sequelae (including death) of above events (interval - not applicable)
D. Events described in manufacturer’s package insert

NOTE: VAERS reporting for the COVID-19 vaccine is NOT required in certain circumstances, as quoted below.

VAERS reporting is not required for the following situations:

  • If a mixed series is given intentionally (e.g., due to hypersensitivity to a vaccine ingredient)
  • Mixing and matching of booster doses (as of October 21, 2021, mixing and matching of booster doses is allowed)

Full details HERE.


More information regarding the vaccine guidelines can be found via the information packaged with it. This may be difficult to find online, but the following site seems to have some of it.

https://vaxopedia.org/2020/12/09/where-are-the-covid-19-package-inserts/

More information, on a per-vaccine/vaccine maker basis, can be found via the FDA information, such as the following:

Moderna https://www.fda.gov/media/144637/download

Janssen https://www.fda.gov/media/146304/download

Comirnaty and Pfizer-BioNTech (US formulation) https://www.fda.gov/media/153713/download

Comirnaty and Pfizer-BioNTech (alternative, non-US formulation) https://www.fda.gov/media/153715/download

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Source Link
Polyhat
  • 325
  • 1
  • 8

The VAERS guideline has this:

What are healthcare providers required to report to VAERS?

Healthcare providers are required by law to report to VAERS:

Healthcare providers are strongly encouraged to report:

  • Any adverse event that occurs after the administration of a vaccine licensed in the United States, whether or not it is clear that a vaccine caused the adverse event
  • Vaccine administration errors

Vaccine manufacturers are required to report to VAERS all adverse events that come to their attention.

The link to that table is:

https://vaers.hhs.gov/docs/VAERS_Table_of_Reportable_Events_Following_Vaccination.pdf

...and in that table, the days required are listed individually by vaccine. The default is seven (7) days, and in no case does the table indicate a reporting time greater than forty-two (42) days. Because the COVID vaccines are not expressly listed, one would assume that the legal reporting requirement was seven days, the default as listed for the final entry in the table.

Vaccine/Toxoid Event and interval** from vaccination
Any new vaccine recommended by the Centers for Disease Control and Prevention for routine administration to children A. Shoulder Injury Related to Vaccine Administration (7 days)
B. Vasovagal syncope (7 days)
C. Any acute complication or sequelae (including death) of above events (interval - not applicable)
D. Events described in manufacturer’s package insert

NOTE: VAERS reporting for the COVID-19 vaccine is NOT required in certain circumstances, as quoted below.

VAERS reporting is not required for the following situations:

  • If a mixed series is given intentionally (e.g., due to hypersensitivity to a vaccine ingredient)
  • Mixing and matching of booster doses (as of October 21, 2021, mixing and matching of booster doses is allowed)

Full details HERE.

The VAERS guideline has this:

What are healthcare providers required to report to VAERS?

Healthcare providers are required by law to report to VAERS:

Healthcare providers are strongly encouraged to report:

  • Any adverse event that occurs after the administration of a vaccine licensed in the United States, whether or not it is clear that a vaccine caused the adverse event
  • Vaccine administration errors

Vaccine manufacturers are required to report to VAERS all adverse events that come to their attention.

The link to that table is:

https://vaers.hhs.gov/docs/VAERS_Table_of_Reportable_Events_Following_Vaccination.pdf

...and in that table, the days required are listed individually by vaccine. The default is seven (7) days, and in no case does the table indicate a reporting time greater than forty-two (42) days. Because the COVID vaccines are not expressly listed, one would assume that the legal reporting requirement was seven days, the default as listed for the final entry in the table.

Vaccine/Toxoid Event and interval** from vaccination
Any new vaccine recommended by the Centers for Disease Control and Prevention for routine administration to children A. Shoulder Injury Related to Vaccine Administration (7 days)
B. Vasovagal syncope (7 days)
C. Any acute complication or sequelae (including death) of above events (interval - not applicable)
D. Events described in manufacturer’s package insert

The VAERS guideline has this:

What are healthcare providers required to report to VAERS?

Healthcare providers are required by law to report to VAERS:

Healthcare providers are strongly encouraged to report:

  • Any adverse event that occurs after the administration of a vaccine licensed in the United States, whether or not it is clear that a vaccine caused the adverse event
  • Vaccine administration errors

Vaccine manufacturers are required to report to VAERS all adverse events that come to their attention.

The link to that table is:

https://vaers.hhs.gov/docs/VAERS_Table_of_Reportable_Events_Following_Vaccination.pdf

...and in that table, the days required are listed individually by vaccine. The default is seven (7) days, and in no case does the table indicate a reporting time greater than forty-two (42) days. Because the COVID vaccines are not expressly listed, one would assume that the legal reporting requirement was seven days, the default as listed for the final entry in the table.

Vaccine/Toxoid Event and interval** from vaccination
Any new vaccine recommended by the Centers for Disease Control and Prevention for routine administration to children A. Shoulder Injury Related to Vaccine Administration (7 days)
B. Vasovagal syncope (7 days)
C. Any acute complication or sequelae (including death) of above events (interval - not applicable)
D. Events described in manufacturer’s package insert

NOTE: VAERS reporting for the COVID-19 vaccine is NOT required in certain circumstances, as quoted below.

VAERS reporting is not required for the following situations:

  • If a mixed series is given intentionally (e.g., due to hypersensitivity to a vaccine ingredient)
  • Mixing and matching of booster doses (as of October 21, 2021, mixing and matching of booster doses is allowed)

Full details HERE.

Source Link
Polyhat
  • 325
  • 1
  • 8

The VAERS guideline has this:

What are healthcare providers required to report to VAERS?

Healthcare providers are required by law to report to VAERS:

Healthcare providers are strongly encouraged to report:

  • Any adverse event that occurs after the administration of a vaccine licensed in the United States, whether or not it is clear that a vaccine caused the adverse event
  • Vaccine administration errors

Vaccine manufacturers are required to report to VAERS all adverse events that come to their attention.

The link to that table is:

https://vaers.hhs.gov/docs/VAERS_Table_of_Reportable_Events_Following_Vaccination.pdf

...and in that table, the days required are listed individually by vaccine. The default is seven (7) days, and in no case does the table indicate a reporting time greater than forty-two (42) days. Because the COVID vaccines are not expressly listed, one would assume that the legal reporting requirement was seven days, the default as listed for the final entry in the table.

Vaccine/Toxoid Event and interval** from vaccination
Any new vaccine recommended by the Centers for Disease Control and Prevention for routine administration to children A. Shoulder Injury Related to Vaccine Administration (7 days)
B. Vasovagal syncope (7 days)
C. Any acute complication or sequelae (including death) of above events (interval - not applicable)
D. Events described in manufacturer’s package insert