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Adverse event reporting for the Johnson and Johnson COVID-19 Vaccine (Food and Drug Administration)

Jordan Bader filed this request with the Food and Drug Administration of the United States of America.
Tracking #

FDA2281373

2022-1470

FDA2281373

Multi Request Adverse event reporting for the Johnson and Johnson COVID-19 Vaccine
Status
Completed

Communications

From: Jordan Bader

To Whom It May Concern:

Pursuant to the Freedom of Information Act, I hereby request the following records:

Records of adverse effects of the Johnson & Johnson COVID-19 Vaccine.

The requested documents will be made available to the general public, and this request is not being made for commercial purposes.

In the event that there are fees, I would be grateful if you would inform me of the total charges in advance of fulfilling my request. I would prefer the request filled electronically, by e-mail attachment if available or CD-ROM if not.

Thank you in advance for your anticipated cooperation in this matter. I look forward to receiving your response to this request within 20 business days, as the statute requires.

Sincerely,

Jordan Bader

From: Food and Drug Administration

*** This is an automated message. Please do not reply to this email. ***
Reference: FDA2281373
Dear Requester,
This is to confirm that you submitted a request for record(s) from the Food and Drug Administration
pursuant to the Freedom of Information Act.
FOIA staff will review your request to determine whether it has sufficient information to be processed;
if so, you will receive another email as a formal acknowledgement of your request, with a control number for your request.
If your request is not sufficiently described,
or if there are any other deficiencies with your submission, FOIA staff will contact you via telephone or email.

From: Food and Drug Administration

Control number: 2022-1470
Please find the attached acknowledgement regarding your FOIA request. Note: Do NOT reply directly to this E-mail

From: Food and Drug Administration

Dear Requester,

FDA received your request for adverse events for a COVID19 vaccine. This information is available at:

https://wonder.cdc.gov/

Please contact me if you have questions about your request. You may also contact the FDA FOIA Public Liaison for assistance at: Office of the Executive Secretariat, US Food & Drug Administration, 5630 Fishers Lane, Room 1050, Rockville, MD 20857, E-mail: FDAFOIA@fda.hhs.gov<mailto:FDAFOIA@fda.hhs.gov>.

Sincerely,

Sarah B. Kotler, J.D.
Director, Division of Freedom of Information
US FDA
301-796-8976

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