{"database": "press", "table": "releases", "rows": [["https://steube.house.gov/press-releases/rep-steube-leads-letter-to-fda-commissioner-requesting-disclosure-of-covid-19-vaccine-adverse-effects-data/", "Rep. Steube Leads Letter to FDA Commissioner Requesting Disclosure of COVID-19 Vaccine Adverse Events Data", "2022-09-23", "2022", "2022-09", "Republican", "House", "FL", "W. Gregory Steube", "S001214", "steube.house.gov", "steube", "https://steube.house.gov/category/press-releases/page/", "scraper", "Rep. Steube Leads Letter to FDA Commissioner Requesting Disclosure of COVID-19 Vaccine Adverse Events Data\n\nWASHINGTON \u2013 U.S. Representative Greg Steube (R-Fla.) yesterday led a letter to the Food and Drug Administration (FDA) Commissioner Robert M. Califf to request full agency compliance with their obligation under law to disclose Vaccine Adverse Event Reporting (VAERS) data for the COVID-19 vaccine. The letter was cosigned by two other Members of the House of Representatives, Rep. Michael Cloud (R-Texas) and Rep. Tom Tiffany (R-Wis.).\n\n\u201cSince the COVID-19 vaccine received an Emergency Use Authorization (EUA), VAERS has received over 1.4 million reports of adverse events following the administration of the vaccine,\u201d wrote the lawmakers. \u201cIf an adverse reaction to a vaccine is identified through VAERS, scientists at the FDA should perform further tests to determine if the vaccine presents an actual risk to public health.\u201d\n\nThe Members continued, \u201cEver since the first COVID-19 vaccine received an EUA, the FDA has been noncompliant in releasing relevant data regarding the safety of the vaccine\u2026The information contained within a VAERS report could be lifesaving. It is unacceptable that the FDA would withhold such important material from the public eye.\u201d\n\nYou can read the full letter here or below:\n\nThe Honorable Robert M. Califf\n\nCommissioner\n\nU.S. Food and Drug Administration\n\n10903 New Hampshire Avenue\n\nSilver Spring, MD 20993\n\nDear Commissioner Califf:\n\nWe write concerned about the reports that the U.S. Food and Drug Administration (FDA) is refusing to provide records and analyses from the Vaccine Adverse Event Reporting System (VAERS), which your agency is obligated to disclose under 5 U.S.C. \u00a7 552(a)(3).\n\nAs you know, VAERS is the early warning database that monitors the safety of vaccines after they are authorized for use by the FDA. Since the COVID-19 vaccine received an Emergency Use Authorization (EUA), VAERS has received over 1.4 million reports of adverse events following the administration of the vaccine. If an adverse reaction to a vaccine is identified through VAERS, scientists at the FDA should perform further tests to determine if the vaccine presents an actual risk to public health.\n\nThe database has helped researchers establish that those who receive the COVID-19 vaccine may be at a higher risk for developing the following conditions:\n\nAnaphylaxis, which is a severe and potentially life-threatening allergic reaction, from the first Pfizer/BioNTech vaccinations\n\nThrombosis with thrombocytopenia syndrome (TTS) after Johnson & Johnson\u2019s Janssen Biotech COVID-19 vaccination\n\nMyocarditis (inflammation of heart muscle) or pericarditis (inflammation of the outer lining of the heart) after COVID-19 vaccination\n\nGuillain-Barr\u00e9 syndrome (GBS) after Johnson & Johnson\u2019s Janssen Biotech COVID-19 vaccination\n\nVAERS has received over 30,700 reports of death among recipients of the COVID-19 vaccine, although no causal link between the vaccine and death has been determined\n\nAdditionally, the system has been able to identify populations that may experience a more severe adverse event after receiving the vaccine based on their medical history.\n\nEver since the first COVID-19 vaccine received an EUA, the FDA has been noncompliant in releasing relevant data regarding the safety of the vaccine. In 2021, a group of medical researchers sued the FDA, stating the agency denied a Freedom of Information Act (FOIA) request to expedite the release of Pfizer-BioNTech\u2019s COVID-19 vaccine review documents. In response to the lawsuit, the FDA proposed releasing around 500 pages of the review documents each month, which would fulfill the organization\u2019s FOIA request in around 55 to 75 years.\n\nIn January 2022, a federal judge ordered the FDA to release at least 55,000 pages of material every month. However, the FDA is still refusing to release their analyses of VAERS data following a FOIA request for the records.\n\nThe information contained within a VAERS report could be lifesaving. It is unacceptable that the FDA would withhold such important material from the public eye. Americans depend on the information provided in VAERS to be able to make conscious decisions about their health and well-being. It is critical that the FDA be transparent and release important sets of data to the public. We look forward to receiving your response within 30 days.\n\nSincerely,\n\n###", 1, "2026-03-30T01:40:41Z", "2026-04-08T03:08:33Z"]], "columns": ["url", "title", "date", "year", "month", "party", "chamber", "state", "member_name", "bioguide_id", "domain", "scraper", "source", "date_source", "text", "has_text", "collected_at", "updated_at"], "primary_keys": ["url"], "primary_key_values": ["https://steube.house.gov/press-releases/rep-steube-leads-letter-to-fda-commissioner-requesting-disclosure-of-covid-19-vaccine-adverse-effects-data/"], "units": {}, "query_ms": 0.8234437555074692, "source": "dwillis/congress-press", "source_url": "https://github.com/dwillis/congress-press", "license": "MIT", "license_url": "https://github.com/dwillis/congress-press/blob/main/LICENSE"}