{"database": "press", "table": "releases", "rows": [["https://www.murphy.senate.gov/newsroom/press-releases/murphy-blumenthal-join-entire-senate-democratic-caucus-in-demanding-answers-from-trump-admin-on-new-review-of-mifepristone-despite-decades-of-evidence-proving-its-safety-and-efficacy", "Murphy, Blumenthal Join Entire Senate Democratic Caucus In Demanding Answers From Trump Admin On New \u201cReview\u201d Of Mifepristone Despite Decades Of Evidence Proving Its Safety & Efficacy", "2025-11-13", "2025", "2025-11", "Democrat", "Senate", "CT", "Christopher Murphy", "M001169", "www.murphy.senate.gov", "chrismurphy", "https://www.murphy.senate.gov/newsroom/press-releases", "scraper", "WASHINGTON\u2014U.S. Senators Chris Murphy (D-Conn.), a member of the Health, Education, Labor, and Pensions (HELP) Committee, and Richard Blumenthal (D-Conn.) joined the entire Senate Democratic caucus in a letter to U.S. Department of Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. and U.S. Food and Drug Administration (FDA) Commissioner Marty Makary expressing alarm over the Trump administration's plans to conduct \u201cits own review of the evidence\u201d on the safety and effectiveness of mifepristone.\n\nMifepristone was approved by the FDA in 2000 and is used in the overwhelming majority of abortions in the United States. Access to medication abortion is more critical than ever in the aftermath of the Supreme Court\u2019s disastrous Dobbs decision that overturned the Constitutional right to abortion and allowed dozens of states to enact extreme abortion bans that threaten women\u2019s health and lives. According to data from Guttmacher, medication abortion accounted for nearly two-thirds of abortions in the U.S. in 2023, the first year after the Dobbs decision.\n\n\u201cDecades of evidence and hundreds of studies prove the safety and efficacy of mifepristone, which is not only the most common method of abortion in the U.S., but is also frequently prescribed to women to help manage early pregnancy loss or miscarriage. We are alarmed by the Department\u2019s obvious attempts to politicize the review, regulation, and approval of mifepristone at the FDA, and we write to request more information,\u201d the senators wrote.\n\nThe letter lays into a recent junk science \u201creport\u201d put out by the Ethics and Public Policy Center (EPPC), an avowedly anti-abortion think tank, that appears to be the basis for the Trump administration\u2019s announced review of mifepristone. The EPPC report parrots anti-abortion disinformation, was not peer-reviewed or published in any medical journal and has been widely criticized by reputable health organizations since its release.\n\n\u201cBy elevating the sham EPPC report as rationale for restricting access to mifepristone, HHS is blatantly undermining well-established science and weaponizing disinformation to fit the Trump administration\u2019s clear agenda to cut off abortion access in any way possible,\u201d the senators continued. \u201cFDA relying on a partisan, sham report as part of the evidence review for any drug is deeply concerning\u2014and in this case, it\u2019s clear that the Trump administration is downright eager to do away with established science if it helps further their extreme anti-abortion agenda.\u201d\n\nMifepristone is already subject to burdensome Risk Evaluation and Mitigation Strategy (REMS) requirements that must be followed for prescribing and dispensing mifepristone\u2014in fact, FDA already restricts mifepristone more heavily than 99.5% of the over 20,000 prescription drugs it regulates. On October 30th, a federal court ruled that the FDA\u2019s explanation for its current restrictions on mifepristone is unreasoned, unsupported, and illogical. In their letter, the senators ask how the administration plans to comply with this ruling and ensure any review of mifepristone is consistent with the court order.\n\n\u201cThat court order reinforces that, in conducting this new review, FDA may not cherry-pick junk science serving an anti-abortion agenda, but must instead look at the full body of evidence both confirming mifepristone\u2019s safety and underscoring the harms of the FDA\u2019s onerous restrictions,\u201d the senators wrote.\n\n\u201cThe bottom line is that access to mifepristone allows patients to receive time-sensitive, essential health care, including abortion care and miscarriage management,\u201d the senators continued. \u201cIf HHS insists on rejecting the science that clearly proves mifepristone is safe and effective, and instead decides to impose additional restrictions on its use, this will force countless women to carry pregnancies to term against their will\u2014regardless of the consequences for their health or lives.\u201d\n\nThe Senate Democrats concluded by demanding answers to a number of detailed questions, including what exactly prompted the administration to initiate the review, what process will be used to conduct it, whether there is any unreported data on adverse events it is considering, and how FDA will ensure compliance with the court order in Purcell v. Kennedy: \u201cThe American people need to be able to trust that any reviews, regulations, and approvals of medication by HHS and FDA are based on science and evidence\u2014not on partisan attempts to attack abortion access. It is critical that scientific experts and evidence are central to any FDA review or REMS initiative. Mifepristone has long been shown to be safe and effective, and there is no new evidence to justify burdensome restrictions that block women from getting the health care they need.\u201d\n\nThe full letter is available HERE and below.\n\nDear Secretary Kennedy and Commissioner Makary,\n\nWe write today with serious concerns about the U.S. Department of Health and Human Services\u2019 (HHS or the Department) announcement that it will conduct, through the U.S. Food and Drug Administration (FDA), \u201cits own review of the evidence\u201d on the safety and effectiveness of mifepristone, which has been approved by the FDA since 2000 for the medical termination of pregnancy. Decades of evidence and hundreds of studies prove the safety and efficacy of mifepristone, which is not only the most common method of abortion in the U.S., but is also frequently prescribed to women to help manage early pregnancy loss or miscarriage. We are alarmed by the Department\u2019s obvious attempts to politicize the review, regulation, and approval of mifepristone at the FDA, and we write to request more information on the details of the review of mifepristone. We are especially troubled by this administration\u2019s clear intent to tee up further restrictions on medication abortion, in light of a recent federal court order holding that the agency has failed to justify its current extreme restrictions on mifepristone and must consider lifting them.\n\nIn an April 28, 2025 letter, Senator Hawley called on the FDA to revisit its existing restrictions on mifepristone, alleging the \u201cresearch showing the safety risks\u201d of medication abortion are \u201cfar greater than the FDA currently acknowledges.\u201d The same day, the avowedly anti-abortion think tank Ethics and Public Policy Center (EPPC) published a junk science \u201creport\u201d that parrots anti-abortion disinformation, was not peer-reviewed or published in any medical journal, and has been widely criticized by reputable health organizations. Based on apparently nothing but the nakedly partisan and easily debunked EPPC report, Commissioner Makary committed to conducting a new review of mifepristone in a June 2, 2025 letter. Secretary Kennedy and Commissioner Makary similarly sent a September 19, 2025 letter to Republican attorneys general, highlighting the EPPC report as alleged evidence of the \u201cpotential dangers that may attend offering mifepristone without sufficient medical support or supervision.\u201d By elevating the sham EPPC report as rationale for restricting access to mifepristone, HHS is blatantly undermining well-established science and weaponizing disinformation to fit the Trump administration\u2019s clear agenda to cut off abortion access in any way possible.\n\nMifepristone has been proven to be safe and effective in hundreds of studies over more than two decades, and this has been backed up by the American College of Obstetricians and Gynecologists (ACOG)\u2014which represents more than 90% of the nation\u2019s OBGYNs, the American Medical Association (AMA), the Society for Maternal-Fetal Medicine, and the Society of Family Planning. While the EPPC report makes unsubstantiated claims about the rate of adverse events following medication abortion, the safety label for mifepristone clearly states that \u201cserious adverse reactions were reported in <0.5% of women\u201d in accordance with the data from 10 clinical trials of more than 30,000 women in settings in the U.S. and abroad. And, the FDA\u2019s own website states that \u201cthe FDA\u2019s periodic reviews of the postmarketing data for Mifeprex and its approved generic have not identified any new safety concerns with the use of mifepristone for medical termination of pregnancy through 70 days.\u201d\n\nThere are numerous serious methodological issues with the EPPC report, whose analyses cannot be verified or replicated due to EPPC\u2019s failure to transparently share its data sources. As the Society of Family Planning stated in a May letter to Commissioner Makary, \u201cthis paper is not a methodologically rigorous, evidence-based resource, and does not warrant consideration, particularly in scientific spaces.\u201d The FDA should be using gold-standard science and evidence when making decisions about medication access for the American people. Typically, the FDA relies on its Adverse Event Reporting System (FAERS) or other postmarketing surveillance data to consider the safety risk of a particular drug, not unverified claims from a debunked report. FDA relying on a partisan, sham report as part of the evidence review for any drug is deeply concerning\u2014and in this case, it\u2019s clear that the Trump administration is downright eager to do away with established science if it helps further their extreme anti-abortion agenda.\n\nIt is also important to note that mifepristone is already subject to burdensome Risk Evaluation and Mitigation Strategy (REMS) requirements that must be followed for prescribing and dispensing mifepristone. The REMS already restricts the number of providers who can prescribe or dispense the drug, and the FDA already restricts mifepristone more heavily than 99.5% of the over 20,000 prescription drugs it regulates, making it more difficult for women to receive the timely access to care they need. On January 3, 2023, the FDA approved a modification to the mifepristone REMS, which included permanent removal of the requirement that the drug be dispensed in-person, and the addition of a new pharmacy certification process to allow qualified retail pharmacies to dispense mifepristone to patients with a prescription. These commonsense changes allow for improved access to mifepristone, yet the REMS criteria continues to impose unnecessary restrictions that cause administrative burdens for providers, which may impede their ability to provide the medication, thus impacting patient access.\n\nLeading health experts, including ACOG and the AMA, have long advocated for removal of the mifepristone REMS, given that the restrictions do not make care safer and are not based on medical evidence or need. ACOG argues these restrictions only create further barriers to abortion care and medical management of early pregnancy loss, particularly for communities that already face structural barriers to care.\n\nAbortion opponents are particularly focused on reinstating an \u201cin-person dispensing\u201d requirement for mifepristone. This would force every patient in the country to travel, in some cases hundreds of miles, to pick up the medication in-person at a health center. This mandate would apply even when the patient has been thoroughly evaluated and counseled by a licensed provider via telemedicine and there is no clinical reason to necessitate a health center visit, and even when it would be extremely burdensome or impossible to arrange the transportation, childcare, and time off work necessary for that in-person trip. Yet, as the FDA itself found, \u201cthere does not appear to be a difference in adverse events between periods when the in-person dispensing requirement was being enforced and periods when the in-person dispensing requirement was not being enforced. This suggests that mifepristone may be safely used without an in-person dispensing requirement.\u201d\n\nOn October 30, 2025, a federal court ruled in Purcell v. Kennedy that the FDA\u2019s explanation for its current restrictions on mifepristone is unreasoned, unsupported, and illogical; that the FDA did not engage with the objections of preeminent medical associations like ACOG and AMA that the mifepristone REMS is medically unnecessary and harmful; and that the FDA ignored peer-reviewed research showing both that mifepristone remains extremely safe when regulated like other prescription drugs and that the FDA\u2019s restrictions significantly reduce patient access. The court also found that the FDA failed to meaningfully address the guardrails that Congress imposed on the agency\u2019s authority to impose a REMS. That court order reinforces that, in conducting this new review, FDA may not cherry-pick junk science serving an anti-abortion agenda, but must instead look at the full body of evidence both confirming mifepristone\u2019s safety and underscoring the harms of the FDA\u2019s onerous restrictions.\n\nThe bottom line is that access to mifepristone allows patients to receive time-sensitive, essential health care, including abortion care and miscarriage management. Medication abortion is a critical option for patients who want to end their pregnancy in a place of their choosing, with access to the medical support and information they need. This option is particularly essential for patients who live in remote or rural areas and those who already face barriers to care due to inequities in our country\u2019s health care system. If HHS insists on rejecting the science that clearly proves mifepristone is safe and effective, and instead decides to impose additional restrictions on its use, this will force countless women to carry pregnancies to term against their will\u2014regardless of the consequences for their health or lives.\n\nAs you review the evidence regarding the safety and efficacy of mifepristone, we request responses to the following questions by November 28, 2025:\n\nFollowing the March 6, 2025 HELP Committee hearing to consider Dr. Makary\u2019s nomination to be FDA Commissioner, he was asked, in a question for the record, if he planned to make any changes to how mifepristone can be prescribed, dispensed, or accessed. He responded: \u201cI have no immediate plans to make changes to regulation of any specific products and would not do so without a fulsome review of safety and efficacy data.\u201d What qualifies as a \u201cfulsome review of safety and efficacy data?\u201d\n\nWhat prompted the Department to initiate the recent review of mifepristone?\n\nWhat studies or data are HHS or FDA relying on to justify restrictions on mifepristone, including but not limited to, initiating a new review of mifepristone?\n\nHave any mifepristone manufacturers communicated to HHS or FDA any changes in the safety and efficacy data for their products?\n\nWhat process will you use to conduct this review?\n\nWill you solicit unbiased expert review and public comment through advisory committees, expert review panels, public workshops, a request for information, the federal rulemaking process, or other avenues? If utilizing an expert review panel, how will you establish that members have relevant expertise, including recent experience prescribing mifepristone? If utilizing an advisory committee, does HHS commit to following all statutory requirements of the Federal Advisory Committee Act (FACA; 5 U.S.C. Chapter 10)?\n\nPlease list all procedural steps you intend to take in the review of mifepristone to ensure public participation and review of all relevant data.\n\nHow will you ensure that this review is based on the best available science? For example, will the agency consider only studies that have undergone peer review?\n\nHow will you ensure that the review is consistent with the court order in Purcell v. Kennedy and FDA\u2019s limited authority under 21 U.S.C \u00a7 355-1(a), (f), and (g)?\n\nThe FDA Adverse Event Reporting System (FAERS) documents any reported adverse events to specific prescription drugs approved by the FDA. Does the agency have additional unreported data on adverse events that it is considering in initiating its new review of mifepristone? If yes, will the agency release the unreported data to the public and to the signatories of this letter?\n\nA recent letter led by Senator Cassidy documented several statements from Secretary Kennedy on mifepristone in a September 4, 2025 Finance Committee hearing. Secretary Kennedy claimed the Biden administration \u201ctwisted the data\u201d to bury one of the safety signals for mifepristone and that the signal showed an approximately 11% adverse event risk. Please respond to this letter with the same information you provide in response to Senator Cassidy\u2019s letter.\n\nSenator Cassidy asked a question regarding a statement by Secretary Kennedy in the same Finance Committee hearing, indicating studies relating to the safety of mifepristone are \u201cprogressing and that they\u2019re ongoing.\u201d Please respond to this letter with the same answer you provide to Senator Cassidy regarding the details of these studies, including the scope, expected timeframe, agencies involved, and type of study.\n\nAt the close of the same Finance Committee hearing, Ranking Member Wyden inquired about Secretary Kennedy\u2019s planned mifepristone review which is \u201cnot based on new clinical trials or data from the scientific community,\u201d but based on one non-peer-reviewed paper from an anti-abortion political organization. Secretary Kennedy responded by committing to \u201cgood science and good scientists\u201d as part of this needless safety review. Please explain how the Secretary intends to meet this commitment and if the preeminent medical professional associations (i.e. ACOG, AMA) will be consulted as part of the review.\n\nThe American people need to be able to trust that any reviews, regulations, and approvals of medication by HHS and FDA are based on science and evidence\u2014not on partisan attempts to attack abortion access. We are seriously alarmed by this administration\u2019s obvious attempts to interfere with the science and politicize the drug review process in order to restrict abortion access. It is critical that scientific experts and evidence are central to any FDA review or REMS initiative. Mifepristone has long been shown to be safe and effective, and there is no new evidence to justify burdensome restrictions that block women from getting the health care they need.\n\nThank you for your prompt attention to this matter and we look forward to your response.", 1, "2026-03-30T01:40:41Z", "2026-04-06T19:52:45Z"]], "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://www.murphy.senate.gov/newsroom/press-releases/murphy-blumenthal-join-entire-senate-democratic-caucus-in-demanding-answers-from-trump-admin-on-new-review-of-mifepristone-despite-decades-of-evidence-proving-its-safety-and-efficacy"], "units": {}, "query_ms": 1.9294030498713255, "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"}