Kenvue stock drops 10% on report RFK Jr. will link autism to Tylenol use during pregnancy

North America
Source: CNBCPublished: 09/06/2025, 04:12:12 EDT
Kenvue
Tylenol
Robert F. Kennedy Jr.
Regulatory Risk
Consumer Health Products
Public Health Policy
Kenvue Inc. Tylenol brand pain reliever for sale at a pharmacy in New York, US, on Wednesday, March 27, 2024.

News Summary

Kenvue Inc. shares fell more than 10% on Friday following a report that Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. is likely to link the use of the company’s pain medication Tylenol by pregnant women to autism in a report to be released this month. The report will also suggest a folate-derived medicine can treat symptoms of the developmental disorder in some individuals. Kennedy has made autism a key focus for HHS, previously taking steps to change U.S. vaccine policy and amplifying false claims about mRNA vaccines. Kenvue stated it has "continuously evaluated the science and [continues] to believe there is no causal link" between acetaminophen (the generic name for Tylenol) use during pregnancy and autism. The company added that the Food and Drug Administration (FDA) and leading medical organizations "agree on the safety" of the drug and its use during pregnancy. The FDA website indicates it has not found "clear evidence" that appropriate acetaminophen use during pregnancy causes adverse outcomes, but advises pregnant women to consult healthcare providers before using over-the-counter drugs.

Background

Robert F. Kennedy Jr. was appointed U.S. Secretary of Health and Human Services (HHS) following Donald J. Trump's re-election as president in November 2024. Kennedy has long been known for his critical stance on mainstream medicine and public health institutions, particularly holding controversial views on vaccine safety. He has publicly questioned the efficacy and safety of vaccines on multiple occasions and has pushed for changes in vaccine policy during his tenure as HHS Secretary. Kenvue Inc. is the consumer health business spun off from Johnson & Johnson in 2023, owning well-known brands like Tylenol and Listerine. Tylenol, with its active ingredient acetaminophen, is a widely used over-the-counter pain reliever and fever reducer, utilized by millions of consumers, including pregnant women. The current report linking autism to Tylenol comes as the Kennedy administration has prioritized autism research at HHS, pledging to determine its causes.

In-Depth AI Insights

What is the extent of a HHS Secretary's personal agenda influencing regulated industries? - Kennedy, as HHS Secretary, making health claims through an official report that contradict mainstream scientific consensus, introduces a new, unpredictable layer of regulatory risk for regulated industries, particularly pharmaceuticals and consumer health. - This approach could undermine the scientific authority of agencies like the FDA under HHS, leading to increased regulatory uncertainty and forcing companies to divert resources to address politically, rather than scientifically, driven policy pressures. - Investors must re-evaluate companies' resilience against scientific controversy and political intervention, especially for those with long-standing, widely used products. What are the long-term brand and legal risks facing Kenvue? - Despite Kenvue's and the FDA's denial of a causal link, the HHS report itself, regardless of its ultimate scientific conclusion, could create lasting negative consumer perception and erode trust in the Tylenol brand. - This negative publicity is likely to trigger a new wave of class-action lawsuits, which, even if successfully defended, will incur significant legal costs and potential reputational damage, creating a long-term 'litigation premium' risk. - Market share could be eroded as consumers potentially shift to alternative pain relievers or non-acetaminophen products, impacting Kenvue's revenue and profitability. What structural impacts might this event have on broader health science and investment? - This could set a precedent for future government officials to challenge other well-established medical products or therapies from their positions, leading to systemic political risk across the entire health industry. - Investors evaluating biopharma and consumer health companies' R&D pipelines and existing products will need to elevate 'political/policy risk' to a level of importance comparable to 'scientific/market risk'. - In the long run, such challenges to scientific consensus could stifle innovation, as companies may become less willing to invest in products that could suddenly face legitimacy crises due to political winds, thereby altering capital allocation within the health sector.