FDA Faces Criticism Amid Innovation Challenges
Written by Emily J. Thompson, Senior Investment Analyst
Updated: 1 hour ago
0mins
Should l Buy PFE?
Source: CNBC
- Regulatory Standards Controversy: Congressman Jake Auchincloss criticized FDA Commissioner Marty Makary for replacing standards of safety and efficacy with fear and favoritism, undermining patient confidence in new therapies and impacting the market launch of innovative drugs.
- Staffing Losses: The FDA has experienced significant staff reductions in its Center for Drug Evaluation and Research, with oncology review staff dropping from about 100 to below 60, which may lead to approval delays and incomplete response letters.
- Decline in Accelerated Approvals: In 2024, the FDA approved 20 drugs through the accelerated approval process, down from 9 the previous year, indicating a direct impact on drug approval efficiency due to the loss of experienced reviewers.
- New Therapy Approval Pathways: The FDA proposed a new system for approving personalized drugs aimed at rare diseases, intending to provide more flexible approval pathways, but this change has sparked widespread controversy, affecting the agency's core mission.
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Analyst Views on PFE
Wall Street analysts forecast PFE stock price to rise
16 Analyst Rating
5 Buy
11 Hold
0 Sell
Moderate Buy
Current: 27.260
Low
24.00
Averages
28.56
High
35.00
Current: 27.260
Low
24.00
Averages
28.56
High
35.00
About PFE
Pfizer Inc. is a research-based, global biopharmaceutical company. The Company is engaged in the discovery, development, manufacture, marketing, sale and distribution of biopharmaceutical products worldwide. Its Biopharma segment includes the Pfizer U.S. Commercial Division, and the Pfizer International Commercial Division. Its product categories include oncology, primary care and specialty care. Its oncology products include Ibrance, Xtandi, Padcev, Adcetris, Inlyta, Lorbrena, Bosulif, Tukysa, Braftovi, Mektovi, Orgovyx, Elrexfio, Tivdak and Talzenna. Its primary care products include Eliquis, Nurtec ODT/Vydura, Zavzpret, the Prevnar family, Comirnaty, Abrysvo, FSME/IMMUN-TicoVac, Nimenrix, Trumenba, and Paxlovid. Its specialty care products include Xeljanz, Enbrel (outside the United States and Canada), Inflectra, Abrilada, Cibinqo, Litfulo, Eucrisa, Velsipity, the Vyndaqel family, Genotropin, BeneFIX, Xyntha, Somavert, Ngenla, Hympavzi, Sulperazon, Zavicefta, Octagam and others.
About the author

Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
- Market Performance Analysis: Pfizer's market capitalization stands at $154 billion, and despite an average annual loss of 8.8% over the past three years, the stock has risen 10.4% year-to-date, indicating some market recovery potential.
- Dividend Attraction: With a dividend yield of 6.4%, Pfizer's steady payment of 349 consecutive dividends, despite a modest average annual growth of 3% over the past five years, underscores the company's financial stability.
- R&D Investment Outlook: Pfizer invested $10.4 billion in research and development in 2025, actively developing 102 drug candidates, with 32 in late-stage Phase 3, showcasing significant future growth potential.
- Operational Growth Situation: The company's recent fourth-quarter results showed a 3% year-over-year revenue decline, but operational growth reached 9% when excluding the impacts of COVID-19 vaccine and Paxlovid, indicating resilience in its core business.
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Pfizer CEO's Statement: The CEO of Pfizer has criticized the current director of the FDA, stating that he is not adhering to the recommendations provided by his staff.
Concerns Over FDA Leadership: This statement raises concerns about the leadership and decision-making processes within the FDA, particularly regarding drug approvals and public health policies.
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- Regulatory Standards Controversy: Congressman Jake Auchincloss criticized FDA Commissioner Marty Makary for replacing standards of safety and efficacy with fear and favoritism, undermining patient confidence in new therapies and impacting the market launch of innovative drugs.
- Staffing Losses: The FDA has experienced significant staff reductions in its Center for Drug Evaluation and Research, with oncology review staff dropping from about 100 to below 60, which may lead to approval delays and incomplete response letters.
- Decline in Accelerated Approvals: In 2024, the FDA approved 20 drugs through the accelerated approval process, down from 9 the previous year, indicating a direct impact on drug approval efficiency due to the loss of experienced reviewers.
- New Therapy Approval Pathways: The FDA proposed a new system for approving personalized drugs aimed at rare diseases, intending to provide more flexible approval pathways, but this change has sparked widespread controversy, affecting the agency's core mission.
See More
- Sales Growth Dependency: Eli Lilly's Mounjaro and Zepbound drugs achieved impressive sales growth of 99% and 175% in 2025, respectively, yet these two drugs account for nearly 45% of the company's total sales, raising concerns about the sustainability of such growth.
- Overvaluation Concerns: Despite the strong performance of Eli Lilly's drugs, its stock price has surged to a price-to-earnings ratio of 44, with a meager dividend yield of 0.6%, indicating that the market's expectations for future growth may be overly optimistic.
- Competitors' Opportunities: GLP-1 competitors Novo Nordisk and Pfizer offer more attractive investment profiles with dividend yields of 4.57% and 6.31%, respectively, and price-to-earnings ratios of 10 and 20, especially as Eli Lilly faces risks from patent expirations.
- Intensifying Industry Competition: While Eli Lilly's success in the GLP-1 space is notable, it may overshadow the risks it faces; as competition intensifies, the strong historical performance of Novo Nordisk and Pfizer could enable them to rebound in the market, presenting new opportunities for investors.
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- Significant Sales Growth: Eli Lilly's Mounjaro and Zepbound drugs achieved sales increases of 99% and 175% respectively in 2025; however, such growth may not be sustainable, introducing uncertainty into the company's future performance.
- Market Share Risk: These two GLP-1 drugs account for 56% of Eli Lilly's total revenue, and with patent protections set to expire, the company may face a substantial revenue gap that could impact its long-term financial health.
- Competitor Dynamics: While Novo Nordisk and Pfizer lag in the GLP-1 market, Novo Nordisk recently launched an oral GLP-1 medication, and its dividend yield stands at 4.9%, indicating its ongoing competitiveness in the market.
- Investor Sentiment Analysis: Despite Eli Lilly's stock price surging due to market enthusiasm, resulting in a high P/E ratio of 44 and a meager dividend yield of 0.6%, analysts suggest that investors consider competitors like Novo Nordisk and Pfizer for potentially better returns.
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- Investor Preference: During turbulent and uncertain market conditions, many investors are turning to dividend-yielding stocks, which typically have high free cash flows and reward shareholders with substantial dividends, indicating a strong desire for stable income.
- Analyst Ratings: Benzinga provides the latest analyst ratings for three high-yielding healthcare stocks, including Perrigo Company PLC, Pfizer Inc, and DENTSPLY SIRONA Inc, assisting investors in making more informed decisions.
- Market Data: Benzinga's analyst ratings page allows traders to sort through ratings based on analyst accuracy, offering a wealth of market data that enhances investor insights into stock performance.
- Attractiveness of Dividend Stocks: High dividend stocks become particularly appealing in uncertain market environments as investors seek to hedge against risks posed by market volatility through stable dividend income.
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