Texas Attorney General Ken Paxton on Nov. 30 filed a lawsuit against Pfizer, alleging that the drugmaker misrepresented the efficacy of its COVID-19 vaccine.
“We are pursuing justice for the people of Texas, many of whom were coerced by tyrannical vaccine mandates to take a defective product sold by lies,” Mr. Paxton, a Republican, said in a statement. “The facts are clear. Pfizer did not tell the truth about their COVID-19 vaccines.”
Pfizer officials didn’t respond by press time to a request by The Epoch Times for comment.
The trial sought to determine how many participants contracted COVID-19 with symptoms after receiving a vaccine, not COVID-19 overall.
Tens of millions of Americans subsequently received the vaccine.
The efficacy estimate was a relative risk reduction for vaccinated individuals when compared to unvaccinated participants.
Of vaccinated participants who had no evidence of prior infection, 0.04 percent tested positive for COVID-19. Of unvaccinated participants without prior infection, 0.9 percent had a COVID-19 case. That meant there was a 95 percent relative risk reduction.
Absolute risk reduction, another way of measuring, is determined by subtracting the post-treatment risk of 0.04 percent from the baseline risk rate of 0.9 percent, which reaches a different efficacy estimate.
Pfizer misrepresented the efficacy by promoting the relative risk reduction number and relying on just two months of clinical trial data, according to the new suit.
“Of 17,000 placebo recipients, only 162 acquired COVID-19 during this two-month period. Based on those numbers, vaccination status had a negligible impact on whether a trial participant contracted COVID-19,” it reads. “The risk of acquiring COVID-19 was so small in the first instance during this short window that Pfizer’s vaccine only fractionally improved a person’s risk of infection. And a vaccine recipient’s absolute risk reduction—the federal Food & Drug Administration’s (FDA) preferred efficacy metric—showed that the vaccine was merely 0.85% effective.”
The FDA has stated in guidance documents that relative risk estimates made reduction “seem large” and that “treatments are viewed more favorably than when the same information is presented using an absolute risk format.”
The agency says drug manufacturers should provide absolute risks in addition to relative risks.
Pfizer also misled the public by excluding COVID-19 cases in the vaccinated if they happened before seven days had elapsed following a second dose, according to Mr. Paxton.
Pfizer was also aware of the lack of evidence that its vaccine protected against transmission but repeatedly made statements and ran advertisements touting it as a way to protect people and their loved ones, according to the suit. The FDA, for instance, repeatedly stated that there wasn’t enough evidence to say the vaccine shielded against transmission.
“Additional evaluations ... will be needed to assess the effect of the vaccine in preventing virus shedding and transmission,” the FDA said in one document.
Federal laws such as the Food, Drug, and Cosmetic Act bar misbranding products regulated by the FDA. Misbranding occurs if advertising or labeling for the product is misleading, including when advertising “fails to reveal facts material in the light of representations.” A Texas law prohibits deceptive trade practices.
In many of Pfizer’s statements, the company didn’t explain the difference between absolute and relative risk reduction.
Pfizer CEO Dr. Albert Bourla also made misleading statements, the suit alleges, such as claiming—after the trial results were released—that the vaccine would “help bring an end to” the pandemic. He also claimed in February 2021 that the protection from the vaccines was “robust” after six months, despite trial data not being collected yet after six months.
“Pfizer’s misleading statements created the false impression that 95% of vaccine recipients would never obtain COVID-19, full stop,” the suit reads.
Later in 2021, data from the drugmaker, Israel, and elsewhere showed that the vaccine protection began to wane within months, leading to the clearance and promotion of boosters and, ultimately, new formulations.
The U.S. Department of Justice didn’t respond to a request for comment on the lawsuit.
“The FDA does not comment on possible, pending or ongoing litigation,” an FDA spokesperson told The Epoch Times in an email.
The suit stems from an investigation that Mr. Paxton announced in May into whether COVID-19 vaccine makers Pfizer, Moderna, and Johnson & Johnson misled the public about their products, including possibly manipulating trial data.
“This pandemic was a deeply challenging time for Americans,“ he said at the time. ”If any company illegally took advantage of consumers during this period or compromised people’s safety to increase their profits, they will be held responsible.”
Mr. Paxton is asking the court to enjoin Pfizer from violating the Texas Deceptive Trade Practices Act, order the company to pay more than $10 million for violations of the act, and decree that fines and penalties against Pfizer are not dischargeable in bankruptcy.
