Fauci Files: Celebrated doctor’s career dotted with ethics, safety controversies inside NIH
Reinstated whistleblower says Fauci failed to get involved when problems emerged on his mgmt. watch at National Institutes of Health
Earlier this month, Dr. Anthony Fauci offered a pointed response to those who have challenged his stewardship of the pandemic as the nation’s infectious disease chief: “I think you can trust me,” he declared, citing his long record of service in government medicine.
That is exactly what Fauci’s National Institute of Allergies and Infectious Diseases (NIAID) agency declared years ago to foster children in New York, Illinois and elsewhere, many of whom were enrolled in an AIDS drug trial without the promised patient protections. An investigation concluded the NIAID’s AIDS research division that reported to Fauci had failed in many cases to provide patient advocates to monitor the foster kids’ health as promised, and in some cases, as required by law.
In other words, a trust was broken.
A Just the News review of three decades of Fauci’s leadership of the National Institutes of Health’s infectious disease arm found that while his agency has achieved many successes in the fights against AIDS and other infectious diseases it also produced several instances — like the foster children research — in which congressional, government ethics and internal watchdogs found safety or ethics lapses on his watch. They include:
- A 2004 internal NIH review that concluded Fauci’s AIDS research division was a “troubled organization” where managers were creating a hostile atmosphere with “sexually explicit and colorful language” and “seemingly being unaware of the need for appropriate behavior, decorum and enforcement of good management practices and rules of supervision.”
- A pregnant Tennessee woman who died in 2003 after she enrolled in NIH-funded research in hopes of saving her soon-to-be-born son from getting AIDS. A review found that doctors continued to administer an experimental drug regimen despite signs of liver failure.
- At least 10 children in a pediatric AIDS drug study died in what an investigation concluded was a death toll “significantly higher” than expected and unexplained.
- An Office of Government Ethics investigation that cited NIAID for failing to review and clear two-thirds of its workers who were moonlighting in private industry for possible ethical conflicts.
- A 1992 Department of Health and Human Services inspector general investigation that concluded NIAID failed to police two conflicts of interest in a vaccine experiment.
In 2005, the AIDS research division under Fauci’s agency was also required to reinstate a whistleblower, Dr. Jonathan Fishbein, its chief of ethics and regulatory compliance, after he and many lawmakers in both parties argued he had been wrongly fired in retaliation for raising safety concerns in some of the agency’s research.
In an interview with Just the News, Fishbein said this week that Fauci failed to take responsibility for the managers and researchers working below him when signs of trouble emerged, allowing problems to persist until others intervened. “Fauci is all about Fauci,” Fishbein said. “He loves being the headline. It’s his ego.”
A spokeswoman for Fauci did not return multiple emails seeking comment about the past controversies. Over the years, NIH officials have acknowledged each of the problems and promised reforms. And while Fauci was not directly implicated in specific wrongdoing, his management has been called into question.
For instance, the 2004 report about problems inside the AIDS research division urged the head of NIH to insist on better management from above. “The overall management of this Division requires careful review,” the report said.
The internal review also concluded that Fishbein’s termination had created “the appearance of reprisal.” Officials have said Fauci did not get involved in the termination.
AIDS drug trials on foster children
Among the more concerning professional episodes in Fauci’s history is a series of AIDS drug trials performed on foster children. Those trials, which were performed in the late 1980s and 1990s, incorporated HIV-positive foster kids from several different states and were funded by NIH. Several of the studies were sponsored by NIAID, a sub-institute of the NIH which Fauci began directing in 1984 and was directing at the time of the studies.
Investigations found the children were very often denied a personal health advocate during the course of their trials, something medical ethicists consider necessary when trial participants are drawn from vulnerable populations such as that of foster children. Government researchers contended that the types of medicine they were using in the trials did not meet the threshold necessary to require child advocates.
The safety concerns surfaced in a series of articles written by the Associated Press and were later taken up by Congress.
Though some test participants died during the studies, authorities later said none of the deaths could be linked to the tested medicines themselves. Still, numerous foster children reported side effects ranging from rashes to vomiting to sharp drops in white blood cell counts, all common adverse reactions associated with those drugs at the time.
Though researchers argued that the young trial participants were given access to world-class medical treatments and medical teams, in at least one case — during a trial involving the drug dapsone — at least 10 children died.
“An unexpected finding in our study was that overall mortality while receiving the study drug was significantly higher in the daily dapsone group,” researchers said at the time. “This finding remains unexplained.”
Years after the AP articles stirred controversy, two biomedical ethicists inside the NIH, Sumeeta Varma and David Wendle, concluded in a January 2008 article the agency did not have adequate protections for vulnerable foster children: “Enrolling wards of the state in research raises two major concerns: the possibility that an unfair share of the burdens of research might fall on wards, and the need to ensure interests of individual wards are accounted for. … Having special protections only for some categories is misguided. Furthermore, some of the existing protections ought to be strengthened.”
Drug trials in Africa plagued by safety reporting lapses
NIH-sponsored AIDS drug trials in Africa in 2002 were discovered to have notable reporting lapses; specifically, the NIH failed to tell then-President Bush that research into the AIDS drugs he authorized to send to Uganda had failed federal safety rules, though the officials did tell authorities in Uganda before beginning the trials.
Government officials at the time “recognized the enormity that this decision could have on the worldwide use of nevirapine to interrupt mother-baby transmission,” NIH’s chief AIDS researcher told Fauci in a March 2004 email. Doctors at the time were experimenting to see if nevirapine could be used by pregnant women to blunt the AIDS disease so that it was not passed on to their children during birth.
It was later discovered an DAID research manager rewrote a safety report from one of his own medical officers, deleting her concerns over the drug nevirapine and substituting his own conclusions that the drug was safe to consume.
Concerns over nevirapine’s safety also arose in 2003, when an HIV-positive Tennessee woman died while on a drug regimen that included nevirapine. NIH officials suspected at the time that nevirapine played a role in the woman’s death, yet her family members did not find out about those assumptions until a year later, following a news report by the Associated Press.
“Ouch! Not much wwe (we) can do about dumd (dumb) docs,” an AIDS division manager who reported to Fauci wrote in an email that angered congressional investigators when it surfaced.
The year before, an independent assessment of the NIH’s Division of AIDS research in Uganda concluded that NIH officials were suffering from “significant problems in the grading and reporting of adverse events.” The analysis also discovered “the possibility that several deaths that occurred during the study” went unreported.
A whistleblower gets fired, then reinstated
[Dr. Jonathan] Fishbein (pictured below), the former director of the NIH’s Office for Policy in Clinical Research Operations, was dismissed from his position shortly after he warned the executive committee of a drug trial that it needed to update its investigative brochure to inform trial participants of the drug’s known risks.
“The adverse events that were brought to my attention involved capillary leak and suicidal ideation,” Fishbein told Just the News. “As I eventually found out, the patients were not being informed. The ones that were on the study, and those that wanted to get on the study, neither were being informed. The fear was, if they were informed, they would drop out.”
“I wrote a letter to the executive committee telling them to update the brochure,” Fishbein continued. “From that point on, all of the sudden, the floor came out below me.”
Fishbein said he attempted to reach out to Fauci as the workplace environment turned hostile. “They said they’d get back to me. He didn’t,” Fishbein said. “He basically ran away.”
Lawyer’s documents provided by Fishbein claim that he was originally told his firing was approved by Fauci, who at the time denied having anything to do with the dismissal. The NIH would also go on to deny that Fauci had authorized the firing.
Notably, Fauci had a financial interest in the drug being tested; he was listed on the patent for the drug, Proleukin, and stood to earn royalties from it.
Following the revelation of Fauci’s financial stake in the drug, he said he had donated the royalties to charity, feeling uncomfortable about receiving a financial benefit from a drug he was involved in promoting. He vowed to continue donating the annual windfall to charity “no matter what the yearly amount is.”
Alleged sexual harassment
Fishbein has also argued that his dismissal was linked to his filing a formal complaint against a division manager for purported sexual harassment. A subsequent internal report written by an advisor to then-NIH Director Elias Zerhouni substantiated Fishbein’s claims that the NIH’s AIDS research division was rife with sexually explicit rhetoric.
Both the DAIDS director and deputy director eventually admitted that they both used “sexually explicit and colorful language” in the workplace, but that “no one had ever complained until [Fishbein].” The deputy director also argued that Fishbein himself spoke similarly while in the office, memos show.
(Following publication of this article, Fishbein told Just the News that that claim had been a “totally false” one for which the department “could provide no evidence,” and that “the only thing [he] ever did was refer to Fauci as ‘Grouchy’ and the grandfatherly Tramont as ‘Grandpa’.”
“I don’t use profanity in the workplace and certainly avoid language that is sexual in nature that could be offensive to anyone,” Fishbein added.)
Sen. Chuck Grassley (R-Iowa), launched an investigation into the allegations of sexual harassment at DAIDS and provided the NIH director with evidence: an email sent among managers with a photo of a woman with an exposed breast.
Ethics violations, failure to report ‘outside activities’
In some instances, NIAID research under Fauci was found to have violated ethics rules within the federal government.
A 1992 report from the Department of Health and Human Services Office of the Inspector General found two conflicts of interest on a NIAID-directed committee studying possible adverse events involving rubella and pertussis vaccines. One member had received “a 5-year stipend totaling $300,000 from a nonprofit medical research fund wholly supported by a major pertussis manufacturer;” another committee member was found to have “made public statements in a legal deposition on the effects of pertussis vaccines.”
NIAID “did not follow Federal regulations to assure the impartiality and objectivity of work performed under an advisory and assistance contract,” the report found, a conclusion that NIH accepted.
In another instance, the U.S. Office of Government Ethics determined in a 2004 review that the NIAID had failed to obtain approval for a full 66% of “outside activities” the institute had undertaken over the review period. Outside activities, according to the NIH, are undertakings that “generally involv[e] providing a service to or a function for an outside organization, with or without pay or other compensation.”
‘Routine close contact’ may spread AIDS, Fauci argued in a bad prediction.
Fauci, who began directing the NIAID in 1984, was known for years for his work on HIV/AIDS, having risen to his directorship amid the first major wave of AIDS infections in the United States. Throughout the 1980s, he was among a team of researchers working to develop an AIDS vaccine. His efforts on that project were highly regarded enough that then-Vice President George H.W. Bush mentioned him favorably by name at an October 1988 presidential debate, calling him “a very fine” researcher and “top doctor.”
Yet Fauci contributed in one case to what two AIDS activists have called the “irrational, punitive” response to the initial AIDS outbreaks in the 1980s. In the Journal of the American Medical Association in 1983, the doctor wrote that while AIDS transmission had been observed largely as a function of high-risk behaviors such as homosexual sex and intravenous drug use, there was still “the possibility that routine close contact, as within a family household, can spread the disease.”
Given that “nonsexual, non-blood-borne transmission is possible,” Fauci wrote, “the scope of the syndrome may be enormous.”
That hypothesis turned out to be wrong. Fauci himself, in a presentation a year later, acknowledged that no cases of the disease being spread through “casual contact” had yet been detected, but the paranoia and fear surrounding the vulnerability of the general population to AIDS persisted for years afterwards. In New York in 1985, for instance, 85% of schoolchildren at one public elementary school stayed home during opening week, while hundreds of parents demanded the school system bar any HIV-positive children from attending classes.
The Zika outbreak that never was
In the years since, Fauci’s later work on HIV/AIDS has been praised for its contributions toward developing treatments and vaccines for the disease and virus. Yet his work elsewhere has in several cases evinced a similar tendency to raise alarm about predictions that did not materialize.
Fauci’s work on the Zika virus — a pathogen the outbreak of which in 2016 caused considerable global alarm — is a case in point. In the summer of that year, the doctor said he was pulling funds from malaria, influenza and tuberculosis research programs in order to fund “a series of four or five vaccines” to counteract the Zika threat. In March 2016 he had warned that the disease “will come again” to the United States and that the country “absolutely [has] to be prepared” for it.
Peaking at a high of about 5,200 cases in 2016, the U.S. has recorded a total of about 550 cases since then, with roughly 80% of those occurring in 2017. The CDC has reported just one case of Zika in the U.S. so far this year. The Mayo Clinic, meanwhile, reported in December that not only was there no functional vaccine for the disease, but that funding for the vaccine itself is “too little, is contributed by too few countries, and may not be sustained,” suggesting the virus remains a low priority for most nations.
Shifting predictions and advice on COVID-19
Fauci’s record of abrupt shifts in public messaging during the course of the coronavirus crisis has only raised further questions.
In late March, for example, Fauci co-authored a paper in the New England Journal of Medicine arguing that, based on the evidence at the time, the infection fatality rate of COVID-19 “may be considerably less than 1%,” suggesting the virus “may ultimately be more akin to … a severe seasonal influenza … or a pandemic influenza.”
Yet in an appearance before Congress earlier that month, Fauci estimated that the virus is fatal in 1% of cases, meaning it would be “10 times more lethal than the seasonal flu.” He repeated that estimate on the Daily Show the day after his article was published.
A source familiar with the writing of the journal article told Just the News it had been authored weeks before its publication, suggesting that by the time it was published Fauci had revised his earlier estimates in light of new data.
Yet the doctor’s initial estimates appear to have been closer to the truth: Health officials today are estimating a COVID-19 fatality rate ranging from 0.2% to 0.6%, with one Stanford professor guessing that the fatality rate for those under 70 years old is just 0.04%.
Fauci himself appears to have moved on from the topic. He recently argued against taking comfort in a “false narrative” of a lower death rate, claiming that even if less people are dying from it, “there are so many other things that are very dangerous and bad about this virus.”
Early in the pandemic, Fauci argued against public use of masks. “If you look at the masks that you buy in a drug store,” he said in February, “the leakage around that doesn’t really do much to protect you.”
That same month he argued against the “misperception that wearing a mask, even if you were in an area where there was transmission, is going to absolutely protect you.” A mask, he said, “is more appropriate for someone who is infected to prevent them from infecting someone else.”
In March, meanwhile, he said that, at the time, “there [was] no reason to be walking around with a mask.”
“If you’re in the middle of an outbreak,” he said, “wearing a mask might make people feel a little bit better. And it might even block a droplet. But it is not providing the perfect protection that people think that it is.”
Since then, Facui has done an about-face, regularly arguing that masks are a critical and indispensable tool for stopping the spread of the virus. At the beginning of last month, he claimed that the wholesale reversal of public health advice over the last several months arose after health officials realized “that we have such a high percentage of people who are asymptomatic and who we know can spread the infection.”
Yet health officials, including Fauci, have been aware of cases of asymptomatic infection and spread since late January at the latest, leaving open the question as to why he and others took months to recommend that the public wear the face coverings now deemed necessary in the fight against COVID-19.
By the middle of last month, Fauci suggested his earlier mask advice may have been influenced by another factor. “The public-health community … were concerned that it was at a time when personal protective equipment, including the N95 masks and the surgical masks, were in very short supply,” Fauci said in June. Authorities didn’t want medical providers “to be without the equipment that they needed,” he said.
Fauci said that “the circumstances have changed” since his earlier recommendations. He also acknowledged why many in the public are skeptical of public health officials months into the pandemic.
“It’s entirely understandable how the public can get mixed messages and then get a bit confused about what they should do,” he said.
The Facts Inside Our Reporter’s Notebook
- foster children in New York, Illinois and elsewhere, many of whom were enrolled in an AIDS drug trial without the promised patient protections
- Fauci’s agency was also required to reinstate a whistleblower,
- two biomedical ethicists inside the NIH penned an article concluding the agency did not have adequate protections
- a safety report
- his own conclusions
- subsequent internal report
- A 1992 report
- a 2004 review
- according to the NIH
- an October 1988 presidential debate
- stayed home during opening week,
- pulling funds
- about 5,200 cases in 2016,
- reported in December
- the day after his article was published.
- just 0.04%.
(TLB) published this article with permission of John Solomon at Just the News
Some emphasis and pictorial content added by (TLB)
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