Talk:Eli Lilly and Company/Archive 1

Archive 1

Do you sell pure ephedrine

Bush family

The connection to the Bush family section is unnecessarily spurious. Shorten it up, give just relevant facts, stay on the topic at-hand, which is Eli Lilly & Co. It looks as if it was largely included to more make the Bush family look "evil" rather than to give info to anyone searching for data on Eli Lilly.

The Bush section is too long and off-topic. It deserves its own page. — Preceding unsigned comment added by 68.236.163.9 (talk • contribs) 20:21, 8 February 2007 ( (UTC)

Global reputation

Along with General Electric and IBM, Eli Lilly has developed a global reputation for attracting some of the brightest corporate managerial talent.

Can this be substantiated with a link ref? — Preceding unsigned comment added by Innovationcreation (talk • contribs) 20:34, 13 October 2005 (UTC)

Medical ethics

Oraflex, the American version of Benoxaprofen, was withdrawn from the market in 1982, just one month after gaining FDA approval. A British medical journal found five cases of death due to jaundice in patients taking the drug and the FDA accused Lilly of suppressing unfavorable research findings. In 1985, the U.S. Justice Department filed criminal charges against the company and Dr. William Ian H. Shedden. Lilly pleaded guilty to 25 criminal counts and paid a $25,000 fine.

Lilly was also cited in lawsuits filed against the manufacturers of diethylstilbestrol (DES), a drug prescribed to women in the 1940s and 1950s to prevent miscarriages. The company was ordered to pay $400,000 in damages from DES even though the complications that developed were not known at the time.

Zyprexa

According to a New York Times article published on December 17, 2006, Eli Lilly has engaged in a decade-long effort to play down the health risks of Zyprexa, its best-selling medication for schizophrenia, according to hundreds of internal Lilly documents and e-mail messages among top company managers. These documents and e-mail messages were soon made publicly available as a location hidden Tor service, and then made available on the public Internet. Eli Lilly sought and obtained a "Temporary Restraining Order" from a U.S. District Court on January 4th, 2007 to stop the dissemination or downloading of Eli Lilly documents about Zyprexa, and this allowed them to get a few U.S.-based websites to remove them. The documents can now only be downloaded from public Internet sites outside the U.S. These health risks include an increased risk for diabetes through Zyprexa's links to obesity and its tendency to raise blood sugar. Zyprexa is Lilly’s top-selling drug, with sales of $4.2 billion last year.

The documents, given to the New York Times by a lawyer representing mentally ill patients, show that Lilly executives kept important information from doctors about Zyprexa’s links to obesity and its tendency to raise blood sugar, two known risk factors for diabetes.

Lilly’s own published data, which it told its sales representatives to play down in conversations with physicians, has shown that 30 percent of patients taking Zyprexa gain 22 pounds or more after a year on the drug, and some patients have reported gaining 100 pounds or more. But Lilly was concerned that Zyprexa’s sales would be hurt if the company was more forthright about the fact that the drug might cause unmanageable weight gain or diabetes, according to the documents, which cover the period 1995 to 2004. In 2006, Lilly paid $700 million to settle 8,000 lawsuits from people who said they had developed diabetes or other diseases after taking Zyprexa. But thousands of additional lawsuits are still pending.

Lilly also instructed its sales representatives to suggest that physicians prescribe Zyprexa to older patients with symptoms of dementia. One document states "dementia should be first message" for primary care doctors, since they "do not treat bipolar" or schizophrenia, but "do treat dementia." Three months after its launch, Lilly's Zyprexa campaign, called 'Viva Zyprexa', led to 49,000 new prescriptions. In 2002, the company changed the name of the primary care campaign to 'Zyprexa Limitless' and began to focus on people with mild bipolar disorder who had previously been diagnosed as depressed, despite the fact that Zyprexa has been approved only for the treatment of mania in bipolar disorder, not depression.

In 2002, British and Japanese regulatory agencies warned that Zyprexa may be linked to diabetes. But even after the FDA issued a similar warning in 2003, Lilly did not publicly disclose their own findings.

Eli Lilly agreed on January 4, 2007 to pay up to $500 million to settle 18,000 lawsuits from people who claimed they developed diabetes or other diseases after taking Zyprexa. Including earlier settlements over Zyprexa, Lilly has now agreed to pay at least $1.2 billion to 28,500 people who claim they were injured by the drug. At least 1,200 suits are still pending, the company said. About 20 million people worldwide have taken Zyprexa since its introduction in 1996.

PRIME

A controversial experiment, Prevention through Risk Identification, Management, and Education (PRIME), was initiated by Dr. Thomas McGlashan of Yale University, and director of the National Institute for Mental Health (NIMH), with funding from Eli Lilly and the NIMH. PRIME investigators tested a speculative schizophrenia prevention theory by exposing healthy youngsters for one year to Lilly’s toxic blockbuster drug, the neuroleptic, Zyprexa (olanzapine). From 1997 to 2003, sixty previously healthy youngsters were enrolled in the experiment: of whom half were exposed to Zyprexa (olanzapine), a drug so toxic it is now costing Eli Lilly over a billion dollars in lawsuit settlements.

None of the youngsters in PRIME met the diagnostic criteria of either condition for which the drug was approved. Absent a diagnosable condition, and absent any evidence to support the assumption that a drug can prevent schizophrenia, these healthy youngsters were exposed to a toxic drug on the basis of speculations. The authors now acknowledge in their published report that the experiment had failed and that Zyprexa did not prevent schizophrenia.

Alan Breier, Vice President and Medical and Chief Medical Officer for Eli Lilly was involved in the PRIME project and was one of the chief medical authors of the clinical trials. Prior to joining Lilly, Breier completed a three-year research fellowship at NIMH.

Prozac

Legal

In one of the only three cases to ever go to trial for Prozac's possible role in inducing suicide, Eli Lilly was caught corrupting the judicial process by making a deal with the plaintiff's attorney to throw the case, in part by not disclosing damaging evidence to the jury.

The case, known as the Fentress Case involved a Kentucky man, Joseph Wesbecker, who was on Prozac and went to his workplace, opening fire with an assault rifle killing eight people (including Fentress), and injuring 12 others before killing himself. The jury returned a 9-to-3 verdict in favor of Lilly. But the judge, in the end, referred the matter to the Kentucky Supreme Court, which later found that "there was a serious lack of candor with the trial court and there may have been deception, bad faith conduct, abuse of judicial process and, perhaps even fraud." The judge later revoked the verdict and instead, recorded the case as settled. The value of the secret settlement deal has never been disclosed, but was reportedly "tremendous".

In 2001 Eli Lilly and Company (Lilly) agreed to settle Federal Trade Commission (FTC) charges regarding the unauthorized disclosure of sensitive personal information collected from consumers through its Prozac.com Web site. The company disclosed E-mail addresses of 669 Subscribers to its Prozac Reminder Service. On June 27, 2001, a Lilly employee created a new computer program to access Medi-messenger subscribers' e-mail addresses and sent them an e-mail message announcing the termination of the Medi-messenger service. The June 27 e-mail message included all of the recipients' e-mail addresses within the "To:" line of the message, thereby unintentionally disclosing to each individual subscriber the e-mail addresses of all 669 Medi-messenger subscribers.

As part of the settlement, Lilly said it would take appropriate security measures to protect consumers' privacy. Lilly's security breach was the subject of a July 2001 petition from the American Civil Liberties Union (ACLU) requesting that the FTC investigate and take appropriate action to remedy the breach.

Medical/Scientific

The signs of violence and suicidality were there since Prozac was tested in premarketing trials. In May 1984, Germany’s regulatory agency (GBA) rejected Prozac as “totally unsuitable for treating depression.” In July 1985, Eli Lilly’s own data analysis—from a pool of 1,427 patients—showed high incidence of adverse drug effects and evidence of drug-induced violence in some patients. In May 1985, FDA’s (then) chief safety investigator, Dr. Richard Kapit, wrote: “Unlike traditional tricyclic antidepressants fluoxetine’s profile of adverse side effects more closely resembles that of a stimulant drug than one that causes sedation.” He warned: “It is fluoxetine’s particular profile of adverse side-effects which may perhaps, in the future give rise to the greatest clinical liabilities in the use of this medication to treat depression.”

Dr. Kapit’s safety review described the clinical trial data from 46 trials with a total of 1,427 patients. He noted under the section, “Catastrophic and Serious Events,” 52 cases of “egregiously abnormal laboratory reports which were the reason for early termination,” and “additional adverse event reports not reported by the company [which] were revealed on microfiche.” Dr. Kapit reported: “In most cases, these adverse events involved the onset of an unreported psychotic episode.” There were 10 reports of psychotic episodes; 2 reports of completed suicides; 13 attempted suicides; 4 seizures—including a healthy volunteer; and 4 reports of movement disorders.

In 1985 Dr. Kapit recommended “labeling warning [for] the physician that such signs and symptoms of depression may be exacerbated by this drug". No such warning was issued until 2004.

On August 18, 2004, a study in the Journal of the American Medical Association (JAMA) showed Prozac and cognitive behavior therapy, in combination, to be the most effective treatment of depression in adolescents. The research, conducted over three years at 12 medical centers, was funded and coordinated by the National Institute of Mental Health (NIMH) at a cost to US taxpayers of $17 million. A total of 439 adolescents aged 12-17 were given Prozac, Prozac plus cognitive behavior therapy (CBT), placebo plus CBT, or placebo alone. After 12 weeks, 71% of those treated with Prozac and CBT showed improvement (defined by the therapists and the subjects' responses to questionnaires). Improvement was reported by 60% of those taking Prozac without CBT, 43% getting CBT alone, and 35% taking placebo alone.

NIMH Director Thomas Insel told the media it was a "landmark study" because "it's the largest publicly funded study and the only study this size that doesn't have pharmaceutical funding", but lead investigator John March of Duke University Medical Center was on the Eli Lilly payroll.

Data to which March et al did not draw attention showed a higher incidence of harmful behavior among teens taking Prozac (11.9%) compared to those on placebo (5.4%) and CBT alone (4.5%). Few stories mentioned that teenagers to whom suicidal thoughts had occurred had been excluded from the study before it began. According to FDA documents posted on the FDA website on September 25, 2003, at least 2 of 48 children treated with Prozac in the NIMH-sponsored trial attempted suicide. NIMH's role in funding a study with taxpayer money was subsequently used by Eli Lilly as court evidence to extend its Prozac patent exclusivity and to obtain FDA approval for treating depression in children.

In 2005 an internal document purportedly from Eli Lilly, and originally published in the British Medical Journal (BMJ) showed that the drug maker had data more than 15 years old showing that patients on its antidepressant Prozac were far more likely to attempt suicide and show hostility than were patients on other antidepressants and that the company attempted to minimize public awareness of the side effects. The 1988 document indicated that 3.7 percent of patients attempted suicide while on the blockbuster drug, a rate more than 12 times that cited for any of four other commonly used antidepressants. The document, which cited clinical trials of 14,198 patients on fluoxetine also stated that 2.3 percent of users suffered psychotic depression while on the drug, more than double the next-highest rate of patients using another antidepressant.

The document was provided to CNN by the office of U.S. Representative Maurice Hinchey (D-New York), who called for tightening FDA regulations on drug safety. "The case demonstrates the need for Congress to mandate the complete disclosure of all clinical studies for FDA-approved drugs so that patients and their doctors, not the drug companies, decide whether the benefits of taking a certain medicine outweigh the risks," Rep. Hinchey said. The BMJ said the documents disappeared in 1994, during the Fentress Case. Each of the four pages of the paper obtained by CNN is stamped "Confidential" and "Fentress," the name of one of Wesbecker's victims.

Evista

In 2005 Eli Lilly and Co. agreed to plead guilty to a federal misdemeanor and pay $36 million to settle charges that it illegally marketed and promoted its Evista osteoporosis drug for two unapproved uses.

The Department of Justice said an investigation that began in July 2002 found that some Lilly sales representatives promoted Evista in 1998 as useful for preventing and reducing the risk of breast cancer and for reducing the risk of heart disease. The FDA had approved neither use.

Thiomerosal

Thiomersal is a preservative that contains mercury and is used by Eli Lilly and others in vaccines. In 1999 the American Academy of Pediatrics and the Public Health Service urged vaccine makers to stop using mercury-based preservatives. In 2001 the Institute of Medicine concluded that the link between autism and thimerosal was “biologically plausible.” By 2002, thimerosal lawsuits against Eli Lilly were progressing through the courts.

Political analysts and the parents of autistic children were baffled when it was revealed, shortly after the passage of the Homeland Security Act in 2002, that a rider to the bill had been added just prior to passage, that would shield Eli Lilly and the pharmaceutical industry from billions of dollars in anticipated lawsuits over vaccines. Known as the "Eli Lilly Protection Act", the provision was designed to force lawsuits over the preservative thiomersal, calling the suits into a special 'vaccine court'. The provision could have resulted in the dismissal of thousands of cases filed by parents, who contend mercury in thimerosal poisoned their children, causing autism and other neurological ailments, but the rider was subsequently repealed when the next session of Congress convened in 2003.

Xigris

In 2001, Eli Lilly's chairman, president and CEO, Sidney Taurel, told shareholders: "No medicine better symbolizes our mission than Xigris," calling it "one of our industry's genuine breakthroughs."

Xigris was designed to fight sepsis, a condition that kills more than 200,000 Americans annually. Xigris is the only approved drug for sepsis, and it costs $8,000 to treat a single patient. Lilly hoped Xigris would be a blockbuster, with sales of at least a billion dollars a year. But after five years on the market, sales are only $200 million.

Eli Lilly used the Belsito & Company public relations firm in a deceptive marketing campaign to promote Xigris, its drug for treatment of sepsis. A report in the New England Journal of Medicine (NEJM) accused Lilly of initiating false reports of a shortage of the drug to boost sales. Belsito and Company spread the word that the drug was being "rationed" and physicians were being 'systematically forced' to decide who would live and who would die. As part of this effort, Lilly provided a group of physicians and bioethicists with a $1.8 million grant to form the Values, Ethics, and Rationing in Critical Care (VERICC) Task Force, purportedly to address ethical issues raised by rationing of the drug in hospital intensive care units. Finally, the Surviving Sepsis Campaign was established, in theory to raise awareness of severe sepsis and generate momentum toward the development of treatment guidelines.

This marketing campaign is especially troublesome because Xigris has been linked to increased risk of serious bleeding in patients who use it as well as other concerns. "Controversy surrounds both the drug study itself and the FDA approval," wrote NEJM editor-at-large Richard P. Wenzel, MD in 2002.. The FDA approved the drug despite the advisory committee's split vote (10 to 10) due to concerns about the validity of the claimed efficacy and safety findings on the basis of a single trial.

Eli Lilly spokeswoman Judy Kay Moore insists that the company did not mastermind the ethics task force or steer the guideline-writing process. It was only a coincidence, Moore says, that the ethics task force and the Surviving Sepsis Campaign used the same public relations firm, Belsito and Company.

References

— Preceding unsigned comment added by RXPhd (talk • contribs) 23:38, 31 March 2007 (UTC)

• Note, this section was added by user RXPhD in this dif on 31 March 2007. Jytdog (talk) 20:07, 19 January 2016 (UTC)

Pharmaceutical brands

This section didn't have many citations, more are needed, especially for more recent products. — Preceding unsigned comment added by Rosalina523 (talk • contribs) 16:53, 12 March 2013 (UTC)

Absolutely

Merge. Lilly must be presented as they are in toto, IN ONE PLACE. Those who seek INFORMATION must be readily apprised of the complete picture; separating the bad from well, whatever else is there, is not serving the interests of accuracy.

Cisum.ili.dilm 17:31, 10 November 2007 (UTC)

BIASED Criticism: check this out!

Unless the Eli Lilly Corporation is pure evil -- which, hey, they may be -- the 'criticism' section is far too long. Now, look what I’ve discovered:

Prior to December 25, 2006, there was no criticism section at all. None. Then comes user 67.82.232.151, who single-handedly wrote the vast majority (possibly all) of its current content. Check out this guy's revision history: aside from minor grammatical corrections, almost 100% of his edits are designed to defame the Eli Lilly Corporation.

Now, that’s fine, so long as he does so in a non-POV manner. He doesn’t. The guy writes with obvious bias, and often (though not always) his statements are unsourced. Most that are sourced aren’t internet-accessible, and therefore cannot be easily verified.

Since this one guy with a grudge has had such a huge effect on this page, I’m adding a POV tag. I know nothing about the industry myself, so until someone can verify this user's rant, we should let people know what’s what.

Here are some of his edits to the Eli Lilly page:

Eli Lilly has been known to engage in withholding internal information on medications, including Prozac, Thimerosal and Zyprexa in order to downplay side effects and adverse reactions in order to boost profits. [11]

Consequently, many critics claim that the FDA approval of duloxetine for Major Depressive Disorder (MDD) and diabetic neuropathy is irresponsible and intellectually dishonest, and is a case illustration of the agency's failure to prevent harmful drugs from being marketed in the name of big profits. [12]

In one of the only three cases to ever go to trial for SSRI indication in suicide, Eli Lilly was caught corrupting the judicial process by making a deal with the plaintiff's attorney to throw the case, in part by not disclosing damaging evidence to the jury. [13]

Over the last decade, the company spent millions of dollars lobbying Congress in hopes of extending its patent on Prozac and some lawmakers even attempted to insert last-minute provisions to omnibus spending bills to grant the company’s wish. Generic drugmakers prevailed, handing Eli Lilly one of its few legislative losses in recent memory. The company, which favors Republicans over Democrats with its contributions… [14]

This same user also started the ‘Controversy’ statement on the Duloxetine page, containing the following outsourced and obviously biased statements:

In the 1980s, [Eli] Lilly waged a successful campaign to get fluoxetine, brand name Prozac, through the FDA even though not a single study submitted to the agency showed the drug to be effective for depression when taken alone. …not only targets serotonin, it also impacts another important neurochemical, norepinephrine. This flatly contradicts the ‘serotonin/good, norepinephrine/bad’ story that launched the SSRI revolution that [Eli] Lilly started with fluoxetine. [15]

He started a ‘Legal’ section on the Olanzapine page with this:

…documents given to The Times by a lawyer representing mentally ill patients, show that [Eli] Lilly executives kept important information from doctors about Zyprexa’s links to obesity and its tendency to raise blood sugar — both known risk factors for diabetes. [16]

He adds this unsourced statement to the SSRI Discontinuation Syndrome page:

Data obtained from 9 clinical trials assessing the efficacy and safety of duloxetine in the treatment of major depressive disorder (MDD) by Lilly Research found that patients with discontinuation-emergent adverse events (DEAEs) were reported by 44.3% of duloxetine patients… No follow up was published by [Eli] Lilly stating the duration of DEAE's longer than one week ultimately persisted for. [17]

--70.17.209.58 09:02, 22 March 2007 (UTC)

This article is a collaborative effort. The controversy section is important to this article and if their are problems with it, it should be fixed, not removed. Neitherday 12:49, 22 March 2007 (UTC)

Gosh, guess I shouldn't have removed it then. Oh wait, I didn't, and never suggested doing so. --70.17.209.58 20:23, 22 March 2007 (UTC)

That should be directed to the person who did. Sorry it came across wrong, and that is my fault. I should not have indented so as to indicate a direct reply. Neitherday 21:06, 22 March 2007 (UTC)

Nevertheless you're right! Also there is a link on the main page to a "El Lilly Controversy" article (in the controversy section). This is content forking and does not follow Wikipedia guidelines ... Content forking. I am also considering putting in Neutrality templates and Dispute templates but am not jumping yet as I do not fully understand the procedure. If a more experienced editor want's to jump ahead of me then fine :) DJ Barney 16:10, 4 June 2007 (UTC) Can't get the links to work for some reason... http://en.wikipedia.org/wiki/Wikipedia:Neutrality_templates http://en.wikipedia.org/wiki/Wikipedia:Dispute_templates DJ Barney 16:13, 4 June 2007 (UTC)

One of the largest corporations?

It's not even one of the largest Pharma corporations!

<img src="http://www.economist.com/images/20050618/CSU885.gif">

http://www.economist.com/images/20050618/CSU885.gif

Pfizer, Glaxo, Sanofi all are far larger pharma companies.

Eli Lilly is 229th largest company in the world. And in the top 40 in the USA [18]. Not bad considering there are over two million corporation worldwide. Charles Edward 00:20, 29 May 2008 (UTC)

Zyprexa

Zyprexa (Olanzapine) is Lilly's largest seller. It used to be the first-place atypical antipsychotic in the U.S. but has dropped to third. This is probably because doctors and patients have learned, through the NIH CATIE study and through thousands of lawsuits, that it has the most dangerous side effects of all the drugs in its class. It causes diabetes, hyperglycemia, and death. 8000 plaintiffs settled with Lilly in 2005 and are still waiting for payment. Many states have sued Lilly for alleged fraud, for not revealing its side effects, and for compensation to their state's Medicaid programs for the costs of the drug as well as the costs involved in caring for people who got such conditions as diabetes from the drug. Lilly has also been charged with alleged fraud in off-label marketing of the drug for children. Many individual lawsuits remain outstanding and will begin to be heard once the 8000 plaintiff suit has been finalized. Lilly states that it will "vigously defend" itself against these individual lawsuits, but a number of them are for death allegedly caused by this drug.

• The New York Times recently reported on this: http://www.nytimes.com/2006/12/17/business/17drug.html?ei=5065&en=51ecabefcf344013&ex=1166936400&partner=MYWAY&pagewanted=print

Should this be included? Frank 16:17, 17 December 2006 (UTC)

I briefly had a contribution up with a typo in it. My profound apologies to all.--Mumbler7 15:41, 18 January 2007 (UTC)

---

Lilly Zyprexa Lawsuit 8 State Countdown May 25 2007

Zyprexa targeted by AG's for Fraud

Utah Latest state to sue Eli Lilly in developing "Viva Zyprexa" Scandal.

Side effects to Zyprexa can include high blood sugar levels, acute weight gain and pancreatitis, according to the lawsuit.

"Utah has paid millions of dollars for inappropriate and medically unnecessary doses of Zyprexa. As a result, Lilly has been illegally enriched at the expense of the State," the lawsuit said.

The state is seeking civil damages and penalties, including $5,000-$10,000 for each prescription that was "not medically necessary."

Lilly also faces lawsuits filed by attorneys general of Alaska, Louisiana, Mississippi, New Mexico and West Virginia alleging that it marketed Zyprexa for unapproved uses or hid the risks of weight gain and diabetes.

Eli Lilly makes billions on diabetes treatment and also gets $4.2 billion a year in sales of their biggest cash cow Zyprexa which has been scandalized as *causing* diabetes as a major side effect.

Not fair!

Daniel Haszard Bangor Maine 4 year Zyprexa user who now has diabetes http://www.zyprexa-victims.com

Re: Prozac

It does not stimulate release of serotonin; it keeps the serotonin that's been released from being reuptaken: reuptake inhibitor. Aleta 01:12, 15 November 2006 (UTC)Aleta

Controversy and medical ethics

These sections below have good potential, but really need more and better citations. RXPhd 23:30, 31 March 2007 (UTC)

Strattera and adult ADHD

In 2002, Lilly began marketing Strattera®, the first non-stimulant medication approved for the treatment of Attention-deficit hyperactivity disorder. It was the first such medication to be specifically marketed to adults with this disorder.

Strattera has been used by more than two million patients. In 2004, Strattera grossed $632 million, or roughly 25 percent, of the $2.6 billion U.S. ADHD pharmaceutical market, and was the fastest growing medication in this market.

Strattera carries a Food and Drug Administration (FDA) black box warning, the highest level of warning a drug can receive, as a result of studies showing a possible link between use of the drug and suicidal thoughts in children, as well as possible liver damage in adults. Lilly acknowledges that the medication has several other side effects, including pain during urination and orgasm, urinary retention, a tightening of the scrotum, mood swings, and dry mouth.

Strattera, a Selective norepinephrine reuptake inhibitor, was originally developed as an anti-depressant, but never received FDA approval for this use. The drug instead was approved by the FDA for use in the treatment of adult ADHD, which has become its more common use.

Lilly owns the domain adultadd.com, which allows visitors to take a test to see if they have the condition, and the company has run advertising campaigns, which have been designed to raise awareness of the condition. This effort has been controversial because there are some medical professionals who believe that ADHD is overdiagnosed and that companies like Lilly have perpetuated this with extensive television and other marketing.

Neutrality

The article has has become heavily biased towards the company. There is a section of accolades (of which there are many) but not a section of critisisms (of which there are many). I beleive someone has unbalanced the article in Eli Lilly's favour due to the recent New York Times articles. I'm rather new to wikipedia editing and don't know the process myself, but could someone more fluent please help with this issue? —The preceding unsigned comment was added by 69.76.170.199 (talk) 04:39, 23 April 2007 (UTC).

There should be a brief overview of some of the controversy surrounding Eli Lilly in this article, though the details should stay in the controversy article. Neitherday 16:11, 25 May 2007 (UTC)

A seperate article is not within Wikipedia guidelines ( Content forking ). The articles should be recombined. I am seeking advice from experienced editors. DJ Barney 13:56, 5 June 2007 (UTC)

Actually, (in jan08 at least) the Content forking page says:There is no consensus whether a "Criticism of .... " article is always a POV fork. At least the "Criticism of ... " article should contain rebuttals if available, and the original article should contain a summary of the "Criticism of ... " article.Mujinga (talk) 17:12, 19 January 2008 (UTC)

This article is a war zone by the look of it! I am putting an Unreferenced tag on the page as it has none. If it is removed then I will face the music. But it looks like this article could go into arbitration (and should?), I must admit I'm not sure of the procedure. DJ Barney 15:41, 4 June 2007 (UTC)

"One of the largest companies in the world"

The above statement was removed from the article, I was thinking it should be readded, but maybe changed a bit. It is 229th largest in the world, and 149 in the US. [19], Hoe about saying it is "A Fortune 500 company, and in 2007 ranked the 229th largest company in the world." —Charles Edward ^{(Talk | Contribs)} 12:27, 29 July 2009 (UTC)

Much better, but does this really belong in the introductory paragraph? Fortune 500 is mentioned later, and "10th largest corporation by global pharmaceutical sales" (also mentioned later) seems to me much more relevant than "229th largest in the world".--Biologos (talk) 13:15, 29 July 2009 (UTC)

Point taken. Good job working on the article too, it is need of a good fixing-up. —Charles Edward ^{(Talk | Contribs)} 13:27, 29 July 2009 (UTC)

Oraflex/Opren

Why has the Oraflex/Opren scandal been whitewashed from this and the Eli Lilly controversies article? Alexi star (talk) 11:39, 10 February 2011 (UTC)

Company history section

The company history originally had just a few inline citations and not much detail beyond the company's early years (pre-1900). I added more content to 20th century as well as adding subheadings. The headings may not be needed, but it may help identify specific periods in the company's long history. I also added inline citations to new content. When I could locate sources, I also added inline citations to previous content that had not been cited.Rosalina523 (talk) 16:53, 12 March 2013 (UTC)

Company profile section

It appears this section should include current information on the company, so I made the company history a separate section.Rosalina523 (talk) 16:53, 12 March 2013 (UTC)

Personnel section

It appears that this section deals with company leaders, so I added info on Presidents/CEOs up to 2012 and subheadings for other company leaders, not sure if those are needed.Rosalina523 (talk) 16:53, 12 March 2013 (UTC)

What about Lilly's impact on the mass production of Insulin?

Yes, hmm? --Word2013 (talk) 01:14, 18 April 2013 (UTC)

Controversy

Eli Lilly is one of the nation’s leading pharmaceutical companies. While the company has played a role in developing a number of progressive drugs and treatments for all kinds of ailments, its most famous product is Prozac, the world’s best known antidepressant. The company spent millions of dollars lobbying the United States Congress in hopes of extending its patent on Prozac. The patent on Prozac was declared invalid on February 2, 2001, in connection with a lawsuit against a generic competitor. The early loss of patent exclusivity allowed generic companies to sell Prozac and Lilly sales plumeted; the corporation is still recovering from this major financial setback. Eli Lilly subsequently released Prozac Weekly and Cymbalta. The company has joined others in the drug industry in continuing to fight for extended patent laws that would protect their exclusive rights to market their pharmaceutical products.

Eli Lilly is also one of many drug companies that give soft money to advocacy groups and political action committees (PACs) to help influence lawmakers and regulators. Historically Eli Lilly favors pro-business Republicans over Democrats with its political contributions (75% to 25% in the last nine US election cycles).

Though the contributions of Lilly and similar large pharmaceutical companies typically are aimed at influencing policies and laws, it is difficult to argue that these contributions are aimed at approving specific new molecules. Approval is handled via the FDA, not congress or any other lawmaker. The FDA's primary source of funding is "user fees" paid by the industry to ensure there are adequate resources available to review and approve these drugs. Many have argued these user fees represent a conflict of interest. It is worth noting that the current system was put in place c. 1990 in response to allegations that drugs were not being approved efficiently; this movement stemmed from gay-rights activists unhappy with the slow progress of HIV treatments.

Other donations sometimes come through the Lilly Endowment, which maintains nearly $11 billion in assets and owns 13% of the company's stock. The grants are portrayed by the company's and nonprofits as "giving back" to patients. The funding usually comes from the company's marketing or sales divisions, not charity offices. Grants often rise with promotional spending as a drug hits the market and fall when sales ebb.

In 2000-2001, the American Diabetes Association (ADA) did not disclose an unusual gift from Lilly: a lent executive, Emerson "Randy" Hall Jr., who moved into ADA's Alexandria, Virginia headquarters and coached the organization on growth strategies, all paid by Lilly.

A Philadelphia, Pennsylvania native now retired and living in Princeton, New Jersey, Hall said he never tried to influence the group and merely helped it market itself, including writing its slogan: "Cure. Care. Commitment." Hall estimated that his work, including diabetes patient research he subsequently shared with Lilly, would have cost "hundreds of thousands" from a contractor. Asked why it did not cite Hall on its tax returns or annual report, ADA spokeswoman Diane Tuncer said: "There is not a requirement to do so."

Another non-profit group, the National Alliance on Mental Illness (NAMI), did not disclose that Lilly marketing manager Gerald Radke briefly ran its entire operation. Radke began in 1999 as a Lilly-paid "management consultant," then left Lilly and served as NAMI's paid "interim executive director" until mid-2001. The group acknowledged this only after being shown Radke's resume listing the job. After NAMI, he ran the Pennsylvania Office of Mental Health and Substance Abuse, and now serves in the Pennsylvania Health Department.

Lilly, which donated at least $2.5 million to the ADA and $3 million to NAMI between 2003 and 2005, called its executive loans mutually beneficial. "The primary goal is to assist that organization in developing a needed capacity or function, but it also often serves to assist in the career development of the employee," a Lilly spokesman, Edward G. Sagebiel, said.

In 2005, as part of a U.S. House of Representatives budget bill that reduces spending on Medicaid prescription drugs, Eli Lilly and other businesses secured a provision ensuring that their mental health drugs continue to fetch top price at a cost of hundreds of millions of dollars to the states.

The provision, inserted by Rep. Steve Buyer (R-Ind.), whose district flanks Lilly's Indianapolis headquarters, would largely exempt antipsychotic and antidepressant medications from a larger measure designed to steer Medicaid patients to the least expensive treatment options. To opponents, Buyer's measure underscores the excessive power that corporate interests wield on Capitol Hill. Critics say the measure also violates the purpose of the budget-cutting bill, which was drafted to give state governments the flexibility to cut program costs in ways that minimize the harm done to beneficiaries. The Congressional Budget Office has estimated that the provision will raise federal drug spending by $125 million over five years, while state officials say they are likely to face far higher costs.

On January 25, 2006, Democratic leader Nancy Pelosi, Democratic Whip Steny H. Hoyer and Ranking Minority Member Henry A. Waxman asked J. Dennis Hastert, Speaker of the House of Representatives at that time, for a congressional investigation into the role played by the Alexander Strategy Group, a lobbying firm closely linked to Tom DeLay and Jack Abramoff, in the passage of the Medicare Prescription Drug Act which was passed on December 8, 2003. With the indictments of DeLay and Abramoff, new questions arose about the role of the Alexander Strategy Group in the passing of the bill. Lobby disclosure forms showed that the largest single client of the Alexander Strategy Group was the pharmaceutical industry, which paid the small firm over $2.5 million, including nearly $1 million in 2003 when the prescription drug law was being written.

The lobby disclosure forms also revealed that the primary clients represented by the Alexander Strategy Group were Pharmaceutical Research and Manufacturers of America (PhRMA) and Eli Lilly during consideration of the Medicare Prescription Drug Act. The person representing PhRMA and Lilly was Tony Rudy, a former deputy chief of staff for DeLay who worked for Abramoff from 2001 to 2002. On January 9, 2006, the Alexander Strategy Group announced that it was shutting down its lobbying operations.

Senior Vice President and General Counsel for Eli Lilly, Robert A. Armitage, is the past chair of the Patent Committee of PhRMA.

In February 2007, the Serious Fraud Office in the UK launched an investigation into allegations of Eli Lilly being involved in the discredited oil-for-food sanctions regime in Iraq. They are accused of paying bribes to Saddam Hussein's regime.

Lilly is paying their debth soon. --Word2013 (talk) 01:14, 18 April 2013 (UTC)

Subjective

There is text in the article that is purly subjective and not backed up by a referrence:

Subjective reference

"Eli Lilly and Company History" from Fundinguniverse.com is used _25_ times as a reference in this article. It would appear this source simply collects material from company profiles. As such, it is not NPOV at all. I think the reference & any quotes should be removed. winterstein (talk) 18:50, 14 June 2013 (UTC)

  I've removed the fundinguniverse.com reference, and toned down some text which relied on it as a source. --winterstein (talk) 08:49, 21 June 2013 (UTC)

Eli Lilly vs the state of Canada

Apparently Eli Lilly has sued the state of Canada for refusing to grant it patents and demands 500M in damages, see Huffington Post: [20]. Shouldn't this be in the article as this has started a debate about whether companies should have the legal powers of countries. AadaamS (talk) 08:06, 18 November 2013 (UTC)

Citation date format

MMM. DD, YYYY ... established in [21] --User:Ceyockey (talk to me) 00:45, 10 September 2015 (UTC)

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Assessment comment

The comment(s) below were originally left at Talk:Eli Lilly and Company/Comments, and are posted here for posterity. Following several discussions in past years, these subpages are now deprecated. The comments may be irrelevant or outdated; if so, please feel free to remove this section.

Indiana assessment This article has be classified as Start class. It has been determined that this article has no in line references which leaves content disputable. The Pharmaceutical brands subsections headers should be removed and make one whole Pharmaceutical brands section. A wikitable could be made for a list for the Other Eli Lilly Therapies. Expand in brief the Controversy section. This article has been determined to be High importance based on the economic impact on the state of Indiana. Assessed by:Jahnx (talk) 06:33, 15 March 2008 (UTC)

Last edited at 06:33, 15 March 2008 (UTC). Substituted at 14:44, 1 May 2016 (UTC)

Revenue by brand

It would be great if somewhere (eg Pharmaceutical brands) it would say which of its brands generate the most revenue. - Rod57 (talk) 13:18, 8 April 2016 (UTC)

Discussion about controversies, company ethics and bias in this article

Much seems to have been archived. Some still seems valid. - Rod57 (talk) 13:25, 8 April 2016 (UTC)

Virapen book

About this, which I have been thinking about for a few days.

Fluoxetine / Prozac

The company has been criticized for supporting the positive studies on side effects of their drugs, in order to speed up the approval of these drugs. Criticism of Eli Lilly was expressed about in connection with the approval of Fluoxetine. John Virapen, former CEO of Eli Lilly and Company in Sweden, wrote in his book "Side Effects: Death. Confessions of a Pharma-Insider" about marketing strategies and corruption of the company during the market introduction of Fluoxetine as an antidepressant.

References

This is a self-published book. I have found discussions of this book on FRINGE-advocating websites like tv.naturalnews.com/v.asp?v=647AC0F97E443BB4BACC91479355F989 this] but not anywhere mainstream. This deserves no WEIGHT in this article. Happy to bring this to RSN if folks disagree, after some discussion here. Jytdog (talk) 00:17, 31 May 2016 (UTC)

• Agree I was wondering about the addition and felt at the very least the material should have been in the Prozac section vs stand alone. Based on what you are saying about the source I support the removal. Springee (talk) 00:43, 31 May 2016 (UTC)

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catalog

moved this list here, per WP:NOTCATALOG and b/c most of this is not sourced. Per WP:BURDEN please do not restore without finding reliable independent sources, checking this against them, and citing them. pls also consider WEIGHT

Additional Eli Lilly drugs

• Alimta (for pleural mesothelioma and non-small cell lung cancer).
• Amytal (a "barbituric acid derivative" introduced in 1925 was "the first American sedative of this kind").
• Bavencio (a "barbituric acid derivative avelumab injection" introduced in 2017 was "the first American sedative of this kind") (in conjunction with EMD Serono and Pfizer) Distribution in Canada.
• Ceclor (an oral cephalosporin antibiotic).
• Cambia (for the treatment of migraine).
• Darvocet (an analgesic for mild to moderate pain).
• Darvon, (an analgesic alternative to codeine, introduced in 1957 withdrawn in 2009).
• Effient (an antithrombotic for acute coronary syndrome in percutaneous coronary intervention); co-marketed with Daiichi Sankyo.
• Ephedrine (introduced in 1926 for the treatment of allergies, including hay fever and asthma).
• E-Mycin (an antibiotic for respiratory and other infections).
• Erbitux (for metastatic colorectal cancer and head and neck cancer).
• Evista (for the prevention and treatment of osteoporosis and for the reduction in risk of breast cancer).
• Forteo (for osteoporosis).
• Glucagon (for severe, life-threatening hypoglycemia).
• Humalog (for Type 1 and Type 2 diabetes).
• Humatrope (a human growth hormone for pediatric growth disorders).
• Humulin (for Type 1 and Type 2 diabetes).
• Jardiance (Empagliflozin) (Sodium-glucose co-transporter-2 (SGLT2) inhibitor) (Treats type 2 diabetes: lowers blood sugar, reduces body weight, lowers systolic blood pressure, and reduces cardiac death.
• Keflex (a cephalosporin antibiotic).
• Livalo (for hypercholesterolemia).
• Lipofen (for Mesothelioma, hypercholesterolemia) and Hepatitis B).
• Moxam (an antibiotic. Introduced in collaboration with Shionogi, a Japanese drug company).
• Mandol (an injectable cephalosporin antibiotic for treating "hospital-acquired infections").
• ReoPro (a cardiovascular drug used during high-risk angioplasty surgery).
• Strattera (a non-stimulant medication for attention-deficit hyperactivity disorder).
• Symbyax (for bipolar disorder).
• Tradjenta (for Type 2 diabetes).
• Vascepa (for severe sepsis) Allergic to Fish and osteoporosis) Introduced in collaboration with Amarin Corporation and Kowa Pharma,a Japanese drug company).
• Xigris (for severe sepsis). Withdrawn in November 2011 after failure to show benefit.

References

-- Jytdog (talk) 07:28, 5 August 2017 (UTC)

unsourced

the following is unsourced; moved here per WP:PRESERVE. Per WP:BURDEN please don't restore without finding reliable sources, verifying, and citing.

A number of global leaders in the fields of health policy, management, and scientific research have worked at Lilly, including:

• Ernesto Bustamante, Peruvian scientist.
• Jose F. Caro, American physician, scientist, and educator most notable for his research in obesity and diabetes.
• Richard DiMarchi, Chief Scientific Officer, Marcadia Biotech.
• Mitch Daniels, current president of Purdue University, former Governor of Indiana and director of the Office of Management and Budget for President George W. Bush.
• Roald Hoffmann, Nobel Prize-winning chemist.
• Michael Johns, former White House speechwriter and Heritage Foundation policy analyst.
• Claude H. Nash, CEO, ViroPharma.
• Peter Nicholas, co-founder of Boston Scientific.

Prominent Lilly board members have included:

• George H. W. Bush, former President and Vice President of the United States of America.
• Martin Feldstein, economist, Harvard University.
• Kenneth Lay, former CEO, Enron.
• William Verity Jr., former U.S. Secretary of Commerce.

-- Jytdog (talk) 18:22, 4 September 2017 (UTC)

Catalog redux

See above, same deal

Additional Drugs

• Alimta, for the treatment of pleural mesothelioma and non-small cell lung cancer.
• Amytal, a Amobarbital introduced in 1923, was the first abrasive drug of its kind.
• Amyvid, a PET scanning radiopharmaceutical compound contaning the radionuclide fluoride-18, recently FDA approved as a diagnostic tool for Alzheimer's disease.
• Actos, a drug co-marketed by Takeda.
• Adcirca, a drug similar to Cialis introduced in 2009.
• Aquaphor
• Axiron, for breast cancer.
• Axid
• Basaglar with Boehringer Ingelheim.
• Byetta, a drug that is co-marketed by Amylin Pharmaceuticals now AstraZeneca.
• Cubicin, co-marketed from Cubist Pharmaceuticals now Merck & Co.
• Cyramza
• Darvon, a drug that was launched in 1955, and later lilly withdraw the drug in 2010.
• Darvocet, a drug that was co-marketed agreement from Xanodyne Pharmaceuticals Inc..
• Drisdol
• Dynabac, a drug that was co-marketed from Sanofi.
• Effient a drug that was co-marketed by Daiichi Sankyo.
• Erbitux, by Merck, ImClone Systems and Bristol-Myers Squibb.
• Eryc, co-marketed by Pfizer and Allergan.
• Evista
• Forteo
• Glucagon
• Glyxambi, co marketed by Boehringer Ingelheim.
• Jardiance with Boehringer Ingelheim.
• Humulin
• Humulin N
• Humulin R
• Humalog
• Humatrope
• Keflex
• Keflin
• Lartruvo
• Livalo, a drug co-marketed by Kowa Pharmaceuticals.
• Moxam a drug that was co-marketed by Shionogi in japan.
• Oraflex
• Oncovin
• Pradaxa co-marketed by Boehringer Ingelheim.
• Sarafem similar to Prozac, launched in 1986, co-marketed by Allergan.
• Saizen with Merck.
• Seconal
• Trulicity
• Taltz
• Tradjenta, from Boehringer Ingelheim.
• Vancocin

-- Jytdog (talk) 07:33, 8 September 2017 (UTC)

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methadone

methadone is not an analgesic but a narcotic — Preceding unsigned comment added by 45.72.206.97 (talk) 13:41, 26 May 2018 (UTC)

Emgality

The FDA recently approved the migraine injection medication Emgality (galcanezumab-gnlm). Would this go under Pharmaceutical brands? Source does a decent job of coverage on some patent lawsuits Eli Lilly was involved with. PcPrincipal (talk) 17:11, 28 September 2018 (UTC)

Footprint in Ireland

Information in this news report: Wei, Daniela; Hoare, Pádriag (2 November 2018). "Eli Lilly partner sees growth". Irish Examiner. Retrieved 4 November 2018. --User:Ceyockey (talk to me) 15:33, 4 November 2018 (UTC)

Elanco

Elanco still redirects here despite being spun off over a year ago. Anyone want to take a crack at starting up a page?CastAStone/^/(talk) 03:42, 8 March 2020 (UTC)

@CastAStone:  Done (finally!) XyZAn (talk) 20:50, 18 July 2020 (UTC)

Zyprexa

I have added a brief overview about Zyprexa to the lead. It is notable, in scope, and adds balance. Ushistorygeek (talk) 14:52, 31 July 2022 (UTC)

@Ushistorygeek: Why is the Zyprexa information from 2009 one of the most important points in the article? See MOS:LEAD. Do you have a conflict of interest (WP:COI) related to Lily? --Whywhenwhohow (talk) 02:56, 1 August 2022 (UTC)

Two reasons. 1)The illegal actions of the organization garnered significant news coverage spanning multiple years and resulted in the largest criminal penalty assessed in the US (for any person or organization at the time), and 2) from the guide you referenced: "The lead should stand on its own as a concise overview of the article's topic. It should identify the topic, establish context, explain why the topic is notable, and summarize the most important points, including any prominent controversies." Ushistorygeek (talk) 19:38, 1 August 2022 (UTC)

It is not clear that these events from 2006-09 are prominent and it is not the largest criminal penalty. --Whywhenwhohow (talk) 21:21, 1 August 2022 (UTC)

The coverage of the controversy coupled with the scope and size of the criminal wrongdoing leads me to conclude it is prominent. (Dedicated sections of Wikipedia articles on the topic support this). The penalty was the largest at the time, as I wrote above. In 2009 the Department of Justice characterized it this way

"The monetary settlement, totaling $1.415 billion, is the largest amount paid by a single defendant in the history of the United States Department of Justice (“DOJ”)."

The DOJ press release goes on to state:

"The information charges Eli Lilly with the misdemeanor of introducing misbranded drugs into interstate commerce between September 1999 and November 2003. The Food and Drug Administration (“FDA”) had approved Zyprexa for use by adults for treatment of schizophrenia and certain types of bipolar disorder. Eli Lilly has admitted that it illegally marketed Zyprexa for uses never approved by the FDA. Among other things, the government alleges that these uses included treatment of elderly patients for such things as sleep disorders and dementia. According to the information, Eli Lilly targeted its illegal marketing of Zyprexa to two types of doctors: those who treat the elderly in nursing homes and assisted living facilities, and primary care physicians. In September 1999, Eli Lilly began encouraging doctors to prescribe the drug for the treatment of dementia, Alzheimer’s, agitation, aggression, hostility, depression, and 2 generalized sleep disorder. Zyprexa was not approved for use for any of these disorders, which, unlike schizophrenia, are prevalent in the elderly population. Nevertheless, Eli Lilly’s long-term care sales force promoted the use of Zyprexa in elderly populations for these symptoms. Because one of Zyprexa’s side effects is sedation, Eli Lilly directed its long-term care sales force to tell doctors that Zyprexa would help patients with sleep problems, behavioral issues, and dementia. They claimed this side effect was a therapeutic benefit, not an adverse event, with the sales slogan “5 at 5,” that five milligrams of Zyprexa at 5 p.m. would help their patients sleep. Then in 2000, Eli Lilly expanded its illegal marketing to primary care physicians with its primary care sales force in the “Viva Zyprexa” campaign, adding even more sales representatives. The goal of the campaign was to make Zyprexa an “everyday agent in primary care” even though the company recognized that schizophrenia and bipolar disorder were not viewed as conditions typically treated by primary care physicians. Lilly instructed the sales force to recommend Zyprexa for all adult patients with behavioral symptoms like agitation, aggression, hostility, mood and sleep disturbances, and depression.

...

"Eli Lilly knew that significant weight gain and obesity were adverse side effects of Zyprexa and that weight gain and obesity were factors in causing hyperglycemia and diabetes. Yet despite written caution from the FDA, Eli Lilly continued to promote these adverse events as therapeutic benefits of Zyprexa use, particularly in the elderly."

...

“When pharmaceutical companies interfere with the FDA’s mission to insure that drugs are safe and effective, they undermine the doctor-patient relationship and put the health and safety of patients at risk,” said Magid. “People have a legal right to know that pharmaceutical companies are marketing their drugs only for uses approved by the FDA and that their doctors’ judgment has not been affected by misinformation from a pharmaceutical company trying to boost revenues."

...

"In a separate civil settlement agreement, Eli Lilly agreed to pay the United States approximately $438,171,543.58 to settle allegations that it caused invalid claims for payment for Zyprexa to be submitted to various government programs such as Medicaid, TRICARE, and the Federal Employees Health Benefits Program and caused purchases of Zyprexa by the Department of Veterans Affairs, the Bureau of Prisons, the Department of Defense, the Defense Logistics Agency, the Department of Labor, and Public Health Service entities for unapproved off-label uses. Also, Eli Lilly agreed to pay various state Medicaid programs more than $361,828,456.42 to settle similar claims."

...

“Today’s announcement of the filing of a criminal charge and the unprecedented terms of this settlement demonstrate the government’s increasing efforts aimed at pharmaceutical companies that choose to put profits ahead of the public’s health,”

...

The civil settlement also resolves four whistle-blower lawsuits filed in federal court here: United States of America ex rel. Robert Rudolph v. Eli Lilly and Company, Civil Action No. 03- 943; United States of America ex rel. Joseph Faltaous v. Eli Lilly and Company, Civil Action No. 05-1471; United States of America ex rel. Steven Woodward v. Eli Lilly and Company, Civil Action No. 06-5526; and United States of America ex rel. Jaydeen Vincente v. Eli Lilly and 4 Company, Civil Action No. 07-1791. Those cases were filed by former sales representatives who identified Eli Lilly’s off-label marketing practices. To encourage individuals to come forward and identify companies and individuals that defraud the government, federal law permits whistle blowers to share in the recovery for such fraud. In this case, the whistle blowers will share in 18%, or $78,870,877, of the federal share of the (civil) settlement. Ushistorygeek (talk) 22:00, 1 August 2022 (UTC)

The tone of the article is inappropriate for wikipedia. The edits reflect bias and contain stale and incorrect information. I am reverting your edits. Please don't add the text back without consensus here. --Whywhenwhohow (talk) 03:31, 7 August 2022 (UTC)

The information you have deleted is notable and reliably sourced. Characterizing past criminal behavior as "mired in multiple controversies" is WP:SYNTH and does not accurately reflect the source. Ushistorygeek (talk) 14:42, 7 August 2022 (UTC)

The added information is factually incorrect and is biased. Please do not add it back without getting consensus. --Whywhenwhohow (talk) 01:40, 7 November 2022 (UTC)

@Whywhenwhohow see the facts quoted above on August 7 of this year. The information you have deleted is notable and reliably sourced. Again, as I wrote in characterizing past criminal behavior as "mired in multiple controversies" is WP:SYNTH and did not accurately reflect the source. Ushistorygeek (talk) 01:20, 8 November 2022 (UTC)

The claims about it being the largest are incorrect.

References

@WhywhenwhohowFriendly reminder to please sign your posts. The text accurately reflects multiple newsworthy sources who reported the judgement at the time. Nonetheless, I've added that qualifier to the article. Ushistorygeek (talk) — Preceding undated comment added 15:21, 9 November 2022 (UTC)

no mention of Dr. Abelardo Aguilar, discoverer of erythtromycin

the entire article reads like the bumpf spewed out regularly by corporate mouthpieces, guided by company lawyers. that this supposedly neutral and factual article does not delve into the shameful treatment of the man is remarkable, especially when one considers the billions erythromycin has brought the company's. perhaps there was a streak of racism as well - the company refused to let dr aguilar visit the production facilities where his discovery was turned into that very highly effective drug, nor would it allow him to visit on his own dime. dr aguilar died in poverty. 70.31.166.89 (talk) 14:53, 19 December 2022 (UTC)

Lede update

In an effort update the lede with notable developments I'm advocating for addition of the following:

In 2022 Eli Lilly experienced a $20 billion loss in value due to a parody Twitter account's false announcement about insulin sales ending in November 2022. In response to public pressure and increased competition, the company took action to make insulin more affordable, implementing cost caps and price reductions.

seeing no discussion or objections I will make this change in the coming daysUshistorygeek (talk) 00:03, 5 April 2023 (UTC)

I have implemented the previously mentioned edits. I welcome editors comments and feedback. Ushistorygeek (talk) 02:06, 11 April 2023 (UTC)

The other editors were right to remove it. This and the section on the 2009 settlement are undue for the article lead (absolutely due in the article body) Springee (talk) 21:30, 23 May 2023 (UTC)

Fellow editors. The lead section of a Wikipedia article serves to provide a concise summary of the article's most notable contents. The events mentioned, specifically the dramatic $20 billion loss in value due to a parody Twitter account and the subsequent actions taken by Eli Lilly to make insulin more affordable, are certainly of significant relevance, especially given their recency and the wide impact they had on public sentiment, company valuation, and potential policy discussions.

Relevance to the Public: The misinformation from a parody account causing such a drastic drop in the company's value highlights the growing influence and potential risks of social media in our digital age. This event serves as a prominent example of how misinformation can affect major corporations and, by extension, economies, making it a highly relevant point for current readers.

Significant Impact on Company: A $20 billion loss in value is not a minor fluctuation but represents a notable shift in the company's financial position. Additionally, Eli Lilly's subsequent actions to make insulin more affordable indicate a major shift in the company's strategy and public relations. This showcases how external pressures, whether from misinformation or public sentiment, can lead to tangible changes in a company's operations.

Balanced Representation: The previous mention of the 2009 penalty is an important historical point, but an update with more recent developments helps paint a more comprehensive and up-to-date picture of Eli Lilly. By including both the historical and recent events, we offer readers a balanced perspective of the company's trajectory over the years.

Lead as a Living Document: Wikipedia is a dynamic platform, and the lead section, in particular, should be adaptable to include recent events that have a notable impact. The incident in 2022 is a significant development in the history of Eli Lilly and deserves a mention in the lead, at least for a period, to inform readers of current and relevant events.

Given these points the inclusion of the 2022 events in the lead, ensuring it's presented in a concise manner. This would provide readers with a comprehensive view of both Eli Lilly's historical and current standing. Ushistorygeek (talk) 17:00, 9 September 2023 (UTC)

References