Preview

Bristol Myers

Good Essays
Open Document
Open Document
479 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Bristol Myers
In my opinion Bristol-Myers Squibb and Sanofi-Aventis seek a settlement rather than let the patent infringement case go to trial because Bristol-Myers Squibb fail to disclose the oral side deal with Apotex and its false certification to the FTC. Going to trial would have cost Bristol-Myers a great deal of money and severe penalties from the FTC. Bristol-Myers knew before hand that the FTC opposes agreements that restricted the introduction of generic drugs which could be anti-competitive. Bristol- Myers was hoping that it could have pursued a settlement with Apotex subjected to FTC approval and delay the launch of Apotex generic drug until its patent expire.
Bristol-Myers Squibb and Sanofi-Aventis should have attempted to pay Apotex to prevent it from launching the generic drug. It seems that BMS only entered the agreement because they felt that Apotex could not get approval. BMS offered Apotex $60 million break-up fee if the agreement was rejected by the FTC (Baron, 2010). To offer such a high break-up fee meant that BMS was very certain of the denial by the antitrust. The deal offered was to prevent Apotex from launching their version of plavix.
The strategy exerted by Sherman of Apotex was considered to be great judgment call on his part as well as the business. I believe he acted ethically in his strategy and negotiated terms that would benefit his business. He performed extensive research and found many distributors who wanted to purchase Plavix at very low and reasonable cost. On August 8th Apotex launched its generic Drug. Sherman states that, “There should be no mistake that our decision to launch a generic of this blockbuster product at risk is a testament to our commitment to patients, consumers and taxpayers (Baron, 2010). Because he was a good business man he made sure that the product was on the market and sales were soaring.
I felt that the FTC and the state attorneys general should have rejected the agreements. Companies must



Cited:

You May Also Find These Documents Helpful

  • Satisfactory Essays

    Trueblood Case 09 2

    • 804 Words
    • 2 Pages

    The agreement states Pharmagen will receive up to $500 million funding for R&D costs as they are incurred solely for the research efforts of a potential new drug “X”…

    • 804 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Biomax Case Summary

    • 1049 Words
    • 5 Pages

    The Company's primary strategy is to get those prescriptions surrendered by other pharmaceutical organizations. Despite the fact that the Company has received 4 standards to screen among the competitors, in any case it confronts the potential danger of disappointment. Drug organizations relinquished these items for a mixture of great reason including security, viability and benefit potential. Why does the Medicines Company have the Golden Finger? There is no such ensure that items which consent to the 4 criteria will end up being a blockbuster product. The Company seems to fail to offer an agreeable advertising arrangement for Angiomax and other future medications that are coming to company regarding to FDA. So we should stay sensible about…

    • 1049 Words
    • 5 Pages
    Good Essays
  • Satisfactory Essays

    The Affymax, Inc. Case

    • 249 Words
    • 1 Page

    The plaintiff in this case is the Affymax, Inc. who focuses on discovering drugs and develops drugs to treat different kinds of health conditions. Between 1992 and 1995, Affymax was contracted to work, research and invent products for Johnson & Johnson.…

    • 249 Words
    • 1 Page
    Satisfactory Essays
  • Better Essays

    An additional issue is what does “active market participant” mean? The Court defined it as someone “who possess singularly strong private interests.” In this case, that appears to mean someone who works in the industry and has an interest in limiting competition in the industry. In summary, the Supreme Court did not make it clear what “controlled by active market participants” meant in the decision, and therefore that is likely to be a major point of contention going forward. As will be discussed later, the FTC guidance will likely serve as a major source of information on this…

    • 1375 Words
    • 6 Pages
    Better Essays
  • Good Essays

    Pfizer has been involved in numerous litigations, which resulted in two things: damaged reputation and enormous payouts. The two biggest litigations concerned the pain killer Bextra and related off-label promotions and illegal drug testing on seriously ill children in Nigeria during a meningitis epidemic. The first was settled in 2008 by paying $2.3 billion in charges and the latter involved paying a fine of $75 million in April 2009. The discontinued projects reflect a loss of resources and also in the perceived inability to complete research projects. From September 2008…

    • 865 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    To determine the appropriate accounting for the Agreement under a R&D agreement, it must be established whether the entity must repay funds regardless of the outcome of the R&D (ASC 730-20-25-1). The PEI is obligated to receive royalties from Pharma not only with future revenues of drug X but also royalties associated with an existing commercialized drug. Therefore, Pharma must repay funds in the form of royalties to the PEI regardless of the outcome of drug X because they have an agreement to still pay royalties for an existing commercialized drug. If funds will be repayed regardless of the outcome, then a liability must be estimated and recognized no matter the means of settlement (ASC 730-20-25-3). Though the Agreement between Pharma and the PEI did not specify whether Pharma is committed to repay a liability, it can be assumed Pharma is committed to repay since the PEI is obligated to royalties. The liability would be recognized on Pharma’s books because they…

    • 427 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Unit 1 Homework

    • 900 Words
    • 3 Pages

    I think with the aspect of economics the company has done the right thing as far as design great drugs in the past, and often even took losses with the making and delivery of those drugs. When it comes to Vioxx, I tend to believe that they should have informed the public and the doctors prescribing and taking this drug with all their findings and notions before the hard evidence came about. I do believe that not telling the whole truth about their findings to the doctors and the pubic goes against my belief in ethics. If I had anything to do with the distribution of the drug before the 2004 removal from market, I would have really studied the reports and warnings, and if I saw what was being reported and said from the scientist, then I would have stopped the sale of it then, and not wait until 2004. I would then have made a public address and told the public and doctors why we are stopping the sale and production of this drug. This would have again put more faith into the company from the public view as well. This is a hard question because if we look at the tobacco companies, they are still selling tobacco that has been proven over and over again to be harmful to humans and animals. I am a smoker and hopefully one day will quit, but for a company to continue to produce and sell a known harmful and deadly product, this is ethically bad for them as well as our government to even allow it. Where is the ethics in all of this? I will never figure that one out.…

    • 900 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Pharmaceutical companies rely on their patents as a source of income that could be reduced by allowing generic companies to copy their drug and make it at a lower cost. If the companies’ profits are cut in half, this gives less money to them and hinders the amount of money they can contribute to the next strain of drugs necessary for those living with HIV. The money they make is used for research and development of these lifesaving drugs are included in the cost of the medication. This is why the prices of the first AIDS drug was twelve thousand dollars per year per patient when it was first released.…

    • 731 Words
    • 3 Pages
    Good Essays
  • Good Essays

    If I was the CEO of Merck I would have disclosed these risks to the FDA as soon as they were discovered so that the patients currently taking VIOXX would have been able to make their own informed decisions whether to continue taking it or not. Merck profits would have dropped, but patients would have lived and Merck’s legal liabilities would have been far less. By the time Merck withdrew VIOXX, they had known of evidence that it lead to increased cardiovascular risks for at least three years and possibly more and had publicly denied that there was any risk associated with VIOXX (Waymor).…

    • 672 Words
    • 3 Pages
    Good Essays
  • Good Essays

    American Dbq Analysis

    • 562 Words
    • 3 Pages

    In my opinion, I believe that it was unnecesarry to jump on board with the decision so quickly. They should have taken more time to justify their…

    • 562 Words
    • 3 Pages
    Good Essays
  • Good Essays

    The drug was a maintenance medication for painful conditions such as arthritis. Maintenance drugs became highly desired by pharmaceutical companies due too long term profitability resulting from no cure CITATION Law14 \l 1033 (Lawerence & Weber, 2014). Vioxx was prescribed to over twenty million people in the United States. Merck posted a seven billion dollar profit in a single year from Vioxx CITATION Law14 \l 1033 (Lawerence & Weber, 2014). Within six years from its release, Vioxx was recalled from the market due to adverse health defects. Merck voluntarily recalled the product resulting from post marketing safety…

    • 1192 Words
    • 5 Pages
    Good Essays
  • Powerful Essays

    an obscure report, but a federal judge upheld the deal as the fulfillment of a valid legal contract.…

    • 4962 Words
    • 20 Pages
    Powerful Essays
  • Good Essays

    violation of the Sherman Antitrust Act. I agree with the conclusion, but I don’t think that it…

    • 430 Words
    • 2 Pages
    Good Essays
  • Good Essays

    Although antitrust laws are good for the market, as in the instance with the federal government’s use of the Sherman Act against AT&T, which led to a communication revolution, there are a couple of issues concerning antitrust laws. The first is issue is the interpretive nature of the federal and state government laws. The Sherman Act, The Federal Trade Commission Act, and the Clayton Act are federal statutes written in general language rather than exact verbiage on code of conduct. In the case of Continental TV vs. GET, Sylvania this general language along with the court’s interpretation of the laws has brought instances where precedent has been changed leading to unknown permissible behavior for companies. The second issue is the increasing…

    • 374 Words
    • 2 Pages
    Good Essays
  • Good Essays

    The pharmaceutical giant and British drug maker, GlaxoSmithKline, has agreed to plead guilty and pay the government three billion dollars in a health care fraud settlement bought by the FDA. This is the largest settlement involving a pharmaceutical company in recorded history. GSK have admitted to committing three fraud charges. They promoted the off-label use of two anti-depressant drugs – Paxil and Wellbutrin. The two anti-depressants are not necessarily considered as bad medicine instead the GSK failed to apply for approval from the FDA. GSK broke the law when they marketed the drug for a non-approved use under the FDA. The second charge that was made against GSK was when they held back data and made unsupported claims regarding its diabetes drug Avandia. The third charge that was made against GSK was when their sales team used inappropriate and illegal marketing tactics to get the doctors to prescribe their drugs. In addition to using illegal marketing tactics, they offered doctors free spa privileges, trips to Jamaica and Bermuda, and concert tickets. The three criminal charges involved Paxil, Wellbutrin and Avandia and included a criminal fine of $1 billion. The remaining $2 billion involves fines in connection with a civil settlement over the sales and marketing practices of the blockbuster asthma drug Advair and several other drugs (NY Times). GSK have not only violated the rules made by the FDA but also committed basic unethical behavior. Even though the $3 billion may seem like a large amount, it represent only a small portion of what Glaxo made on the drugs. According to IMS Health, Glaxo’s diabetes drug Avandia racked up to $10.4 billion in…

    • 872 Words
    • 4 Pages
    Good Essays