Comparison Of Pfizer And Johnson & Johnson

Improved Essays
i. The two companies that were selected are Pfizer and Johnson & Johnson. First of all, Pfizer, Inc. is a research-based, global biopharmaceutical company which it focuses in improving the health standards locally or globally by manufacturing vaccines and injectable biologic medicines. Basically Pfizer operates under a few business segments such as Global Pharmaceutical, Global Vaccines, Oncology and Consumer Healthcare and Global Established Pharmaceutical. Unlike Pfizer, Johnson & Johnson is an investment holding company which focuses its interest towards health care products. Therefore, it engages in research and developments to improve the manufacture and the sale of personal care hygiene products, pharmaceuticals and surgical equipment. …show more content…
As Pfizer and Johnson & Johnson were among the top ten companies, the total revenue generated in 2016 is equivalent to 5.2 percent of the market value. Firstly, as Pfizer, Inc, the world’s second largest pharmaceutical company, the New York City-based company only had generated approximately 53 billion US dollars of the total revenue. This reflects the vulnerability of Pfizer towards the local economy because the major production of well-known drugs were carried out within US such as Lipitor, Lyrica, Enbrel and Viagra. In addition, with an extensive level of research and development within and outside of US, Pfizer is exposed to global economy where 60 percent of its total revenue, almost 26.4 billion dollars were generated from abroad. To illustrate, Pfizer has over 500 subsidiaries including research and developments departments and manufacturing companies and also with the total 98,000 employees in operations throughout the world. Due to Pfizer operates internationally, Pfizer faces foreign exchange risk, geographic risk, and also legal risk. The exposure of foreign risk was due to over 60 percent of Pfizer’s total revenue is from non-U.S. markets. Pfizer able to reduce its geographic risk by operating globally, so any changes of economic condition of one market would not affect others and also Pfizer is vulnerable to legal risks such as patent rights and trademarks. With having drug manufacturing as their core business, the company faces many legal issues related to

Related Documents

  • Improved Essays

    To capitalize on the success of their super bowl ad campaign for Old Spice body wash, Procter and Gamble developed and implemented a project to interact with fans and customers of their commercial. The idea of the project was simple, over a series of 2 ½ days (July 12-14 2010) the Old Spice guy would respond to comments given to him by his fans via social media. Procter and Gamble’s main reason for implementing this project was to generate brand awareness for Old Spice and therefore increase the volume of sales for Old Spice Body wash.…

    • 509 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    In addition, pharmaceutical industry is getting more competitive due to more merge companies and harder to get product approval by FDA. In addition, the number of new IND application is increasing in every fiscal year and FDA does not ease the regulatory or expedite the NDA review…

    • 544 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    Introduction In August 1983, the U.S.-based pharmaceutical giant Merck & Co., Inc. acquired Banyu Pharmaceutical, a major producer of penicillin and antibiotics in Japan, as one of the first acquisitions done by a non-Japanese company. “Upon conversion of the bonds, Merck would own 50.02% of the company” (Harvard Business Review, 1989). Both companies have been active leaders and investors in R&D projects; the constant innovation was especially important in the U.S. in regard of the patent law restricting ownership to 17 years (Harvard Business Review, 1989). The acquisition of Banyu Pharmaceutical arose out of the two companies’ long history of corporation of thirty years, and had itself been kept quiet by both firms until the final step…

    • 1078 Words
    • 5 Pages
    Superior Essays
  • Decent Essays

    Bill Jenison, president of Pharmacy Gold, said the pharmaceutical company-PBM mergers will allow his independent PBM to "leverage more enrollment because of our clinical objectivity and independence." With existing PBMs prepared to handle increased market share, and new PBMs forming, the arguments that the manufacturer-PBM mergers increase the barriers to entry into the industry, or foreclose unique products or services, are weakened. Additionally, no pharmaceutical company makes every drug on a formulary list, so the possibility of strict foreclosure is diminished because the PBMs must maintain supplier relationships with other manufacturers. A different issue arises from these continued supplier relationships concerning more subtle ways in which…

    • 6621 Words
    • 27 Pages
    Decent Essays
  • Improved Essays

    Ofra Sherman Case

    • 904 Words
    • 4 Pages

    Discussion Board # 3 Johan Rivera Liberty University The industry of pharmaceutics is a very competitive field. Moreover, corporate mergers and acquisition are a complex method to gain corporate advantage over it’s competitors. In this case the company Wellcome agreed to merger with a larger company, Glaxo. Promedico, an Israeli company was in charge of the distribution and medical registration of Wellcome.…

    • 904 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    In October 2015, two major players in the healthcare industry announced a possible merger between the two. Pfizer is known for its products as Lyrica and Viagra; similarly, Allergan is known for its Botox and Restasis (La Monica, 2015). If those two major players were two merge, a health care oligopoly could be the result. By allowing the merging of these two companies, they would become a major rival to the industry’s leader which is JNJ. Additionally, by sharing a small number of producers in an industry a fixing of prices could occur, which would affect American consumers and since the health care industry affects every American household, these implications could be dangerous.…

    • 236 Words
    • 1 Pages
    Improved Essays
  • Improved Essays

    An example of key stakeholders might be directors, funders, elected or appointed government officials, heads of businesses, or clergy, and other community figures who wield a significant amount of influence. Stakeholders within the PharmaCARE scenario In the case of PharamCARE, based on the group division of stakeholders mentioned above, following will be the determination of who can be primary, secondary and key stakeholders of PharmaCARE: • Primary stakeholders: those who has a direct impact on the operation of PharamCARE such us shareholders or investors who are investing, employees including the Colberians working for the company, the several healers, managers, supervisors, accountants, pharmacists, doctors or physicians, customers includes patients related to Medicaid and Medicare, the low-income consumers, beneficiaries of the PharmaCare foundation, vendors can be suppliers and distributors. • Secondary stakeholders: those who have an indirect impact on the operation of PharmaCARE such as the local communities in Colberia, the media, the state government in New Jersey, the government of…

    • 1853 Words
    • 8 Pages
    Improved Essays
  • Superior Essays

    Big Pharma Pros And Cons

    • 1533 Words
    • 7 Pages

    Big Pharma: The FDA’s Ineffectiveness and Corruption Cleveland State University Jesse Craciun Professor Bonsky BUS 351 20 March 2017 Big Pharma: The FDA’s Ineffectiveness and Corruption Introduction “The number of people killed by FDA-approved pharmaceuticals since 9/11 is equivalent to dropping a nuclear bomb on a major U.S. city,” says Mike Adams, author, scientific researcher and director of CWC Labs. While this claim might appear to be an over-exaggeration, it is actually a relatively accurate depiction of the harsh reality of FDA-approved pharmaceutical drugs. In a study published in the year 2000 by the American Medical Association, an estimated 106,000 deaths occurred per year from “non-error, adverse effects of medications”…

    • 1533 Words
    • 7 Pages
    Superior Essays
  • Decent Essays

    The Glaxo-Wellcome situation to me is much simpler than the reading presents it. I believe that for the sake of continued success going forward, it is in the best interest of both Wellcome Israel and Ofra Sherman to pursue their interest in completely becoming the newest team members of Glaxo. While Wellcome is considered successful, falling between 10th and 20th worldwide in revenue (Jick, T. & Peiperl, M., 2011.), its is not uncommon for these rankings to change dramatically overnight. Wellcome’s stable of income producers all having glaring flaws going forward into the future, not including the one major constant of the threat of instability in their region. With the U.S. methamphetamine epidemic, increased government regulations on sale of Sudafed and Actifed will be problematic, as well as the potential negative stereotypes associated with “crystal meth.”…

    • 647 Words
    • 3 Pages
    Decent Essays
  • Improved Essays

    Over Medicated Essay

    • 512 Words
    • 3 Pages

    Last year, pharmacist filled 4,468,929,929 prescriptions in the United States that is an 85 percent increase from just twenty years earlier (Carr, Rabkin, and Skinner 38). With these kinds of numbers, it must be obvious the process to develop drugs in America is working like a well-oiled machine, or is it? Prescription drug companies, the Food and Drug Administration (FDA) and independent research companies including universities all work together to develop improved medications. Each one has an unbiased, independent role to play in the process, however, over the years the unbiased independent part has become blurred. The Federal Government has made changes to regulations and health care policies, consequently, the prescription drug company’s…

    • 512 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    Securities and Exchange Commission (SEC) filings to mirror the new typical in cybersecurity. The Big Pharma lays out the circumstance doubtlessly: "As a worldwide pharmaceutical organization, our frameworks are liable to continuous assaults. " That announcement is one of three noteworthy changes to Pfizer's latest danger variable area on IT, the word check of which has dramatically increased since 2011. Other Big Pharma organizations have additionally extended the scope of IT security dangers they convey to financial specialists. In any case, the perception that being a worldwide pharmaceutical organization places Pfizer in line for "successive assaults" is not a concern, regardless of the fact that the announcement itself is obvious (Anderson & Choobineh,…

    • 1015 Words
    • 5 Pages
    Improved Essays
  • Improved Essays

    Johnson and Johnson is known to consumers by its multifaceted line of healthcare products ranging from Band-Aids to Tylenol. Johnson and Johnson is touted as a “family” oriented company with significant brand loyalty. While its product line include much more than prescription drugs (J&J is made up of around 250 subsidiaries and 129,000 employees), it has a formidable presence in the drug market drug market. It falls among the highest revenue makers with 2013 revenue of $71.312 billion and a preceding 2012 year of $67.200 billion (www.fiercepharma.com/special-reports). The pharma division provided most of last year's growth; this included rheumatoid arthritis medication Remicade and the HIV treatment…

    • 456 Words
    • 2 Pages
    Improved Essays
  • Superior Essays

    Clinical trials have been performed at many sites around the world for many years to obtain approvals in multiple countries. The harmonization of regulatory processes developed by the ICH, drug patent laws, and country specific regulations is very important steps towards the product development, such as drug discovery, early development and preclinical testing, clinical trials and marketing authorizations. Nearly every country agrees to accept the ICH technical necessities for registration of pharmaceutical products for human use. Taking this into an account makes very easy to perform worldwide clinical trials by outsourcing and offshoring models to achieve the numerous regulatory and commercial incentives obtainable in many countries. The perfect time to build a regulatory strategy is before submitting an Investigational New Drug (IND) application.…

    • 1496 Words
    • 6 Pages
    Superior Essays
  • Great Essays

    esentation analyses the events leading up to the 2004 merger between the pharmaceutical companies Sanofi-Synthelabo and Aventis. It reveals the social, commercial and political complexities and challenges of a merger process in which the defence of French national interests and regional capabilities competed with traditional ‘commercial’ narratives before the deal was closed. presentation critically evaluates the competing criteria adopted by government and industry to justify different merger scenarios and considers the implications for pharmaceutical innovation, industry consolidation and M&A theory The American economy greatest market for the pharmaceutical industry in 2004 the tax cuts and the lower interest rates stimulated expansion…

    • 1499 Words
    • 6 Pages
    Great Essays