Wonder Drug (book)

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Wonder Drug: The Secret History of Thalidomide in America and Its Hidden Victims
Wonder Drug - The Secret History of Thalidomide in America and Its Hidden Victims book cover.jpg
Author Jennifer Vanderbes
CountryUS
LanguageEnglish
Published2023
Publisher Random House

Wonder Drug: The Secret History of Thalidomide in America and Its Hidden Victims is a nonfiction book authored by Jennifer Vanderbes and published by Random House in 2023. It tells the story of how Frances Oldham Kelsey of the Food and Drug Administration (FDA) found flaws in thalidomide research. Contrary to the initial opinion that the FDA declined the drug a license for morning sickness in pregnancy and the US was therefore spared the thalidomide scandal, Vanderbes claims that the drug was still widely distributed there in the late 1950s and 1960s. As a result, many more babies were affected by phocomelia than originally believed. [1] [2] [3] [4] [5]

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<span class="mw-page-title-main">Food and Drug Administration</span> United States federal agency

The United States Food and Drug Administration is a federal agency of the Department of Health and Human Services. The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco products, caffeine products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), cosmetics, animal foods & feed and veterinary products.

<span class="mw-page-title-main">Thalidomide</span> Immunomodulatory drug known for its ability to cause birth defects

Thalidomide, sold under the brand names Contergan and Thalomid among others, is an oral medication used to treat a number of cancers, graft-versus-host disease, and many skin disorders. While thalidomide has been used in a number of HIV-associated conditions, such use is associated with increased levels of the virus.

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Mifepristone, also known as RU-486, is a medication typically used in combination with misoprostol to bring about a medical abortion during pregnancy and manage early miscarriage. This combination is 97% effective during the first 63 days of pregnancy. It is also effective in the second trimester of pregnancy. It is taken by mouth.

<span class="mw-page-title-main">Pharmaceutical industry</span> Industry involved with discovery, development, production and marketing of drugs

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<span class="mw-page-title-main">Ivermectin</span> Medication for parasite infestations

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<span class="mw-page-title-main">Grünenthal</span> German pharmaceutical company

Grünenthal is a pharmaceutical company headquartered in Aachen in Germany. It was founded in 1946 as Chemie Grünenthal and has been continuously family-owned. The company was the first to introduce penicillin into the German market in the postwar period, after the Allied Control Council lifted its ban.

<span class="mw-page-title-main">Frances Oldham Kelsey</span> Canadian-American physician and pharmacologist (1914–2015)

Frances Kathleen Oldham Kelsey was a Canadian-American pharmacologist and physician. As a reviewer for the U.S. Food and Drug Administration (FDA), she refused to authorize thalidomide for market because she had concerns about the lack of evidence regarding the drug's safety. Her concerns proved to be justified when it was shown that thalidomide caused serious birth defects. Kelsey's career intersected with the passage of laws strengthening FDA oversight of pharmaceuticals. Kelsey was the second woman to receive the President's Award for Distinguished Federal Civilian Service, awarded to her by John F. Kennedy in 1962.

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<span class="mw-page-title-main">Lenalidomide</span> Pair of enantiomers

Lenalidomide, sold under the brand name Revlimid among others, is a medication used to treat multiple myeloma, smoldering myeloma, and myelodysplastic syndromes (MDS). For multiple myeloma, it is used after at least one other treatment and generally with dexamethasone. It is taken by mouth.

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<span class="mw-page-title-main">Purdue Pharma</span> American pharmaceutical company (1892–2019 bankruptcy)

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Jennifer Vanderbes is an American novelist, journalist and screenwriter.

Numerous governmental and non-governmental organizations have criticized the U. S. Food and Drug Administration for alleged excessive and/or insufficient regulation. The U.S. Food and Drug Administration (FDA) is an agency of the United States Department of Health and Human Services and is responsible for the safety regulation of most types of foods, dietary supplements, drugs, vaccines, biological medical products, blood products, medical devices, radiation-emitting devices, veterinary products, and cosmetics. The FDA also enforces section 361 of the Public Health Service Act and the associated regulations, including sanitation requirements on interstate travel as well as specific rules for control of disease on products ranging from animals sold as pets to donations of human blood and tissue.

<span class="mw-page-title-main">Fenoprofen</span> NSAID analgesic and anti-inflammatory drug

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<span class="mw-page-title-main">Pomalidomide</span> Chemical compound

Pomalidomide, sold under the brand names Pomalyst and Imnovid, is an anti-cancer medication used for the treatment of multiple myeloma and AIDS-related Kaposi sarcoma.

<span class="mw-page-title-main">Thalidomide scandal</span> Medical condition

In the late 1950s and early 1960s, the use of thalidomide in 46 countries by women who were pregnant or who subsequently became pregnant resulted in the "biggest man-made medical disaster ever," with more than 10,000 children born with a range of severe deformities, such as phocomelia, as well as thousands of miscarriages.

The Food and Drug Administration is a federal agency of the United States, formed in 1930.

Aducanumab, sold under the brand name Aduhelm, is a medication designed to treat Alzheimer's disease (AD). It is a monoclonal antibody that targets aggregated forms (plaque) of amyloid beta (Aβ) found in the brains of people with Alzheimer's disease to reduce its buildup. It was developed by Biogen and Eisai. Aducanumab is given via intravenous infusion.

<span class="mw-page-title-main">George P. Larrick</span> Commissioner of the Food and Drug Administration

George P. Larrick was Commissioner of the U.S. Food and Drug Administration (FDA) from 1954–1965.

References

  1. Klass, Perri (22 June 2023). "Review | Thousands of children were maimed by thalidomide. A new book explores why". Washington Post. Archived from the original on 31 August 2023. Retrieved 31 August 2023.
  2. Spink, Geoff (27 July 2023). "Review: Jennifer Vanderbes's deft and thorough Wonder Drug maps the thalidomide tragedy". The Globe and Mail. Archived from the original on 20 September 2023. Retrieved 31 August 2023.
  3. Rascoe, Ayesha (23 June 2023). "Jennifer Vanderbes on her book 'Wonder Drug'". www.npr.org. npr. Archived from the original on 20 September 2023. Retrieved 31 August 2023.
  4. Thomas, Katie (23 March 2020). "The Unseen Survivors of Thalidomide Want to Be Heard". The New York Times. Archived from the original on 20 September 2023. Retrieved 31 August 2023.
  5. Olszynko-Gryn, Jesse (30 June 2023). "Thalidomide in AmericaWonder Drug: The Secret History of Thalidomide in America and Its Hidden Victims". Science. 380 (6652): 1329. doi:10.1126/science.adi5325. ISSN   1095-9203. PMID   37384679.