Age, Biography and Wiki

David Bailey (pharmacologist) was born on 17 March, 1945 in Toronto, Ontario, Canada, is a Canadian runner and pharmacologist (1945–2022). Discover David Bailey (pharmacologist)'s Biography, Age, Height, Physical Stats, Dating/Affairs, Family and career updates. Learn How rich is he in this year and how he spends money? Also learn how he earned most of networth at the age of 77 years old?

Popular As N/A
Occupation N/A
Age 77 years old
Zodiac Sign Pisces
Born 17 March 1945
Birthday 17 March
Birthplace Toronto, Ontario, Canada
Date of death 27 August, 2022
Died Place London, Ontario, Canada
Nationality Canada

We recommend you to check the complete list of Famous People born on 17 March. He is a member of famous runner with the age 77 years old group.

David Bailey (pharmacologist) Height, Weight & Measurements

At 77 years old, David Bailey (pharmacologist) height not available right now. We will update David Bailey (pharmacologist)'s Height, weight, Body Measurements, Eye Color, Hair Color, Shoe & Dress size soon as possible.

Physical Status
Height Not Available
Weight Not Available
Body Measurements Not Available
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Who Is David Bailey (pharmacologist)'s Wife?

His wife is Barbara Bailey

Family
Parents Not Available
Wife Barbara Bailey
Sibling Not Available
Children 3

David Bailey (pharmacologist) Net Worth

His net worth has been growing significantly in 2023-2024. So, how much is David Bailey (pharmacologist) worth at the age of 77 years old? David Bailey (pharmacologist)’s income source is mostly from being a successful runner. He is from Canada. We have estimated David Bailey (pharmacologist)'s net worth, money, salary, income, and assets.

Net Worth in 2024 $1 Million - $5 Million
Salary in 2024 Under Review
Net Worth in 2023 Pending
Salary in 2023 Under Review
House Not Available
Cars Not Available
Source of Income runner

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Timeline

1945

David George Bailey (March 17, 1945 – August 27, 2022) was a Canadian track and field athlete, and subsequently a recognized pharmacologist, who pioneered the research of grapefruit–drug interactions.

1965

He was two-time Canadian Universities Track and Field Athlete of Year (1965, 1967) and two-time inductee into the University of Toronto Sports Hall of Fame (individually 1998 and team 2003).

He was a member of 9 Canadian national track and field teams, competing at:

1966

He was the first Canadian to run the mile in less than 4 minutes (3:59.1) in San Diego, CA on June 11, 1966 and the first Canadian to run the mile in less than 4 minutes in Canada (3:57.7) in Toronto on July 22, 1967.

1967

A resident of North York, Ontario, he won the bronze medal in this event at the 1967 Pan American Games and the silver medal in this event at the 1967 World University Games.

1968

Bailey represented Canada at the 1968 Summer Olympics in the men's 1,500 metres.

Bailey completed undergraduate studies in Pharmacy (1968) and graduate work in Pharmacology (M.Sc. 1970; Ph.D. 1973) at the University of Toronto.

1986

After post-doctoral training in Pharmacology at the University of Saskatchewan and work in drug development for the pharmaceutical industry, he returned to academia in 1986 at the University of Western Ontario, Canada.

He was a full Professor in the Departments of Physiology & Pharmacology and Medicine.

His research focused on mechanistic and translational clinical pharmacological investigations related to drug interactions.

Bailey's notable publication of grapefruit–drug interactions has been cited more than 300 times.

Grapefruit decreased drug metabolism in humans, which likely represented the first clinical example of a food producing such an effect.

Clinically, the concern is that a single judicious amount of grapefruit ingested even many hours beforehand would noticeably boost oral drug bioavailability and cause overdose toxicity.

Research findings have demonstrated that grapefruit produced a clinically relevant interaction with more than 40 medications.

Formal product information for a number of highly prescribed or essential medications now warn about the risk of a grapefruit-induced adverse drug interaction.

A label stating, "Do NOT take with Grapefruit Juice" is often affixed to prescription vials.

Bailey's research was prominently discussed in such prestigious journals as Nature Medicine and the New England Journal of Medicine.

1999

A research study in the elderly received the William B Abrams Award from the American Society for Clinical Pharmacology & Therapeutics (1999).

2002

The initial publication in 2002, which has been cited more than 100 times, supported a new model of intestinal drug absorption and novel mechanism of food-drug interactions.

Bailey showed that the major flavonoid in grapefruit, naringin, was an important clinically active inhibitor of intestinal OATP1A2.

This appeared to be the first example of a single dietary constituent modulating drug transport in humans.

Bailey died in London, Ontario on August 27, 2022, at the age of 77.

2004

A review article of his on the topic of grapefruit–drug interactions was republished in a special 2004 Anniversary Edition of the British Journal of Clinical Pharmacology, which reprinted only 14 publications that were considered of major importance over the past 30 years.

2005

Bailey was the recipient of the Senior Investigator Award from the Canadian Society for Clinical Pharmacology (2005).

Moreover, this research is now well known to the public through numerous articles in the lay press.

2006

Some were in the most influential and trusted publications including The New York Times (March 21, 2006), National Geographic (March 2007) and the Wall Street Journal (November 27, 2007).

Thus, this research has received significant scientific, clinical and mainstream stature.

In later years, Bailey shifted the focus of his research slightly to assessing the effect of fruit juices on other potentially important mechanisms of drug absorption.

Research found that grapefruit and other juices (orange and apple) inhibited a specific intestinal drug uptake transporter (organic anion transporting polypeptide 1A2; OATP1A2) to diminish oral drug absorption discernibly in humans.