Google Search could diagnose unknown drug side effects
Google could soon be helping diagnose otherwise unknown drug side-effects. The search engine might be looking for a SEO manager to sort out its own Google rankings,
bizarrely, but the Food and Drug Administration in the US is turning to
the company's search powers to help it uncover otherwise elusive drug
side-effects.
Bloomberg spotted the unusual pairing in the FDA's public meeting notes of 9 June,
which show that senior Google research scientist Evgeniy Gabrilovich
was in attendance for the "Google/FDA Adverse Event Trending
Teleconference" -- "adverse event" referring to the unknown side-effects
that only transpire once a drug is in widespread circulation.
The
idea is, with enough data, serious contenders for additional drug
side-effects could be whittled down from among all the paranoid search
entries the public type everyday. The FDA was beginning discussions with
Google on "identifying adverse event data, using Google's technologies
and data," Bloomberg reports FDA spokesman Chris Kelly as saying.
Kelly added to WIRED.co.uk: "The
agency met with Google for a high-level, general discussion of their
technology and data capabilities. The teleconference was for each side
to introduce themselves and for the agency to begin a discussion on how
we might collaborate with Google on identifying adverse event data using
Google’s technologies and data. There will be a follow-up
teleconference with Google in the future."Now, it seems the FDA wants Google to do its work for it. The agency is responsible for checking every drug in circulation in the US has been clinically tested on numbers large enough to get population-wide side-effect predictions. However, this is not an assurance that there are no side-effects outside of those already discovered. Additional side effects can be highlighted through official channels, but it's a slow and inefficient system. Creating a robust alternative that collates vast amounts of data on side effects could lead to them getting added to lists faster, or even alert the FDA to a side-effect that could potentially lead to a drug being stripped of safety approval.
Data miner Gabrilovich co-authored a paper in 2013 that looked into the viability of such a robust system. It argued that, rather than relying on "spontaneous reports by patients and health care providers" of side effects, which may only come about as a result of long-term use (not accounted for in clinical studies) or use alongside other drugs, a "low cost, fully automated method" that could be run continuously would be far superior. It would mean the FDA could look specifically for the different potential reasons behind the side-effects, including whether they are being taken alone or in conjunction with other common drugs.
While clinical trials generally look at a few hundred or thousand patients, Gabrilovich's experiment ran 176 million search results. He was able to validate the findings by also testing for common side-effects of particular drugs. In the end, he concluded that the most serious early-onset side effects would be more likely to be reported to and picked up by the FDA and others. But that "less acute later-onset ones are better captured in web search queries".
Two
years later, it looks like the FDA is taking notice, and finally
looking into collaborating with big tech to solve this unwieldy
challenge.
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