French drugmaker, watchdog on trial for diabetes pill deaths

French drugmaker, watchdog on trial for diabetes pill deaths

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PARIS: France’s medicines watchdog will join a pharma firm in the dock from Monday on fraud and negligence charges linked to the deaths of multiple people prescribed a diabetes pill for weight loss despite safety concerns.

At least 500 people are thought to have died of heart valve problems in France after taking the drug, Mediator, in a major health scandal that became the subject of a 2016 French movie called “150 Milligrams”.

Legal experts have concluded the drug may cause as many as 2,100 deaths in the long term.

The criminal trial, with 12 individuals in the dock, will focus on 91 victims, four of them deceased, for whom lawyers believe a link can be shown between their illness and Mediator.

The medicine was on the market for 33 years, and used by about five million people.

Though initially intended for overweight people with diabetes, it was widely prescribed to healthy individuals as an appetite suppressant.

Safety alerts were first flagged in the mid-1990s, but the drug was only banned in France in 2009 — long after being outlawed in the United States, Spain and Italy.

Victims “want to understand how this medicine could have been left on the market for so long,” said Charles Joseph-Oudin, who will represent about 250 complainants in the trial expected to run for six months in the Paris criminal court.

Drug manufacturer Servier and nine subsidiaries are charged with fraud for allegedly concealing Mediator’s risks, while the ANSM drug watchdog is being pursued for negligence and allegedly dragging its feet in suspending the drug.

At the end of the trial, both risk a fine or an order to compensate victims.

“Servier knew that it was selling poison,” said 71-year-old Joy Ercole, who took Mediator for six months ten years ago, and said she suffered heart damage as a result.

“The unlucky ones, like me, are condemned to a slow death. My life is ruined.”

Francois de Castro, a lawyer for Servier, said the company was “keen to come and explain that they did not identify the risk before 2009.”

Pulmonologist Irene Frachon had alerted French health authorities of heart problems among patients who had taken the drug. She published a book in 2010, which became the basis for a documentary

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