150 Milligrams

150 Milligrams

Year: 2016

Runtime: 128 mins

Language: French

Director: Emmanuelle Bercot

Drama

Working in a hospital in Brest, France, a lung specialist uncovers a disturbing connection between a series of unexplained deaths and a state-approved medication. Determined to expose the truth, she embarks on a solitary fight against powerful forces, risking everything to uncover the full extent of the danger and ensure justice is served.

Warning: spoilers below!

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Timeline – 150 Milligrams (2016)

Trace every key event in 150 Milligrams (2016) with our detailed, chronological timeline. Perfect for unpacking nonlinear stories, spotting hidden connections, and understanding how each scene builds toward the film’s climax. Whether you're revisiting or decoding for the first time, this timeline gives you the full picture.

1

Opening surgery observation

In the university hospital in Brest, doctors perform open-heart surgery. Dr. Irene Frachon observes that the heart valves of patient Corinne Zacharria appear severely damaged. She notes this valve damage in other patients who had taken Mediator, suggesting a possible link between the drug and the heart condition.

opening scene Brest, Northern France
2

Pattern across patients and hypothesis

Irene realizes the pattern extends beyond a single case and there are multiple Mediator users with similar heart damage. She determines that an epidemiological study is needed to prove the link.

early investigation France (across multiple hospitals)
3

Formation of the research team

A research team forms, bringing together several colleagues who contribute to the investigation. Dr. Antoine Le Bihan's work is highlighted as especially significant in building the study.

shortly after Brest, Northern France
4

Findings support the hypothesis

Their research findings strongly support Irene's hypothesis that Mediator is linked to the heart pathology. The team compiles epidemiological evidence across cases to demonstrate the connection.

during data collection Brest, Northern France
5

Presenting to the regulator

They present their findings to AFSSAPS, the French health regulatory agency, in hopes of regulatory action. Servier's representatives scrutinize the presentation and push back against the conclusions.

after findings presented Paris, France
6

Regulatory setback

Despite the intense scrutiny, Mediator is not removed from the market, leaving Irene disappointed but undeterred. She remains committed to pursuing the evidence and advocating for patient safety.

after regulatory scrutiny Paris, France
7

Persistence in the face of inertia

Irene presses on with her campaign, drawing support from her family and colleagues. She refuses to back down in the face of regulatory inertia.

following regulatory inertia Brest, Northern France
8

Self-published book

Irene self-publishes a book detailing their research and the team’s findings. Servier responds with legal pressure in an attempt to halt publication.

after book publication Brest, Northern France
9

Media attention and support

A Le Figaro reporter, Anne Jouan, supports the investigation and helps bring attention to it. Her coverage amplifies public scrutiny of Mediator's risks.

after media involvement France
10

Regulatory and clinical support

An AFSSAPS member, Catherine Haynes, offers support to the effort, bolstering the regulatory side of the inquiry. Her involvement signals some regulators' alignment with the clinicians' concerns.

after media involvement France
11

Health-insurance data support

A CNAM informant from the national health insurance fund backs the investigation. The informant provides data and context from the health system to strengthen the epidemiological case.

after CNAM backing France
12

Deaths linked to Mediator revealed

The investigation reveals around 500 deaths connected to Mediator. Most of the victims are women.

late in the investigation France
13

The gravity of the issue

The scale of the deaths underscores the gravity of the issue and the stakes of regulatory debate. Irene remains determined to pursue justice and safer drug practices.

late in the investigation France
14

A turning point toward ongoing scrutiny

The revelations set the stage for ongoing scrutiny of drug safety and the handling of such cases in France. Irene's work leaves a lasting impact on how patient safety cases are approached.

conclusion France

Last updated: February 20, 2026 at 12:18

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150 Milligrams (2016) Timeline Questions Answered – Chronology FAQ

Find frequently asked questions about the 150 Milligrams (2016) timeline, including chronological order, nonlinear jumps, cause-and-effect links, and scene sequence clarifications. This timeline FAQ helps explain when key events happen, how moments connect, and why the story unfolds in that specific order.

Q1

Why was Mediator originally prescribed if it was linked to heart problems?

A.

Mediator was developed by the pharmaceutical company Servier as a medication for diabetes and weight loss. It was marketed as an appetite suppressant for overweight diabetic patients. However, the drug's active ingredient was later found to cause severe heart valve damage, leading to the deaths of around 500 people, most of them women. The drug remained on the market for years despite early warning signs because it was initially approved as a diabetes treatment and continued to be prescribed even when its dangerous side effects became apparent.

The opening scene showing severe heart valve damage in patient Corinne Zacharria establishes the clinical evidence that Frachon would later connect to Mediator use.

mediatorservierdiabetesweight lossheart valve damageprescription
Q3

Why did French health regulators not remove Mediator from the market immediately?

A.

When Frachon and her team presented their epidemiological findings to AFSSAPS (the French health regulatory agency), they faced stiff opposition from Servier's representatives. Despite clear statistical evidence linking Mediator to heart valve damage, regulators were reluctant to act against a pharmaceutical product already on the market. The film depicts the tension between patient safety concerns and corporate interests, with bureaucratic inertia and political pressure slowing the regulatory response.

The earlier scene showing the formation of the research team and their data collection builds toward this confrontation with institutional power.

afssapsregulatory agencyservierdrug safetyclinical evidencebureaucracy
Q4

What role did the epidemiological study play in proving Mediator's dangers?

A.

The epidemiological study conducted by Dr. Frachon and Dr. Antoine Le Bihan was essential because it provided scientific, statistical proof that the heart valve damage was not random but directly correlated with Mediator use. By gathering data across multiple patients and hospitals, they transformed individual clinical observations into measurable evidence that could not be easily dismissed. This rigorous methodology converted bedside concerns into credible scientific data that could be presented to regulators.

The timeline of forming the research team and collecting patient data directly supports the credibility of their final findings.

epidemiological studystatistical evidenceantoine le bihanscientific proofmedical research
Q5

Why did Servier fight against Dr. Frachon's self-published book?

A.

After regulatory channels proved slow and ineffective, Frachon self-published a book detailing her research and the patient stories behind the cases. Servier responded with legal pressure, attempting to halt the publication because the book threatened to expose the company's knowledge of the drug's risks. The publication also aimed to empower patients and alert the broader public, making it a significant threat to Servier's reputation and commercial interests.

The earlier regulatory setback and Frachon's determination to continue despite institutional resistance sets up her decision to take the fight public.

servierbook publicationlegal pressurecorporate cover-uppatient awareness
Q6

How many deaths were ultimately linked to Mediator?

A.

The investigation revealed that approximately 500 deaths were connected to Mediator, with the overwhelming majority of victims being women. This stark statistic became the driving force behind Frachon's crusade, transforming her personal medical concern into a public health imperative. The scale of the tragedy underscored the gravity of the regulatory failures and corporate negligence.

The film builds toward this revelation as the culmination of years of investigation and data analysis.

500public healthmortality rate deathswomen victimsmedical tragedy
Q7

Why were women particularly affected by Mediator's side effects?

A.

Women constituted the majority of Mediator-related deaths because the drug was primarily prescribed as a weight-loss aid to women, particularly overweight diabetic patients. The medication's appetite-suppressing properties made it popular among women seeking to manage their weight, which meant they were disproportionately exposed to the drug's toxic effects on heart valves. This demographic pattern became evident as the investigation compiled data on victims.

The early patient cases mentioned in the film, including Corinne Zacharria, establish that women were the primary recipients of this medication.

women patientsgenderweight loss medicationdiabetic patientsdemographic impact
Q8

What was the significance of the CNAM data in the investigation?

A.

A CNAM informant from France's national health insurance fund provided crucial data that strengthened the epidemiological case against Mediator. This health system data allowed Frachon and her team to triangulate their findings with independent, large-scale insurance records, providing additional statistical weight to their conclusions. The CNAM support represented a breakthrough in accessing comprehensive, system-wide information that validated their research.

The timeline shows CNAM involvement coming after media attention and regulatory support had already begun to build momentum.

cnamnational health insurancedata triangulationhealth system recordsepidemiological evidence
Q9

How did media coverage by Anne Jouan influence the Mediator case?

A.

Anne Jouan, a reporter from Le Figaro, played a critical role in bringing widespread public attention to Frachon's findings. Her journalism amplified the investigation beyond medical and regulatory circles, creating public pressure on authorities to act. Media coverage transformed the story from a specialized medical debate into a matter of public concern, helping to build momentum for regulatory action and keeping the pressure on Servier.

The self-published book and legal battle with Servier created the newsworthy content that Jouan was able to investigate and report on.

anne jouanle figaromedia attentionpublic pressureinvestigative journalism
Q10

What were the broader implications of the Mediator case for drug safety?

A.

The Mediator case exposed systemic failures in pharmaceutical oversight and regulatory processes in France. Frachon's fight highlighted the conflict between market forces and patient welfare, between precaution and speed in drug approval, and between individual courage and institutional inertia. The case led to increased scrutiny of how medications are approved, monitored, and removed from the market, leaving a lasting impact on how patient safety cases are handled in France and beyond.

The concluding timeline points toward ongoing scrutiny and reform in drug safety practices following the revelations.

drug safety regulationspharmaceutical oversightinstitutional reformpatient welfaresystemic failure
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