Their daughter, exposed to Depakine, a treatment for epilepsy, was born with malformations. Sanofi, its manufacturer, was sentenced Thursday, May 12 by the court of Nanterre to compensate his family up to 450,000 euros. The judges considered that the risk of autistic disorders in connection with Depakine were known to the laboratory, at least in 2005, and that consequently it had the duty to mention it in the notice, according to the judgment consulted on Saturday May 14 by the AFP. The mother, followed for epileptic seizures, took this medicine since 1982. In 2004, during her pregnancy, she took 4 tablets a day.
When she was seven months old, her daughter was hospitalized with bronchiolitis. It was then noted an “overall delay in acquisitions”. Delays in psychomotor development were then observed throughout his childhood. In 2016, his parents took Sanofi to court. Used since 1967 in the treatment of epilepsy and bipolar disorders, sodium valproate (active ingredient of Depakine) increases the risk of physical malformations (lack of closure of the spine, cardiovascular anomalies, etc.) neuro-developmental (language delay, autism spectrum disorders, etc.) in children exposed in their mother’s womb.
“A turning point for the individual recognition of each of the children exposed to Dépakine”
“This decision to condemn the laboratory marks a turning point for the individual recognition of each of the children exposed to Dépakine”, reacted to AFP, the family lawyer, Me Charles Joseph-Oudin, calling on the group to ” change behavior in all procedures”. According to him, the laboratory “must now line up with reason and take care of the families hard hit with dignity” by the drug. According to the judgment, the laboratory recognized that from 2003 it was aware of the risks, in particular neuro-developmental, so it therefore had a duty to inform patients in the instructions.