ELECTROCONVULSIVE THERAPY (ALSO KNOWN AS ELECTROSHOCK THERAPY)
Received Jul 3, 2025
Report MW5172224 · MDR key 22395783
Device
Generic name
Device, Electroconvulsive Therapy
Manufacturer
UnknownProduct problems
- Patient Device Interaction Problem
Patient
54 YR · Female
- Memory Loss/Impairment
- Anxiety
- Depression
- Sleep Dysfunction
- Cognitive Changes
- Confusion/ Disorientation
- Suicidal Ideation
- Memory Loss/Impairment
- Anxiety
- Depression
- Sleep Dysfunction
- Cognitive Changes
- Confusion/ Disorientation
- Suicidal Ideation
Narrative
Description of Event or Problem
IN 1998 I FOLLOWED DOCTOR (DR.) INSTRUCTIONS TO STOP TAKING ZOLOFT OVER TWO WEEKS. I STARTED EXPERIENCING SYMPTOMS I HAD NEVER HAD BEFORE: EXTREME ANXIETY, OBSESSIVE-COMPULSIVE DISORDER (OCD) AND INTRUSIVE THOUGHTS, DIFFICULTY, SLEEPING, CONCENTRATING, WORKING, CONVERSING. INSTEAD OF BEING RECOGNIZED AS WITHDRAWAL, I WAS MISDIAGNOSED AS A RECURRENCE OR WORSENING OF MY "ORIGINAL" CONDITION. I WAS PUT BACK ON ZOLOFT AND IT DID NOTHING FOR ME. I WAS COMPLETELY DYSFUNCTIONAL AND COULD NOT GO OUT IN PUBLIC FOR AT LEAST SIX MONTHS. I LOST MY CAREER IN CLIMATE CHANGE POLICY. IN THE NEXT YEARS I WAS PRESCRIBED OTHER SSRIS (SELECTIVE SEROTONIN REUPTAKE INHIBITORS) AND SNRIS (SEROTONIN-NOREPINEPHRINE REUPTAKE INHIBITORS) - CELEXA, LEXAPRO, PROZAC, VENLAFAXINE - BUT I CONTINUED TO HAVE DEBILITATING DEPRESSION, ANXIETY, DECLINE IN COGNITIVE CAPACITY, MAJOR SOCIAL DIFFICULTIES, VERY UNSTABLE RELATIONSHIPS - NONE OF WHICH I HAD BEFORE OR DURING TAKING ZOLOFT. I WAS HOSPITALIZED THREE TIMES DUE TO SUICIDAL IDEATION AND INTENT. I WAS GIVEN ELECTROSHOCK THERAPY BECAUSE NOTHING WAS MAKING ME BETTER. THE ELECTROSHOCK WENT WRONG, AND I BECAME CATATONIC AND HAD TO BE HOSPITALIZED AGAIN. THE ELECTROSHOCK FURTHER DAMAGED, MY MEMORY AND COGNITIVE CAPACITY. AS MY DOCTORS WERE CONTINUALLY SWITCHING MY MEDICATIONS OVER THE NEXT 15 YEARS, MY SYSTEM WAS CONSTANTLY BEING PROVOKED INTO WITHDRAWAL. I WAS GIVEN THE MESSAGE THAT I WAS ALWAYS DESTINED TO BE SEVERELY MENTALLY ILL, WHICH DID EXTREMELY GRAVE DAMAGE TO MY SENSE OF SELF. IT WAS NOT UNTIL 2021 THAT THERE WAS ENOUGH LITERATURE, AND DOCUMENT DOCUMENTATION, FOR ME TO LEARN THAT WHAT HAD HAPPENED TO ME WAS PROTRACTED WITHDRAWAL. WITHDRAWAL THAT RUINED MY LIFE, KEPT ME FROM HAVING CHILDREN, KEPT ME FROM GETTING MARRIED, TOOK MY CAREER. NOW THIS MANY YEARS LATER, I AM SUFFERING, LONG-TERM ADVERSE CONSEQUENCES FROM BEING ON ALL OF THESE MEDICATIONS, AND I AM BEING FORCED TO TAPER THEM. AT LEAST NOW THERE IS SOME BETTER INFORMATION, IF YOU KNOW WHERE TO FIND IT. THERE ARE VERY FEW PROVIDERS WHO KNOW ABOUT HYPERBOLIC TAPERING, OR ANY OF THE KNOWLEDGE THAT HAS BEEN ACCUMULATED BY FELLOW PATIENTS AND A FEW RESEARCH RESEARCHERS. I HAD NEUROCOGNITIVE TESTING DONE WHILE LIVING IN (B)(6) SPAIN IN 2019. THEY TOLD ME THAT MOST OF THE PEOPLE WHO THEY SEE IN MY AGE GROUP (I WAS BORN IN 1971) WHO HAVE THIS LEVEL OF COGNITIVE DECLINE, OUR PEOPLE WHO'VE BEEN TAKING MULTIPLE PSYCHOTROPIC MEDICATIONS FOR MANY YEARS. THEY ALSO SAID THAT THERE ARE NOT REALLY ANY GOOD STUDIES ON ANY OF THIS, SO ALL THEY COULD REALLY OFFER ME WAS THEIR ANECDOTAL EXPERIENCE. I HAVE BEEN SERIOUSLY DISABLED BY THE WITHDRAWAL THAT I SUFFERED FROM ZOLOFT AND SUBSEQUENT MEDICATIONS. I GRADUATED FROM (B)(6). I WORKED IN THE (B)(6) ON INTERNATIONAL CLIMATE CHANGE POLICY. I WORKED AS A CONSULTANT FOR THE (B)(6) ON CLIMATE CHANGE. FOR YEARS AFTER THAT, I COULD NOT WORK AT ALL. THEN I WAS A PART-TIME DANCE TEACHER. NOW I AM AN ARTIST BECAUSE THAT IS ONE OF THE ONLY THINGS THAT I AM CAPABLE OF DOING. THIS MEANS THAT THIS WITHDRAWAL SERIOUSLY DAMAGED MY ABILITY TO EARN A LIVING. THE FDA NEEDS TO PROVIDE BETTER LABELING ON THESE MEDICATIONS THAT MAKE PEOPLE AWARE OF THE POSSIBILITY OF VERY SERIOUS WITHDRAWAL. THERE NEEDS TO BE BETTER EDUCATION OF PROVIDERS AND PATIENTS AS TO THE POSSIBLE RISKS, AND ALSO EDUCATION ABOUT HYPERBOLIC TAPERING., AND THE IMPORTANCE OF KEEPING UP-TO-DATE ON WHAT WE ARE LEARNING ABOUT HOW TO COME OFF OF THESE MEDICATIONS IN A SAFER MANNER.