Over a decade ago, I had a head injury and post concussion syndrome before being injured permanently by an off label antipsychotic prescribed for severe insomnia and anxiety caused by the concussion. It gave me a neurological involuntary movement disorder called tardive dyskinesia that is a bit like Tourette's and Parkinson's disease combined, and pretty much permanent. It goes into remission but to say it's been hell with the horrible disfiguring involuntary movements and symptoms is an understatement. 😢💔
My GP polydrugged me with a lot of psychotropic medication at the time, and I was in severe distress caused by all the post concussion syndrome symptoms. As a last resort to help with severe anxiety and insomnia, she prescribed an off label antipsychotic for a week, and told me not to look up the side effects, as she knew I'd literally not take it (as I'd said I was worried about adverse effects). There was no patient information leaflet in the medication box either.
I had a chat with a solicitor about a decade ago, and was told they could possibly look into a case to claim something. But i didn't know how stressful it might have been, and I had a reply and apology from my GP after I wrote a letter of complaint to the surgery, and she covered her arse pretty well, outlining the reasons she had to prescribing the medication she did
I guess it has been extremely difficult to live with a medication induced movement disorder, and perhaps any financial compensation might not have really helped me to get some ways of feeling better/closure about it all.
Maybe I'm just feeling sad about the fact my life was permanently changed and it makes my ongoing health problems (perimenopause etc) harder to treat, as I'm now more sensitive to medication side effects etc.
I'm not sure what I'm posting here, apart from a rant! Maybe just the question of whether i could have pursued a claim.