Weird thing, You can still get trobalt in countries like Mexico and Dominican Republic.
Well @david14433; I have just come back from Malaga in Spain, and it is still available from the pharmacies there, and they are still selling it without a prescription. It is a bit expensive though.
As I understand it retigabine has been taken off the market, but is there anyway I can get my hands on this stuff. It seems to work wonders for some people with tinnitus. I would probably cycle its use to prevent serious side effect problems.
Retigabine is being redesigned by Dr. Tzounopoulos of the University of Pittsburgh for the treatment of tinnitus. The original drug was not intended for tinnitus and has monstrous side effects as others have mentioned here.Is there a particular pharmacy there that still has it in stock?
Others have also mentioned finding it in Mexico and Dominican Republic, although that was in 2018.... if any of you are still around and remember which pharmacy you found some, that would be very helpful.
Am trying to find some tablets to try, as a remedy of last resort.... Thanks.
Is there a particular pharmacy there that still has it in stock?
Others have also mentioned finding it in Mexico and Dominican Republic, although that was in 2018.... if any of you are still around and remember which pharmacy you found some, that would be very helpful.
Am trying to find some tablets to try, as a remedy of last resort.... Thanks.
I think they would more likely allow a personal importation of a not yet approved device than a discontinued illegal drug.
Offtopic: Bob, I see that your T was triggered by Amitryptiline. My doc wants to try nortriptyline (the sister of ami). Do you discourage it?
I not available anymore. Trobalt has very hard side effects that why it was discontinued. I tried it myself and it gave me some of the more quiet days i had ever had and at some points i thought it might cure me. Soon i realized that the effect is only transitory and you have to keep raising the dosage. it finally affected my eyesight (floaters) so i stopped. Yes before you tell me that you rather had floaters than tinnitus, i will tell you me too but at the expense of more side effects and the effects of trobalt on tinnitus been transitory and dosage dependent i can 100% tell you that knowing what i know now i would not take it. I do think that the more successful road will be something related to trobalt but without the side effects because it indeed works (there was at least in my case a direct relation of taking trobalt and my tinnitus going from 7-8 of ten to zero!!!!). its a shame that more serious studies at least to my knowledge, are not being done for drugs similar to trobalt that might alter tinnitus perception or production through kv channels.Where is Trobalt available? Which country ?
They are actually. See this thread.I not available anymore. Trobalt has very hard side effects that why it was discontinued. I tried it myself and it gave me some of the more quiet days i had ever had and at some points i thought it might cure me. Soon i realized that the effect is only transitory and you have to keep raising the dosage. it finally affected my eyesight (floaters) so i stopped. Yes before you tell me that you rather had floaters than tinnitus, i will tell you me too but at the expense of more side effects and the effects of trobalt on tinnitus been transitory and dosage dependent i can 100% tell you that knowing what i know now i would not take it. I do think that the more successful road will be something related to trobalt but without the side effects because it indeed works (there was at least in my case a direct relation of taking trobalt and my tinnitus going from 7-8 of ten to zero!!!!). its a shame that more serious studies at least to my knowledge, are not being done for drugs similar to trobalt that might alter tinnitus perception or production through kv channels.
This gives me hope for the reformulated version.Apologies for the bump.
I took Trobalt in 2016 for 2 months, 3 x 400mg. It permanently reduced my spike to baseline but never got rid of tinnitus completely. I'm having another spike but only have like 3 weeks worth of supply left, I already used 1 week and it is still lowering my tinnitus (even tough it expired 2 years ago).
I was hoping to add another 1 month of supply. If anyone has some spare left, please let me know as I'm willing to purchase it off your hands.
Thanks.
Also gives hope for the treatment that is ongoing through the trials for kids' epilepsy.This gives me hope for the reformulated version.
Will we need it if we can regenerate the cochlea though?Also gives hope for the treatment that is ongoing through the trials for kids' epilepsy.
Yes. We haven't proved regenerating cochlea can significantly reduce tinnitus. Don't forget tinnitus is a brain issue. Not everyone gets tinnitus with hearing loss. No reason to not have more options.Will we need it if we can regenerate the cochlea though?
I took it for a few weeks. I thought it was super fucking weird and then it caused me pelvic floor muscle problems that persisted for 2 months.People that have used Retigabine, where are they now? And how are they doing? Benefits from the short time using it? Are they mostly dead? Lasting side effects?
I need to know. I'm at the end of my rope.
EDIT a day later:
Guess everyone's better or dead that took Retigabine.
Thank you for your time.I took it for a few weeks. I thought it was super fucking weird and then it caused me pelvic floor muscle problems that persisted for 2 months.
I'm still alive and as far as I know I may still have most of a bottle of Potiga locked up with drugs somewhere. It's expired, I think it's dangerous garbage, and if it didn't already get turned over to the cops during the last "dump your prescription meds" event, it will be next time.
It's not a panacea. @Danny Boy is indeed dead, though, not Potiga related as far as I know.
I don't think it does anything for my tinnitus that substantially less dangerous GABAergic drugs don't also do, and I think the primary mechanism that Potiga caused relief by may have as much to do with GABA as potassium channels.
I took Retigabine for over a year. While on the drug, it killed my tinnitus and seemed to help with my hyperacusis. It also improved my mood. It has a weird kind of 'high' like effect, but not as inhibiting as THC or alcohol. I had an ophthalmologist monitor my eyes before, during, and after doing a visual exam, OCT, and dilated fundus photography. No negative effects on my vision, although at higher dosages I did notice some visual side effects a few times that were dose dependent.People that have used Retigabine, where are they now? And how are they doing? Benefits from the short time using it? Are they mostly dead? Lasting side effects?
I need to know. I'm at the end of my rope.
EDIT a day later:
Guess everyone's better or dead that took Retigabine.
I'm curious, when you say it "killed" your tinnitus while on it - Was it gone gone or at a really low level?I took Retigabine for over a year. While on the drug, it killed my tinnitus and seemed to help with my hyperacusis. It also improved my mood. It has a weird kind of 'high' like effect, but not as inhibiting as THC or alcohol. I had an ophthalmologist monitor my eyes before, during, and after doing a visual exam, OCT, and dilated fundus photography. No negative effects on my vision, although at higher dosages I did notice some visual side effects a few times that were dose dependent.
It's difficult to say if it had a long term improvement on my tinnitus, but it helped me habituate to it. That is until my tinnitus got even worse and I added on new tones for unrelated reasons long after discontinuing. Had it not been discontinued, I would have been tempted to keep taking it.
Your mileage may vary. Some people did seem to get long term side effects even after discontinuing the drug.
What dose were you on @Alue?I took Retigabine for over a year. While on the drug, it killed my tinnitus and seemed to help with my hyperacusis. It also improved my mood. It has a weird kind of 'high' like effect, but not as inhibiting as THC or alcohol. I had an ophthalmologist monitor my eyes before, during, and after doing a visual exam, OCT, and dilated fundus photography. No negative effects on my vision, although at higher dosages I did notice some visual side effects a few times that were dose dependent.
It's difficult to say if it had a long term improvement on my tinnitus, but it helped me habituate to it. That is until my tinnitus got even worse and I added on new tones for unrelated reasons long after discontinuing. Had it not been discontinued, I would have been tempted to keep taking it.
Your mileage may vary. Some people did seem to get long term side effects even after discontinuing the drug.