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#1 | ||
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Junior Member
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Has any switched from Gabapentin to Gralise? My PCP has suggested I talk to my neurologist about it so I won't have to take so many pills throughout the day. Rather, take it in the AM and it lasts all day. I would be interested in others experience.
Thanks. |
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"Thanks for this!" says: | pinkynose (11-01-2016) |
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#2 | ||
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Junior Member
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I'm taking Gralise and I think it was a good switch. I was on 3600mg of Gabapentin, 1200 three times a day, and I would notice more jitteriness and nerve activation when there was a change in my blood level, especially if I was late with a dose. Gralise keeps me much more even in those regards.
I was instructed to take it with dinner and that the 1800mg of Gralise I'm taking is equivalent to my previous 3600 of Gabapentin. Dinner times can vary wildly for me (like, between 6pm and midnight), but I have some straight Gabapentin I can take if it becomes too long since the last dose. I've also taken Gralise without food (such as the night before a colonoscopy), and that's also been fine. Gapapentin is better absorbed when there's fat in the stomach. Horizant is another time-release Gabapentin with once-a-day dosing. Haven't tried it, but maybe others can weigh in. And you've probably seen Lyrica mentioned. It requires only twice a day dosing, and I'm told it hits the exact same receptors in the body as Gabapentin does. It didn't work as well as Gabapentin did for me, and I think it was making me gain weight, so I switched back to Gabapentin. As they say, your mileage may vary.
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May all beings have happiness and the causes of happiness. May all beings be free from suffering and the causes of suffering. May all beings rejoice in the well-being of others. May all beings live in peace, free from greed and hatred. |
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"Thanks for this!" says: | Joe Duffer (11-10-2016) |
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#3 | ||
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Junior Member
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Do it ! I take 1,200mg before bedtime & have been a very satisfied customer. No more peaks & valleys so to speak of. No more foggy periods during the day, for me it works great.
It took me fighting with my insurance company for almost a year to get it approved. Good Luck
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My PN is considered Critical Illness Neuropathy. In October 2010 I left for a golf trip not feeling well, woke up in a hospital 21 days later. I was in an induced coma for treatment of Legioneers Disease. First day out of ICU I noticed the pain in my feet and as they say the rest is history. |
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"Thanks for this!" says: | Joe Duffer (11-10-2016) |
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#4 | ||
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Junior Member
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Quote:
Thank you both for your replies. |
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"Thanks for this!" says: | echoes long ago (11-02-2016), MikeK (11-03-2016) |
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#5 | ||
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Junior Member
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I was not able to get Gralise. My neurologist said they don't prescribe it because of the cost. I was able to get tested for SCN9a and should have results in a couple months. My neurologist said he would put me on Carbamendine if the test is positive. I don't see that as making any progress though. Just a different drug with worse side effects. I also just got the shingles. I did get the vaccine in 2013 and was put on Valtrex within 3 days. This tells me my immune system is weak. Not sure which way I will turn next but will keep trying.
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Junior Member
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Junior Member
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