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Amitriptyline / Perphenazine
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Amitriptyline drops numb mouth?
I was just prescribed Amitriptyline in an oral liquid form. I was told to take three drops and I did so by placing them in a spoon and taking them that way. The taste was awful and instantly my mouth and throat went numb and dry. Is this normal?
I was just prescribed Amitriptyline in an oral liquid form. I was told to take three drops and I did so by placing them in a spoon and taking them that way. The taste was awful and instantly my mouth and throat went numb and dry. Is this normal?
swimsalot
in
Anxiety Support
6 years ago
My senses are more alive now I have off Amitriptyline!
It's taken weeks and I am still not completely free of the Amitriptyline inside me but thankfully I am over the worst of the withdrawal symptoms but I am angry. I have been out of the world for so many years thinking the bad thoughts I woke up with every morning was part of my depression but I now realise
It's taken weeks and I am still not completely free of the Amitriptyline inside me but thankfully I am over the worst of the withdrawal symptoms but I am angry. I have been out of the world for so many years thinking the bad thoughts I woke up with every morning was part of my depression but I now realise
Lizzypick
in
Anxiety and Depression Support
6 years ago
Severe coccyx pain
This has been going on for prob about a year now. It's worse at nite and I have to pay on my back with various cushions due to agonising hip pain. The past wk I've been woken twice by the sheer agony, couldn't sit up but thankfully my crutches are next to my bed so I can use them. I'm battling the rheumy
This has been going on for prob about a year now. It's worse at nite and I have to pay on my back with various cushions due to agonising hip pain. The past wk I've been woken twice by the sheer agony, couldn't sit up but thankfully my crutches are next to my bed so I can use them. I'm battling the rheumy
RAgemz81
in
NRAS
6 years ago
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Worried about what options I may have great endo
I recently underwent a TURBT procedure for a cancer scare in my bladder, after biopsy found out it was endometriosis inside my bladder. Urologist has referred me to gynachologist. After lots of reading and am concerned what my options maybe to treat the end o because I have had the mirena coil fitted
I recently underwent a TURBT procedure for a cancer scare in my bladder, after biopsy found out it was endometriosis inside my bladder. Urologist has referred me to gynachologist. After lots of reading and am concerned what my options maybe to treat the end o because I have had the mirena coil fitted
Poppy1973
in
Endometriosis UK
6 years ago
Weaning off Amitriptyline - what are the side effects?
My Dr has asked me to decrease my dose of Amitriptyline from 50mg by 10mg every week so i can start a different medication. I am getting the worst migraines of all time. What is the common side effects of going down a dose of Amitriptyline?
My Dr has asked me to decrease my dose of Amitriptyline from 50mg by 10mg every week so i can start a different medication. I am getting the worst migraines of all time. What is the common side effects of going down a dose of Amitriptyline?
Nataliesg1
in
Anxiety Support
6 years ago
Shingles as well as Crps and rheumatoid arthritis
Hi all. Just found this group tonight. I have so many questions ATM. Hope u don't mind. I have had Crps for abt 10 yrs after right wrist was fused. Also diagnosed with Rheumatoid arthritis 8 yrs ago. Yesterday I was told I now have Shingles, right side. My concern is and any connection between Crps
Hi all. Just found this group tonight. I have so many questions ATM. Hope u don't mind. I have had Crps for abt 10 yrs after right wrist was fused. Also diagnosed with Rheumatoid arthritis 8 yrs ago. Yesterday I was told I now have Shingles, right side. My concern is and any connection between Crps
Southafrican
in
Pain Concern
6 years ago
Hello everyone.
Diagnosed in 2010 with RRMS. First noticable symptom was in 2008. Which was ON. But I wonder if I've had it longer because, thinking about it I had a bought of PBA in the late 90s early 2000s. My next neuro appt I am gonna let him know that. I'm on Ocrevus. First half dose was in Apri second half was
Diagnosed in 2010 with RRMS. First noticable symptom was in 2008. Which was ON. But I wonder if I've had it longer because, thinking about it I had a bought of PBA in the late 90s early 2000s. My next neuro appt I am gonna let him know that. I'm on Ocrevus. First half dose was in Apri second half was
dailygrump40
in
My MSAA Community
6 years ago
Feeling overwhelmed!!
Hi I was diagnosed with hypothyroidism in March this year. Within a few months leading up to and after diagnosed I went completely bald. I was put on 50mg thyroxine and retested 8 weeks after and the dr said my levels were fine now with no mention of testing again January this year I was 10 stone I am
Hi I was diagnosed with hypothyroidism in March this year. Within a few months leading up to and after diagnosed I went completely bald. I was put on 50mg thyroxine and retested 8 weeks after and the dr said my levels were fine now with no mention of testing again January this year I was 10 stone I am
Ziggy12
in
Thyroid UK
6 years ago
IBS is going to be the end of me
It started 1 year ago. I was 26 and had already suffered for 2 years with an extremely impairing disease (intrinsic rhinitis) which got so bad that I almost couldn't breath, spending my days gasping for air, and living reclused in my dark-lit bedroom. After 2 surgeries and finally breathing again, proving
It started 1 year ago. I was 26 and had already suffered for 2 years with an extremely impairing disease (intrinsic rhinitis) which got so bad that I almost couldn't breath, spending my days gasping for air, and living reclused in my dark-lit bedroom. After 2 surgeries and finally breathing again, proving
Hans7
in
IBS Network
6 years ago
Put on weight whilst taking Amitriptyline?
Have other people found they have put on weight whilst taking Amitriptyline? My doctor increased my dosage to 25mg due to my pain level, but it doesn't seem to help. I had wanted to change to Gabapentin but he was not keen for me to do so. Thanks. Daphne
Have other people found they have put on weight whilst taking Amitriptyline? My doctor increased my dosage to 25mg due to my pain level, but it doesn't seem to help. I had wanted to change to Gabapentin but he was not keen for me to do so. Thanks. Daphne
Flory28
in
Thyroid UK
6 years ago
My fight against augumentation
Hi all just thought id let you know about my last 5 weeks fighting above, ive been on parpeximole for 5 yrs starting with one then reaching 6, far too many, so in last 12mths my rls has increased to the point if not sleeping at all some nights, so i decided i would come off parpeximole as i thought i
Hi all just thought id let you know about my last 5 weeks fighting above, ive been on parpeximole for 5 yrs starting with one then reaching 6, far too many, so in last 12mths my rls has increased to the point if not sleeping at all some nights, so i decided i would come off parpeximole as i thought i
BLUES60
in
Restless Legs Syndrome
6 years ago
I have fibro but need a painkiller to help me cope never had pain killers before do they work?
Ive had it for about 10 yrs just used amitriptyline but need better pain management now ?
Ive had it for about 10 yrs just used amitriptyline but need better pain management now ?
Fibrospark1962
in
Fibromyalgia Action UK
6 years ago
Amitriptyline
Has anyone experienced a sore throat while taking amitriptyline?
Has anyone experienced a sore throat while taking amitriptyline?
99am
in
PBC Foundation
6 years ago
Daily headache & migraines
I’m at the end of my tether! I’m 51 & have had headaches & migraines since my teens. I’ve tried painkillers, triptans, amitriptyline, propranolol and I’ve been on Topamax for a year (100mg a day) and the daily headaches are back with a vengeance. I’m desperate. The pain is really bad and is ruining my
I’m at the end of my tether! I’m 51 & have had headaches & migraines since my teens. I’ve tried painkillers, triptans, amitriptyline, propranolol and I’ve been on Topamax for a year (100mg a day) and the daily headaches are back with a vengeance. I’m desperate. The pain is really bad and is ruining my
fixit
in
National Migraine Centre
6 years ago
Amitriptyline
I was told by my consultant taking amitriptyline for nerve pain was absolutely fine, (been on it for about 9 months), but read on another site that their liver was affected by amitriptyline. Does anyone have any experience with this drug x
I was told by my consultant taking amitriptyline for nerve pain was absolutely fine, (been on it for about 9 months), but read on another site that their liver was affected by amitriptyline. Does anyone have any experience with this drug x
Mnoye
in
PBC Foundation
6 years ago
Anyone got any ideas about what I should do now?
I was diagnosed with RA in 2006 and later Fibromyalgia. Since then I've been on Sulfasalazine, MTX orally, Hydroxychloroquine, MTX subcutaneously, steroid injections. At the beginning of the year I was so bad I could hardly move, I was put on 4 months of Prednisone, and started on 50mg Benepali - which
I was diagnosed with RA in 2006 and later Fibromyalgia. Since then I've been on Sulfasalazine, MTX orally, Hydroxychloroquine, MTX subcutaneously, steroid injections. At the beginning of the year I was so bad I could hardly move, I was put on 4 months of Prednisone, and started on 50mg Benepali - which
annie0261
in
NRAS
6 years ago
Embarrassing symptoms
Although I’ve not been referred to a specialist my GP suggested that my symptoms pointed to fibromyalgia and left me to self manage. I tried Amitriptyline and gabapentin, neither of which I felt helped. I have managed living with the pain medication free however recently my symptoms have changed. My
Although I’ve not been referred to a specialist my GP suggested that my symptoms pointed to fibromyalgia and left me to self manage. I tried Amitriptyline and gabapentin, neither of which I felt helped. I have managed living with the pain medication free however recently my symptoms have changed. My
Paffette71
in
Fibromyalgia Action UK
6 years ago
Vulvodynia - new member trying to gain some insight with people suffering similar symptoms
I'm so glad I've found this site as I too have been searching for cases where vulvodynia seems to be just itchiness and not stabbing pain like a lot of other women seem to experience. I'm 30 years old and last December (2017) I started to experience itching. It was initially treated as a UTI then thrush
I'm so glad I've found this site as I too have been searching for cases where vulvodynia seems to be just itchiness and not stabbing pain like a lot of other women seem to experience. I'm 30 years old and last December (2017) I started to experience itching. It was initially treated as a UTI then thrush
ejp1006
in
Pelvic Pain Support Network
6 years ago
Endometriosis: at a loss on what to do
Hi, I've not been on here for a while but feel like I need some support so I've come back onto this site. I'll start by telling you a bit about me; I'm 20 years old and was diagnosed with Endometriosis when I was 18 I'd struggled for years and was so tough to get medics to take me seriously. I've tried
Hi, I've not been on here for a while but feel like I need some support so I've come back onto this site. I'll start by telling you a bit about me; I'm 20 years old and was diagnosed with Endometriosis when I was 18 I'd struggled for years and was so tough to get medics to take me seriously. I've tried
endowarrior_x
in
Endometriosis UK
6 years ago
so tired
Hi everybody, im Lou Lou and im new on here. I was diagnosed with fibromyalgia in november 2017 after being in pain for quite a few years , every day now i feel like im dragging my legs around and last night i couldnt uncross my legs without using my hands, im having physio and doing exercises at home
Hi everybody, im Lou Lou and im new on here. I was diagnosed with fibromyalgia in november 2017 after being in pain for quite a few years , every day now i feel like im dragging my legs around and last night i couldnt uncross my legs without using my hands, im having physio and doing exercises at home
lou_lou2018
in
Fibromyalgia Action UK
6 years ago
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