Dry, Itchy, Peeling, and other skin problems
#1
Posted 30 August 2007 - 07:13 PM
Here's my issue:
Even though I try to stay hydrated, my skin seems to be drying out... no visible rash, just prickly feelings like you get when you need to moisturize or when you are about to get a heat rash, and horribly itchy pits (again, no visible rash). I don't usually use lotions, since I am allergic to a lot of stuff. I am using Dove Sensitive skin bar soap and Dove Sensitive skin deodorant, both with the 1/4 added moisturizers.
Has anyone else gone through this with Lamictal? And, which lotion is best to use while on Lamictal?
Any advice would be appreciated...
thanks!
Current Daily Meds: 150mcg Synthroid, 25 mg topamax x 3 daily (introduced 1/10/13, titration dosage), 100mg Wellbutrin x 2 daily, .25 to .5 mg clonazapam prn.
#2
Posted 30 August 2007 - 08:05 PM
"Ah, war. God's way of making Americans learn geography." ~ Jon Stewart, The Daily Show
Dx: Bipolar Something (depends on who you ask...), ADHD- inattentive type, some anxiety stuff, PTSD
Alt Dx: "Nutty as squirrel poo." (quote from Harry Potter and the Deathly Hallows)
Rx:Seroquel- 200 mg at bedtime, Klonopin .5 mg prn, Adderall XR 10mg/day, adding Wellbutrin
Favorite things: Harry Potter, Seroquel, flannel sheets, House, Lost, The Office, my Tempur-pedic bed, pajama pants, massage, music, reading, Coca-Cola, Starbucks, sleep
Dr. Wilson: Beauty often seduces us on the road to truth.
Dr. Gregory House: And triteness kicks us in the nads.
#3
In_Remission_beachgal
Posted 31 August 2007 - 12:26 PM
Well, since rash is always an issue with lamictal and you don't want to use anything that would set that off, I'd go with something very gentle. I recommend Eucerin Calming Creme. It's thick and works well and it's gentle. it's fragrance free, too, which is a good thing.
When I was on Lamictal I used Eucerin Calming Creme, but it didn't help me. I got a bunch of little tiny bumps under the skin like orange peel, which is why I started using that creme. I had it for several weeks and thought it was weird cause I always had smooth skin. Well, to make a long story short I ended up with a rash and had to go off Lamictal after 8 1/2 months. I don't know if that bumpiness is a precursor to the rash or not, just be watchful.
#4
In_Remission_bd1972
Posted 02 April 2008 - 06:04 PM
I'm not on any other meds and can't think of any lifestyle changes recently.
#5
Posted 02 April 2008 - 07:39 PM
Just in the last week or so, ever since I went up to 400 mg of Lamictal, the skin on fingers and palms to a lesser extent has started to peel slightly. It's not to the point where it's freaky or anything and I don't (and never did) have a rash of any kind, but I'm wondering if I should be concerned. It's not peeling anywhere else on my body to the best of my knowledge. I would certainly think if it was related to SJS it would have shown up during the last 6 months while increasing my dosage. The only physical issues I've had until now were some pimples in weird places like upper thigh, chest, etc.
Please go to the Lamictal page and look at the picture of Stevens-Johnson syndrome (SJS) in progress.
You can be on Lamictal for years at the same dosage and that bastard of a syndrome can strike.
Of course it could also just be a case of an anticonvulsant just messing with your skin in a freaky way.
I am not a doctor, nor do I play one on TV. No doctor, nurse, pharmacist or lawyer was harmed in the creation of this post. No warranty is expressed or implied. Not valid with any other offer. Void where prohibited.
Straitjacket T-Shirts: When you're crazy enough to let your meds do the talking for you. Straitjacket Annex for mugs & bumper stickers.
Current meds: lamotrigine 200mg, topiramate 325mg, protriptyline 50mg, EPA 800mg, methylphenidate 5-10mg, lorazepam 1mg PRN
Past meds (likely incomplete): Abilify, clonazepam, desipramine, diazepam, Gabitril, lithium, Neurontin, Paxil, prochlorperazine, Provigil, Prozac, Risperdal, Seroquel, Serzone, Strattera, Trileptal, Zyprexa
#6
In_Remission_bd1972
Posted 04 April 2008 - 07:15 PM
#7
In_Remission_bd1972
Posted 08 April 2008 - 08:30 AM
Please go to the Lamictal page and look at the picture of Stevens-Johnson syndrome (SJS) in progress.
You can be on Lamictal for years at the same dosage and that bastard of a syndrome can strike.
Of course it could also just be a case of an anticonvulsant just messing with your skin in a freaky way.
You were 100% correct Jerod. I went to my general prac today and she stopped midsentence when she compared my symptom to Lamictal side effects. She told me to immediately discontinue it and not to start it again. Here's my concern though, she told me to stop cold turkey. I mentioned to her that I heard it can seizures if you don't tapper off and she told me that's only if you were taking it for seizures. I'm currently at 400 mg. Should I be concerned?
#8
Posted 08 April 2008 - 09:49 AM
You were 100% correct Jerod.
I hate it when that happens. Sorry.
She told me to immediately discontinue it and not to start it again. Here's my concern though, she told me to stop cold turkey. I mentioned to her that I heard it can seizures if you don't tapper off and she told me that's only if you were taking it for seizures. I'm currently at 400 mg. Should I be concerned?
If one is epileptic and not on another anticonvulsant the odds of having a seizure are pretty damn good.
If one isn't epileptic there is still a chance of having a seizure. A short-term prescription of clonazepam would be really helpful, just to be on the safe side. Plus there are the rebound mood swings, headaches and other crap that will make you feel like shit. Clonazepam just would make your life easier.
I am not a doctor, nor do I play one on TV. No doctor, nurse, pharmacist or lawyer was harmed in the creation of this post. No warranty is expressed or implied. Not valid with any other offer. Void where prohibited.
Straitjacket T-Shirts: When you're crazy enough to let your meds do the talking for you. Straitjacket Annex for mugs & bumper stickers.
Current meds: lamotrigine 200mg, topiramate 325mg, protriptyline 50mg, EPA 800mg, methylphenidate 5-10mg, lorazepam 1mg PRN
Past meds (likely incomplete): Abilify, clonazepam, desipramine, diazepam, Gabitril, lithium, Neurontin, Paxil, prochlorperazine, Provigil, Prozac, Risperdal, Seroquel, Serzone, Strattera, Trileptal, Zyprexa
#9
Posted 08 April 2008 - 04:37 PM
My GP completely over re-acted when I thought I had 'the rash' and wanted me to discontinue lamictal immediately even tho he said it's not SJS. I refused and my pdoc agreed it wasn't SJS. That's why I ask because what is the technical term they used to warrant going cold turkey?
Aside from the possible seizure due to abruptly stopping, are you going to taper down? Is there a game plan on what to put you on next?
I'm really curious because my dose needs to be adjusted and I wonder if you went from 300mgs to 400mgs abruptly if that what may have brought this on.
Rx: Lamictal 300mg, Valium 20mg, Abilify 15mg, Gabetin 300mg, Butrans 15mcg
Ex Rx: Zyprexa, Seroquel, Cymbalta, Nortryptaline, Effexor, Topamax, Klono
#10
In_Remission_always_doing_laundry
Posted 12 November 2008 - 09:39 PM
The only thing I can figure is a new sensitivity of the kind that occurs just because it is a new reaction -- or that my allergy to yellow dye No. 5 is cross-reactive with the yellow oxides listed in the info for generic lamotrigine 150 mg tablets. It sorta freaks me out, but I don't have any other issues; already take vistaril at night; claritin during the day prn; and otherwise tolerate it well. I haven't experienced headaches, brain fog, cognitive changes, anything bad at all other than the recurrent itchies that pop up in different places every day/throughout the day. This is the best drug I have taken. I haven't had a big seizure in four years, though I had a breakthrough kind of episode 18 months ago and a few auras that didn't materialize now and then. I also take neurontin and klonipin.
Any thoughts? Is this one to call the doc about, since I don't want him to take me off it -- but I don't want all my skin peeling off and feeling all stinging and sensitive, either.
#11
Posted 13 November 2008 - 12:22 AM
I notice it most when I shower, which I did today ... my skin is almost paper-thin these days (which isn't typical, as I have olive complexion), and literally rubs off -- with a washcloth, my fingers, when I use lotion (it collects with the lotion as I slather it on). I have always experienced rashiness with Lamictal/lamotrigine, and I continue to, but I haven't even been subject to significant (any, really) sun exposure, and my dose was decreased.
The only thing I can figure is a new sensitivity of the kind that occurs just because it is a new reaction -- or that my allergy to yellow dye No. 5 is cross-reactive with the yellow oxides listed in the info for generic lamotrigine 150 mg tablets. It sorta freaks me out, but I don't have any other issues; already take vistaril at night; claritin during the day prn; and otherwise tolerate it well. I haven't experienced headaches, brain fog, cognitive changes, anything bad at all other than the recurrent itchies that pop up in different places every day/throughout the day. This is the best drug I have taken. I haven't had a big seizure in four years, though I had a breakthrough kind of episode 18 months ago and a few auras that didn't materialize now and then. I also take neurontin and klonipin.
Any thoughts? Is this one to call the doc about, since I don't want him to take me off it -- but I don't want all my skin peeling off and feeling all stinging and sensitive, either.
Assuming you have experienced no fever and that your skin is neither burned looking or blistered... my internet wonk guess would be that you need to get your ass to a doctor. You are having a drug reaction to a severe enough degree that it is expressing itself in your skin (your largest organ).
"The" rash that everyone flips out about is called Steven Johnsons. If it is left untreated, it can progress to another nastiness called TEN, or Toxic Epidermis Necrosis, wherein a person's skin blisters, peels, and falls off. Oh, and their internal organs fail, too. If you had that, you wouldn't be typing on a chat board. But you have epidermis something. Seizure control or not, you need to fess up and get it biopsied.
Dymphna
Yes, my name really is Dymphna.
I'm not a doctor, nurse, pharmacist, or therapist.
I can find you an answer and I won't blow smoke up your ass.
St. Dymphna is the Patron for brain maladies.
I'm the Enforcer.

#12
In_Remission_always_doing_laundry
Posted 13 November 2008 - 06:11 AM
#13
Posted 13 November 2008 - 09:32 AM
It took a bad liver panel to get me to stop taking Lamictal. Pay no mind my nose had been bleeding every day for a year... (or that my fingertips were peeling, or my feet and palms were itching, or that I had a wicked rash on my face, etc. etc.).
It will all work out.
D
Yes, my name really is Dymphna.
I'm not a doctor, nurse, pharmacist, or therapist.
I can find you an answer and I won't blow smoke up your ass.
St. Dymphna is the Patron for brain maladies.
I'm the Enforcer.

#14
Posted 13 November 2008 - 10:29 AM
To give you some hope here, I had to stop lamictal a couple years ago for sjs, and I literally cried.
But, I've found a new cocktail that works for my symptoms, and I"m pretty stable now. You probably have lots more options.
Hopefully it's something unrelated, but you really need to get it checked out.
Good luck,
Anna
Diagnosed Bipolar Type I, most recently Mixed.
Current Meds: Seroquel, Risperdal, Neurontin, Provigil.
#15
Posted 13 November 2008 - 10:41 AM
The only thing I can figure is a new sensitivity of the kind that occurs just because it is a new reaction -- or that my allergy to yellow dye No. 5 is cross-reactive with the yellow oxides listed in the info for generic lamotrigine 150 mg tablets.
On the off chance that the problem is due to your allergy hating the lamotrigine coloring, you have two options: going back to brand or the ever-expensive compounding. Both of which would have to be reintroduced at a slow titration.
Obviously the pros who can see what your skin looks like are the only ones who can tell you if those are even options or not, but you might have a slim chance of keeping Lamictal.
I am not a doctor, nor do I play one on TV. No doctor, nurse, pharmacist or lawyer was harmed in the creation of this post. No warranty is expressed or implied. Not valid with any other offer. Void where prohibited.
Straitjacket T-Shirts: When you're crazy enough to let your meds do the talking for you. Straitjacket Annex for mugs & bumper stickers.
Current meds: lamotrigine 200mg, topiramate 325mg, protriptyline 50mg, EPA 800mg, methylphenidate 5-10mg, lorazepam 1mg PRN
Past meds (likely incomplete): Abilify, clonazepam, desipramine, diazepam, Gabitril, lithium, Neurontin, Paxil, prochlorperazine, Provigil, Prozac, Risperdal, Seroquel, Serzone, Strattera, Trileptal, Zyprexa
#16
In_Remission_synapticgap
Posted 13 November 2008 - 02:50 PM
I notice it most when I shower, which I did today ... my skin is almost paper-thin these days (which isn't typical, as I have olive complexion), and literally rubs off -- with a washcloth, my fingers, when I use lotion (it collects with the lotion as I slather it on). I have always experienced rashiness with Lamictal/lamotrigine, and I continue to, but I haven't even been subject to significant (any, really) sun exposure, and my dose was decreased.
The only thing I can figure is a new sensitivity of the kind that occurs just because it is a new reaction -- or that my allergy to yellow dye No. 5 is cross-reactive with the yellow oxides listed in the info for generic lamotrigine 150 mg tablets. It sorta freaks me out, but I don't have any other issues; already take vistaril at night; claritin during the day prn; and otherwise tolerate it well. I haven't experienced headaches, brain fog, cognitive changes, anything bad at all other than the recurrent itchies that pop up in different places every day/throughout the day. This is the best drug I have taken. I haven't had a big seizure in four years, though I had a breakthrough kind of episode 18 months ago and a few auras that didn't materialize now and then. I also take neurontin and klonipin.
Any thoughts? Is this one to call the doc about, since I don't want him to take me off it -- but I don't want all my skin peeling off and feeling all stinging and sensitive, either.
I've just starting taking Lamictal and I have had weird skin reactions/sensitivities. I have a patch of dry skin on my chest which randomly appeared and I have had a relapse of dyshidrotic excema which I had as kid but hadn't had in at least 10+years. Obviously Lamictal and skin issues go hand in hand.
#17
In_Remission_always_doing_laundry
Posted 18 November 2008 - 08:15 PM
The question I have now is whether anyone else has had unusual sensory experiences with even slight tapering: In particular, smells. For instance, Ivory soap that normally has little to no scent to me, smells like watermelon. Coffee smells like tuna. It can be almost anything, unexpectedly and not in particular pattern. I will experience an incongruent smell, or a smell where there really isn't anything to smell. Or, a family member may have a really offensive personal odor that only I notice. I also feel a little emotionally labile inconsistent with any previous experience/pattern. It's very weird. I feel sorta hyper-aware, which extends to the smell thing and the emotionality. Has anyone else had this happen with medication changes of any kind?
#18
Posted 18 November 2008 - 09:17 PM
Definitely worth mentioning to pdoc sooner rather than later, I would think...
Anna
Diagnosed Bipolar Type I, most recently Mixed.
Current Meds: Seroquel, Risperdal, Neurontin, Provigil.
#19
Posted 19 November 2008 - 12:09 AM
Since you just dropped your dose, and you are epileptic, my vote would be on mild EEG changes?
Dymphna
Yes, my name really is Dymphna.
I'm not a doctor, nurse, pharmacist, or therapist.
I can find you an answer and I won't blow smoke up your ass.
St. Dymphna is the Patron for brain maladies.
I'm the Enforcer.

#20
Posted 19 November 2008 - 12:28 PM
Two separate things: Phantom smells and smell perversion. Smell perversion (such as you describe) is common with all AEDs. Phantom smells (smelling smoke when there is none, smelling cat pee, etc.) can occur both in MI and with seizures.
And having both at the same time makes it difficult to sort out. The two occurring simultaneously? Phantom smells overwhelming true smells, so it's not truly smell perversion? Or
Since you just dropped your dose, and you are epileptic, my vote would be on mild EEG changes?
Not enough data for me. All three have equal probability as far as I'm concerned.
I am not a doctor, nor do I play one on TV. No doctor, nurse, pharmacist or lawyer was harmed in the creation of this post. No warranty is expressed or implied. Not valid with any other offer. Void where prohibited.
Straitjacket T-Shirts: When you're crazy enough to let your meds do the talking for you. Straitjacket Annex for mugs & bumper stickers.
Current meds: lamotrigine 200mg, topiramate 325mg, protriptyline 50mg, EPA 800mg, methylphenidate 5-10mg, lorazepam 1mg PRN
Past meds (likely incomplete): Abilify, clonazepam, desipramine, diazepam, Gabitril, lithium, Neurontin, Paxil, prochlorperazine, Provigil, Prozac, Risperdal, Seroquel, Serzone, Strattera, Trileptal, Zyprexa
#21
In_Remission_always_doing_laundry
Posted 19 November 2008 - 03:32 PM
The kids don't notice; they don't smell the tuna-like coffee; and when they sniff the bar soap, it still smells like Ivory/nothing. The day can randomly continue just fine, with no weird smell things that I notice, then I'll go to chew a piece of gum (from the same package of Trident White peppermint I've been chomping from) ... and it will smell like pineapple and "metal," (whatever that smells like), and I will be convinced that the Cadbury Adams folks have had an assembly-line/mechanization error that accidentally landed tropical chiclets in my peppermint package.
#22
Posted 20 November 2008 - 01:14 AM
I call this my "oh my god, the chicken is RAW" smell.
Talk to your neuro: it sounds like you need an adjunct med.
D
Yes, my name really is Dymphna.
I'm not a doctor, nurse, pharmacist, or therapist.
I can find you an answer and I won't blow smoke up your ass.
St. Dymphna is the Patron for brain maladies.
I'm the Enforcer.

#23
In_Remission_always_doing_laundry
Posted 20 November 2008 - 03:50 AM
... I have actually had the "chicken is RAW smell" ... hamburger, too (a raw meat in general thing ... as in everything smells like it).I call this my "oh my god, the chicken is RAW" smell.
I feel so much better calling the nurse with the knowledge that this is not a solitary experience and they won't send little men to lock me up. This forum is great ... it helps me feel more validated that something is weird, and that it isn't melodramatic to call the doc. I keep learning that the brain is pretty amazing ... makes me wonder how it all manages to work just right in so many folks every day. Thanks, everyone.
#24
In_Remission_ssplash
Posted 26 March 2009 - 06:04 AM
Has anyone researched a way a way to minimize dryness (skin, mouth, eyes) caused by Lamictal? There must be something that can be done without Lamictal losing efficiency. What's causing it, I wonder?
Also, I know about the binding with melanin. I'm biracial, it might affect people of colour more, don't know. What do you think?
I want to manage secondary effects a bit better. I'm bipolar II self-taught
Thanks!
oNE LoVE
Greetings from Madrid, Spain
#25
Posted 26 March 2009 - 09:07 AM
I've tried a couple of moisturizers, but I haven't found anything that really works. Suggestions?
As far as dry eyes go, lubricant eye drops work well and are safe. The ones we use are called Thera Tears, and they come in individual vials, not a bottle, so you are always using sterile drops. I don't know whether they have them in Spain, but I am sure there is something similar.
I drink a lot and suck on sour candies or chew gum for dry mouth.
Bipolar NOS, ADHD, migraine
900mg Lithium CR, 5mg Abilify, 50mg Latuda, 20mg Adderall BID, 300mg Wellbutrin XL, .5mg Xanax XR prn
#26
Posted 26 March 2009 - 10:24 AM
Lips do well with any balm that you are accustomed to - remember, don't add new make-up & toiletries when you have just started Lamictal.
The best solution is always to drink more water. Not soda, coffee, tea or anything else - just water. If you get totally bored, get fizzy water (but don't take your meds with fizzy water: it can hasten the meds out of your system).
Dymphna
Yes, my name really is Dymphna.
I'm not a doctor, nurse, pharmacist, or therapist.
I can find you an answer and I won't blow smoke up your ass.
St. Dymphna is the Patron for brain maladies.
I'm the Enforcer.

#27
In_Remission_ssplash
Posted 26 March 2009 - 12:25 PM
Yes, your advice is great as well.
I was also wondering in bio-chemistry ways, you know. If anything could be done to foster protection to the skin and eyes, mmmhh. I'll search on this a bit further and will report soon.
Cheers and keep well
oNE LoVE
#28
Posted 26 March 2009 - 03:46 PM
I have super dry skin pretty much all over, including my scalp. And with that comes itchiness. Like I-just-slammed-some-dilaudid itchy, without any warm and fuzzy feelings.
I've tried more lotions and moisturizers than I have meds in search of relief. Apparently I'm not in the least bit rash prone(so far).
So far, for me, I've found Eucerin Calming Cream(Rite Aid brand is just as good, btw) is very helpful for my dry skin. Aveeno is decent as well, but it's a bit pricey and the store brand seems to have more alcohol in it. Which is no good for itchy dry skin. If I take a bath, I also put baby oil in the water, which works well. It's also important to avoid any harsh soaps, shampoos, and other skin products and to look for products that are specifically formulated for sensitive skin. Eczema lotions are good too.
Sorry this is kind of scattered, though trying to write this post just reminded me to take my Focalin.
-- George Washington, 1776
'I don't want to be lonely, I just want to be alone.'
Working Dx: MDD, Bipolar NOS, ADHD, LD-NOS
#29
Posted 26 March 2009 - 10:20 PM
You can't slam Vitamin E or A while on Lamictal, but you can eat more fish, which can help with natural conditioning.
D
Yes, my name really is Dymphna.
I'm not a doctor, nurse, pharmacist, or therapist.
I can find you an answer and I won't blow smoke up your ass.
St. Dymphna is the Patron for brain maladies.
I'm the Enforcer.

#30
Posted 27 March 2009 - 08:08 AM
I'm not a cynic, I'm an optimist with experience.
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