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Found 14 results

  1. Does anyone know what actually causes Lamictal-induced acne? Lamictal gives me the most god-awful acne on my back, shoulders, and chest. I got off of it for a few years after I had just totally had it with the horrendous, almost cystic acne that it caused. It cleared up finally after a few years, but not completely, and finally cleared up almost completely after I got off Zonegran. But when my pdoc recommended recently that I give Lamictal another try due to my recent decline in mood, I reluctantly decided to give it a try, with the idea in mind that my physical appearance (covered by shirt nearly 99.99% of the time) was less important than my mental stability. Sure enough, after about 3 weeks or so, these zits are popping up on my back, shoulders, upper arms (even over my tattoo), and chest. They're not as bad as it was when I got off Lamictal last, but they're definitely there, and they're definitely getting worse. I'm only on 25 mg bid (twice a day), and she may want to increase the dose the next time I see her (here in a few days), as this dose isn't doing anything to help my depression. I saw a dermatologist for years while I was on it the last time and she couldn't figure out anything out to help it. I tried the following medications: Oral doxycycline (Vybramycin) 100 mg bid (didn't really help at all) minocycline (Minocin) 100 mg bid (helped mildly for a little while, then quit working) sulfamethoxazole/trimethoprim (Bactrim DS) 800 mg/160 mg bid (this was the only thing that put a dent in the acne but I wasn't able to take it long because it caused blood test abnormalities) Topical salicylic acid (no help) adapalene gel (Differin) 0.3% (helped mildly) BenzEFoam Ultra (micronized benzoyl peroxide) 9.8% (no help) benzoyl peroxide/clindamycin gel (BenzaClin) 5%/1% (worked decently, but bleach-stained my clothes) benzoyl peroxide wash 10% (both generic and PanOxyl brand) (no help) tretinoin topical cream 0.025% (no help) clindamyycin phosphate lotion 1% (Cleocin T) (some help combined with benzoyl peroxide and adapalene) erythromycin gel 2% (A/T/S, Emgel, Erygel) (no help) I don't think topical medications are really the answer, really. Plus it was a PITA to reach around my back applying these topical meds on my back and shoulders every day twice a day with some of them. There were several medications we tried to try, but my insurance wouldn't cover it... like dapsone topical I think was one of them... I was just wondering if anyone knew the root cause of Lamictal-induced acne so I could address it with my dermatologist when I start seeing her again. Or is it just something I would have to just deal with?
  2. Hello everybody, I started on Lamictal a few weeks back. My doctor had me up the dose by 25mg every 10 days. The first 10 days were okay aside from an intermittent sore throat and a few random aches and pains. When I went up to 50mg though, things got a bit weird. The first day, I woke up with a few tense muscles. And then a few days later, I had some noticeable swelling on my tongue. I ended up stopping the medication. My questions are, do you think this is the result of me going up too quickly? Has anybody else experienced this and was then able to successfully titrate at a slower pace? Should I be willing to give Lamictal another shot?
  3. I'm not sure if I'm posting this in the right place: I came across this site while searching for a new manufacturer for this drug Lamotrigine. The local pharmacies are quick to tell their customers, "We no longer have a contract/buy from, that manufacturer", but don't give out what manufacturer makes the drug and where to purchase it. All I get is, "I don't know. That's not something we are associated with," but can't give me squat for information. This drug intended purpose is for seizures. Now for Bipolar. I wasn't diagnosed with Bipolar, but I do have some of the tendencies behavior, (not enough to make Bipolar diagnosis), which I was tested and my new diagnosis is PTSD. If your not familiar with most recent studies, it can be a cause related to anything traumatic in our pasts. Yes, this is me. I have military retired insurance coverage and I'm trying to find who makes this drug to see who sells it and to try and have my insurance cover it. Damn, this is hard for a patient to do. I thought pharmacies or doctors do this.But what do I know? I'm just a nurse who cares for retired/disabled Vets. Suggestions/recommendations?
  4. About three months ago, I was prescribed Lamotrigine for General Anxiety Disorder. I have had no other issues aside from my anxiety. As would be expected, my dosage was gradually increased. However, after about four weeks something just didn't seem right. I ended up stopping at 75mgs per day. I continued that dosage for about a month. Sometimes, I'd wonder if my vision wasn't quite right. About four weeks ago, I was out on a walk with my son and realized that I could barely see more than twenty feet ahead of myself. Something just was not right about my vision. If I tried focusing on something, it would almost feel like I could go cross eyed. I did some reading on other people's experienced with this medication, and was alarmed to find a lot of information on vision issues. I decided to taper off the Lamotrigine. There were a number of medical sources saying to reduce by 50% per week. I figured going with 25% per week would be safe. I also met with a doctor, who confirmed that 25% per week was super safe. About four or five days after decreasing my dosage, my eyes began to feel immense pain. Especially my right eye. It felt like the most intense sinus pressure, or a migraine, or some incredibly severe tension. The issue with not being able to focus became much worse. I saw an eye doctor, and also had an eye exam done. I was told both times that my vision was completely fine. They did mention that I had really dry eyes, and I'm currently using a heat compress that they had recommended for treating this. However, the eye pain has been constant. I have barely been able to interact with my family, work, or even read. At times I can hardly look at the page of a book, it is so incredibly difficult to focus on. Yesterday, I was in such terrible pain that I could barely handle being awake. Now, I have a constant ringing in my ear. My ears also feel very clogged, almost like sinus issues. I'm honestly not sure how much more of this I can handle. Does any of this sound familiar to any of you? I could sure use some peace of mind. I am pretty concerned that I have permanent hearing issues, let alone that my eyes will never feel normal again. Any insight would be much appreciated.
  5. Hi, im not a forum person and also from Sweden so if theres already a thread about this or info somewhere point me in the right direction anyway, i was diagnosed with cyclothymia alittle more than 2 years ago and been on lamictal since. worked wonders since im able to have friends now and on the verge of joining the workforce again anyway, seems lamictal doesnt work for me anymore :/ been having bad headaches and feeling shitty overall for over a month, stopped taking them for 5 days and headache/feeling shitty went away, started taking it again today (at lower dose) and got headache and feeling shitty again... and ive never had issues with headaches at all in my life before and im actually having a pretty healthy lifestyle these days so i see no other connection than it being the lamictals fault so it seems i have to switch meds. im seeing my psychiatrist again in two weeks and of course i will make decision in discussion with him but I wanna go there prepared so... anyone have suggestions/experience what med(s) to take instead of lamictal? ive been googling alot and reading on crazymeds so im somewhat aware what meds are out there but its hard for me to tell which ones would be similar to lamictal tried virtually all SSRI's, SNRI's and Bupripone (together with lamictal) and they all make me crazy and/or feel awful, also been on aripiprazole and wasnt pleasant either. sorry if rambling/broken english. /Nils
  6. I’ve read that angioedema can be a very rare side effect of Lamotrigine. I figured this was a bigger pool of people and there might be at least one other with this issue. That’s my biggest goal here I’d rather not get off it if I don’t have to. My doctor isn’t sure it was related, but now thinks it’s okay to try taking me off to see if my swelling goes away. I have a history of living with a low level of constant panic that triggers to severe panic easily (I’m now agoraphobic). But the angioedema can make my airways swell at ransom, so it may be worth the risk. My experience: I was on Lamotrigine for 5 months when I went from 100 to 150mg. I had a strange cough that ended up lasting all of June (felt like asthmatic bronchitis, but my lungs were clear), a week after the upped dose I had a few nights where I looked and felt just like my arms and chest had a bad sunburn. My doc put me back down to 100mg. By July 1st, I had idiopathic angioedema. My lips, tongue, throat would swell with anything I ate or with brushing my teeth. Any pressure. I went two months eating a few bites or nothing but pedialyte. I had to get off lithium cold turkey because of how sick it made me to take on an empty stomach. It’s better controlled now, but the anti-inflammatory (dapsone) I was taking caused anemia and I had to get off it. The next step is a monthly shot that is extremely expensive (I’m unemployed and uninsured). If there’s a chance getting off Lamotrigine will help, I’ll try it.
  7. Since upping my lamictal dose (only to 75) I gradually noticed increading strange muscular pains and cramps, akin to what I imagine arthritis to be like. I obviously have noticed that lamictal side effects tend to dissipate after a while after a dosage change, and of course had much more intense pains, headaches and other such things around the increase time howhever these particular ones appeared after the initial S/E subsided and have progressively worsened. These are focused on my legs, primarily my calf and knee joints, and have affected my gait. Alongside this I've notices strange muscular twitches and sharp pains, primarily in the leg areas but occasionally other muscle areas. I have noticed there is some info and muscle pain does seem to be a known side effect of lamictal, but was wondering if anyone has experience in treating this? Am wondering whether to reduce dose, which is a difficult choice as 75 is the highest dose I've been able to tolerate and is still pretty subtherapeutic. I should probably note on the list of odd side effects that I also have a crazy range of odd head, neck and jaw pains, alongside ocular aura w/out migraine (like a dull pain behind the eye accompanied with a feeling of a round orb or spot sorta behind vision), although these are harder to pin on the lamictal... Fun times...
  8. I have mild reflux, something like GERD or LERD, for the past six months or so. Mostly no pain, just really bad smells at the back of my throat and occasional vomit burp. It recently (past couple months) started giving me vague gut pain and bloating after meals, so I saw a dr, got scoped, and was diagnosed with reflux. No erosion/ulceration was seen though, just stomach juices bubbling up my esophagus a little. So, I got some prescription strength probiotics and started putting chia seeds in my drinks. (The goo really soothes all that mess.) My reflux was more or less under control with just that, until I finally decided to go to a psychiatrist for my (years long untreated) depression. Now, after a week at 5 mg escitalopram and 25ish mg (I'm trying to quarter 100 mg pills, it's not so accurate) lamotrigine in the AM, my stomach is MAD. Putting anything in my stomach makes it bloated and painful. And the past couple days it's even worse. Last night, probably two hours after eating I had a wicked vomit burp. Like the food in my stomach wasn't moving down AT ALL. This morning I even woke up bloated. I have a long history of gut unhappiness, but it's usually my bowels/large intestine and this stomach pain shit is really making it hard for me to do anything. Like, I'm so bloated I'm scared if I get up and move around I'm going to vomit. (But I don't have nausea, weirdly enough.) And I think all this clenching my stomach against the bloating and pain is making my asthma worse. Is this a start up side effect that will go away? Anyone know of anything besides PPIs that can help it? I think the problem is that my digestive tract just isn't moving, not that I have too much acid, and besides PPIs give me wicked diarrhea. When I had a big cup of coffee with breakfast yesterday morning, my big hearty breakfast didn't cause me any problems at all. Coffee usually makes my digestive track tweak the fuck out and puts me on the toilet, I think in this case it brought my gut back to normal speed. But I can't do that with dinner. My doctor actually wants me on 10 mg escitalopram already and I'm scared to go up because I don't want this to get worse. Also I have medication phobia and want to stay at the lowest doses possible for everything. But I really want to give the meds a chance to work.....
  9. I have finally decided to go off Wellbutrin (Bupropion/Zyban) as I just cannot live with this anger and rage attacks any longer. I spend my day swearing, (I can’t fit enough swear words in a sentence), clenching my hands until they are rigid, screaming and hurting my throat, telling myself I wish I was dead and having even more intrusive thoughts than normal, even thoughts that wake me up in the middle of the night and I respond by telling myself to fuck off while I‘m laying there in bed. The anger has alarmed me and I can feel the cortisol surging through my body. I’m getting off this medication by myself without help because I went to see my psychiatrist the other day sand he virtually dismissed me and was clearly annoyed with me for having too many side effects and he was frustrated at how difficult I was to treat. There was no sympathy whatsoever. He said we’ve exhausted all avenues. I felt like a fool for not responding correctly to medications that he thought should work. It was a waste of money seeing him and I’m sick of doctors telling me it’s worth having numb genitals or inability to orgasm if you find a pill that gets rid of your depression. The doctor was frustrated with me before for all the pills I’ve been on that I couldn’t tolerate because of sex issues. The Wellbutrin didn’t do anything negative for me sexually (it seemed to have a big improvement on me sexually, actually), but the insane anger is just too much to live with. The anger was over the most minor of things, such as the vacume cleaner cord getting tangled, or losing internet connection. I’m currently on Lamotrigine 200 mg by itself which I hope will help my depression/anxiety.
  10. Does anyone have any experience specifically with the Depakote+Lamictal combo (with or without other medications). I've been on Depakote now since about November of last year but we're swapping out the Trintellix for Lamictal because my new insurance in July might give me a hard time about covering Trintellix. And we (my pdoc and I) figured that demonstrating an approved medication doesn't work (if it doesn't work that is) should be something we should try before submitting the step therapy paperwork for Trintellix. For this new insurance, they not only require that you try at least two other generics, but the "Restricted Access" meds also are only allowed to be used for FDA approved indications (i.e. Trintellix is approved for MDD but I'm BP2). I started Lamictal on Thursday. 25mg every other day for 2 weeks. Then 25mg every day for two weeks. Then we'll decide if we want to increase it again to 50mg for another two weeks or if we want to increase the Depakote or Rexulti. I don't recall Lamictal having such a difficult startup when it comes to GI discomfort. I remember the antsy almost anxious feeling, and I remember the headaches, but I'm also having nausea, some mild stomach cramping, diarrhea, but fortunately no vomitting. Has anyone else ever taken Depakote and started Lamictal and found they had a hard time. Better yet has anyone ever taken Lamictal both with AND without Depakote and found it less tolerable when taken with Depakote? I am aware of the medication interaction between these two meds. So I know that Depakote is going to increase Lamictal blood levels and might amplify some of these side effects. It's just more difficult than I remembered from the last time I took it years ago when I wasn't on Depakote and I wasn't really expecting it to be this much worse. Granted, I've only taken two doses at this point. So I might be jumping the gun and might find that I feel better later this week. But I'm also supposed to be discontinuing the Trintellix on Thursday. And if I'm still having a hard time adjusting to the Lamictal, stopping Trintellix at the same time could make me miserable, and I know that. Anyone have two cents?
  11. Hi There, I'm not much of a poster. But, I've noticed when you are trying to look up people's personal experience with meds, usually the reports are from people who have had really bad experiences, and so you don't normally get the full range of experiences. I'm assuming, the people who are fine, on certain meds, don't really post anything, because they've had no problems with it. Also, I wanted to post about Fetzima, because there is basically not a lot of information on it, so I felt like I wanted to share with the community to help others out who are deciding what to do. And, these forums were always helpful for me on my med research, so I wanted to contribute. I was on Fetzima for probably 3 years. My main medicine was Lamotrigine/Lamictal 150mg, which controlled my depression crashes. And, I needed a depression booster because of my dysthymia. I was on 40mg the whole time of Fetzima. I learned over the years, the SSRI's did nothing for me. I tried everything in the book. Finally, this, actually, good psych doctor recommended an SNRI, Fetzima. I remember in the beginning, my only side effect was cold sweats. Like wake up in the middle of the night, drenched in sweat. It was not that fun. But, my depression improved and I was finally stable and felt good for the first time in my entire life. And, I told myself, I'll take the cold sweats, if it means I feel like a normal functioning adult human being. But, after a while, maybe 2-3 weeks, the cold sweats subsided. After that, Fetzima worked! It was great, the first depression med that I ever felt good on, didn't feel weird, was happy, held a job, friends, etc. Amazing! Then, I worked really, really hard with my therapist. I did everything I could possibly do to get better. I never wanted to be on meds. I wanted to treat myself and get better, and the end. I have severe trauma as a kid, and in result, suffered from severe depression, suicidal ideation, couldn't move or function, anxiety, social anxiety, and pretty much everything that goes along with that. Although, on the outside, you would never suspect it; I have a master's degree, I'm outgoing, friendly, etc. (Just trying to give you guys a picture of the situation). So, yes, I, personally, would recommend it. And, had no problems with it. Although, because it's a newer med, and no one has ever heard of it, there is no a lot of research on the long term effects. Obviously, medicine is different for everyone, but Fetzima worked for me. I finally felt good enough and stable enough to try to get off my meds, 3 years later. I recently tapered off of Fetzima, 20mg for 1 month, and then off. It was not that fun, but, it wasn't horrible, and it is not the horror stories that I've read from others online. I had one day of a pretty bad depression crash (maybe two), although, I knew it, and I knew what was happening, and I just reached out to everyone to help me through it. And, I know that a side effect of withdrawal is depression! Because your body is used to the meds, and then it doesn't have it anymore, so it takes a while for your brain to even out. The other very seriously difficult part for me- was the brain fog- brain cognition defects. I've never had anything like this before in my life, always good in school, always able to concentrate. I never even pay attention to that one on the list of issues that could arise. But, I was in a class that week, and it was rough! I couldn't concentrate, couldn't focus, fidgety, I felt like my brain was at 80%. It was a big struggle. I was scared my brain was going to be like this forever, and kept having to remind myself that it's the withdrawal. I, also, decided I'd rather deal with the withdrawal, then be on this forever, so I put up with it. And, probably after a week or two it went away. And, that's it! My emotions are okay! No depression! I'm very proud of myself, and I feel like the trauma therapy really worked! (So, I'd recommend that too). A lot of people "poo poo" talk therapists, and honestly, going through a lot of them since I was a teenager, a lot of them are pretty bad. But, once you find a good one, which can take a bunch of tries. It pretty much changed everything for me. Took a solid 4 years, I'd say of serious talk therapy from 2014-2018. But, I am a happy/content human being now! And, it was worth everything! And, I have someone I can check in with now, but don't need to go regularly, which feels amazing too! The meds teach you (or, taught me) what it was like to be stable and content. Which, I had never felt before in my life. And, then once you get off of them, your brain has been trained to know what being stable and content is, (and you've added the skills and tools you need to, through talk therapy to help yourself through), so, it'll go back to where it needs to go. Obviously, some people will need to be on meds forever, and that's okay too. I'm just sharing my personal experience. I'm now feeling strong enough to taper off my Lamotrigine 150mg. Which will be 125mg for 3 weeks, then 100mg for 3 weeks, then 75mg, 50mg, 25mg each for 3 weeks, and then 0! We're just doing it very, very slow. And, I hope it goes well! So, I'll share that experience too, in a couple months. Anyways, that's my review of Fetzima! And, it worked for me, while it needed to.
  12. Hello - I've been on Lamictal (50 mg at night), Prozac (20 mgs in the morning) and on Klonopin (0.5 mg at night) for treating anxiety and depression. I've been on it for 4 years, and during the last 3 I got extreme fatigue and brain fog. It is now debilitating me - I could not go work. I will talk to my pdoc, however, I'm thinking to tapper of from Lamictal or Klonopin. I've read a lot of bad stuffs on the tappering of both and I'm now concerned; however, I can't keep the way I'm now. Is there someone at the same mix? Given the dosage and period I've been on it, what do you think I should tapper off? thanks
  13. Hey guys, I am tapering off lamotrigine at the moment. Down from 75 to 25 mg (though taking 37,5 every second day). Been at this dosage for a week and a half. I am experiencing fatique, anxiety, akastheisia/internal restless (severe), depression (minor), nausea, headache and dizziness. I am also very stressed, which could create some of these symptoms as well. does it sound like stress or withdrawal? Which withdrawal symptoms did you experience? Any similar stories?
  14. Hey guys, I am tapering off lamotrigine at the moment. Down from 75 to 25 mg (though taking 37,5 every second day). Been at this dosage for a week and a half. I am experiencing fatique, anxiety, akastheisia/internal restless (severe), depression (minor), nausea, headache and dizziness. I am also very stressed, which could create some of these symptoms as well. does it sound like stress or withdrawal? What withdrawal symptoms did you experience? Any similar experiences?
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