Welbutrin symptoms and conditions

I posted a couple of days ago about the hair loss I've experienced with Welbutrin and I have since went out and bought the GMC Ultra Nourish Hair since it's been recommended from those on this site. I also stopped the Wellbutrin last week (by slowly winging myself off) and I've actually lost MORE hair. It's all over the place when I shower and style and I have bald spots on my scalp (it's thinning evenly)...which is sad for a 29 year old woman (or for any of us experiencing this). I was hoping to hear back from anyone who has had this experience and stopped Wellbutrin. How long did it take for the hair loss to stop and for the hair to grow back? Will it grow back? It's so upsetting to shower and style my hair anymore because I lose so much.

Also, I wondered if anyone used any shampoo that helped? I did go to a Dermatologist and she said that I had Dermatitis and prescribed a shampoo which isn't working at all. I honestly think it's the Wellbutrin.

Any help or advice would be very much appreciated! Thanks so much.

I posted a couple of days ago about the hair loss I've experienced with Welbutrin and I have since went out and bought the GMC Ultra Nourish Hair since it's been recommended from those on this site. I also stopped the Wellbutrin last week (by slowly winging myself off) and I've actually lost MORE hair. It's all over the place when I shower and style and I have bald spots on my scalp (it's thinning evenly)...which is sad for a 29 year old woman (or for any of us experiencing this). I was hoping to hear back from anyone who has had this experience and stopped Wellbutrin. How long did it take for the hair loss to stop and for the hair to grow back? Will it grow back? It's so upsetting to shower and style my hair anymore because I lose so much.

Also, I wondered if anyone used any shampoo that helped? I did go to a Dermatologist and she said that I had Dermatitis and prescribed a shampoo which isn't working at all. I honestly think it's the Wellbutrin.

Any help or advice would be very much appreciated! Thanks so much.

*****For those of you posting in the future - and even those who have posted and are now reading this - could you please be specific on whether you are taking Wellbutrin or bupropion and what mg. Would be interesting to see if there's a noticeable pattern!*****

So glad I found this site. I too have had marked hair loss on this drug, with the exact symptoms most of you describe. I was on 300mg of Wellbutrin (the brand name) and had no problems. I switched to the generic (bupropion) and my hair starting thinning and falling out until you could easily see my scalp. For other reasons (I didn't put it together until recently), I went down to 150mg of the bupropion and my hair started growing back in. I went back up to 300mg and it fell out again - so I am now 100% convinced it is this drug. I too ruled out - with tests - all other causes: hormones, vitamin deficiencies, side effects of other meds, etc.

Here's my focus now: it seems to me, and many other people have noted this, that it is the generic (bupropion). When I was on the Wellbutrin, I had no hair loss. However, I noted several people said they had hair loss on "Wellbutrin" - so even though this wasn't the case in my experience, I'm so freaked out right now about the amount of hair loss that I decided to go off completely. A shame because I was doing really well.

I'm wondering ... when people are saying "Welbutrin" - is it really Wellbutrin? Most pharmacies will automatically switch it out. Maybe some of us think we are taking Wellbutrin, or are just calling it Wellbutrin, but really are taking bupropion. Generics and brand names differ in "ingredients." I noticed a definite difference in the "feel" of the Wellbutrin vs. bupropion - but it was a $50 vs $7 co-pay! It would be great to sort this out because those of us doing well on bupropion but have hair loss could switch to Wellbutrin - albeit a more expensive route.

Maybe its both? Either way I'd like to know. The doctors are no help. I love my doctor and brought this up to him several times. He did not think it was the meds. If he had simply gone on the Internet and typed in "Does Wellbutrin cause hair loss?" - like I did, it's impossible to totally dismiss it!

Thanks so much for sharing and letting me share. Oh - and please note, at least for me, even when I went down to the 150mg on the generic, my hair totally started growing back in. So, at least in my experience, hair regrowth starts immediately after reducing/eliminating the drug. And my hair loss was (and now is again) really bad.

I am so relieved to see these posts. My husband started Wellbutrin 2 weeks ago. We are at the beach and yesterday he started experiencing itchiness followed by rash and welts that have spread and are huge now. He has them on his legs, under arms, around waist and on feet. This morning his right eye became extremely swollen and now his lips are HUGE.. At first we though an allergic reaction to seaweed until it started getting worse. I googled benadryl and wellbutrin to see if they could be taken together and found this sight. He has also been complaining the last week with chest pains and I see some people also experienced that. Thank you all for sharing for now I can see what is causing it and we are stopping Wellbutrin now.

I've been on Wellbutrin for about two months. I notice that I am quick to anger, and seem to suffer memory loss. I was beginning to think I was in early stages of Alzheimer (I am 45) as it runs in my family. I couldn't remember names and it terrified me. The doctor subscribed it due to the weight gain I experienced on Prozac, and I have lost weight on Wellbutrin. I have been diagnosed with mild to moderate depression, due to excessive crying that I could not control (especially at work). The Wellbutrin has helped keep my crying under control when crying would be inappropriate. But still feel it is excessive when I am in a more relaxed atmosphere. Prozac was certainly my "happy pill".

I had forgot to pick up my wellbutrin at the pharmacy and I went about a week without it. I started having nightmares every time I went to sleep. I didn't put two and two together till my sister asked me what medicines I was on then I remembered that I had forgotten to get my medicine. I like this medicine and it has worked well for me. I started taking it when I lost my Dad two years ago. It was a very difficult time for me and my family, and I honestly think that wellbutrin kept me going. I just need to remember to take it. lol

I was prescribed Paxil and started out at 10mg. then they gradually increased it up to 60 mg a day. Later on they added I think it was 200 mg of Wellbutrin. I was on Paxil for I think 2.5 to 3 yrs. What happened was I was so out of it I didn't know what day it was. The HMO would have to call me to remind me to come in that day for my doctor visits. I slept most of the time and was just worthless. I didn't care about anything much and didn't have the energy to do much of any thing. This was a drastic change in me and my family hung in there with all this. I actually drove which is not a good idea at all. But when they put you on this you don't realize how bad you are on this stuff and once you are on it for so long then you are either a captive at home not able to do anything or you try to take back some part of your life. You also can't just go off of it cold turkey at 60 mg. I tried and it got bad and went back on it. After I got really bad all I did really is drive to therapist appts or to nurse practitioner who managed the Paxil and Wellbutrin. After being on 60 mg of Paxil and Welbutrin for awhile/months and I was so out of it, that is when they said we need to back me off of it. I think it accumulates in your body and I think you can kind of have an overdose in a sense. They didn't really monitor it that well and took their sweet time recognizing it. But they didn't say anything about it. I think that is what happened to me but no one at the HMO said that. Instead they got me scared that I was going to run out of therapy sessions allowed while on Paxil and that is why they were going to back me off of Paxil. I guess another patient had that happen to her and they didn't want that to happen to me. I then say my therapist very rarely while I was backing off of the Paxil. She acted like I was ready to handle everything on my own. I had no idea that suicidal thoughts were in my future when backing off of this drug. But they sure knew it, a lawsuit in California had been filed the month after I started taking the drug and it was all about the lack of disclosure about the withdrawal issues. First I got off of Wellbutrin and then they slowly backed me off of Paxil. It was physically wrenching. Throwing up and diarrhea all at the same time. Painful is not the word. I have given birth to two kids and pneumonia and this was much worse! Chills, tremors, I felt sick all the time. This went on for months. When I talked to nurse practitioner they pretended that it was no big deal. I wasn't sure what was happening. I finally got pissed off about the whole thing and never called them back and they didn't follow up either. Not even therapist. They hoped I would go away quietly which I did. When you are in the throws of this and you know who did this to you, you really don't want any more of their harmful help. It took at least a year to feel better. There is this uneasy weird feeling and zinging noise that lingers for a long time. But my memory is a fraction of what it was. My short term memory is very difficult. I know that Paxil was responsible for this. How do I know? Well when you are on Paxil and if you have a recall on a bad incident and you start to emotionally react to it, Paxil will offset it by making you sleepy. It literally targets your emotional reactions and those thoughts connected to it. It tries to disconnect the feelings from the thoughts. These disconnects also disconnect your ability to remember other things. Even after I got off of Paxil I noticed that I would get sleepy when I thought of stressful things. It has taken me about three years and I am talking better and can remember many more words. I talked very simply for so long since I couldn't recall basic conversation. It targets emotional responses and I got to a point where I was really numb about a lot of stuff due to the constant tapping down by Paxil. I feel like it disconnected those connectors to your brain that talk to each other. My family made jokes about me and how simple I got and how I couldn't remember anything. They are worried that I have alzheimers disease or will get at this rate. I could not work on Paxil at those high doses I was on and while I was withdrawing. I found that afterwards my memory was so bad that I missed so many simple things that I would have never missed before. I am concerned that my memory lapse will cause a big mistake that may hurt someone. I was out of work for so long. I volunteered to keep myself busy until I got too bad. It would keep me busy. I also noticed that while on Paxil I was uninhibited and said things that hurt folks and I was unable to monitor myself like normal and couldn't determine what was not appropriate to say all the time. I had an emotional disconnect to myself but also to others. This hurt some folks and cost me a job. My memory is so bad that I have to write down important things if I really want to refer to it again. I also have given up on going back to school. I couldn't test well at all. I can not remember what I did 5 minutes ago let alone a chapter I have read. I am only 52 now and I feel so much older due to this. I suffer from Fibromyalgia and IBS. I was so upset with my doctors at HMO since they didn't warn me of the withdrawals. When they put me on Paxil I was adamant about not taking an addictive drug. My family has had a history of addiction and I was not going there. I know how bad it can get. Paxil's withdrawals is very much like the withdrawals that addicts go through. I was devastated by not only how doped up I was on Paxil but also all time I wasted on it and with the year just trying to withdraw from it. Then the time just trying to get some of my memory back to function. I am mad that there is no way I could go back to school to better myself. I am mad that no one warned me of any of this and if they would have I wouldn't have taken it. How many of you would take a drug knowing that you memory would be messed up? Not many. Certainly not me. My daughters know what a tyrant I am about drugs and alcohol. This is not something I would have opted for if the whole truth were known. They certainly don't warn you that your memory will be like swiss cheese afterwards. No one in my family has had such memory loss. No alzheimers disease. In fact quite the opposite is the case. My grandmothers were very clear at older age, so menopause can not be a big factor and beside this happened before menopause. Also grandfathers and father were very clear getting older. My family noticed a definite change while I was on and after Paxil. The irony was that when I started to go back to HMO for regular care which took me a long time to trust them enough for them to do even that, someone at HMO had put in my automated chart that I was allergic to Paxil. They won't say who put it in either. I was not allergic to it but they are now saying that I had a bad reaction. But what I say is after seeing so many "bad reactions" on websites like this I am convinced that this is more than isolated cases but rather the norm of what happens to patients who take it. HMO doesn't want to admit wrong doing. Paxil seems to have kept a lid on it. Besides how do you measure a bad memory and how do you prove it after the fact? You are getting older and who is to say it isn't genetic. But I was on it for maybe 2.5-3 years. I was so out of it I don't remember how long I was on it. I also was suicidal when coming off of it. I even called a crisis line since I couldn't trust the HMO. I was irrational. For those of you still on it I think you are doing more harm than good. I don't believe all the facts have come out about the side affects from these types drugs. Who would be doing the studies? Certainly not he drug companies, FDA is a joke and if you think the attorney generals are doing much think again. Yeah a couple states like CA an NY they did settle on suits about suicide for kids but they settled quietly. The doctors who prescribe these drugs also are in a catch 22 like my HMO. They don't want to be linked in this and will avoid it too. What attorneys can afford to go up against all those high powered attorneys for those loaded drug companies? Not many. No one is actually dying from this and that is another reason there won't be much done on this either. Fortunately today we can hook up online and share our stories and this is the first step in documenting what is really happening to patients.

Be so careful coming off of these drugs. Give yourself plenty of time to get normal. Make sure you are seeing a therapist you can trust and is trustworthy. It takes an alcoholic about a year to rid their bodies of the toxins that have built up in their tissues. I do believe that is also true of Paxil. Be kind to yourself and get good support while doing so. It can be a very lonely physcially and mentally anguishing time. Think of yourself like someone who has had a brain injury or stroke. You need to practice to get things to reconnected as best as possible considering. You will never be like before you took Paxil but with time and patience and hard work it can get better or you can develop ways to compensate or work around or cope with such memory loss. Financially this can be devastating and it was for us. The loss of income and finally a bankruptcy. We paid dearly for taking this drug. It can be very frustrating and you have to look long term. I think it is very easy and cheap for HMO's to pass out pills rather than schedule needed appointments for therapist and other alternatives. Before they started to take me off of Paxil I was warned by my HMO that I had exceeded my number of appts allotted for a 2 or 3 yr period. So I may end up without any therapy while on Paxil. That is the reason why they decided to back me off. I had apparently used something like 32 appts in two or three years and I was getting close to not being able to have any for a long while. This was interesting approach since by then they knew that suicide was linked with Paxil. They will put you on Paxil and they will leave you high and dry without at therapist if you actually use one regularly and use up a normal amount of visits. I have very little compassion for HMOs. What was amazing was listening to the nurse practitioner tell me if these drugs don't work there are lots of other ones we can use. These are the easy going drug pushers of today and they prescribe these drugs without much thought. They make it cheap and easy and they will swear to your face they aren't addictive but are basing it on very little research. They regurgitate what ever the drug companies tell them. The cost cutting with HMO's is almost frightening. I also have problems sleeping too. I wonder if the drug messes up your serotonin levels since it does make you sleepy so much of the time and when you are off of it the brain is fried from all that artificial serotonin that it no longer knows how to manufacturer it well. I think that is what maybe causing my Fibromyalgia since this is a condition where you muscles never repair themselves at night due to lack of sleep is one theory. I was always a deep sleeper before all of this. I think there maybe a connection.
Finally depression. When you can't remember what you did 5 minutes ago or simple things it gets more than frustrating, you get depressed at how limited you are now. The pain from the fibromyalgia is constant and that too is depressing. I wish someone could put together the data on this to prove the link to memory loss and how it has affected our serotonin levels.
The only way you can stop companies is to sue them. Government won't do it really. A class action suit might work.

NOW I SEE I AM NOT CRAZY. I JUST GOT OUT OF BED AT 3:30 A.M. - another sleepless night. I thought, I wonder if it is the singular - let's get up and do research. So here I am writing this is the middle of the night. I am a 56 year old female. Have been taking allegra for years, no complaints. History of smoking caused asthma-like symptoms which disappeared about a year ago due to improved lung function. I no longer need the albuterol, inhalers, etc. Two months ago I went to the dr. primarily to talk about depression and anxiety. History of depression and I've been taking welbutrin for the past six months. I decided not to change presc for depression. He suggested that I take singulair and switch to zyrtec.
WELL I CAN SEE THAT THIS IS JUST GREAT! I'm ill with everyone, depressed, have loads of anxiety, have three uncompleted projects in my house and was considering a fourth when I realize - now this is a problem! Wake up! So I find these postings and I am angry that all of this suffering has occurred, esp to children who can't explain that they feel different, etc.
So now I am going cold turkey, going to stop singular and zyrtec immediately. I am retired so I can take benadryl most times if I need to and I look forward to getting some good sleep tomorrow. (Will it leave my system that fast.) God bless you all and your children.
OH I FORGOT TO MENTION THAT MY MIGRAINES - WHICH WERE LONG GONE - HAVE COME BACK WITH A VENGEANCE. The nausea has been slight. OH - I'VE HAD TERRIBLE THOUGHTS WHEN I PICK UP A KNIFE IN THE KITCHEN WHILE PREPARING A MEAL. I INTENTIONALLY SHAKE IT AND WONDER WHY IN THE WORLD I WOULD HAVE SUCH A THOUGHT. I am so upset with dr. and pharm. companies. We need to take ownership of our own conditionsl.

After about three weeks of taking the generic form of Welbutrin, I too broke out in a horrible case of hives. They started on my trunk and migrated all over my body. After two miserable days, I went to a redi med clinic late one night because I couldn't take the itching. The doctor said it wasn't the Wellbutrin, said it might be some type of allergic reaction to something else. They gave me steroid shot and sent me home with a steroid pack of pills to take over the course of a week. Three days later, no sign of the hives going away or becoming less irritated. Found some relief using the Target version of Gold Bond powder and benadryl every four hours. That's when I found this site. I immediately stopped taking the Wellbutrin and guess what? Twelve hours after I skipped my Wellbutrin dose, the hives were 80% gone. Today, 36 hours since the last Wellbutrin pill, the hives are almost all the way gone. This should certainly be listed as a possible side effect! I have never been so miserable in my life with itching!! If you have hives and are on Wellbutrin tell your doctor!

My teenage daughter was taking generic Wellbutrin (manufactured by Watson pharmaceuticals) 150 mg. daily for about 3 weeks or so and started having serious hair loss on the top of her head. The prescribing psychiatrist told her to stop the medication and after about 2 weeks, the hair loss has stopped almost completely. I have read a number of blogs including this one that indicate that hair loss is a side effect yet the Wellbutrin trials only listed hair loss as a side effect for less than 1% of patients. Given the U.S. Supreme court ruling today that says that even if the FDA has approved a medication, a pharmaceutical company is still responsible for fully reporting side effects and can in fact be sued in individual states if they do not provide sufficient warning, I would be interested in hearing ideas of how we can put more pressure on the manufacturers of Wellbutrin and its generic equivalent so that they give better warning of this side effect.

I had my second Lupron shot this last mid October that lasts, supposedly, 3 months. So I will be 5 months in this mid December and I have to say I was one of the people who was fine with Lupron...up until now. I had and have all of the typical side effects of hot flashes, headaches, memory loss, mental fog, etc. Then I had my first ever migraine a week ago that knocked me on my butt for 2 days. My memory loss and depression are by far, by far, the worst side effect I have experienced. At this point I am concerned my memory problems and mind fog will not go back to normal, which has already adversely affected by daily life. I was one of the people who spoke positive of this injection even after reading all the horror stories but now I am beginning to wonder if they were right on some levels. When reading all the different experiences I would get confused and wouldn't know what to believe. I am not saying I would change things, the jury is still out as to whether the benefits will outweigh the difficulties, but my personal experience and symptoms have been getting worse just in the last few weeks, so that would be between month 4 and 5 on it. I could lead a pretty normal life up until recently and I'm a pretty tough person, I clean houses for a living and work hard with a packed schedule so I am not just stating little symptoms I experience but ones that actually have affected my daily life. Just being honest so you know what to possibly expect, depending on your body's reaction. That is a point to keep in mind, everyone's body reacts differently but if the majority of people are saying the SAME side effects, makes you wonder if there is a consistent pattern.

One thing I will tell you that has helped me is B vitamins regularly in your system and staying as active as possible. Write things down to remind you for the memory issues, don't over-commit to things because of the mental affects-it hits you hard when you can't follow through, and try to watch your sugar intake, which messes with your emotions. Hope this is helpful.
I would love to know from someone who has the same symptoms (which looks like almost everyone who is on it) and who is now off of Lupron for at least a few months, if the symptoms of memory loss and mind fog go away. Is my memory permanently damaged?

I was taking Wellbutrin for about 2weeks (i had taken for about 7yrs previously) from Effexor because of sexual side effects. The Welbutrin worked to get rid of that problem and my Dr in the hospital warned me about generic Budeprion, but my regular PA-C said that the 150's were different and made by Glaxo. Huh???? Like an idiot i got the generics and 5 days later I feel like i have no anti-depressant in me. Im having panic like "emotional attacks" where i just cry if I hear or see something that triggers an emotion, sleeplessness (i don't need any more of that), weight loss (what's food and why is my stomach gurgling) and over all lethargy. I hate this drug, its useless beyond belief, I really wonder who got paid at the FDA to pass this one through.

I took Wellbutrin 300 mg for two years before to quit smoking and for mild depression. After the initial (weeks 2-4) side effects of nausea, dizziness and headaches - I felt great. Not drugged and not overly emotional. I had been crying all the time and felt hopeless. I felt much better (and didn't want to smoke at all). I quit it for about 2 years and now I am back on Wellbutrin for the last 7 months. I started with Cymbalta - but hated the loss of sex drive (not able to orgasm - so who wants to have sex, right?) and felt drugged. So Wellbutrin was a welcome "old friend" I didn't have bad side effects with switching and have been pretty happy. EXCEPT for the one very scary side effect that I have experienced just a handful of times - but I really am curious if anyone else has had this HEAD TRIP WHILE DRIVING: It has happened when I'm on the interstate and/or bridge when I am driving at fast speeds, and my head feels whoozie all of the sudden and my brain seems to shift sideways - like on a roller-coaster, up and down, sideways - and I am amazed that my hands don't go with it and drive me into the wall! It takes intense concentration and wheel gripping to get myself where I can pull off the road. What the?? I don't want to ever experience this again - but it is so OCCASIONAL. The only variable I can think of is that I have not been faithfully taking the WB at the same time everyday (I'm more and more forgetful) and have skipped a day. Has ANYONE ELSE had a similar experience???

During the three weeks I was using 150 mg. Wellbutrin, ringing in the ears gradually increased, mild headaches on top of my head, occasional light spasms around my mouth, constipation, and bladder problems. My sleep was unaffected, and my depression did not lift. My dose was increased to 300 mg, and by the fourth day, I was having serious facial spasms, intense headaches, louder and constant ringing in the ears, almost 'round-the-clock wakefulness, anxiety, difficulty thinking and completing sentences, pounding heart, amplification of sounds, jitters and quaking. I felt like a car, perpetually idling so roughly that all my parts were about to rattle right off the chassis. On the fifth day I took nothing. I've had some chills, a little nausea, headache, neck-ache (Isn't that weird?!) and some ringing, but at a lower volume that's hardly noticeable. This is the fourth day with no Wellbutrin, and I haven't had facial spasms at all in the past couple of days, have less nausea, and the very funky smell produced in my urine from the second week I was on the meds has calmed down. If I'm still in a depression it's been overshadowed by the most awful side effects I could have imagined. It felt like the spector of death was overtaking my body by day four of that 300 mg. dose. I had been on a hefty dose of Zoloft daily for almost ten years and never experienced anything unpleasant other than weight gain, my reason for trying to switch meds because I couldn't quit putting on weight no matter what. I am going to try SAM-e, and suggest that anyone looking for a natural alternative, with the prospect of few and insignificant side effects, do an online search. Whether I find success with the SAM-e, or if it falls short of what I need, I'll post here to let you know what happens. A month ago I thought the depression was the end of the world; I think the cure was worse than the disease.

would anyone who has experienced sleep apnea since being on wellbutrin, please let me know?

pitbull lover2

I've been taking Zoloft for nearly a month. My sex drive has not decreased but it takes me a very long time to have an orgasm. It is frustrating because my partner and I have always had a very active sex life. Now, I'm hesitant to have sex because it takes too long to have an orgasm. Any suggestions?? Sexually Frustrated

I've been on Welbutrin for about six months, along with Zoloft. I had tried it because of the lack of motivation and the lithergy I was feeling (I suspect) as a result of the Zoloft. I came across this site after a search for memory loss connected with Welbutrin. I believe I'm having that problem. I don't seem to have the quick grasp of words I did. In a phone conversation today, I could not remember a certain medical term that I have been using rather frequently over the past six months. There are some other cases, but that incident put me on the trail of memory loss research. I actually suspected that it was the Ambien I had been taking for sleep (I have not completely ruled that drug out). But all the posts here seem to indicate that the welbutrin could be at fault.

I'm on 150mg, twice daily. However, in the morning, I will actually take one and a half pills (225mg) to get me going. I have noticed CONSIDERABLE jitters, hand tremors, enough that if I'm doing delicate work of some type, I have difficulty continuing ti complete the task. At the 225mg, I do seem to become over amped a bit, but it improves my motivation. A St. Johns Wart capsule will usually calm that, but you see the problem of one drug, helping one problem, but causing another, so you take a third! I have tried numerous other antidepressants and they all caused more side effects than they were worth.
Celexa cause an eventual complete lack of ANY motivation! Plus SERIOUS sexual side effects. Zoloft has been the best with the least side effects and I have always returned to it. But the sleepiness can just be extreme with me.

I have run out of Welbutrin and the result is return of the lithergy. I also believe that the Welbutrin may be causing my occasional up tick in anger. Possibly spreading the dosage will help. Not mixing it with caffiene may also help because caffiene can make me explosive if I don't limit my intake to about a cup of coffee. Most of you know that Zoloft, Prozac and the like increase the available seritonin in your brain, a calming neurotransmitter. Welbutrin increases the available norepinephrine, a stimulating neurotransmitter, akin to adrenalin. (Research for yourselves those facts, remember, I posting this because of a problem with MEMORY! :) So it makes perfect sense that people can become overstimulated with Welbutrin. The memory aspects of it, I don't yet understand. I'm going to experiment with dosage reduction and possibly replacing the Welbutrin with the amino acid L-phenylalanine. I hope this little post can help some of you as much as the other posts here have helped me!

Burt

I just HAVE to add my story here!! I was on Lexapro 20mg for 2yrs. All was pretty well. It somewhat controlled my anxiety & panic attacks (I have GAD) and it helped stabilize my moods (I am Bipolar), BUT I DIDN'T like that it made it to where I couldn't cry when I wanted to but yet cried at inappropriate times! I basically came to a stand-still with the lexapro and it KILLED my sex drive, so bad that my relationship was at risk (well, thats what I think, cuz no man is happy with NO sex!!) So, I SLOWLY came off them over a month, and even though it was very slowly, the WITHDRAWAL from this drug is just a horrible experience that I hope none of you that are taking now, will ever have to go through what I did!! I seriously thought at one point I was going to die!! I was severely sick for one week-- nausea, vomiting, the runs, hot flashes, cold flashes, the shakes, internal tremors, severe migraines, dizziness when I sat up or stood up, and I got bad electrical zap feelings in my hands & brain (which, even one month & 3 weeks later, I am still having!!) But to you all still on them, I also had weight gain on them, head rushes, dizziness, headaches, internal tremors, and I didn't like that it made me generally dumb!!! Since coming off, I still have the "duhhh" moments, getting less & less, thank goodness, now if only these darn "Zaps" would go away. But yeah, the side effects of this & the withdrawals are HORRIBLE!!! I will never take this again!! So much for newer drugs eh!!

I've been on a lower dose of Wellbutrin XL in combination with Zoloft. Stopped taking Zoloft and upped my dose of WB to 300mg and then to 450mg. I felt good w/no side effects on the 300mg. I'm not sure if it was the WB, but after a couple weeks at 450mg, my head started to feel really weird. Not dizzy, not a headache, just feeling like I need to shake my head to clear it. I dropped back to 300mg and it's been a few days, but I've still got the weird feeling. Can't really focus. Anyone else have this feeling?? I don't know how to describe it other than maybe a head full of cotton balls.

I was on SSRI's for a while (lexapro, zoloft) when I finally couldn't take the tiredness, weight consistency, and NO sex drive. So I tried Wellbutrin SR 150 2x a day. Started off at 150 for a few days and felt like I was given a new life! I had never felt so good. Then it was time to increase my does to the 300mg. I started getting headaches, dizziness, my ears are ringing so bad I can't hear very well anymore. So I went back down to 150mg per day. I don't feel as tired, but it's still there. The ringing won't go away and I am still dizzy. The funny thing is, is that I can almost guarantee it's the same time everyday. I get the dizziness and headaches around 3pm, they go away(most of the time I have to lay down) and by about 5pm they're gone, but by about 10pm they're back. And it happens every day like clockwork. I like the way I feel (minus the headaches and dizziness, and ringing) my brain doesn't feel "numb" like I did on the Zoloft or Lexapro, and I have lost a few pounds which doesn't hurt, but I don't think I should feel like this everyday. I want a medication that I can feel good on without headaches and dizziness. And PLEASE no ringing in the ears. It's good to know that other people are experiencing these side effects, I really thought I was the only one.

I am 30 years old and have been put on Depo Lupron after a laproscopy to help with endometriosis. I am 2 months into a 6 month course (one shot every 3 months) of Depo Lupron and my life has drastically changed. I started feeling life altering hot flashes and night sweats two days after the first shot and nearly drown myself in sweat 24 hours a day. I experienced a little postpardum depression after giving birth 6 years ago but have found myself sunk into a sinking hole of depression and anger like I've never felt before. I bawl at McDonald's commercials and become enraged if the dishwasher isn't loaded properly! I am ecstatic one minute and severely depressed the next. I have even had thought of suicide since being on this shot. I am normally a very outgoing, athletic, cheerful, happy person - but since taking this shot, I have become a stanger in my own head. I tell my family all the time that I need to "go stick my head in the freezer" to cool off because of the horrific hot flashes. I have to carry a handheld fan with me 24 hours a day and sleep with ice packs to keep cool. Since the shot started 2 months ago, I have lost all sexual drive, am thoroughly exhausted by 9am and find myself crying at my desk at work by late afternoon because I am so tired. My family thinks I am going crazy and I've never fought more with my husband. My daughter has gone to grandma's for awhile because I'm just so tired and irritable that I feel like an awful mother. Migraines have also come full circle since the onset of the shot as well as blurred vision and shaky hands. I'm a little achy throughout the as well. I know that everyone responds to medication differently, but I'm finding a lot of people with the same side effects as myself and have to wonder why the doctors don't warn patients about these types of problems before prescribing medications such as Depo Lupron. I don't think I'll be going back for the second shot. Could it get any worse?

I started taking 300 mg wellbutrin sr while weaning off of effexor xr (another nightmare) about three months ago. The past few weeks I have been extremely agitated with everyone in my life. I have also had the worst migraine of my life that will not go away. I'm not sure if this is a side effect of the welbutrin, or just more painful effexor withdrawal? My husband swears that my anger has made me a different person. I hate the way I feel, but don't know if the Wellbutrin is making it better or worse. Anyone have any input?

My insurance changed and i was substited budeprion for the other generic for Wellbutrin which was buproprion. The first thing I noticed is that I was extremely irratable and downright mean to people. I never used to be like that while on Wellbutrin. I cried easily and this new pill just did not help me like the old original. But the most annoying side effect I have noticed is that it has given me an awful odor. It took me awhile to put two and two together but I noticed the budeprion has an awful smell in the bottle as soon as I took the lid off. Then I noticed my urine had a horrible strong smell which I associated with the same smell as the pill. Now I also am afraid it is being excreted thru perspiration as well. I am certainly not going to continue to take this budeprion if it is making me smell bad! Has anyone else noticed this side effect?

I took 300 mg. wellbutrin about 1 1/2 years ago and did not react well to it.
I just quit taking cymbalta after about 3 months because of sexual side effects, but here is the kicker. I started on a lower dose of wellbutrin about a week ago (175 mg xl) after only 3 days I was so screwed up it was a no brainer that I could not take it. It has been 4 days since I quit and I am still getting waves of disorientation and mild panic. How long will this last. Damn I only took it for 3 days and the side effect have lasted 7

There is an important point that everyone here is missing. I had been on Toprol XL for years, brand name. Recently, a generic version by Sandoz has been issued. It is the GENERIC metoprolol that is causing the side effects, the racing heart, etc. If you can get the doctor to write "no substitutions" on the prescription, and get the original Toprol, you will notice the difference. the problem is, health insurance wants to push the generic, so you will pay more. but it's worth it to feel better!