Nervous energy symptoms and conditions

Wellbutrin SR 200 mg. two times a day. Intensity. Nervous energy. Inability to focus sometimes. Memory loss. Speech can be disjointed and it's difficult to form complete sentences. I will often struggle to find the right word to complete a thought or trip up and not be able to finish a complete sentence smoothly. If I wait to take my second dose in the middle of the day my speech improves so I'm going to experiment with the time I take the drug whenever I have an important meeting.
From reading these posts I have now realized the hair loss that I have been experiencing is the result of Wellbutrin. I had no idea and have been experiencing this every since I've been on Wellbutrin. The texture of my hair is much courser and I shed hair at a much faster rate.

I have been taking lexapro, lamictal, and wellbutrin for about 2 1/2 years for a lifetime of depression and anxiety/panic disorder. I had tried medication at age 15 and experienced all side effects and no benefits. But then at about age 21, I was so desperate that I gave it another shot...figuring there might be a difference in the past 6 years.

I started off with lexapro...and the first week I was soaring! I was jogging at 1AM and going out and enjoying life! I remember going to the movies with friends and laughing FOR REAL and having REAL fun!

At some point of course you level out and that was fine...but then it wasn't enough anymore so the lamictal and wellbutrin got added on.

Recently, my psych raised my (generic) wellbutrin to 300 XL from 200 SR.

I definitely noticed the difference between the XL and SR.

The real function of wellbutrin for me was getting me up out of bed in the morning. It gives me nervous energy, but that has been better than none at all.

But now I've recently realized some other fun side effects!

Memory loss and motor function impairment.

It's kind of funny because I think it has been going on for a good while, but I just didn't REMEMBER enough of it to piece it together. AHA good one right?

I am a hairdresser. A damn good one I'd say. Or...used to be?
I trained for and alongside of the best educators in the industry. I wrote the haircutting curriculum for one of the top education academies.

Now I feel like a f***ing idiot.

I've cut my fingers more in the past week than in the past 6 years. I find myself getting completely lost while doing someone's hair...like I've never been in that situation before.

Sometimes I have tremors that keep me for being able to hold my comb straight and still. My fingers seem to move more slowly and with less grace or control.
I type sooo much slower now.

I've also gone from having excellent spelling, grammar, and range of vocabulary...to forgetting common words...not being able to finish my sentences...and I find myself trying to sound out a word to figure out how to spell it. This doesn't work out too well.

I feel just plain dumb in general. I can't do relatively simple math in my head without getting confused. I can't process or answer a question under pressure.

Now I'm telling my DR. to stuff it, and try to wean myself off of this madness.

I really hope that these side effects aren't permanent. Then I'm just screwed.

I stopped a few times during this post at a loss for words.

Yeah so it stinks that I have lost my substitute for motivation.

Thanks for sharing everyone...you've made me feel like less of a failure.

OH YEAH!

The original story I was going to post was that today I went to the deli to get lunch and I got everything I was going to get for my coworkers...and forgot to get my sandwich. The check out lady is mean to me so I didn't go back. :\

My time on Biaxin was one of the most TERRIFYING experiences of my life! (And I’m a cancer survivor, haha).
It all started when a doctor put me on Biaxin (500mg) for having Pneumonia. I was to take one pill at night and one pill in the morning for a week. The 1st day on the Biaxin was fine. Then the second night, I started to experience changes in my behavior. I began to cry and become extremely emotional to minor things.
The 3rd day I woke up and took my pill and started to feel extreme pressure pushing on my brain. I also got very agitated, grumpy, hyper, and over stimulated. That night I took my Biaxin pill and got 0 hrs of sleep. I was up all night paranoid, scared, hallucinating, crying, shaking, nervous energy, pacing back and forth, thinking in my head “what is happening to me!” The next morning, I took my Biaxin pill and then experienced the same horrific side effects. I was calling my family and telling them that something is going wrong in my head and I need help. It was as if I was having a panic attack. My stomach cramped up, my head hurt, and my heart was beating 10x its normal pace. I also felt hopelessness, couldn’t concentrate, shortness of breath, and worst of all the feeling of paranoia and the thought that my mind is being possessed.
Finally, I got on the internet and looked up “side effects of Biaxin”. Thank god I found this website and was able to see I wasn’t alone. I called my family and told them it’s the Biaxin making me crazy. That day I went and saw my doctor and he said, “Yes, Biaxin can cause emotional distress and all of those other horrible things you are going through." He says it is rare to get that many crazy side effects, but it is possible. He said to stop taking it, and go home and rest. I needed to allow my body to recover from what has happened the last 4 days.
I will never take Biaxin again for as long as I live. I literally thought I was going insane. The feelings and thoughts I was having was absolute torture and an emotional rollercoaster. I thank this website and all of you for your posts. This website truly helped me discover that Biaxin is a dangerous drug that is not intended for everybody. Especially not me!!!!!

I have been taking a generic version of Wellbutrin SR 150mg for almost 2 months now. I also take Zoloft 50mg. Before I started the wellbutrin, I had been taking zoloft for over a year to help with depression. The zoloft was working very well for my depression, but it completely killed my libido and as a newlywed, I felt something had to be done as it was beginning to affect my relationship with my husband.
So my doctor prescribed the wellbutrin. For the first couple of weeks I experienced a lot of nervous energy, a shortness of breath, a bit of nausea, forgetfulness and confusion. I almost stopped taking it because I didn't feel it was helping my libido either. But I stuck with it and after 3 weeks, it felt like it was definitely having a positive effect on my sex life. My husband noticed it too. He mentioned how much more responsive I had become when we were intimate. After 2 months, I am absolutely convinced that it has changed our lives and our relationship.
It is not, by any means a miracle drug though. I have a few complaints about it, the main one being the CONFUSION that I experience for hours after I take it. I was taking it in the morning before I went to work and everyday I noticed that I was not as sharp and efficient as I usually am. I figured this was a temporary side effect so I kept taking it as usual, but it never went away! I kept forgetting everything, lost focus easily, had dull headaches, and generally felt as if I could not connect to what I was doing.
SO...about a week ago, I thought I would try to take it at night...when it's not as important to be sharp and focused (and more important to be turned on). And it has turned out great! I'm so glad I started to do it. It doesn't affect my sleep...in fact I think I sleep better. And when I wake up in the morning, my dull headache is gone and I feel less foggy. At work, I feel normal again. My short term memory has recovered and I don't get confused as easily.
If you suffer from a lot of memory loss and confusion from this medication, I definitely suggest taking it at night. It has really helped me! Thanks and good luck!

Hello,

I have 3 friends who have liked the Mirena, so on their testimony and after talking to my OB/GYN, I decided to give it a try. I have a history of a J Pouch surgery when I was 19, and I'll be 37 in June. My husband and I luckily have one little girl, but it's doubtful we'll have more due to multiple reasons, and I was doing this so that we could finally have spontaneity. We've been together for nearly 18 years.

I had it in for only 5 days. I suffered things I've NEVER suffered: raging hormone headache, bloating like I couldn't believe, anxiety, a panic attack, not just crying jags - SOBBING jags that would come on in a panic, a "doom" feeling and this horrible feeling of loneliness. I was jittery... I don't drink caffeine, but this felt like I'd just had 15 espressos... I had all this nervous energy, but no focus.

After just 5 days, I went in and had it removed. After removal, I continued with the headache for 4 days, these were headaches unTOUCHED by any pain meds, bloating that finally abated and fatigue like you couldn't believe. I never nap, and I spent one full day on the couch without any motivation to do anything, and I also napped everyday and slept at night for 10 hours three nights in a row.

My doctor and nurse were understanding. They said I might have been "Hormone Naive," as I've not been on any kind of birth control, but whatever... it was a horrid experience and I'm so glad it's out. My doctor said I was in the minority of people with this kind of experience to birth control, but she didn't deny its existence, nor did she persuade me to try to "give it more time," and for that I was thankful.

This is both one of the BEST and WORST drugs for anxiety/depression. I was on Paxil CR 37.5mg for five years for moderate anx./dep., and yes, the weight gain (10-15 lbs.), vivid dreams, sweatiness, etc. were all side effects. But the Paxil so thoroughly balanced out my anxiety and depression that the side effects seemed a fair tradeoff.

(P.S. Nothing kills a libido like Paxil.)

And then, I went off the Paxil b/c I was changing insurance companies. Having read all of the terrible withdrawal symptoms, I scheduled myself a full four months to taper off. I lowered my dosage every week by only 2-3mg at most. (This involved cutting up the pill, which *they* say never to do, but of course *they* also claim that there are no withdrawal symptoms.) As a result, my withdrawal symptoms were negligible at best.

This past year, I went back on the Paxil CR 37.5mg and for a short while it worked again. And then it suddenly STOPPED. *They* don't want us to know that once you've been on, then off, Paxil, when you return to it, its chances of working again are slim to none. I took less time (only 2 months) to withdraw this time around, and the withdrawal symptoms were HIDEOUS. I've never felt so scared of what my body exhibited--unbelievable dizziness, terrible electric "shocks," headaches. And abject rage that I've never experienced before in my life. So much incredible nervous energy that I couldn't sit still. A rotten memory and confusion. Horrible symptoms. And yet, while I was withdrawing, I could see my body improving in other areas--far less appetite, for one, far less need for sleep, and less exhaustion.

While my anxiety and depression have returned, and while I'll probably need to be put on a different pill, I now at least know to research not just "official" medication Web sites but also patients' anecdotes. If I'd done so the first time around, I never would have stopped the Paxil at all. Pharmaceutical companies are just pimps who own doctors, so drs. are never going to warn you about the bad side effects of what they prescribe!!

This is the drug from hell! Nothing really happened after my first one-month shot, just a few mild hot flashes. My doctor had wanted to give me the three-month shot, but I insisted on the one-month to see how my body reacted. A month later I was given the three-month injection. The hot flashes increased dramatically. About a week later I started to feel like I was truly going insane. I was having serious panic attacks, I could cry over absolutely nothing, and I had this wierd disconnected feeling. Couldn't sleep, was exhausted yet had nervous energy, palpitations, feeling of unease all the time. This was pretty intense for a few days and was quite frightening. I had severe headaches, and I am not a person who gets headaches very often. Worst of all, I have had SEVERE joint and muscle pain. Twenty years of fibromyalgia was NOTHING compared to this. I had never had neck and back problems before, and now I'm experiencing pain all the time. I get weakness in my arms and legs, and often I feel a strange twitching feeling in my legs and neck. It has been over two months since I had that three-month injection. I'm due to go back for another one in early July, and I've already decided against it. The hot flashes seemed less intense for a little while, but now they're increasing along with night sweats. Nothing helps with the vaginal dryness, so my sex life is non-existent (not that I really care since this has killed my sex drive anyway). I had read about some of the scarier side effects before going through with this and asked my doctor about them, and he brushed my concerns off, saying that this stuff doesn't happen, I would likely just get some hot flashes. I'm very upset that I was pushed into having the three-month injection because now I'm stuck with this poison in my body. I think the pharmaceutical companies push the three-month injections. They got paid by my insurance company, that's all they care about and there's nothing I can do about this now. Anybody know if the doctors are getting kickbacks for pushing this on patients? For me this was follow-up treatment after having surgery to remove endometriosis and to remove one ovary that was severely affected. With that ovary gone I don't even know how necessary it was to follow up with Lupron. I'm 42 and will probably be going into menopause in a few years. Despite endometriosis I was able to have a baby at age 37 and was then free of endometriosis for almost four years. I will say I would probably think this was all worth it if I was going to try to get pregnant again, but I'm not, so I think this was all an unnecessary risk to my health. Anybody with similar experiences or info on Lupron, please feel free to email me at ****** Good luck to all!

I'm taking Methylprednisolone to combat the rash that developed from my Poison Oak exposure. My dosage is 6, the first day, five the 2nd, 4 the 3rd, etc for 6 days. I am having a hard time concentrating. I feel like my mind is racing, and my body is full of nervous energy. I have no pain, and the rash is fading fast.

NOOO sex drive!!! Almost repulsed by the idea! Will it ever return? I'm up to my fourth shot. Hot flashes every hour on the hour, you could set a clock to them, not to mention extreme coldness in between the flashes. I barely get any sleep. Extreme tiredness, and very moody. A constant feeling of nervous energy or anxiousness. On the other hand, no cramps! No cramps! It's a trade off. Oh, also loss of memory. I'm going to get fired if I don't remember converations from one day to the next.

I took ultraset yesterday and was up all night...no sleep and had lots of nervous energy...it did help me get lots of chores done around the house...