Twitch symptoms and conditions

I was diagnosed with Optic Neuritis in my left eye, at the time of diagnosis, I felt fine. Had an MRI to check for lesions on the brain, there were none. I was put on IV solu-medrol for 3 days, then 90 mg of prednisone for one week, with a rapid taper the second week. 6 days into the prednisone, I started have shortness of breath, etc. Went to the ER and my white count was 22,000. Had bronchitis and the beginnings of pneumonia. Because of the breathing problems, I only did 2 days of taper (doctor's advice). I have lost site completely in the left eye and now I have blurred vision in my right eye. Extreme fatigue, and a mental fog I just can't explain. A "twitch" in my left left hand and muscle weakness. I just don't feel "right". How long does it take for this drug to leave your system? Has anyone had a similar experience? My eye doctor was considering another round of prednisone for the optic neuritis, but I am not so sure I can survive it.

I'm 43 years old, 5'3" and weigh 165lbs. My doctor started me with Zocor 40mg. I stopped sleeping through the night about a week after taking it, but thought it was work/stress related. About 2 weeks after taking it, I could only sleep for about 3-4 hours, wake up, and then lay about another 2-3 hours hoping for sleep again. I didn't think any of this was drug related. After two months of insomnia, I began suffering very bad neck and back pain. It felt like someone stabbed me in my spine and it was excrutiating to roll over or get out of bed. I thought maybe it was my bed/pillow. I ran out of Zocor and my symptoms went away in about a week. I figured this was all stress related. After a month off, my doctor insisted on increasing my dosage to 80mg. Within 2 weeks of the increased dosage, the insomnia returned, my eye developed a "twitch," and I started feeling pains/aches again in my neck, shoulder and back. I refuse to take this drug further.

I have been on this medication for 3 months now. I am a 28 year old male, 6'2", weigh 211lbs, and in overall good health. My blood pressure average is 144/72 without the medication, but on the medication it seems to stay around 136/66. It took about one week for the blood pressure medicine to start working and when it did I felt very tired (which is normal). Now, in my third month I have started to notice new symptoms like severe headache in the right front lobe, severe tiredness, cold fingers and toes (in warm conditions), severe lower back pain, mood swings, blurred vision in the right eye (same location as headache), and a occasional twitch in my right thumb (probably not related to the medicine). When I first started this medication I did read all of these post and figured that everyone was crazy and/or nuts, but know I am thinking that I would rather stop the medication
and start seeking out for a better medication.. I know medicine has side effects but damn!!! Anyone else have cold fingers and toes while they have been on the medication..thanks

I took reglan in 1990 for the treatment of escophagitis (sorry if spelling is wrong). Had severe life threatening reaction (acute dystonic) and was rushed to hospital. Basically, it started the day after taking it. My face was stuck in a permanent Joker-like smile and it was painful. Thought I was going nuts, I was only 18 at the time, and then took another pill as prescribed. Later, my face stuck in an open mouth gaze position, I could not shut my mouth, it would spring right back open. Then, I lost my speech and spoke like a baby. At that point, my parents realized there was something seriously wrong (they had previously thought it was just me being nervous or something) and called the doctor. I was rushed to the hospital, and on the way I couldn't breathe. My bottom jaw shifted to the right, and my top jaw shifted to the left, and the pain was excruciating. I chipped my front tooth right off. My face was all twisted.

This went away after I was given Benadryl in the ER but I then developed the facial tic associated with Reglan, on the left side of my face. I am 36 years old now and a trial lawyer and singer who is always in the public eye. Luckily, the twitch is slight and only affects my left side, and mostly when I speak because it involves muscle movement. I was prescribed this drug 14 years before it was approved by the FDA. I would tell everyone I know never to take this drug, not even once. Its so dangerous and if I knew of the side effects I would have ever agreed to take it. Its very, very embarrassing to have this twitch. No one ever told me how dangerous this drug was. Hope this post may help someone. Thanks for reading.

im a 20 year old male who was given prednisone to reduce the inflammation around my spinal cord in my neck from a herniated disk. 60MG in the morning for 4 days and 40MG in the morning for 3 days...... no real weening process which im seeing probably should have been administered. while i was on it the mood swings were nuts and i noticed feeling muscle weakness and joint pain along with the occasional burning or tingling. ive been off it for 6 days and now the muscles in my legs and feet twitch and im still crazy in the head with little sleep and sinus headaches that don't quit. how long does this shit go on?

I have a question to any and all of you who have posted. I have similar symptoms to just about all of you minus any rash but mostly I have pain and some weakness in my right side particularly my shoulder and arm with some tremors in my pinky and ring finger and some pain and weakness in my right thigh. Insomnia and anxiety have also been a big part of the symptoms. Additionally when I take a hot shower my fingers twitch really bad then subside after about an hour...weird. My question is to some of you who have been going through this for some time is does this subside or even better go away over time? I have been off this stuff for just about a month now and things seem to be a little better but it might be that I am just getting used to the symptoms. Thanks

I've developed a twitch in my right eye in the five days I've been taking Yaz. No other new elements have been introduced to my routine in that time. I'm going to stop taking it today, the sensations are too distracting.

I'm a 21 year old mother of one 4-year old. I recently got my Mirena put in on March 11, 2008. Insertion was painful but the cramps went away pretty quick when i left the doctors office I tried to feel for the string but i never felt it so i assumed that my fingers were to small to reach so i just forgot about it. My boyfriend and i had sex the next week and it felt much much different. It felt as if his penis had doubled in size or something. I just know that it HURT a little more but it was still somewhat enjoyable. Since then I got my period last monday March, 26th and I'm still bleeding 9 days later! It's very frustrating. My head is spinning all of the time, I black out, and i twitch like something is wrong. I've gained weight, I have intense migraines, and i'm scared!!!!! Today is the 4th of April and i want it removed so badly. I just left the doctors office for my follow up, so that he could make sure my Mirena is in place. GUESS WHAT.... HE COULDN'T FIND THE STRING to the Mirena....so now i've got an ultrasound appointment on Tuesday. I'm terrified that this thing is floating around somewhere in my body doing damage. My significant other is devestated because he is in fear that we can't have children together and he has already made himself distant. It's a very stressful situation. I'll keep you updated....

I am a 25 year old, who was perfectly healthy prior to recently when I was diagnosed with Nephritic Syndrome and Minimal Change Disease and possibly FSGS (kidney diseases) I was put on 60 mg of Prednisone for 1 month then I was lowered to 40 mg for one month and I am then dropping to 30 mg. I am also taking Fosamax for my bones and a Vitamin D pill because my last lab test showed low vitamin D levels.

I am dizzy constantly and can not live a normal life, I can not drive or do any activities that I had previously done. My chest is so tight and constricted all of the time, my heart rate is so fast and pounds at my chest. I have no energy to do anything, I can barely open a door at times. I am beginning to grow unwanted hair on my face. My abdomen is always bloated. I have pain in my rib cage, and shoulders. I feel very sore throughout my entire body. I do not really sleep at night, so I look very tired all the time.

I have actually lost weight, I have no appetite at all. I am down 10-15lbs.

Now for the Pro- my Kidney Diseases are currently in remission and this has happened much faster than the Nephrologist had thought.

I am very anxious to getting my life back to normal and getting off the Prednisone.

Has any one else experienced increased heart rate, chest tightness, or rib pain?

I wish everyone the best in their roads to recovery!!

I just got my Metoprolol XL 25 refilled. The druggiest gave me Metoprolol ER 25 . My heart rate is up and i get more PAC, this drug is not working the same . What gives I am going to ask my doctor to put me back on the name brand drug Toprol XL 25 I don't care how much it costs.
the muscles of my legs twitch

Geodon was not worth it for me. I took 60 mg in the evenings and noticed I had a clenched jaw, anxiety, blurred vision, late menstrual periods, and HORRIBLE insomnia. I took myself off it with no problems.

I am 47 and have been on Lipitor now for about 7 months. For the last week or so, I have been experiencing upper shoulder, neck, and elbow pain. I passed it off as possibly the way that I sit at my computer. 1 week ago I went to the doctor to have the normal liver blood tests and she (the PA) asked if I had been experiencing any pain in my legs. At the time I didn't, and I didn't think anything of asking about my upper shoulder and neck problems, so I said "No, I feel fine".
Now today, I have been experiencing a constant twitch (for the lack of a better term) in my left foot. It's not like a normal twitch, in fact when my husband asked me to describe the sensation, I said that it felt like my nerve endings were twitching. I have also had a lot of dull headaches lately (which is very uncommon for me). I decided to search for Lipitor side effects and found this site. The thing that worries me more than anything is that my mom (which is 80 years old) has been on Lipitor now for approximately 4 years. She complained of her knees hurting but, chalked it up to her age. She contacted the doctor and he said that it wouldn't cause the kind of pain she was describing. It was most likely due to her age. I am so thankful I found this site and that everyone has taken the time to share their story. I am hoping that there is a healthier alternative. I read somewhere (maybe this site) to start taking CoQ10 and Vitamin C to reduce your cholesterol naturally. Hope this helps. Also, your natural CoQ10 is reduced considerably when taking statins. Thank you to everyone that has posted here. If I hear anything new I will let you know. God Bless and best wishes to everyone.

I was given this for a root canal. All I can say is stay away from it, ask for lorcet or percocet if you are in pain. This stuff made me feel like i needed to throw up but couldn't. I ended up sticking my finger down my throat at 4am just to get some sleep. All my motor skills were delayed and my balance was off. I was easily startled and agitated. I would be lying on the sofa sleeping and would suddenly get the feeling that someone was standing over me. I woke up and just about jumped off the couch in fright, and of course there was nothing there. Extreme Dry Mouth, and the medication blurred my vision at times. I also had no sense of time and was very disoriented. I also had some of the strangest dreams in my life while on this medication. My right hand would twitch at times, but not very often. This should be labeled as a roofy, not a pain killer.

hey me again. I forgot to mention why I am on topamax. I have a wierd face twitch, used to be a deliberate looking wink which now involves an entire head jerk to theleft and an inability to open my eyes, that my neuro thinks my be the result of focal seizures, also I have regular migraines and daily, literally daily headaches. Because of some other more personal issues and symptoms I feel like I might have Tourret's instead. Last week I had an EEG done. My face was moving so much it was unreadable. I had a second one done. I fell asleep and the twitch slowed down, then I had an MRI done. I find out the results of it all in two days. Will topamax help if it is Tourret's? Does any of this sound familiar? Thanks

oct 1 2007
wow.
thanks everyone for sharing your stories and for taking the time.
my son has been on singuair for a yr now and rite from the onset
he developed a twitch in his neck and face muscles.
sincee his dad had just left to go to iraq i figured it was nerves
or lack of attention or some emotional reaction.man oh man...
after reading all your expierience...and seeing that they are too
similar to deny we are off this drug... and zyerteck too.
i just hope his asthma can be managed with out him having to be
a guinia pig for drug companies anymore.
God bless all of you with children who suffer too.God bless all of you adults
who were smart enogh to quit . God bless those with whom this stuff still works.and God bless the people who are trying to find cures for asthma

I really, really regret ever having started Lamictal to begin with. Even though lamictal has greatly helped me with my social anxiety/ocd/gad/whatever it is I have (lol), it has caused too many damn side effects.

I started taking it sometime July and now it's September 21st, so it's been in my system for a couple of months now. When I first started on the starter pack, the 25 mg didn't have any effect on me- and then it started making me really, really anxious. I'd have super big physiological reactions to stress, but then I was advised to take it at night. Of course that started insomnia, and when I increased it to 50 mg I was really sensitive to light. It also caused my eyes to twitch and not stay closed when I tried to sleep- which was really, really annoying.

When I was first doing the 100 mg, at one point I became manic (I couldn't stop talking, I had racing thoughts, energetic- felt like I was on top of the world) and then I crashed. It was really hard going from being manic to really depressed, but that's the shit that happens on lamictal lol.(for me at least)

Anyways, so finally the 100 mg started to level me out- but I still have the rapid mood swings. I also feel incredibly spacey all the time and have trouble focusing/concentrating. Oh yeah, and my short term memory is shot. And my libido- which is really important to me. I hate having freakin' vaginal dryness and not really wanting sex- so irksome.

My advice to anyone reading this: don't ever try lamictal- it's not worth it.

I had a stye/ staff infection in my right eye. It was swollen and severely hurting me. Well, my doctor put me on sulfameth and a eyedrop antibiotic. I don't mind taking the eye drops, but these pills are making me feel horrible. I am on 1 pill twice daily for 10 days. I asked the doctor and the pharmacist if this stuff causes constipation and they both said no. Well, I haven't been able to use the bathroom well since I started it. My muscles twitch, my eyes are sensitive to the sunlight, I can't go to sleep easily, I've been itching up a storm, and I have headaches. I want to just stop the medication but if I do then I will never get rid of this infection in my eye. I figured I'd stop the meds in the middle of the week. I hate feeling bloated and constipated. Has anyone else had the constipation effect?

Okay, tried the Nuvaring for 7 days at first I was super happy because it didn't make me throw up like other birth control, but day 5 I started getting mild cramping and spotting, a headache and a twitch in my bottom lip!!!! Today is day 7 and I just took it out because I cried all day, the bleeding is now bad enough to use a tampon, the twitch hasn't gone away, I still have a headache and I told my ex-boyfriend that I f--king hate him and I don't even cuss usually!

I was just given the NuvaRing to try yesterday, I did not even last 24 hours! Literally 4 hours after I put it in, my eye started to twitch, constantly. I started have chest pain and pressure, almost like when you have bronchitis. My legs felt crampy, my back hurt, I couldn't sleep, and I had the worst headaches. Seriously. I hoped it would pass by morning, but no luck, so I called the GYNO and she said to remove it and wait to see if the symptoms go away. I removed it this afternoon, and this evening, I am still feel crappy, but at least a tad better.

I read and re-read the Nuvaring packaging looking for my side effects, and there were none. I am so disappointed with this. It was the worst experience I have ever had with birth control!

I had been taking Zocor for 10 days when I woke up in the night with heart palpitations, wobbly legs, a severe headache and dizziness. Shortly afterwards, my legs began to twitch on their own and cramped up. This happened several nights in a row. Then the twitching spread into my arms and neck. My muscles became very sore, then weak to the point where I couldn't stand up long enough to take a shower or get out of bed without help. Thankfully after being off of Zocor for 3 weeks I am getting some of my strength back, but I am plagued with a constant headache and dizziness, sometimes nausea and vomiting. Tests for muscle enzymes, liver damage, etc. have all come back with normal results. I am 21 years old and Zocor has made me feel about 75. Like others on this site my doctor did not think the problems had anything to do with the Zocor, but helpfully suggested I try incorporating more fat into my diet.

Can anyone tell me from experience how long I can expect these side effects to last? I've been out of work for 3 weeks and can't go back until I stop feeling dizzy and can stand up/walk for a full 8 hours.

I've been using the ring for a week and a half now. I am taking it out tomorrow. Since I started, the first couple days were without side effects, but now I am tired ALL the time, even after exercising, napping...I just want to sleep and sleep. I am also extremely and uncharacteristly moody. I feel as though I want to snap at people over the smallest things, and the tiniest irritations make me rage. This is not like me at all. I feel horrible, like there is a tick inside me making me twitch. I also have almost zero sex drive now. Just not interested. I dont care. I never felt like this before I started using the ring when I wasnt on any birth control. I had a feeling all these changes were due to the ring, and after reading everyone else's bullitins, I know my gut feeling was right about this damn ring. It's coming out tomorrow. Whats the point of birth control if you dont even want to have sex with your partner? I am finding another way of birth control that doesnt use hormones.

Hi everyone,
Today was not good a day for me. I just feel like lately alot of my symptoms are creeping back up even on the Lexapro. I have a question that I am scared to ask but really curious. Has anyone on here feel back to their original self? I know people say they feel better and are getting through the day but does anyone feel completely back to their old self again without the anxiety at all. Sometimes I get so scared that I will never be me again. I look at old pictures, well actually not even that old just from over the summer / before Yaz days. I wonder if I will ever be able to sleep without pills or A/D, will I be able to go months without having any anxiety, will my muscles ever stop shaking and feel weak. Will I ever just feel like 100% me again? I found so many websites with people that have been through hell from the Yasmin and yaz but I still yet to see someone that has recovered fully and says they are back to their old self. Well the people who suffered with severe symptoms anyway. My muscles since taking the Yaz feel so damaged. At night they twitch, during the day i have annoying flutters throughout my body. Does anyone else have this? I never had any of this before Yaz. I just worry I will never be the same again and that something in the pill really damaged me forever.
Sarah,
I think it's great what you did with the forum. I will definety post my story on there. WE need to get to as many woman as possible. Plus it helps to know we are not alone.

i was on seroquel for 2 count tnem 2 days and my heart would pound and ache and my muscles would twitch and ache like i had run for 5 miles, nothing was ever so scary and i was always hungry, i mean i gained 3 pds in 2 days. I am quiting this crap, at this rate i would be dead in no time welcome back anxiety at least i'll be able to feel that. Oh and also horrible horrible action dreams.

hi kim123,
i am sure it is a symptom of your anxiety levels. the excess adrenalin circulating in your system causes muscles to twitch,tense and shake and tingle just like they would if you were in real danger (although you are not your body thinks you are because of the constant high anxiety state) i used to have twitching in my legs,they would jump and shake all the time. i also used to get tingling and numbness in my face. how is it going with the lexapro? is it helping you at all?

sarah

Burning in right shoulder blade; neck pain (burning) diagnosed as arthritis; pain in left heel after sitting too long; sensation of cold behind temples; various occasional facial twitches--currently left nostril, for several weeks it had been one eye that would twitch; sensation that something is on face like a strand of hair when it is not there; slight trouble in thinking of everyday words or saying the wrong word.