Couple of minutes symptoms and conditions

im having cough and then wheezing for a couple of minutes. My doctor thinks its common allergies, but I wasn't having my usual allergy attacks. She put me on Singular and It's been 3wks now and I've been feeling worse than ever.

I've only been on topamax for about a month and a half and already I'm feeling some interesting side effects. In the first week of taking the medication I had such pressure behind my left eye I thought it was going to pop. It eventually went away and has not come back (thank the Lord). I also experienced some pretty nasty numbness, tingling, and uncomfortable pins and needles in my fingertips and toes/sole of my foot. The tingling in my hands usually lasted a few hours and the tingling in my feet only lasted for a couple of minutes. This tingling is never predictable.

Eventually the tingles went away and I was tingle free for a while. But in the past few days they came back. It actually coincided with my PMS. The tingles came back and with intensity about three days before my period started. I was wondering if it was common to have a side effect return or increase in intensity around your menstrual cycle? My hormones are pretty nutty and the reason I'm on topamax is to stop severe migraine auras and slight seizures that are tied to my menstrual cycle.

The feet tingles are the worst. It feels like I'm being jabbed with needles and I hate when it happens while I'm sleeping because it wakes me up and I can't fall back asleep again until they go away... they are that irritating. The hands I can deal with because I'm used to my left arm going numb when I was having the auras.

My sleep patterns have been disturbed because of topamax... I'm not too peeved about that. I still manage to get enough sleep. However there are times when I'm out with friends or having conversations and I'll know the word I want to say and I'll just bust out the wrong one. Like for example saying symphony instead of sympathy. My friends have gotten used to it and know what I'm trying to say. It cracks them up when my word salad produces sexual innuendos on accident when I really mean something else. BUT it's really messing up job interviews at the moment. I'm a bright and articulate person who is getting her BA in Anthroplogy and Archaeology, minor in History and am trying to get research assistant jobs at museums and universities. It's really hard to get a job when you are sitting there sounding like an uneducated moron high on crack.

I haven't had problems with memory, thank the Lord. Even though I've got the word salad going on (and it's strange... the word jumbles are only when I'm speaking... I'm super coherent when typing) I'm not forgetful. I was able to make it through finals week perfect, while juggling a full work load. I hope I don't start losing my memory.

I haven't lost any weight (AW SHUCKS!!!!!). I was looking forward to that one. How soon should I expect to lose weight by, if I do in fact lose weight? I'm a difficult duck when it comes to weight loss. I've been at a stable weight since I was 13. I'm an athlete so my body is my temple sort of thing. But in the past two years I've put on a little bit of unwanted weight in certain areas when I stopped hitting the weight machines :( My question is, if I haven't lost it yet... will I lose any?

I'm also classified as type II bipolar, obsessive compulsive, and anxiety disordered. I've noticed my mood has stabilized. I'm not as all over the place as I used to be. My highs could get pretty high and when they would get up there my obsessive compulsive would almost go on a little joy ride. And when I was low, I was super low and my anxiety would take the depression out for a spin. But now I feel a calmness and a zen that I never felt previously. It's not an apathy I can certainly tell you that. I feel like I am in control of my life. I thank topamax for that.

Reading all of these posts I just worry that the honeymoon period of my medication maybe over. I worry about other side effects cropping up. I think that I can deal with my tingling extremities and that I can manage my word salads. I don't want the pressure in my eye to come back. I also don't want to start exhibiting the other side effects. What is the possibility that I will start exhibiting more side effects or are you generally stuck with what initially presents in the first month or so? My doctor also does NOT intend on increase my dosage. He thinks 50mg once a day will do me just fine. Oh and one last question, anyone else experiencing the side effect increase coinciding with PMS?

Sorry for the super long post! All replies are welcome!

I cannot stand for even a couple of minutes without my feet tingling/burning for the rest of the day. Walking seems to help therefore I thought it was circulation but vein docs say it is not. Symptoms got seriously worse during ivf treatment (3rd ivf, 3rd baby), and now one year later I have a baby but symptoms are worse. I thought drug effects are short term but maybe they are not. I am suspecting lupron but i could not find much info on its long term effects and how to counter those effects, or it could be something else. Saw neurologist who wants to do nerve conduction study but that just sounds very painful and not necessarily helpful.

if you have any feedback, would love to hear. thanks

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 had an agonizing migraine this Saturday, with all the usual delightful symptoms: pain, violent vomiting,... Went to the ER. After many hours I was hooked up to an IV with Tegretol (an anti-seizure med that's effective with migraine) and Reglan (for the nausea). Within a couple of minutes after the IV drip started I realized something was wrong. My migraine pain was actually increasing. I felt a desperate sense of being connected to this IV that was feeding me drugs whose effects were suddenly unexpected. Then things spiraled from there. I went into a panic. This sense of panic was unlike anything I have ever experienced in my life (and I've had my share of hospital horrors). I thought my heart was going to explode. Luckily my friend was next to me. I told him to get a nurse. I told the nurse frantically that I didn't know what was happening to me, I was freaking out, but I begged him to do something. He said I was probably having an "anxiety attack", which can happen with Reglan ("anxiety" sounds like a euphemism for what I was living through, but whatever...). He moved quickly, and hooked up some Benadryl to the IV. I also asked him to get me out of the dark, airless room I was in, as I felt like I was going to choke from the claustrophobia. Between the Benadryl (which apparently counters the panic effects of a Reglan reaction) and standing out in a spacious, well-lit hallway, I felt a couple of degrees removed from hell. Anyhow, there's my Reglan tale. R.M., Newton, MA

I got all those problems but the higher the dosage the more attacks i had.Another neurologist think that i just have pseudoseizures-paranoia attacks.Anyways the doctor screwed me up,he gave me 5 years ago something different and my seizures started daily than switched me to lamictal.I must say that sometimes i have or HAD electricity in my left hand all the time and once a women touched me and got stunned lol.anyways lamictal is bad,i didn't have any side effects like loosing hair but i did have A LOT of head hecks.I must share something with you,when i read epilepsy.com it seems that my seizures called myclonics in the end they are not but they similar in effects.Myclonics its seizures that happens only in the morning.Heres the catch for me,i figured out that if i won't close my eyes the first hour after i got up and went to the sun outside than i didn't have seizures.Its not a real solution so i decided to raise the lamictal from 175 which was ok for me to 200-250 like the good doctor said,just made me worse.Now i started dropping it by 25 mill each week and i must say i feel better only a little tired after 5 years that my body got used to it.Anyway if any of you have myclonics than don't close your eyes.BTW i have AURA-feeling before the seizure but luckily for me after a second if i open my eyes nothing will happen although i don't always take notice of it.In midway it would happen if i seat in front of computer and will lose attention if someone will call me or whatever but its a mill-sec seizure,barely noticible if at all and i never get "disconnected" from reality!!!
the ONLY thing which is bad for me is that except that im sick now my blood pressure is huge-140/82 and pulse 106 which is being like that for couple of days but i will get trough that.Since i lowered my dosage my midway seizures stopped,now im on 100.

P.S=Check yourself with the neurologist with a different one preheps.IF you can describe the whole seizure it means you don't dispatch from earth which mean it might be psydo seizures which are psychotic and not epileptic,the most important thing is that if someone takes lamictal or any anti apileptic drug even tho he doesn't have real seizures the medicine can do this.I got screwed and now i try to get over it,the doctor trowed me on woods with tablets after having a first seizure WHICH IS WRONG because you sepused to get tablets only after 3 attacks and after describing seizures and doing eeg tests to make sure that you DO have the problem.

Anyways remember what i said about the closing eyes in the morning part,if you close your eyes and feel weird keep them open at least those that have them after they wake up,that was a solution for me and it can help you to...MY doctor said everyone like me but i think he is laying,the other neurologist said my doctor was wrong probably about the seizures,i think i have both but i do know that believing and saying that you don't have anything WILL help you and lower your seizures,after speaking with the doctor i actually started to believe i don't have anything and walla i have almost NADA,today i had zero!!!! :D

OF course don't lower dosage without first consulting with someone expert,but since i know i can control basically every seizure i have and i know what to do to avoid it i let my self start dropping dozes!!!

GOOD LUCK my friends believe in yourself and if you want some personal info leave your msn i will add you and try to answer you the best i could,i was researching my self trying to figure out the core of the problem for 5 years but after 6 months knocking my head in the pipe when i washed my face i learned what i should avoid to minimize the chance!!!Try that

I have been on Levaquin over 6 times in the past 2 years for upper respiratory infections. I just came off another levapak 750mg for 10 days and my biceps were feeling really tight. I mentioned this to my doctor but he said it was a common side effect. After researching this today I am shocked about the tendon damage. I have had distal bicep tendon surgery on each arm on separate occasions in the past two years. Now I am terrified this is going to happen again. None of the surgeons could figure out why someone my age (41) could do this twice in under 2 years. Has anyone found a way to reverse this? I am terrified to go back to the gym or even lift anything. My biceps are so sore and I have been off the Levapak for 3 days and my biceps seem to be getting more tight and sore each day. I can't face having another surgery. This drug should be taken off the market.

I am a female taking narcotic pain medication due to a back injury. Those pills make it hard to pee. My doc put me on Flomax to help me empty my bladder. I have had swollen sinus every night when I sleep. I have extreme elbow, wrist and finger pain that lasts all day/night long. My legs and knees are very stiff and sore. If I stand on my feet for more than a couple of minutes, my soles ache. I feel extremely tired and exhausted. DO NOT TAKE THIS DRUG!! Now that I am off of it, my retention problem is worse than ever before. I wish I would have seen this web page before starting this horrible drug.

I took Yasmin for 2 years and about 6 months after starting Yasmin I started getting migraines at least 3 x per week and sometimes 5 x per week (before not even really getting many normal headaches). I thought it might be my birth control and saw my OB who referred me to a Neurologist who put me on a medicine for migraines. About another 5 months later I noticed I had a small bald spot in my hair line. Saw a Dermatologist who diagnosed it is alopecia. I immediately stopped Yasmin and migraine meds and decided to get an IUD (GREAT CHOICE!) My migraines stopped almost immediately, however my hair loss continues to progress. I now have 3 additionally bald spots on my head and areas on my scalp that are very thin. I feel great otherwise, no headaches, no depression (other than losing my hair), no anxiety, appetite is normal. I'm so desperate to find someone else that has had this specific problem as no one believes the hair loss is connected to Yasmin. I just pray after awhile the hair will grow back. Please if anyone has experienced this same situation please post what might have helped you get through it and if it does ease up! One more thing - I have scalp pain, like burning on the front and top and back part of my scalp, wide spread, not only in the bald areas.

I had Avelox prescribed after severe pneumonia. It kicked the pneumonia, but there has to be a better option. I am a little scared right now. I took my fourth (and last) pill this morning, feeling pretty good. The last 3 nights I have not slept despite being wiped out from pneumonia and type A flu. I was hallucinating mildly, as soon as I close my eyes or turn the lights, I get a real light show and weird images coming at a frantic pace. My heart races, my neck feels stiff and pressured, I can not concentrate, and I just feel too weird to describe.

1 hour after taking the medicine this morning, all these symptoms returned, stronger than before. I now feel a bit depressed. I started studying Avelox as soon as these symptoms returned. If you are reading this, I hope you were smart enough to research Avelox before taking. There is a ton of scary stories about this poison on the internet. I am now experience heart palpitations every couple of minutes, though I have had arrhythmias before, but not consistently. I have looked at a lot of websites with patient feedback on drugs, and I never imagined that anyone would proscribe a medicine with so little positive feedback and some many horrible stories. Good luck to all of you who are in my shoes.

My 4 yr old son has been on Singulair for 2 years now After having what was close to pneumonia, his pediatrician decided that we should try Singulair. He suffered from allergies all year round and both sides of the family also have a history of allergies. We went over the indicators to decide whether or not there was a good chance that he would develop asthma. Yes, we found there was a very good chance. We were told that Singulair is the one drug that could actually prevent him from developing asthma - so OF COURSE we said okay. He started so young, that we never really realized that this wasn't just his "personality" - you know terrible two's, then independence, then along came his baby sister...on and on. Anyway, he has always been an overly-emotional child, hyper, etc., but then it was like every little thing bothered him and he would throw fits about "nothing". One day I told him to stop acting this way and while crying he said he couldn't stop and asked me to help him to stop. How heartbreaking! He goes to preschool and can't sit in a circle for more than a couple of minutes without being reminded by the teacher to sit down. He has been especially aggressive - saying how he just wants to kick something or push his sister down. He has always been a restless sleeper, but just recently he has been telling me about his terrible dreams - things you would never expect to hear from a 4 yr old. I thought he was a hypochondriac b/c he was always complaining about something hurting. I was reading about ADHD and decided that maybe this was what he had - everything fit quite closely to these same behaviors. I called the pediatrician's office to see if this may be his diagnosis and instead they told me about the possibility that Singulair might be to blame. They told me take him off of it and see how things go. It has only been 3 days. I have not seen any improvement and his is very itchy and scratching like crazy. I'll let you know what we find out.

I have been going through the nightmare that is Yasmin for 2 months now and have been trying to help my body as much as possible. I have been taking a multivitamin plus a B Complex and a supplement that includes zinc, magnesium and calcium. Here is my question: about ten or twently minutes after I take all three vitamins I feel extremely nauseous for a couple of minutes and I have to lay down and wait it out. I have not actually gotten sick but this happens nearly every day. I have tried everything...taking the vitamins together, apart, at the end of the meal and in the middle.

Has anyone else struggled with this? Does anyone know if vitamins do cause nausea and why? I am nearly positive it is the vitamins because the nausea always happens right after I take them, no matter what time of the morning I take them.

Also, is it normal to still struggle a bit with anxiety even if I am not ovulating or menstruating at this time in my cycle? I do feel much much better on the whole, but I just want to make sure that even though I feel quite good most days, that it is still considered normal to have some hard moments. I think on my good days I get in the mindset that I am all better, and then I freak myself out if I do feel a bit of anxiety. I sometimes feel like I have to attribute the anxiety to that time of the cycle, due to coming off Yasmin, but if I am not in that part of my cycle, I get scared that I am crazy and that it is not Yasmin even though I know in my heart it is.

Any feedback from those who have gone through this nightmare would be appreciated!! Take care, everyone. You are ALL in my thoughts, all the time.

I HAVE BEEN ON TOPROL FOR 5 YEARS SINCE MY FATHER AND MOTHER HAVE PASSED. BOTH HAD HIGH BLOOD PRESSURE AND I HAVE TWO SIBLINGS WITH HIGH BLOOD PRESSURE. BOTH SIBLINGS HAVE HAD HEART ATTACKS. ONE SIBLING HAS CHF THE OTHER REFUSES TO GO BACK TO DOCTORS TO GET EVALUATED FOR MEDS.

ANYWAY - MY SIDE EFFECTS HAVE BEEN VERY SLEEPY SOON AFTER TAKING, VIRTIGO, COLD FEET AND HANDS, SLEEP IS SOMETIMES INTERRUPTED BY DREAMS, WEIGHT GAIN HAS BEEN 15 POUNDS OVER MY ORIGINAL WEIGHT (NUMEROUS DIETS DON'T HELP). I AM HAVING DOUBLE VISION AND HAVE BEEN FOR 2 YRS - I HAVE HAD MRI'S/MRA'S ULTRASOUNDS, FLORESENE TEST - MY MUSCLES HAVE BECOME WEAK IN BOTH EYES TO THE POINT THEY THINK I MAY HAVE MYASTHENIAGRAVIS DISEASE - BLOOD TEST WILL CONFIRM WHETHER OR NOT BUT THAT RESULT IS 2 WKS AWAY. I HAD TO BE PUT ON ZOLOFT TWICE AND COULDN'T TAKE IT DUE TO ANXIETY ATTACKS WHILE DRIVING IT ALSO LOWERED MY PULSE BELOW 44. PULSE IS NOW AT 56 WITHOUT ZOLOFT. WHILE ON ZOLOFT I HAD REALLY CRAZY DREAMS EVERY NIGHT. I STILL HAVE PANIC OR ANXIETY ONCE IN A GREAT WHILE WHEN I AM DRIVING AND I HAVE TO PULL OVER FOR A COUPLE OF MINUTES TO RECOUP. I HAVE LIMITED MEMORY SOMETIMES. SEEMS LIKE SHORT TERM IS RARELY THERE.

I was on effexor for a year to treat dysthimic depression and general anxiety disorder. My dose started low but was upped every few months until I was on 150 mg.

The side effects I experienced were:

- Dizziness
- Inability to sleep soundly at night (I would wake several times and have difficulty falling asleep again)
- Inability to stay awake during the day (probably as a result of the previous side-effect. this was so bad that i even fell asleep once while i was standing up!)
- A "fuzzy" mental state; everything looked cloudy, I had no concentration, poor attention span
- Frequent vivid nightmares
- This weird sensation that happened every couple of minutes. It wasn't quite like dizziness...it was more like my brain was doing a flip-flop in my head.
- I was ALWAYS exhausted
- My libido disappeared

The withdrawl affects of the drug were similar but also accompanied by twitching, nausea, increased dizziness, more frequent "brain flips", and occasional fainting or blacking out.

Worse was that I had to take the drug at the same time every day, or else I'd enter withdrawl almost immediately. If I took the drug at 7:00 AM every morning before school, and then slept in until 10:00 AM on the weekend, I would wake up in withdrawl, even though i was only a few hours late!

When I tapered off the drug, the withdrawl affects were almost unbearable for a couple of weeks, but eventually I returned almost to a normal state, except that it took over a year for my libido to return, and even though I've been free of the drug for a couple of years, I still have difficulties in that area sometimes.

Hello everyone. Firstly I have to say that I'm a hard one to deal with. I don't trust doctors for the most part, I find that they're the legal drug pushers. Out of the blue 2 years ago, I developed Asthma. Without any testing they put me on advair 125. After reading your postings..wow... I thought I was taking crazy pills until now. Lately, due to enjoying the odd cigar... I've found that I've had to increase my usage (I've since stopped the run of cigars)...and as of late I've had a funny aching pain in the center of my chest. it comes, it goes, it comes it goes... it seems like every couple of minutes, but it does eventually stop. by stop I mean it doesn't last continuously for 24 hours, but it has been happening at least every day. i've gone for stress tests, MRI's... and a host of tests, ut yet they say my heart is normal. I've also noticed that some days within 2 minutes of taking my advair it seems like my heart flip flops... again, it usually only lasts for a few minutes but it's scary as hell... the only thing is that it does help me breathe easy... I've also noticed that the past 2 years of using it... I"ve had a ton of foot cramps on the bottom ball of my foot leading into the toes... painful as hell and at 3am it'll shoot me out of bed so I can walk it off and put as much pressure on it as possible in the hopes of fixing the pain. Is this really normal...or rather are these really that normal of side effects for using Advair. If so... that's it...I'm going natural in my search for an asthma cure. What kind of crap are the drug companies trying to put into our bodies.