Second time symptoms and conditions

I am a 55 year old female. I had a heart attack in July -08. I had a stent placed. Since then I have been on Plavix, Lopressor, Lisinopril and Lipitor. I have been back to the Hospital 2 times since then. The first time they found nothing. The second time I had to have another stent place because the first one didn't work. This last time they did another catheter and found nothing. I have episodes every couple days of Light headedness, heart pounding, stomach upset, confusion , really bad burping and sometimes diarrhea. I am at my wits end. I have lost 30 lbs and am weak most of the time. I was very active before all this and can't get back on my feet. When I ask about the medicines, the doctors say I don't think it's that. Someone please help!

So far i am a 14 year old boy facing prednisone and have been on this drug over 4+ month periods at 10 mg first time and 100 second time. I have chrons's disease and it is hard to treat when it has a flare, so they have to put me on prednisone. I have experienced some of the worst side effects imaginable along with many other suffering victims of this drug, and they include: Headache, Severe Acne, Flu-Like Symptoms, High Blood Pressure, 50+ Pounds Gained, Moon face, Stomach Pains, and Much More. After i have been weened completely off i have notice these: SCARY Heart Palpitations, Out of Breathe, Feels like something is beating in my stomach, and feels like my heart drops to my stomach like pacing.

I was wondering if anyone else was having the same experiences and then I came across here!!! Hopefully there will be someone out there who will be able to relate to me. I had my Mirena placed in August 2008. It wasn't that bad going in, actually went right back to work after that. About a month into it I just wasnt feeling right. In September I tried to get it taken out, but the hospital talked me out of it (military hospital, and said the cost blah, blah, blah, blah...) Well since then my life has been a living hell. It started as a small little headache but has literally grown into a DAILY dizziness and headache "fest" that is so bad that it's effecting my daily life. has anyone had this??? I've had CT scans, MRI's, spinal taps.. All says i'm ok... Plus "foggy brain" to go along with it.

Took Limbrel for 1 week and started experiencing fevers for 7+ days some of which were over 103+. Had significant body aches, diarrhea, weakness and fatigue. Stopped taking the Limbrel, but did not make the connection until the second time. Same thing happened. I stopped and got well, but I also used many other remedies such as homeopathy and vitamin IVs. Stayed off for 3 weeks. Then decided it couldn't be the Limbrel, so tried it the third time. The first one I took gave me a fever about 12 hours later. I am calling my doctor first thing in the morning to report this. Very dangerous.

I just had the mirena inserted for the second time. I have had it for five years and have not noticed any side affects. I have barely had a period. Libido has been up and down but I think it is more a result of being a busy tired mom. Had my old one removed and my new one put in today, no more uncomfortable than a pap smear. I feel kinda yucky since, minor cramps, and a little bleeding. I m not at all worried. It is easy birth control, but of course there is a downside too. It cant be good having a foreign object in your body. Good luck to everyone!

I had my Mirena inserted in the beginning of july after having my second child. I made a horrible mistake. I had cramps so bad that I would actually be in so much pain from I turned pale and cry whenever they happened. I constantly bled from the day it was inserted until the day I had it removed which was Oct 29th. Almost 3 months. Some days would be worse than others. Right before I had it removed I had to go to the hospital because I was pouring out blood as if I was peeing. It made me have severe mood swings. One minute I'd be extremely happy then the next I was really hateful and wanted to punch someone. I would get light headed a lot from loosing that amount of blood right before it was removed. It made me tired all the time.I had a lot of migraines. It affected my sex life for the obvious reason I couldn't because I never stopped bleeding besides the fact I had no desire to.

But since I've had it removed from I guess the lack of hormones I am having hot flashes and nausea and getting shivers wile changing from being hot in cold ever few minutes. Its subsided though since I started a new birth control last night. I'm only 20 and I didn't obviously know what a hot flash even was and it scared me i remember I went out to the hospital for a second time because of it lol. Now that I know what they feel like I really don't look froward to going through the change. I'm getting better and better each day since I haven't had it in. I just feel better and my bleeding has subsided.

I would never recommend Mirena to anyone.
Since I've had it removed I feel a lot better

I have been taking Methimazole for exactly 1 week. I am 26. This is the second time to take these same drugs. Methimazole along with a beta-blocker, Propranolol. My thyroid had been back to normal for 2 years. This time, I started off taking one three times daily, then just one a day, now I was instructed that I should take three once daily. My tests just came back and I am extremely thyrotoxic and have Grave's Disease. I have had headaches on and off this week, today I have had a headache most of the day. My heart is still palpitating but my strength is coming back. Last week before starting the drugs was much worse. I could barely move my body hurt so bad, felt like I had a fever, fatigue...the works

This is the second time I have switched birth control in the last year and looked for side effects online. I started the nuvaring 6 days ago and yesterday felt sick all day, had abdominal cramping, and was so moody and irritable. I haven't been sleeping well either for the past few nights. Today at the gym, I was getting dizzy and tired during my workout when it was only a Zumba class and not very strenuous (I work out everyday). I also just have that overall "weird" and tired feeling. I had these exact same side effects when I tried Yaz earlier this year. If you switch back to the pill, I suggest Desogen, which I will start taking again since I just took the ring out after reading similar stories - I have never had any side effects or problems with it and can't find websites that have bad experiences like this one and the one I found for Yaz earlier this year.

I started Nuvaring in June of 2008 and it hasn't been that so far but I have had severe depression where I can't get out of the bed I just cry and cry and I'm very moody. Sometimes during sex I have cramps that won't go away until maybe the next day if I'm lucky. I've also gained at least 20 to 30 pounds since I've started. I noticed that I could eat and still feel like I never ate a bite.The only plus is that my period is regulated and my cramps aren't that bad but is it really worth it?

Hello everyone

Well I thought I could find some help on this forum and I definitely did. I started the NuvaRing last month and had no problems. This second time I have had vaginal irritation and itching. It feels like little cuts are there at times and I also have had increase secretion and anytime its there thats when the itching really happens. Im glad im not the only one who has had some issues. The NuvaRing will be removed tonight. Thank you

I have had a mirena before it was okay the first time besides that i couldn't lose my pregnancy weight. I have one now and it is worse than ever. I weighed 120 lbs back June when I got the mirena for a second time. I now weigh 156 lbs concedering I'm only 5'3. I have tried asking my doctor several time if that is normal. They have continued telling me that it has nothing to do with mirena. They claim my metabolism has slowed down. I am 23 years old and have never had weight problems. I am so glad that I have found this web site because I have been super depressed about this. It is terrible to gain weight and go up 2 pants sizes in just a few months. I have even tried exercise like the doc ordered and it isn't helping. I have had massive headaches. I can't concentrate on anything when they come. I even experience foggy vision. I have a sex drive but I loss it easily. I can be so ready and then just something as simple as a cough will just take it all away.the only good thing about this so far is that I have no period and craps are down to a minimal.

Taking Z-pak for the second time this week. Each day has gotten worse. I take them at night, figuring that the worst of the effects would be during my sleep. Well, that's not so. Starting about 9am each day, I get horrible dry mouth, chills, and pain in my chest that rivals any pain I've ever felt. I have trouble eating and I feel super weak - including some tingling/pins and needles in my hands and feet. It usually goes away by about 6pm and I start feeling better. I do take my Claritin at about 8am every day. Could there be an interaction? It seems odd that I feel OK on waking up, but feel terrible for hours after taking the Claritin while on the Z-pak. Has anyone ever experienced this? Any advice on how to handle it? I have company in this weekend and I can't even function to entertain them!! Thanks!!

Okay...so I first posted the day I had Mirena inserted, Oct. 1. ( and had wished i found this site prior to installment)
It has now been two weeks. So lets up date:
I bled for only a few days, maybe 5 days tops. Which was great, I just thought " hmm maybe I'm a lucky one, maybe they put it in right, or maybe my body is handling it better than I though it would" But then 5 days later I started bleeding again.
Like I said, I have had this thing in for TWO WEEKS.. and I've had sex.... TWICE! I don't even want to have sex, no wonder it is so good for birth control.
The first time was great. My boy friend didn't feel anything, and was enjoyable for the both of us.
Needless to say, the second time was great... until it was over.
The second it was over, I was doubled over in pain. Literally, 30 seconds after sex, I had a severe hot flash, and felt like i couldn't breathe. I started shaking, and started crying. I felt like the " insertion part" was happening allllll over again. ( insertion, is miserable.. that alone makes me not want to recommend it to ANYONE) I thought i was going to pass out, and standing felt impossible, I couldn't even roll over. A few minutes later I stood up and went to the bathroom, I was nauseated and felt sick. I tried to pee, and couldn't. It just burned and felt like my whole body was trying to squeeze this thing out.
I went back to bed and layed there for about 45 minutes in agonizing pain. My fiance was so sad, he felt completely guilty that he "caused" the pain... he thinks it should be removed immediately. And so do I.
The one word to describe this pain was INTENSE.

To add, I have noticed dry, itchy skin. And my skin is now sooo fragile. My scalp is sooo itchy that when I scratch I actually bleed and scab.. it is DISGUSTING. And yes, my hair is slowly getting worse. Everyday I notice a little bit more shedding than usual. My complexion is not getting WORSE, but the few pimples I have are deep, painful, and are actually scaring. Never before did I scar.

I also feel the extreme fatigue, and occasional mood swings, I will admit, I have Always had an attitude but this is a little more than even I am willing to except.
I have not gained any weight, but it's only been TWO WEEKS and, I have intentionally weighed my self everyday... and I am now fluctuating 6 lbs a day in water weight.My belly is 23/7 bloated. The only time I am not bloated is after the first pee in the morning for about 45 minutes, and then it starts allllllll over. People have noticed my fingers are chubbier, and are sore. For 2 days my toes and feet were a light blue-ish color... that "symptom" was enough to make me WANT to go to the E.R. but I opted not, as there was no discomfort.
A major discomfort, like i said was sex, and the random times throughout the day when I bend over or wiggle into a chair... it just feels like it is STABBING the right side of my body. There is truly no comfortable way to sit without favoring my right side.
It is weird, painful, and is getting really old.
I tried calling my doctors all day today, and it was still left on their " night time recording" so, I am a little angry.
I thought about pulling it out myself, but this time I read " REAL PEOPLE INFORMATION" and apparently its not a good idea. SO DON'T, if your thinking about it. lol.
Anyone that has had it removed, is it painful? Does it feel anything like the insertion? I am scared to death.. and I am a little upset that i have to continue to wait to get through to my nurse practitioner. I just want this to be over with. The last thing I need is to have it get " lost" like so many other women.
I tried, but I'm listening to my instincts, and this just isn't right.

This is my second time to use Topamax and I am having a different side affect now. I am getting very hot and breaking out in cold chills at the same time. The top of my head was so hot yesterday I had to wet it before I came to work. Has anyone been having problems like this? It says decreased sweating but mine is the opposite.I have the increased body temp. I thinkl.

I had an injection into a Bursae about a week and a half ago. My face was hot and bright red for about three days, if i went out in the sun it made it worst almost like i was allergic to the sun. I have had headaches daily, since. Vicodin will not help these headaches, my heartburn was so bad i stopped taking all medicines, birth control, antibiotic, pain meds. My stomach hurt so bad the second night that i could not make a sudden movement. and i couldn't stand straight up. i have been so nauseated, ive thrown up twice, once i was taking a sip of milk to get rid of the side effects and as soon as i swallowed i puked, the second time i just smelled something. i have been bouncing around in the bed all night. and so depressed i need to be committed. my head has hurt so bad many days i don't want to hear my one and a half yr old speak. but i am stay at home mom and i have to do what i have to do. i had told my doctor that i had these effects, but another physician treated me. i told him and he assured me it would be a very small amount. also a my ankles hurt especially, feel like they are gonna snap, as well as all my other joints when i come off of these. someone email me plz *******

I have felt poorly since October 2006. Sugar levels ranging from the 450-550 range. My G.P. who is a fantastic dr. put me on Januvia in January of 2007. Range of sugar levels did not change much Sent me for blood work found many abnormalities and in March 2007 I was diagnosed with a bone marrow plasma cell cancer call multiple myeloma (not a side effect of Januvia I'm sure). I am I'm the hospital now for a second time because of severe abdominal cramping. Looks like lower bowel problems. Have not been on Januvia for five days now. ***************My right shoulder feels better, I can raise my arm above my head, no night sweats, no bloody nose, my eczema is clearing up, no pain in joints or rest of my body (thought pain was associated with cancer which is considered inactive since April 2008, I have slept through the night, no pain meds for the last three days, no nightmares, no stomach pain, no coughing, chest not feeling congested, I can get out of bed w/out having to stand for a few minutes by the bed-side because of dizziness, not feeling like a truck ran over me in the middle of the night in the last three days, and most of all I have more energy. To many side effects !!! All of these side effects I thought were a possible result of my cancer although my oncologist did not think so and we still believed that there was some other underlying problem(s). THE UNDERLYING PROBLEM(S) IS JANUVIA !!! Thanks for reading. God Bless You All. Great Health to All.

This is my second time taking Chantix and I had a horrible experience with it the first time, but thought after a 20 year plus habbit at 33, I needed to do something. I am on day 15 of taking Chantix this time and quit last week, so 7 days ago. I am doing better this time, the nausea is manageable and I am using Dum Dum suckers for the hand to mouth urges.

I have been taking the generic form of Wellbutrin (social anxiety with a touch of ADHD) for just over six months and as much as I hate to admit it, I believe that the bad is finally, convincingly, outweighing the good.
The good things that came along with 150mg of the SR every morning at 11:00: Weight loss (but only after an initial one month period of eating every form or carbohydrate I could find), it seems to brighten the whites of my otherwise cloudy eyes, helped me maintain conversations with people that I would have normally cut off early, and possibly--but only possibly--helps me focus (although the hyper focus that I used to get via the ADHD is gone. Completely. Non-existent.)
Which brings me to the bad: This goes against most of what I've read other people experience on Wellbutrin but lethargy has set in. And it feels like it's here to stay. It's not really a sedated lethargy but more of a false contentment that everything is just fine the way it is. No progression, no improvement, and looking to the future is almost impossible through the fog. I too, during the first two or three weeks, had the speedy, productive reaction to the medication. But that has subsided. Next, hair loss has become a concern. I'm in my thirties and it could be just how it goes but I truly doubt it. Mild constipation may seem bearable but I miss regularity more than I have time to describe. Ringing in the ears. Impaired memory. Confusion. Forgetfulness to a fault. Mild hives on the back. Irritability. A marked shortness of breath. After one month on Wellbutrin, I could barely run a mile on the treadmill when I've been accustomed to flying through three to five with ease. I feel weak, vulnerable even. Working out has therefore fallen to the wayside. And last, but probably the worst, this medication has seemed to cultivate a serious craving for other drugs. I can't explain it but I can't take it anymore either.
Like most people on a medication, I have read numerous posts and some people share some of my concerns but mostly, it seems that the people who report in are the speedy folks on day two or week two. That is, in my opinion, only a bit helpful, since these effects are usually short-lived. Wellbutrin started out with promise but while parts of me look into the mirror and see an improvement, underneath it all, I know that it is purely a nicely dressed form of prescribed avoidance.
I haven't posted this to discourage anyone. If it works for you--great. Really. But I also haven't read anyone's experience that matched my own so I figured it might help someone who is going through any of the same. Good luck.

I've heard nothing but good things about Yaz. The commercials make it look like a DREAM drug......one I truly needed. I'm 34 and getting married for the second time. My PMDD has become horrible. I started YAZ 7 days ago because I didn't want to be on my period for my honeymoon but mostly because I wanted to be a normal woman. I have 1 good week out of the month. I'm so tired of the mood swings and everything that is associated with PMS/PMDD. Well after day one I was horribly nauseated just like I was when I was pregnant. That has been daily. My stomach felt very"anxious" like I was nervous all the time and that is NOT me at all. It never dawned on me it could be the YAZ I thought it was nerves because of the upcoming wedding. I felt depression that I hadn't felt in a while since getting engaged. And it was almost a "hopelessness". Last night when I was driving home from work, day 6, I started coughing for no reason. I haven't been sick at all. It was like I couldn't quit. My left chest area was on fire and radiated to my back. I finally started thinking what in the world could this be so I got online and researched side effects of Yaz and boy am I glad I did. It blows my mind at the poor women who have either suffered threw a blood clot, or have died from it and ALL the other side effects I see on here that are just like mine. I'm so glad that I found this because today the Yaz went in the garbage. I refuse to take it anymore. I was worried all night I had a blood clot in my lung that I could barely sleep. I don't think anyone is aware of these problems associated with this medication. I hope they recall it soon!

My 9 1/2 yr old son started Singulair in July 2004 when he was 5 yrs old.Looking back now we realize that he started showing signs immediately. We only gave him Singulair in the fall when he had the most trouble with his asthma. His asthma was under control immediately but was not worth the damage that was done. He complained of pains in his legs that I just thought was growing pains. He would sometimes run a fever with no other symptoms of being sick and then the fever would go away. He would also feel like he always had to go to the bathroom, especially after he went to bed. I gave him Singulair at 7pm before he went to bed. The biggest change we noticed in him was the signs of attention deficit. We first noticed that he kept getting out of his seat at dinner time. No matter how many times we told him to sit down he would sit down and then a little while later he would get right back up. We realized after a while that he wasn't doing it to be defient he just couldn't help himself. I asked his Kindergarten teacher if he had trouble sitting in his seat or with attention but she didn't think he was any worse than any of the other Kindergarten kids. In 1st grade, at the beginning of the year, his teacher said he had trouble keeping his attention but then by January she said he was a different kid. We usually stopped giving him Singulair in December. The same thing happened with his 2nd grade teacher. I question his allergist in the fall of 2nd grade but his allergist said Singulair wasn't the cause for his ADHD symptoms. When his 3rd grade teacher contacted us in Oct 07 with the same complaints I realized that it must be the Singulair. I looked online for Singulair side effects and came across this website. I couldn't believe it. I was so disappointed in myself for not doing it sooner but we took him off Singulair immediately. I called his allergist the next morning and questioned him for a second time and he told me that sometimes parents of kids with ADHD just look for something to blame for their childs behavior. I couldn't believe he said it to me. We made an appointment at Children's Hospital Boston to have him evaluated for ADHD just in case but couldn't get an appointment until Feb 08. When we had him evaluated he had been off Singulair for over 3 months. The neurologist said he did not have ADHD. When I asked him if he thought Singulair could have been to blame for the symptoms he was showing and he said there was "compelling evidence" that showed Singulair does cause ADHD symptoms in some children. We were happy that he did not have ADHD but were so sad that we gave him this medicine for 3 years without realizing what damage it was doing. My biggest fear now is that there may be long term damage. All his symptoms have gone away but sometimes he still seems a little out of it and I don't know if it is just his age or his personality or if it might still be some long term effect from the Singulair. He is such a sweet, loving, caring boy and I hope that I didn't do any long term damage by giving his this horrible medicine. I hope that something will be done soon to get this medicine off the market. My prayers go out to all the families who lost children on this medicine. I can't even imagine the pain you are feeling but I thank you for getting your story out and saving other children! I am thankful that I was able to get informed by this website because God knows my allergist wasn't looking out for my son! His asthma has been under control since being off Singulair and just seems like a happier child over all!
Thank you!

I took Doxy for about 2 weeks as a remedy for a bump on my eyelid. This first exposure to Doxy seemed only to cause a little skin sensitivity and burning in my fingers, no big deal.

When my eye problem didn't go away, my eye doctor prescribed Doxy for a second time a month later. This time my side effects were much different. Within a couple hours of taking my first pill I felt a bit off, I felt anxious and unsettled. I Continued on the medication for a total of five days. During this time my side effects progressively worsened. The first few days I had very abstract thoughts, and began feeling strangely claustrophobic. By day three I was beginning to feel paranoid and fearful over just simple everyday things. Day five is when it all hit the fan. I started having difficulty breathing and feeling extreme tightness in my chest. My feelings of claustrophobia had also worsened to the point where I began having panic attacks, like I was trapped inside my own body. It was at this point I made a desperate attempt to search the internet for a possible cause, in hopes it might be the Doxy medication I was on. I was somewhat relieved to find this website and read that others had similar symptoms, maybe I wasn't losing my mind. I immediately quit taking the medication, but unfortunately the symptoms didn't go away for several more days. That night I was unable to sleep, I had mild nausea, and would wake up in the middle of the night in a panic and would shake uncontrollably. Lovely huh. It gets worse. I began to feel extreme fear and paranoia like I was going to die, or lose my kids and family. I began to feel if this didn't go away, I would not be able to go on. Thank God it did, and by day eight the extreme thoughts began to subside. I continued to have the breathing difficulty and mild depression for several days after, but the worst was over. Within a month I was back to normal.

I write this as a warning to those who are taking this med and feel anything close to this... stop taking it! I am a healthy, normal, 40 year old male, that has no history of mental issues, other than a "blue" day from time to time, and within six days I was entertaining thoughts of suicide. The psychological side effects of this drug NEED to be addressed. This is very serious stuff!!!!!!! Though it may be a small percentage of people that are susceptible, for those who are, it is a deep dark hole.

this is the second time i have taken the zpack for bronchitis...first time no symptoms, this time however......i am having verrrrry dark brown/ red urine, diarrhea, headache, stomach cramping, and body sweats....i don't know if this is due to my illness or due to zpack, but i HATE these symptoms/side effects

daily headaches, waking every hour till 2 am, vision, but mostly the headaches are what are bothering me the most. This is my second time on methadone. the 1st time was 8 months start to finish with 3 years clean then a relapse. I realized that both times I had headaches. Why the headaches? I feel like I am losing it. I'm trying to be a wife, mother to 3, independent rep and so on. Am i alone?

well, i guess i am not alone. this is the second time i have been on it. i weighed the pros and cons and figured that the migraines were worse than the depression, mood swings, and the inability to compute simple math. well, i feel differently now, and i think i am going back off of it again. my sex drive is also gone, but i have had a problem with that and the depression for years, just not this bad. i feel i have yelled at my children way too much lately, cuz it is making me so crabby, and i don't think that it is worth it. after reading some of your posts, it has helped me make the decision to go off of topomax for good. i could deal with tingling, bad taste, and weight loss (the only good side effect), but not the other horrible effects.

Topamax may help some people, but for me it is poison and I've tried it twice! This second time around I tried it longer and went to higher dose. I'll just list the bad side effects that I had this time, although I had some of the same the first time. By the way, I took it for migraines. The first time a couple of years ago I was on 25 mg a day. Then, this time decided to try again since migraines were so bad thought I would give it another chance. I went from 25 mg to 100 mg a day slowly increasing as directed. The side effects started occurring right after the first couple of days, numbness in my hands, jaw area. Then sometimes numbness in my feet. Started to feel bloated in my stomach, waistband on pants a little tighter, and also noticed a little fluid retention in my fingers and ankles. I would forget a word here and there, or when typing, type the wrong word. Eventually it got so bad that I would sit there and think to myself, ok I know this is the right word but should I actually say it or type it? Friends thought I was in a bad mood when I wasn't. I would get very very quiet and I didn't want to leave the house. Thank goodness my husband was understanding. We knew it was the drug. And we knew I would stop taking it! Sometimes my back and sides would ache which is unusually for me, and I drank a lot of water. I lost my appetite completely but still did not lose weight at all like others say they do, if anything I think I gained in fluid retention. The skin on my ears started to burn and itch, then the skin on my face started to itch. I felt nauseous almost every day. I also felt like I was completely encased in cement, this is about the only way I can describe it. You just do not feel like yourself at all. You have that foggy brain feeling people mention. You know you don't feel like your normal self, but you feel so lousy you almost don't care. It's a scary feeling. This was all in one month, I figured I had given it a chance but that was it. Even with the warnings about seizures I quit taking it immediately. I would rather have migraines than have all of those side effects. Also I wonder what is it doing to your other vital organs if it can have those effects? For those who do not experience any of this, I'm glad, but I have to say very surprised.