Different places symptoms and conditions

My 18 year old daughter had a terrible allergic reaction to omnicef 2 weeks ago after a 10 day regimen. Sadly, it happened 2 weeks after my nephew had an allergic reaction to the same medicine. His situation did not end so well. He was taking the medicine for strep. The allergic reaction started with hives and got worse. After some aggressive research on my brother and sister-in-law's part, my nephew was diagnosed with an allergic reaction to omnicef followed by rheumatic fever. I should have refused the omnicef for my daughter, but who knew.
My daughter is 2 weeks into annoying hives that continue to pop up in different places. Her feet are swollen and we are very concerned. She has taken steroids, Kenelog cream, benadryl, as well as prescription strength antihistamines. Tomorrow she is going to see another doctor to find out what is going on. Cefdinir/omnicef is no longer welcome in our extended family.

Does anyone here ever had any tingling issues? I had total thyroidectomy in Feb. 2009. Felt good the first month or two and have gone down from there! Some days are good, some are bad. Never know from day to day how Im going to feel! I started out for about a month and a 1/2 on 125 levothyroxin.....then my doc lowered it to 100.......as of July 14th, Im now taking .88. The tingling Im getting is all over my body, different places, here and there. Ive had some heart rate issues for a couple of months now too and finally had my regular doc send to me see a heart doctor.
Thought maybe the tingling could be from low calcium.....it was normal, CBC was normal, ECHO was normal.....waiting on the holter test results right now. The heart doc gave me a prescription for Toprol. I told him I wasn't going to take it cuz sometimes my heart feels like its barely beating and Im afraid it will make it worse. Im glad I didn't get it! Ive read of too many side effects.
Palpitations, kinda fast heart beat with pounding.....sometimes it feels likes its barely beating! Most of this occurs when first laying down......every now and then while sitting, etc. I do not exercise.....and should but just don't find the time. I switched jobs around the time I found out I had several nodes on each side of my thyroid. I was getting tired a lot and just thought i worked too much. I went from a physical job to a sit down, 12 hour, graveyard shift. Since the surgery, Ive felt it more. Im tired of feeling like crap all the time......I was already going thru some perimenopause stuff before all of this! Before I ever found out about my thyroid, I did have real light pounding of heart when laying down and tingling every blue moon, but very mild as well.
Now with no thyroid.......and medicines with all the side effects......IM GOING NUTS!!! Right now the moodiness and tingling are whats bothering me the most. Some days Im really tired, others Im ok. My body gets hot off and on, no fever. The past 3 days my calves, feet, and ankles have started to swell........never before! Plus I get some throbs and pains in my legs and arms and under my arms here and there. I probably need a new doc and I change of medicine......but Im afraid.
For one, Ive decided to go back to a physical job........and hopefully it wont screw with my heart rate even more. Ive read up on tingling........Im guessing maybe its from all the damn stress since my calcium was normal. Does anyone here have any suggestions?????

Just want to survey everyone and ask for responses for the following 3 questions:

1. how long did you keep your Mirena and if you no longer have it, why did you have it removed?

2. how many of you had your thyroid checked? who's came back abnormal? what were the levels?

(I'm a medical student doing research on this one since I believe the levonorgestrel affects our thyroid hormone. My TSH was elevated to 5.2 which is considered "subclinical HYPOthyroidism". This was mid cycle when my natural progesterone AND synthetic progestin were cumulatively high. When I had it rechecked 6 weeks later (around my period when any natural progesterone level is gone) it was normalized at 1.5. So I think that the P+P screws up our thyroid and can throw us into a high TSH and "hypothyroid state". The opposite effect may be true during menstruation and we can become HYPERthyroid for a few days... hence the really bad anxiety?!)

3. where is everyone from? perhaps we can have support group meetings?

I share the scare - I developed a bacterial infection after surgery and had an allergic reaction to first two antibiotics so was given Avelox. About an hour after the 1st dose my eyes became bloodshot, my joints ached like I had the flu or severe arthritis and I started having jolts of pain in different places, legs, groin, neck. I became disoriented and developed tiny blisters on bottom of feet, behind knees, on neck they faded, and at base of my fingers. The second dose caused severe joint and neck pain, disoriented feeling and again blisters. My doctor had me break the pills in half to take twice a day with benadryl. I also took large dose of Ibuprofen an hour after taking Avelox. That helped lessen severity of side effects. Final straw was the fifth dose - took before sleeping, woke at 4am and could not move from neck pain. My husband pulled me up so I could use the bathroom with me crying from pain. Sitting on the commode, I threw up and started to pass out. I managed to get downstairs and take an 800 mg. Ibuprofen and passed out for about 30 seconds. We went to ER. The attending physician decided I was having a muscle spasm and dismissed my fear it was the drug. They gave me a muscle relaxer and sent me home. I slept like the dead. My doctor called me that afternoon and told me to stop the Avelox immediately. You can imagine after missing 5 weeks of work for surgery, then having to miss three days last week and who knows this week how bummed I am. I am 46, have a wonderful family (a husband and 4 kids), a job I love, and life is good. I hope my body can recover soon as I am not used to inactivity. I cannot seem to function normally anymore.

I stopped taking Yasmin about a week and a half ago. I assumed it was the cause of two anxiety attacks I had, constant lump/tightness, weird tingling feelings in my throat and chest and overall body aches and ill-feeling. I haven't felt anything severe since stopping except for a dizzy spell when my period came. I'm wondering if anyone has any idea as to how long these side effects could go away. Off and on, I still get a tightness/heaviness in my chest, and although I don't get a lump in my throat anymore, it's like a numbness and constriction in different places in my neck, and sometimes a clogged up feeling in my ears. A friend told me it takes three months for the pill to leave your system, and I have a Doctor appointment this Friday, but I'm just hoping to hear any advice/suggestions. I had an EKG, cat scan and chest x-ray and everything looks fine in my body. It's just really scary and hard to shake the worry that something worse may be wrong with me. Reassurance would be much appreciated!

Earlier this summer, I developed a case of shingles. It went away, but about a week ago a similar rash broke out. I thought that it was a second bout of shingles, but my doctor assured me that it would be impossible to contract the disease on different parts of my body. Because I am not home with my ordinary doctor, I had to see another doctor, who was unsure of what the rash could be, but nevertheless prescribed with with 50mg of Prednisone daily. I took my first dose today, and am reluctant to continue. I don't want to be a victim of any of the side effects, but am unsure as to whether there is another way to go about getting rid of the rash. Any advice that could be given so as to not have to continue with the Prednisone would be great. I don't want the rapid weight gain, depression, mood swings, etc.

I've been on simvastatins for about 2 years after TIAs. I'm 56. I had two small Strokes about year ago despite being on simvastatins. Had brain scan which showed two small areas of scarring and carotid artery scan- arteries fine. Started experiencing dizziness last year and GP diagnosed vertigo and gave me seasickness pills which didn't do much good. Since then I've experienced headaches which last for weeks, increasing fatigue (now struggle to get out of bed in morning) muscle pain which is getting really bad and sore feet (?). Increasing memory loss, confusion, lack of concentration, eye problems (when I first wake in morning my vision is blurred for ab out 30 minutes or so. I've been worried i mmay be developing Alzheimers. I've also piled on weight and the texture of my hair has changed - it has become very soft and silky and become thinner - normally my hair is very thick. Also I've had two perms in last 6 months which won't hold curl - been having perms for years and never had this problem. I've had several blood tests including for under-active thyroid and they have all been clear. I've been really worried about all these problems and did some research and came up with this site. I am beginning to think my problems stemm from taking 40mg Simvastatins so am going to stop them and book appointment with GP. Any comments/advice would be appreciated.

I was prescribed Simvastatin 40mg four weeks ago and had horrendous side effects almost immediately eg deep depression, diarrhea, bad stomach aches and night cramps in my legs. Last week my doctor prescribed Lipitor 10mg and I feel no better in fact probably worse. The worst side effect for me is the stomach aches and constant diarrhea and complete lack of appetite. There can be absolutely nothing in my stomach any more. Does anyone else have these symptoms? After reading peoples experiences on here I feel I should stop taking this medication immediately!

Karen

For the last 2 yrs I had a horrendous cough that plagued me night & day. My Dr. didn't know what was causing the cough, couldn't give me any cough medicine to alleviate the condition. In addition to coughing, I would lose my voice. I went to an ENT specialist. She found me to have pre-polyps on my vocal chords, diagnosed me with 'vocal chord dysfunction' & told me surgery would be useless as the pre-polyps would reappear. This last June, I had a bout with bronchitis, severe enough to seek medical aid from the Emergency room Dr.'s. While there, the Dr. treating me asked about my cough. After listening to my list of aggravations, he asked if my Primary Dr. had told me that 'coughing' is a side effect of Lipitor. NO! I hadn't been told that!! --But, I QUIT taking Lipitor that day, haven't taken it since & though I still cough, somewhat, it's NOTHING compared to what I'd been suffering--for two years!!..

Hello ladies. I'm a 19 year old college student and I was having problems with fainting and it was suggested that I get the IUD put in because some women start to faint while taking the pill.

I've had it since December 2007, and I absolutely hate it. I have extreme mood swings, one minute I'm happy and the next I'm not. I feel like Ive come into a deep depression that I cant get rid of. I have extreme pain in my right ovary area, my back is constantly hurting, I probably have a headache more than not, I cant sleep at night, and I have a horrible odor that can be smelled through my clothing.

I'm so angry at the doctor who put it in. He told me nothing of these symptoms and even told me that women loved the mirena. I went online and it seems that on every forum women are hating it. I almost feel like marching in and giving him a dosage of the pain I've been going through these past few months.

I would NOT recommend the Mirena to anyone. It just simply is NOT worth it. But, does anyone know of what we can do for the symptoms? I want the IUD out, but my mother paid for it out of her own salary, so I feel obligated. Thanks for all the help ladies!

has anyone experienced twitching with the Wellbutrin

I have been taking Remicade for years. At first it was getting the job done. I started having severe pain that seemed to migrate to different places in my body. Sometimes the bottom of my feet would get so tender I could barely walk. My finger would bend while sleeping and I could not straighten it for days and it would hurt real bad. Knees and ankles would do the same things and then move onto other parts of my body. I thought it was more of a tendon problem, but the pain could also be in any random spots on my body, like shins or maybe a random place on my back. My wrists seem to be a favorite place too. The pain can set in fast and sometimes leave fast. Prednisone is the only thing that seems to help these symptoms. I have been taking 5mg a day for years and when I am having problems that is not enough. I went to a Rheumatologist and he says it is not the Remicade but another antimmune problem. My family doctor thinks it is a side affect of the Remicade and I tend to agree with him. I am going to have my damaged pouch removed in hopes of getting off all medications. I have been living with a colostomy bag for the past three years and it is the least of my problems. Before that I had all my large intestines removed and a pouch which worked well for approx 15 years. I am one of the early people to receive that kind of surgery. I can only pray for all of you that are suffering and lend hopeful advise to your journey.

My 16 yr old son was prescribed this drug 9 days ago for a severe sinus infection. He came home from school yesterday with several small raised welts on the creases of his arms. I took him immediately back to his Dr who said he was having an allergic reaction, prescribed steroids and said it would get worse before it got better. Within a few hours his elbows had visible knots in different places, then his knees did the same thing, then his feet started getting knots on the bottom and he had different whelps breaking out on his torso and lower stomach. We immediately took him to the ER last night when he said his tongue "felt funny". The attending immediately diagnosed an acute severe allergic reaction and gave him a huge steroid and Benadryl dose. He released him because the itching had stopped and his tongue no longer felt funny. Last night he kept drenching himself with sweat during sleep. Today so far some of the whelps are gone but he has some pretty severe joint involvement with visible knots around the elbow and knees and feet.

I have been taking 200 mg of lamictal for about 3 years. I am on no other medication. I too have the dry hacking cough that never ever goes away. All day and all night. Dry hacking cough that sometimes leads to gagging. It is terrible. I have had chest xrays, breathing tests and no one can find a reason for the cough. It started about the same time I started this medication and I believe it is the cause. I also experience pain in muscles, it's a roving pain that seems to show up in different places daily, sometimes muscle spasms. My stomach is always nauseated. Very little short term memory, runny nose all the time, constant feeling of having a cold, blurry vision, sensitive to light, little red bumps that appear on my skin, itch, then when they disappear, a scar is left like a cigarette burn. I am reducing the amount of lamictal I take as of this week. I am now only taking 175 mg and will for another week then go down to 150 mg. I am hoping some of these side effects will go away, if not I have to get off of it altogether. It's funny, because I didn't have all these side effects when I first started taking it. Seems the longer I take it the worse it gets. Just can't handle it anymore. wf

Rash ???

I am under Treatment for Bi Polar using Lamictal-
200 mg in morning and 200mg at night before I go to bed. (totally 400 /day),
300 mg of trileptol at night and
100 mg of Zoloft in the morning.
I have taken the Lamictal for about 5 mos ramping up steadily( 25 mg,50 mg etc) as per directions to prevent the infamous rash. I used to take 1200 mg of treleptal and depakote before that.

Rash? I don't know what you call it. I get the feeling of a bee sting sensation periodically on my neck and collarbone area. To say the least, it itches and I have redness ( i don't know if this is from the scratching or a side effect)
Ouch!!! ( I have it now)I use ice to soothe it but it seems to progressively get more annoying. The little stings occur every 2 minute or so, isolated in a 2-3" square area, they will occur in different places at different epsiodes that occur about once every 48 hours. but always on the neck /collarbone region The Psychiatrist says it is not the rash that everyone talks about. When I was on Lithium 22 years of 1500 mg starting in 1977, I remember a similar rash at times.
I remember a rash that itched on my stomach about a month ago - I figured it was just a bug bite.
( I once attended a BPSA meeting and declared that lamectal is just lithium in disquise)

feed back, experiences and comments welcome

I was placed on Doxycylcine for Epididymitis, which is an inflammation or infection of the epididymis, a convoluted duct that lies on the posterior surface of the testicle. I took Doxycycline for one week. 100 mg twice daily. I ate a meal with every pill. I did not experience nausea or vomiting like I see many did. I did however have fatigue, loss of appetite, diarreha, increased anxiety (I have anxiety and panic attacks), depression, agitation, pains shooting down the back of my quadriceps, abdominal pain and some acid reflux type symptoms towards the 4 th day of taking this drug. It has been a little over a week since I finsihed this drug and I am still having pains down my right leg in in different places, when I sit or lay down is when it is most painful. The doctor can only describe it as a possible slipped disc. How? I was bed ridden for a week! The pain in my leg is not severe but very annoying! Like others here my doctor says that he does not see how Doxcycline could cause this. I will never take this drug again! I will from now on request Zithromax. I have had to use Zithromax quite a few times in my life and have had no problems with it.

I never had any swelling of the hands, feet, legs, arms, etc. My face swelled but I gained the weight everywhere. I've lost 31 1/2 lbs. so far being off of pred. From what I've read, alot of people swell in different places. I'm surprised too that it took a year to swell in your legs and feet. Usually it's really soon after u start taking pred. Hang in there.

I've been on Wellbutrin XL for about 9 weeks now and I originally started out on 150mg a day and now my dose has been upped to 300mg a day. I was put on wellbutrin to see if it would help me quit smoking and also for depression. Previously I was on Zoloft and Buspar together. (I won't even get into the side effects with those two)

1. After about a week on 150 mg I experienced sharp and short headache pains in different places but that has since gone away.

2. I am on a computer at work for 8 hours a day and sometimes it seems to take me a few seconds to catch up with the words/numbers I'm typing and at times It seems like I'm re-arranging letters or numbers around backwards without really noticing it unless I check it as I type. Hopefully this will go away it seems to be slowly disappearing.

3. I've also noticed an increased sensitivity to light.

4. I've also felt very energetic, pulse racing and keep thinking my heart is going to jump out of my chest and sometimes there is some slight discomfort.

5. The oddest thing to happen and this only started happening 4 days ago is that I've started having heart burn symptoms and I've never really even had heartburn before maybe once or twice in my life. I think it has to be the wellbutrin but I'm not sure if thats a HUGE side effect or happens to most people but I did see a couple of people mention that in the previous posts. It's really starting to make me nervous and I've been taking tums etc. like crazy and I hope this side effect goes away as soon as possible.

6. An additional note to line 5 I've also experienced constipation.

7. I did experience a decrease in appetite for a couple of weeks but that seems to have stopped. I haven't noticed any weight loss or weight gain at all. My weight has stayed the same for the most part give or take a couple of pounds.

8. Sex Drive: orgasms are more intense

9. Dry mouth: that has stopped completely

10. I do drink alcohol and smoke regularly and due to the risks I was told not to suddenly stop drinking etc. due to reverse side effects of the wellbutrin and what could happen and I'm still drinking here and there so maybe thats causing the heart burn along with the wellbutrin; I'm not completely sure.

I have not experienced any joint pain, loss of hearing or ringing in the ears, hives, increase in acne or seizures since I've been on wellbutrin. The only side effect I'm having trouble dealing with is the Heart Burn and it has to be the Wellbutrin since I've never experienced it really before or I could just be getting older. (27) Either way it is has been almost intolerable at times.

All in all it's not a bad drug so far and hopefully as time goes on the side effects will lesson.

If you have experienced heart burn as a side effect feel free to respond I'm very curious to see how common it is.

This site has really given me some insight about this medication.

Best Regards

I did not see anyone posting with my problems so I don't know if they are side effects. I have been on Yasmin for 21 months taking the active pills only the entire time. I am taking it because I suffer from menorrhagea (unbearable pain during periods) and was unable to even leave the couch or bed for 2-3 days a month. Pain medication did not work and I bled so heavily that I had to change my super tampon every half hour. Sorry to be graphic but I want to make it clear that I am taking this for pain and as an alternative to surgery. Yasmin really helped at first. I had breast tenderness but my gyno told me to take evening primrose oil and it took care of that. My debilitating cramps were gone and I got my life back. My husband was so happy because now we could actually do things without having to consult the calendar. I have only taken the active pills this entire time so I should almost never have a period but I have been getting intense breakthrough bleeding lately. I used to get it only every 6-8 weeks or less but now it's about every two weeks or more often and I have terrible cramps, headaches and abdominal swelling prior to it. At least one day is heavy bleeding. This just started recently. The blood used to be really dark but now it is like my period used to be just not as heavy. I also have developed a sensitivity to dairy products (gas, bloating, diarrhea), headaches, crying jags, short temper, dark patches on my face, and my feet hurt. It seems like I just started to have side effects in the last four months. I also get quick sharp stabbing pains that make me gasp at different places on my body; sometimes on my thigh, sometimes my arm, etc. Has anyone who has been on Yasmin for *over a year* started to have side effects after having none? Breakthrough bleeding getting increasingly worse? Stabbing pains? Please let me know. Also, does anyone know of another BCP that stops your period? I am desperate because I really like this pill and I am terrified of getting an operation. I had suspected that my ailments were related to taking it and found this board last night. Most posters seem to be new users and all BCP's made me sick at first so that's why I'm asking for the experiences of those who have taken it for at least a year. Thank you.

i have been taking it for 3 days. My first dose was in the hospital as an I.V. Then from the pharmacey. I have heat in certain parts of my body at different times. Like sides of arms(hot to the touch like a burn).
Different places at different times. Really weak and confused. Haven't sleep for 3 days I will not take another pill would rather die. Really. That's what it feels like . It is horrible . Heartburn non stop. Just pain everywhere. Bones and muscles are very sore to the touch .Gosh this is scary