Agony symptoms and conditions

My husband had a cyst on his face. His primary doctor gave him Bactrim. The first week was fine, but then he got really sick and had to to go the ER. He was doubled over in agony, screaming, nausea. He was admitted. They scoped his stomach, CAT scan, X-rays. He got better ('cause he stopped it while in the hospital). They discharged him with a script for MORE Bactrim. He took it and ended up back in the hospital!

He has thrown it all out. He had chills, aches, he moved like a 90 year old man. He was very sick to his stomach with agonizing stomach and abdominal pain. He's still moving really slow and feels terrible. He says he can't taste anything sweet, either. We hope that resolves soon.

Hi Guys

I am taking Yasmin since May 2006. I have been suffering from chronic daily headaches since March 2006 and wondered if Yasmin could be a factor in this? For my headaches I have tried so many different things and not been successful and hadn't looked at the possibility that Yasmin could be a problem until I started to google it. What do you guys think? Could Yasmin be adding to my problem of chronic daily headaches? Cos I have the headaches all the time.

Any responses would be greatly appreciated!

Regards
Warda

My son became soo aggressive 3 days after starting Singulair, that he was almost banned from soccer for life because of attacking another player on the field. It resembled what I had heard of 'roid rage'. When I questioned the doctor immediately, was told there was no connection. After months of the aggression, then came depression and self mutilation. My 15 yr old was secretly burning himself to 'punish' himself for things he done wrong or "disappointing" those around him. He now has permanent scars all over his arms from these burns. The depression took to drug abuse and my A student fell to an F student in 6 weeks. He completely lost his will to live and thrive. After 4 months of hell, the dr informed us that the FDA just warned physicians of this side effect. Im furious now that I read through the court documents and find that the drug company knew this all along. I know I am a luckier parent than some whose children committed suicide, but still wish that the FDA would get off their BUTTS and do something to take this drug off the market. I was told by a rep at the FDA that Merck will not take it off the shelf until they're made to because even if they had to pay parents millions for their child's suicide, they would still be pocketing more profit than our children's lives are worth in the court system. Not sure WHY we even HAVE an FDA, they won't do anything to protect us from these money hungry drug companies. A YEAR to do an 'INVESTIGATION" are you kidding me? If the CEO of Merck had to bury his child, it would come off the shelf THAT DAY.

ok I posted a few months ago about my experience with this pill. Well Im now back to say it is starting not to work. My period started about 8 days ago and has not stopped but get this I am not taking the brown pills so I should not be getting a period @ all. Go figure. Also my breast which were large before I started this pill is HUGER now I take pictures from the neck up cuz I l look like Im swollen. I am now taking two pills a day to stop the bleeding so we will see but when this pack is gone im off these for good. I have had horrible cramps as if i was not on the pill. I can say the bleeding was considerably light considering I cannot leave out side my house when Im on my period usually. But the reason for me starting the pill was to not have periods at all!!!

didn't have Mirena, but another kind of IUC or IUD whatever you want to call it. I sure hope young women know they could die. Sorry to see these things back on the market. At age 21 I had complications, the device embedded in my uterus and became infected. No one wanted to admit it was the iud. The infection turned into acute peritonitis which is usually fatal. I did live, but had to have a complete hysterectomy. A bit extreme for a 21 year old. Spent 3 months in agony in the hospital. Took 2 years to recover. I had all the side effects associated with premature menopause - premature wrinkling, loss of interest in sex, not to mention no more kids for me.
I later did some research to find out that stones were inserted into camels to prevent pregnancy during long trips. The camels died screaming in agony in the desert from the stones. It works about the same on women.

I cannot believe I did not make the connection sooner, I went on jasmine for 6 months and was incredibly weepy and so emotional. I had pains in both breasts for about 2 weeks of every month, the pain was unbearable so much so that going over a speed bump was pure agony, I ended up having a Mammogram as I was convinced I had Breast cancer, (there is a very strong history in my family), so that worry coupled with my emotions being all over the place I really was not in a good state of mental health. Not to mention the spotting and Migraines,and my poor new husband dealing with awful mood swings, I even brake down uncontrollably in the Doctors. I had no Idea all these other people have experienced similar symptoms. It is outrageous these are being given to Women. How have these not been removed from the market?

Started Simvastatin 20mg Jan. 08, just quit June 16th. I 've had all the problems the rest of you have had, arm, chest pain, thought I was having a heart attack for about a month, eye problems,no sex drive, memory loss, weird thoughts, stomach problems, so tired I could barely move, just could'nt wake up. Since I've been off this stuff I'm up one day and down another. I can see some progress, but it seems slow. Does anyone know how long it takes to get this stuff out of your system? Talked to a friend of mine who was on a statin, he quit , and told me it took him 6 months before he felt right. It does'nt seem to go away over night. Anyone else feel this way?

Hi all,
I have spent the last 2 days on the Internet reading about Mirena; as a matter of fact, I had mine removed 2 days ago. For the last 10 months, my life has been horrible. I had the Mirena inserted in November of 2007, I was also coming out of a divorce, so I (and my doctor) was attributing my extreme depression, anxiety attacks to it. I started noticing that my hair was falling out and it just kept getting worse and worse. I went to see my doctor again and she said I had anemia (I was having very heavy periods and bleeding through my periods). Doctor said anemia causes hair loss. I went through different tests, saw a dermatologist, I always mentioned I had the Mirena, but no one seem to relate that to anything. I actually went on the Mirena site a couple of times, but the side effects listed there were very mild so I discarded the thought that the Mirena was causing my depression and my hair loss. There is no mention whatsoever about hair loss. Months went by, I kept seeing different doctors since my hair loss was getting worse and worse, my once beautiful, thick hair had become extremely thin, I have two holes on my scalp. I continued to bleed heavy and my ob/gyn said to give it some more time. My life was a complete mess, going to work was a struggle, dealing with my kids was a struggle, some days I would just lay in bed and cried for hours, I started to believe that my life had no purpose or reason. I was truly in agony, I am sure those of you who have gone through this know exactly what I mean. Anyway, I can't believe in all this months it never occurred to me to google mirena and hair loss....or mirena and suicidal thoughts, etc., etc. I thank you all for sharing your stories and I hope we can figure out a way to let all of those mirena users out there suffering that the answer to their agony is simply to have the Mirena removed. I look forward to my new life, new hair. It has been 2 days and I don't know if it is a state of mind, but I feel so much better already.
Thx
Jessica M.

Checking in again. Been off the lipitor 3 weeks now. It feels good to feel better. I feel my old self coming back. I laugh sometimes. HOORAH!!! Pain in my legs 50% gone. Hips still troubling. Legs are still weak. I don't know if its from not using them much over the past 8 mo. or the poison lipitor. Still sapping life forces from my body. My life is a wreck . I can tell life is starting to get better. The only thing different, is off the lipitor. Lets get this stuff off the market. It is debilitating, painful, causes depression, to the point you are thought of as lazy, unmotivated. The pain and ache is all you can muster to deal with on a day to day basis. it is indescribable agony. I want to kick something. For the months that I have lost of happiness. Something has got to be done. There was a move awhile back to sell this stuff over the counter. What will they think of next. I am just thankful that I am feeling better. moonman

Checking in again. Been off the lipitor 3 weeks now. It feels good to feel better. I feel my old self coming back. I laugh sometimes. HOORAH!!! Pain in my legs 50% gone. Hips still troubling. Legs are still weak. I don't know if its from not using them much over the past 8 mo. or the poison lipitor. Still sapping life forces from my body. My life is a wreck . I can tell life is starting to get better. The only thing different, is off the lipitor. Lets get this stuff off the market. It is debilitating, painful, causes depression, to the point you are thought of as lazy, unmotivated. The pain and ache is all you can muster to deal with on a day to day basis. it is indescribable agony. I want to kick something. For the months that I have lost of happiness. Something has got to be done. There was a move awhile back to sell this stuff over the counter. What will they think of next. I am just thankful that I am feeling better. moonman

Just an update about the class action suit discussed previously, and Aamaya had provided us with the Florida attorney, Justin Wikin: I got a letter in the mail yesterday stating that they would not be pursuing suit against them. They said that they deal mainly with wrongful death cases and it does not mean that the case does not have merit, just that it is not their specialty. I will be doing some research here locally in Ohio to see if I can locate a practice to pursue this. If anyone comes up with something, please let us all know.

Trying to figure out if my back pain is like others. The pain is in the lower left side and groin area of both hips. I have trouble reaching my feet to put on shoes and socks. Ive been on Lipitor 20 for about 5 years and have never had a problem before. This started about 6 months ago and even with heat and stretching it seems to get worse. It hurts when I stand for any length of time. It hurts to walk or run. It hurts very badly if I try to straddle something like an ATV or a horse. When I sleep (if I can) I sometimes have to put a pillow between my legs and lay on my side because it hurts a lot to bring my legs together. Feel free to email me at ******

Alright. After observing my daughter for two full weeks after discontinuing Singulair, I have decided to share our story.

Our daughter started taking Singulair last August (2007) to relieve her allergy symptoms. I'd like to add she is an identical twin, whose sister did not need to take the medication, for she had mild allergy symptoms that were easily relieved by taking Allegra. So we clearly have a side-by-side case study where one twin took the Singulair and the other did not. About two weeks later we noticed changes in her behavior and thought it was due to the new school routine and changes, etc. Then she started not eating, and when she did eat, she ate very little. Both girls are in a select soccer league are physically active 4-5 times a week.

Long story short - she stopped eating, lost weight, stopped growing and is now 2.5 inches shorter and 15 lbs. lighter than her identical twin. They are fifth graders, I might add, so 15 lbs is ALOT of weight at their age. She was withdrawn, known to have deep depressive episodes, reacted adversely to everything and, in general, wasn't acting herself since last August. She was not enjoying life at all.

She is usually a quick-witted child, one with a sunny disposition and who interacts with others very well. She is joy packaged in a colorful bottle, ready to share her thoughts with you.

We took her to her pediatrician, a nutritionist, a psychologist and all said she was clearly depressed and that is what led to her changes in eating. No kidding, I thought. But why? What has happened that could have changed her so drastically?

I had never felt so far away from my child as I had with her during this time period. We are a close family and we pride ourselves on being able to freely express how we feel.

My dear mother-in-law saw that the FDA was probing the side-effects of Singulair with children and she mentioned it to me, because she knew that is what my daughter was taking was taking. I never thought about the connection, because I take Singulair. I will add I also take an antidepressant and have made an appointment with my doctor to discuss all of this.

After talking with our pharmacist and getting an exact date as to when she started taking it, I called her pediatrician and discussed it with him. We had not been to him since October, because we took her to everyone else (psychologist, etc), so he had not known exactly what was going on with her mental health. He did, however write in his notes (and told me when I called), "Discontinue Singulair if symptoms persist." Hmmmm. Exactly why I wasn't told this from the beginning, I don't know and am very bothered knowing he wrote that on her chart.

Well, after taking her off it two weeks ago she is now back to her happy, connecting and eating self. People (her father, twin, and I included) noticed a change in three days from stopping use of Singulair.

She has changed IMMENSELY since getting off the Singulair that it has been easy to pinpoint her taking that medication as the reason she has been absolutely miserable for the past SEVEN MONTHS. I thank God it wasn't longer and that she didn't suffer any longer than she already did, but it was a true hell to watch her go through what she did and to watch her decline and to not know (professionals included) what to do. Words diminish how we felt and how we feel now after having her back.

So there you have a side-by-side comparison. One identical twin thrived while NOT taking Singulair and the twin who did take it suffered terribly, physically and mentally, while she was taking it.

The allergy relief she experienced was clearly not worth the internal suffering she endured while taking Singulair. I wish we could turn back time and give her those seven months back.

I am 28 and just suffered a pulmonary embolism (P.E.), very unusual for someone my age. I went into the hospital three times before they found it. I had severe pain in my upper left back, shoulder blade and neck when I first went in and the doc told me I was just having muscle spasms...I played Division I basketball for 4 years and am now a coach...I told him it wasn't a muscle spasm, but he sent me home with Ibuprofin....The second time I went in, I had worse pain two days later and told him it wasn't going away that something was really wrong. They did lung ex-rays, MRI and didn't find anything. They did no ultrasound or CT...hmmm. The third time I went in, I had terrible pain in my right side as though someone was stabbing me in the side. Couldn't catch my breath and was in absolute agony.
Finally they did a CT and ultrasound and found it at 6:30am on a Monday evening. I am very lucky that the third time I was admitted into the ER after a week, that they did a CT that found the P.E. I very easily could have died.

I was on Yasmin birth control for a year, unusual for a clot to occur after taking birth control for that amount of time, so they are not sure if that caused it and are still uncertain of the cause for my P.E. Maybe a blood disorder that I have not yet been tested for.

At the beginning of my warfarin treatment, I didn't experience headaches. Now though, after about 3-4 weeks...I am experiencing headaches in the middle of my forehead that are driving me crazy. I'm wondering if it is stress from all that I have gone through...an extremely painful experience...or a side effect of the drug.

Also, pain in my legs have been a problem. They feel heavy, like carrying around lead and I don't feel like I have much energy. I don't have much of an appetite anymore either. I have always been extremely active, stay at a healthy weight and have wanted to eat meals! Not so much anymore.

I'm not a smoker, and eat healthy foods...This is all very uncharacteristic for me and I'm extremely frustrated. I understand that it will take a while for me to recover from all of this, and inpatience with the matter could be a problem causing stress.

If you have any feedback, please let me know.

DISASTER! WITHIN 45 DAYS AFTER 4 MONTH SHOT I HAD LOST ALL UPPER BODY STRENGTH, QUIT GOLF . PRE-LUPRON I WALKSED 2-4 MILES EVERY DAY, AFTER THE 2ND SHOT , I COULDN'T WALK 100 YARDS, WAS IN 24 HR., AGONY FROM LEG PAIN, DEVELOPED NEUROPATHY. SIMPLY, IT TURNED A VIGOROUS 83 YR OLD INTO A FEEBLE OLD MAN IN 5 MONTHS.

I had Mirena inserted in Feb. 2007 and it was the most painful experience of my lif (and I have 2 children). I cramped and bled for weeks. All of which I was told was normal. I would have sharp pains that would come and go as well. On or about December 17, 2007 I was having terrible pains and became nauseated and was vomiting uncontrollably. I told my husband something was wrong and that I needed to go to the hospital. As he was trying to get the kids ready to bring me to the hospital I fell on the floor in pain and could not walk. My husband called the ambulance to have them bring me to the hospital. When I got there they thought I had a stomach virus or a ruptured appendix. After completing an MRI they found that the MIRENA was lodged in my fallopian tube and I needed to have emergency surgery to have it removed. I had to wait in agony and pain until the next day for them to perform the surgery and I am still recovering. DO NOT GET MIRENA!!

We need to file a class action suit to get this product off the market. It is harmful and they lie and say there is a less than .1% chance of this happening which just isn't true.

I was part of a class action lawsuit that was about the price not the side effects. I got a small check as I just had a so-pay.
Anyway, I have to reiterate that LUPRON takes about 1 year to leave your system. I had a huge boil where the injection site was. (i had 3 shots, 3 weeks apart)
My tiny fibroid was not my problem. I had HEAVY, LONG (10 day) periods, the worst cramps ever, I was gaining weight although I rode my bike 10-15 miles a day, and swam 5 miles per week. I had a balloon ablation first, then the Lupron for another surgery that did not happen due to my uterus shrunk too much.
I then went to a fertility/endocrinologist specialist. He asked if I had my thyroid tested by my OBGYN. I said "no".
That was my problem! All that agony for 2 years and all I needed was a $20.00 blood test.LUPRON SUCKS...give it to your doctor~

I was prescribed Cipro for a UTI on 1/25/08. I took 500 mg for 7 days. About day four I began to experience intermittent "little pains" in my hands and feet. I thought it could be a side effect of Cipro but no big deal and would subside when I finished the prescription. Boy was I wrong. It has been two months and every week that goes by I feel worse. I have pain and mild cramping in my arms, hands, legs and feet on and off all day. The muscles in my neck and the back of my head tighten up and I get very lightheaded. When I get up in the morning I am extremely stiff and do not feel like myself most of the time. I have read many comments by others who have used this drug on several websites and I am quite worried at this point. Can I expect these symptoms to gradually subside or am I on the road to becoming an invalid? Sorry to sound dramatic but this is very upsetting. Has anyone found anything to help with these sort of symptoms or does anyone have any suggestions? Thanks.

I was on Prednisone for a year and weened myself off because of the side effects.I'm back on it now and can't wait to be off again.Not that i felt that much better off of it.They started giving it to me through my i.v. in the hospital about 2 weeks ago.I was admitted for a Crohn's Colitis flare up and dehydration.The first 3 days were ok but then i felt the Prednisone kick in.It wasn't that bad until i left the hospital and started 40 mgs by mouth.I couldnt really sleep at all.Really bad panic attacks.Crazy dreams, hearing voices.I'd wake up every 20 min. dripping with sweat.I'd panic all day and night.Now I'm being weened off and am taking 20 mgs.I'm really weak.Can hardly type this.Its hard to walk.My arms and legs feel so weird.I'm having a really hard time concentrating.I feel like I'm on drugs all the time.Really dizzy,every things funny looking.Its like a really bad panic attack that never goes away.I have 2 more days then I'm down to 10mgs.Then another 7 days then I'm off.Hopefully this will all pass and i can be normal again.I can't live like this.I don't even know if any of this is making sense.I hope all is well with everyone of you and will keep you in my prayers.Hopefully we'll all be normal again soon.God bless,Carl

I'm a 47 year old male and have been on 20Mg Daily Lipitor for about 4 years. Everything was mostly fine until about 1 year ago when I started experiencing severe hip and groin pain. I played hockey regularly up until that time and assumed the problem was a hockey related injury, though never remember any specific incident that may have been directly responsible. I told my doctor I thought it was a sports hernia because the symptoms and suspected cause held a close resemblance. X-Rays, MRI and Bone Scans were all negative. Physical Therapy was a useless waste of money. I was in agony for over a year and barely able to walk some days. Could no longer participate in hockey or other sports. Even coaching youth sports was a challenge due to the pain that greatly limited my mobility. The maddening part of it all was the doctor's had no explanation and just wanted me to continue with Physical Therapy. My wife casually suggested to me that maybe it was the Lipitor as she had heard some recent news on TV related to Lipitor and muscle pain. I told her she was being ridiculous and that's when I started to do some internet research and came across this site. It's all starting to add up. I've been off Lipitor for a week and the pain on my left hip is almost completely gone while the pain on the right side has shown significant improvement. While I am seriously happy that I think I have found the cause of my pain, I am incredibly angry that not a single doctor (I saw a total of 3) even suggested the possibility that the problem might be the Lipitor. They all new I was taking it. I know the drug has had highly positive affect on most people and saves lives but I feel that I've lost a year of my life to it.

I've been experiencing severe stomach pains (not period pains) for the last six months. Symptoms are very similar to that of an ulcer (pain after eating, severe heartburn) except the doctors can't find anything wrong with me. Every day I'm in agony. I started taking Yasmin 2.5 years ago and it's been good for me (other pills have made me depressed and gain weight, daily period pains). I was advised to take 3 packs back-to-back then a 7 day break.

Could all this be caused by Yasmin? If so can anyone suggest a suitable alternative contraception?

I took Levaquin 500 mg for 10 days for pneumonia starting Jan 23, 2008. It got rid of the pneumonia but after about a week being on them I ached all over but especially in my biceps, moving was agony. My doctor said I must now have a virus but I've never had a virus that made my biceps so painful. Yesterday my left knee swelled up twice its size, today after being off it for 18 hours it is still just as big. Sleep is impossible, everything hurts and feel wired. I've been off the Levaquin for five days now and symptoms are still progressing. Was going for a battery of tests today, then last night my daughter who is an RN found this site and said there is your problem. Don't know what to do. Any suggestions?

I had bacterial pneumonia a few weeks ago they gave me Levaquin as well, After the hospital I notice some pain in my left arm. A week later I was unable to straighten my arm now the pain has moved up to my neck and back and is slowly reaching my right shoulder. It seems that though you ask doctors question you never get answers and yes its true about this pain I have been in agony for almost a month now and can not find any type of relief. I was treated with a 7 day regimen of medication and I don't know what is worst the pneumonia or the pain. If there is any where to find relief as a natural source please post it

Thank you

I don't know what to do, I have been on Levaquin (750 mg) for approx. 8 days now, I have 6 more days to go. I was prescibed this drug due to being diagonosed with MRSA. However the infection has gone away, I began to have extreme pain in my both knees. Sleeping has been difficult as well waking up with night sweats. I will bare the pain for the 6 remaining days. But if the pain tends to get worse, I will need to consult my physician

I was on Celexa for about 5 weeks for panic attacks and anxiety but wasn't getting much better. My doctor switched me to Zoloft, I was on it about 10 days but I decided to discontinue it yesterday because it was causing extreme drowsiness, horrific headaches, weird crying spouts, and more anxiousness. Today, the first day being off Zoloft is harsh, I was in bed half the day and I feel like I'm in a dream and the headache is still there. Although , its about 630pm now and I feel a little better than earlier but not much. Hopefully tomorrow will be better? I'm also on Ativan.