Suffering symptoms and conditions

that medicine has killed me ,i have been taking doxycycline from last 6 months and since 2 months i start having severe joint paints thou i started feeling little pain when i started that medicine but i didn't pay attention but now i feel my self very old my whole body hurts and i m only 25 but i feel like killing myself ...my each part of the body hurts ,i stop taking doxy from last one week now i m taking Motrin to get rid of my body pain i don't know how long it will take for me to recover ,even my throats hurt everything of mine gives me pain ,i m very depressed i wish i get over with my body pain soon :(

My 12 year old son had a lactose intolerance and because he loved dairy - especially skim milk, mac and cheese, ice cream - we decided to help him with the intolerance side effects of diarrhea, cramps, gas - and try the store brand of lactaid. The ingredients were identical to the brand name. the pills & worked great for about 3 weeks. This past week, he had horrible stomach pains, diarrhea again and nausea, so bad he had to miss school. He had an appetite, no fever, but was assaulted with the side effects from taking the lactaid pills. I thought I was helping him, yet only the reverse! I am grateful to have come across this web site and shared blogs. Now I know how to solve my son's problems that caused so much suffering. In addition to the stomach pains, diarrhea & nausea, he also complained of bad headaches. As a mom, my instincts are correct and I attribute all of this to taking the lactaid pills. Thankfully, my son will not have to endure the horrible episodes anymore. Lactaid pills are banned from our home!

I was on Yasmin for about 3 years, and during I noticed I was real depressed which was not normal for me. I also during my last year on it started having what physicians thought as "Panic disorder" which once again was not normal for me. I didn't tie the two together until after being off the pill and not having depression or anymore attacks, that the pill had caused it. And almost a year later, confirmed, Yasmin has been recalled! I am so sick and upset to know that all of that suffering I went through was from a pill that my doctor prescribed. I was scared that every time I would have these "episodes" that I was going to die. And it sickens me that they are still advertising everywhere these commercials to get on this wretched pill!!

i have never taken lipitor and i never will but here's a warning for everyone- there is actually a company that sells reports for stock investors and they are advising people to invest in the company that makes the one of the only drugs used in the management of ALS. they predict that the ALS patient population (code for customers) will grow as a result of all the people on lipitor.

ok, aside from the fact that it made me sick to my stomach that wall street views the potential suffering and death of ALS victims as a business opportunity (what else is new?), this is a pretty good indication that there is a link. it will probably take years for "science" to conclusively state the connection and for the FDA to take lipitor off the market

in the meantime, save your own life. if you're not taking it, don't start. if you are, stop NOW! cholesterol is not the enemy

Just started my six year old son on Zyrtec again. The dr. said he could take the adult pill now 10mg. The last few nights he has wakened with terrible nightmares/night terrors. And after reading these posts i remember taking him off for the winter (he was on the liquid 5mg) and i remember him always itching his arms and legs. i remember giving him oatmeal baths. Now i know it is from stopping the Zyrtec. I am calling the doc tomorrow about these nightmares. He was also on Singulair 4mg for 1 1/2 years then one year ago was upped to 5mg. Within one dose we noticed he was very depressed and cried easily. After a week called the doc about it, stopped it then had our son back in a few days. Will Never give Singulair again and now stopping Zyrtec. All these meds are so scary. A part of me feels these meds are created because it is a HUGE business. They have side effects then you have to take other meds for those side effects and it is a never ending circle i feel purposely created by pharmaceutical companys to make money. And we are all suffering because of their greed. Shame on them

I was given Levaquin for a kidney infection. It seemed to help break my fever but after only one dose, I broke out in rash and later that night had tingling in my legs. My hand felt numb. When I called the oncall doctor she told attributed to anxiety. I told her I was anxious because all of a sudden my hand had gone numb and knowing that was a danger sign I refused to take anymore. Later that night, I could not walk or stand or bear weight on my legs. My shins and Achilles tendons were burning and only because of the internet did I know what was happening to me. Only 1 out of three doctors would agree I was having a drug reaction. For some odd reason, the doctors REFUSE to believe or acknowledge this was caused by Levaquin. No wonder the side effects are "rare" if no doctor will acknowledge the pain their patients are going through....how can the drug companies get any real feedback. Funny thing is only after I sent an email out to my team essentially warning them about this drug did I find out my coworker who had been on medical leave had suffered the same fate of torn achilles tendon and only after 3 months of PT is finally walking without pain. WHAT IS WRONG WITH our world when no one will listen to us. Thank God for the internet. I can walk now and have no pain standing (lasted only 2 and half days) but I am scared about the future as I know the results are lingering. I have been exhausted this whole weekend and wonder if its just me recovering as my PCP had me quit all antibiotics even at the risk of getting my kidney infection back. Well nice to know our stories are the same...and its not in our heads. BTW, my ER doctor told me it was a good drug and very unlikely the cause of my leg pains. They rather believed I had pneumonia or lyme's disease before they would believe it was caused by their beloved drug. All I can think now is I hope one day they are given this drug and it cripples them like it has so many others. Sometimes that is the only way they will acknowledge the truth. It has to happen to them or someone they love.

Hi, I am a 47 year old female. Last month (June 2009) I went to the doctor because I had a bad migraine that wouldn't go away. After a week of suffering I went to my Doctor and my BP was high, so she put me on Benicar. I took it for 3 days and then I refused to take it anymore. After taking it I couldn't hardly get off the couch, and I was dizzy, and had a tightness in my chest with chest pains. The doctor changed my prescription to lisinopril and the chest pains got worse along with that deadly cough. I went back to my doctor and told her that I wasn't going to take lisinopril any more because of the chest pains and the caugh. She said that she didn't think it was the medicine and she gave me an EKG and I failed it. I went 2 days later and had a nuclear stress test and failed it too, then I had a heart cath and the cardiologist said that my heart was perfect, it wasn't my heart. Needless to say it was the meds that the doctor had put me on, those nasty side effects. Now I just moniter my BP and I'm to scared to take anything because of the side effects. I wished I could make the doctor pay for all the test I had to take. She should have just listened to me when I told her it was the meds. After failing 2 test, I thought that I may be really having a heart attach, Very scary. Just listen to what we are saying " DON'T TAKE LISINOPRIL" Oh yea after heart cath I called my doctor and told her that I was not taking Lisinopril any more because that was what was causing my problems not my heart and she said just to let all meds get out of my system and come back in a week and we would try something else. yea right. She's not getting any more of my money. I've come to realize that every thing has side effects, so before I take anything else I will look it up first. Be careful what you take!

My mother just died from all of the secondary effects of prednisone. She was diagnosed with glaucoma 4 years ago but no one ever did a sed rate blood test to find out that she had giant cell arthritis. So once they found out, they treated her aggressively with 60 mg of prednisone. She swelled up immediately and had terrible pain in her legs. Then she became diabetic with big sugar swings that couldn't be controlled. Then s he got thrush in her mouth and couldn't eat or drink. Then she became dehydrated. For pain they gave her constipating pain meds and this caused a bowel impaction. She had tremors and then she had mental confusion. Then her skin started splitting everywhere but wouldn't heal. Then she started losing fluids from her skin. Then her bowels got impacted again. Then her colon ruptured and she got sepsis. Her sugar levels went haywire. Her heart wouldn't slow down, her skin tore up worse, she lost more fluids. And finally she got pneumonia and fever. She died in my hands after so much s suffering - it was just ungodly.

I hope she's ok now and happy and having no pain and is in God's loving arms.

I will never forgive this doctor.

Please be careful with this drug. It is so incredibly dangerous.

Hi everyone, like almost all of you I was so glad to stumble across this site. I had my mirena put in 4 months ago and when I was getting it put in my partner took the day off work and decided to tell his boss it was because he was coming with me to get the Mirena (I was horrified that he told him at the time!). But it turned out to be a blessing because my partner came home 3 days ago and told me that his boss asked him whether I had been getting deep pimples that never come 'to a head' and that his wife had them all over her face and couldn’t get rid of them and that she had put it down to the Mirena. I said to him, "Don’t be ridiculous, the Mirena does not give any side effects", and that was that. See I was told from my gyno that "The Mirena is perfect" and she said that the only people that go back to her to go off the Mirena "are people that are never satisfied with any contraception". And then over the past three days I realized that the bumps on my face that are deep under my skin have only appeared in the months after I got my Mirena and I have had worse pimples than ever before, and they have been untreatable with new ones appearing every day and I had never before had lumps that remain under my skins for months. It also wasn’t until I got onto this website that I realized the anxiety I have been feeling in the last couple months, weight gain and itchy skin have also all come about since the Mirena. I am tired all the time and never want to move or do anything and hate getting out of bed even with 14 hours sleep!!!!! Also - I have been pulling clumps of hair out of the shower drain and my comb over the past couple months - yet have had the same hairdresser and hair routine for the last 6 years.... I could not figure out why I was losing my hair and ended up having it cut from a mid-long length to above the shoulders 3 weeks ago, because there was just hardly any hair left. Also - about 2 weeks ago I told my partner (in an emotional uncontrollable episode which has become a frequent event since Mirena) that I had no reason to live anymore and just didn’t want to go on. First time I have ever felt like this, it was awful. I am normally the happy person at work who gets along with everyone and yet now I cant stand the look of any of them or even the sound of their voice makes me want to scream at them. WHOA, CRAZY!!!!!!! I have also lost any interest in self appearance and in the past few months have completely let myself go. I have also had sex twice since going on it. YES thats right - SEX TWICE IN FOUR MONTHS, aaaaaarrrrrgh. And to the most disgusting part of all - I have been getting an awful discharge that smells bad. I am a really clean person and was considering going to my gyno in the coming week to ask why it was happening….. I have been on many pills and the depot and whilst I experienced side affects with all of them, none of them were anything like this, I would get a side effect here and there on the others, nothing like this. Biggest waste of $800 ever. p.s. I wear panty liners every single day and night of the week.

Has anyone had side effects pop up after 3 years? Yes, you heard me. Three years. Hair falling out. Joint pain. "Foggy headedness." Chest discomfort. Gotta be that. Please share.

I have been taking 40mg Omeprazole (by APOTEX) for one week. At 3am Saturday 6/20/2009, I woke up with a severe itchy rash from head to foot. Over four hours, I took 125mg of Benadryl, but the rash got worse, At noon, I went to the Emergency Room at UPMC Shady side. They gave me intravenous steroids, but this had no immediate effect, After three more hours, they admitted me to the hospital. It wasn't until almost midnight before I began to have relief. I was discharged the next day. I have been instructed to never take Omeprazole again.

As i read some of the news reports on the new FDA comments,i see we are referred to as a handful of reports,the very words handful conjure up a picture of 10 not the thousands that there actually are.Also i noted missing from the news reports was ,that this drug is largely given to children,as young as 6 months,not for 10 days or 2 weeks but everyday,for as long as they need it.i know myself trying to convince my doctor,that my sons depression,insomnia and anxiety,came from this drug was impossible,so i fired him.I am wishing the best to everyone that has suffered,and ask all to please report your adverse effects to the FDA

I have to comment..... look at how many entries there are showing side effects.. so many people have the same symptoms. does this not open the eyes of others to accept that it can be a real problem to some people, admittedly not all, but it obviously doesn't agree with all of us. I could not believe my ears the other week when the local GP said that it's rare there are side effects, then 4 hours later a DR. in a hospital emergency department stated that statin drugs are very common for muscle problems, in particular one named brand (need I say more??) Couldn't wipe the smile off my face after hearing someone finally admitting it..
Come on professional people, start listening and accepting that people do know their own bodies and can see and feel so many vast changes in their day to day activities. Maybe guide people to a better understanding of diet and lifestyle before dishing out meds. so quickly. Give us some credit......some of us exercise regularly, we want to live healthy too and all this has done is put a stop to that luxury.
I have to add, I posted earlier this month, I AM getting much better each day, clearer thinking, vast improvement in mobility, so please stay positive and take care of yourselves, obviously we all need a little patience, hard to do after some long term suffering i know, we want overnight fixes just to feel normal again.. :-)

I have been on Birth Control since May 29, 2007. I was first put on Errin Tab .35mg, which went well, but was very depressed and angry. I had very few symptoms, but very severe headaches, and mood swings with this birth control. Then on August 4, 2008 I had the Mirena IUD inserted.
About 1 ½ months after insertion of the Mirena IUD, my mood starting really getting severe and bad. Now, this was the biggest issue for me because I have always been a person to lets things roll off my back. I have never once in my life felt the least bit depressed. Other than PPD with the birth of my daughter. I am noticing that I am just not feeling myself mentally or emotionally and I am crying very easily. I even yell at my husband and my daughter about the stupidest things and it’s like I am watching myself from the outside doing this and wondering why the heck am I yelling, but I can’t seem to make myself stop. I know something is wrong. I am also very lethargic and fatigued all the time. I also feel that I can’t ever seem to catch my breath. This still continues today, and is very distressing to me. My PCP has diagnosed me in the past week with Asthma, with no conclusive proof that Asthma is the issue. I haven’t had allergies since I was about 12 years old.( I am 35 now) I can only catch my breath when I lay on my left side. I constantly struggle for air, which cause’s panic, heart palpitations, and anxiety.
I have severe depression due to this situation and have been put on 5 different anti-depressants and sleeping aids as well, however it seems like I am a basket case, over anxious and often times a nervous wreck. There are days when I have uncontrollable crying episodes, off the handle severe mood swings. I have no patience with anyone or anything. This is usually around when my menstrual cycle will begin, then at the time it begins, I have horrible persistent bleeding, pain, cramping, coffee ground blood clots the size of a quarter. I will bleed for about 10 days and then stop and start again in about 8 more days. I have persistent abdominal pain, occasional fever, and unusual vaginal discharge, itching, and odor. It makes it very difficult to have sexual relations with my husband. It is very painful to have sex, and I just don’t have the libido for it as well. Sex drive is completely gone.
Since the insertion of the Mirena IUD, August 4, 2008, I have had horrible constipation, that will last for about 1 to 1 ½ weeks, and then for 2 days, I will have horrible and severe diarrhea, and then have no BM’s for the next 1 to 1 ½ weeks again. I also have severe headaches, that hit at anytime. I have lost a lot of my hair, it used to be very thick and strong. I break out in hives, rashes. I also have swelling of my face, hands, tongue, throat, and ankles. Not to mention again the not being able to breathe.
I also have a horrible time eating, I will eat, and then feel like vomiting for the next couple of hours. Sometime’s I do have to vomit, so I try not to eat at all, cause I just hate feeling that way. It just isn’t worth the discomfort for me.
I am withdrawn, and scared to socialize with friends, which that is not me at all. I am always depressed, have anxiety, severe acne, NO sex drive, angry all the time, very easily angered, and I have basically become a totally different person. I used to be a confident women and now I am a total train wreck.

In conclusion I am incredibly concerned about is the emotional side effects that I have experienced! I have slowly become a basket-case. I have at different times experienced the following side-effects : anxiety, minor paranoia, racing heartbeat, MOOD SWINGS! unexplained crying episodes, foggy thinking, and panicky feelings.

I was diagnosed with pneumonia in Nov 2008. When I was released from the hospital, my doctor prescribed bactrim (2pills 3x daily).
After a short time I had noticed body aches and my legs and joints felt as if I had been hit with a bat.
The primary side effect was a rash like skin irritation all over my body.
What started as itchy red marks, began to dry up and my skin was flaky and hard (back, arms, chest, legs, stomach, neck, face and ears).
I was admitted back into the hospital.
The rash and itchiness cleared up. Yet, now my body is full discolored with dark blotches where the rash was (back, arms, chest, legs, stomach, neck and face).
I'm totally humiliated when I'm in public because the discoloration is clearly visible and it looks as if I have a disease.
In addition to that, I can't even wear most of my wardrobe anymore because I hate to expose my skin.
Looking at my before pics is a sad reminder that I've been scared for the rest of my life.
I've consulted an attorney who quickly told me that I had no legal recourse.

I had the same symptoms you all list here: heart palpitations, lack of sleep (leading to emotional meltdowns at work), acne, and inability to lose the last baby weight despite a near perfect diet and miles & miles of running. And of course, my husband was at his end with my crying and constant stress. I also couldn't focus on my children b/c I've been consumed with myself, my apparent stress, and hours spent running.

Finally, a friend told me that my weight is stuck b/c of my hormones. Knowing that the weight came off easily after my first baby, I had the "a-ha".

Literally, I searched on "mirena side effects" this very morning, found this site, and read your stories. I called the doctor and had it removed before lunch.

I'm so relieved that it's almost over. I will be doing a cleanse to expedite that process. Can't wait to have my life back.

Please spread the word. No more suffering. No other women should experience what we know all too well.

I am new on here and am so thankful to have found this site and read other stories. I am only 2.5 weeks into my first course evr of Yasmin and can't believe what it's doing to me. I predominantly went on it to try and fix my adult acne, but so far my skin is getting worse and worse, so much so that I don't even want to leave the house! I'm 31 and it's so embarrassing and hurtful suffering like this. But, I'm definitely going to throw away the remaining Yasmin tonight, as my mood swings!!! Unbelievable, I'm a very level headed, calm, friendly happy person and for the last 2 weeks I have done nothing but cry and cry for no reason what so ever and bite at all my friends. It's a horrible horrible drug. I just really hope I can find something out there to help my acne. Any advice would be more than appreciated.

Well on 2-15-09 my sister in law died just shy of turning 39. She had severe depression, As of three years ago she began starving herself. She would go weeks without eating or drinking anything. She was in and out of the hospital through out the years. She started taking Lamictal six days prior to 2-15-09. The Dr. said she had made a mistake and wrote 100mg where it should had been 25mg. The doctor's later stated it didn't matter if they wrote 1mg it would have happened eventually.

Now we had called her on her birthday three days prior to 2-15-09, and she said the medication made her feel weird. That night she fell to sleep and did not wake up but for only a brief minute in the hospital. After being asleep for a day she was rushed to the hospital were a battery of test were run. She had begun to have liver failure and sepsis. The doctor's had her airlifted to a hospital four hours away where liver specialist were available. She arrived there and withing a few hours her lungs collapsed, her kidneys began to fail, and she had two heart attacks where she finally died at 11:10 pm on 2-15-09.

So I am here to make you aware. This is the side affect no one has talked about yet. Now she had no rash. She had weekend her system by not eating. Other than her depression she was OK. The doctor's don't know if she had an allergic reaction or not. The autopsy will be arrive in 40 days. With just some fatigue and weird feelings she continued to take the medication for the six days. I read on and on and I see so many symptoms, this would be a great time to evaluate with a profession because lets face it we really don't know the long term affects. It could be doing damage to your internal organs, or not. I feel if your body is showing you signs that are not normal than it is a good indication that your body is telling you that is cant tolerating it to well. So at least your getting the signs you might want to see what else is out there. As God is my witness we wanted her healthy and to not suffer so I really do have only good intentions for you all.

The funeral is today.

I am 71 years old, I have been taking 80mg of ZOCOR ( Simvastatin ) for the past 16 years. five months ago I started to hurt in my lower back, hips,Knees,thighs, for two months then it traveled to my shoulders, wrist, hands, fingers. the Dr. gave me a round of prednisone (one shot and 11 pills) the pain stopped and everything was wonderful for two weeks,the Dr. stated that I had avused my body in the years gone by now the pain has started back in my shoulders, wrist, hands the pain is very strong,and my legs are starting to get weak again, I am taking Naproxen 500 mg two times a day and also taking Hydrocodne10mg every four hours also have Oxycodone 10mg to take every four to six hours, I have mentioned the results that I have read about the Statins in this forum but the doctor, does not act like it has any significance. does anyone have any suggestions??? if so please let me know, this pain is killing me, if you have any info. please email me at. ******

Doctor prescribed 500mg 1x day for Upper Respiratory Infection. I took it the first 7 days. I experienced insomnia, anxiety, loss of taste and smell and loss of appetite. After a meal, food just sat there and bloated my stomach for 10 hours. I also was shocked to experience increased sexual desire and that is the last thing I wanted while in the dark mental state of panic induced by Levaquin. It's a horrible drug.

I found this site and stopped taking it. I called the doctor, who said he did not agree that Levaquin caused those symptoms. It's time for a new doctor.

I have read the dreadful Levaquin experiences of others here. May some good come out of the suffering of these folks and may this site serving as a warning to prevent others in the future from ever taking Levaquin. God bless everyone.

It seems most people on here are blaming their "side effects" on the medicine. Could you quite possibly have health issues anyway? what about those people that don't take Singulair and have the exact same symptoms? Is it because they are THINKING about it?
It's one thing to be informed about medication. It's another to go overboard.

I have not heard what the FDA's findings were regarding their recent investigation. I think it is an outrage that so many people have suffered from this drug. My 4 year old child too was a victim of this nasty drug. No child especially young children should have to suffer. My doctor had no clue as with the pharmacist that singulair changed their pamphlets. It just inferiorates me. Merck stated that they were committed to safety and had communicated that information of changing the pamplets. Funny how so many doctors missed that!

Wow! I must be the latest in a long line of Lipitor users and apparently pain sufferers. I have been on Lipitor for over a year. I am 56 years old, active and healthy (thank God). Around November 2008, I noticed a "twinge" in my left hip while sleeping. This has gotten progressively worse over the months and I thought it was due to arthritis (which runs in my family). But after reading these blogs, I am not so sure. If anyone has anything definitive regarding this, ie: tests, studies, etc., I would really appreciate a point in the right direction for more information. I was thinking (until today) that I was headed for hip surgery or something equally drastic. Now that I have a clue that it may be the Lipitor, I want to investigate further and then, if necessary, change to another medication that won't break me down like this. My heart goes out to anyone that has suffered through hip pain. It is a miserable, painful condition that saps your energy and your desire to even move sometimes. I appreciate any help you can offer. God bless all of you. - L. B. ******

My 3 year old son was just prescribed Singulair today. After reading the pamphlet that came with the trial pack, I decided to do more research. All of the side effects that most people have mentioned on this post are listed in the pamphlet. I don't know if I will put my son on this medicine but thought I should mention the importance of actually reading the pamphlets that come with your medicine.

I have also gone to the FDA website and filled out the form about the side effects of the Mirena. I urge you to do the same. If they get enough people reporting, maybe they will do something. I cringe thinking about the hundreds of thousands of women with the Mirena in who are suffering and have NOT made the connection just like all of us at one time. MOST people would not make the connection to the Mirena esp. when their doctors never would!!