Money symptoms and conditions

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.

I am a 51 year old male. November 2007 jaw pain sent me to the hospital where they found a 99% block in my right coronary artery, yep 4 stent's. Three month late the same this time 2 stent's and two weeks later 2 more. I now have 8 stent's. My DR. put me on several meds including Zocor. The zocor made me very tired and headaches. He change it to Lipitor 10mg. I have been on it for 7 months and a few day's ago I have notice pain in both knee's and hip. I once again find it hard to concentrate, feel sluggish and have headache's. I NEVER have headache's. Stopped taken the Lipitor, hope the pain goes away. It a shame that the medical field is so quick to put us ALL on drug's, how about herb's instead. I'm going to look into a natural way to lower my cholesterol.

I am so glad this site is here. I started to think I was crazy. I got my Mirena put in on June 30th. Since then I've experienced excessive bleeding, stomach cramps and recently began to experience nausea as if I were pregnant. My bleeding has been so excessive that prior to having a baby I never really had long periods nor did I bleed heavily enough to go through a pack of pads. Now, I got through a pack of pads in two weeks. The nurse at by GYN says to take 800 mg of Ibuprofin inorder to stop the cramping and excessive bleeding. Ive found that taking 800 mg in the AM and at night stops the bleeding and cramps but, does this mean I will be taking Ibuprofin throughout my time with this birth control??

I was so sure I was pregnant I went out and got a pregnancy test to check. Thank god it was negative. I just had my first child May 8th and I'm not ready for another child right now. I've recently relocated to a new area and I'm still enjoying being on an extended maternity leave. Not to mention... I scared the heck out of my husband!! I feel so unsure about Mirena but I'm willing to try it out a little longer but, in addition to Mirena I'll certainly be using another birth control method for back up like a spermicide or something.

email me at ****** i would love to get in on a class action lawsuit cause these people need to be stopped they messed my body up and ladies don't need to have this as an option

I am a parent of a 14 year old son. He has been on many meds due to having migraines, adhd, seizures, and asthma. For 3 years his ADHD meds have been switched. Now Thanks to a friend she told me about singular side effects. OH MY GOD. it blows my mind reading this stuff. He has been on singular for 3 years and never once did I think all these problems were caused by that drug. Flipping out over the smallest things, arguing with us his parents, his friends, being mean to us and a real smartass, depression, and MAJOR attitude. Getting upset over nothing at all then crying for no reason What was his Dr. thinking? Needless to say, I took the singular while she was telling me this stuff about her own son, and threw them away, I will never allow my son to take that shit again. I hope in three days like all of you say, that my son will be that loving, caring, friendly person he use to be ! Singular free is how he will be!!

My eight year old daughter was recently diagnosed with precocious puberty. This is devastating to my family...She was on singulair fo asthma for almost 4 years...Noone in the med profession will comment on how this happened but the internet is filled with other parents dealing with the ame dilemma. I am so furious right now.

MY sister is not even thirty yet and has has a full hysterectomy (sp) and will no longer be able to have kids. She started with headaches, cramps, ect after she stopped having periods a year into her mirena use. Then they thought she had cyst, the day of her surgery the found the were malignant (sp) tumors....she fully believes it was due to the mirena.....now i am seriously wanting the one i have out. My hands go numb, lack of energy and now that a year is coming up my period is getting unusual. I was recommending this now i am scared for myself, i have no medical so i is just a matter of getting the money to have it removed and get on new bc. I definitely would not recommend this to anyone. We share the same ob and they assure me it is not the mirena.....and that i should not worry....but after reading more......i know it is the right choice.

Thank you so much for your website. I cannot begin to tell you what this drug has done to ruin my life.

I had been on it for over 4 years on a misdiagnoses (Never should have been on it) and was told
“It was no worse than Tylenol.” Ok I thought as I was suffering from a few swollen joints every
now and then but was fine otherwise.

Then one day I was working and someone noticed my face was swelling. I looked in the mirror and
low and behold my face was rubbing my glasses. I asked my doctor and he said “it will go away soon.”
I am very athletic so I continued to run and work out as I slowly went from a 30” waist to a 50” inch waist!!
People at my office thought I was on a food binge like no other. My wife was stunned on how fast this
happened as was my family. Now the problem had gotten much worse. Constant body aches and swollen ankles.
After a year I went from jogging, to walking, to using a cane to using a walker…how sad my family felt
for me and no friends insight. my company then laid me off as I used the walls as a walker and simply could
“perform up to par.”

Next came the extremely high sugar, blood pressure, Glaucoma and I suddenly noticed I was having problems
seeing. Went to the eye doctor and was told I was getting cataracts but it would take a couple of years to form.
90 days later I could not drive and could barely see in both eyes, now I was almost blind.
Now 80lbs overweight almost blind with Glaucoma, high blood pressure, diabetes and cataracts. not to mention severe depression and mood swings that were unbearable, and yes still using a walker from severe muscle pain.

Well the time came where I lost my health insurance and was unemployed. I was out of Prednisone
one day and called my doctor. He said come in for $320.00. I said I didn’t have it and pleaded for them to call
in a 30 day supply, I was told that they “weren’t a charity” and “go to the emergency room” click!! My wonderful
doc was gone. Well I went to the emergency room the next day and was told “they don’t give refills.” I had been
off prednisone for a day and as some people know if you stop that high of dose for that long you may die from
adrenal crisis. So I stood in the emergency room for 12 hours waiting to go into this crisis! Finally a nurse convinced
a doctor to see me for 30 seconds, gave me a refill and a list of welfare clinics and booted me out the door. They
hated my appearance and hated me for no cash.

One day I decided to end this nonsense and tread everything I could from sources I hadn’t read that were very old
regarding what was wrong with me. I went on self imposed diet of 1000 calories a day and lost 60 lbs…yes!!
I stated weaning from the Prednisone and took a ton of supplements I had read about. I got down to 7.5mg every
other day. Yes, suffering tremendous total body aches, severe mood swings, dizziness, severe hunger and
confusion but I plowed though. By the way I don’t recommend this but I couldn’t get a refill for a prescription from anyone
because I ‘had made to much money.” So I turned to the Internet for everything. I bought 500 5mgs for $23.00 screw the doctors I don’t need their prescriptions. I am now totally off for 6 weeks I do have some bad stiffness, muscle aches and mood swings but after 4 years of pure hell I am truly thankful to be off this dangerous drug, it ruined my life.

So I went to a new Doctor finally and my diagnoses was a food allergy and simply had a small stint of bursitis a total mis- diagnoses from my first Doctor! Doctors aren’t gods so take it from me trust yourself first and do your research.

My prayers to all who suffer from this drug. Damn the incompetent doctors who wrongly prescribe it!

Dan

PS Does anyone know how long these severe body aches last after completely stopping. Its been 6 weeks and its just a little better. My doctor told me to fight it out or get back on pred. NO WAY!!

Hi all. I would just like to agree that PredniSone sucks but it is the best out there for these diseases especially the auto-immune diseases. Drug companies do not make any money on prednisone because it is generic and there is no patent. I know I picked up 98 10mg prednisones yesterday for $5.00. Believe me when there is a better steroid that works as well and has less side effects it will be available to us all. It will cost tons but it will be sold. Researchers have been working for so many years trying to find an alternative, some have been found but do not work well enough. As bad as the prednisone makes us feel it does work on the diseases. You always have the choice to say no - that is why we should all have a health care power of attorney - just remember that when you decide not to take the prednisone you are agreeing that the disease may worsen and may be life threatening. I hate to sound so morbid but patients must be informed. When you are at the physician ask about the side effects, ask if they can give you something to counteract any mood swings, ask what lotion is best for the itchy skin (AmLactin works well for me and is over the counter). Also, my physician advised me yesterday that the side effects are worse on women due to our precarious hormones. I have told my husband to just stay out of the way and don't piss me off because I am not sure how this next 7-8 weeks is going to fare for him. I am 4ft 10in 110lbs and he is 6ft 1in 200lbs and believe me he is scared for his life. I am using prednisone for my ulcerative colitis so now that I am feeling better physicially I can return to exercise and that has definitely helped. So has turning up the music really loud and dancing and singing poorly. Yelling at the tv helps me whether it be politicians, soap operas or idiots on game shows who get the wrong answers. I also have been keeping a journal of all the rage I have and what kinds of things I could do to people who keep getting in my way at the store, on the road, in line at the pharmacy - I guess I need to put that in a safe place so it can't be used for evidence :}

I'm trying to wean myself off Geodon and I had a minor, panic attack,. My doctor won't help me because she said I need to see a psychiatrist but I can't afford to see one. Does anyone know how long the side effect last when you get off Geodon. I am a single parent and have a job I need to function at so any advice will help. I have ,anxiety, all the time the doc had to prescribe some anti-anxiety medicine which I never had anxiety like that before. My symptoms on the medication is sleeplessness, restlessness, loss of appetite, can quit moving, racing thoughts, depression.

I was a healthy 42 year old male who took Levaquin for a sinus infection. The same day as the Black Box Warning was issued; I was having my third tendon reattachment surgery. I have to wait at least 6 weeks before I can undergo yet a fourth tendon rupture reattachment. At least it takes my mind of the Achilles Tendinopathy, joint pains, headaches, uncontrolled muscle twitching etc. I consider myself one of the lucky ones since so far it has not affected my kidneys, liver, heart, eyes and other side effects that many are dealing with from this class of drugs. I would urge a real journalist to take the time and look at the real number of cases. The Fda numbers are misleading. The clinical data coming from other counties are showing much higher rates of tendon ruptures and other life threatening side effects.

I just started my 3rd pack of Aviane. One of the reasons I started taking birth control was to lighten up my period due to anemia. Well, so far its only made my periods worse. The first pack i had breakthrough bleeding for almost 2 weeks. It was heavy, the cramps were worse, felt sick, and worse depression/anxiety. I went to the doctor and he said this was "normal" and that I should continue the pill. During the second pack I bled for over a week and it was heavier, bad cramps and a headache for a week. Not to mention my "period" never came during the placebo pills but I know it can take time to regulate. I just started my 3rd pack of pill and I'm not feeling well. Just nauseous, sick and depressed again. Just last week when I was on the placebo pill I felt just fine and now i've started Aviane again and i feel horrible. All I know is that if bleed irregular/heavy this month again, i'm either going to go off this horrible stuff or go to the doctor to find a new birth control that doesn't make me feel sick and depressed all the time!

After reading these posts, I am glad I didn't change my mind about having the MIUD removed. I have had all sorts of problems since that evil piece of plastic was inserted. I didn't think much of it at first and thought maybe I am just tired because I have my period and cramps alllllll the time. The relationship I was in was bad and thought maybe I was tired and moody because of that. After a couple of months - boyfriend free - things didn't change. I had horrible mood swings, my concentration was shot. My work ethic went down the toliet, I felt like a 10 year old kid with ADD. No energy, back hurt on a regular basis, carpal tunnel came back with a vengence and TMJ (I don't know if that's related but I've never had it before), acne, weight gain, no sex drive, and a constant itching around my neck. I am sure the NP was ready to try to talk me out of it and wait the full 6 months for "side effects" to go away. Well, the last 5 sucked, I really didn't want to deal with this crap any longer, besides with the price of gas, I can't afford the money for the regular buying of feminine products. I am only 6 hours free of this and I am already feeling a little better. I don't have that "pressure" you feel in your belly and a have bit more energy. I am so looking forward to the next few weeks when things start to get back to normal!!! If you have any doubts about this thing....get rid of it. Its really not that bad to get it out, 99 times less painful than getting it inserted!!!

I have had asthma for about 12 years. It has progressed fast but don't believe it is emphysema yet. Stupidly I still smoke...or try to. I have used mostly salbutamol regularily and every now and again my doctor will try other types. I too have gained weight, lots of it, have leg pains and restless leg syndrome, blurred vision and fatigue. Many days I barely make to and from work. And all of these in just since taking Advair. I trust the doctors too much. Reading all of these are scary. It seems many doctors don't really have our best interest at heart. It begins and ends with money doesn't it? Another problem I have is because I am so sensitive to different thing, how can I know what is causing what??? I went for allergy tests last month and I could have told them more than what their tests showed and then some. I have since tried not to smoke and seriously looking into alternative treatments...stop the smoking for sure withpatches if I have to.

Hello... I am on my third pack of loestrin 24. Im 19 and have never been on BC. the first pack i spotted and did NOT get my period on my brown pills. the second pack i got my period about the second week and bled for 2 weeks straight. it went away for a week and i DID get my period on the brown pills.. i was excited, i thought i was regulating finally. i am currently on my third pack the second week and i got my period last night and have cramps. i don't not really want to switch and go through this again. i lost my appetite( i don't mind) my drive has increased and i lostt weight. my skin is great im happy not moddy. i am hoping since loestrin is 24 days of hormones not 21 maybe its taking longer to regulate. I hope i regulare im scared i wont. has this happened to anyone... has anyone been normal. my only problem is this constant crampy bleeding! please help.

I was prescribed Levaquin in Feb./March for 30 days. I have had tremendous pain in my heels since then. I am walking slower as every joint and muscle in my body hurts. I can barely stoop down and it is getting worse. I can not sleep. I thought I was just going through some depression and stress until I started reading about it in the WSJ and now realize I fit many of the symptoms being discussed.
We all need to take some action as this is only going to get worse for everyone.
FDA?????????????????

Lipitor an all Statins deplete the natural enzymes from your muscles.
Your Heart is a muscle. I haved been on Lipitor for a number of years
with many of the side effects posted here. I have had Heart Failure fo
a year now and the best doctors could not help me. My son recently
researched an found a possible solution the indicated Statins deplete
th heart muscled of COQ10 a natural enzyme in the Heart Muscle.
This depletion over time can caused Heart failure due to weak walls.
Since my doctors could offer no solution, I decided to try it for 90 days.
I am off Lipitor an taking 400mg of COQ10 per day.
I am now in day seven an have slept in my own bed with my wife for the first time in a year. I am less restless, an have ha no recurrence of Heart Failure. The drug companies know the problems but thy have
deep pockets an the best lobby to get laws passed and FDA approvals.

They have now received approval to get kids on Statins so they can
make even more money before the patient run out. Thy should be ashamed but they are not!!

I went over to Lisinopril when I transfered insurance carriers recently. The new carrier was going to charge the max allowed for using Altace and Lisinopril is way cheaper. So I went back to Lisinopril and have been on it for about a month. When I first tried it many months ago I had a sick gall bladder that has now been removed. The side effects at that time include a rash on my chin, burning urine and crotch area. Within two days of stopping, the symptoms were gone. Since I don't have the gall bladder problem I decide to try it again to save money (ha). After a week I notice my BP was increasing. I was taking 10 mg so I went up to 20 mg of Lisinopril and that didn't work - my BP kept going up! I keep talking more of the stuff and my BP keeps going up. This morning I took 40 mg and my PB was 200/90 and I suddenly thought it's the meds as there is no reason in the world that my BP should be going up crazily like this. Then I found this side and several folks mentioned their BP had gone UP. No more Lisinopril for me. I'm so glad I found this site! Thanks all for being independent thinkers and sharing your stories!

I have been on Levoxyl for about 9 years and have felt awful. I have had weight loss, dry hair, thinning hair,dry skin, muscle aches, migraines and the list goes on. I just got out of the hospital Monday after 4 days of testing of my heart and lungs. I was admitted for racing heart. The doctor's conclusion was anxiety! They said that Levoxyl has nothing to do with my rapid heart rate. The endocrinologist prescribed taking levoxyl .050 on day and .075 the next also a beta blocker, Xanax and Zoloft. I can not take any of these meds b/c they make it almost worse. I KNOW it is not Anxiety and it from the Levoxyl but what do I do?? I am a mess right now can not be in this condition with four young kids and a husband. None of the doctors would say it was the Levoxyl and instead prescribed more and told me to check up with blood work in 6 weeks. I took the .050 yesterday around noon and by 7:30pm my heart rate picked up again and continued until 4:30 this morning. I can not sleep more then 2 hours at a time and wakeup feeling like I am crawling out of my skin. PLEASE let me know of any solutions.

My father is currently in the hospital for his second internal bleeding from coumadin. He had a GI bleed and was discharged a month ago, put on coumadin AGAIN , supposedly monitored and wound up in ICU again, this time he had trouble breathing and was intubated and sedated for two days. I really thought Coumadin killed my father and in reality it almost did.....Now the hematologists are saying he is extremely sensitive to it, and his only other option is heperin shots which he refuses to do (that also has risk of bleeding). he is going to live with the chance of stroke rather than take coumadin a thrid time which is what they are suggesting. (idiots) . he has atrial fib and needs to be on blood thinner but at this point he would rather take his chances or take aspirin even though the doctors are saying it won't work as well. Hopefully there will be new anticoagulants out in the market soon like there are in Canada and Europe.

Coumadin KILLS....8,000 people a year bleed to death from coumadin......yes, it helps people too but judging from this site the side effects are awful...if you can avoid coumadin you should...

I have been on BC for about 4 years and was last on Ortho. So when I told my GYN I wanted to be back on BC, she said that FEMCON FE was just like Ortho and to take it the exact time everyday. I found it strange that she told me that I had to take it the same time everyday; something I did not have to do on Ortho. So after taking it the first week and still experiencing bloating and other side effects I thought nothing about it. However, when I took my pill later than scheduled two days in a row, I started bleeding. In addition to the bleeding I developed other side effects...same as mentioned by others. After various comments from co-workers about my complaints that were very similar to pregnancy symptoms, I became very concerned and decided to research this pill. After finding this site, I immediately stopped taking the pill. It's been close to 3 weeks now since stopping and I've seen a world of difference. I am done with BC pills, condoms will just have to do. I already suffer from migraines so that is the only debilitating, uncontrollable issue that I am willing to deal with right now.

I am also convinced that GYN's are making their pockets fat by pushing this BC with their patients...a theory that does not sit well with me, because I had a lot of respect for my GYN before she prescribed this packet of side effects to me.

After being on Synthroid for a few years and getting NOTHING from it, I was switched to Levoxyl for several more years, and got NOTHING for it either. They are some of the most useless medications ever made, and all they do is put money in the pockets of the maker. Armour is what made a HUGE difference in my hypothyroid. ******

I just started using Singulair a few days ago. I am 54 years old and just started coughing at night only. I would be fine during the day and then never failed, at night I started to cough keeping me awake. I was given antibiotics, narcotic cough syrups but it only helped temporarily and then I went back to coughing nights only again. So as I mentioned, I started taking Singulair a few days ago because my physician thinks I have developed allergies and Singulair is noted to help night coughs. It is helping my night coughs but I still cough a few times at night and now I cough quite a few times in the day when I never use to cough in the daytime. Wondering if Singulair is worth taking as the symptoms are becoming opposite? I hate taking drugs and don't know if I should find a safer alternative? Help, anyone? Thank you

About 1 1/2 years ago my allergist recommended I switch BPM from Lisinopril to Atacand because of congestion problems associated with Lisinopril. I made the switch and had no problems with Atacand other than my co-pay was considerably higher. Because of this I asked my family practice MD to switch me back to Lisinopril because I remembered it worked okay. However this time - a couple of days after the first dose of Lisinopril I developed flu-like symptoms (aching, congestion, fatigue). I thought I was coming down with the flu AGAIN. After about three days I started having chest pain, a headache that wouldn't go away, blurred vision, dizziness, shortness of breath, very shaky, weakness, couldn't sleep. I thought I was on the verge of a heart attack at times. The fatigue and weakness worsened. I often felt that I couldn't get off the couch or out of bed. My legs felt like weights. It wasn't until I checked out the side effects on this website and read the comments of other users of the drug that I realized what was most likely happening. Needless to say, I called my doctor and asked to be switched back to Atacand. I'm more than willing to pay the extra $'s to feel better.

I was given Bactrim at the ER where I was diagnosed with a staph infection. They gave me 800 mg twice a day for 7 days. On day 8 I returned to my regular GP because another boil had appeared. He said the dosage the ER had me on was not high enough. He doubled me to 3200 mg a day. After 4 days on this high dose I began to feel terrible, flu like symptoms, all of my lymph nodes were swollen and painful to the touch, especially the ones at the base of your neck/head. That night my eyes started itching like crazy and began to swell. I went back to the doctor she said it was allergies in my eyes and prescribed some expensive drops, told me I had a virus causing my body aches and fever, and lanced my other boil, she then put me on Doxycycline. That night I broke out in a terrible rash from head to toe that was itchy, then became more like a very painful sunburn. I thought I was allergic to the Doxycycline, so I called the doctor who switched me to Levaquin, wow,,,I sure have spent a lot of money on medicines to discover tonight on this forum that all of this was due to Bactrim. I will NEVER take it again as long as I live.