Hospitals symptoms and conditions

I had back surgery in July and caught two infections from the hospital, Staph and pseudonymous. I had a picc-line put in and was put on Cipro oraly and Ancef. I got Steven Johnson syndrome from the Cipro and almost died. I looked like a burn victim and swelled from head to toe that was three weeks ago. They pulled me off the Ancef and Cipro. It took a week of me running 103 + temps and the dr. kept telling me its a virous until the rash showed up and my tongue swelled and private parts and throat started to swell shut before they decided to admit me. Then once all that was done and they figured it out they put me on impernem to kill both infections. They pulled my picc-last week and put me on Doxycycline. I have done my research and know that the two are related I asked my dr. what the chances were of a reaction again he told me less then 1%. Ha! I am seeing an infectious disease dr. by the way. Since I started the Doxycycline last Thursday I have developed hives I called the dr. and was told they are not worried about it because I am not running a 101 temp and I am not swelling, plus they don't even know if the Pseudonymous is cured. What do I do? If I go off the antibiotics I will die and if I stay on them I am probably going to die. My joints hurt all the time now and I am only 31. Do I look for a new dr.? Can someone please help me? This is the only website I have found so far where people have had the same reactions as me. These antibiotics are dangerous they need to be taken off the shelf. Thank you and good luck to everyone who is struggling with this.

My daughter is now 20 years old. she received her 1st gardasil shot in 3/08 and the second in 8/08. She didn't get the last one and will not be getting it. From the day she got the first shot we should have known something. She nearly fainted immediately after both shots and complained of weakness and flu like symptoms. Started feeling poorly in the days and weeks to come. It was the end of her senior year the doctor tested her for mono. and it was negative but she had an extremely heavy schedule at high school. He chalked it up to the stress of that. Between the two shots she started having numbness and pains in her hands,elbows and arms. She continued to feel poorly and terribly irritable in the upcoming months. We saw a orthopedic doctor for her pains in her arms. He referred us to a neurologist. She was beginning her first year of pharmacy school and we put off the neurologist because she didn't have much time until spring break. During her 1st year of school after her 2nd shot. Her personality changed completely. Became insecure, moody, very anxious , constantly complaining of flu symptoms, bladder infections and had a hard time urinating. When my daughter returned home from her first year away at college I knew immediately that she had changed. She had been a very bright, intelligent, independent daughter and came home the daughter from hell. I couldn't believe what I was seeing. She was miserable, disliked pretty much everything. I had been talking with the doctor and friends over the course of the year and they all said that she was in a very stressful field (pharmacy) and college life takes some time to adjust. Then just a few weeks home from college she was complaining of dizziness, light headedness, headaches and saying she was having an episode. I thought maybe low blood sugars.....until I witnessed one. She was having Myoclonic seizures. She could feel them coming on but couldn't move or react. By the time I witness one of them she hadn't slept in 3 days. She was diagnosed within a week seeing a neurologist and having 50 to 60 a day. It took 4-5 weeks to get them under control in and out of the hospital . She has been on many seizure medicines it seemed like if it worked to stop the seizures she had crazy side effects. She was diagnosed with Juvenile myoclonic epilepsy. No one in our family has ever had seizures. I asked about the shot right away everyone said no and it was dropped. Since last July 08 we have been trying to help our daughter get her life back and it has been the worst year of our lives. She was unable to return to pharmacy school. The first fall 08 she was completely disabled. It looked as if she had had a stroke. They were saying it was the meds or maybe she had a breakdown of some kind. I am learning that it was side effects of this horrible shot. This is why I am posting this lengthy message because I wanted to let other people know that you and your daughter are not crazy!! We just started 2 weeks ago investigating the possibility of the gardisil shot being the reason for this madness. We have learned many things and are very sure that it was the shot that change our daughter.. I was contacted by a friend of a friend about a similar girl having the same pains in her arms and the focal seizures. I am learning more and more everyday about similar situations.. If this information can help one person it was well worth the time to jot it down. I will be praying for all of your families out there dealing with side effects from this vaccination.. I will let you know what we hear when we visit the neurologist at the end of the month. Any comments or information that may help us help our daughter can be sent to ******

My daughter had her 2nd shot in August, 2008, she started having problems November 10, 2008.Since then, she passes out at least 5 to 6 times a month, she has Bradycardia, arythmias, vagal vasal syncope, and Heart Block. She has been in and out of hospitals. The only answer to fix this is a Pace Maker. Shes 18 years old, cannot drive, go onto college (at this time). She could not even go to her graduation ceremony because she was passed out in the bathroom and wouldn't wake up. I cannot find one doctor to connect this to Gardasil, I wonder why it cannot be traced back to the shot. I would love to voice my opinion to the public about her experience since this shot. Out of all the doctors that see her, not a single one can explain why this is happening to her heart, they say she is a difficult but interesting case.

My eldest son was diagnosed as a Severe Asthmatic at the age of 3. He was put on Flovent 110, 5mg of Zyrtec and Singulair. I cried thinking about my little guy having to be on daily meds for who knows how long. I decided that I would just try the Zyrtec and Flovent 110, it worked wonderfully. When my eldest was 4, my other son, 2, was put on Flovent 44. Never gave them to my youngest because I knew it was not asthma. I ended up lowering my eldest's dose to the 44 and giving him 1 puff a day with the Zyrtec, he is now 7 and is still under control. As for my younger son, he was not asthmatic, he had sleep apnea, had his tonsils and adenoids removed and is now perfect. Just be careful with these doctors, they seem to diagnose these little ones too quickly......most of the time they are not even right. My eldest went through many many doctors before he was finally diagnosed in the ER and sent to peds for 2 weeks. My youngest went through many doctors too, none would do anything, I had so many excuses as to why my son was such a heavy breather and why he had difficulty swallowing and sleeping. Sorry guys, I ran off here, just want you guys to know that all that are diagnosed with asthma do not necessarily have asthma and I believe way too many drugs are prescribed for these little ones.

Well, let's see now.................
I am a 48 year old female who has always been healthy.
4 months ago I went to the clinic for stomach pain that was gnawing at me. That's when my nightmare started. I was told to go straight to the local hospitals ER room because my Blood Pressure was 238/127
I was kept for 2 days in the cardiac unit. Tests were run and they all came out perfectly fine. I was then put on 50 mg toporol along with 20 mg Lisinopril. I was sent home and couldn't hardly function. Nauseous and dizzy, I was hanging onto walls just to go to the bathroom. Doctor switched me to Diovan instead of the lisinopril but insurance would not cover it. So once again I was switched to Avapro taken along with toporol.
By the second day on Avapro I was itching extremely and my skin was on fire. I called the Doctor once again and he said to Quit the Avapro and just take the Toporol alone. Well, within 4 days I ended back up in the emergency room with an elevated bp of 204/107. Once again, I was kept overnight and put on Labetelol (an alpha and Beta Blocker).
I did quite well on this med for a month and then the bp levels started to rise once again. I called the doctor this evening and was told to take 20 mg of the Lisinopril I had in the medicine cabinet along with the Labetelol.
It's been two hours and I'm starting to itch from the Lisinopril now....sigh.
Thank God I go to the clinic in the morning!!
I am really getting anxiety problems from dealing with these meds!!
Hopefully I can get everything straightened out. I am willing to hang in there until I can find something that works. It is obvious to me that I need HBP medication. I just wish They could find the right ones for me without having to go through all this . To all of you that have high BP, Hang in there. If one med doesn't work, keep trying!!
God Bless All Of You!!!!

For 2 years I delt with body numbing pains! I literally thought I was dying. I lost weight, could not eat, was having diarrhea everyday. I am a small person 5'2 and 100 lbs. When i started loosing weight I was down to 89 lbs!! I thought I had a bug inside of me. I went to 5 different hospitals in 1 year b/c of the pains I was having. Each hospital said I had UTI infections or I my blood pressure was up. I noticed these pains mostly come around when I am supposed to get my periods. I finally went to a OBGYN and the OBYGN told me that I had PMS and put me on birth control pills. I felt like the doctor didn't listen ot what I was saying about my pains. I went to another OBGYN and she listened did tests acted like her actually cared! FINALLY! She said that I had 5 ovarian cysts on my left ovary and 4 ovarian cysts on my right ovary and the pain must of been from them popping. None of the cysts were large enough to be surgically removed. The doctor determined that they were all bynine. 2 months later I had a check up appt and explained Im still in pain around my cycle (I would never get my period - I always had a irregular period) She reviewed my tests and determined that I was slightly anemic and that it sounds like I have Endometrosis. She put me on a birth control pill that did not agree with me so I went back and she gave me 2 options: The Mirena or The Ring. I chose the Mirena because it sounded like a better option. I mean 5 years without pain?!?! Im all in! She tried inserting the Mirena in her office and was no successful. She said b/c I never had any kids before my cervix was to closed so I had to go to out patient surgery and get it surgically inserted Aug 2008. For the first 2 weeks I was fine. No cramping no bleeding no pain. Then it hit me! I started bleeding real heavy I was crampy all day no matter how many IBP I took. Within the first month I had to go back b/c I was bleeding a little to much and with all the weigh lost I had in the last couple of months they wanted to monitor me. She said because she tried inserting the Mirena in her office I must of gotten an infection that is causing my cervix to bleed and not heal properly.I wish I told her to remove the Mirena at that point! For the next 7 months I bleed everything single day!!!! I would get real dull pains in my legs to the point where I couldn't even stand any more, my back would hurt if I was to sit down for a long period, I got headaches to the point I was sick, I would cry at anything (and still do). Instead of getting a normal period I get this thick brown gunk that comes out of me for days. I thought the Mirena is supposed to make your boobs bigger? I LOST a cup size! The only think positive I can say about the Mirena is that I gained weight and I am not in pain from the Endometriosis! I am definitely going to get the Mirena removed ASAP!

My daughter-in-law had the Mirena inserted November 2008, when my grandson was about 7 weeks old. Our lives have been hell since, after months of headaches,nausea, fatigue,and just always pale, weak and lethargic. Many trips to Doctor's and hospitals, never any answers. March 12th 2009 blood test showed kidney failure, low hemoglobin requiring transfusions, and platelets so low they had to do plasma exchange every day for almost a month. Our answer TTP, this is a very rare blood disorder- in this case caused by the mirena IUD. 32 days in the hospital, after the Mirena was finally removed on day 26 her counts returned to normal ..with tons of lasting effects she came home, she lost her kidneys from damage that went on to long for her body to take, she is 20 and will never have another child, and continues to have lasting heart problems, as well as needing a kidney transplant. Please know that those of you who have it who have never had a child, that's not supposed to happen, its only recommended for women who have had a child. The list of side effects and who should and who shouldn't have it is not getting to the patient. Here is a link to a petition I found and continue to forward and post everywhere I can. Please keep this going so we can get the FDA to take this poison off the market.

******

Has anyone been in contact with any doctors, hospitals, or researchers who are willing to recognize that Singulair targets a receptor CysLT1, with known genetic variations? As you know, I have been posting that I know of researchers who are doing work about how the genetic variations can determine the efficacy of Singulair. If genetic variations cause differences in efficacy, then, of course, these variations can also cause unpleasant to very serious side effects. These seems to be some kind of disconnect. How can the genetic component be recognized in the area of efficacy and ignored in the area of adverse drug reactions?

Since having the Mirena inserted 6 months ago, I have gained 30 lbs, my hands and feet swell terribly, I get headaches, suffer from insomnia, I have no sex drive, I cry all the time and other times I want to be as mean to someone as I can. I have developed heart palpitations and undergoing stress tests, ECG's, blood pressure monitoring. I have dry course skin and hair and developed acne and I either bleed or spot so have had to be monitored for low blood iron levels. I use to healthy and happy and feel like I spend all my time at appts or in hospitals. I have mentioned my beliefs concerning what the Mirena does and feel as though it reaches deaf ears. Today was a terrible struggle talking my ob/gyn into removing the Mirena. I will have to go for surgery to have it removed and have become very vocal about the Mirena overnight.

I have been getting Kenalog injections on and off since I was a teenager. I am now 38 years old. I get these injections about once a year and depending on how bad my allergies get, sometimes twice a year. It is the ONLY MEDICATION that I have ever been able to take that has completely relieved my allergy symptoms. I to have got the "dents" into my skin at the injection sites, which over time have resolved on their own. My hips ache as well but fortunately only just sometimes. Exercise relieves the pain. I am a nurse and know full well the "adverse" side effects from this medication and am reminded by my physician every time I go for the injection. The misery of dealing with my seasonal allergies when nothing either prescription or over the counter helps makes me incredibly grateful for this medication. Everyone will react differently to every medication. People need to realize that it will not work for everyone and there are serious side effects. That is when YOU need to decide if the risks are worth the potential benefits. For me they are, every year I dread spring and summer and will dread it even more if the FDA pulls this drug.

I am a 56 year old female & have been on toprol for 7 or 8 years. I was a small business owner & under a lot of stress. I had couple of times where my heart would race & pound & I felt really strange. I went to the ER where they of course checked my blood pressure. It was a little high, but I was stressed out! After the second time this happened they put me on 50mg of toprol. I have since weaned myself down to 25 mg. I think I was having a panic attack, which I had never had before. I regret the day I ever started taking this poison. I have had such shortness of breath that I can hardly walk to my mailbox & back. I feel like I can never get enough air in my lungs. I feel a tightness in my chest all the time, sometimes my heart feels like it is beating abnormally. I am always aware of my heart beat which I never was before this med. I have gained about 20 to 30 lbs, which is very hard to lose when you feel like you are dying if you exercise. I have pain in my left shoulder, which I don't know if it is from the med or not. I do not sleep well at night & am so tired all the time it is hard to get through the day. I just overall feel like crap! It seems doctors are no help they just want to try you on other meds, I have tried that too. They are all poison I felt even worse on some of the others. I don't want to go through the rest of my life like this. Has anyone successfully gotten off this stuff? I would love to hear from you. Thanks, K. L.

Hi everyone, I have just read all thirty pages of posts to try to find some answers to my crazy reaction to prednisone. My thoughts are with you all since I have had an usually severe reaction to prednisone. I was on prednisone for 1 week in October 2008 at 60 mg/day for a sinus surgery. I am still having the following side effects at full force:

Axiety to the point I can't socialize
mood swings
hot/sweating even in freezing weather
whole body shakes
severe migraines
tooth sensitivity
muscle pains
extreme thirst (I drink almost 2 gallons/day)
hungry all the time
moon face
water retention around waist
acne
hair loss
rapid heart rate
dizziness
nightmares
night sweats
high blood pressure
high hear rate

I'm not exaggerating, my parent's can contend to that. I do have a history of having sever reactions to medication and I've had all the gland and blood tests which all check out. I never had a single one of these before the prednisone - I was a healthy 22 year old.

I was wondering if any could tell me when this hell will end - my job and well-being depends on it!

My daughter received her first shot on 6/20/2007 when she was 14 years old and second shot on 12/27/2007. During this time frame she complained of having headaches daily. On 1/8/2008 my daughter had a seizure. She had been a healthy, dancer and scholastic student. Since her shot she has had a total of 12 seizures and has been in and out of hospitals numerous times. She was diagnosed with epilepsy in March of 2008. She has been on Topamax, Keppra, Lamictal and Zonegran and continues to have seizures. The side effects from the medications that my daughter has suffered with along with depression has been tremendous.
We thought we were protecting our daughter and found that we have only hurt her. The doctors need to stop pushing the shot and it needs to be taken off the market. Because of this shot she has to be dependent on more drugs. She has missed so much school, which were important years (freshman & sophmore) that she will never get back. How many more girls need to suffer!

I am 20 and had all 3 of the shots. I was going into my freshman year of college, and in September became very sick. I refused a blood test because I hate needles. By November I could barely walk on my own. The hospitals kept giving me medicine for bacterial infection, but it just kept getting worse. My fever stayed at 103 before I went back to the ER. A blood test concluded I had mono. Just figured I got this from being a freshman partier. During this time I also had an abnormal pap smear for the first time. My mom did research and found other girls who had cases of mono after the 3rd shot too. Very, very rare. Now I have to go to the gyno every 6 months because they found pre-cancerous cells. I also failed my first semester of college because I was so sick. This is all thanks to the Gardisal shot. I do NOT recommend. It should be taken off the market now!

google the class action lawsuit for mirena. i joined in. so should you. it has ruined a part of the happiest time of my life. don't let them get away with it.

Hello everyone.. I am so sad..Would you like to know why? I believe it is because the mirena I got put in after my second child. I talked all things over with my doctor and he strongly suggested I go the "Mirena" way. Keep in mind I'm 22years old. Good Health, never had a serious illness or anything out of the ordinary ever happen with my health. Well 2 weeks after mirena was incerted into me I began feeling very tired, lack of motivation, irritable, and the best part of it all is I have extreme anxiety now. I never had ths in my whole life, until Mirena was implanted. So I immediately go to obgyn and ask why??? He said it had absolutely nothing to do with mirena, that mirena has no side effects like that . So he put me on an anti depressant. Well that did not help at all. Let me tell you about panic attacks in case you don't know what they are. They are episodes of extreme panic, dysphoria, nausea, chest pain, muscle stiffness, near fainting, you down right feel like you are going to DIE.... No Joke, There is nothing you can do. But take meds that damn near knock you out. Now, panic attacks will not kill you. They just feel like you are dieing. I going through this for two years now.!!!! From med to med, doc to doc . No Body seems to know why??? So I got the Mirena removed. They magically went away for two months.. I was thanking GOD, it was a miracle..Just two weeks ago I began having them again. So I go back to my doctor. She puts me on busprone and ativan...To stop the attacks. But the meds don't work and she wont listen. Im just so sad because, this has cost me my marriage, My husband left me, we have a two year old beautiful daughter named destiny. She has suffered all this, she doesn't understand why?Why mommy has panic attacks, or why mommy is crying, and having to rush to the doctors or hospitals. I just feel like Mirena has ruined my life. A life I can never get back. To anyone reading this who hasn't gotten the mirena yet....Stop right now and do something else.... My husband and I would still be together if it wasn't for this mirena.Though, I pray it never happens to another soal..It could happen to you too.

I was encourage when i read the post of the lady a few posts down,who picked up her prescription and it was covered in stickers telling her of post market side effects,a long time coming yes ,but it is happening none the less.Several articles on merck have noted flat Singulair sales,due to safety concerns,the word is getting out slowly but surely.I know we have been frustrated with how slow it is all happening,but it is happening.One of our hospitals here in cleveland now will list a doctors affiliation with a pharma company,important news for us that know what the implications of that could mean.We have had an education in the medical system,which quite frankly i found shocking,i don't think any of us will every fill a prescription again with out research,we have learned ,we are not the same,we must continue to change a system that is broken ,the dollar must be secondary to the health of all of us.I again urge all that still have issues to file a report with the fda,Keep on fighting

WOW! My jaw is on the floor. I have been taking Simvastatin for 4 years! At around that time I started feeling ill. I ended up in the infection clinic. There they did 6 spinal taps since they could not understand why I had this major headache, and stablike pains.
I was hospitalized for 2 weeks and during the last 4 years I have been in and out of hospitals and doctors.
After they found 'nothing' they told me that I might have LUPUS/RA. So they started me on drugs to treat reumatism. I was on 2000mg per day! Complained and said that the meds where not working and I needed help and someone to listen to what I was saying. Then one of the many doctors I had was telling me to shut up and go see a psychiatrist. That got to me and so I started writing letters. I got a 'new' doctor and he said odd. Told me he was only interested in my joints. After the second time w him he passed away and so I met a fresh doctor, on that was right out of med school.
She looked at me and said...*You cant go on living like this, this is no life.* she sent me to the hospital for 2 weeks so that I could get the right treatment. There they realized that I have no sings of reumatisum but rather a connection w Simvastatin.
They right away told me to stop taking all the reumatisum medication and they will now focus on removing Simvastatin.
I am blown away.... I was so sick, so may hours lost from work, family and friends. I almost left my husband because I felt like I was just 'there' not ever being able to do things. I was so sick all the time.
Wow is the only word I have in my head right now- I am in a shock.

I was put in the hospital November 8th, they were giving me Levaquin through IV's and then after they seriously hurt the back of my hand, I demanded to take meds by mouth-I had already had around 5 days of this through the IV-I was diagnosed at the emergency room with a ruptured appendix, and it had been that way for 3 weeks-it took 1 doctor and 2 hospitals to diagnose that!! really makes we wonder about the medical profession these days! so when I was released from the hospital after a 6 day stay and appendix still in me, they gave me a prescription for Levaquin for another 10 days-well, I took it for 8 days and had to stop all together-I have been so weak and from my knees down kill me! I have bad joint pain in my knees and hips, but I thought maybe this could be from sitting in a hospital bed for all those days-now that I've read all these complaints, I'm wondering if I should have taken this stuff at all! I hadn't taken any kind of antibiotics for over 3 years-have been ok up til now. I am so scared of the pain and tingling in my feet, thought maybe it could be blood clots in my legs from not moving around as much as I'm used to-my grandmother recently passed from a blood clot and my cousin also at the age of 33 died from a clot after knee surgery! so what do I do?? is it a clot or is it the dreadful drug "Levaquin" that is causing me all this pain?? any suggestions out there?? and I have no insurance either! what a terrible experience!

Thank you all for posting your experience with Levoxyl. My mother started to take this med about a year ago or so. She has experienced all of the side effects listed in postings. I thought she was going crazy. She actually found this site and e-mailed it to me. WOW!!!!!! We have been in and out of doctors (numerous) and hospitals for testing. All test results came back with nothing being wrong with her. She actually just went to Catholic Medical Center in NH (this hospital specializes with heart problems) last week because she too thought she was having problems with her heart. Thankfully all is o.k. She has now taken herself off the Levoxyl. It is amazing what we think will help us can do so much harm to a person. Good Luck to anyone who prescribed this medication. DO YOUR RESEARCH FIRST!

D.NH

I just started on topamax and it has done wonders for me i suffer from cyclic vomiting syndrome and have suffered for many years making my teenage years absolutely horrible in and out of hospitals all the time, despite some minor side affects i have my life back i can go on vacations i can spend the week end at a friends house without being scare i might end up in the hospital its an amazing miracle drug and i thank my doctor for finding it and prescribing me it.

Oct. 9,2008. I was given Avelox Monday Oct 6,2008 from my family Dr for a sinus infection . I went home & took the prescribed dose of 1, 400 mg tablet, and15 minutes later I felt a burning sensation coming from my toes to my face , I was having problems breathing , I suffer from asthma when I have any kind of sinus or cold type illness. ,I thought that was what was happening,but the inhaler did not help,, I couldn't stand up ,I couldn't sit up , I couldn't talk , I went into seizures,& started puking . I honestly thought I was dying , I couldn't even call 911 , thank God for memory call, my mother called 911 as I was home alone with my 5 year old granddaughter .
I was so incoherent ,I couldn't tell the EM"s what happened, all I could get out was anti.. The EM's thought I was either overdosed or having cardiac arrest . In the ER,the doctor's gave me all the anti allergens ,and I started coming out of it. I was soaked w/ sweat from the burning, I couldn't
speak right, it was if I had a stroke . My legs and body hurt so bad, I never experienced this much pain . 4 days latter I still am not alright . My entire body was red , I was so afraid to take even an Advil the next day . Then I heard the ER Dr. told my husband they're having a lot of problems w/ this Avelox! I asked an attorney if this is a suit and he said not unless it becomes a class suit! How on earth did the FDA approve this stuff ???
I would tell everyone ,this stuff is not worth the risk ! I came close to dying over a sinus infection ! DO NOT USE THIS AVELOX !

Here is our daughter's story, and believe me the tears are pouring down my face as I am writing this.
Our daughter, who had completed her series of 3 vaccinations has been experiencing considerable hair loss. Her first shot was in May 24, 2007, the second on July 26, 2007 and the third and final on November 27, 2007.
Here are the other specifics....our daughter was 13 turning fourteen.
She has had every blood test imaginable to rule out the obvious which may cause hair loss such as thyroid disease, polycystic ovary disease, diabetes, and the list goes on and on. Everything came back negative. We even have a future appointment scheduled with a rheumatologist this coming November 08. We have seen the Endocrinologist and two dermatologists (a scalp biopsy proved negative to any infection, disease, etc. Granted, she had a typical amount of stress during the school year, as any young teen would, but nothing to cause this. Everyday our daughter says to us, "you should see how much hair fell out in the shower today". She's so afraid to brush or comb it because of the extreme shedding. She literally, to date has half the amount of hair she had one year ago. Let me tell you she had beautiful hair. The hair loss is becoming quite visible at the forward part of her scalp. This has been devastating, hair is everything to a teen. (to anyone this is devastating) We must also mention that her periods have been totally out of whack. She went 6 months at one point without one. It finally came back, but it is so sporadic, getting every two weeks, at times extremely heavy, etc...
She also complains of intermitent dizziness. We are reporting this to Merck today (the Co. who makes this horriffic vaccine), along with the FDA. If anyone else is experiencing anything close to what we are, we all need to pull together and make the public aware of what's happening so we can prevent this from happening to our loved ones.
Please share your experiences. Feel free to write me if someone you know is going through this same tragedy.

I was hospitalized about four months ago for a total of three days due to a massive kidney infection, during three days in the hospital I was pumped full of Levaquin. I began suffering what the doctor believed was a migraine on the second day, let me tell you it was far worse than any other migraine I had ever had. So not only did they send me home with a prescription for Levaquin they sent me home with a migraine prescription. I took Levaquin for a week after my departure from the hospital, I am young and very naive when it comes to doctors and hospitals and I had faith in my doctor that the medicine they prescribed me was good for me. After suffering from a migraine for almost two straight weeks I began to suffer from blind spots in my eyes, and a kind of slowing down effect. I would get up and it would cause my head to feel like it take my mind and my eyes a couple minutes to catch up to my body, vertigo. Well I returned to the hospital and was told I was suffering a migraine, once again, no migraine I had ever had caused blind spots. They referred me to a neurological ophthalmologist who took the time to look at my eyes, and diagnosed me with Pseudotumor Cerebri. He told me that the medicine had caused pressure to build up in my head and caused hemorrhaging in the back of my eyes, hence the blind spots. I have a scheduled MRI to validate the doctors concerns, but the treatment he is telling me may reverse the affects is a long term treatment, and has a possibility of not being successful. So for a medicine I was given to treat one thing I acquire something far worse and all for trusting a doctor to have my interests in mind

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.