Last thursday symptoms and conditions

Am on day three of Omeprazole for pangastritis, ulcers, acid reflux disease and duodenitis. I have cried every day. This is not like me. Mother died of stomach cancer so am afraid to stop taking medication following endoscopic diagnosis last Thursday. After reading this I believe I will have a discussion with my gastrointestinal specialist about just cleaning up my diet to the 'n'th degree.

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.

I am 44 years old and have been taking singulair for about 4 years. 3 months ago I started experiencing crushing chest pain, tingling in my lower limbs, and felt very stressed out. I went to the ER last Thursday and was checked out for angina - the ER doctor told me I was suffering from chronic severe anxiety. I took Ativan for 4 days and felt better, but now the drigs are gone and I again having constant chest pain. In doing some research I found that anxiety can be caused by imbalance in adrenaline, and so started looking online to see if any of the allergy/asthma meds I am taking (adviar, singulair, allegra) can affect adrenaline. That';s when I found this website. Although i find the testimony compelling, I wish more folks would have poted about how their symptoms improved (or didn't) AFTER discontinuing singulair. Also I've noticed many of the stories are about children not adults; many people are taking more than one med for asthma, and most people's symptoms seem to come on right away whereas I have been taking sinulair for years and only recently have anxiety. I will stop singulair tonight and see what happens, but am wondering if anyone has come across further research that correlates singiulair with anxiety? My job life is really peaceful, I am otherwise happy, work can get hectic but that's true of any job, and I am out of ideas as to why suddenly at age 44, when I eat right and exercise - why get anxiety? Thanks for the posts, I'll try to remember to follow up after I am off Singulair for a few weeks.

I love Mirena, I am 29 years old with two children, and I had mirena twice, I actually have less cramping than usual with mirena and my periods are lights and regular. I just had it removed and I am looking forward to conceiving again.Also, I am able to conceive right after I have it taken out, I don't have any spotting or pain after removal.

Lamictal with lithium was the latest sentence for a lifetime of depression. Not only did the depression then intensify over anything I've dealt with for the last 40 years, but anger, rage, weight gain, memory loss, difficulty communicating, (could this be dementia at 60 yrs?) and loss of taste especially coffee and chocolate were now defining my life. I had been a happy, productive, exciting, witty, professional self-employed woman. So, I've been reducing my 250 mg dosage for the last 6 weeks with Dr. oversight. My last dose of 25 mg was last Wednesday. Throughout this experience, I've experienced confusion, head aches, zombie days, spatial disorientation, muscle weakness, muscle spasms, jumbled speech and thinking, and THE FOG. But, guess what? Today, I'M BACK. My head is clear, I have a plan for the day and I'm 4 pounds lighter than I was last Thursday. The surprise about the weight is that we went to dinner in restaurants twice in this last week and I haven't taken any special steps to lose the pounds. I knew it was time to evaluate myself without medication when the Dr. wanted to add just one more medication to level off the mood swings. Of course, this is a continuing drama, but it's great to be able to see me without the drug-colored lenses. I would not have done this without Dr. supervision, and I'm so glad he co-operated with my wishes. Sometimes you just have to throw the project away and start fresh. Have a beautiful day.

I had my Mirena placed almost exactly 3 years ago. For about the last year, I've had pelvic pain almost constantly. I've gone to my gyno and she's given me several ultrasounds. All show that I have multiple follicular cysts on both ovaries. I am starting to worry that I have endometriosis and my gyno won't give me a laproscopy to find out-you won't believe her reason. She says because I don't have a problem with fertility (I have 3 children), that she's pretty sure that isn't what's wrong with me. So, I was talking to a friend who has endometriosis and she gave me her gyno's name. I have an appointment on 18 August and the nurse told me to consider, in the time I'm waiting for my appointment, having my Mirena removed. I have battled depression for quite a while, I've never been able to lose my baby weight (my oldest turned 4 last month) and recently, my pelvic pain has become so bad that I have considered going to the ER a few times. Also, I have lots of cramping in my back. And something that I never considered being a symptom of the Mirena, I'm having a lot of trouble remembering things. If I'm trying to say something sometimes, I can "see" the word I want to say but I can't get the word out. But I've seen a lot of other posts here that describe the same thing. I was honestly afraid I had some horrible brain tumor. I have recently gotten divorced, so I don't need the BC anyway. I had another ultrasound last Thursday, with the same results, only this time, my gyno told me to go see a gastroenterologist (sic). Basically, I felt like she was saying "don't bother me anymore because I can't help you". She never, ever suggested removing the Mirena and stupid, gullible me never considered it because I trusted her that it's not the Mirena. However, now, reading these experiences that are so similar to mine (and my sister, who also has a Mirena and is having the exact same symptoms), I am going to call the gyno on Monday and tell her I want it removed at my appt next month. Thanks for sharing, ladies.

I on it for ms and it was iv and i went off it last Thursday i have numb lips numb belly sore legs sore back legs feel like they are on fire all the time tired all the time do not want to get hoping it leaves my system soon

April I started Singulair last Thursday night and felt tired and depressed
29th on Friday but thought it was something going on in my life. On
2009 Saturday, I had severe, throbbing headaches all day but took the
Singulair for the third night. Sunday, I again had throbbing head- aches so looked up this web site and thought, "Aha!" I stopped
the medicine but had dull headaches on Monday and felt tired. On
Tuesday, I woke up and had trouble breathing. I went to the doctor
who ended up putting me on a nebulizer, giving me a shot of
steroids and prescribing an inhaler that I'm to use 3 times a day as
needed until the Singular is out of my system. I was only put on
the Singular in the first place because my doctor thought my
hoarseness might be from an allergy. What a nightmare!
I also suffered from apprehensiveness, and also
sleeplessness, and a fever. Never again!

I was put on Lipitor 10mg 2 weeks ago after my bloodwork from my yearly physical came back that my cholesterol went up again. Levels are HDL 61 LDL 176. After the first week I called my MD to advise that I was having chest pain and muscle pain in my legs and forearm. He said to cut the dose in half which I did last Thursday. Yesterday all of a sudden I had heart flutters the entire day! I am a 43 female who goes to the gym 3 times a week doing 30 minutes of cardio and weights. I eat right and overall I am in great shape except having high cholesterol. My blood pressure is great, had a stress test and echo last year both negative for any problems. I called my doctor today and advise that I was still having fluttering in my chest and that I am stopping the Lipitor. What good is being on a medicine that helps with one problem but then causes others that you may need more medication for???
I have been feeling like crap ever since being put on Lipitor and I believe that it is the medication that is giving me the problems. Last year my MD put me on Zocor and I stopped that after having the muscle pains. I am now hoping that things will get back to normal and I plan on telling my doctor that these "statin' medicines are not for me and there has to be something else.

ive had mirena since nov. 2008 i had it placed 6 weeks after having my 1st daughter in sept. it hurt going in and since then i have had nothing but bleeding since it was inserted. its put me in the hospital twice, 1st time doctors said it was a cyst on my ovaries ( i refused a pelvic exam) then last Thursday night i started having horrible cramps on my right side in my ovary area to the point where it hurt to walk. went to the ER they did an ultrasound CT scan and a pelvic exam turns out i have a bacterial infection in my uterus. and i remember my obgyn telling me that if it cause an infection i needed it removed so all in all i made an appointment to talk about removing it tomorrow.. i thought it was the best thing in the world but they don't really tell you every side affect. i cannot wait for it to be removed although im not going to like taking a pill everyday!

I happen to stumble across this sit after googling DIZZINESS and forgetfulness oh did I mention slightly slurring at times!!! I am a school teacher the kids would giggle all the time so thought to myself okay there is definitely something wrong here. I have ZERO patience and you need buckets full of that in my job. I also have a MIRENA I had mine put in after being convinced by my OBGYN and a family friend. Back in July 2006 I haven't felt right ever since. I am so glad I have come across all these wonderful and open women. I am making my appointment today to get it removed maybe I will start feeling normal again.

I was started last Thursday for sinus infection. I ended up in ER on Sunday with what I thought was a migraine headache with nausea and vomiting. Which I have a history of. Thank God the doctor on call did not give me the normal shot which I usually get and send me home. He was did blood work and found out the my liver function test was so high that it was not safe for me to go home so I spent two days in the hospital to get my liver functions back to safest enough level to send me home. And they are not normal yet. So be ware of this meds or any meds that it is related to

Both my children, girls ages 6 and 9 are currently taking 800 mg. a day of Amoxicillin for double sinus infections. My girls are normally upbeat, happy kids and I have noticed that over the last several days they seem gloomy, quiet, fatigued and frankly rather depressed. As this is unusual for them, I can't help but think it is the medication. I can't wait until they finish the dose.

I am just in tears right now... Finally to know what is wrong with me is so overwhelming. I had Mirena put in Oct of 2008 after my son (third child) was born. No other bc had worked for me and I had miscarriages and two other children at age 24 because of this. My doc pushed Mirena like there was no other option on the planet. He raved about it and was VERY quick to just give it to me without discussing any negative side effects. In fact all I heard were positives, I went home AFTER it was in and looked at the official website to see what the side effects may be.
The hair loss started almost immediately, which like many others I chalked up to hair loss that you get after having a baby. I had pains all over my body, but I had a fall at the hospital (off a broken toilet seat with my numb epidural legs) but I didn't know why I was just...sore everywhere. Achy just all the time almost similar to when you have a fever but not quite. Then the memory loss began. This I thought was because my son had been born with Persistent Pulmonary Hypertension and had to be put on ECMO. I thought the stress of it all was just causing memory loss and confusion. The fatigue was constant, never ending no matter how much sleep I got. And like I've read by so many others, thought I have 3 kids and I'm a full time student, my husband works 70+ hours a week, I'm just busy and exhausted. The mood swings, anxiety, and just overall feeling of being crazed started around Christmas time (I thought it was the holidays!)
So I began to cut down on SO much. Like my cleaning, I tried to make the simplest meals I could (I DREAD cooking something that used to be a passion of mine) just getting done what my body allowed. And week after week my body let me do less and less.
Today after an entire weekend of ocular migraines and getting 10+ hours sleep every night and feeling like I have gotten less than 2, fighting with my husband because I'm such a wreck and have ZERO sex drive, constant pain, and after my shower this morning looking at my hair just bawling seeing how much I have lost, I just googled all my symptoms.
I'm so thankful I did, I'm so glad I know that this stupid piece of plastic is what is sucking the life out of me! Thats what its like! Its like RAPID aging. A part of me is outraged too. Why does it take us having to do our own research to find this out? This is SERIOUS. This stupid thing has practically cost me my marriage, I can no longer do school work because I can't remember ANYTHING, I can barely take care of my kids, I make it through the day by the skin of my teeth and honestly I was thinking today if I can't live like this anymore. I mean that. If this got any worse...I don't want to think about it. This should definitely be told to anyone considering Mirena. Yes, it may be a miracle for some people, but there is the chance and I don't care how slight, we are living proof that it happens, that it will suck the life out of you and consequently destroy it. I'm changing docs and getting this thing out ASAP.

i took citalopram for approx. 8 mos, and about 3 wks ago i talked to my doc about getting weaned b/c i want to get pg. she told me to cut them in half and take a 1/2 every day for a week, and then the second week take 1/2 every other day. i finished them last Thursday and for the last wk. i've felt fuzzy and unfocused, and whenever i turn my eyes w/o turning my head i feel like i might pass out. want to cry about EVERYTHING, i thought that would go away when i was weaned b/c i seemed to be doing okay before stopping the pills. also, when i first started taking them i couldn't decide whether to take them in the am or pm b/c shortly after taking it, i would get almost manic, wanting to clean etc, and then after about 2-3 hrs, i was knocked out cold, didn't hear the kids, nothing.

I had my Mirena inserted in 9/07. I was fine until 6/08. In 6/08, I started to experience strange urinary symptoms of urgency and frequency. I addition, I had pain on urination. No UTI present. I had a cysto to r/o interstitial cystitis. The physician said that it did not look like IC because I did not scream when fluid was infused into my bladder. For the last 5-6 months, I have been dealing with my strange symptoms. The GU speculated that my problems might be due to my dropped bladder, but he seemed very unsure.

A few week ago, everything changed. I started having the most severe urethal pain. I was in tears all day long with 3 kids to care for. I have wbc and rbc in my urine. ALL cultures were neg. The Dr. even cultured me for STDs. Last Thursday, I had my Mirena pulled out after reading this message board. I'm hopeful that it hasn't caused irreparable damage to my body. I still have the same symptoms 3 days post Mirena. Please let me know if anyone has had relief post Mirena.

Thank you!
K.

Thank you for this site...although it is too late being I already poisoned myself with my 1st dosage - I know better now to STOP TAKING THIS DRUG IMMEDIATELY.
31 y/o male - non smoker - In good overall health.

What happened...(brief history of what got me to the point of being prescribed this horrid drug)
I caught a cold a few days after drinking quite heavily at a wedding (Aprox 1 month ago). It was severe enough for me to take a trip to this new doctor that is in my network and nearby (how I wish I could use my old family doctor that is out of network).
Symptoms then were congestion in my head and upper chest, cold sweats, runny nose. The doctor told me to take some over the counter stuff and try to fight it off w/ Mucinex, and Zyrtec - and lots of liquids. If that didn't work, he asked me to return.
It took about 5 days, and I seemed to kick the cold.
Approximately 2 weeks went by where I was feeling fine, then it seemed as if I was coming down with something again. (Last Thursday was when I started feeling ill)
I think what brought it on this time was breathing in excess dust at work opening some skids of paper in our warehouse.
Anyhow, this time around I had a pretty serious cough, felt feverish, and fatigued.
Sunday morning I woke up and took two Mucinex to break up the cough (which work great by the way)...and I hacked up something awful enough to call my doctors emergency line and have him paged. I was ready to go to the ER. It wasn't just phlegm or mucas - it was a soild mass of lord knows what containing blood. It look like an organ from a small critter.
Doctor said to keep taking the Mucinex and if I didn't feel better to come see him.
The coughing got worse on Monday, and the mucus I was spitting up wasn't pretty.
I went to see him yesterday afternoon (Tuesday) and he said its time to start you on an antibiotic and diagonsed me with an Upper Respiratory Infection.
He gave me Avelox, and Advair, and I asked for some of the good cough syrup w/ the codeine. He also sent me for a chest X-ray.
I got home around 4pm, made some food, then took some syrup and tried the advair.
I waited to take the Avelox til later on in the evening so I could set up a routine as I work nights and 9pm would be good.
I took the Avelox, around then, along with another dose of the cough syrup.
Around 1 hour later I felt extremely nauseous. I would burp, and feel almost ready to vomit...it was my body rejecting this horrible drug. The nausea came and went, came and went - then I got tired.

I laid down around 11pm and then the REAL trouble started. I must have fell asleep for about 30 mins, then woke up suddenly gasping for air...It felt like my heart was about to stop. I sat up in the bed panicked. I then got a little nervous, but calmed myself down, drank another glass of water and tried to fall back asleep. Sure enough just as I was about to drift off, the same sudden feeling of my breathing or heartbeat was interrupted and I sat up again. I had tingling in my chin area and in my arms. Walking to the bathroom I felt slightly disoriented and dizzy, and my legs and whole body felt weak. I also started getting itchy in my legs and groin area. Now I'm scared to go to sleep so I come to the computer and started researching this Avelox. It's 3:30 am now as I'm writing this. I looked at this site and http://www.fluoroquinolones.org/ before decided to post my experience.
I am still very itchy, slight nauseous, and feel disoriented. I'm scared to lay down to sleep now, but hopefully that will wear off soon - but I feel very nervous, uncontrollably. I almost want to induce vomiting to maybe get out any of the drug that is left in my stomach, but hate vomiting.
I will not take another dosage of this Avelox, no matter what this doctor tells me...and will give him a piece of my mind for prescribing this instead of something like ammoxocillin or just penicillin.

For me having the Mirena removed just last Thursday was the right decision. I was not using it for birth control but as hormone therapy for heavy, crampy periods. I had it inserted in July 2008 and bled every single day for the entire time, I had it removed last week and now I am bleeding very heavily but hopefully that will stop once all those hormones are out of my body.
While on Mirena I lost all sex drive, I became severely anemic and with that fatigued terribly, and moody, crying at nothing and screaming at my kids or husband for stupid reasons, I felt bloated and gassy and didn't have those problems before.
I am 42 years old and I hate my heavy bleeding in fact I want a hysterectomy, but not sure now what I will do.

For those of you who had the Mirena removed, how long did it take to stop bleeding afterwards? This is draining every last ounce of energy for me and I am taking iron supplements.

What sucks is the cost of this, Even with insurance I ended up paying a lot out of pocket to get this thing and then all the Dr. visits due to bleeding and side affects in the 4 months it was in and now the removal of it. I am wondering if there is any way that we can get a Class action lawsuit against Bayer for this horrible thing they are trying to sell to women.
I know there are some out there who have not suffered all these horrible side effects at least not yet or that they are aware of, but I truly believe that there is nothing good about this IUD and those of us and there are a lot of us who have suffered with this should be reimbursed or compensated for the pain and loss of parts of our lives and expenses with this. Does anyone else have any thoughts on this?

I finally had mine removed last Thursday and it was quick and painless. The doc still refused to believe any of my side effects were from the IUD - needless to say he is now on my EX-DOCTOR list! I should have printed this website for him. I had a very light cycle on Sun/Mon and then it stopped. I mentally and physically feel better. Now I can focus on losing the 40 lbs I gained over 1 year on the IUD without severe lower back pain, achy joints, bloating and acne in the way. My best friend has an IUD and 3 kids and loves it ... so go figure!! She is one of the few lucky ones.

Started taking it last Thursday, and with a previous bout with depression, and a pending ending marriage, I decided that I would go ahead and cut this off at the pass and get on some medication early. Paxil made erections difficult, so I got off of it back in 1998, and then within 5 days of taking budeprion, I am noticing the same side effects. Including what my doctor called, "the inability to finish."
Getting off of it now, wellbutrin worked in the past.

I had my Mirena put in on 9/11/08 last Thursday. I got it done on the recommendation of two of my co-workers that recently got theirs a few months ago. I had been having stomach problems, found out I have food allergies and than suddenly couldn't stomach my birth control that I had been taking for several years. Mirena seemed to be the answer. I had it put in on Thursday which hurt like hell. I was a little sore Friday and only spotting from my 2nd day on my period. By Saturday I was very sore and felt nauseous. By Sunday I was bleeding heavily, nauseous and had migraine headaches. By Monday I couldn't keep water down and had the worst headache. I called the doctor and she told me that the side effects were normal and I needed to give it time. I had read these post from Saturday and was getting worried. On Tuesday I couldn't even lift my head off the pillow. I woke up with my hands in a cramped position and couldn't feel them or my feet. I had tingling and numbness in my hands, feet and lips. I called my regular doctor who got me in right away. I had to be rolled in a wheelchair to his office because I couldn't even walk. I throw up about 4 times on the way down to hall to his office also (thankfully they had trash cans along the way). He immediately took the Mirena out and I got feeling in my hands and feet about 10 minutes later.

I was finally able to go back to work today after being out sick. I still have a dull pain on my right side around my ovaries and my stomach is very tender. I have felt like I was in a fog all day today and still a little sick to my stomach. I hope these symptoms wear off soon.

My first injection gave me generalized bodyache, but after the 3rd day it was absolutely wonderful, I am 49 years old, 120 pounds and 5'5, and I felt my legs extremely energized like when my knees were not injured. Then I went to the 2nd injection, when the medication was ejected in the joint, it was extremely painful. I had to have help to excert my self. I was not able to squat down. In the mornings,the posterior side of my muscles, below the knee, felt like it was shrunk down to a third. Every step was excruciating pain, especially when walking down just a few steps. Before the shot,I had pain in the lateral side of the knee. Now the pain is in the internal side of the leg, starting below my knee all the way down to my big toe. If I would have known this pain would have occurred, I would have never taken the second injection. My condition got even worse than before I ever had any injection. I am so devastated I have come to the bridge of crying and feeling crippled. I had the last shoot about two weeks ago and my legs feel very heavy when I take a step. Now I hope and pray for a miracle.

I had Mirena placed just last Thursday and I wish I hadn't. The pain was excruciating, nearly passed out. Ever since, I have been nauseous, headaches, cramping/sharp pains in lower abdomen (not like menstrual cramp) and excessively tired as well as dizzy. I will give it the three to six month trial but as of right now I would not recommend this to anyone. I should have stayed on the pill!!!!!

I am not sure if my side effect is from using Singulair or not. I just started taking the Singulair 10mg last Thursday only in the evenings. After 3 days my face was swollen to the point that I couldn't see. I went back to the doctor and he didn't think the Singulair had anything to do with it since he was treating me for a contact dermatitis chemical burn so I still continue to take the Singulair but the swelling hasn't gone away yet and it has been 3 more days. If anyone can shed some light on if this is a side effect from using Singulair it would be appreciated. I also am taking Xyzal in the mornings so therefore I am not sure if this is what caused my face to swell. Any replies would be appreciated.

I am a 38 Yrs old and I took myself off Yaz 2 nights ago after being on it for 2 weeks. I still need to call the gyno and inform her. My personality completely changed, my moods terrible, snappy and extremely short fused, i think i'm officially banned from the dunkin donuts at the end of the street after yelling at them for screwing up my order-normally i'd let it go and just get it fixed, no patience whatsoever. I'd never been on birth control before, and I'll never go on it again after this experience. I didn't even want to be with myself. I can't believe my boyfriend didn't dump me after Sunday. The side effect i find odd and worrisome the most is, and I still have, pressure in my head and throat and tongue, it's dissipating as of today but started last Thursday (about a 1.5 weeks on the yaz). Has anyone else experience the head pressure?