Horrible pain symptoms and conditions

Someone help! I've had my Mirena IUD for almost five months now and at first I thought it was wonderful but lately I'm thinking I've changed my mind. Every few days I'll get these lower back aches which feel like pre-contractions, and I get this horrible pain on my right side between the bottom of my ribs and my hip (more towards my hip). This is debilitating pain, where I have to put my son down and either sit or lay down. I have an appointment this week with my doctor but I was just wondering if anyone else has experienced anything like this. Occasionally I'll bleed during/after sex. Also, I started working out again and after a three mile walk (pushing the stroller) I came home and was bleeding pretty bad, then about ten minutes later the pain on my side started again and my lower back pain started up. I don't know whats going on and my nurse practitioner acted like it was NBD..... its a big deal to me and I'm freaking out about it.... anyone???

Have been taking Fosamax for 2 years until stopping 5 weeks ago at the advice of my gynecologist. It never occurred to me to associate my joint and muscle pain to this medication, it felt like I had generalized arthritis. I started to get informed online, to find out that my terrible problem stated with Fosamax. I am now feeling better from most of the pain, however I am still suffering from extreme pain in my right buttock muscle, keeping me up at night, to relieve the pain I am taking tramadol which only helps during the day. Is there anyway that this Fosamax side effect can be reversed? If anyone is experiencing what I just mentioned, please let me know, I am afraid that this horrible pain is permanent.
Many thanks.
A. R.

Mirena inserted December 07, 6 mo. after my son was born. Was not even dressed after procedure when a severe wave of pain took over. Asked nurse, said "discomfort" was common. Thought to myself, I've had 2 kids, this isn't discomfort. She gave me a "super" Advil. No clue what it was, took it because I felt like passing out from the pain, Called husband on way back to work, in tears, thought I was going to vomit from pain. Got much worse, had to pull car over -- afraid I was going to black out. Mustered up strength, got to work. Took additional 3 hours for cramps to subside. Completely exhausted. Next night, out of nowhere, horrible, horrible pain -- never had ovary issues, but it was to one side, thought my ovary was exploding. Went to urgent care cetner -- didn't know what else to do. They took Xray (no ultrasound available), nothing out of the ordinary. Called dr. -- she was perplexed -- never heard of this before. Next 6 months a blur. Every single month, at completely random times, horrible pains would hit again - nothing I could do. So bad, thought I would wreck my car when driving, felt like throwing up from pain, had to lay completely still, take 4 ibuprofen and WAIT for it to go away--up to 3 hours each time. This left me exhausted and extremely scared for the next month. Waited the standard 3 months -- up to 6 months. Finally gave up, asked dr. to remove it. She did. Have not had a SINGLE episode like this again. IMy body doesn't react like this to new things, so I was shocked when my I didn't adjust. I have no other way to explain this, but I am interested why the side effects were so unheard of by my ob-gyn. She reported them to the FDA and pharm. manufacturer. WEIRD.

I am 22 years old and I got the Mirena April of 2008. I got it put in because I have a blood clotting disorder and this was the only option of birth control that was safe. I don't have any kids. When I first got it put in it was the most horrible pain I have EVER experienced in my life. I bled for a couple months on and off but it was just spotting. I still have my period but its way lighter! I LOVE THE MIRENA! Ive had some side effects but not to the extreme you ladies are saying. I was on the pill for 4 years and I have the same side effects as i did on the pill.. The only thing that I dislike about the mirena is the bad ODOR! I don't like it. I feel like I can always smell myself and Its embarrassing! I use summers eve and clean myself out probably more then I should, but I cant help it. Does anyone have any suggestions?

I have UC, and was diagnosed in April after a Colonscopy. I was put on Prednisone and was never able to get past 20mg without getting very sick again.I changed everything I DID, my diet, everything. they finally put me on Imuran. But the prednisone is making me loose my hair, they started before imuran. Also give me horrible pain, in the bone and muscle. I take all my vitamins, and it helps a little but it still hurts. they run regular blood test. Some days I feel like I can;t walk. Make sure to cut your salt out. It also made my face horribly round and fat. and i got a fat hum p on my back. The acne sucks, and it messed with my period too!

So like i just told the lady that thinks this site is a joke, I am happy for her that she hasn't had any negative side effects. For the rest of us though, this site is a blessing. I am a 27 year old with one daughter who is 2 1/2. I got my mirena put in at about my six week check up as well. For me, it took at least a year for me to really notice any symptoms, I guess before I just thought it was new mama syndrome. Now I am losing tons of hair (now when I say tons, no one can tell but me, like when i pull out handfuls when i shampoo or blow dry), I have horrible fatigue, depression that i am taking medicine for with little relief, discharge, and about once a month i have horrible pain on my right side about where my ovary is. Oh and not to mention no sex drive, which is not normal, and moody, moody, moody.

So my point pretty much is that I am a REAL WOMAN, not someone paid by a drug company, and I was looking for answers. Maybe the lady that is posting nastiest about this site is paid by Mirena? Hmmmm.....

Started taking Levaquin Friday afternoon for a bad UTI. That night I had trouble sleeping. The next day I woke up with horrible pain in my mid and lower back and in the backs and sides of my legs. My right ankle was also in a lot of pain. I took 4 doses. By now I am completely miserable. My stomach hurts and I'm bloated and quite nauseated. The pain in my back and legs feel much like labor pains. Today the back of my knees and down my calves hurt. It's hard to explain the agitation feeling I'm having. I feel miserable. I looked up side effects today and realized it's the Levaquin. Good grief, why don't they tell people this?? I cannot wait for these side-effects to be gone.

They are switching me to yet another anti-biotic which I start tomorrow with much apprehension! But, my cultures came back very high and I will need to continue on something for another week.

I was put on 20 mg twice a day to combat my Crohn's Disease. A few days in, I began having trouble sleeping because of a heart beat that was making my whole torso and head throb. Exactly one week in, I woke up with a bad headache and nausea. I got out of bed and my heart started racing. I couldn't take my pulse at the time, but my estimate is about 150 beats/minute. The doctor accelerated my tapering in response to this episode. Right now I am taking 30 mg a day, but I still experience a heart rate in the 130's and chest pain several times a day unrelated to physical activity. I will say, however, that all the symptoms of my Crohn's Disease have really been diminished by this drug, and so far I am willing to accept these side effects.

I am 19 years old and I have depression. I had a Laparoscopy done in January to remove a rather large cyst... during the surgery they found that I have endometriosis mainly on my right side. After about two months of horrible pain (after the surgery) my doctor decided to put me through the 6 months of Depo Lupron. After a week the nausea was horrible and I actually vomited at work. The hot flashes have been horrible and my body hurts all over all the time. About a month or so into the treatment, my depression intensified to the point that I didn't want to live any more. I would sit up at night just thinking about how I could make it all stop. Crazily enough I stopped taking the depression medicine while one the shots and I felt a little better. I still have some bad days but it is better. The night sweats have gotten worse the past two months. I have a consult in a couple of weeks to figure out where to go from here in my treatment. I've read several "testimonials" and it seems that I'm not alone in the way I feel. My friends and family haven't exactly been understanding about it either. It's nice to hear that other people can sympathize with me.

I started taking this garbage in May of 2009. I would go to the Dr and my BP would be 180/110. Let me say im still on Lisinopril BUT stopping tomorrow. Let me tell you my story.

35 year old male, diabetic and HBP. After years of not taking care of my self i went to the doc, i started taking Lisinopril. With in weeks i got a hacking cough and my BP was still crazy high. They up'ed my dose to 20MG and then hell started.

Constant blinding chest pain, strange electrical shocks in my back and head, went to ER and was admitted, they said i may have had a PAST hart attack Weeks of in and out of the hospital a 3 day stay in the cardiac ICU! Then i had a CT angiogram with dye and that reviled MY HART WAS FINE. I still had this horrible pain in the chest and legs and hands and my gut, electrical shocks and night mares and freak out for no reason at all. Problems with erections and slow hart beat. Unreal panic attack that i think i was about to die or GO insane. The past few days i have had intense pains in my upped back and gut. I went to have some blood work done to see how my new diet is doing. All the numbers were amazing, BUT my LIVER IS HURTING! Now i do not see a doctor for 5 day to review it all BUT i know this pill has mad my life hell for the past 2 months. MY LIVER WAS FINE BEFORE i took this pill.

I was able to make my diabetes VANISH with diet, i must try that with HBP. STAY AWAY FROM THIS PILL.

I have been on Warfarin since October 20th of 07 after being bedridden for 3 weeks in excruciating pain in my hip/butt which kept me from moving & i'd drag my left side of body from my waist down, into our bathroom in excruciating pain unable to turn to flush a toilet or stand for more then a minute. I begged my primary doctor to "give me an mri as my back was in so much pain with the hip/butt". I had been getting epidurals for what doctor assumed was a herniated disk.i was in a wheelchair now & my husband took me several times to E.R. AND THEY SAID "WHY ARE YOU CRYING IT'S ONLY BACK PAIN." I labored more & more just to breath. I couldn't get my breaths. "Frightening" finally Then, I walked myself into the local E.R. and told them "I think I have a clot in my lung because I don't have a cold or a bronchitis & I've been in bed so much I believe it is a clot." It was two clots in my right lung. My lung hurt a little more each day I recall I went about two weeks gradually having more & more difficulty getting my breaths. I was hospitalized and then my primary wanted NOTHING to do with my care when E.R. doctors called him.local hospt. took care of me & the clots resolved. I am still on warfarin for coumadin. I really do have a memory problem I fear now, "short term", especially now after 2 yrs on this med. Also, Last time I went in the sun I was so wiped out exhausted like it beat me up. I am afraid to go back to the beach. I get headachs also and one time when my INR. went up over 3, my ankles got these little red spots and also on my chins of both legs like blood specks showing thru the surface.Still there but not as evident. My avg. INR is 2.4 I feel most comfortable at.I try to maintain. Back in 1998, I got two clots in my left leg after a botched knee surgery to repair a torn cartledge and awoke with an in place fractured knee cap.. two weeks later horrible pain in my left leg revealed two clots one at ankle to groin in my vein=d.v.t. and the other at the side of my knee in artery to groin when the tornaquat was.

I took Januvia for 4 very long weeks. At first I experienced rectal itching so I increased my fiber, which helped. After the 3rd week, I had horrible pain in my arms, I was bloated to the point that my pants did not fit and the gas was unbelievable. I stopped taking it about 2 weeks ago, the pain in my arms are gone but the bloating and gas are still present. You can also add nausea, now, every morning. Having read here that it takes a month to work its way out of your system I hope to be back to normal in a couple of weeks.

I feel so relieved to have found this website. I am going to call the doctor and have my Mirena removed ASAP! I have been experiencing many different random health problems lately. Which is strange because I am an extremely healthy person. My husband was laid off from his job and we lost his health insurance, so through all my symptoms I have just been suffering through it because I couldn't afford to go to a million doctors and have a million different tests run to find out the source of my symptoms. It started with itchy hives on all of my joints, elbows, knees, knuckles, toes and fingers. Then a symptom I had gotten during my pregnancies called PUPPP which is basically ugly, little, red bumps that ooze a clear liquid and itch like the dickens on my hands, fingers and legs. Then a big knot developed under the skin on my right wrist. The pain started on top and started radiating all the way around my wrist. Then the numbness, tightness and pin-prick pain occurred in my fingertips, then my hand, then my entire arm went numb from the elbow down. I also had horrible pain in my reproductive area on two different occasions that had me doubled over in pain. It felt exactly like contractions. I also have been bleeding every day for several months. Not enough to call it a full blown period, but bleeding every day. Some days, blood streaked mucus, other days full on blood clots would drain out of me. I've has horrible back pain and have been very fatigued even when I am careful to take care of myself. I also am naturally a very optimistic person who can handle bumps in the road of life, but lately, even though I hate to admit it, I have been down-right depressed. I have lost interest in all my interests, have a hard time shaking off life's set-backs, find myself on the verge of tears a lot, and basically have just wanted to pull the covers over my head and not wake up until I can just feel like myself again. Then last night my lips started to tingle, numb and swell. Then the same thing happened again tonight. I told my husband I am just falling apart and don't know what's wrong with me! I have never had any health problems before and now it's a new symptom practically daily. He said he had been doing some research and that he thought I was allergic to my IUD. I immediately Googled "Allergic reactions + Mirena" and found this website. It is such a relief to know that I might actually have an answer to all my problems. I can hardly wait for the doctor's office to open in the morning, I want this thing out right now and I want my life and ME back!

I am 21 and am in the second week of the second pack of pills. I have to attend a low-income based women care and either these docs don't really care or are out of their minds. i have been having problems with cysts on ONE ovary (left) about a year and a half ago the cyst got 2 inches in diameter. It supposedly went away on its own. I ended up in the ER again a few months ago and found out there is another cyst on my left ovary (which i have reason to believe its the same damn cyst, just flaring up and down)
Anyway I have had horrible side effects on just about EVERY BC i've been on. depo and numerous diff pills. I even had a 2 month period while on the depo. but with Loestrin I have had countless side effects that incl:
hot flashes, anxiety, depression and mood swings, cold sweats, restlessness, sore and swollen breasts, constipation, heart burn, almost constant back pain and ovarian pain and worst pain when on my period. I had 2 periods my first month, missed ONE pill in the beginning of my second month and had a second period within 2 weeks with the most horrible pain. The only good side effects are an increased sex drive and a change in appetite.
I really don't know what to do. try a different bc pill or just stop altogether considering all the problems i've had.
i've thought about ortho-novum, girls my age seem to have less complaints about it....
this is so frustrating!!!

I've been on NuvaRing for a little over 2 weeks now, before that I had been using the OrthoEvra patch. The patch was working just fine but it's less convenient in the summer (esp in TX) because sweating does cause the sticky stuff to ooze around the edges and I often found the patch stuck to my clothing. So, back to the ring...the first few days I swear I could feel it inside me but I gave it some time and figured I would get used to it which I have. I haven't experienced any of the other symptoms you all are sharing about but I have had horrible pain in my hips. It's not a joint pain, I think it is actually swollen lymph nodes. My OB/GYN said they had not heard of this type of side effect and suggested Tylenol and fluids and of course to call back if worse or if no better in 3 days. Is anyone else having hip pain or issues with their lymph nodes (hip area)?

Was on Prednisone for 11 days for an injury to my neck. I knew nothing about the drug except what my doctor told me that it would reduce inflammation in my neck and help with pain.

Well, it did nothing for the injury and pain in my neck. BUT.... I had HORRIBLE menstrual cramps and got my period 8 days early. I've had my period for 9 days now AND terrible pain in my upper left leg. I thought the pain was related to my leg and as the days went by I realized it was in my left hip! It's so bad I can't lift my leg without extreme pain. I KNOW IT'S FROM this awful drug.

I've been off of it for 4 days and the pain is still with me. I called my family dr. and was told Prednisone doesn't do that. BULL!! The paperwork I got with it from the pharmacy show "Changes in menstrual periods" "muscle/joint pain" "bone pain".

I wish I knew this BEFORE I ever took it.

Does anyone know if these symptoms and problems will go away after stopping it? I called the pharmacy and was told it will take 2-3 weeks for it to get out of my system!!

Has anyone had problems that eventually went away after stopping the drug?

Thanks and I hope everyone else is okay soon! This drug should be off the market. I received no help for my neck pain at all!!

ok, so I am 28yrs old just had my second lap for endo and my doctor has recommended lupron, after reading this I am soooooooooo scared to even get near this med. Its like you either take this with the hope of saving fertility and no pain..or not and have endo ravage your body and you will live with unbearable pain!!! I have no idea what to do, my post-op surgery appt is this week, and i am so scared after reading this. Is there anyone that did not have weight gain, headaches etc...anyone that can testify that lupron actually worked for them? Cause right now its my health on the line, my ability to have children, my ability to have a normal life free of endo pain or these crazy, horrible side effects...please help me!!!

I made an appointment today to see whats going on.I have been on yaz for about 3 weeks..yes i too have all the same symptoms however i also have a horrible pain right in between my breast..it feels like someone is standing on me.i wake in the night in tears cause i cant roll over i cant pick my 3 kids up cause the pain is always there.... maybe its something else but at the same time im thinking it might be this pill.. as of today im off it.. and when i find out what my doctor says i will let everyone know.. i personally think out of the blue im seeing all these commercials on this pill and doctors are pushing it like crazy so im feeling a little like a ginny puig and no one will tell us this pill is causing all this crap in our lives! so im off to
the docs to see whats hes going to say not too hopeful...

I have probably had THE WORST experience with YAZ, than anyone else on this site. Please GOD do not go on this drug. It is pure poison, save yourself!!!! I am having horrible pain as I am writing this. OK, I have been on YAZ for about 9 or 10 months. My Doctor draws labs every year on all of her patients (just run of the mills things, to make sure you are still healthy.) By the way I am ONLY 21 years old. I was on Ortho Tricylen for about 3 years, but wanted to try something new. While on Orthotrycyclin, I had normal blood pressure, normal lab levels, painless periods and ovulation. This drug almost killed me, it might still. Within one year, I went from being a healthy 21 year old, to having my blood pressure increase every month until the doctor put me on a blood pressure med, which didn't help, so she increased that dose, which didn't help, so she added a water pill as well, which doesn't help. The highest my blood pressure went was 158/110. The doctor did a kidney ultrasound, everything was fine. I was having constant cramping on the left side of my pelvis for 3 months, the doctor did a uterus and ovary scan, and those were fine. the doctor ran blood work on me, My TRIGLYCERIDES (the fat in your blood) had TRIPLED in 9 months. That seems impossible to me, considering I had not gained any weight, in fact I had lost 10 pounds, and my cholesterol was not elevated, but was low. At the advice of the doctor I stopped taking the Yaz over a month ago. My period is almost 2 weeks late, and i am not pregnant. I am still having constant severe pain in my left ovary in my pelvic area. I had no sex drive on Yaz, and increased anxiety. I developed a strange fungal infection on my chin while taking Yaz. I do not have any diseases, and should NOT be developing a fungal infection on my FACE. I just hope my period comes back, I want to have a baby one day. I am very sad and hate myself for taking Yaz, please take this seriously.

I just had my 2nd lupron shot, and I have to say I am fine, no negative side effects. My first shot, it had stop my hot flashes and I was sleeping better, after getting close to the 28 day mark , I started to feel the pain and discomfort that I had before the shots and agree to the 2nd shot. I was having hot flashes before the 2nd shot and still have them, but the most important thing is I am not having the pain which was horrible pain that I needed tylond codeine to help me. I have not seen any weight gain, I stay active and work out even harder , no increase in appetite, so I will take it and see each month if any side effects come upon me, but so far I am good. I have to say that I was already into menopause before these shots.

After being on YAZ for about 7 months and realizing how it was harmin my mind and body, my doctor told me to stop taking it immediately, even though it was mid-cycle. he put me on Loestrin24fe because "there has been a much higher success rate with a lower dose of estrogen" NOT IN MY CASE!

i started taking it on a Tuesday, it is now the following Monday and i have already experienced:
harsh aches and pains throughout my body, unbelievable mood swings from cryin until my eyes hurt for NO reason to sitting and talking calmly within 5 minutes of each other, once again a complete lack of sex drive which i *just* recovered from with YAZ, not being able to eat yet having extreme weight gain??? my stomach is completely round when i have had a 6pack for my entire adult life and my jeans will not get past my thighs anymore, my skin and hair are oily and i have broken out worse than i did when i was a teenager ...

and the BEST one yet! Severe Panic Attacks during the night to the point where i am terrified to sleep because of waking up hysterical and actually "feeling" my dreams. i woke up from a nap yesterday crying uncontrollably because i was convinced i snapped my spine/neck because i dream it, felt it snap and HEARD it snap in my dream. it is all too real and i am on lack of sleep AND not eating for a few days.

Needless to say, i have stopped taking the pill as of last night. i am hoping to get back to normal in about a week because i clearly cannot function like this. I missed a gorgeous Easter day yesterday because i was having a low grade panic attack ALL day and couldn't eat or even talk to anyone.

i am not going to let another bc pill ruin my life this year. its not worth it but i must ask, where do i go from here? i am concerned about getting an IUD because my body seems to have every side effect possible with any type of birth control but i think the IUD is my only option besides complete abstinence.

I was prescribed z-pak for a horrible cold I had. Immediately I had stomach cramps, horrible pain that would come and go...but I kept taking the medicine. Each day the stomach cramps were worse than my cold. By day 5 I broke out in a rash on my upper chest, shoulders and upper back...they were like pimples that itch. I am assuming since the zpak stays in your system for 10 days that this stomach pain and rash will continue. PLUS the zpak has not helped my cold/cough. I will never take the z-pak again and told others to never take it.

My 12 year old daughter completed the 3rd round of the Gardasil shot in late August of 2008. School started the next week. A couple of weeks later, she became ill and I rushed her several times to the doctor and to the emergency room only to have the doctor say she had a virus. After 2 weeks of horrible pain, nausea, and headaches, I took her to the emergency room at Wake Forest Baptist Medical Center. She was referred to a Gastroenterologist where she has been going ever since. The doctor has had her on pain medicine since December to help her cope. I analyzed all of her information and compared it to the 12,000 cases in the VAERS database and I am convinced that the shot made her sick. NO DOUBT! The database is located at http://www.medalerts.org/ and you can run the lot # of the dose given to you through the database to determine if their has been any adverse effects noted. The first dose that Lauren had was listed 78 times. Her second dose was listed 70 times. Her third dose was listed 74. I researched the ingredients contained in the shot and the one that I am concerned with is Aluminum. After researching the effects of aluminum poisoning, I believe that she has all of the signs. I begin treating my daughter at home with sublingual (dissolves under the tongue) Vitamin B12 and Vitamin C tablets available at the local drug store over the counter. My daughter has been sick for 7 months and has missed almost her entire Eighth Grade year. As you can see, since starting the vitamins, she has gone from being sick 97% to only being sick 28% of the time. This is a BIG improvement and this may help other young ladies who are affected. I don’t think it will help all, but as sick as these girls are, I don’t see how it could hurt. Her doctors at Wake Forest are aware of what I am doing and agree.

Month Sick Well
SEPT 93% 7%
OCT 97% 3%
NOV 83% 17%
DEC 87% 13%
JAN 71% 29%
FEB 43% 57%
MAR (WK 1-3) 28% 72%

My daughter has been referred to Duke Medical Center now and will go for her first appointment in about 1 month. The FDA and CDC need to pay attention to what is going on and pull this drug off the market. If you have been affected, please ensure that you report your reaction to the VAERS Database. Your doctor is required to report adverse effects, so demand that they do so.

I hope this helps, and if anyone tries the vitamins and it does help or if you would just like to ask me some questions about my daughters experience, email me at ****** and let me know. I will update the doctors at Wake Forest and Duke. Hopefully, if we band together, we can get to the bottom of this and figure out what to do help these vaccine injured girls.

I started taking Topamax for migraines. I had been on the medication (about 25 mg 1x/day) for 7 days. On the 8th day, my doctor told me to double my dose and take 2 - 25 mg pills each day. I did that on the 8th day.

It was Memorial Day, 2006, and I had taken a pill that morning. By about 10am, I was dizzy, had blurred vision, a pounding headache, and slurred speech. When I got home, I went straight to bed thinking I could sleep it off. I woke up about 2 hours later with the most horrible pain you can imagine and was completely blind. I called for my husband, who rushed me to the hospital. I spent 4 days in the hospital completely sedated. I threw up constantly and subsequently lost 14 pounds in those 4 days because I could not keep anything down due to the pain. I saw every kind of doctor and no one knew how to help me or what was wrong.

On the 5th day, the hospital had me see an eye specialist. He took one look into my eyes and ran out of the exam room. He returned shortly and told me that I had acute angle glaucoma and that I was lucky I had come in to see him. He told me that if I had waited, I would have been permanently blind in a matter of a few hours. He had to do laser surgery to blast holes into the backs of my eyes to relieve the pressure that had built up.

He asked me what medication I had been on. I told him Topamax. He did some research and found that glaucoma is one of the side effects of the medication. When I went back 3 weeks later for a follow-up visit, I had started getting my eye sight back. The doctor told me that since I had been in, he had 2 other people with the same diagnosis all brought on by Topamax. He then called the FDA and told them they needed to list that side effect in a more visible place on the drug pamphlet.

I'm VERY glad I found this too! I started taking it one week ago today. Took one dose that day, in the evening. Then I took 2 doses the next day, Sunday. One in the morning and one in the evening. I woke up the following morning, Monday, at about 5 am with horrible, horrible pain in my upper stomach/esophagus area. This lasted the entire day. There was terrible pain that flared up every couple minutes or so. I could hardly breathe and sometimes cried or yelled out because of the sheer pain. The pain has lessened considerably since Monday, however, it is now Saturday, and it still hurts every few minutes and hurts to eat/drink. I have never had anything like this happen to me IN MY LIFE, and it suddenly does a day after I begin taking this medication? Sorry, that's more than a coincidence. I called the office that gave it to me, was referred to a nurse, and she said that that was, "Not a normal reaction" and to "take it with a big meal." I'm so scared. I don't have insurance, and I'm beginning to fear that my stomach/esophagus has been severely damaged by the doxycycline. After reading this article (******), which I admittedly do not fully understand because I am not a physician, I am even more afraid because the doctor who wrote it said he hospitalized one of his two patients who experienced these symptoms. If anyone has any advice, I'd be so grateful.