Acid reflux symptoms and conditions

I am 20 years old.

I was put on Loestrin when I was 17 to prevent pregnancy. I had very light periods that lasted a day maybe every month. Until I completely stopped having a period altogether for about 8 months while being on it. I enjoyed it, but started to get a little concerned so I went to my gyno and they gave me a pregnancy test (standard procedure) which was negative (I knew my body and knew I wasn't pregnant and it was just the pill that made me not have a period but still wanted to check).

I was 18 at the time and they switched me to Yasmin. I started having a normal period again. But I had awful side effects with Yasmin..HORRIBLE depression and mood swings....soooo bad that I went back to the gyno and switched to Yaz...I don't remember much about Yaz but I didn't take it very long because I wanted to be back on Loestrin again.

My script ran out when I was 19, and I never went back to get another script...to give my body a break from BC.

I just turned 20 and recently went to the gyno and asked to be put back on Loestrin again. I have been on it for three weeks so far. I've have some mood swings and slight depression. I also have had some very light spotting, nausea/heartburn/acid reflux this time around....which i don't recall having when i was on it before... but i'm sure my body is just getting re-adjusted and I plan on waiting it out, considering I had a positive experience with it before (minus the nonexistent periods..which wasn't even a problem to me)

I also had mild acne before BC, but when I take Loestrin it completely clears up (Which is a huuuuuuge plus for me..obviously.) When I wasn't taking BC for a year, my acne came back! It was awful! (to me at least) Big difference! But it has once again diminished once I started taking Loestrin again.

I have tried Loestrin, Yasmin, and Yaz..and will swear by Loestrin over the other two....especially Yasmin (that was awful). For those of you who have only tried one brand of BC and hated it.. i suggest you switch to another one before completely saying goodbye to BC pills forever. Thankfully I did switch and try other brands..because I now know that Loestrin is right for me. But everyone is different. Good luck :)

I am a 52 year old female and my bad cholesterol is fine but my good cholesterol is low. I have been taking Lipitor now for a few years and have numb hands and feet to the elbows and knees. My feet are extremely sensitive, worse at night and now I'm getting sharp pains that feel like a bug just bit me. My tongue is also always numb and I do get migraines.I have insane stomach issues and food intolerance. I also take medication for high blood pressure, acid reflux, & thyroid. I have now been diagnosed with type 2 Diabetes but control that with diet so far. Until four years ago I had nothing wrong with me. I am slim and healthy. I had a lump in my thyroid which was removed and there was a trace of cancer. Then like dominos all the other conditions lined up. I have had MRIs and all the tests and doctors insist that I am not a severe enough diabetic to have neuropathy. I can hardly wear shoes now and it hurts when I wear runners while I walk and exercise. Does any of this sound familiar to anyone? I hate that my health has become so much a part of my daily life. Does anyone have neuropathy as a result of Lipitor and am I even taking the the right medication since I don't have high cholesterol?

I was surprised and enlightened to read the side effects of Zoloft (or its generic) from other users. I took Prozak for years. It didn't seem to be having the same effect so I asked my dr. about changing it. My brother takes Zoloft and it does wonders for him, so I asked to try Zoloft. I am taking a generic form now. Since starting taking Zoloft, I have experienced an almost uncontrollable urge to eat. Not just when I am hungry, but eat until I am miserable. It was comforting at the time, but discouraging to see my weight increase. It was very difficult for me, since I have always been able to control my weight and to lose weight when I tried. My gastroenterologist told me that I should lose some weight, that the extra weight around the middle would cause pressure and add to my acid reflux. I also experience a feeling of "fuzzy" headiness, with difficulty concentrating or remembering things. Some nights, I find it very difficult to sleep.

I have been on this medication for 5 days now for acid reflux (or at least, that is what the dr. assumes I have. The doctor told me to take two 20mg pills in the morning before breakfast, and it seems to have helped some, since the Pepsid prescription did not seem to help me. I also am getting terrible pains on the side of my neck, and my throat hurts. Also have an ear ache that feels like an icepick being stuck in the canal. I also have a red spot now above eyelid like a rash, and all day i feel anxiety. I don't know if I should quit taking this. The stomach burning was terrible and is why I was put on this med. to begin with. So I am afraid if I quit taking this, the stomach burning will return. The dr. said 2 weeks of this, but I don't think i will last that long.

BTW...also have had major weight gain with Lamictal...loss of sex drive, tired all the time (there could be other things that affect this but)
I also take high BP med, acid reflux med but I don't feel they contribute to this problem with Lamictal. I've been on those meds way longer than L so...I think I just would like to "start over" and see how I can feel better.
I used to think L was exactly what "the doctor ordered" (no pun intended...again, glad I can sorta laugh at this but...) BUT I DON'T FEEL GOOD!!
Another doc prescribed me Provigil and didn't really explain what it was. She said I needed it bc I was tired all the time. I actually went there bc I thought I had Fibromyalgia and all I got was a 'script for Provigil and sent on my merry way. Got it filled, took my first 200 mg pill and thought I was goin' out of my freakin mind!! OMG!! Told my psych doc and he was like, "P not good for BP patients" so...BUT I did cut the dosage down bc it was SO nice to have energy to make it through the day but still, I do not suggest taking the stuff.
Anyways....just thought of this after I posted walla go...tx!

ps Im not sure the L works that great on the depressive side of BP

I've now taken 12 days of 21 day course of treatment. After struggling with acid reflux, nausea, etc., I thought I'd share some things that I found that helped me tolerate it better in hopes it may help others.

I take a pill as soon as I get up and then another as soon as I get home from work - 5:30 a.m. and 5:30 p.m. I drink a good 4-6 oz. before I take the pill and another 8-10 after swallowing the pill. I try not to eat any later than 2 hours before going to bed, which has dramatically reduced and mostly eliminated the acid reflux.

I've been following the instructions to the letter - not eating 2 hours before or 1 hour after taking the pill and no dairy for 2 hours in hopes it would give maximum absorption to get rid of the Lyme Disease. However, I've found that by keeping something on my stomach during the times I can eat, my nausea has also been lessened. I was really struggling with nausea about 45 minutes after taking the pill, but have found increasing the water to the levels indicated above helped reduce the nausea.

All that said, I'm feeling some fatigue, am a bit lightheaded and my stomach is bloated and a bit tender. Still, it's not nearly as bad as some of you are reporting and while I wondered at Day 4 if I could complete all 21, I'm now hopeful I'll be able to make it. I will, however, be doing a happy dance when I take the last of the pills next Friday. Good luck to all - hope maybe something I've suggested may help someone!

i was told i was hypothyroid,but i felt fine! dr. put me on 88 mcg's of levoxyl and i all of a sudden came down with the worst case of acid reflux,which i did not have b4.also,heart palpitations.i choked down this med for 3 years,experiencing hours of burning after my daily pill.i could not take it any more! i put myself on a trial month without levoxyl ,and the burning and acid feelings are gone! i feel gr8! i dread being scolded by my doctor for going off it,but i could not take that burning anymore.ive been to 2 gastroenterologists,plus my general practitioner,all of whom said it was impossible for levoxyl to cause g.i distress.if that is so,why has the burning gone now that i stopped taking it?if u have experienced burning with levoxyl,could u kindly email me/i want to know-am i crazy,or is heartburn an issue for other levoxyl users also/plus,i never felt/looked ill in the first place,so even tho my thyroid functioning may not be optimal,did i really need medication yet?maybe someday i might,but i feel fine,i have long thick hair,decent fingernails,full of energy and not cold all the time-so why do i need meds at this point?(if i ever have overt hypo symptoms,i will have to take something,but why fix what is not broken?) ps-my b/p and cholesterol all very good too,altho apparently ive been hypo about 5 years.

I've been prescribed 100 mg. of Doxycycline Hyclate twice a day for 21 days for Lyme Disease. I was tested to rule that and rheumatoid arthritis out because of hand pain - and I don't know who was more surprised when I tested positive - my doctor or me. Any symptoms I had, including the hand pain, I attributed to the aging process (51/female).

Took the first pill in the later evening on a Friday and waited the 30 minutes before going to bed (instructions said not to lay down for 30 min.). I woke up in the middle of the night with terrible acid reflux, which I've never had. I found it difficult to time taking pill after not eating for 2 hours and waiting 1 hour afterward - never realized how often I ate small snacks. Same thing the next two nights - I also had heartburn, which is rare for me.

I realized it would be far easier if I took the pill immediately after rising and as soon as I came home from work. That has greatly reduced the heartburn and eliminated the acid reflux.

I am fully committed to taking the pill to have the best results in eliminating the bacteria from Lyme Disease, so I'm taking it exactly as prescribed on an empty stomach. This is causing some stomach upset and nausea, which is the worst in the hour after I take the pill while I wait until I can eat - especially in the last 15 minutes, when I feel on the verge of vomiting. I try to keep myself busy, but even without looking a clock, I can tell where I am in the hour. I am hopeful that by taking the meds on an empty stomach, I'll get maximum absorption - but it's been a struggle for me.

One other discovery I've made is that the nausea is less the rest of the day if I eat - and carbs seem to be what is most appealing. I'm far more easily nauseated during the entire day, some days more than others. I feel some fatigue, but nothing that is so severe I'm not able to function and go to work. I feel bloated and my stomach just vaguely hurts, so I'm trying to wear loose clothing.

I'm finding this drug therapy a bit difficult, as I felt pretty well beforehand. My doctor has recommended I give this my best effort, as it is the "go to" drug for Lyme Disease, but has said if I can't handle it, she will give me an alternative. I am trying to stick this out, partly out of determination and silly pride, but also because I am allergic to a lot of drugs and since I seem to be able to tolerate it, albeit with some discomfort, I figure I should suck it up. I have a little bit of the tingling, am occasionally feeling a little flushed - usually when I'm highly nauseated (which is a typical reaction for me), but nothing horribly bothersome.

I'm hoping I don't develop the sleeplessness, anxiety or depression that many of you have reported, as I feel terrible for you. That would become a deal breaker for me.

Unless it's my imagination, my hand pain is reducing and some achiness I just figured was normal has been lessening. If this was the result of Lyme Disease and I can get rid of that, this (hopefully) temporary discomfort will be worth it. Good luck to all.

I have had the Mirena IUD for 2 years. I have notice lately that I have had vaginal dryness during intercourse. I have extreme dry scalp, and I have had about three bacterial infections in that time. I have been irritable for so long everyone in my house has gotten use to it. I am getting the IUD out next week. I am looking forward to the change.

My allergies caused nearly constant painful sinus pressure, drippy nose (I should have bought stock in Kleenex to profit from my box-a-day use), asthma, getting gradually worse all the time--it was as though I'd had the flu for 10 years (I'm 54). I was taking Claritin in the morning and Zyrtec at night, which only toned down the most severe symptoms. I was on Prilosec as well, as one doctor though acid-reflux might exacerbate the asthma. My family and I are avid hikers, but I haven't been able to breathe well enough to join them for years, even with daily Ventolin and Flovent. I've only been taking Singulair for two weeks, but it has made all the difference. I feel "normal" instead of sick for the first time in a long time. So, for me, it does work. But my stomach's been killing me--like a bleeding ulcer (which I had 25 years ago). I'm hoping that will subside or going back on Prilosec (expensive!) will counteract it. I've also had the weirdest dreams--very vivid and disturbing. Because I did research online before taking Singulair (Doctor uttered not one syllable about side effects), I recognize the dreams are from the Singulair. Because I understand what is causing them, I can easily set them aside when I wake up. I think anyone who's had mental or emotion problems could be sent over the edge by the dreams unless they had a clear understanding and acceptance that the allergy drug caused them. I would be easy to think something was wrong with you to dream such bizarre, violent stuff. (I'd give examples, but I've truly trained myself to forget all about the dreams as soon as I wake us, so I don't remember the dream events now.) I'm quite concerned about children taking this drug. Maybe not everyone has this disturbing-dream side effect, but how could you explain them away to a four-year old? How would you even know if a younger child was having them? Even children old enough to comprehend shouldn't be subjected to horrific mental images, like the 16 year old above. A tip for people who Singulair helps, but they have the weird dreams--try Melatonin (over-the-counter supplement) at bedtime. I've used it to help me sleep in the past when life events kept my mind too active to sleep for several days at a time. Unlike sleeping pills, it doesn't make your tired the next day, you can wake up easily, and it's not habit-forming--it just lets you drift off on days you otherwise can't. Since I'm concerned about the long-term effects of anything taken frequently, I don't take Melatonin very often, but I did try it after the fourth day of Singulair dreams. I had no memory of weird dreams when I woke up, so it seemed to work, and I didn't remember dreaming the next night either. I only tried it that one day because, as I said, I've trained myself to not be bothered by the dreams.

First day in I had cramps and upset stomach. Second day in I had cramps, upset stomach, and acid reflux. I never have acid reflux. The cramps got so bad and the pressure from the ring inside that I took it out.
Why can't it be a little more bendy and less springy? That picture is a side view of it flattened, on the directions. It was almost all the way extended inside and boy did it hurt.

I took one 100 mg tablet one night just before bedtime with a little water for my acne, bad idea! I should have taken it with a lot of water and should not have lain down for at least 30 minutes after.
I felt as if something was stuck in the middle of my chest and wouldn't go down no matter how much water,or ginger ale I drank. I could not go to sleep that night, and the feeling of having something stuck in my chest lasted for about 2 days, although to a lesser degree than the first night.
I took pepcid the next day because I thought I had acid reflux or heartburn even though I have never had this feeling before. Doxy makes me dizzy if taken on an empty stomach or not enough liquid. Always take with lots of fluids and make sure you do not take it on an empty stomach.

I have been on both Diovan 160 mg and Diovan HCT 160 mg / 12.5 mg, started having trouble swallowing right away. After a couple years on this med suffered severe acid reflux so bad it burned through 2 prilosecs a day. I thought I was going to die of esophageal cancer. One day I forgot to take the Diovan and had no reflux. Doc switched me to a new different pill so now the acid reflux has vanished. Yes Diovan does cause acid reflux! Also joint pain, and I am wondering if it caused me to have an enlarged uterus as well, that I developed on the med. No fibroids or cancer, just hyper-uterine lining the tests revealed.

I am 48 years old. I have been asthmatic since I was 10. Never in my history of having chronic asthma, have I had to take prednisone.I started with 10 mg for the first 8 days. After a trip to the emergency, my Dr. found it necessary to up my dose to 40mg. I took this dose for 17 days. My face is round, I have had the worse acid reflux in my life, I have had mood swings..was up all night for 2 weeks and I still can't breath that good. I am weaning myself off of this prednisone and I am looking for another doctor. I am down to 10mg and I plan never to have to take this awful medicine again. I guess It would be okay if I was breathing like a champ, but I'm not. So there is no use in having all these bad side effects if I am still having trouble breathing. It's just seems that even a Pulmonary Dr. would want to take the fast way out. There are other safer meds to use.

After reading all of the comments, I am embarrassed to say that I have taken omeprazole for the past 2 years. Originally, I began taking it for nausea from GERD. I began taking it soon after the death of my cousin (as I figured the anxiety from her death caused my stomach issues). I began to become depressed shortly after, which I also attributed to her death, financial issues, etc. However, when life got better I was still depressed and anxious. Two years passed and I still couldn't figure out why I felt so bad mentally. Not to mention I was mildly nauseous most of the time and NEVER had a normal appetite. I would only know it was time to eat when I felt faint. Light-headedness, stomach cramps and lethargy were also side-effects that I experienced almost daily. The worst part was that I didn't know if the nausea was caused by my stomach issues or by the omeprazole. It was obviously the omeprazole. About 2 months ago I switched to Prevacid which caused much less nausea but many of the other side effects were still there although a little less. I weened myself off completely (which I would recommend to anyone) and I actually feel like my old self again mentally and physically. I didn't realize how low my energy was until this last week that I've been off those meds. I'm actually HAPPY again, I WANT TO EAT something, I have ENERGY, and no light-headedness or stomach pain at all. It saddens me to think that I spent over the last 2 years feeling this way needlessly and thinking that I was crazy. There ARE other alternatives to acid reflux, GERD, etc out there that are much safer and more tolerable. If any of you are experiencing some of the symptoms that I or others have described, explore other options before you just "get used to" feeling like crap.

this drug gave me extreme bloating in my mid abdominal section to the point where I couldn't eat much. I lost a lot of weight because of that. I'm taking it because of acid reflux but is defeating the purpose since the bloating is putting pressure on my stomach and making my food come up.

My name is Katie, I am 31 years old. I have been suffering with what doctors call Chronic Idiopathic urticaria for 16 years now. I was prescribed Zyrtec 14 years ago and remained hive free until I had my first son. After a complicated pregnancy and emergency delivery the hives returned full force. The doctor prescribed Singulair in addition to the Zyrtec.

The hives went away; however, I have so many other problems now. I have been seeing a specialist thinking I have lupus or some other disorder, but all my tests are normal. It wasn't until I had my singulair refilled yesterday that I realized instead of symptoms, what I am experiencing may be side effects.

-- I have gained 60 lbs.
-- I have horrible headaches almost daily
-- I am so tired that when I am not working it is impossible to even make myself leave the house
-- I have taken myself to the hospital 3 times thinking I was having a heart attack and told I suffer from acid reflux
-- I have so much pain in my legs/feet/back that I can hardly walk
-- My hands and feet like to go numb for no apparent reason
-- I am always anxious & moody.
-- Can't sleep
-- Clearly I am not myself. Lately, I have felt the quality of life I am leading is horrible.

Wouldn't it be something that I have spent all this time & money trying to figure out what else is wrong with me when it is the medicine I thought was keeping me well really making me sick. Why do the finest doctors not realize when your symptoms are actually side effects?

I am pretty out raged at this point. I would take myself off this medication today if only I knew how to control the edema.

I am 35 years old and I have high blood pressure. I am taking Inderal and Lisinopril. I have been taking Lisinopril for about a year now. I have had a cough for almost a year now. Have had chest x-rays and ct scans that show nothing is wrong. I was taken off of Lisinopril and put on Diavan but my feet and ankles were swelling so I went back to Lisinopril .
I still have cough, dizziness, light headed, hot flashes, fatigue, weakness and chest pain. I cannot go to the grocery without everyone staring at me coughing and the people at work are getting annoyed with it. I cough to the point where I vomit. My doctor has sent me to a specialist for acid reflux and has even went as far as telling me I have sinus or allergy problems. I will be going back to the doctor next so I will be suggesting being taken off of this drug and put on something else. Thank you to everyone on here. Everyone thinks that I am crazy because I am only 35 and I have all of these symptoms but no one knows what is wrong with me.

I am SO glad I ran across this site.I am not crazy! My Mirena was put in about 3 months ago after my gyno finally put it together that my birth control pills were causing menstrual migraines. I will say the Mirena helped with the headaches, but lately I have not felt like myself. I have gained 10 lbs. in 3 months (even though I have been eating well and exercising more to avoid this side effect), my hair is oily, I have little dry itchy patches on my skin, fatigue, joint pain, no interest in having sex (after we do have sex sometimes I get horrible cramps and pain, like when the Mirena was inserted) I am super moody, and have anxiety/depression/anxiety problems, bloated almost constantly, and I feel like I can't focus or concentrate on anything! I called my gyno this morning because I do not want to feel like this anymore, and told her about all my symptoms. The only thing that makes sense to me is that Mirena is causing all my problems, since I never had any of them until I got it put in. The gyno tells me its not Mirena, that it definitely does not cause all that, and to get my thyroid checked because that is my problem. However, after reading all these stories, I am convinced that it is Mirena, and I am definitely getting it out. There is no way so many women can only have Mirena in common and have the same problems, even if they are not listed as side effects on the Mirena brochure.
So I am definitely getting it taken out, but I am curious about experiences after having it removed. How long till you feel like yourself again? Do the side effects go away quickly? Does it hurt more or less than getting it put in? Does the weight come off easily?
Hopefully this post helps someone as much as the other posts helped me. Thank you all for taking the time to post.

Hi,

I'm fit, tough and extremely healthy. Tried Mirena. Ok for one year then within six months I experienced increasing upper abdominal pain and ultimately the sensation of something bursting central chest and the first of three Emergency Hospital admissions. Bloods clear. Xrays clear. ECG's clear. Endoscope clear (had experienced severe and sudden onset gastroenteritus/IBS acid reflux, extreme food intolerance.) Also had a large cyst needed draining (and multiple smaller) appeared in left breast. Lymph glands in neck up. High histamine, raised albumin, white blood cells relating to allergy/parasite. Allergic reaction/systemic rejection of coil?
No uterus pain at all.(Not had period for over a year)
So very ill after sixteen weeks being consistently told it wouldn't be the coil I took it out. Hard to describe but an extreme sense of relief, reduction in pain from entire GI tract swelling/sensitivity.
QUESTION.
One week on huge improvement but I still have continual upper body/chest pain (diaphragm?), and additional pain sharp pain through left ribs to shoulder blade, worse with sudden movement. Anyone had residual/slow to improve nerve damage? Need to be fit for my job.

Thank you for reading.

PS. Its not a 'coil'. Its a nasty sharp edged piece of plastic.

I am a 36 year old white male - generally good health. Could use to lose a few pounds but not overweight. I've been taking Singulair for a little over a year and since then (I also take Zyrtec - over the counter and Nasonex) all are for allergies. I since developed acid reflux - went to my pharmacist and she said that most people with this mix of allergy drugs form acid reflux. Anyhow, I am generally a moody person-have always been - too intense and most of the time I am not a go with the flow person-since I've been taking Singulair my mood swings amplified horrifically - I blow up at my wife over stupid assanine stuff - after reading these posts..today is the last time I am going to take Singulair. Wish me luck. I hope the mood swings decrease.

I started off taking Tenormin 50 mg 1 x a day and Lanoxin 25 mg 1 x a day about 21 years ago. I continued to have constant palps and skipped beats even though I was on these meds. I wound up developing vertigo after about 5 years that got so bad I had it daily. I ended up with severe sinus problems and was given a cortisone packet of pills (the kind that decrease each day you take them) to take. The vertigo left for 6 months, coming back again with a vengeance. I begged the docs to put me back on cortisone pills again, once more helping to stop the vertigo. However, at the same time I also stopped the Lanoxin. ??? I totally believe that Lanoxin was part of the problem causing the vertigo. I now only have it from time to time, maybe only a few times a year. I still blame the Toprol that I now take for the left-over vertigo. I was taken off of the Tenormin after about 10 years of taking it and put on the Toprol at that time and have been on the Toprol xl for the last 11 years. The docs said that I needed to be on Toprol XL, as it was an extended release and would help me much more around the clock. I did not notice much difference throughout the switch, but looking back I do believe that a lot of the things that I have been dealing with through the years are side-effects of the medicines. I have had irritable bowel syndrome, told I have fybromyalgia, then told I did not have fybromyalgia, hip and back pain, skin problems on one of my hands that started with the Toprol, headaches, tiredness, horrible weight-gain (without overeating!! Honestly.), I have averaged 5 lbs. a year and the docs never even listen to me when I voice my concerns, I have been diagnosed with anxiety, joints ache, ankels, feet, face and hands swell, stomach bloats something terrible, acid reflux, hiatial hernia, and I had a tumor removed that could have been a problem off my rectum (who knows what caused it), I have had CTs and MRIs of my head, twice, for the vertigo and what I was told was probably psuedo-tumor cerbri (because of months of severe headaches), told by my eye doctor that he wonders if I have beginning MS, everything came back fine and things seem to resolve and go into something else. I have been passed from my general physician, to a cardiologist, to a ENT, and a neurologist. No one can ever find anything physically wrong, but they did conclude that I definitely had benign positional vertigo. LOL, that means they could not tell me why I had it. I put a stop to testing when they wanted to do the spinal taps.

Now I am experiencing tightness around my lower rib-cage and feel as though I am sucking for breath, I have a terrible time falling asleep at night, I wake up gasping and swearing that I am dying. My rib-cage is numb around my right side, not so much the left side when I lay down to go to sleep at night. After a few bouts of this I finally fall asleep and sleep all night most times. My blood pressure is now on the rise 150/99 at the highest. I have been working out lately with a few positive effects, more energy, more endurance, less aches and pains, muscles are starting to tone up, however, no weight loss. I thought my bp was starting to lower, but found out it was actually up. I went to my family doc and she listened to me really good, realized at last that I was not shedding the weight despite the efforts I was making. She cut my toprol to 25 mg 1 x a day and put me on lisinopril, I did not tolerate the lisinopril so she switched me to dyazide, lowest dose 1 x a day. I have great positives ...no more swelling, weight loss, lower bp, HOWEVER, I am now having jitters, anxiety (somewhat), no appetite at all, a few muscle spasms in my arms and legs, nothing painful or severe, dizziness, slight headache that comes and goes especially through my eyes. I am also experiencing coughing, and raspiness...but I am also coming out of a bout of bronchitis, which got really bad with the lisinopril. I believe it is partly due to the meds.

I called my doc today to tell her about the twitching and buzzing feeling and to ask about the dyazide. My feelings are that I am experiencing a lot of different things, first the bronchitis, and all the meds I was taking for that...albuterol, musinex, tylenol w/codeine, and biaxin, then the decrease of my toprol xl, the bad effects of lisinopril (coughing and raspiness), and now starting the new drug dyazide (generic form). I really want this to all settle down and work out for the best, but it is getting to me now (after 2 weeks). Last Saturday I would up in the ER with shooting pains through my chest that left me very pale and lightheaded when it happened as well as very tight throug my chest and sucking for air. The ER did chest xray, chest CT w/contrast, bloodtests, urine test, bp's sitting, standing and lying down (it is highest while sitting), everything came back good. No heart attacks, no blood clots, no bronchitis anymore, nothing. Blood work was good, urine was good. I am beginning to think that perhaps my body is reacting to cutting the Toprol xl in half. Sort of a withdrawal. There is really nothing else it can be and I really don't think that the dyazide is that bad of a drug and probably not causing all of my problems now, maybe just a part. Which are the tingling, dizziness, anxiety, twitching, and coughing. I have only had 3 of the dyazide medication. But have read that withdrawal symptoms of Toprol can cause these problems for a while. I am also thinking that the shooting chest pains last week were also withdrawal of the Toprol as it had been 1 week at that point that it had been cut in half.

Any opinions, if anyone can make heads or tails of anything that I have wrote. Sorry for the length and if it is confusing.

Wavy feeling of anxiety in my head (like I used to get from codeine). Fuzzy feeling in big toes. Dry, choking cough when I lay down at night. Now, I am morbidly obese and have bad acid reflux. If I don't take Prilosec every day, I cough. I also have sinus/allergy problems. So I take Claritin-D. And for health benefits, I take baby aspirin. So I'm wondering if it is the combination or if I am getting ready to have a stroke. It's my own fault for being so overweight, but it is frustrating. I also have swollen ankles and legs. And lately I feel like I have to pee too frequently and that I'm not quite able to finish. This worries me because I was feeling like this before I found out I needed surgery to remove an ovary due to a very large cyst. I wonder if I am getting another one.

32 year old male here. I was prescribed Levaquin 500mg 2 days ago for 10 days after being diagnosed with cellulite which is a bacterial infection in the blood. I had a swollen and sore groin on the right side. I already take prilosec once a day for acid reflux. Since starting Levaquin the infection seems to be clearing up, but the heartburn is pretty vicious. Yesterday I thought to myself hmm, maybe I didn't take my prilosec but I thought I did. So, I took a second prilosec but with no results. Today again as listed on the bottle I waited two hours after taking the Levaquin and then took my prilosec, but no luck. I've since taken a second prilosec and a couple of tums. As I drove home from work the heartburn started reoccurring. Thats when I googled it and came to find this site and that I'm not crazy. I also had sharp pains in my wrist and hands today and feel really run down and almost mildly depressed. I can live with joint pains and feeling a little run down, but the heartburn really does effect your eating and sleeping. I guess I'll have to see how the next 7 days go.