Left leg symptoms and conditions

I took ortho-tricycline low for 6 years with no problems whatsoever. At 18 my doctor switched me to Yasmin, by my 28th day on Yasmin I had a intense dull pain in my left hip/groin area and the of my knee and calf area. After two weeks of putting it off as a sprain, it had only gotten worse, my entire left leg was swollen to about twice the normal size and had purplish discoloration and I was could barely walk or sit. I was taken to the ER where they diagnosed me with a DVT the size of a softball in my left thigh. I spent two weeks in the hospital on narcotic painkillers and IV Coumadin before they would let me go home. I spent an additional 6 weeks at home on light duty and bed rest. I stayed on Coumadin for a year before it almost killed me as well. Today I am 23 years old and still feel the effects of the clot I had 5 years ago. My leg a calf are still swollen, though not nearly as bad and anytime I'm on my feet or have to sit in a chair all day I have to deal with moderate pain. I wasn't on Yasmin on Yasmin long enough to experience any other side effects but I would strongly advise you do your research before taking this medication.

I was on Yasmin for 1.5 years. Ended up with chest pains, severe Vitamin D deficiency, B12/Folic Acid deficiency, elevated potassium and unbelievable fatigue/exhaustion along with muscle loss. I have now been off for almost 3 years and do not feel completely recovered. I'd encourage folks to google Yasmin/Yaz lawsuits as they are just beginning and I expect will eventually come off of the market due to finally, recognized increased risk of these pills with pulmonary embolisms, stroke, heart attack and blood clots. Also, if you google Yasmin Survivors, there is an international forum of women who have been sharing and contributing now for last 3 years as well.

Where do i start? I've been on coumadin for 13 months for a huge clot in my left leg which leads up into my groin. I have experienced dizziness, lightheadedness, unable to concentrate, diarrhea, headaches,stomach pain ( when i was taking it at night before bed), hair loss was a biggy at first. I lost a lot of my hair! joint pain. These of course are all at times. Didn't always feel crappy, but a lot of the time. Especially when they changed my doses or I changed the times of the day I would take them. Any doctor or pharmacist I've asked about these side effects say they don't exist! ya right! ask someone who actually takes the stuff! Hope this blog helps someone else.

My daughter has been on Sulfatrim for about 2 years, she was diagnosed with bilateral urinary reflex or (VUR) grades 4 and 5. I'm concerned for my daughter's health. I noticed that my daughter (about 4 months old at the time) had started having what looked like seizures, after being on the drug. She would and still does lay on the floor and draw her left leg up in to her side, while her right leg is straight out and stiff. She puts her head down and sometimes she headbutts the floor. She sweats when she does this. She alert though. We went to doctor and she had a test done to rule out seizures. We keep going back and they can't seem to find out what is wrong. This is not a normal thing or "tick" that my daughter does. I would like anyone else with these systems to come forward and talk with me please. V

The mirena coil has destroyed my relationship. At the beginning my partner told me he could feel it and it hurt us both. But when i told the doctor he said my partner was making it up as it is not possible to feel it. Im made to feel like a liar, and im sick and tired of them lying to me. I get sharp stabbing pain all the time, every day where the coil is. Sometimes i can not sit down as it hurts so much. I have no sex drive, i also get this weird pain at the top of my left leg near the fallopian tube. I bleed almost everyday and have constant cramps. Which is causing my spine to curve, due to not been able to sit up properly. My partner has left me as it has been going on for 3 years. I can not even begin to start a new relationship as sex is very painful and i bleed heavily afterwards, which lasts for weeks. I have a connective tissue disorder called Ehlers-Danlos vascular syndrome. And the hormones that are in the mirena coil react to my condition and i shouldn't be having the this coil. But my Dr refuses to take it out. I am deeply depressed by this as my life has been ruined by the mirena. I also suffer with headaches and i burn up and i start to sweat quite bad. Which can be very embarrassing. I didn't really want the mirena but i was pushed into by my doctors, as they thought they knew best. I told them that it wasn't recommended as i have EDVS. But they don't care what i think. I have begged for them to take it out but they will not do it. Im at my wits end as i don't know what to do anymore. I am 33 years old with a disable son to look after. And it can interfere with me looking after him as the pain gets too much. I want it out and i want my life back before i have no life left! Ladies please do your homework before making any choices. Dr's are not super human and they do not know everything. They are only human and make mistakes just like anyone else.

I took 1 Levaquin pill 500 mg one evening in September 2007 for a kidney, UTI infection. My left side went numb and started tingling, my left hip hurt, I could not put weight on my left leg, had to limp to walk. I had severe pains shooting through my head, felt dizzy, nauseous, weak, had to stay in bed for 3 days after taking medicine. I could only limp to eat and bathroom. I called doctor, they said KEEP TAKING IT. NOT. They told me that these were normal side effects. I read on the internet that these are NOT NORMAL side effects. I didn't take anymore and read about alternative medicines. I was still in a lot of pain in my kidney and bladder. So I asked for Bactrim, a sulfur based drug. It worked great on the kidney/UTI. But since I took the Levaquin, my joints hurt and pop, my achilles tendon is painful everyday, my shoulders have excruciating intermittent pain and my hip hurts inside when I move it. Also, there is a lot of crackling and strange sounds in my joints now. My wrists have been having a lot of soreness as well. I just read about Levaquin causing these problems for years after you take one pill. I didn't know all of these symptoms might be connected to the Levaquin. Does anyone know how to get the Levaquin out of your body and joints???

Hi I posted this on the Coumadin site when I should have been here,

I am a 66 year old female and up to a year ago I felt 20 years younger now I feel 20 years older.

I fell and broke my hip June '08. Had a hip replacement and developed a blood clot (DVT) in my left leg.

They put me on Coumadin and when that didn’t do the job they added Lovanox (another blood thinner requiring shots in the stomach).

Not only has they not helped but my blood clot is growing.

My symptoms:
daily headaches, debilitating leg pain (the pain is so bad that it is crippling me), fatigue (an overwhelming feeling of tiredness, I set down for a few minutes and wake up hours later.), loss my concentration (trouble doing simple crosswords), can’t study simple directions, numbness in toes and hands. I can go on.

And the doctors? “It’s all in my head. It can’t be the blood thinners.”

I am going to copy your blogs and take them to my doctor and demand something be done.

Thanks again to this site and all of you. I was beginning to think there was something wrong with my mind.

I'm not crazy!!!! Thank you..

I fell and broke my hip June '08. Had a hip replacement and developed a blood clot (DVT) in my left leg.

They put me on Coumadin and when that didn’t do the job they added Lovanox (another blood thinner requiring shots in the stomach).

Not only has they not helped but my blood clot is growing.

My symptoms:
daily headaches, debilitating leg pain (the pain is so bad that it is crippling me), fatigue (an overwhelming feeling of tiredness, I set down for a few minutes and wake up hours later.), loss my concentration (trouble doing simple crosswords), can’t study simple directions, numbness in toes and hands. I can go on.

And the doctors? “It’s all in my head. It can’t be the blood thinners.”

I am going to copy your blogs and take them to my doctor and demand something be done.

Thanks again to this site and all of you. I was beginning to think there was something wrong with my mind.

I cant Walk this crap disabled me! I have nerve damage to my left knee.Dont take this crap.Period It can Kill you.there are a bunch of greedy people making a ton of money on the sale of this crap.We seem to have no Rights??? I was i a lot of pain like someone shot my knee off pain.Plus my lower left leg too all the way from ankle to my Thigh joint.It really sucks too when doctor blows you off.I went and sen another one for second opinion he had never seen a Knee swollen 5 times the size of other right knee.Class action Lawsuit anyone.I,d sign on.I was forced to take this poison.by insurance company.I was on Benicar for last two years.that worked for me.But for costs I was told I had to change over or die was my choices.Well to save a couple bucks its going to cost a lot more getting my extra doctors bills.plus attorneys fees I hope.

THis website has been a tremendous help for me. Two days after I was prescribed 500 mgs of Bactrim twice daily, I started feeling really odd. First the achiness, then my left leg began to swell. I am not taking the meds anymore, but am now so fatigued, and sore, I feel as though I have had the flu for a week. I honestly do believe that it also has a negative effect on the liver. Just from the almost constant ache , I have on my right side. I just want to sleep all the time. I have not taken the meds for two days, and yet, the effects remain. Beware of this nasty medication. I don't know why the FDA allows its distribution!!

I had a lap done last year in May and my doctor removed an adhesion that was hanging above my uterus. Also a fibroid (3 cm) was found in the muscle and is located right against my bladder. My doctor could not remove the fibroid because of its location and because of a risk that I might have scar tissue and could be a problem to get pregnant. He also said that I could have some other complications, like lose a lot of blood. I feel like he is not being straight with me. I also have ovarian cysts which is common in the women in my family. Since a teenager, I always had really bad cramps and heavy bleeding. As I got older, it became worse. Before I had the lap done, I bleed for 6 weeks straight. I was changing pads every 30 minutes. Then my stomach extended so far out that I looked pregnant. I could not sit or stand. My husband had to take me to the E.R. An ultrasound was done and found that my uterus was enlarged (9 cm). I was put on Nothridone to control the bleeding and to treat endometriosis. After taking 2 months of this drug my doctor did a vag lap and abdomen lap. Everything was good that is what he said. I believed it. I was doing better. I was working and had no pain for 8 months. Then it all changed for the worse. I started to have really heavy menstrual bleeding and lots of blood clots. I felt week all the time and sick. The bleeding went on for 8 weeks and finally my doctor said that I had to take Lupron injections. I asked my doctor if he could just do a myomectmy and he said no because that was should be the last result. I could no longer stand the pain and I asked him what kind of side effects come with this drug. He made it sound like it was not bad and that there are very little side effects. He gave me a some information about the drug and I read the information and I did a lot of research. I was terrified but I had to make a choice. I was calling in sick because I could not work with the pain and worrying about embarrassing moments when my pads failed to keep me from overflowing. So I took the 1st shot in May along with add-bak therapy which is Nothridone. The bleeding tapered off slowly and the pelvic pain decreased. I did not feel any side affects right away until the second week. I started to forget things and would just stand in the middle of a room feeling confused. I always had headaches since a child but now they are pounding headaches, which I cannot stand any noise. I also can't stand the light. I have body aches like I have the flu and have problems with my right hip all of a sudden. I had a x-ray done because my doctor thought I might have fractured my hip. There was no sign of a fracture but my pelvis id tilted. I have some arthritis in my spine which I do not understand how that happened. Sometimes I cannot walk and I have to use crutches to get around. I cry all the time because I am extremely sensitive and confused. I use to be a very strong person and now I just cry all the time. I called my doctor to tell him what I have been experiencing and he said its all normal. I have already had a total of three Lupron injections and the symptoms just get worse. I have been spotting here and there, sometimes I have a pinkish discharge, and now the pelvic pain is back. My doctor knows this and he just says its normal. I requested for another ultrasound because I am worried something is wrong and he said that I have to wait until I get the 6th injection.I feel like my doctor is insensitive but he is supposed to be the best GYN doctor where I live. I also want to say that I have gained 20 pounds in three months. My sex drive is gone. My hair is thinning. I lost my job because I ran out of FMLA. This has been a nightmare! I am losing trust in my doctor. My poor husband and family are having to put up with what I am going through. I pray all the time to help be stay focused and think positive. I just do not know what to do anymore. Is there anyone out there that can give me some advice?

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 am 26 years old. I've been on warfarin for almost eight years. I wish I had seen a site like this eight years ago when I started on warfarin (after DVT and P.E) I may have had some insight into the hellish two years that were to follow: hair-loss, depression, weight-gain. But I attributed all this to stress (it was pre-med varsity and I was under a lot of pressure academically).
Anyway, now my life is more settled, I eat right, exercise furiously 5 times a week...but I have digestive problems. Bloating, gas, overall discomfort in my stomach almost every night. I've cut out milk, wheat, coffee...nothing.
But tonight I started thinking...could it be the warfarin?
Does anyone experience or know about possible side-effects of warfarin on the digestive system, and does anyone have some useful advice????

Hi, I am a 47 year old woman and started Warfarin and Lovenox June 29th as a result of blood clots in my left leg from knee surgery. I was able to go off the Lovenox July 4th (Yay!) because my INR levels were above 2. I thought the Lovenox was the cause of the nausea I experienced, but apparently that is not the case. I keep telling the clinicians at the Anticoagulant Clinic about the nausea and their response is that they haven't heard of it as a side effect. Thank you all for posting to this website, there is some comfort in learning you are not alone with these strange side effects. I also experience dizziness and have difficulty finding words. I think I will switch from Warfarin to Coumadin to see if the side effects are less, though many of you have written about weight gain ~ yikes. For those of you bruising with Lovenox I was told if the needle is dry when it goes in there is much less bruising. And to everyone my thoughts and prayers are with you. Oh yeah, I also have nerve pain in the bottom of my left foot, the compression hose do help website is ******

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!!

I'm sitting here in tears reading all of your posts because I've also been on prednisone and have horrible side effects. I was diagnosed with metastatic breast cancer in my lungs in June of 2002 and, after starting at 60 mg/day then, I have been on 20 mg/day for years now. The very first posting that I read mentioned problems with the femur bone. Besides all of the other problems associated with this devastating drug, in December, 2007, I broke a bone in my left foot with no known cause for it. Then I started experiencing pain standing or walking in my left leg and was diagnosed with a fractured femur bone and after several months of trying to get it to heal (including an ultrasonic bone healing system), it just kept getting worse until an orthopedic surgeon recommended that I have a 16 inch rod put into my leg which I did and it ended up to be one of the worst decisions that I have ever made. After experiencing all of the prednisone side effects for almost seven years including depression, severe fatigue, weight gain, moon face, thin skin, cataract surgery on both eyes, hump on my back, mood swings, etc., the pain and suffering that were caused by that operation brought me to seriously consider suicide. I was also diagnosed with chemical neuropathy in both of my legs also which makes my legs so weak that I have to crawl up any steps and have trouble just standing. I actually have an appointment for this evening to have an x-ray done to see what is wrong with my knees and did not realize that this also is yet another side effect. I never make it through the night without waking up in pain and getting a pain pill and then getting up in the morning is almost unbearable with that "burning" pain. I am now on Cymbalta for depression, Xanax for anxiety, Percocet for pain, and of course 20 mg of Prednisone. I was told that I would have to remain on Prednisone for the rest of my life because of the lung scarring and COPD. After reading all of your comments, I have decided that I would rather put up with any breathing problems (and I don't even know how slight they may be at this point) than to remain on the Prednisone. I have tried weaning off several times but get so fatigued that I can't move and that's dropping one mg every week. I'm affected by the decrease but it gets out of hand when I get to 14 mg and I get so frustrated and depressed at not being able to do anything that I just go back up to the 20 mg/day. If you have been able to wean off of it, would you please let me know how you did it and what you had to go through? I'm 65 years old now but I have two wonderful granddaughters (ages 4 and 6) who I can't do any normal "Grammy" things with anymore at this point and I have to change this condition for them and for me. Obviously, the doctors don't recognize the severity of the drug because they just keep prescribing it and out of a regular doctor, an oncologist, an orthopedic surgeon and a neurologist, they can't seem to get together to come up with a solution. I have to say that I haven't considered suicide lately but I do wish that I would just die and be out of this pain. My family and definitely my granddaughters and wanting to see them grow up are the only things that keep me going. There are probably things that I'm forgetting but I'm sure that one of you have covered it in our posting. Although my family is so supportive, no one and I really mean not one of them, realizes knows what we all go through because of this drug. How could they know that something that is supposed to help you could cause these problems? My life is a living hell, all because a pulmonary doctor prescribed prednisone seven years ago and I trusted him to only do what was right without informing me of what was to come. I more than sympathasize with all of you. I sincerely appreciate the time that you took to post to this site and so thankful to know now that this knee pain is not something new that I have but another side effect of the prednisone. I wouldn't have known that if it wasn't for this site because I'd be willing to bet that after I would have had this x-ray done, one of my doctors would have just prescribed another medication to take. Please feel free to contact me directly with any comments or especially any help that you can give me. I know that all of you are going through the same thing so if I can do anything for you, even just listen and understand, please contact me also. Sometimes that's the only thing that people can do is to listen and someone who is in the same situation can always understand. I'm here for anyone who needs a hug for the day.

This is my second time writing in. I wrote about symptoms in Feb. and now have MORE to add. I have had Mirena in for a year and a half and things are starting to add up! I still get a period though it is a little lighter than before. I am still spotting (even after all this time and there is no knowing when this will happen), heart burn, hair loss, heart palpitations (even have gone in to ER and had test run with no conclusion except I need more sleep and less stress - ha - been a mom for 9 years and haven't slept forever, why would this happen only now?) dizziness, back pain, constipation, bloating (my stomach will not go back to pre pregnancy size), gas, fatigue. My doctor says no way related! More needs to be done to make women aware of these side effects! Especially when they tell you before that there are no side effects!!!

I would just like to say that, even though I just started it, I love Microgestin(generic Loestrin). I'm finishing my first week of pills and things are already getting better. I had been on the shot for my 9 months when I couldn't take it anymore. In the week that I've started taking it, my depression has seemed to melt away. While on the shot I suffered from severe depression and mood swings. Also, I am no longer spotting after having spotted for almost the entire 3 months I had had my last shot. The only thing I noticed was that I had a little more discharge than I normally do and that my appetite may have gone up a little more..although I am trying to gain weight. Also I had some pain in my left shoulder and left leg? I don't know if it was related to the pill though. Just so you know, the shot makes you eat like a pig. I gained almost 15 pounds over the course of 9 months. I started out 5'7 105. I'm now 5'7 118. The shot also gives you hot flashes. Terrible terrible hot flashes.

Hi everyone, I have been taking omeprazole for eight years. The past year my amount was increast to 40mg from 20mg. My very first side effect was itching all over but most of all around the rectum. i have had pains in my chest.Had camera put down behind my heart had all clear. I have high pulse rate been admitted to hospital when it reached 150 a min.Still suffer from this. Tinging in hands, whole left leg tingles when I touch my leg to moisturize it has a pins and needle effect. Had brain scan for blurred vision. Have diarrhea most days.Get dehydrated because of this I am for ever drinking. My muscle cramps are so bad I cannot do baking any more. Cramps in my legs and feet.I have bad fatigue.I am not interested in sex.My whole life has changed completely over a gradule process. I thought it was down to my age 61.My e.s.r.blood rate is raised I have had every test available I have taken steroids to lower it.It worked at first but then graduly went back up even being on steroids made no difference.
I had no idea this was down to this drug.
From reading this site today I am going to cut down first to 20mg a day. Change my diet and drink plenty of water ,If this makes a different on my state of health I will be back to tell you

I am a 43 year old female, I got a couple of clots in my left leg, caused by taking birth control. I was taking the bc to control my menstrual cycle, I took it against my better judgment, even though my dr. said it was not a high risk since I didn't smoke. Well that wasn't true.
The side effects are extreme dizziness, I went to walk down a set of stairs recently and almost fell down them, That would have been tragic, Thank god my friend grabbed my arm. I know for a fact that it is a side effect from the coumadin because prior to this dvt I had no dizziness, as a matter of fact I was very healthy, I exercised 4 times a week, boxing, weight lifting ect. I was "NORMAL" I can't wait until the doctor says ok, stop taking the blood thinner. I want my life back. I just want to get back to the way I was before my dvt.

I have had serious hip pain, especially when extending my left hip, and even worse with abduction of my left leg. I had absoluetly no pain before taking Fosamax. My doctor insists, the pain is only arthritis, and had nothing to do with the Fosamax.

I have been reading on here. I got my mirena in July 2008. I had really heavy periods and terrible cramping. Also, my doc said it was a treatment for ovarian cysts, which I also have problems with. I had bad cramping for 2 months after getting it and spotting. I have no desire to have sex and I've been battling depression and anxiety. I am 26 with 2 great kids. My husband had a vasectomy, so this was only to prevent periods and cysts. However, I haven't enjoyed sex since. Not only do I get pain afterwards, but the pain sends a terrible pressure down my left leg. My husband says he feels the iud during sex. The pain I get after sex lasts for up to 2 weeks...Has anyone had something like this? I have been referred to a specialist, but the docs look at me like I am crazy. Sometimes I feel like I am.

After many months on Zocor, I began to experience sore knees, stiff legs and sore lower back. All at once, in about a one week period, I could no longer walk. My leg muscles were completely gone. I have been for xrays, MRI and more. I am convinced it is the zocor and have quit taking it, however after almost a month without, I still cannot walk without support. My upper body is fine..Right leg better than left leg, left leg almost useless. No more statins for this 71 year old and used to be VERY active male. I hope I can get it all back.

I have had the minera coil for about 5 or 6 years over the past 4 years pains; have got so bad i am due a scan on this Friday. I have very sharp pulling pains each side of my belly button ;a swelling on my left side a dull ache on my left side ;psoriasis dry skin ( and it used to be greasy) ;blotted cant loose weight ;sore boobs tiredness cant get on with house work ; my back aches all the time ;if i lift anything iy brings the pain on cant stand for too long ; this brings the pain on. i cant take this anymore the stomach cramps are so nsty i feel sick i now have thrush piles and just woke to a very sore burning bottom and have a small hard lump in my rectum. one of my gp;s thinks i could be worst off having the coil removed ;how i ask.when the pain is so bad i can hardly lift my left leg for the pain on my left hand side. please has anyone else suffered kile me.

I'm so glad I found this site. I was prescribed doxy for a rash I got in the Dominican that they thought lead to some sort of infection. The first couple days were fine but one night I took the medication before bed and was up all night with the worst chest pains. I have been nervous ever since that when ever I take the pills I'm going to get the same reaction. I have had chest pains the past couple days and I've been really careful with what I take them with and have been making sure I drink at least two bottles of water with each pill. But today I feel so weak. The last week on the medication I've been so tired I want to take naps when I get home from work which is unusual for me. Today my head feels heavy and my leg feels like it's about to twitch but it doesn't. I've felt some tingling in my left leg and my left arm. I thought this was from whatever infection I had since the rash was on my left ankle, but I think it's from the doxy instead. I've also been feeling a dull pain in my thigh every once in a while. I normally have some anxiety but a couple days after I started the doxy I put myself into a panic and spent the entire day at work researching tropical diseases on the internet because I thought I had one from the rash. I've also had some shortness of breath. I have asthma but it feels nothing like that. Also the doxy made my birth control stop working and I started my period. I thought I just had bad cramps but I'm starting to think they were more stomach aches from the doxy. I've had diarrhea also. And I feel so light headed that I'm going to pass out but I don't. I'm definitely calling my doctor today to get a different antibiotic. Thanks everyone for your posts!