Burning sensations symptoms and conditions

Was prescribed Cipro for a diverticulitis infection. Took the first dose right before bed and had immediate vertigo (could tell when I turned over in bed that my balance was off), slept and woke up remembering unusual vivid dreams. Had vertigo bad enough to call out sick. The vertigo continued so I called my doctor had asked to be switched and was given Levaquin. Didn't like the known side-effects of that either. Legs felt like tree stumps but that went away. Took Levaquin 2x without anything overt happening and infections cleared up. Recently had the same infection, once again prescribed. Skin started to have a burning, tingling sensation about 3-4 hours after taking. Woke up with hives on right arms and swollen tingling/burning lips with rather slight tingling/burning sensations off and on on face and body. I am allergic to penicillin, developing an allergy mid-way through a dose (having taken in before without any problems) where I broke out in itchy bumps all over my body, including the undersides of my hands and feet. This happened when I was around 9 or 10 years old. So even if a med is safe once you can still develop symptoms later. I have a call into my doctor, have no idea what they will prescribe next. I get bronchitis a lot and they usually given me the 3 days dosage of antibiotic, which *never* works and they they put me on a 10 days. Not as powerful but that might work. This bought of diver doesn't seem as bad as the past and already my gut feels better. I hate these meds but what can you do when you have a nasty bacterial infection that could kill you?

i have been on mirena for 2 yrs and along with everyone else have all the symptoms from hair loss to very serious cramping in the top of my thighs. i know this is a side affect because as soon as i had it put in i have them since and telling the doctor he said child birth could have caused my pains he calls cramps. it almost felt like a hot needle in my thigh and lasted for a little over two weeks. well let me tell you something this is no ordinary cramp it is a burning sensation and does come and go like cramps but it last anywhere from 1 hour to 10 hrs or even longer. these pains are sharp and burn almost like someone is setting your legs on fire. i can't wait till i get to see the doctor again cause this is coming out one way or another.

Hi, Im an 18yr old female. I recently went to my gyno because im starting college in a month and a half and I thought getting on bc would be a good idea. I went in on the 24th of June, and she told me to try nuvaring. She told me to start that day when I got home. she told me to leave it in until the 1st of July then take it out and wait to the 5th to put a new one in, and progress in that cycle.
Well, less than two weeks into having the nuvaring, I got a really bad uti infection , I have had a history of utis..so i try to do the most I can to prevent them, but this was different. I felt like my bladder was going to explode!. It was so painful and it felt like it was contracting, I was spotting blood and I felt like I was going to pee my pants all the time.. . and horrible burning sensations. I put the ring back in on the 5th, and that day I spotted blood a little heavier and clumpy but not a period. I took it out on the 9th because I did not feel like the infection was getting any better...the ring has been out for 3 days now and I feel so much better bladder infection wise, but I have been having horrible headaches, and nausea. Any ideas?
The only problem is that I have no idea what is gonna go on with my period.
Before the ring, I would usually start anywhere between the 10-14..and I have not had unprotected sex.
Anyone have any ideas on the whereabouts of my period?.

I started taking doxycycline hyclate 100mg twice daily for 10 days for a respiratory infection. After about 7 days I started noticing tingling in my hands and feet and feeling like I was being misted with water on my arms. The tingling became worse and is now very painful in my hands but more so in my toes. It is especially worse at night when your trying to go to sleep.
It feels like the nerves in my hands and feet are raw and going crazy. Nothing relieves the pain. I took my last pill this morning and will never take this medication again.

I was taking doxycycline for a lesion on my face. I started to have tingling of my feet and fingers but did not associate it with the medication. I only used the doxycycline for two weeks. The tingling in my feet lasted for almost 5 weeks.

Several months later I went on Doxycycline because I thought I had lyme disease. After being on the Doxy for one week I started up with burning sensations of my hands and feet. Puffy, red hands...burning on different parts of my body. My Md said it was anxiety! An immunologist said it was peripheral nueropothy from drinking too much!!! I knew both diagnosis were bogis....then I started to research doxy and came upon this site...thank God. I finished the month of the Doxy. I have been off the med now for two months and the symptoms are finally starting to subside.
I can remember waking up one night and my entire chest felt like it was on fire. Wearing shoes was so painful that I wore slippers to work...I was a burning tingling mess and I am convinced it was the doxycyline.

Please, help me! I went ER three times.. I'm looking for someone having symptoms like cold and heat on the body, burning sensations, and chemical reactions.(I could not take any medicine and vitamin and mineral) I was off taking this medicine 2months ago but I've suffered with these symptoms and I could not sleep well..A lot of sweating... Getting weaker and weaker..
HELP ME PLEASE!!!!!!!!

Sorry, I'm new to this! I was wondering if anyone else has experienced vaginal burning sensations with Mirena. I had mine removed yesterday after six months; I've had a problem with burning on and off since November 2008. It's been particularly bad since the beginning of January 2009. My doctor said Mirena's not causing the burning, but he can't find an explanation for it yet, and I've already tried 4 different creams - none worked for long. My instinct said that Mirena was the problem, so I'm going to wait and see if my symptoms go away. Comments welcome!

I had the Mirena put in a year ago. Experienced bleeding for approx 3 weeks.Not really seen my period since(Wooohoooo),except for some light spotting round "that time of the month". I recently have been experiencing very bad acne breakouts.Have always felt that my tummy is bloated and have a very low sex drive. But my BIG QUESTION is Has anybody experienced a burning sensation in either of their bum cheeks,(especially when sitting,feels like it's on fire)which is unexplainable by numerous doctors and endless tests I have had done. Not sure if it's related,but so desperate for this burning to stop.

OH MY GOD!!!! I thought I might be imagining things. I was prescribed Levaquin and clyndamycin on December 15 2008 for a urinary tract infection that appeared to have gone systemic. After 2 days my right knee swelled up. I went back to the Dr the next day and he looked up both antibiotics in his little book and said the clyndamycin could cause joint swelling and pain. He told me to stop taking the clyndamycin and take 600 mg of ibuprofen for the joint paig. His little book said nothing about levaquin. Well I kept taking the levaquin and the pain spread literally to every joint in my body. I could not walk and had trouble even holding a coffee cup. The pain was unreal. I completed the 10 day course of the levequin as instructed. The joint pain was getting worse. I called the Dr. again and they did blood work to rule out arthritis and stuff like that. He put me on prednisone which has significantly helped with the pain. He said it may be a coincidence that I have developed arthritis and that it had nothing to do with the UTI. Well as I was watching TV last night I saw a lawyers commercial for a law suit against levaquin and cipro. Then today got on the internet and found this site. I am going to call the Dr. and tell him to update his little book he looked up the levaquin in. My fear is how long after you stop taking this poison does the joint pain end? I wish I would have known all of this sooner. I will never take this drug again.

Muscles spasms, sensitivity to light, burning sensations up and down my arms and legs, racing of heart, horrible sinuses, migraine headaches, chronic fatigue, hair loss, dry skin, Candida, acidity (low PH), low immune system, acne, joint pain, and the list goes on and on.....
My doctor told me I was fine and suggested I go on an anti-depressant. I am not depressed I told her. Since my doctor and other conventional doctors weren't helping me (all they wanted to do was prescribe more horrible drugs) I decided to seek an alternative MD. He said all these symptoms can most definitely be from my birth control. I went off Triphasil (Trivora) 3 weeks ago and am taking some herbs that are supposed to help correct the damage the medication has done. I now have a whole in my kidney, cysts in my ovaries, spots on my lungs, and an infection in my stomach (yeast also known as Candida). I have been sick for over 6 months now and am finally ready for this to be over. I can no longer go to the gym, work a full time job and enjoy social functions/outings. It is emotionally and physically damaging. Those of you who are on it...please stop! It is ruining your insides and making you weak. I am 30 years old and was on Trivora/Triphasil for 6-7 years. What a mistake. This is the ONLY drug I take and I used to be perfectly fine. As a matter of fact, I used to run 10 miles a day and now I can't even walk 30 minutes in the gym. Needless to say, I am very angry at the doctors for prescribing such medication to me, for the FDA for approving it and for our government for not doing their due diligence.

Cipro is a chemotherapeutic agent that is stored in fat cells and is reabsorbed into the bloodstream when burned and can potentially damage any system it comes in contact with. I took this for two weeks.and had horrible pains and kept having what could best be described as partial seizures and heart palpitations as well as peripheral neuropathies. As the drug recycles every few months back into my blood the symptoms start over and sometimes new ones occur. I am currently experiencing floaters, brain fog, vision problems, burning sensations, panic attacks, partial seizures, dizziness, depersonalization and extreme fatigue even nine months after taking 27 pills over the course of two weeks. Cipro is used to kill anthrax and should not be used on people even though Bayer is making a killing in its sales. You don't have to look far to find thousands of people who have had their lives destroyed by this drug. Remove from the market ASAP.

I have been taking Singulair for 5 weeks and stopped after developing high blood pressure, numbness and tingling all over my body, flushing, anxiety, memory loss/difficulty concentrating, skin burning sensations, fatigue, "heavy legs" feeling, heart palpitations. I have been off of this drug for 3 days. I still have the side effects and hope that they will go away ASAP. I am also a very well-controlled 28 year old diabetic and when I had neuropathy-like tingling sensations in my extremities (from Singulair) I became worried and angry. I am seeing a doctor tomorrow for a full exam. If this drug has caused me permanent nerve damage I intend on filing a lawsuit against the drug company.

Most of the "side effects" are die off responses (sometimes referred to as a herxheimer response similar to that which occurs when treating syphillis) from bartonella or borrelia. Levaquin is a potent intracellular antibiotic...where these and other organisms can hide. These can be subclinical infections where (at this time) you are not even aware you are infected. If your "side effects" start around the 3rd day into your prescription...rejoice...and suffer for a while, you are killing something really bad.

I had Mirena put in July 6, 2007. It was 2 months after the birth of my son. I felt wonderful before it was put in. I was excited about being a mom to child number two and surprised at my energy level. Three weeks after getting mirena on July 28, 2007 I went to church feeling normal when suddenly I started having severe cold chills. I had to leave the service. It was hot that day and I went outside and sat in the hot sun. I couldn't get warm enough, I laid flat on the hot sidewalk to absorb the heat. Next I put on a sweatshirt, then a jacket, next I sat in a hot car until I got sick from the heat. I got nauseous and a horrible headache from the heat. When church let out we drove home. I slept for two days straight. When I finally got out of bed I was dizzy. I stayed dizzy until yesterday--two days after I had my IUD removed, One year after having it put in. I also had many other symptoms including the following: extreme fatigue, slurred speech, loss of coordination, numbness-tingling-burning sensations-in my limbs, blurry vision, brain fog, inability to comprehend simple questions such as "what is your name?", excruciating muscle pain and stiffness, joint pain, depression, short temperedness, acne, bloating, decreased sex drive, sinus congestion, shortness of breath, psoriasis, and probably more. I didn't think the IUD was responsible because I was told it was virtually side effect free and that the hormone in it was "localized" and didn't circulate through the body. Because of that misinformation I can say that this has been the hardest year of my life. I started out bonding wonderful with my newborn son, however it is hard to bond with a newborn when you are so dizzy you feel like you will drop him. Let alone the fact that I couldn't see straight, had no coordination, and was extremely tired among my many other problems. I'm not saying we didn't bond, we did, it was just so challenging. The only way I could was to lay still with him. I am usually a fun and energetic person and my baby didn't get to see much of that during the first year of his life:(. I wish I had been informed about the possible side effects or at least been treated like it could be a possible cause. Instead, I was told there was absolutely no way my Mirena could be causing my side effects. Well, now I know otherwise because every symptom I listed above has either gone away completely since I had the Mirena taken out or at least subsided dramatically. It has only been out for three days. Another thing that causes me concern is that for the first couple months of my sons life he was a very happy baby and very content. A couple of weeks after I got the IUD he became a very fussy baby. At first I thought it was colic because it was around the age that babies get colic. The fussiness lasted until I stopped breastfeeding him. I have a feeling he was having some side effects also. I wish I would have researched the Mirena more. I actually wish I had prayed about it because I have a feeling I was supposed to. I just want to say that if you or someone you know is having any health issues and they have the Mirena, please have it taken out before you do anything else. It may save you a lot of grief. I have been to the doctor so much. I have had my thyroid tested, blood tests, seen a neurologist, diabetes test, been back and forth to my doctor and a chiropractor for the muscle and joint issues I had. All I needed to do was lose the Mirena. I was told I most likely had Lupus, fibromyalgia, or MS. I am so angry at this point. Why can't they just say that it is a possibility that Mirena could cause all the side effects people are having. My children would have had so many more good memories if I had been told that. Good luck ladies! I hope Bayer finds itself in a class action lawsuit and all the doctors learn something from it!!!!!!!!!!!!!!!!!!!

21 lb. weight gain, hoariness, night sweats, extremity cramping, hair loss, numbing, tingling and burning sensations in arms, hands, face and scalp, clearing of throat consistently, joint pain, muscle aches. Advair 250/50 for 9 minuths.

I am a 54 year old male who was put on Lipitor by my Dr to treat cholesterol levels of 6 to 6.5 around august 2007. I used the drug through until early Jan 2008 when I started to notice continuous muscle pain and injuries especially in my lower back buttocks and arms. I constantly had tingling/burning sensations in my large leg muscles, finger tips and hands. My eyesight was deteriorating rapidly and I had a constantly fuzzy brain which was hard to focus and concentrate. I thought that I had rapid onset Alzheimer's or similar. I was finding difficulty controlling/getting nerve instructions to muscles such as bowels, prostate, mouth. My Wife accused me of slurring words and my balance became unstable and I had a series of minor falls.
I started to wonder about my medication and as I only used two and Lipitor was the newer one of the two I stopped taking it. With in Five days most of the symptoms were disappearing or rapidly improving. After ten days I decided to reintroduce Lipitor and within four days they were all rapidly returning. It was at this point that I started to do a lot of research and found all of the sites highlighting the varied side effects attributed to this drug. None of which had I been informed of by my doctor or Pharmacist and most of which I was experiencing. Needless to say I now no longer take the drug and most things have returned or are returning to normal including the eyesight, balance and nerve control. This drug needs to be withdrawn from use before too many people suffer lasting debilitating damage or even worse, death.

I have been on the NuvaRing for 4 months...I have had the worst side effects ever! I couldn't figure out what was wrong with me. I actually found this website and took the damn thing out- THANK GOD! I already feel better. I can't believe the countless number of accounts on this site- women who are suffering from this BC like me. I knew I was irritable. My Symptoms: ANGER, road rage, impatience with my family and friends, feelings of laziness, extreme uncertainty and anxiety about the smallest decisions. I couldn't figure out what was wrong with me..just knew I was WAY WAY off balanced. I thought I might be becoming a manic depressive. The last thing I suspected as the problem was the NavaRing...why????????????... because it's claim on the box that it is less likely to causes moodiness and other side effects than other forms of BC. Not only was I acting like a total bunny boiler but I also broke out several times, gained 10 lbs, had constant UTI's, burning sensations in my vagina and strange odor.

This is the worst form of BC I've EVER EVER tried. I warn any woman that feels strange- TAKE IT OUT!

61 year old female, on Lipitor 2002-2005 10 mgs a day. Doc increased dose 2006-current to 20 mgs a day. No muscle problems BUT hair has thinned out dramatically! Doc called today and reduced dose back to 10 mgs for 6 weeks as liver enzymes up with tests last week. Also have tingling in feet. Haven't read all the posts here yet as just found site today but anyone else losing hair and taking drug? If you had hair loss and quit the drug, did your hair come back? If your liver tests were higher and you cut back on the dose, did your numbers go down?

I have been on synthroid for about 6 months now. Some of the side effects I have been experiencing are numerous.I have hair loss, sometimes I get so ill that no one can stand to be around me, my weight has gone up about 30 pounds, my cholesterol levels went sky high so now I'm taking Crestor, I'm bloated most times, I have episodes where my face flushes and gets so red that it feels like its on fire, and now I've just started experiencing burning and aching of the legs, I'm tired a lot too! My doctor said I would lose the weight but every time I go for check ups and get on the scale it just keeps going up. I would like to know if anyone else out there is experiencing the burning and achy legs because I have been tested for everything and they can't find out what is going on. They of course say it's not the medication.It seems to never be. Does anyone feel me??

I was experiencing high b/p so the doctor prescribed, Metoprolol 25 mg a day. I took it for one month and was having burning sensations in chest below breast bone, palpitations, tightness in chest like I could not get a full breath of air. Stomach pain, gas nausea and upset bowels. I complained to my doctor and he switched me to Toprol XL and upped it to 50 mgs a day. Still having palpitations, burning sensation in chest and stomach upset. I am hoping the side effects will diminish and my body adjust to this pill. The doctor has told me to give it some more time to allow for this.
kittietoes

I have experienced burning sensations from Celexa.

Well, I thought that I was really enjoying the NR until yesterday, there was a Lawyer from NY in the hotel that I work with a women. They were discussing a case against the new stop smoking drug and he said something about the Nuva Ring. I tuned in to hear that he has had cases over the NR as well as the patch. I thought that my dizziness was just because I hadn't ate anything in a while. I haven't gained weight. I have actually went down a pant size but I am really lazy and I do like to sleep a lot more now. I get dizzy and head aches. Sometimes I get the burning sensations like I am breast feeding. I have horrible mood swings. I feel really bad because I am so mean to my husband and kids. I get cramps and back pain. and I have no sex drive. Yeast infections and discharge. I feel like you name it I have the symptoms. I thought that I was going to have to have my blood sugar levels because the dizziness is getting so bad! I am about to call my DR.

I have been on NR since July 18 of this year. I was diagnosed with PCOS and Insulin Resistance. I am also on Byetta. My experience with NR has not been good. First of all I was skeptical about constantly having a foreign object in my body especially such a sensitive area. Symptom 1, decreased sexual desire! Symptom 2, burning sensations down there. Then itching, and a horrible discharge and smell!! At this point I kept thinking how much worse can it get. Well it did, I should be loosing weight from the medication finally regulating my insulin levels, after all I work out 5 times a week and follow a healthy eating plan. My lower tummy is swollen as well as my hips and thighs. Not to mention I have pains in my hips, like they need a massage. On top of this all I have an increased resting pulse rate and blood pressure as well as tighten feelings in my chest. I really feel like this birth control is not safe for me. I was previously on yasmine, and loved it. My endo suggested NR due to the PCOS and IR they feel like it works best with Byetta! WRONG!!! I am waiting for the DR to return my call I am requesting AGAIN that my BC be changed.

I was recently diagnosed with Hoshimotos Thyroiditis. It's only been three days since I have been on the Levoxyl (100 mcg), but I am feeling slight chest pain and tingling in my face. My heart isn't racing though; it's just a dull pain! I am nervous that it will continue to increase and that other symptoms will come about. Just reading about people's experienced on this site has made me nervous too! Has anyone ever experienced this and if so, did other symptoms follow?

Thanks for your feedback!!!

Hello! My name is Tyra from Chicago. I started using Nuva Ring 4 months ago. I notice a week before I begin bleeding, I started to have bad gas problems, sometime I get such a bad gas pain in my stomach I couldn't barely move,unable to sleep and missed work. I have no sex drive, I do not want to have sex at all; when I do, it's so painful and got alot of burning sensations afterward. Sometime I feel disoriented, confused and slightly depressed. The ring is causing all of these symtoms. I am going to have to discontinue using this. One thing I will miss is having light and short period, but I rather bleed longer and heavier in exchange to my old self back! I am just going to go back to same old condoms..my boyfriend will have to compromise.