Skin sensitivity symptoms and conditions

About 4 months ago I took 7 days worth of Levaquin after my sinus surgery. It was a preventative measure, I never had an infection. A few days into the prescription I started having tendon pain in my knees & ankles. I couldn't sleep, I was having nightmares, I was emotional, anxious and drained. My doctor told me to stop taking the Levaquin immediately. 4 months later and I am still suffering from entire body tendonapathy, neuropathic pain, joint pain, skin sensitivity, severe migraines, temperature sensitivity, twitching (muscles convulsing), basically my entire body hurts. Some days are a little better than others but not by much.

I have been to rhuemetologists, neurologists, pm & r doctors, physical therapists, acupunture, orthopedic surgeons, & allergists (in Chico Ca, & @ UC Davis in Sacramento Ca). NONE OF THE DOCTORS KNEW WHAT TO DO. My general physician actually told me to "go home and wait it out" because there was "no hope of finding help" (I'm not kidding). I've had tons of blood tests with fairly normal results. Thankfully I have a wonderful neurologist who has taken some interest in my situation. All of the other doctors told me that my case was very rare & that they had heard of such side effects but had never seen any patients with them! After some research on the internet I seriously doubt that my condition is as "rare" as they claim.

I am only 28 years old, I can't walk, I can't work, and my life has been turned upside down. I was very healthy before, I don't have a family history of health problems, nothing like that...it was the Levaquin.

Here is what I am currently taking: Lyrica for neuropathic pain, twitching, not being able to sleep etc., and oral morphine for the severe pain, Milk Thistle to promote glutathione (important because it helps your liver detox), Magnesium Malate (also helps detox), a multivitamin, vitamin c, and fish oil pills. I also attend acupuncture 2x per week (honestly feel some relief from it). Also, I heard that glutathione infusions are helpful but I haven't tried them yet. At this point I will try anything.

IF YOU HAVE HEARD OF ANYTHING OR ANYONE WHO CAN HELP WITH THESE DEVASTATING SIDE EFFECTS PLEASE LET ME KNOW.

~J.

March 3, 2009
I returned to the doctor today to get a different antibiotic because Avelox made me worse off than the sinus infection I had. I stopped taking it about two weeks ago and still have side effects from the drug. My doctor had given it to me about two other times. The last time I recall was in November. I didn't finish taking my prescription then either.
I thought maybe I was having flu symptoms also, but it was the drug making me more ill. RASH, HIVES, RED HANDS, SWOLLEN TONGUE THRUSH, BUMPS ON MY TONGUE, TINGLING IN MY BACK, VOMITING,HEADACHES, PAIN IN MY STOMACH NOT LONG AFTER TAKING A DOSAGE. FREEZING HANDS, THROAT FEELS LIKE IT'S CLOSING UP AND DIFFICULTY SWALLOWING, COULDN'T GET OUT OF BED, MUSCLE FATIGUE, ACHES WEAKNESS, JOINTS HURT, TINGLING IN HANDS, ANXIETY,CRYING SPELLS, NIGHTMARES, SKIN SENSITIVITY, INSOMNIA, THEN EXTREME FATIGUE, DIZZINESS AND LIGHT HEADED UPON STANDING AND/OR GETTING UP FROM A SITTING OR SQUATING POSITION. EVERYTHING HURTS ALL THE TIME IN EVERY MUSCLE...... I BASICALLY FEEL LIKE I AM DYING.
My fiance thought I was totally losing my mind. I was moody, aggressive, irritable, depressed etc... I felt like like a different person.. My fiance of course got sick also and his doctor prescribed it to him. His side effects included muscle aches and pains and extreme fatigue and mood swings. I looked up some side effects when I was started taking it a few weeks ago, but didn't pursue the research until the side effects got worse. I took it for 7 days this time. My fiance took it for three days. I called him at work after seeing this website and told him to stop taking the medication immediately. I am still sick with a sinus infection, and a whole slew of other crap going on. I called the doctors office and went in right away to get a different medication. To no avail, when I went to my doctors office there was a rep from Avelox there. I said don't give that Avelox to anyone sarcastically. I then saw his tag on his shirt and his bag full of Avelox samples. He asked what type of symptoms I had and I told him.. He said he would report it to the company.... What do you think they will do about it? MOST LIKELY NOTHING. I am an educated person with the capability and time to research anything I need to and I will do my best to dig up the most dirt I possibly can about this horrible medication. They need to stop pushing these meds on doctors to give us and make us more ill than we were to begin with. I JUST HOPE MY AILMENTS AREN'T PERMANENT. People try to make light of the situation because they don't want to be sued. I think the FDA needs to be revamped and the Government should stop letting these pharmaceutical companies poison us. I AM NOT EXAGGERATING EITHER! DO NOT TAKE IT.
I have been going to my doctor for about fifteen years and she never gave me any medication that had made me this ill. I get samples a lot because I have no insurance. Sometimes she gives me scripts. Today I got Zithromax which always worked well for me in the past. Very little side effects. I realize that everyone reacts differently to certain meds, but come on now! It isn't just a coincidence that all of us commenting and complaining here are imagining these horrible side effects! Today I got Zithromax which always worked well for me in the past. (Very little side effects).Then why did I ever have to take Avelox if there are other antibiotics that will make me better not worse. They push these meds on doctors to give to us that's why! I always trusted and admired my doctor. She always treats me well and does right by me. What is going on with these medical companies?! SOMETHING HAS TO BE DONE ABOUT THIS!

I was prescribed amoxicillin for a sinus infection. (3 x 500mg / day) The good news is that the sinus pain was relieved within two days. On the other hand, I developed several side effects, which seem consistent with other reports I've read on this site. These include the common complaints of diarrhea and upset stomach. In addition, after about two days I started to experienced symptoms of a fever, including general body aches, slight head ache, chills and skin sensitivity, especially on my back. The strange thing is, I don't have a fever (temp. 97.9F). These symptoms seem worse at night. I suppose I could have some type of virus along with the sinus issue, but it seems strange that the onset of symptoms was so coincident with the amoxicillin treatment.

I took Doxy for about 2 weeks as a remedy for a bump on my eyelid. This first exposure to Doxy seemed only to cause a little skin sensitivity and burning in my fingers, no big deal.

When my eye problem didn't go away, my eye doctor prescribed Doxy for a second time a month later. This time my side effects were much different. Within a couple hours of taking my first pill I felt a bit off, I felt anxious and unsettled. I Continued on the medication for a total of five days. During this time my side effects progressively worsened. The first few days I had very abstract thoughts, and began feeling strangely claustrophobic. By day three I was beginning to feel paranoid and fearful over just simple everyday things. Day five is when it all hit the fan. I started having difficulty breathing and feeling extreme tightness in my chest. My feelings of claustrophobia had also worsened to the point where I began having panic attacks, like I was trapped inside my own body. It was at this point I made a desperate attempt to search the internet for a possible cause, in hopes it might be the Doxy medication I was on. I was somewhat relieved to find this website and read that others had similar symptoms, maybe I wasn't losing my mind. I immediately quit taking the medication, but unfortunately the symptoms didn't go away for several more days. That night I was unable to sleep, I had mild nausea, and would wake up in the middle of the night in a panic and would shake uncontrollably. Lovely huh. It gets worse. I began to feel extreme fear and paranoia like I was going to die, or lose my kids and family. I began to feel if this didn't go away, I would not be able to go on. Thank God it did, and by day eight the extreme thoughts began to subside. I continued to have the breathing difficulty and mild depression for several days after, but the worst was over. Within a month I was back to normal.

I write this as a warning to those who are taking this med and feel anything close to this... stop taking it! I am a healthy, normal, 40 year old male, that has no history of mental issues, other than a "blue" day from time to time, and within six days I was entertaining thoughts of suicide. The psychological side effects of this drug NEED to be addressed. This is very serious stuff!!!!!!! Though it may be a small percentage of people that are susceptible, for those who are, it is a deep dark hole.

My 6 y/o daughter has been taking Singular for approx. 2 years. She began to have regular stomach pains shortly there after. She was sent to Children's hospital where they put her on a laxitive which made things worse. Then we began testing for food allergies only to find out that she tested positive for a 3 page list of foods. We eliminated those food and had her tested again. She was subsequently allergic to the foods we eliminated. She was recently down to rice, a few meats and some vegetables. Guess what, she is now allergic to those foods.

All this time she has been complaining of severe leg pain, eye pain, throat pain, numbness and tingling in her hands a feet, all of which come an go. I have reported this to all the doctors and specialists we have seen. She had undergone countless blood tests to rule out autoimmune disorders and all come up negative.

She began to develop severe anxiety and just had the blues most of the time. She would be crying and saying off the wall things like, "I don't think my fish is happy". She couldn't stand to be away from me and would stress out about even weather or not she would sit by me at a restaurant. I mentioned this to all of the doctors. They said to not make too much of it. One suggested she see a psychologist. NOT ONE DOCTOR EVER LOOKED AT THE SINGULAR.

Finally about 4 weeks ago my neighbor who is a scientist at a pharmaceutical company called me and told me about the "black box" warning that had just come out on Singular. I took both of my children off of it immediately. My daughter went through about a 10 day period where her anxiety got worse and then it was just gone. We are adding foods back into her diet and at this point she has not had any severe allergic reactions.

The last 2 years have been a complete nightmare for her and for us. I am a medical professional and I have had doctors treat me like a hypocondriac, hypersensitive, attention seeking mother. I feel so justified and saddened by the recent findings all at the same time. Most of all I am so grateful that we figured this out before things go even worse.

Please let me know if anyone else is suffering food related reactions as a side effect.

Dealing leg pain and swelling fpr over 6 months - having 2 DVT test and 3 MRI's they finally found that I did have a DVT in my left leg and now I am taking Warfarin as of May 30th 2008. I now have severe joint pain, sore skin/sensitivity, my vision is going I can hardly read anything all of a sudden, so exhausted, sleeplessness - even after taking an ambien and getting some sleep, I can take a shower dry my hair and I am ready to go back and lay down because I am so tired. the doctor says thin blood does not carry oxygen as well so this is why I am tired. I am not anemic as I just had that checked. I can feel my muscles getting weaker. From reading what everyone else says it must be this drug, but I don't think I could live without it since my clot is so massive. I feel like my life will end soon I am getting weaker by the day...is this just my imagination? I know I am depressed but I do think all of the symptoms I am having is from the warfarin(besides the pain from the DVT which is still very painful)

Anyone have extreme skin sensitivity? The right side of my face and scalp have a minor burn/itch feeling. I also seem to have some small goose eggs on my head. I'm seeing the OB today. Should be interesting.

Hi all! I just began taking YAZ two weeks ago and things were fine up until two days ago. I started experiencing itching on several parts of my boy an last night, realized I had hives on my waist at my back, near my underarms and have serious itching all over the rest of my body including the palms of my hands. Please, please, please if anyone reads this an has had similar side effects, please let me know. Furthermore, I did not take the pill last night as I knew this could be the only thing causing these issues. Does anyone know the reprecution of stopping the pill mid month? Please let me know and thanks for your help!

I'm not sure whether this is Sporanox side effect, but after taking Sporanox I'm experiencing Skin irritation & skin sensitivity. Rashes formed without the known reason, once scratch the redness canot fade & spread the whole body, & itchness that non-stop. Tell me what to do!!!

I wouldn't try the patch because of skin sensitivity, shots just seem really wrong to me, but I have been taking different oral contraceptives for nearly fifteen years. Fortunately I haven't had a pulmonary embolism which was definitely a risk because I was a smoker the whole time. Every time I switched pill brands, it was because of insurance copays, it would be non-preferred. However, I was still diagnosed with endometriosis and had one ovarian cyst removed laparoscopically and one ruptured on its' own. Endometriosis is less common in women on the pill because of the ovulation regulation...so I imagine things could have been so much worse. I was able to ask to take the pill continuously, meaning I'd skip the sugar pill week. Oh heaven! Without the pill I have severe cramps, PMS, heavy bleeding, pain and numbness in the crotch area, diarrhea, and was emotionally unstable. Although I suffer from depression, I don't feel that the pill has affected that much at all. I've recently quit smoking, and now am on the Nuvaring because of drug interactions. I've been spotting for 10 days now at least, and been on the ring for a month. I know there is a transition period, but this is not acceptable. My request to my doctor is to get back on some sort of pill on my insurance's preferred list. I'm starting to break out too. I want my pill back!

I am sooo relieved that I found this site. OMG. I was on the NR before for about a year and 3 months. I didn't have any side effects whatsoever. I went of the NR because my boyfriend and I broke-up and I wasn't having sex. About 4 months later, I developed 2 ovarian cysts that ended up rupturing in my right ovary. BTW, I turned 30 in the same month. I was in so much abdominal pain, hot flashes, painful menstrual cycle, passing huge blood clots, depression, crying all the time, thoughts of suicide, anxiety attacks, very irritable, easily frustrated, inability to concentrate, and nausea. I had NEVER had any bouts of depression, crying all the time, thoughts of suicide, anxiety attacks in my life before. NEVER! My OB/GYN told me my hormones were all out of wack and that I should go back on the NR to regulate my hormones. So, I went back on the NR, my cysts went away and I felt 100% better immediately. Now it's 2 months later and I'm having all the same symptoms I had before the NR, although, it’s not as bad as it was before. Apparently, I'm still ovulating while on the NR although the NR STOPS ovulation. I have developed more cyst(s), haven't gone for the ultrasound yet, in my right ovary, even though my last ultrasound showed that the last 2 cysts went away. Right now, I am emotionally drained and physically in a lot of pain. I think that if I get off the NR my symptoms would be a lot worst. I’m allergic to the patch because of the adhesive, coming off of depo caused too much pain, and I forget to take the pill. So I don't know what to do.

Hi! I am a 36 year old female and have been on this HORRIBLE HORRIBLE drug (prednisone) for 2 1/2 years now..... Hopkins doctors still arent sure exactly what i have. My immune system is attacking my liver so to speak. My body is basically looking at my liver like it doesnt belong and is attacking it with large multiple lesions that is eating it away... the good thing is that it hasnt interupted the functioning of it yet but is leaving horrible scar tissue. I have been in and out of the hospital 13 times, have had just about every test imangable, 12 liver biopsies and they STILL have NO clue! They are leaning towards Church Straus desease and Wegners but the weird thing is i have half symptoms of both. The first year they had me on 80 mgs of prednisone a day which had seemed to put me in remission for about 4 months and then they came back even worse so i was put back on the prednisone, 80 mgs a day AGAIN along with 100 cc's of Methotrexate, another not so nice drug... i had EVERY SINGLE BAD SIDE EFFECT OF BOTH DRUGS!! This second time around was ALOT WORSE for some reason!!! My body DID NOT LIKE IT!! Nausea, hair loss, moon face, gained 40 pounds (and i was in great shape, worked out, i am 5'4 and was 110 pds!), EVERYTHING was swollen, legs, ankles, arms, neck, face, had the camel hump, fingers and especially my belly!!! UGH!!! Have bone, muscle, and SEVERE joint pain! Kaliedescope vision, dry eyes and then had mucus discharge (kindof like pinkeye), headaches, intestinal problems.... VERY CONSTIPATED and then the opposite!!! I literally felt as if i had turned into a man in my behind!!! Sorry to be so gross but thats how bad it was!!! Jaw problems, teeth and gums as well, skin sensitivity and have little bumps all over my skin (kindof like tiny little moles), itchy, broke out with acne and pretty much NEVER had more than 1 pimple a month, had facial hair (VERY DISGUSTING!!!! HAD IT WAXED EVERY WEEK!!!!) and then on top of all of that the swelling of my liver not to mention the PAIN! I was recently in the hospital again with 12 new lesions, pneumonia, and 104 fever. My doctors said the Methotrexate was the cause and i was having a bad reaction to it so they now have me on 100mgs per day of Azathiroprine. I am now finally down to a maintenance dose of 5 mgs of prednisone cause my body was starting to reject that as well. I thank god that i am now down to that dose!!!! It as only been 2 wks and the withdrawl symptoms are horrible worse then they were but i know what is to come =) loosing all this fluid and all of the HORRIBLE side effects i listed above. I will have to be on the maintenance dose of 5mgs the rest of my life and can live with that cause when my body gets back to somewhat normal i wont even notice that im on this CRAP!! I will be on the high dose of Azathiroprine for a few years and then on a maintenance dose of that as well for the rest of my life to keep whatever this is that i have under control.... the scary thing is is that they arent even sure that all of these meds will even work...... im a guinea pig..... The only thing that i am on out of all 25 pills/meds that i take everyday that works is my pain meds. Oh and i also forgot to mention that i had to be put on some "HEAD CASE" medication (thats what i call it =) ) for depression. Its a low dose but it does seem to help... I am terrified of what the future holds but continue to be strong and have an amazing support team... my fiance and family =) I dont even want to think about how i would be without them. I go back on the 25th of this month for my MRI so please who ever reads this keep me in your prayers as for all of you are in mine. I feel for each and everyone of you that has to endure this horrible drug everyday and i hope that everything works out you. =)

Sue =)

I am a 39 year old female. I have been taking Advair for about 4 years now, since a bad attack landed me in the hospital. My pulmonologist initially put me on the 500 strength and told me to take it twice daily. After a couple of week of that my skin broke out in small bumps all over the place - my face, my chest, my back, even on my scalp. I suspected the Advair, told my doctor, and she advised me to reduce to once daily. I did, and the bumps were gone within days. After a few months she decreased me to the 250 dosage and I remained on that for 3 years with no debilitating side effects. Unfortunately my doctor retired around this time and another doctor took over her practice.

About a year ago I noticed that my joints were weaker, specifically my knees, and I had one bad fall caused by complete loss of strength in my left knee. My new doctor said I might be experiencing cartilege loss but did not mention it may be from the Advair.

Then a few months ago I had got an upper respiratory infection which went into bronchitis. My doctor put me on an antibiotic that I'd never taken before and increased my Advair to 500 again. Almost immediately I began experiencing racing heart, joint pain, extreme skin sensitivity, sore throat and ear pain. I also got a yeast infection, which is something I have never had before. I still did not suspect Advair as the culprit. Although I reported all these symptoms to my doctor, he also did not mention the possibility of Advair playing any part in them. He told me it was acid reflux, although I've never had a single GI problem in my life. He told me the muscle pain was stress, for Heaven's sake. I wasn't very comforted by his diagnosis, but couldn't think of what else I could do.

One morning a few weeks ago I woke up and for some reason decided to Google Advair, and found copious documentation from reputable sites like Mayo Clinic that detailed all the possible side effects of the drug. I was floored to see that I have been experiencing so many of them.

I have now taken myself off Advair. It's been a week thus far and my breathing has not gotten any worse but the heart racing has already gone away. I also feel less ear pain. The joint pain has remained. I suspect that bone and cartilege damage done by this drug will not be reversible.

Tomorrow I have another appointment with my doctor and plan on showing him the information I printed out from the Mayo Clinic site on the effects of Advair. I do not plan to resume taking that drug.

I had severe flu like symptoms (fever, body aches, bronchial congestion). My doctor prescribed zythromycin as a precaution since my son currently had pneumonia. Within a day of starting the 5 day dosage, I started having severe skin sensitivity. No other way to describe it but a bad sunburn over my body. It hurt just to have clothes touch my skin. Not sure if it was from the Zpak (my doctor didn't think so) but it sure seemed coincidental if not. Pain lastest for days even after going off meds.

It has been a monthan a half since I finished efudex treatmnt. Whenever I take a hot bath or get overly warm , the areas to which i applied the efudex will get red again. Ha anyone elseexperienced this and if so how long idi it take to go away?

I've taken Zpak several times (4+) and each time, it worked like a charm to cure ear, nose & throat infections. I think it worked better for me overall because of the short-dosage cycle which made it easier for me to take the full course prescribed (2 first day, 1 every day thereafter for 4 days). Side effects: diarrhea, cramping, headache, feeling "high" or medicine head--taken with or without food. Hard to say if these effects are attributed to meds or to the infection itself. Boyfriend taking Z-pak right now--he reports severe body ache, skin sensitivity (to touch), and feeling like crap. Again--hard to say if from med or virus/bacteria.

yes i am having the same flu symptoms and today i broke out in a body rash. had a headache yesterday and body chills. skin sensitivity, head ache, dizzyness, loss of appitite, sleeplessness, fatigue, nausea. i believe it is an allergic reaction. glad i found this place so now i know i'm not sick like i thought i was. i have three days left on the medicine and i'm not going to continue to take it

Skin sensitivity. Have to take for 3 weeks for Lyme disease. Am willing to put up with tiny side effects over those from Lyme disease. I think many of the symptoms people have been complaining about here are directly unrelated to Doxycycline.