Cold water symptoms and conditions

So relieved to find that I am not alone with my symptoms. These include severe sunburn, esp. nose & vitiligo spots. Nose got very red last time I took this and I ended up with decent case of rosacea...and my nose grew larger. Cold tingling irritating feeling in my hands, feet, arms, many places. Cold water or pool feels terrible to me. I am on vacation...had to stop taking it in order to be able to enjoy myself. Before I didn't know that the med is what caused the rosacea. Now I know... I will not be taking this med again if I can avoid it. I am wondering what the long term damage is, and why there is not a warning about these symptoms on the med info sheet I rec'd. Are any of these issues causing permanent damage?

Wow, I thought I was going crazy. I've been so sick the last week but didn't think it would be this new medication. I'm taking 150 mg once a day for 15 days. I have three left of which are going in the garbage. I missed a family reunion today because I'm so tired I can't function. It's like someone gave me a sleeping pill. I've taken three pregnancy tests of which they were all negative thinking I was pregnant. The nausea is horrible. Just talking about food makes me vomit. I have stomach cramps, severe lower back pain, my heart feels like it's doing flip flops at night. My face feels very hot at times. My hands feel like raw nerve endings when put in cold water or wind blows over them. My arms tingle and hurt when exposed to the sun. I just want to lay in bed and not face the world. I've been dieting and lost 15 pounds prior to starting the medication. Boom, all that stopped. Still doing all the workouts and carefully eating but have gained 4 pounds back. Very disappointing. I am so glad I found this site. You won't find this information on the manufactures website.

I started on the NuvaRing in April of this year, so this is my 4th month on it. The first month was great! I loved that I didn't have to think about it daily and my libido was through the roof! The only side effects: I noticed immediately that it increased my discharge, which was a little uncomfortable on a day-to-day basis but was very nice for making love. The discharge was also a whitish color, which threw me off because I'm used to it being clear but my doctor assured me that all was normal. Also, it would occasionally fall out during more passionate sex, which wasn't a big deal. I just washed it off with cold water and reinserted it. The second month, things seemed great until the last half of the month. I noticed that there wasn't as much discharge and I would get a slight burning sensation after sex. About a week later, I came down with a full blown yeast infection. I hadn't had a yeast infection in 10 years! I treated it with an OTC 3 day suppository, which seemed to help it a little. I removed the NuvaRing like normal and a few days later I started my period. Things seemed to go back to normal and a week went by without much problem. The middle of the 3rd month I was slammed full force with yet another (or the same) yeast infection, plus bacterial vaginosis as well. I asked the doctor about the NuvaRing and it possibly causing/aiding yeast infections. She assured me that it wasn't possible for the ring to cause infection. She gave me instructions on how to properly rinse it off in case it ever fell out again. She prescribed me 2 doses of Diflucan for the yeast and an antibiotic for the BV. I took both and afterward things seemed fine for another 2 weeks. This week, I noticed that I had a weird itchy feeling down there before bed and sure enough when I woke up in the morning it appeared I had another yeast infection. I called to make an appointment but the nurse just called back and prescribed me 2 more Diflucan pills and told me to give one to my partner. I asked again about the NuvaRing perhaps being an aid in the appearance of these infections and again she told me that it wasn't possible. At this point I am really confused. I don't know if I have a really bad yeast infection due to the ring or if my boyfriend and I are simply reinfecting each other. I also asked about whether I should discard this NuvaRing and start a new one after the infection clears up and got a very vague response of "it's your call". I really don't know whether to can the NuvaRing or keep going a little longer to see if this is all a big coincidence. I just think there isn't enough known about the NuvaRing...by my physician anyway. More side effects to note in the fourth month: weight gain, loss of sexual desire, vaginal dryness (the discharge was short-lived), irritability, crying fits. I'm just at a loss...I really wanted this to work for me...

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.

After taking a 500mg Niaspan last night 1/2 hour after taking it I had this reaction: Hot flush in my upper body, face,neck and arms.
Happened out of the blue. got scared.
Went to the bathroom and washed my face with cold water.
Came over to the iMac (computer) Googled Niaspan allergic reactions, found this site and was mentally relieved to note that this was a common side effect of this drug.
Consumed 10 oz of water calmed down and fell better within 6 or 7 minutes.
While some people curse the amount of info on the net I am not one of them.
I am really glad that people share info like I am doing.
I suggest though if any of the side effects are worse then mine yo go to the ER and if you cant hit 911.

I am so relieved to hear that I am not alone!! I was outside in the sun the other day, slathered with SPF 35, and I felt like my skin was burning off! After I moved inside, my lips, hands and even feet were tingling. The tingling worsened whenever exposed to cold temperatures (ie. cold water, freezer, even refrigerator). It is 3 days later and my lips and hands are still sensitive. I have a dark complexion and rarely burn. I'm glad I can blame the medicine and not a sun allergy!

a few hours after i took levaquin, i went to BK and got a cheeseburger. i had just had a csection and was having a hard time recovering. i thought the pain i was having had something to do with the surgery but i started to realize it was the levaquin. it was like everything i tried to eat kind of got stuck going down. it hurt so badly i just stopped eating. i was so weak and my muscles were so weak. ias so weak that i had to concentrate really hard on my breathing. i didn't realize it was the levaquin until later that night. i started getting giant red spots on my arms and on my forehead. they were on fire and it was miserable... my husband had a bowl of ice cold water and ice packs and rags in the freezer. he was running around like a mad man trying to keep bringing me cold rags. every time he would put them on the red spots, the rags would be hot within seconds. my mom thought i should just jump into the cold shower but i had to explain to her that i was also freezing at the same time. finally my mom did some research and found out that this happens so the doctor said to take benadryl for a few days until the medicine wears off. i will never take that crap again... it was such a weird and terrible experience.

I took Levaquin for about two weeks, I started out with 500mg.. and went down to 250mg once a day. I had MRSA and that has healed up nicely.. but I developed the rashes.. on the backs of my hands and arms for some relief I put peroxide on then rinse with cold water, and pat dry then I put Calamine lotion on which is used for rashes, poison ivy and such.. the pink stuff.. It helps a lot with the itching and the pain from itching it. The rash on the back of my hands is almost gone now, I have been putting the calamine on my arms. The rash on the back of my hands ive had for about 2 weeks.. try the peroxide and the calamine lotion.. it really helps to relieve the itching.

I was prescribed 750 mg. for 3 days of Levaquin for a UTI by a doctor (not my regular) I did notice the slight dizziness but wasn't too concerned. I also had some insomnia but didn't connect it to Levaquin. Then in the a.m. after 21 hours of taking the first dose, I had elevated heart rate and blood pressure along with nervousness. Scary! I've taken 250 mg of Levaquin for sinus infection previously (3 days) and never had any side effects. I even asked for this prescription...can you believe that. It's New Years Day so I can't even contact my regular doctor but I am stopping Levaquin and requesting to not ever prescribe this drug to me again!!!!!

Attention!
I used Lupron protocol for IVF the last year 07. I began to have side effects a couple of weeks after I finish it. I had hot flashes, headache, insomnia and gain weight. However, on October 07 I began with burning sensation in both legs, which do not allow me to sleep or rest during the night or day. I went with 2 neurologists and I had a lot of blood tests done, also 2 nerve conduction study, 3 MRI… and until now November 08, No diagnosis. The burning sensation in my legs is not a joke! I need to try to keep my legs cool or my life is miserable, even in the winter my legs and feet are hot. I soak my feet almost every night in bucket of cold water and ice because they are practically burning. This year on November 08 I received again lupron as microdosis lupron protocol. Immediately, I begin to have the hot flashes 5 or 6 days after start it. The last year was after few weeks to finish the protocol. Also, the burning sensation in my legs is worst this second time. For a couple of weeks before use the Lupron again, the sensation in my legs was very light. Actually I cannot sleep at night and normally I wake up during the night because my legs feel on fire. Please if someone knows more about it, write in this blog. We need to figure out what is going on.

I started Adoxa (generic form of Doxy) about 2 weeks ago for a cyst. About 5 days after taking the med, I was swimming and my hands had the weirdest sensation... After I got out of the pool, my feet were on fire as were my hands. Thought I just had gotten sunburn, though I don't normally burn. A couple days later, I had a severe tingling/burning in my fingers and toes. Couldn't sleep because of the pain. This lasted 2 night and I stopped taking the Adoxa. Went to Urgent Care because the burning was not subsiding and and my toes and fingers were EXTREMELY sensitive. I couldn't even open a pop can. Dr. said I had Periphrial Neuropathy and it is not a side effect of the Adoxa that I was taking. Told me I had symptoms to a bigger problem. I have been off Adoxa now for 4 days and the tingling/burning/sensitivity has all gone away! I know that it is the Adoxa and will not ever take it again!!! Remember to trust your instincts when you take medications!!!!

I was wondering if any of you are experiencing tingling in your hands and feet, which increases during sleep. I have been on this medication for two months and have just started noticing this sensation.