Blisters symptoms and conditions

I took cipro 500 mg just this past thurs Sept 25/2008 only 3 pills. One thurs lunchtime, one that evening and then another fri lunchtime. By Friday morning I was starting to experience a sore throat and flu like pains.When it came to that evening my throat had red really red blisters and swollen glands. I didn't take that pill friday night. I stayed up all that night and at 4 am realized my sore throat and swelling had subsided. I called my pharmacy Sat. morning and told them what I had experienced. They said I did the right thing. I then had to contact my doctor to get another RX for my kidney infection. I have since had pain that hasn't went away. I have had a ultrasound on sept 9 and bloodwork on Oct 1 and a CT scan. All tests were ok. I was told just now on the phone to finish the new antibiotic and then 48 hrs later get another urine culture. I had to be given pain relief patches from the doctor.

I have been put through the wringer with Crohn's. 15 surgeries, all of my terminal ileum removed, 1/3 of my large bowel removed, etc., etc,- Those with sever Crohn's know.

I spent years on high doses of Prednisone, Imuran, Sulfasizine and other drugs and nothing worked.

I was even retired from the US Air Force due to its severity.

Remicade has help tremendously. However, some of the side effects listed above, I have also been through. Some of them, have been explained through other factors and those attributed to the Remicade I take other meds to offset them.

For example, Head aches. I figured the head aches were from allergies that I have had for some time. I attributed some of the headaches to the Remicade. The head aches are very sever after my infusions and decrease to a dull roar after that. I take four aspirin and Sudifed PE and this leaves me with a dull roar shortly after the infusions and does away with them till the next infusion - perhaps this will help some of you.

The muscle soreness is horrible and I take aspirin or Tylenol, but that barely takes the edge off.

I started get those little red dots. Then the dots turn to blisters. I get these on my hands, feet and scalp. My GI Doctor said it wasn't the Remicade, but a Dermatologist showed me a recent article that should Remicade could cause Psoriasis. I take Clobetasol Propionate for these and it has cleared them up.

I took the Remicade years ago and then it was stopped - it was the way it was done then - not constant, just three doses spread out over three months.

I got the tingling fingers during those. A neurologist attributed it to the Steroids I had been on. The nerve damage is permanent.

A few years later, they started the infusions again and I experienced no muscle soreness, headaches, etc. and it did not help the Crohn's as it had before. When I talked to my GI doctor he showed me a study that people build anti-bodies to the Remicade over time. They doubled the dose and it started working again. For those who are experiencing the Remicade not working - perhaps this is what has happened to you.

I get the mood swings, but had never considered it might be the Remicade. I will talk to my doctor about this one.

I have the blood pressure decrease during my infusions, but it has not been sever.

More recently, my joints have begun to ache and initially the Remicade had helped to stop the minor joint pains I already had. Come to find out, I have had bone thinning due to the Crohn's.

The one symptom I have started getting this week is random, sever pain in odd locations - not joints.. They have been deep and feel like they are in the bone. One midway up on my shine, one midway down on my foreman and one in my right thumb. Has anyone experienced this. The pain has been horrible and it does scare me.

I also suffer from depression, but have had it for years prior to the Remicade treatments.

i'm a fourteen year old girl, who has been completely healthy my entire life. about a week or two after i got the gardisil shot, i went on vacation in the outer banks. when i returned i started experiencing severe abdominal pain, feeling nauseated, fatigued, having muscle pains and confusion. i went to my family doctor, who diagnosed me with the flu and gave me antibiotics. days later, i wasn't getting any better so my mom took me to the emergency room where i was put on an iv for dehydration. i was sent home with medicine for the abdominal pain, which gave me no relief. i returned to the emergency room several days later due to the same issues, and was put on an iv for dehydration again. they took blood to test for a bunch of different things, but everything came back normal. i was sent home again, and over the next month i was referred to a gastroenterologist, where i had a CT scan of my stomach, an upper gi/barrium swallow, an upper endoscopy with biopsies, a MRI of my brain, and tests done on my liver and gall bladder, all of which came back normal. i was admitted to the hospital on august 20th, the day i was supposed to start high school. i was put on an iv again, and had liquids dripping in me for about 12 hours. my gastroenterologist seemed to think i was bringing everything on myself and might have a minor case of IBS. the doctor made me talk to a psych, who basically told me i must be stressed and had to be bringing it on myself. the doctor sent me home, telling my parents to force me to go to school. i cried the whole way home from the hospital, no one was even trying to make me feel better, and i hated the doctors for thinking i could bring something like this on myself. i started my first week of high school later than everyone else, i felt completely exhausted and threw up in the bathroom between classes. a day at school takes everything out of me, and i have to spend the next day in bed. my mom and i just saw all these side effects of the gardisil shot and are convinced that's what caused all this. i couldn't try out for the volleyball team, i've lost 14 pounds, i might have to re-do my freshman year because i'm missing so much, i can't hang out with my friends, i can't even go to homecoming and im honestly depressed because of all. this has ruined everything for me. don't let anyone tell you it's all in your head, its not, this is real and its effecting a lot of girls. please think twice before getting the gardisil shot

I was taking Doxy. Hyclate for 3 days prior to a breakout of an allergic reaction. Initially, the small bumps resembled flea bites or could even be mistaken for pimples; however, they later manifested into blisters onto my legs and arms. As with other (skin) allergic reactions, the bumps were red and itchy. I immediately notified my physician and began using hydrocortisone cream and benadryl to minimize the discomfort.

My 1 year old son got into my box of chocolate Ex-Lax and ate about 3 or 4 pieces. Called Poison Control and they didn't have any suggestions except to keep him hydrated. I put him to bed that night, he was still in a diaper, and he had a bowel movement during the night. In the morning his butt had huge blisters where his stool had laid. The senna in the Ex-Lax caused severe chemical burns. He had to be admitted to the burn center at Akron Children's hospital. Most people aren't aware of how dangerous this product is because adults wipe after using the bathroom, but imagine what this chemical in Ex-Lax is doing to the inside of your stomach, intestines, and colon. I would like to make people aware of the seriousness of this drug, especially parents whose kids, like mine, will eat anything chocolate. I always assumed Ex-Lax was so safe, as they even claim on their box and that it would just cause you to use the bathroom without harm(as obviously even the Poison Control Center doesn't know the dangers), but Ex-Lax is very dangerous!

In 1999, Ex-Lax company changed the main ingredient to senna because the old main ingredient caused cancer. Ex-Lax and other senna-containing product companies don't want people to know about this. It's not even labeled on their box or website! They definitely know about it because I have called the Novartis Company and they have also had many other similar incidences. Please pass on.

V. Donaldson

I'm an adult female with severe sinus polyps, adult onset asthma and allergies. Initially Singular seemed to be helping my nasal polyps, when nothing else helped in any way. I made several attempts to use Singular, and proved repeatedly that this medication did, in fact, cause me severe side effects - even when I used a childs dosage. While using an adult rx for Singular, I immediately began experiencing horrific nightmares (which I have never had in my entire life). I also had extreme knife like pains in both ears, which made me feel like I had a severe ear infection, chest pains where it felt like a cinder block was lying on my chest, and migraine like headaches (which I've never had). I stopped the medication after about a week and the nightmares went completely away, but it took me a couple weeks to recover completely because I developed what felt like a respiratory infection and ear infection as soon as I stopped using it. Because Singular seemed to slightly reduce my nasal polyps on my first attempt, my allergist suggested I try using it again - almost a year later. When I first began, I completely forgot about the negative side effect and why I stopped using it in the first place, and just gave it another try. I again experienced the same horrific nightmares, ear pains, but this time got a strange rash/cluster of blisters under both eyelids which my eye doctor confirmed was an allergic reaction to something I was using. Singular was the only medication I had changed. My allergist thought I should give it longer to see if the symptoms went away (because they probably weren't caused by this medication - and were due to something else ???). Fearing going to sleep, I decided to try taking the medication in the morning instead of night, and had my physician reduce my rx to a childs dosage (5mg). The nightmares lessened, and the blisters under my eyelids went down, so I continued using Singular for about a years time. What I didn't realize, was that over this time I was becoming depressed, fatigued, and became easily agitated and short-tempered, which was very different since I was normally a very happy, energetic mom. My nasal breathing seemed to be slightly improved, so I just kept taking the medication - not realizing that it was causing all of the other problems I was experiencing. I became so fatigued and depressed feeling, that all I wanted to do after I got my kids off to school was to sleep until it was time to pick them up in the afternoon. I was also experiencing stomach pains for unknown reasons. I was certainly not myself. I didn't realize that while I was using Singular I had lost complete interest in everything that I normally loved in my life. And please note I'm 45 years old, and I was using a childs dosage. ( I can only imagine what this medication does to a child. )Fortunately for me, I accidentally forgot to refill my prescription for a few days and noticed that my depression started to improve. I decided not to refill my rx and stay off it to see if I continued to improve - and I have. Unfortunately, even though my depression has all but gone away, I'm experiencing symptoms which must be from withdrawal of the medication - and they are just as scary as the side effects were. Now that I'm not taking Singulair any more (and I've made no other medication changes), I have extreme fatigue beyond belief, and ache everywhere. My muscles are in such pain that I'm having difficulty doing things I would normally do. I have extreme weakness in both arms and legs, and my back aches almost constantly. And strangly enough, my asthma and allergies have slightly improved since stopping Singular - I thought for sure my allergies/asthma would worsen when I stopped completely - but they did not. All I can say is - please trust what your body is telling you - even if your physician tells you otherwise, and do not use this medication or any other if you experience adverse side effects to it. I would never give this medication to a child that wasn't old enough to tell me what he/she was experiencing, and would document the childs temperament, ailments if any, and what changed once the medication was started - and discontinue it immediately if even one adverse side effects occurred. One last note - I am still experiencing vision problems, which I feel are due to using this medication. Hopefully, no other permanent damage to my body will result from the Singular that I've already used - and I hope you Singular users will recover completely too from its dangerous side effects. Wishing you the best of health!

Ear busing, pain and swelling on my left ear down and a golf ball un my throat, short pin pain on my kidneys and legs first noticed swelling of my lower lip with small blisters after one pill SMZ/TMP DS 800 –160 TAB QUAL
biolence, headache,

I had some really odd-ball side effects from Lyrica. I was on 150mg twice a day for fibromyalgia, and it seemed to work initially. I was feeling pretty good, and thought I, too, had found an answer to my aches and pains. After about two months, I noticed that my hair was falling out and turning gray (I was 39 at the time). I hadn't had a menstral period that second month, either. I told every doctor I saw about these strange symptoms, but was prompty ignored.

The third month, I began to gain weight like crazy. I ended up gaining a little over 20lbs during the year-long treatment. My skin was dry and thickening around my thumbs and heels. My energy level began to really go down (it was never that high to begin with). My fingernails became brittle and broke with the slightest provocation. The grayer and falling out hair was coarser, too. I also was either sleeping all the time for days, or then couldn't sleep at all for days.

By the sixth month, I noticed that my wounds were also taking longer to heal. Being diabetic for the last 29 years, I thought that maybe neuropathy was starting to set in. Up to that point, I had never had any signs of neuropathy, and always was in good control of my blood sugar levels. Now, I was beginning to get worried.

The eighth month forward brought cracked heels, cracked toes, cracked fingers and thumbs. I began to have pitting edema, which I immediately informed my Rheumatologist about. I have chronic renal insufficiency, though not diabetic related. It was a gift from my OB/GYN during pregnancy when I became eclamptic. The edema was so bad that blisters appeared on my ankles and would not go away, no matter how high up I rested with my legs. My skin hurt all around my legs, and soon started to notice my face also swelling. Still, no comments from any of my numerous doctors.

After a year of all this strange stuff, I took myself off of the Lyrica. It was a hard choice, as the meds helped to silence the strangling pain in my muscles. Within a month after discontinuing the drug, my period came back. Three months later I noticed that both my hair and nails were stronger, and my hair wasn't falling out as much.

Six months later, and I notice now that my wounds heal like they used to. My hair isn't as coarse, and my nails are much stronger. My sleep schedule is still not right, and I still have the deep cracks and crevices to my thumbs and heels, but it is much better than it had been. I have also since tried Lamictal, but am having tachycardia and shortness of breath, along with a marked rise in my blood pressure. This, too, I discontinued and am feeling somewhat better. The muscle aches and pains and fatigue are back with a vengeance, but I will put up with them as long as I can. I am on so many meds anyway, that my body is probably kissing my toes in thanks!

Luck to all who are on this drug, and hope it works for you without all the weird side effects I put up with!

I had my parotid glands washed out with saline and because they were still dirty the surgeon decided to swab them with Betadine. When I came around from the operation I was panicking in the recovery room. Later, I was put into a side ward, luckily with my sister in attendance, and took a minute sip of water. This caused me to choke and I could not catch my breath. Assistance was sought and I was taken away to get help with my breathing. My whole face swelled up and my eyes had huge sort of blisters under them, which affected my sight for about 3 days; my hearing was also affected temporarily. The sides of my face, where the parotid glands are, were absolutely solid, my lips were distorted and I looked like I had been in a fight. My vocal cords were also swollen, which resulted in very poor speech for 24/36 hours. I had to be put on continuous oxygen, and have frequent nebulisers. I was given steroids, antihistamines, antibiotics and other treatments which I am not sure of. What should have been a 45 minute operation and 2-3 hour recovery resulted in a week's stay in hospital. When I was discharged, I had to return the following day, as the swelling had come back up again and I had to have the steroid medication I was sent home with doubled and Piriton and Omeprazole prescribed as well. I had intense pain at the top of my head, over my left ear, at various times during the week, resulting in me having to take Oramorph. All of these effects caused my diabetes to go out of control, with my blood sugars running over 20 for the first 2 days and well over 10 for the rest of the week. All in all I was very unwell.

I had my mirena fitted April 08, and four days ago I had it removed... What a relief! A week after it was fitted, i went to a gyn because of the cramps and they scanned my uterus. Everything was in perfect order. But the cramps didn't stop and I was bleeding more or less all the time. Sometimes I could feel it when having sex, and my boyfriend did too. I also had that PMS feeling for about three weeks before having my period, getting irritating and moody. Before period I got acne and blisters in my mouth (never had any of it before!). I had to convince the doctor to take it out, she said it was such a good birth control.

Now I am feeling happier with no mirena in my body. But I am bleeding quite heavily. I can't find any information about what happens to your body when mirena is removed?

Hello all,
I'm in the same boat but near the end.... I was given Bactrim for a UTI. I woke up after 2 days with horrible aches in my joints and muscles. I was immediately taken off the Bactrim and put on Doxycycline. I was then put on Prednisone for the aches (which helped). I developed blisters and a rash after a few days. My aches went away after about two weeks but now I have itchy, sore and peeling feet, buttocks, mouth, and genitals. Stomach upset as well. I have been tested for everything (STDs, Lyme Disease, West Nile, etc, etc) and everything has come back negative. I was diagnosed with Stevens-Johnson Syndrome from the allergic reaction I had to the Bactrim. It has been 3 weeks since the first dose and I am finally starting to feel better (except for the insane itching). Good luck to everyone. Never again!

I was diagnosed in April 2006 with congestive heart failure and End Stage renal Failure. Out of the blue! One month before I was diagnosed I began bruising severely, and just not feeling well overall. I have maintained uncontrollable hypertension for about 3-4 years now.

I have been on at least 15-20 different medications, not all at the same time, but in different combination. I have adverse reactions to everyone I have been on in some form or fashion. ie rashes,, sometimes in the form of blisters from my hands up to my elbows, severe deep itching, headache, nausea, vomiting or they simply do not work. The only medication that I have been on for the entire time without stopping, only changing the dosage is Clonidine.

I am very sensitive to a lot of chemical drugs, even the chemical form of folic acid!

I recently had a biopsy done on my kidney. I came back positive to chronic and acute inflammation, causing scarring of the kidney. Therefor causing my kidneys to shut down to about 7% activity. There is still some active inflammation. Could this be from the clonidine? Since it is the only thing that has been a constant for the past 4 years?

It has certainly raised a question in my mind.

I tried Neutrogena Energy Renewal Day Lotion with Helioplex and broke out in a terrible burning rash all over my face. It has caused hives and small blisters. It itches and has dried my skin in some places so that it is peeling off. It has been like this for nearly 5 days.

This needs to be taken off the market.

I have been on Lamictal for a few months and I started out on 50 mg and went up two 100 mg within two weeks time - Everything was fine until I went off of it for 5 weeks and then back on it pretty suddenly. Ever since then I have had chronic nausea (constant feeling of car sickness). There are times when I wake up with it in the morning and go to sleep with it at night. Nothing will help except fountain coke (I don't know why, but it works) but the pain always winds up coming back within a few hours.

I ALSO HAVE BEEN EXPERIENCE THE FOLLOWING AS WELL

• Memory Loss ***
• Messing Up Words + Speech Comes Out Backwards ***
• Loosening of Teeth
• Sores and Blisters on Inside of Mouth
• Soreness and Heaviness in the Legs + Occasional Muscle Aches
• Headaches (Not so much anymore)
• Heart Racing + Mind Racing
• Trouble Writing + Spelling ***

I am 31 yrs. old and this is month 4 on the NuvaRing. I have been on several different types of BC over the years the side effects had been so severe I decided to give up on BC all together. When my doctor recommended NuvaRing I was leary, but I tried it anyway and was quite pleased until recently. I am not experiencing head aches, nausea, or irregular periods, but I am experiencing problems with my moods. Most of the time I am sad or I get agitated very quickly for no reason. I was shocked to read about some of you experiencing loss of energy. I thought I was going crazy. I don't seem to have any energy...I am tired all the time. I have been taking vitamins, but they don't seem to be boosting my energy any. I have gained weight in my stomach and seem to be gasy and bloated. My jeans are so tight...It is depressing! In a matter of 2 weeks my breasts have grown in size...I am sure I have gone from a 36 C to a D! What I am most concerned about is the blisters that appeared about 2 1/2 weeks ago on the exterior of my vagina. They are very painful and over the counter creams are not working. I am not sure if this is due to the NuvaRing. I have my anual checkup with my OBGYNE tomorrow. I plan on getting all of my questions and concerns addressed. My delima is do I stay on NuvaRing...I like that I don't have to worry about popping any pills and I don't get any major side effects. What should I do?

I'm taking Doxycycline 100mg 5x/day. Started a little over 2 weeks ago for Chronic Lyme. I have a 4 month course to complete.
In the past 14 years after that tick got me I was the living dead, those with Chronic Lyme know what I mean. I have virtually the same side effects as everyone else here and wonder if it even matters how much you take a day. A lot of you have the same doses (100mg 2x/day) and the same degree of side effects as I do. My side effects are headaches or a pain in my right temple whenever I cough, severe itching EVERYWHERE, blisters on my hands from itching, burns on my skin wherever the sun shines on me (I live in Florida), vomiting daily some days worse than others, mood swings, crying for nothing, nausea almost constantly, gassy (both ends), I have a bladder infection that started 2 days ago that after reading this can be attributed to the Doxy, asthma symptoms are getting out of hand, I also have this odd swelling/pain over my liver/gall bladder area that's been coming and going, ears ring, noise bothers me and actually starts a headache, diarrhea the first week and constipation the second week, skin feels tight and there's noticeable swelling all over.

With that said I want to say that yes this is not one of the more pleasant drugs to be on however in my case if I don't get these bugs out of me I am going to die so would rather deal with side effects knowing these bugs are being killed and I will be off them someday unlike the Lyme I will have for eternity. Lyme people and other chronically ill people on these meds say this is called "herxing" and this comes and goes also. You feel really bad and then you feel good, then bad and then good again and so on. I started out on this drug keeping in mind that any sikness/side effect was telling me those bugs are dying so in a sense I almost welcome them.

Good luck everyone:)

My daughter 8 has been on Advair 3 years for asthma. Prior to, she was always a happy little girl, fit and healthy.

Some of the new things I noticed as the months progressed were severe mood swings, weight gain, and unexplained reoccurring rash on her feet,legs and thighs. They appeared like Mosquito bites and turned into blisters, not the pediatrician or even an Dermatologist could diagnose it, yet it would appear almost monthly. She has complained of "bubbles" in her eyesight, she developed this squinting, we had her eyes checked several times by eye doctors but told there was nothing wrong.
She has also experienced blackouts, after extensive tests a Neurologist concluded that she had Aura (sp?) migraines and referred to her squinting as a tick.
I feel like I have lost 3 years of my child's life that I cannot get back. She finally has been weaned off it. It has been only a few days with no Advair. I hope for no lasting adverse affects.
My 5 year old daughter has just been diagnosed with asthma and I noticed he is no longer prescribing Advair for children, I would refuse it, if he did.
Veronica, CT

Good god. I had some long-named-not-quite-acne thing growing on my face around my nose and mouth and the cream prescribed didn't help so I got Doxy. Today, after having taken it for almost a month, I had the last-straw symptom appear. Blisters on my hands. I spent some time in the sun, with sun screen over what little wasn't covered but I guess the sun screen washed off my hands and where they were exposed is now blistering like I someone threw scalding water on me.

Other symptoms: At first I was nauseous and learned to take food first, then I had the burning hands, feet and face, and now this. I'm done. I'll let you know what horrible things I go through now that I'm going off.

MARCH 17TH MY MOTHER WAS A VERY HEALTHY ACTIVE FUN LOVING PERSON AS OF TODAY SHE IS TOTALLY CONFINED TO THE BED. SHE TOOK 4 PILLS OF LEVAQUIN FOR A MINOR CHEST COLD AND GOT A VERY BURNING RASH AND BLISTERS ON HER ARMS NECK AND CHEST AFTER THAT THE SORE THROAT AND EXTREME MUSCLE FATIGUE KICKED IN .HER DR. PUT HER OFF SHE WAS SMART ENOUGH TO QUIT TAKING THE DRUG ON HER OWN ON APRIL 8 SHE WAS HOSPITALIZED WITH THE ABOVE SYMPTOMS WHICH HAVE ULTIMATELY MADE HER UNABLE TO USE HER MUSCLE SHE CAN NOT SWALLOW HAD TO HAVE A PEG TUBE PUT IN SHE HAS NOW BEEN WEENED OFF OF THE 120 MG OF PREDNISONE SHE HAS BEEN ON AND NO END IN SIGHT ON RECOVERY. I HAVE NO MEANS TO TACKLE A DRUG COMPANY BUT I WILL TELL MY STORY AS OFTEN AND AS I CAN. 50 DAYS LATER WE ARE STILL TRYING TO GRASP ALL OF THIS

I have been on 200mg per day for 7 months! Seems too long for anyone to be on an antibiotic, since antibiotics can deteriorate your gut and colon. However, I suffer from pemphigus vulgaris, which is an autoimmune blister disease, whereby the body no longer recognizes the skin as part of self and attacks it as an invader. The doxy will make me severely nauseous without food. I have experienced the burning from the inside out, tingling and new blisters from the sun because of the doxy. It has been a long run, I imagine the anxious, depressed emotions could be from the doxy, however I am unsure. Always feeling tired has been quite common. I tried to stop, especially if I were going to be in the sun, but the consequences were severe with new sores appearing from my pemphigus. So in my case apparently the benefit outweighs the risk, for now. I have noticed in my 6 month that my knees and hips are in pain. Is that a side effect of long term use of this medicine? Not that may be worthy of reconsideration, if it is responsible for joint and bone deterioration.

My daughter is 12 and got her first shot on May 23rd, 2008. The next day in the evening her face was severely red with a bad rash all over, looked like blisters and pimples. Since then she is achy, headache and nauseous. So I am assuming that is from the shot, there is no other reason to get such a bad rash.

I received a shot on the 21st of march and was told by my dr that the side effects were minimal and I have now been on my period for 18 days straight called my dr and they said thats not normal call your ob dr. Now that I have found this web site I see that I am not the only one who has had this problem. I have always thought it was a dr responsibility to worn you about side effects like this but I guess NOT. And to top it all off the shot didn't even work for me I am stili in alot of pain in my back. THIS SUCKS

I was on Lamictal for 4 years and after the first year I suddenly started having all kinds of teeth and gum problems for no discernible reason. But since Lamictal has the possible side effect of "sores or blisters on the inside of the mouth" I wondered if it could be related.

I did a Google search and am coming up with no experts yet, but lots and lots of posts connecting anticonvulsant meds, particularly Lamictal, Topamax, Neurontin, and Depakote, with dental problems. Dilantin is well known for causing gum disease and breaking down tooth enamel, loosening of teeth, and even breaking down of jawbone tissue.

I don't think the experts have connected the dots yet, but is anyone else having this problem?

I was put on this medicine for a bladder infection ,(*whicn by the way was really a yeast infection I learned later ) after 3 days of taking it , the whole side of each cheek and roof of my mouth ,plus just behind the tongue ,and on the tongue sides , broke out in the worst blisters I have ever experienced in my whole 80 yrs , also the vagina area was blistered too, I stopped the meds 3 days of taking it and called my doctor she put me on a yeast infection med that cleared up the bladder infection right away ..the mouth completely peeled off every blister but remains very sore and hard for me to eat ..this sulfameth drug needs to be removed from the market or stronger side effects need to be listed aslo as a more of a warning in big letters ...!!!!

I have been on Topamax for 4 months and so far the migraines I have suffered for 40 years are gone. Great Some side effects like can't stand carbonated drinks. Reaction time is a little slower. I stress out a little more then I used to. I get really tired at the end of the day. I used to be a night owl but now love my sleep. Question to you all. Any one had problems with their teeth? Such as pain, fillings falling out? Let me know.