Mild case symptoms and conditions

I'm a male in my mid 50's. I started Zyrtec and Nasacort on the recommendation of my MD to deal with itchy, red eyes and other general allergy. Most other meds hadn't worked. These did and stopped the symptoms cold. However, I started noticing that I'd pretty much lost any desire to exercise and that I felt very lethargic in the mornings. I decided to drop the Zyrtec. The first day off, I had a mild case of hives. The second and third day I've had itching. I figured it had to something to do with Zyrtec so I started searching the internet and found this site. I don't plan on going back on Zyrtec unless I have a serious allergy flare-up. Even then, I may consider shots instead of meds.

I have been taking Topamax for atypical trigeminal neuralgia for about five weeks - starting at 25mg and working my way up to 100mg each night. The first three or four days I was a bit headache, nothing unbearable but just kind of uncomfortable.

Right from the beginning I had this great side effect that I haven't read anyone else here mention - this feeling of clarity in my head, as though I've always had noisy background static that was now suddenly switched off. I just love it! I was not even aware of this noisy static that had apparently been going on in my head all my life until it had been switched off! And now I feel this wonderful sense of peace and calm. So I have no idea what that is all about, but I'm not complaining. I do remember once reading about generalized anxiety disorder and wondering if I perhaps suffered from a mild case of that (not a very severe case of it), if that is the case, that could perhaps explain the static-y background noise in my head - that is now thankfully gone after taking Topamax. So, I can happily say that I have a pleasant side effect from this drug (sounds like I'm one of the few from reading this forum!)

I'm not sure if it's a related side effect, but I feel more calm and more peaceful. Like it takes a lot to upset me. It's kind of funny, I'm watching my husband get all cranky and fired up about something and I'm just watching him and waiting for him to calm down, whereas once before I would have got hooked and gotten all cranky and fired up myself. Now I just don't get it and I'm thinking to myself "why's he getting so upset about this?" And he's looking at me all quizzically like "why aren't you getting all upset about this?" But it all just kind of slides right off... Interesting because some of the other posters are saying quite the opposite about feeling aggressive on Topamax...

Another really good side effect for me is being able to sleep really well at night, something I've never been able to do (I've always been a really erratic/light sleeper), I don't remember ever sleeping this soundly. I swear I now sleep with a big smile on my face : ) I'm just so happy to be sleeping soundly! And I actually think I might now be less sleepy during the day than before (so unlike other posters) which is likely to be because I'm sleeping better at night. Although if I'm having a lazy day at home, it is very easy to have a big daytime nap (but that’s not really that new for me!), and I definitely get very tired at bedtime, but otherwise my energy levels are quite okay, probably more than before Topamax, rather than less.

I'm still not sure yet if the frequency of my atypical trigeminal neuralgia is less as I usually only get it about once every ten - fourteen days. I think it has been less frequent but I will need to be on it a little bit longer to know if it's working for sure.

I had a scary experience one day after I'd been taking it for about a week or two where it felt like a water balloon had been popped in the back of my head and the water was running down the back of my head and neck. It was the creepiest experience and one that I didn't immediately attribute to the Topamax but after reading some of these posts made me think that maybe it was?

The tingling in my feet has been pretty bad, not just your regular pins and needles but really very uncomfortable/almost painful. Yesterday was the first day I didn't have it, I'm not sure if it was because I've been drinking more milk (I read that calcium could help) or taking potassium supplements. I'm also being mindful not to cross my legs or sit on my feet as I usually do. I've also been very constipated so I'm making sure I'm eating a lot of All Bran every day.

My biggest concern has been the cognitive side effects because I'm due to start my doctoral degree in a few months and need to be extra sharp. I have definitely not been feeling sharp! Again, yesterday was probably about the first day I started to feel a bit better with that side effect too. I've been taking folic acid supplements but I also took the advice of one of the other people who posted here who suggested taking the Topamax with food, so I take it with my dinner and maybe that's what's helping? I'm not sure, but I don't feel quite so dumb! One of the things I felt most ditzy with was time perception, I don't know whether other people experienced this also? Whether it was being aware of the day or the month I just couldn't work it out...

I'm also less hungry - loving that. Weight loss is very slow though (but all weight loss is good), maybe 2kg (4.5lb) in 5 weeks. I was on holiday for 3 of those weeks in my favorite food eating destination surrounded by all my favorite foods and I was pretty much uninterested - now that's a first. Normally I come back from this trip with an extra 5kg! If I wanted to I could still eat, but it definitely makes it easier to abstain, so I know I won’t have to worry about getting dangerously thin as some other posters have written about.

My side effects have definitely changed over time, I'll get something for a few days and then it will go. So I'm hoping that I'll continue to get the good ones and that the bad ones will go. Overall, I'm very satisfied so far with Topamax and seem to be tolerating it quite well, so fingers crossed that it continues to go well. Perhaps different people simply tolerate different medications differently. But from all the reading I've done on Topamax, here's a few tips I've picked up which seem to be helping me: I take it only at night (to help combat daytime tiredness), I supplement with a multivitamin, folic acid, potassium and make sure I'm getting enough calcium, I take my Topamax with dinner, I drink a lot of water, plus I don't take any other meds. I hope these may help some other people reading this and I wish you all the best of luck with your migraines/trigeminal neuralgia/epilepsy or whatever other nasty ailment has you taking Topamax. I’d also love to receive your replies to hear if any of you have experienced any of the same side effects as me.

I stumbled on this site while doing research on DVT's. I am a nurse and was on YAZ continuously (skipping the inactive pills and going straight to a new pack) to control my migraines for about a year. I developed 3 DVT's in my left calf and behind my left knee. I have been having charlie horse cramps as well. I am now on lovenox injections 2 times a day and 7.5 mg. of coumadin to deal with the clots.I have also had the issues with heart palpitations, chest tightness, and feeling like i can't catch my breath. I read in one of the posts where it was described as she "had to think to catch her breath". I totally agree! I thought this drug was great, until now. I stopped it last wed 1/7/09 when they found the clots in my calf/knee. Can anyone with experience tell me how long it took them to recover from the palpitations and breathing issues. I am a very health person, non smoker, with no prior or family history of any clotting issues. Thanks for all the info on here and God Bless everyone who has suffered!

I had a mild case of laryngophrayngeal reflux (reflux into the larynx) with no heartburn. My PCP prescribed 20 mg Omeprazole to be taken once a day. I experienced terrible muscle numbness, nausea, gas, burping, fatigue, lightheadness, anxiety and depression. I stopped after 6 days. The symptoms continued. After another 6 days, I had a panic attack and went to the ER. It has been over 20 days since I stopped this awful medication. I still cannot eat normally. I now experience heartburn after almost every meal. I still feel light headed and disconnected with the world. I tracked down the manufacturer of the Omeprazole that I took by asking my pharmacist. The manufacturer's rep wrote up a side effects report for the FDA with my consent. I urge everyone to do the same. You can also contact the FDA directly. This is the only way that we can force the FDA and the drug industry to retest the safety of this drug. Best wishes to all.

My husband was recently prescribed Bactrim from his family doctor for a case of the ful. We thought it strange, since flu is normally not treated with antibiotics, viral we thought. Anyway, we felt Doc knew best, so he took three doses. His original symptoms of the flue were simply nausea, vomiting and a bit of diarrhea. After taking the bactrim, he developed a very high fever, headache, pain in legs and feet, burning eyes, chills so severe his whole body shook with a vengeance. He was sent home from the ER and told this was "worsening flu symptoms" and to continue the medication. We didn't follow the advise, and thought it might be the bactrim. He still continued to get worse, and went back to ER next night, bad stomach pain and all other symptoms worse. We found out it was all due to the bactrim, which shouldn't have been given in the first place for a mild case of the flu. He also suffered decreased kidney function, which has taken some time to come back to normal (luckily). His heart rate is still increased after several days, and may remain so permanently, requiring him to take beta blockers for the rest of his life. The doctors won't admit this is from the bactrim, but i have found medical literature stating otherwise. His doctor said it was his fault for not reading or understanding the little insert that came with his medication from the pharmacy. A lot of this information wasn't even on it. There are so many other choices of antibiotics to use, which do not chance a horrible reaction, permanent medical problem, or a fatality, which seems to be the case more often than it should from the medication, bactrim.

I was prescribed Levaquin in July 2008 for a kidney infection - 500 mg for 7 days. I experienced insomnia, muscle cramping in my calfs, and aching a chilies tendon while taking the drug. Approximately 5 days post Levaquin I started having generalized muscle twitching (head to toe) which is intensely noticed at rest, severe anxiety, burning sensation, vibratory sensation, and most recently weakness accompanied w/ pain in my right arm. I have seen 4 separate doctors in 3 months and have had blood work done along with an MRI of my brain. All tests came back normal... I am scheduled for an EEG and EMG this coming week - which too will probably come back normal. Between all of my doctors I have been diagnosed w/ a virus, anxiety disorder, fibromyalgia, and a mild case of Guillain-Bairre Syndrome. Luckily all the doctors have agreed that they do not believe I have MS or ALS. Before the kidney infection I was healthy and RARELY made a visit to the doctors. I have issued a Medwatch Report to the FDA as I am completely convinced that my medical issues are related to Levaquin. I have been dealing with these symptoms now for 3 months and would appreciate any feedback from individuals who have experienced the same side effects and what they may have done to ease the symptoms.

Ok....I just took this pill 100mg this morning with a cup of coffee and sure enough, 25-30 min later....I got dizzy and extremely nauseated!! I even ate a slice of toast to try to calm my stomach, but nope, still felt sick and I chucked it all up!! Now last night around 9:30 and after dinner I took my first pill and felt absolutely fine?? Im still feeling a little weird right now so not sure if Im gonna continue or not??

I was prescribed the 4mg methylprednisolone pack along with 50 mg tramadol for acute tendinitis in my wrist. I took the first 3 days of the prednisone and only 2 doses of the tramadol over the three days. For a total of 60 mg of prednisone.

The first day I had hot flashes and insomnia but attributed it to the tramadol because I had never taken it before and had taken the prednisone several years ago for poison ivy with no adverse reactions. I didn't take the tramadol the second night and then took it again last night along with my daily dose of prednisone. I had extreme difficulty falling asleep, heart burn, hot flashes; and tossed and turned all night trying to fall asleep. At around 2am, I began to have difficulty breathing, tightening in my chest, confusion, and racing thoughts. It felt as though my throat was closing up on me. My anxiety progressed to the point that I was pacing back and forth. I woke my husband up and told him to prepare to take me to the ER. After calling my insurance's 24 hour help line, it was recommended that I go to the ER. I had an x-ray, blood work, urine drug screen, and echocardiogram. Luckily, everything was negative. The ER doctor told me that I likely had a reaction to the prednisone and commented that some people will experience these symptoms when taking it. He stated that he had a similar reaction when he took it and it felt like he was climbing the walls, which is an accurate description of my experience that night. He recommended that I either stop taking it altogether or call my primary care provider and cut it down. He prescribed me xanax and administered some to me at the ER which greatly helped. The next day I stopped taking the pred but am still having dizziness, chest tightness, hot flashes, and mental dullness. I have decided to never take this medication again. Fortunately, I don't have any of the physical sx that some have experienced, and my heart goes out to you. I think the mental symptoms were traumatic enough for me and can't imagine having both as I would be a basket case. I have mood swings, some melancholia, and am very fatigued.

I think it is imperative to research any medication that is prescribed to you before you take it. Many providers will say that side effects are rare, but my experience is that side effects are more common than rare. My prayers go out to those of you who are going through what I am going through. I hope that it clears our systems quickly because this is no way to live. I'd rather put up with the pain of tendinitis or carpel tunnel than to have these symptoms.

My personal experience with Cipro is what they say is a mild case. To me I felt I would die. I've documented everything blow by blow on a new website ****** I was so angry with the medical profession for crippling me, so I took the time and channeled it into the only thing I could. My daily report. 6 weeks and I'm well on the road to recovery. To all of you who say it can't be done, it can. To all of those who say it will recur, perhaps, but I have great faith in the power of natural supplements to heal and support the body in it's repair. If you are suffering and reading this, make sure you visit my site and make your own decisions on what course of action you will take.

The experience has changed me forever, I will no longer have blind faith in the medical profession. We can't fight in the courts, but people have power in numbers. Share your experience, share your pain and help warn others about the toxic substances doctors hand out like candy.

YOU call the shots with YOUR healthcare.

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 am sooo glad I found this site; I have been thinking I am going crazy. For the last six months (since starting NuvaRing for the first time). I have had a mild case of depression (I am not one to struggle with depression , NO sex drive which is unusual for me, my boobs have gone up two sizes, I ma always tired and I am a fairly energetic person. My stomach is always bloated and I can not loose a single pound and I have been doing weight watchers and working out. I have one week left with the ring and I will NEVER use it again!!

I have two children 5yrs. and 10 months. I decided to use Mirena after my August C-Section seemed to result in awful, heavy, long periods with excruciating cramping, which I never had before. I was using the Nuvaring and felt Mirena would be easier, more cost effective over time, and lighten or obliterate my terrible periods. I had Mirena placed a month ago and just went for my check-up today. I haven't had a lot of negative side effects so far. Just light spotting for about 1 1/2 weeks and cramping the first day I got it inserted. The procedure was quick, although NOT AT ALL PAINLESS! I have been serious in trying to lose weight for the past 2 months since I am still carrying around some baby weight. I work out about 5-6 times per week and eat 1200 calories or less per day. I have lost 14 lbs., and until I read these postings, didn't even know Mirena caused weight gain, although I researched the product prior to insertion. Evidently, I should have dug a little deeper! I do however, have a mild case of acne now, that I thought was from sweating constantly at the gym, now I know it could be the Mirena. Furthermore, I came to this site because my husband swears he's getting stabbed & I can feel what he's talking about, its NOT the strings. Does anyone know if it needs to be "tucked" or something? I am going to withhold judgment but remain aware of any new negative side effects. I'll keep ya'll posted!

I have posted in the past about my 9 yr old dd who was taking singulair for 3 yrs. Upon finding all this information about singulair and way before it hit the news .My dd was being tested for many different problems nuerologically wise. Trying to rule out depression,bipolar and ADHD. She had an eeg and labs done a few days after stopping singulair. And just today we went in for results and nuerologist says labs are normal but eeg was not . Meaning that she could possibly be having seizures. BUT NOW I AM WONDERING IF IT WAS SINGULAIR CAUSING THIS? I read somewhere that seizures can go unnoticed if they are very mild. But she did having trouble sleeping and concentrating. And at times even just stared off into space after we spoke to her repeatedly. My question is has anyone had any similar experiences with singulair ? Please respond.

Okay so I'm reading all of your postings and I about to totally flip out. My 6 yr old was diagnosed with a very mild case of asthma (an occasional cough that got worse with colds) when he was around 3. The doctor prescribed him Singular and I'm almost positive they started him at 5mg and now I'm reading that it's not recommend at that dose until 6yrs. He is very prone to severe mood swings....one minute screaming "I hate you!" and making commits like "I'll get a knife and kill myself!" to acting like there is nothing wrong and the previous outburst had never occurred. As a rule he is an extremely lovable kid but has these sudden outbursts. Having said this he has been off the medication since October with out any noticeable change. My concern is that if this medication has these types of side effects could it have long term or permanent effects on such young and still developing children. Has anyone else out there had their child off the meds for more than 6 months and not seen improvement in their behavior?

After prolonged use, my spouse seemed to loose all feelings and emotions. It was as if he didn't care about anything. Has anybody else had this happen?