Meds symptoms and conditions

i, too had the head zaps with lexapro. they happened when i stopped taking it and also if i missed a dose. i thought i was the only one who had them and i could never really describe them to anyone else. they sucked though. i also gained about 15-20 lbs on lexapro but i'm not sure if it was related to the meds. when i was on lexapro it kinda made me a sociopath...i didn't really care about anyone or anything. it didn't make me happy or unhappy...just made me not care about anything. i almost ruined my relationship. honestly i never really felt like i needed medication. so i was on it for about a year and one day just decided to stop taking it...not the best idea cuz the withdrawal symptoms were pretty bad. in addition to the head zaps, i had migraines and walked around in a fog for awhile. i was also super cranky bc i stopped taking the Pill at the same time so some of the side effects could have been hormone-related. needless to say i was kind of a mess for a few weeks afterward. but i'm fine now.

I have been on Yasmin for a little over a year. I also have suffered from migraine headaches for a few years. My doctor kept putting me on different meds to help with my headaches but nothing has worked. These headaches I've been getting lately aren't at all like my normal migraines. I get sharp pains in only one side of my head and it feels like there is so much pressure that my head is going to explode. It hurts to breathe through my nose, and if I sit up or stand it gets worse. I have been depressed and irritable so he put me on anti depressants. Then I find out all of these things that I have noticed happening like my legs feeling weird and my pains in my chest are happening to other people on the same pill. I have an appointment next week and I'm definitely bringing all of this up.

I have hypothyroid. Have been taking Synthroid for about a year, 0.075MG a day. Had my levels checked 3 times since on the meds and still have never gotten to normal, but a lot closer. I have gained 20 pounds that I can't get rid of, which for me, is crazy. I have never had a problem dropping weight, and for the past month or so, I have started losing my hair. Not just losing it, but the texture and everything has changed. No matter what I do it looks dry and flat, and even when I condition it and also use a leave in conditioner, it still knots up and tangles. I have NEVER had a problem with tangles. It's coming out in handfuls. Im not taking any other meds, so I imagine it has to be the Synthroid. My problem is..What else can I take? I mean, I have Hypothyroid, so I can,t just leave it untreated, But I have no wish to be fat and bald either. Please...anyone know of others meds without these side effects?

I take Lamictal for seizures for 3 years. I had my first unexplained seizure at 25 and another 6 moths later. Both times I had drank heavily two nights in a row. After the second seizure I was put on the Lamictal. I was slowly ramped up to 100mg in the morning and 200mg at night. On occasion, I get horrible "poop pains" as I call them. It feels like my insides are being ripped apart. I can sit on the toilet and poop incredibly runny stool, then I have to wait up to 15 minutes for the second batch. The pain doesn't subside until the second batch but it is immediately gone. It usually only happens when I wake up in the middle of the night. I have tried to correlate it to foods that I have eaten and can't match anything up. I also have horrible short term memory. I sometimes tell the same person the same story twice and they will be like "you just told me that." Also, golfing is the best example. I have a hard time remembering my strokes. My long term memory is fine. As fair as hair loss, I was already on track to lose my hair before I was on the meds so I don't know if they made it any worse or if this is a natural progression. It seems somewhat rapid but I never loose it in quantities or clumps. I just notice it in my hats and beanies every once in a while. I also have a hard time falling asleep on occasion and if I wake up in the middle of the night I have troubles falling back asleep as well. The bottom line is that this drug WORKS. I can live with the side affects cause they are random and not that often. I am a volunteer Fireman and cannot risk loosing that again so I am too hestitant to change meds as the doctor said Lamictal has the least side affects of the seizure drugs.

I just posted and forgot to add regarding the kidneys/adrenal glands. I asked an OBGYN (not reg doc - won't go back to her again) about this med and she said it was pretty much benign to the body. She stated though that if I did want to become pregnant to be sure to get off first. I was curious then and asked exactly what Lisinopril does to a fetus. She stated - pretty much the kidneys don't develop at all during pregnancy. I then retorted - "that only makes me wonder what this med is doing to MY kidneys now!" She just smugly had nothing to say. You cannot tell me that this is not hurting people. I am going to lose weight now and get off all meds. I only take this and I know with diet/weight loss and exercise it's possible for me. Besides sometimes when I check my BP it's high still and other times, like the day of surgery, it was lower than normal.

I just started taking Lisinopril 2 weeks ago for my high blood pressure, I'm coughing all the time with mucus, my left rib cage feels like somebody is continuously stabbing me in the same spot and then afterwards I would get a weird tingling sensation, I've lost my voice, I'm hungry all the time, I urinate way more than usual, I get irritated easily and start yelling at people when they haven't done anything, I'm exhausted from doing nothing. This medicine is terrible, I'm going to my doctor tomorrow and tell her that I'm going to stop taking it, I don't care, it's just not worth all the side effects.

I have had great experiences with Levothyroxine. I am no longer tired, achey, grumpy, constipated. I feel great. I am only 27 years old and got my hypothyroidism from having my first child. I am excited that my levels are now normal after 3 months (TSH was 25.89). I was on .50 mcg now I am on .75. Feel great!
I am a medical technician and have found that a lot of people who start on a certain medication for hypothyriodism, such as Synthroid - do not fair well if they have to switch. My doctor always says NOT to switch...not EVER. She repeats over and over again to check my prescription every time I receive it. That means checking the pills against each other, because hypothyroidism medication is one of the highest missed - filled prescription. If I were anyone who has had to switch, I would demand to be put back on your original meds. Have your physician write up your symptoms with the new meds and make a recommendation to the insurance company that you NEED synthriod.

Jan. 4th, 2009
4:35 am
I have been on wellbutrin 150 for several month's now and I have extreme dry mouth, sometime's unable to swallow without taking a drink. Itching, strong urine odor, hand's shake badly when drinking and sometime's eating, headache's, dizziness, lightheaded, balance is bad, nausea, depression seem's to be returning, weight gain, short term memory, leg cramp's bad enough that I have to get out of bed and walk them off, burning spot's on my lower leg's. Including the wellbutrin 150, I take about 27 or 28 pill's a day and it seem's like every time I go the doctor they add more pill's. I now also have nighttime incontinence and barely make it to the bathroom in time, but still have leakage or worse going to the bathroom, having trouble getting to sleep and if I get awakened it sometime's take's 2 or 3 hour's to get back to sleep.
--By floridapeach / Reply / Private Message Me

I would like to know who is NOT experiencing side effects from Singulair.
We are not.
My 7 years old started Singulair three months ago because of allergy issues. She had asthma attack every other week, running nose all the time, she was so miserable, she missed many days of school and she couldn't exercise .Since she started to take SIngulair her allergy improved, no more asthma, no more running nose. SIngulair did not change her way to be. She is doing very good in school (she is above the average..) she does piano, ice skating, she is purple belt Tae Know Doe, speak two languages, she is doing great in everything. Of course she has her "bad moments" but which child does not?
I tried homeopathy, but it did not work, she got worst and worst. I was supposed to give SIngulair to my daughter a year ago, I did not because I was afraid of the side effects. But I wished I had started before because I could have avoid so much steroids since she had asthma most of the time. The doctor convinced me to use this medicine when she said " You think SIngulair has side effects, yes sometime it does, but do you know the danger of using steroids so frequently in a little body?" Then I thought I had to give a try. I am glad I did. Of course I keep watching my daughter behavior closely and reading all the possible side effects of this medication. I forgot to say that beside singulair my daughter is also taking Pulmicort, two puffs once a day.

Well, after reading all of the postings here, I feel like I just dodged a major bullet! I took Singulair for a little less than a week in combination with a couple of other meds to get a bout of uncontrolled asthma reined in. All was well for 4 or 5 days and then suddenly I began to itch like crazy - I had a massive outbreak of hives (and this was while taking Prednisone, which is used to TREAT hives). Well, long story short, the doctor felt that it was most likely the Singulair and told me to stop taking it. I did and did not have another outbreak of hives. Now I'm actually rather thankful to have gotten the hives if it meant getting me off this medication before it could cause more serious issues!

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!!!!!

Seems like I'm in the same boat as a lot of people here. My dr. started me on Lipitor 40mg last year then raised it to 80mg. I started getting slight buring type chest pains with some sharp pains on the upper right side on my chest. The sharp pains increased when he raised me to 80mg. In Feb. 2008, I started to complain. He blew me off at first and then I ended up in the hospital for 2 days taking tests in March 2008. All the tests came back fine and my dr. explained the pains as "spasms" caused by "low flow" and told me to ignore then because it wasn't my heart...WHAT?? He gave me 2 other meds for the spasms. In Nov 2008, the sharp pains were daily and throughout the whole day. I started to research chest pains with lipitor and could believe the stories I read. It was as if I wrote them myself. I stopped taking lipitor on Dec 2, 2008 and within 2 weeks the sharp pains are almost by gone. I'm still having the slight burning feeling sometimes and was wondering how long this will last take to completely go away.

Hello, told my doctor today of leg cramps, facial rashes and numbness in feet....and specifically asked if they were related to Synthroid? He said no, I have been on it for 2months...and just upped script to .50mcg....and cramps are worse....I am going off the meds. I am in excellent health @ 64 and only went to this Doctor because of back pain.....was tested for a myriad of things...I had none of the symptoms for hypothyroidism.....what natural remedies are there for this . E.

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.

Hi....I am a 48 year old male just starting on Lisinopril 10mg daily. Have taken it for 7 days now. Blood pressure before was 184/120 in the doctors office. Have seen it spike to 200/129 at the dentist plus 220/149 at the Oral surgents office removing a tooth. First day of taking Lisinopril it knocked down my BP too 123/75 thought that was great. Since has mellowed out now at 140/90. Im sure on my second visit the DR. will up my dosage which I will question. So far reactions have been that scratchy throat right of the bat that everyone discribes. Plus my stomach just groals the first hour as it trys to disolve. Takes about 4 hour before I can see it lowers my pressure any. Have been trying different times of the day best I can to find the best time to take it which I now have settled on right after noon lunch about 1 hour works best. I also have had alot of tiredness from it, which is different from the weakness I also get from a condition they say I have called N.A.S.H. (non alcholic steatohepatitis ) which basically is too much fat in your liver that drains me of energy worse each year. But why I bring that up is the feeling is different a tiredness compared to a weakness feeling I dont seem to like. The weakness I can jack away with some caffine but this tiredness nothing seems to help so far. Have had some dizzyness getting up which is something I can live with til it makes me faint or fall at some point then I surly will cry wolf get me off this. Getting blood work done soon to see how it affects my liver counts will update you on that later.

I am a 39 year old female in relatively good health. In the past year since taking Lipitor, I have had SEVERE thinning of my thick hair. I have lost nearly 2/3 of it, and luckily I had a lot, but I am thinning more quickly on the top of my head and you can now see my scalp. After reading this, I am stopping my Lipitor, tonight. I hope that my hair returns ... I have also had chest pain, leg pain, trouble sleeping, trouble with eyesight, trouble focusing, unexplained weight gain and extreme fatigue. I think I would rather take my chances with high cholesterol than be bald at 40. Nice eh? I complained to my doctor when my hairdresser called this to my attention, and she poo-pooed it and referred me to a dermatologist- who after months of waiting rescheduled. I will be BALD!

I was diagnosed with Diverticulitis and put on the usual regime of Levaquin (500mg a day) and Flagel. The case turned worse and was admitted to the hospital (they thought I had a blockage but turned out did not) and was put on IV of the same medication. Released from the hospital 4 days later and stayed on the Levaquin as prescribed. When I ran out, I called my regular doctor who sent in the renewal prescription. However the his aide made an error and the bottle read 500mg 4 times a day…nobody including the pharmacy caught it. So for 3 days I was taking 2000mg a day of Levaquin. When I started getting worse (truly thought I was dying), I got to the doctor and he said I had taken turn for the worse and could not figure out why. He asked if I was taking the meds and I said yes 4 times a day…his face when white. I had the bottle with me and he panicked. They apologized for the error and I was told to stay off my feet, no heels, they ran ekg’s that day and the following Monday, blood work to check the kidneys etc.

Subsequently, I have had extreme pain in my joints and muscles – everyday, all day. Some days I just cry it hurts so bad. If I bend down I can hardly get back up because of my right knee. I have talked with a doctor I happened to run into about this and she said that Levaquin dosage has saturated my body and gotten into the joint and muscles and takes a long time to work it out. I can hardly lift my arms above my shoulder without severe pain. Stabbing pains in my knees, shoulders, arms and hands.

I have not gone back to the doctor because when I mentioned the pain the when I was in that last time…he just wanted to give me more meds! I have been seeing a massage therapist who specializes in deep tissue restoration and repair. It helps some, but he as well says this is going to take a lot to time to work out.

I have depression to the point of feeling like I am a nothing and what good am I to anyone feeling like this. So like snoop45...that is exactly what i feel like!

dawn62

J.

I'm on bactrim for a kidney infection. The first day I was fine. I was in so much pain, after 2-3 pills it made me feel a lot better, I'm taking bactrim 2x a day for 7 days. I'm on day 4 and feel like crap. My backache is back, headache, cramping, stomach ache. I feel worse then I did before the meds. I stopped it this morning, but go so sick I had to take one. They make me feel better for a moment, until everything kicks in. And I cant do this with a 5 month old to care for. I go to the doctor in 2 days....I will be stopping tonight. Thanks to everyone elses answers!!

Wow, i cannot believe what i'm reading. I have been taking Simvastatin for almost three years. My Doctor never mentioned any side effects. It has gotten bad enough for me to seek information on the internet. What medicine cause all my symptoms; Tingling in the hand and feet, weakness of muscles, dropping things, dizziness, memory problems, sore muscles, sinus problems sore knees, arms, shoulders, stomach,numbness, sensitivity to light. I'm sure glad i have found this web site. I think i am going to take myself off of it for a week and see if things improve. Drug companies must be making a killing on this medicine since they refuse to warn potential patients.

Hello All. Diagnosed bipolar in 2004, been on and off meds realizing that I guess I can't really be off of them, though having a hard time dealing with it. Been on Lamictal, Lithium, Geodon, and several anti-depressants and others I can't remember honestly in the past, now just Geodon, 80 mg at night (can't do it in the morning, can't work). It's now 2 a.m. and I'm desperate. I feel worse on my meds than I do off, though I get suicidal and sabotage my life and my marriage and kids. I have experienced insomnia, tired in the morning, my muscles ache, I dance all morning long and my co-workers think I'm crazy ( I guess I may be). I have landed in crutches because my "dancing" has caused shin splits. I hold a good job and I have two kids that I need to tend to. My husband travels a lot and I just can't seem to deal with the Geodon. All others caused similar issues. I'm desperate on my meds, but I suffer schitzo symptoms off meds. Any suggestions would be greatly appreciated. BTW, just found two great doctor's, one for therapy and one for med admin. Only been back on my meds and doctor's appts for 2 months after being off meds for 9 months and suffering another "great" relapse. Help me!!!!

Yaz is AWFUL I took it for 5 months and it made me have headaches a lot, feel dizzy, diarrhea, throwing up and anxiety. It also made me feel like I didn't want to do anything and just really tired. It started making me feel really different the past month and I just realized that it was the birth control because i'm not on any other meds and that was the only other possible thing. These birth controls are not good for anybody to be taking. The FDA are using us to see what side effects it will have on us, I don't know about you but i'm not going to be there lab ratz anymore.

I have been on Advair since Feb. of this year, I have had a lot of these side effects but didn't really realize it was from this med. At first I was told to take it 2x a day, reading the directions it says it has to be 12 hours exactly apart. My work schedule didn't allow that so I just took it 1x....Working 2 jobs I just thought when I couldn't sleep and was always tired, it was from working a lot. When I told the Dr. about not being able to sleep more than 4 hours, I was told since I was taking the meds 1x a day that wasn't it. After a bad cold and bronchitis I was told I had to take the Advair 2x a day, now i'm more tired than ever, still can't sleep and have a headache that won't go away even with migraine medicine. I'm even jittery and forgetful--kinda ditsy now and itchy off and on all day...After reading this blog site I see its not in my mind and i'm going to stop taking this med. I think i'm going to the health food store and find something natural.

i got a bad sinus infection for the past month after starting lisinopril, on many meds for this, i switched from avapro to lisinopril as i wanted to join the walgreens plan for cheaper drugs, the doc put me on lisinopril instead after i sent him the walgreens list of available drugs that they use, the avapro was not on the list,, ive been to my ent and allergy doc for this sinuse thing that is well over a month now and getting better, but i have spent more $ for drugs to combat this infection that r not on the walgreens list over $300 spent out of pocket but with a discount for switching to the lisinopril from the avapro that ive been on for about a yr,, it was not worth it,, BUT my cardio doctor thinks it ws just a coincidence that i got the sinus infection about the same week that i started lisinopril, he asked me to tell my ent and allergy doc about this, the ent thinks i shld go back to the avapro if ii feel that it may have started the infection with the little cough, i have not talked to my allergy doc about it yet, has anyone felt they got these symptoms with lisinopril????? i am still taking it all thru this sinus thing, MRI and 2 inhalers and antibiotics, narcotic cough med, sinus wash and musilex r doing ok and on the mend, i have no other symptoms and on the 5 mg , what do u all think? and anyone else have a sinus thing going on when starting the lisinopril??? D.

Hi, just wanted to give all an update....day 8 off the Doxy, by the end of the 6th day off the doxy, I began to get a clear head again....I would feel great, then all of a sudden a fog would come over me for about 5 minutes with ear ringing, and go away....this happened about 3-5 times...my left arm and left side of my face felt hot, but i did not have a fever....thats when I knew the doxy was leaving my system...day 7 i felt fine, but went into a slump...laid in bed for about 12 hours, I think this was due to still having no appetite and barely eating for 3 weeks, I lost a bunch of weight . I felt mentally clear finally, the bout of depression that the doxy put me in was lifting, but still felt physically weak. Today, I woke up feeling fine, ate a croissant for breakfast, forced 4 sliders down for lunch, and finally was able to eat some dinner. The good part is that another user on this board was kind enough to mail me letting me know that she went through the exact same side effects, and assured me that they would subside with time, especially the loss of appetite and depression/anxiety...takes about 2-3 weeks off the meds for everything to start getting back to normal....She also told me that the doxy has a very long half life...so it does stay in the system awhile....but im starting to feel slight improvements as the days go by...the bad news...i don't think the doxy cured everything. Im considering taking ionic silver instead of any more antibiotics....one other caution...beware of Levaquin...I was on this at first for 5 days along with the doxy, and that drug truly is (in my opinion) dangerous. I read some of the side effects people were having, including myself and was horrified....I thought something was weird when my middle finger on my left hand went numb for a day, left hand was warm, right hand was ICE COLD, sudden and sharp pains in the back, like I pulled a muscle, that left me unable to move for a few days, and severe diarrhea. Anyways, please feel free to mail me if you have any questions....support is the most important thing a person can have because of the fear and anxiety these drugs put you through.

Hello, I have read over most of these side effects and i would have to agree and be afraid of most of it. See I was diagnosed with bronchitis/pneumonia, they prescribed me these pills along with steroids. I have not taken the steroids yet but I did take my first dose of levaquin about 12 hours ago around 8 pm. With my dinner and plenty of water and fluids. I went to bed late with my fiance but not cause of the medicine, we decided to stay up and watch movies. Although, it did help my coughing and breathing, I felt bloated or ballooned up all of a sudden and it was starting to hurt my stomach. I figured it was the food I ate and all the water I have been drinking. So, next I noticed some minor vaginal discharge of which looks like when I'm ovulation so I pasted that as that. Now I woke up at 5:30 in the morning when I went to bed at 2 am and I can't go back to sleep! I woke up from a nightmare to see things in the dark to scare the %$^* out of me. I had this really bad taste and dryness to my mouth I felt like it was suffocating me. I cant seem to think straight or type well (I had to go back and review what I wrote but I might not have gotten all my mistakes) I feel like I have ADD I keep forgetting how to spell simple words... I mean the list keeps going and going. I am writing now because I am currently on it. I will not be taking this medication anymore much less the steroids but if anyone reads this, I hope you read first then take.