Preventative measure symptoms and conditions

I recently had been prescribed macrobid for a uti I developed a cough after 4 doses that really hurt. After finishing the course of it I came down with the flu ( cough fever,body aches, etc.) and a rash all over my legs and arms of tiny bumps that itched. 2 weeks later I was given macrobid as a preventative measure by urologist to take for 30 days. I took the 1st dose before I went to bed at about 11:30 pm. the next day by 10am i couldn't finish my morning oatmeal due to sudden loss of appetite and nausea. Then I noticed I was starting to get body aches and my temp was elevating by noon. I took some aleve. By 2:30pm my I had a terrible cough that hurt my chest and my heart felt like it was beating out of my chest. Since I work for my PCP I told him about the symptoms and that I thought it was related to the macrobid and that this was listed as some of the side effects he checked my pulse and it was 133. I went home sick and he called to check on me around 6p.m. by then I was much worse my fever went up and I was coughing to the point that I was short of breath. I had headache dizziness, lightheaded and my whole body ached. and i was so hoarse I could barely talk and had what felt like a bruise on my left hip. He told me if I didn't start to feel better or got worse I should go to the E.R. I woke up at 10pm feeling worse and my heart rate was 120 after waking up from sleep. Went to the E.R. and my pulse was 142. they totally disregarded the fact that I told them this was side effects of the macrobid and they told me that could not be. That night I was diagnosed with bronchitis and uti. I was perfectly fine the day I took this med. I have never had bronchitis before. And my urologist had checked my urine 2 days before and said it was fine. i wasn't even having uti symptoms this was supposed to be preventative med. My PCP says he had his doubts but after looking at the side effects of this med in his MPR, I had almost every one that was listed. I will never take this med again. Antibiotics are supposed to help, not cause infections this should be taken off the market.

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.

it caused a robotic personality in my husband. he had no empathy and no sex drive. he had cheated on me with a woman who was on prozac herself. I guess they tired of taking drugs together and became bored - no sex, nothing in common. people need to deal with life and get off these type drugs. taking something every now and then is not bad. but a drug that is to be taken everyday to help one cope is another "outlet" and unrealistic. it almost destroyed several families.

So far I haven't seen anything in regards to my symptoms with Yasmin.

After going the past two years and having only two periods, I was diagnosed with PCOS. My Gyno told me that the only way I would be able to have a period, and delay the harmful side effects of this disorder would be to go on Yasmin. I agree that my mood swings the 1st month were terrible. I almost punched my own mother in the face because I didn't like one of her jokes. That's not me. But that is something common with BC. They are hormones your body takes in to regulate your cycle. And because my body doesn't' regularly produce the hormones needed for menses, I expected mood swings. The catastrophic depression and PMS were the main reasons I stopped taking the pill years ago.

My problem is a bit different. I haven't gained weight. As a matter of fact, I think I've lost a bit. My problem is my skin. Before the pill, I had flawless skin. It was always really sensitive, but because I was cognizant of this fact, I took every preventative measure to ensure its healthy appearance. But now my skin in a mess. I have a rash spreading all over my body. My eyelids have a hard crushed rash of skin folding over, and my under-eyes are the same way. All across my face, I now have raised red patches of skin that burn, and the only change I've made to my daily care regimen is popping that little pill every night. The rash is now spreading to my shoulders and a bit on my legs.

Has anyone else developed skin problems, or could this all just be coincidental in my case?

I

5 year olds do not talk about suicide...period!!!

My child was on no other medications. I have reported this to Merck and the FDA and have also changed pediatricians after a lengthy discussion with her. I cannot speak for others.

The issues with Singulair are far from over. Stay tuned.

I can't believe it's taken me so long to find this site. I have been on Lipitor for the past 5, going on 6 years. My doctor thought it would be a good preventative measure as 22 year old sister had recently had a massive heart attack.My cholesterol levels were all great but a CRP test indicated that I was on the high end of normal. Nearly three years ago, the muscles in my right arm became very achy and I could not rely on it to lift many heavy objects or even my 2.5 year old son at the time. The doctor recommended i see an OT, who, in turn, was not able to figure out why I always felt like I slept on my arm funny. After months of getting nowhere and chalking up to pulling a tendon while throwing a baseball, I decided to live it all. That summer, I also started having a hard time focusing. So, I saw an eye doctor, who said that I was slightly near sighted and that glasses would help strengthen my vision. I had never had any vision problems prior to that and it seemed like it came on suddenly. But, I figured that I was getting older and people need to have glasses sometimes as they age. Then, last summer, I began to get these crazy rashes, which I now know where hives that bacme irritated by touch. The rash would pop up any time, any where and never in a way that i could relate to anything I ingested. Then, all of my joints began to ache unbelievably. I looked up some symptoms, wondering if I contracted something through my son's preschool, which was dealing with a little fifth's disease breakout. My symptoms seemd in line with what an adult can experience if he/she had fifth's disease. The doctor was stumped and had me have blood drawn, which indicated my liver levels were a little high, but they could tell me "What you don't have"... lyme disease, any viruses or lupus. Okay. I was to have more bloodwork done in a week or two, but decided to see how this rash, etc. would play out. The pain went away (except of the arm on that started a year and half or so earlier) and the rash was something I thought would dissipate soon enough. After three months it did subside. We bought a house and my son started kindergarten and it finally seemed like I was on the upswing. Now, six months later, the rash resurfaced. I was completed disappointed. At first I thought the Fifth's was making a comeback. I looked online and found a site that showed different types of rashes. That is when I came across a picture labeled "Drug Allergy" and began looking into the two drug I was on. By the weekend however the pain started in, especially in my legs, the calves, and my ankles hurt so bad. I was having spasms in my arms and legs and noticed within the week, two bruises on my thighs that I am certain appeared on their own. I did not bump my leg at all. I became very nervous and thought that I was going to experience a blood clot as my mother had one at 34 years of age. I am 32. But, after researching and reading forums like this, I am convinced that I, too, am experiencing serious Lipitor side effects. On Saturday,I did not take my usual 10mg and saw the doctor. She recommended that i go off the Lipitor for now and have blood work done. I have been off it since then (not very long) but by Monday I was feeling almost normal. Today, I feel some cramping in the legs, but I think it will take a long time for this drug to rid my system. I have to go back on Friday for a follow up, but I haven't heard anything alarming about my bloodwork yet.
Again, I can't believe it has taken this long to find this wonderful site. Best of luck to the rest of you in your recoveries and a Lipitor-free life.

I am 51 year old female. I have been having similar side effects that everyone is posting. The cough just started. And I am having cramps in my legs and back that I never had before. I also have been a little depressed. I just stopped taking the medicine yesterday. I am at a place called Optimal Health Institute. They put you on raw veggies and juice and fruits and nothing else for a week to 3 weeks or as long as you would like to be here. Also mild exercises to help you cleanse and you juice wheat grass 2 times a day. I decided to go off my meds yesterday (been taking 10mg for about 4 months) and my blood pressure reading just registered 119/78. It has been running 135/85 with medicine average. I just started but after reading all of these posts and my own side effects, I am definitely going off this junk. I hope this cleansing works. I am going to be here for 2 weeks.

IA huge thanks to you guys for putting this info out there, because I'm sure the Singulair website wouldn't go into detail about this, and tell about side effects it has: FYI -->

This was what I found on the Singulair website, no more, no less (see post below this one please)

'm really sad to hear that these things happened to you guys and your children.

My 8yr old (55 lbs) son got a cough that ended up lasting about 4 weeks, so i finally took him to his pediatrician. He gave him a breathing treatment and hinted at him having asthma- but he wasn't sure. We have no family history of asthma and in my mind i thought it was pretty far fetched, but we continued the breathing treatment for about 2 weeks and my son cleared right up.

We came back in the Friday after Thanksgiving for a check up and his doctor said that my son sounded much better. The doctor said that looking over my son's medical history (not much of anything) he said he could have asthma-but he wanted to put him on Singulair for the next 3 months until the winter is over.

He said it would be a preventative measure to keep my son's symptoms from "flaring" up. The doctors said " This is not a steroid, and there are NO side effects. Its a once daily chew able for children." I thought-hmmm that's a first, a drug with no side effects. Then I was thinking" "What symptoms was the doctor referring to?" He had a really bad cough he got while visiting his dad's family (bug going around). But I held my tongue and just nodded. He wrote out the prescription, and I left. I heisted as I pulled out in front of the pharmacy and then kept driving.

I felt uneasy about the whole thing. Giving him a daily medication for a condition (asthma) I doubted my son had. Glad I did my homework, I decided to not fill the prescription. I don't feel the least bit guilty for not giving him the meds.

My 8yo son has been on Singulair for his asthma for about 2 weeks and he has complained of a 'sick tummy' regularly, ending up in tears because he can't do things. We have had a long run of this, perhaps due to the 8 lots of penicillin for tonsillitis, and some tummy bugs going around the schools I work in. The doctor has been suggesting irritable bowel syndrome so we didn't think of the Singulair side effects until it has got so bad that he is not going to school.He has been unusually clingy and almost paranoid about small things that don't usually worry him over the past couple of weeks. We were trying these tablets as he has been on steroid based preventer since he was 3 and we wanted to get him off the cortisone stuff. After reading here he is off the Singulair today and we will report the side effects to the paediatrician.

I am also currently taking doxycyline as a preventative measure because my boyfriend had NGU. I am taking 100mg twice daily. I experienced very mild nausea, I felt very bloated and had extreme gas. You just feel very heavy when taking this medication. I felt full all the time and my stomache was semi hard and when I put pressure on it, it caused burping and farting... sorry to be so graphic :)

Our doctor prescribed Singulair for our 4 year old as a preventative measure for bronchitis this past Friday (July 7th). That night, she was up every 2 to 3 hours saying that she's scared and that her legs hurt. She has slept through the night since she was 6 weeks old, so this was shocking to us. We just thought that because she was sick she wasn't sleeping well...even though other times she's sick this didn't happen.

Saturday, Sunday, Monday went by and each night she woke every few hours...crying and crying. She was dreading bedtime (this was also strange). On Tuesday, I found this site and read all the stories....and many of them were similar to our situation. My wife and I talked about it and we decided to take our daughter back to the doctor on Wednesday to let her know that we'd like her to try an alternative medication because of her reactions to her meds. She listened to her lungs and said just to stop the meds...she sounds ok now.

Wednesday night...still woke up....but fewer times. Last night...slept from 8pm to 8am!!! Was in a great mood, no talking about nightmares or achey legs!!

Beware of this medication....we will not be using it for our little girl ever again!!! Thanks to eveyone who shared their story.

In Janyary 2001, I was diagnosised with diabetis. Besides the diebetic medicine the doctor put me on plavic and zocor as a preventative measure as my cholesterol was normal it was always between 160 and 189. I was 66 yrs at that time.

After taking the zocor for six months my legs and feet began to swell and I developed a bone spur in my right heal and could hardly walk. By the end of the year my legs were hurting, tingling, burning , numness and I could not stand on my feet for more than an hour. When I would discuss this with my doctor , he said I probably needed potattisum and calcium.

After a while I began to notice that my purse seemed too heavy for me to carry. I was suffering from depression and it took a lot of effort for me do do anything. I still had no idea that the zorcor was causing the problems. I got a walker to help me walk. My back hurt me so bad when I was on my feet that I found it impossible to keep up with my house work.

I began to have breathing problems, so I was put on oxygen.
I was gaining weight very fast over 103 pounds in three years. I was hungry all the time. I could not open my eyes in the morning. The muscles around my eyes just didn;t want to work. I would have to rub them and sometimes use a wet cloth so that I could get my eyes to open.

As of this year, I am no longer able to do my own shopping, or drive my own car. Using my walker to walk from the front door to the car is painful and leaves me breathless. My son has to help me into the car and buckle me up, while I am trying to catrch my breath. My last blood work showed my cholesterol to be 136. I stopped taking zocor about a month ago after seeing someone on TV that said they could hardly walk from using zocor. I was taking 40 mg daily since 2001.
I am now dependant on a wheel chair to get around the house . Will I ever be normal again and able to walk?

Hi. My name is Vicki & my husband David is a Type 1 diabetic.
David started taking 10mg. of Lisinopril daily on 7/4/04 as a preventative measure. Eventually his doctor wants him on 40mg. a day. He experienced the common side effects of a cough, fatigue and dizziness. The fatigue has become overwhelming for him and he wakes up saying I don't feel good. Not his normal happy self.
On Saturday 7/24 he woke up with blurry vision in his right eye. Later a floater appeared in the right eye. Sunday morning he woke up with a larger floater and a film over his eye. He cannot see details or read with his right eye now. His eyes were in good conditon before this.
His doctor & ophthlmologist say they have never heard of any
side effects affecting vision with this drugand want him to continue using it!
Thank you for your site and letting me know that there are others who have had similar problems.
Please e-mail me if you've had a similar problem on this drug. ******

Not been here for a couple of months and very interested to see all the new postings, some quite alarming. Still on 5 mg. a day. Re: Rosemary's post. Yes, I too have a high reading at the doctors - we usually have a joke about it now (but not to the level of yours Rosemary). My decent quality monitor at home, best reading last week 124/72. About the worst 140/85. Have had to take another Zantac (ranitidine) tablet today - due to excess acid - cannot source this down to any particular food I've eaten over the past 12 hours or so. Hair loss? Still out on this one as I tend to have thicker growth in Summer and thinner in Winter (in UK). The annoying thing is that I've been on Lisinopril now for 18 months as a purely preventative measure. But this is a Catch 22 situation now. If I stop taking it, in my innermost thoughts I would think: "am I shortening my life, or my good health? Should I carry on with these tablets for the sake of my wife and kids?"

I was prescribed Levaquin the first of April 2003 as a preventative measure, and around the 20th of May 2003 lost my ability to taste, just a weired metallic taste, and noitced I tired very easily and was short of breath with very little exerction. Was advised by a Dr. friend of mine to have some blood test done which showed that my immune system was very depressed. Abnormal platelets, very low RBC (2.95), very low WBC (1.22). Just about every entry on my CBC is low, with exception of two items which were high and these have remained unchanged for the past two weeks. I have had four CBC's done in the past 14 days with virtually no change. I am going for a bone marrow biopsy as soon as I can get in. (no insurance) Does anyone have any suggestions?