Medication symptoms and conditions

Hi,

5 days ago I was diagnosed with staph, MRSA. I went to my doctor, who put me on Augmentin, didn't work so he added Levaquin. I ended up in the ER on Thursday with my arm worse and intravenous drugs. To make a long story short, after my second dose of Levaquin I told the doc I woke up that the night before at 2 AM, soaked in sweat and asked if it could be a sign of the Levaquin. He said no, and to continue taking it. Needless to say, I took a dose tonight, I am up, anxious, my heart is beating out of my chest and I feel dizzy. It is now 3:00 AM and I just got off the phone with the nurse hotline because I know it is the medication and I am scared. She told me to try and stay calm, don't take anymore, and report it to my Doctor. The thing is I did report it, and he told me the effects I was suffering had nothing to do with the drug. Same thing with the ER doctor, he told me the same.

DON'T TAKE THIS DRUG IF YOU KNOW IT IS HURTING YOUR SYSTEM. IF YOU FEEL STRANGE, DIZZY, WEIRD. I JUST WANT THE DOSE I TOOK TO BE OUT OF MY SYSTEM.

I also started taking Welchol, two in the morning and two in the evening. I started noticing that I can not get an erection, and I know it's the medication. Can someone out there tell me if i am the only one or is someone else having this problem due to Welchol?

In August I started taking Topamax and every week i am to up the dosage now I am taking 50mg in the morning and and 50 mg at night because my headaches was so bad that I had to quit my job because I couldn't serve food and vomit at the same time. Now that my headaches have gone from everyday to about every other day I have noticed the indigestion. Because I had because sick so long the doctor suggested I had a reflux and it would correct itself.I started looking at all the medication I was on and the list from the pharmacy never indicated indigestion on as a side effect for Topamax.My appetite is non.Weight lost about 20 lbs but I could afford that and then some. I try not to use the upstairs of my home if no one is there because of the dizziness.And simple chores around the house go undone.I have bounce $130 in bank fees this month and can't figure out how and gave the finances over to my husband to keep up with and I am a math major in college this semester.This is how bad things have gotten some simple words i can't recall how to spell . I have to use the dictionary. It's bad.

Hey to All.
I know that the ALA study got everyone upset and I am happy we all emailed her.We all pretty much got the same response from Heather,defending the study and the integrity of the results.If only this investigation would conclude!
The Merck company contacted our Senator and indicated there was a conclusion and then ,they never got back to her before the weekend.I will have news early in the week.Please everyone just keep on voicing your concerns by reaching out any way you can.Sometimes it seems unbearable and I have to take a break with the communications on this website but,I continue my communication with my local contacts and the FDA.
I would love quick results and everyone would love this to get the publicity this story deserves but,if you look at how far we have come getting attention focused on this drug it is amazing.
This website has been here for years and people have complained and nothing has been accomplished until now.Our system is so broken it will take time to fix it.Drugs get approved everyday and when they are put out for multi use,the population benefit -risk ratio changes and there is little oversight on this matter.
The problem is much bigger than just notification of updated side effects,which indeed is why our son died from this drug.It is reporting adverse events to the FDA and the drug company and following up on your report.We can only fight within the system of the government that is in place at the moment and push for change to take place in there programs.
This is what has take place as of this year,The FDA's new 'Safe Use "iniative(which when it gets further developed will increase our partnerships with physicians as well as patients) and the July 2008 AAM report" Education in Safe and Effective Prescribing Practices" which aims to address the education of the next generation of physicians on how to best use medicines.This may help in notification practices and over prescribing but, we want the drug companies to lose the unprecedented control over the clinical research and and evaluation of there own drugs.What other company in the USA, gets to self regulate.Change will come ,we have asked for accountability by having a signature exchange when new and updated side effects are found.Full disclosure of all reported adverse events to doctors from the company representatives,with signature required upon full understanding of the benefit -risk ratio change. A prescriber should know all the good and the bad about a medicine they have chosen to dispense,if not then they should not be able to dispense it.If we were not knowledgeable about selling mushrooms and we sold the poisonous ones ,because we did not take the time it would take to educate ourselves about them,would we not be legally responsible for our actions.
Accountability is what we are asking for and maybe the candyland doctor prescribing practices would stop.They seem to ,not have a responsibility to their patients and the company has no responsibility to the prescribers,so who is responsible for our safety?
I will keep fighting for real change and all you people must do the same ,make an appointment with your representatives and have them contact our Congress representative of NY,maybe with enough onboard we can get the legislation we need to put a law in place for proper notification practices.Kirsten E. Gillibrand Member of the US House of Representatives 120 Cannon House Office Builing Washington, D.C. 20515
This is how change is made ,if you want to help please go forward and do this and don't stop until they listen.I am always willing to do whatever I can,it is physically exhausting and sometimes I just have to step away but, my daily review of this site has not stopped and my fight will continue.Dave and I sit here and our hearts just break for all but, we need people to push their Representatives they do work for the people just remind them of that.Any one with questions or that wants to communicate via private email just ask for my email address or phone number or leave me yours and a time and I will be sure to contact you,Kate M.

My first injection gave me generalized bodyache, but after the 3rd day it was absolutely wonderful, I am 49 years old, 120 pounds and 5'5, and I felt my legs extremely energized like when my knees were not injured. Then I went to the 2nd injection, when the medication was ejected in the joint, it was extremely painful. I had to have help to excert my self. I was not able to squat down. In the mornings,the posterior side of my muscles, below the knee, felt like it was shrunk down to a third. Every step was excruciating pain, especially when walking down just a few steps. Before the shot,I had pain in the lateral side of the knee. Now the pain is in the internal side of the leg, starting below my knee all the way down to my big toe. If I would have known this pain would have occurred, I would have never taken the second injection. My condition got even worse than before I ever had any injection. I am so devastated I have come to the bridge of crying and feeling crippled. I had the last shoot about two weeks ago and my legs feel very heavy when I take a step. Now I hope and pray for a miracle.

Just read an FDA article out today, I believe. The FDA is looking to publish quarterly a list of "potential problem drugs". That is fantastic! But where will this information be posted, and how often should a medical prescriber visit and hunt for such information?

I still maintain every medical professional with the appropriate credentials to prescribe any medication should be required to register with an email address with a database within the FDA to immediately communicate this new-found quarterly list, as well as any investigations launched (as with Merck/Singulair). Wow - what a concept.

I suppose I should be somewhat more optimistic with a slight move in the right direction - but I know with all my heart neither my daughter's pediatrician, nor my personal intern will receive, nor be aware, of any of the quarterly "lists".

Will keep trying to get a change within the FDA.

I am a 51 y/o white female that has been on Lipitor for 2 years. I am 5' 1" and when I had to go on it my cholesterol was 267 I weighed 112 lbs. I was shocked.... my doctor told me weight had nothing to do with cholesterol. She kept a close watch on me and my cholesterol came down...... and then my ex-husband of 17 years and I re-connected and got back together and I moved so I had to get another primary care physician. I took all my meds to her, she also kept a close watch on everything. At this time my cholesterol is down to 109 and I asked if I could stop taking it, as I take quite a lot of meds, due to different things and if I could stop anything it would be great, but she said it I stopped it, my cholesterol would go right back up. So since I am not experiencing any side effects I'm okay with continuing it.

I surely hate to hear what you all are experiencing with your Lipitor..... could your doc try another cholesterol medication?

The only one of my meds that is giving me any problem is TOPAMAX........ that we are using as a Migraine preventative! HORRORS!!! Today is pretty good day. But my cognitive abilities are in the trash... I say the wrong word when I mean something else...... I search my mind looking for a memory...... I am also on disability since 2002 because of the Migraines....... I have has them since 1978, but they got progressively worse over the years until I was sick more days per week, sometimes more than 7-10 days at the time, having to be in the hospital being rehydrated and on IV pain meds.......... and as awful as the TOPAMAX is.....it has been reduced the migraines to approx 2 per month and they do not last nearly as long.

So sorry, I got waaay off topic, but I know that it is not the Lipitor that is giving me the side effects as it the last med I had to go on and I had no new side effects....... but that TOPAMAX is kicking my behind.

I was on 10mg of Lisinopril for 6 weeks (switched from Azor). After the first 3 days, I was having trouble swallowing . . . this went away 2 days later. Then, I was having trouble breathing, sinus problems, dizziness and constant FATIGUE during the course of the 6 weeks. I am a very active, energetic, 30 year old male. I'm not overweight, and play basketball 2 or 3 days a week. I really think I have White Coat Syndrome (170/110 at dr's office - 130/75 at home), but better safe than sorry.I could not even run for more than 5 minutes straight without feeling like I might pass out. I would have to say during those 6 weeks, I was functioning about 50% of normal, at best. I tried to stick it out to see if the side effects would go away; they only seemed to get worse over time. My Doctor said it was the "summer fever" and allergies. I felt it was the medication, especially after reading these posts, so I switched doctors. My new doctor took me off of this medication. He said Lisinopril can has been known to effect your lungs and cause breathing problems. He is located in the same practice as my previous doctor. Why she didn't inform me of any side effects, I'm not sure (thanks for nothing). All of my terrible symptoms were gone within a week. I am now taking Bystolic (5 weeks), and feel normal again. My father has been on 30mg of Lisinopril for 12 years, and never had any problems. I believe everyone reacts to medications differently. I am now on my 3rd medication in 7 months, and think I have found the one that works best. I guess I'm just one of those people that has trouble adjusting to medication. Good luck to those of you that have not found the right medication yet.

These side effects are scary! I just got off of the drug LISINOPRIL! PLEASE, PLEASE look it up if your doctor is changing your current medication to LISINOPRIL! There are 1,800 entries from people who got very sick on it! He now gave me a scrip for this and no way I am taking it after reading these side effects and seeing how sick it is making people. Thanks to everyone to for posting on this site! I am making drastic lifestyle changes with diet and exercise so I don't end up in the hospital.

My daughter began taking Singulair in 2003 for asthma and allergies. I slowly watched her deteriorate from a lively, intelligent, and outgoing young woman to a depressed, withdrawn and self-mutilating person who said that she hated herself and everybody else in the world. She was an athlete, a straight A student who had received an academic scholarship to college, she was fluent in German and had been teaching herself Japanese, and she was a staunch supporter for equal rights for children with disabilities and gay and Lesbian teens. On February 3rd, 2007 my daughter hung herself after working at the local community center. I no longer recognized who she had become. I have a degree in psychology, my father is a retired police officer, and my mother is a retired R.N. We were all trained to recognize the symptoms of depression and suicidal thinking, but we were never able to connect it to the medication that she was taking.We must all ban together to prevent other people from suffering the way that our loved ones have! Educate everyone that you know about what Singulair can do to you. They are still prescribing this drug to people without any notification of what the side effects are.

HELLO EVERYONE....IM SITTING AT WORK AND JUST DECIDED TO RESEARCH THIS DRUG LISINOPRIL...BECAUSE I AM REALLY BORED....WHEN I GOOGLED THE NAME I CAME ACROSS THIS SITE.....OMYGOSH...I THOUGHT I WAS GOING CRAZY...I HAVE BEEN TAKING Lisinopril FOR ABOUT 6 MONTHS NOW....I ALWAYS READ THE INSERTS THAT COME WITH THE MEDICATION BUT I NEVER SEEN THE SIDE EFFECTS THAT WE ARE HAVING ON THE INSERT...I SING IN THE CHURCH CHOIR AN I ALWAYS WONDERED WHY MY VOICE WOULD BE SO HORRIBLE AND MESSED UP..I AM SO HAPPY I GOOGLED THIS DRUG...DOSE ANYONE KNOW HOW LONG IT TAKES BEFORE YOUR BODY GOES BACK TO NORMAL AFTER STOPPING THE DRUG....

Was previously on Micardis HCT; dr. switched to generic Lisinopril HCTZ 12.5 in 11/07 when I went on Medicare & was concerned about cost of Micardis. Since that time I've put on 10 lbs. and had increased pain/muscle fatigue and general lethargy. Unusual, as I've exercised 4-5 days per wk. (incl. aerobics/strength trng/flexibility.) for 20+ yrs. Also, frequently, have problems swallowing pills due to feeling of obstruction in esaphogus tube. In July '08 I awakened to slight numbness/tingling in lips and my lips then proceeded to the swell to the point of pain and my lips (in profile) protruded further than my nose. I received steroid injection and prescription for steroid pack. Diagnosis was possible allergic reaction to new cosmetic product. Today (9/3/08) I woke up with the same symptoms and again had to go to the dr.for a steroid injection & meds. Diagnosis this time (different dr.) was possible side effects of "blood pressure meds." Has anyone else experienced edema of the lips, wt. gain, and problems swallowing?

I was on SSRI's for a while (lexapro, zoloft) when I finally couldn't take the tiredness, weight consistency, and NO sex drive. So I tried Wellbutrin SR 150 2x a day. Started off at 150 for a few days and felt like I was given a new life! I had never felt so good. Then it was time to increase my does to the 300mg. I started getting headaches, dizziness, my ears are ringing so bad I can't hear very well anymore. So I went back down to 150mg per day. I don't feel as tired, but it's still there. The ringing won't go away and I am still dizzy. The funny thing is, is that I can almost guarantee it's the same time everyday. I get the dizziness and headaches around 3pm, they go away(most of the time I have to lay down) and by about 5pm they're gone, but by about 10pm they're back. And it happens every day like clockwork. I like the way I feel (minus the headaches and dizziness, and ringing) my brain doesn't feel "numb" like I did on the Zoloft or Lexapro, and I have lost a few pounds which doesn't hurt, but I don't think I should feel like this everyday. I want a medication that I can feel good on without headaches and dizziness. And PLEASE no ringing in the ears. It's good to know that other people are experiencing these side effects, I really thought I was the only one.

I had my Mirena placed in Jan. 11, 2008. I had my son Sept. 20, 2007. Since I had it placed I gained over 15 pounds, after losing most of my baby weight. I had continuous bleeding for about 4-5 months and than really bad odor started that medication didn't cure. I have very dry skin and unusual amount of acne, I've always had pretty clear skin. I've had a noticeable amount of hair loss and regular headaches. I've also had really low energy and different forms of depression and irritability. Also the biggest thing that really bothers me is I have very low to almost non-existent sex drive.

I just called my doctor tonight to schedule an appointment after doing some research on my symptoms. I will never get an IUD again.

My son has been taking Singular for a few years for mild asthma and recently in the past few months all of the sudden he has been having a hard time falling asleep,anxiety at bedtime taking hours to get to sleep with me having to stay in the room. We took him to his pediatrician who ran blood tests and referred me to a sleep specialist who suggested he may have OCD or Anxiety. I just thought it was just something that would pass after 4 months it still has not passed. I am removing him from Singular TODAY. After all these visits with these doctors who knew he was on the medication and never said anything to me about possible side effects . I cant believe it took an article my husband saw in the paper for this to come to my attention.

I just read an article dated 9/1/08 that stated that the American Lung Association just cleared Singulair as causing depression and suicide. They had researchers study the results from the original test trials because they are supposedly more accurate than after market reports. The article is at ******. I cried when I read this report. My now 8 year old daughter has been on this medication for mild asthma since she was 4. We have thought the stomach aches and tantrums were related to moving to a new town around the time she started taking singulair. But, 3 months ago, she all of a sudden started having depression, ocd about germs, afraid she might hurt herself and then depression and suicidal thoughts. She has been off meds for 8 weeks and still has some problems with thinking she wants to hurt herself and feeling down. She is normally very happy and our family is happy and normal, but dealing with this is difficult. How long does it take to get out of their system?

I have been on simvastatin for about 1 month. I have some stomach discomfort and what bothers me most is the awful taste in my mouth in the morning. I take this medication before bed.

I have been on Lisinopril for about 10 months. I have really not felt well the whole time and have developed some side effects that i have gotten use to and just lived with and couldn't figure out what was wrong with me. I had fatigue, problems concentrating, headaches, chest pain, blurred vision, body aches and overall didn't feel like doing anything. I also noticed a small rash on my stomach/chest when i would get out of the shower but figured it must have been soap or something. I even tried not using soap and it would still be there. Friends and family started telling me I never feel good etc. So about 3 weeks ago I got really sick with diarrhea, nausea, vomiting, chest pains etc. Kept thinking i had a virus or something. A few times i was so sick I layed on the floor wondering what is wrong with me. Finally got into my doctor today and he also said it was a virus. A few people said they thought i was my blood pressure pills including my chiropractor. The doctor ran a sleu of tests today and i should get the results tomorrow. I have also had itching all over my body and a vaginal infection so i thought that would not go away. From reading all of this I realize everything is a reaction to the medication and I did not take a dose tonight but 2 benadryl instead. I always noticed throughout this that i always felt better towards the evening of course because that was when my medication was due. I will not be taking anymore of this and I am not happy that so many people are being given this everyday without any knowledge. Thank goodness people are responding and telling their stories so we don't think we are going crazy and hopefully feel better and maybe save a life!

I think some of the severe symptoms reported here are just that.. severe, and as advised on the drug information insert they can happen, and should be reported to your doctor. We are led to believe our doctors will stop the meds and try something else. If they are not willing to do that, or try to convince us it's all in our heads then... we should stop the meds ourselves and find another dr. These side effects are real, and scary. I've stopped cholesterol meds for that reason. I don't need a dr. to tell me to stop... I know my body, and how I feel and know when something isn't right.

I've been on Lisinopril for two weeks now. I was initially on the diuretic Hydrochlorothiazide, but had so much arrhythmia that I thought my heart would jump out of my throat. The dr. discontinued that after less than a week, and put me on Lisinopril. I am a bit dizzy sometimes, and do have a mild cough, but I had the cough before the meds so I can't really blame it on that. However, for all those with the problem of coughing and headaches... I read at drugs.com that you should take this medication with a full glass of water, and drink lots of water throughout the day. This tip was not in the drug handout and I thought that odd. Something so easy, and yet left out. Luckily, I drink water at my desk all day at work. This weekend while home I didn't drink water and had a horrible headache the entire time. I never connected it until I read that you should drink lots of water. Back to work today and drinking water and my headache is gone. It's worth a try, it might help. My husband is on Lisinopril/HCTZ combo, has been for at least 3-4 years with no adverse side effects.

We are all different, medication effects all of us in different ways. I hope I never experience the kinds of side effects I'm reading about here. If so, I'll be off the drug in short order. My dr. told me there are loads of other medications we can try. While there are side effects to everything we take, mild is ok but no one should put up with life altering and/or life threatening side effects like what I am reading here.

My husband has been prescribed Meprozine for a back injury, and since he has been on it I have notice a major difference in his moods, he is edgy, and temperamental. He has started yelling at my daughter for stupid kid stuff and arguing with me over small things and we never argue. He has had weird dreams and twitches in his sleep. When he is on the medication he doesn't seem like the man I married and when he is off its like hes going through withdrawals and trying to go un-noticed. He is also on Soma and Zanaflex. I don't know what to do. Im worried for him. He is also becoming depressed, and has had a severe migraine for 3 weeks now. He wont listen to me when I tell him not to take it. I would not recommend this medication to anyone, especially if they want to keep their relationship.

I have been on Synthroid since 1983--varying dosages. Side effects have included: weight gain, heart palpitations,adrenalin misfires, extreme reaction to heat (sun burns) and body feels hot all the time, fingers go numb in cold weather. Just recently have not been able to regulate dosage--fluctuating between hyper/hypo. I would like to try a new medication with few side effects. Anyone had any luck finding a different med that works?

started taking simvastatin 3 months ago after having a stroke straight away started feeling nausea and diarrhea was told at the time while still in hospital it was probably the tablets but nothing was done about it, since then i have been back to the docs twice, had 2 different types of anti sickness pills, none have worked, which is worse when awaking in the mornings, when i run gagging to the toilet, plus diarrhea tablets, which i am having to take at least 3 to 4 times a week, was told i could not stop taking the simvastatain tablets as i needed them, surly i am not supposed to live my life feeling constantly sick and the rest of the time sat on the toilet, plus panic attacks and depression of which i am also on medication for and my migraine attacks have gotten worse. and a awful taste in my mouth all the time all in all not a happy bunny

I apologize that the summary is not ready yet. At this time, I am inclined to believe that the FDA will "black box" Singulair. Maybe, I am just hoping but we will see. I also believe that the FDA will also investigate the entire category of drugs with genetic components and warn doctors that these drugs do NOT behave AS EXPECTED when the patient has a genetic variant.

I am posting this again.

I just wanted everyone to know that I am still here and concerned about everyone who is having side effects from Singulair. Sometime within the next few weeks I am going to post a summary and conclusion about all of the research that I have posted. I hope to come up with a well organized concise statement about why everyone who experiences side effects from Singulair should stop using the drug immediately. Not everyone has an adverse reaction to this drug. For those who do, it is very dangerous to continue this medication even for one more day. STOP IMMEDIATELY IF YOU SUFFER SIDE EFFECTS FROM SINGULAR. WHEN YOU SUFFER SIDE EFFECTS FROM SINGULAIR, THE REASON IS THAT YOU ARE NOT COMPATIBLE WITH THE DRUG'S GENETIC BASED MODEL. Singulair targets the CysLT1 receptor, which is a gene. This gene is not the same for everyone. If your doctor does not understand that the mode of action of Singulair has a genetic component, then tell him/her.

I've just started taking sertraline a couple months ago, I've worked up from 25mg to 100mg, and I see a bit of difference in my mood levels. The best way I can describe it is that my low points aren't as low as they used to be and my general level of anxiety has eased. I just recently changed over to the 100mg dosage a couple days ago and I'm feeling what I hope to be the initial numbness, which I hope will go away soon. One thing that is fairly concerning is that I havent' been able to cry since I started on this medication. I'm usually prone to crying jags during low points and within the last couple of months I havent' had one or had the urge to have one.

I think it's from my inability to stay concentrated on a single subject for a period of time, like others mentioned, I've noticed that I zoloft has decreased my attention level. Eh, but I"m not sure if the fact that I can't cry is a good or bad thing, we'll see how everything turns out once my dosage is stabilized.

HI, I am a 56 year old woman with elevated BP. I was put on Lisinopril/Hctz about a year ago. I am not exactly sure when the cough started, since I am an asthmatic and have trouble with coughing already, but this cough is different and much worse than my asthma coughing. I like many others on here cough in the night and mornings until I vomit, cough up fluids, gag and can't breath. The cough was so bad on Friday I broke the blood vessels in my face, the coughing spell lasted for 30 minutes. It was just yesterday that I looked at the Warning for this medication as I picked up my refill on Friday. There on the warning was dry cough. So I looked on this site and there was my answer...most of you described exactly my symptoms....I feel so much better now that I think I know what has caused it, since my doctor was chalking it up to the asthma. I have emailed him with my new info, and hope that he will change my medication ASAP. I also have researched cronic fatigue sys....because I am always tired and unable to get anything done.....I was never like this before. Good luck to the rest of you, thanks for sharing or I would never know that this medication could cause all my problems.
DL