Relapse symptoms and conditions

I have been prescribed a 20 day course of flagyI. I was prescribed this med for a uterine staph infection caused by an iud...as you can imagine I was ready for any antibiotic that would bring relief. I tried a few antib's (Cipro, Macrobid, Doxycyline) before flagyl while the drs waited for the culture to return from the lab...flagyl brought immediate ( 24 hours) help with the staph but causes metal mouth, a woozy feeling and a strange aching in my feet. In my situation the side effects are worth it...Also the severity of the side effects have been temporary, as the bacteria die off the toxins they leave behind will leave your system and ease the side effects. It is important to replenish your natural bacteria while taking antib with probiotics in yogurt and supplements this helps me with the yeast problems also taking Caprylic Acid and coconut oil have kept yeast under control. Stopping your antib treatment before the course is through can cause a relapse in your symptoms worse than the original illness and can cause antib resistant bacteria...MRSA (bad stuff!!!) I hope this helps you.

Thanks everyone here for your comments. I experienced severe insomnia, restlessness, and anxiety while taking Flomax. Also, stuffy nose, swollen throat, and shortness of breath. Since insomnia, restlessness, and anxiety are not widely reported side-effects of Flomax, at first I didn't think that was the cause. Instead I thought I was having a relapse of the major depression that I recovered from 10 years ago, which began with similar symptoms. That scared me! Then I talked to my doctor, and he told me to STOP taking Flomax. I did, and within 24 hours, the insomnia and restlessness are gone. I don't know what our next treatment option is going to be, but it sure won't be Flomax. Flomax had me flummoxed!

Hello ladies. I just wanted to share that I got my MIRENA taken out about 2 hours ago. I didn't feel a thing when she did it. Since the dr. tried so hard convincing me to leave it in ((that these symptoms were all in my head)), I made her show it to me just to make sure that thing was gone from my body!! I'm not bleeding and feel no pain as of now. I think even if I were, it still would be sooooooo worth it to have that thing gone. The only thing I feel now is RELIEF!! I'm excited and very much looking forward to having myself back. I just want to thank everyone so much for their stories on here and wish you all luck. I thought I was going INSANE, but it was just that "personality killer" they're calling MIRENA doing it to me. GOODBYE EVIL MIRENA!! HELLO TO BEING NORMAL AGAIN :)

I've been on it for about 2 months, the first month nothing really happened...but the last month its just been getting worse and worse. Light headed, sweaty hands, cold feet, tinglinging in the fingers, heart palpitations, etc...the worst are the heart palps, and light headedness (I feel like I might pass out right now!). I stopped taking it today, my last pill was yesterday morning, so hopefully the side effects will subside today or tomorrow.

for those who went off the drug, how long did it take for the side affects to disappear?

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!!!!

I am trying to find out if there are any law suits filed against the makers of this horrible medication. Does anyone know of any??

I stopped Lisinopril 40 mg Aug 28th after reading comments from from this site. My life has changed drastically -- I am "ME" again. I started in Feb 2006 at 10 mg and gradually increased to 40 mg in early 2007. I became increasingly tired to the point of severe exhaustion which started with a hoarness of voice and instantly all energy just drained from my body. I became depressed in a way I knew that medicine would not help. I had diarrhea that seemed to me was caused by a change in the GI medication that changed because my insurance would not cover the one I had been on for several years. My family became concerned about my confusion, loss of caring about just about anything and refusing to leave the house only when really necessary. I was tested etc. for so many times and all tests were normal.
I am still having some relapse into the above problems especially when I get really tired but I am tired because of overdoing. I am having so much fun living again.

I took paxil when I was around 24 years old. The stupid psychiatrist (who was so cold, and never smiled, and then asked me to tell her how I felt) at the time never warned me about NOT stopping it cold turkey. So one day I did stop and I experienced symptoms already described by other people: extreme relapse into depression and anxiety, felling like I "wasn't real", social phobia, agoraphobia and feeling suicidal. Now I am on Effexor and my doctor says "there are no withdrawal symptoms". I was put on Effexor due to a diagnosis of major depression last 6 months ago and I believe it was all precipitated by hormonal birth control. All the doctors and psychiatrists I spoke to about the possible link between hormonal birth control and depression and anxiety told me there was no link (or that it was very rare). I hate the attitude of the medical community:(

I have had alot of the similar side effects with the mirena as have the rest of you. I had it put in sometime in June 08. My doctor said it was my only birth control option because i had a blood clot last summer after i had my baby. So i went with her on it, i had it put in, well right away, i started bleeding, constantly, and still am, cramping, im so tired, ive horrible mood swings, acne,bloating, and back pain. Ive associated the mood swings with my bi-polar disorder, i thought i was having a relapse and started taking my meds for it again, which i am so glad i found this site, because now i know it was the mirena. I went in the middle of sept to have my mirena checked out and i told my doctor i wanted it removed i couldn't handle the mood swings or the constant bleeding. She told me that the mood swings had nothing to do with the mirena, and that she could give me some pills to stop the bleeding, that where i had got the mirena put in my body was out of sorts and needed some medicine to get back in to a rhythm. I said okay. Well i took the hormones for a week, that ended Wednesday night, and here it is Saturday and im bleeding badly again, and cramping so bad, i can hardly sit here and type, so i am defiantly calling Monday to get it removed. When i went in last time she couldn't even find the mirena, i had to have an ultrasound, its been traveling upward in my uteras, and theirs no strings on it that they can see, so i have no idea how they are going to remove it, and i pray it don't take surgery. This is the biggest mess i have ever gotten myself into. I so wish i had done some research on this, besides mirena's pretty little website, before i had gotten it pt in.

daily headaches, waking every hour till 2 am, vision, but mostly the headaches are what are bothering me the most. This is my second time on methadone. the 1st time was 8 months start to finish with 3 years clean then a relapse. I realized that both times I had headaches. Why the headaches? I feel like I am losing it. I'm trying to be a wife, mother to 3, independent rep and so on. Am i alone?

What a Godsend this website is. I am a 48 year old female, and I have been taking Advair (the lowest dose) for about 2 months now, with steadily worstening side effects. Although I have to admit, my first dose of Advair was like a much need "breath of fresh air", the side effects are not worth it. In fact, I just got off the phone with my doctor, telling her I will no longer be taking the Advair. These were the side effects I have experienced: rapid heartbeat, rib pain, joint pain in my legs and fingers, loose bowels, and a noticeable change in weight / body shape. I have always been complimented on my tiny waist and flat stomach, but as of late I have noticed my waist size increasing, despite my usual exercise. In addition, the most serious and most disturbing side effects are insomnia and the onset of severe depression / anxiety / paranoia. I had issues with depression as a young woman in my 20's with anorexia, with no relapse until I began this medication. Yesterday, I had to pull over to a store parking lot to cry for no reason! If it were not for this website, I would have blamed myself for some sort of mental weakness or unhealthy thinking. Also, I have never experienced anxiety in my life, and while on this medication I have had several episodes of intense panic, where I was convinced I should immediately draft a last will and testament. My vision has been blurring in and out considerably, my voice sounds as if I have larynxitis daily, and I have also experienced profoundly increased thirst and urination. I have not had my blood pressure checked, but I feel like what must be an increase in this, as well. Lastly, the past few days I have noticed severe hair loss, which, until I read this website, I attributed to my recent dieting. (I have been desperately dieting and increasing exercise to try to regain my figure that this medication is apparently ruining. Until this time, I have weighed the same and had the same or stronger body than high school school (5'4'', 115 - 120 lbs.) God bless everyone who has contributed to this website to educate others about the horrors of this medication. My doctor wants to see me to "give me something else", but I am going look into alternative therapies (yoga, breathing exercises, teas, etc.) The comment that made the most sense on this website was the person who wrote "break up with your asthma...begin by taking a deep breath and telling yourself you no longer have asthma." Also, I have seen that God / Jesus can heal anything, so I am going to turn to Him in prayer instead of the doctors. After all, Who created our bodies to begin with? I will add you all to my prayers, and that God will help us all heal from this... both the asthma and the suffering created by Advair.

Hi All - I have been off prednisone for one week and I am not doing as well as I thought I would be at this stage. My symptoms are not flaring, which is a very good thing but I am so tired and feeling very depressed and low energy. I thought I'd feel great once I was off the evil prednisone but so far I am feeling almost as bad as when I was on it. My moon face has not started to go away, which sucks, but I guess I have to be patient. I am so tired of this situation as it feels never ending. Part of the problem is I have continued to work throughout my ordeal, and it's been very hard at times to carry on like a normal person who is not sick. I have been sick since last November (with an autoimmune disorder) and I had really hoped by this time that I'd be on my way to being better :( Prednisone saved my life but the side effects are horrendous, as are the after affects of it. Good luck to all who are taking it. I share your pain and frustration.

My son has been on Concerta 54 for 2 years now. His grades have drastically increased and his attitude is great while he os on the meds. I do notice that he comes down from the meds in about 8 hours and his relapse is not fun. He becomes extremely emotional and violent. He will cry at the drop of a hat when things do not go his way. He also wants things to perfection. I also notices he picked up some bad ticks like popping his knuckles or clearing his throat. He is very negative when he comes down from the meds and has a hard time falling asleep.

age 72 had MI angioplasty and stent.On lipitor for 3years but recently noticed increase in muscle and joint pains and then lightheadedness and walking unsteady and tending to go slightly from side to side.Also a tendency to have nasal congestion.I am an MD and will stop the statin and assess the progress.

What side effects? I have taken Lamictal for 6 weeks. I am on a steady dose of 100mgs. I started out with severe depression (unipolar), and have also been diagnosed as bi-polar and borderline personality disorder. So who knows what I have other than to say that I have felt like a train wreck for 3 yrs. All the other meds I have taken did not help my constant cycles of severe depression. I felt like I was in a fish bowl and the world was going on around me, I could see it but was not a part of it. It was hell on earth. Other meds would help somewhat on certain symptoms, but nothing ever brought my life back to a level where I could say I felt joy and was truly happy until I started Lamictal. 2 weeks into the start of Lamictal (50 mgs), I woke up to a miracle. I realized I felt joy, I was laughing without trying to. I felt refreshed and prepared to go out in the world and face the day with a positive outlook on everything. My side effects so far have been nil. Not one thing...no pain, no headaches, no weight gain, no memory loss, no dizziness, no hairloss. Am I the only one? I know these meds effect people differently but wow, I am in heaven. I hope all of you eventually find something that works for you because I really felt ( before Lamictal) that I would never feel good again! Hallelujah! I do! bless you all!

wow, reading these posts made me realize that i'm not alone in this. I was fine the first few months of being on Yaz, but then i started to become depressed, gain weight, have tenderness in my breasts and nipples, and feel like i am constantly bloated. I went to the doctor for a physical and talked to her about the depression, which I thought was a relapse of post partum depression. I am on lexapro now and emotionally feel like myself, but maybe it was the Yaz all along. I'm calling my OB tomorrow to see what else there is.

What's the safe replacement drug for Singulair? I took my son off it before and he had his worst asthma attack ever. I see all the same symptoms in my son who's 9 and has been on it for 4 years now. It's so scary. We're off to the doctors to see what can be done. My Pharmacist has never indicated that there was ever a change in the side effects to Singulair. Thank you for all your helpful postings.

I have only been on Singulair for allergies for 4 days. This was added to my Symbicort inhaler (for maintenance) along with a Proventil inhaler (rescue inhaler). About the same time I changed my make-up and facial cleanser. Day 2 of the new meds...Singulair and Proventil I have developed a breakout of hives all around my mouth, jawline, chin, and upper neck under my jawline. I seriously thought it was the makeup and soap until I read some of the posts here.

As for other side effects, only a headache but that seems to be after the Proventil puffs.

I am 30 y/o and only recently found out that I have asthma and severe allergies and probably have my whole life. The last 7 years have been hell, with one "upper respiratory infection" after another.
Thank goodness I found a new doctor who took the time to find out what was really wrong with me, but I am upset that he prescribed the Singulair, as he should be aware of the side effects.

As of tomorrow I am done with this drug and we will see if the hives go away. I do not want to get to the point that some other patients have gotten to, with the stomach pains, moodiness, etc.

I only the last year got the depression and irritable bowel syndrome under control and do not need a relapse.

Thank you to all who post and God bless.

Hi I'm 26 years old and just started 60mg pred treatment for Kidney condition called Nephrotic Syndrome. This is my 8th Relapse since i was 7years old.

Started Tabs 27th Dec and now they are really kicking in with side effects! I have a beautiful little boy and just got married and was soooo Happy. Now I'm feeling so depressed, I cant sleep , My Face has started swelling and I've eaten all inside my mouth cause I'm so hungry!! Been having a few Cramps but nothing like I've experienced in the past.
I'm trying to reduce the tablets myself so I'm not on them too long but its just not working!
I just WISH I could stop the moon face I'm developing, Its the main problem for me (causing depressed thoughts)

Update - 7th day with zero Toprol. Feel just awful... Breathing has not improved, tight band feeling around chest keeps coming and going like before. B/P spikes, headaches, etc. The Diovan (80mg) was making me cough and making chest tightness worse - so she tried me on Dyazide - made me dizzy and sick to my stomach. This has been just one of the WORST experiences of my life. I was SURE all my problems were related to my (4) years on Toprol - but on day 7 with NO TOPROL and not feeling better I am depressed, discouraged, and just want to curl up and cry and cry and cry. I have ended up in the ER three times since the weaning began - once for breathing, once for pulse (over 215) and once for severe abdominal pain. My family thinks that I am 'mental' and that it is all in my head???? I cannot take much more of this.....

O>K> here i am again. After taking Levaquin back in the spring I SUDDENLY developed a severe case of arthritis!!! Imagine? I had a UTI and then wham!!! Can"t walk joint painb beyond belief! Now it"s Almost November and my knees are still killing me and my hands, the joints are so swollen,. The doctor can"t understnad why this happened. She sent me to a rheumatologist and my counts went so drastically up he thought the lab test was a mistake. ThankYou, Levaquin!!!! Marsh

I have had my third relapse of mania and will be on geodon for life. It has been a godsend and no side effects i can tell except when i take 80mg at night i get wobbly at some point when i stand up. During day i take 20 mg as I am still on 6 mg of klonipin, hoping to taper off by end of year. Geodon has been a godsend

My daughter is 5 years old and has been on singulair for 1 week. i have already noticed a dramatic change in her behavior. she has become irritable, mean, nasty, and emotional. she has had me in tears on a daily basis. she has turned into a monster. we will be calling the doctor in the morning!

Hello- I was Dx with Sarcoidosis in February, 2007. My lung specialist put me on 20mg Prednisone, increasing to 40mg within two weeks. My Sarcoid symptoms were from enlarged lymph- extreme trouble breathing, middle and lower back pain, kidney pain. Within a week of being at the 40mg level my heart rate and BP became so erratic that he had to start weaning me down. Initially I had extreme energy which felt good after suffering from fatigue but was short lived due to the cardiac problems.

The Prednisone has resolved much of my inflammation for the Sarcoid but I will not go on this again. I have been weaning now for over three weeks. Down under 5mg of Prednisone and it is almost unbearable. Each time I took a drop my mental symptoms became intolerable. Anxiety, extreme fatigue with extreme weakness, irrational thoughts, blurred vision. Within the last couple of days I could hardly get myself out of bed. My weight has increased steadily, bloating stomach, stiff joints, skin rash.

My biggest complaint is that doctors are not giving us enough information as to how this will affect from a negative side. Yes, it takes care of the inflammation but no one prepared me for these awful side effects and withdrawal symptoms. I feel like a nut case most of the time with no coping skills.

Hi, My name is Scott and I am 58 years old. I had a severe case of Bronchitis four years ago. I was so sick my Doc. sent me to have a chest x-ray thinking I might have pneumonia. He prescribed Levaquin...one tablet a day for 30 days. I immediately started taking the antibiotic. I was so sick I did not realize any reaction immediately. I just felt horrible, but attributed it to the bronchitis. The infection started to come under control, but I was starting to feel worst physically. I got so bad my wife took me to the emergency room. I was slurring my speech, my muscles ached, I had night sweats and I lost my coordination. It had also affected my memory...both short term and long term. The physician who saw me at the hospital was 99% sure that I had suffered a stroke. I was admitted to the hospital and spent 3 days undergoing blood-work and testing to see if they could determine what was happening to me. Upon release I was sent to a neurologist and had MRI's of my brain. All came back negative.

I took the medicine for 26 days before it dawned on me that it could be a reaction to the Levaquin. I went home and researched Levaquin and was blown away by what I read. All of the weird symptoms I had been experiencing were right there in front of me. I immediately stopped taking the antibiotic and within days started to feel better. I continued to get better until I was feeling almost normal. This took about three weeks. I still experienced problems with my memory and had residual effects with my coordination, but otherwise felt 100% better.

Approximately three months later I had a severe relapse. It came out of the blue. I was not taking any medicine, but was taken to the hospital and admitted with the same symptoms I had experienced before. Again the Doc's had no idea what the problem was. I did explain about my reaction to the prior use of levaquin, but that was dismissed as not probable and they released me after three days with no idea what was wrong.

I continued to have relapses for the next 2 1/2 years, every three or four months. Each time was not as bad as the last. Finally I traveled to Boston and saw a very well known neurologist who explained that he had seen this before. He called it a post infection syndrome. He was the first person who agreed that it was a reaction to my long-term use of levaquin. I finally felt vindicated!

If you check the manufacturer warnings online, you will see that they do know about these reactions. It a small percentage so they think the benefits out way the adverse reactions of some patients. As a person who has suffered with these reactions, no percentage is worth the risk!

For those of you that are experiencing adverse effects, there is hope at the end of the tunnel. It does take time, but it does get better. I can live with my memory problems and although I have some residual muscle and tendon problems in my legs, my life is almost back to normal. I have not had a relapse in the past year.

Good luck to everyone and keep the faith!

Scott

i started taking seroquel about 2 years ago, and with being steadily increased in the dosage i have gaine 100 pounds, and i cannot lose anything. I have tried every diet out there, besides surgery. I am afraid to go off them because i have insomnia and deppression, and anxiety soo bad that i can never sleep. and now in reading other persons' effects i am starting to wonder if all my other problems are an affect of this medicine. I take 800 mg. a night just so i can sleep 7-8 hours. How crazy is that??? i am so afraid...