Beats symptoms and conditions

I have been on Lisinopril 20 mg for the past 9 years. I can't believe I have taken it for such a long time. I noticed some strange chest sensations 2 years after taking it but pushed through it. Then I developed breast cancer and went through the chemo and radiation while continuing to take it. In the last 2 years and more recently in the last 3 months, I felt so many skipped beats that I had to check it out and I also have had significant hair thinning. I had a holter monitor, resting EKG, lots of bloodwork and was told that everything was normal. Normal???? Then why was I feeling so rotten and scared every time my chest decided to heave or get funny sensations in my throat. Doctors do not want to hear these types of complaints especially when you think it is related to a medication that they ordered.
So I decided to try an alternative approach. I have been taking fish oil, coenzyme 10, cholesterol nutritional supplement, Vit C, Vit E. I started these about a month ago while still taking Lisinopril. I finally stopped the Lisinopril yesterday so I'll see if I have any improvement of my symptoms.I also went to a website that showed 1% of people can have skipped heartbeats while on Lisinopril Here is the URL
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Hope this helps many of you who have similar episodes. MHS

this is probably the worst thing Avelox caused, besides death, which would have happened without help..

7th day on Avelox for sinusitus - massive pain back of my head, sweating so much my clothes were soaked, threw up 2 times, legs were uncoordinated when trying to walk

Called 911 - paramedics took blood pressure - guess what.. 210/180.. something was definitely wrong. Rushed to hospital - passed out in ER - woke up with wife and family present - CT scan found my brain bleeding and brain surgery was performed to remove the clot..

But wait, it gets better... 2 days in the ICU my brain swelled from the surgery and the fluid stopped circulating.. I was semi conscious in the ICU for probably 4-5 hours and nothing was done. My wife came in early in the morning and thought I was sleeping, but could not wake me.. The nurse said that a doctor was called and will be there later. I'm DYING right before their eyes in the ICU!!! My wife demanded I get a CT scan immediately. If she didn't I would have stopped breathing. Later CT showed my ventricles enlarged with fluid backed up so much that my brain and brainstem was ridiculously squeezed so much, my head was all ventricles and barely any brain showing in the CT. I attribute my current brain damage to this episode.

A shunt was placed in my head for about 3 days.. basically a needle is inserted into my brain and left there to drain the excess fluid.. After my condition stabilized, the shunt was removed.

Spent 1 week in the hospital, then transferred to another hospital to stay in for inpatient PT and treatment. I didn't know left from right, had double vision, was throwing up constantly, was hot, then very cold, my legs hurt, had hallucinations (was believing certain things were happening, that really weren't) was incontinent, had a new catheter inserted every single day, was taught to walk again, had to use a wheelchair.

I had always been healthy, was vegetarian and did not smoke cigarettes.. I exercised regularly, did not use drugs (i.e. - cocaine or methamphetamine which can cause high blood pressure leading to a stroke)

Didn't know what happened to me, but realized I had to be there.. After 1 month, decided to go home (the hospital was becoming too stressful, somebody was always screaming and yelling at night and the daily catheters were uncomfortable), to be back in the lifestyle I knew.. my wife, my granddaughter, my house, my dog, cats, and other pets were sorely missed.

Once home I found that I couldn't do what I used to anymore - could not mow the lawn, drive, speak well, walk properly, had double vision, a tingling on my face, a metallic taste in my mouth so bad that good food tasted bad.

My wife set me up for physical therapy three times a week daily outpatient at the hospital I was at. Vomited regularly from the daily dizziness.

This was most disturbing, I developed a pain in my left hand and left shoulder, to the point where I could not raise my arm above my head and had to sleep with my arm straight down for at least a year. After playing guitar for 30 years, I found myself unable to play my guitar anymore. My left hand had lost all its dexterity and was not usable. I did not realize what happened to me until my wife explained the entire thing to me.

In the next few weeks I spent each day trying to put "2 and 2 together" and figure out why this happened to me. When doing research on strokes, I realized that certain things happened to me that were not consistent with having a stroke. In my brain damaged condition, I remembered taking the antibiotic Avelox, based on a physicians prescription. I researched the adverse effects and to my amazement, the listed side effects were consistent with what happened to me.

I began a quest to file a lawsuit - was unable to find a lawyer willing to tackle such a huge case.. although one lawyer did file before the 2 year time limit expired.. I had MRI's performed on my hand and shoulder which revealed scarring and previous ligament tearing.

During the time of having more outpatient and in home therapy, I regularly visited a psychologist and my physician confirmed that the Avelox most likely caused the brain bleed, tendon tears, and other mysterious symptoms when I presented him with my research. I was unable to work and my only income was from monthly Social Security Disability benefits that didn't begin until 6 months after the incident.. leaving me with no income and unpaid bills for 6 months. The mortgage payments fell behind and soon foreclosure notices arrived. We decided that an alternative would be to sell the house.. it could not be sold after 1 years attempt, so my wife and I moved to an affordable apartment. I put household items in a storage facility. I either sold to pay bills or threw away much of my personal things,since I was devastated by what happened to me, I didn't think I was going to survive long after reading statistics on strokes.

While in the apartment, I needed an income and was forced to take what was in the scpoe of my limited ability. I accepted an early morning paper route and then made deliveries for a courier company using my own vehicle.. That was a 12 hour work day. Being completely upset over what happened, losing everything including my house.. I decided to attempt to escape the overwhelming things that happened and were still happening. I found a house for rent that was less than the apartments rent, except it was in North Carolina. At the time that seemed perfect, a 3 bedroom house located in a far away place where I could forget everything that happened and make a fresh start. Only problem is my wife not want to go, but I was adamant upon doing it. She helped me move everything, including all storage items.. I had moved to North Carolina, but soon found being alone and unable to find suitable employment unbearable. I was being contacted for back rent owed, but could not do everything alone - I became more depressed to the point of feeling suicidal, so I called my aunt in NY and she said just leave everything and get myself to her house. I did, leaving everything behind, and stayed with her for a month until my cousin invited me to stay with him.. which I did. I stayed with him for 3 months, all the while searching for employment.

With help from my family I moved back to my familiar area in NJ in the summer of 2008. I had lost everything..unable to be physical with my wife and being seperated for 18 months, she has requested a divorce. Currently I live by myself and am still slowly recovering, yet my left arm and hand are uncoordinated, my talking is difficult, slurred and gravely (diagnosed with dysarthria), my balance is bad and am dizzy every single day for the past 4 years.. Although brain damaged, I am attempting to rejoin the computer support business again.

My entire past, everything I knew and did, everyone I knew, who I was, etc.. is all a strange hazy memory. If I don't take a sleep aid, I wake up around 4am with racing thoughts, unable to sleep.. My depression and anxiety are so bad, it is difficult to function and interact with others. My psychiatrist has diagnosed me with post-traumatic stress disorder and prescribed Zoloft and Xanax.

Upon proper research, I have to blame the prescription and subsequent use of Avelox for causing the brain bleed which led to my life being completely and utterly destroyed. My intentions are to file suit against the manufacturer Bayer and/or the hospital for allowing me to die in the ICU

My 13yr old niece has always been a healthy, active and straight A student. Then on 11/5/08 during a routine physical, she received her 1st dose of Gardasil. On 11/28/08 she started to complain that she felt weak and had a headache. Since it was 2 days after Thanksgiving we thought that she was tired from all the holiday activities. On 11/29/08 she had a headache and stayed in bed all day. She got up that afternoon & had 2 seizures. She was rushed to the ER.
As of today, March 8, 2009 she is still in the hospital in Intensive Care Unit. She has been in critical condition since. Within 2 days after her seizure, she lost the ability to eat,speak,walk and communicate in anyway. She is completely unresponsive. She is on the ventilator, she is basically in a coma. We do know she has an viral infection with a shadow on the left side of her brain. All of the testing that has been done all show negative for any illness or diseases.
We are still unsure if she will come out of this. This has been completely devastating to our family.
We have no answers from doctors. Even though we know in our hearts that this was a side effects from Gardasil. I don't know if they will ever fully admit it.
We are left to watch and wait. That is what the doctors tell us daily..

On wellbutrin for about a week. My heart has been more then fluttering. It has been skipping beats and I have trouble sleeping. How long before side effects subside?

I was prescribed Toprol for an irregular heart rhythm (eventually diagnosed as premature ventricular contractions) that developed suddenly when I was 54, despite an active lifestyle, low-normal weight (110), low stress levels, and low blood pressure (100/60). I felt as though my heart was skipping beats, and the "catch-up" beat was so strong my entire chest seemed to vibrate. The Toprol stopped 98 percent of the PACs virtually immediately. But within days I noticed occasional numbness in my legs, and my hands and feet turn icy cold for no obvious reason. I'm also quite tired till late afternoon (I take the Toprol around 10 p.m.), and I just feel "blah." No suicidal, but generally unmotivated. I am often sleepy--at least until around 1 or 2 p.m, when the Toprol starts to wear off. I'm not ready to stop taking it yet--though these reports are sobering--because the PACs made a normal life impossible. But I'm going to be cautious, and if other side effects appear, look for other options.

I am a 21 year old female. I have been on 25mg Toprol (twice a day) for over a year now. I was having intense heart palpitations from scary panic attacks... this drug basically cured my heart irregularity. When I first started taking Toprol I experienced some muscle cramps but that lasted less than a week. Overall I have NOT experienced ANY negative side effects from this drug. It is one of the best things I have ever done for myself. I was so scared before due to having at least 5 ‘episodes’ a day with my heart… now I may only have 2 – 3 per week. Such a wonderful improvement! It has really changed my life for the better.

OMG. I guess I am lucky that this is the first site i found! I am 22 years old and i have had Mirena since may of 2007 since i delivered my youngest son. I stopped having a period (which is great) but i started having some symptoms that were completely out of the ordinary for me. I started what felt like panic attacks, it feels like tightness in my chest with pain high in my chest. I'm having heart palpitations very often, and sometimes when my heart palpitates (it feels like it stops for a second) i partially black out. i have been attributing it all to stress because i am a full time college student with 2 toddlers and a house to run but now after reading all of these comments i'm not too sure. I have a really hard time focusing, it's like my eyes slide out of focus and i just stare into the distance. I've been having sleep trouble as well... i'm always fatigued but i have a really hard time falling asleep. My mood swings have inreased tenfold. i get so angry at the littlest things and i just can't help myself. the last and most important side effect (at least in the eyes of my husband) is that i have absolutely no sexual appetite. I find myself dreading sleeping with him because i just don't feel like it anymore. I love him dearly and I really think it's not normal for an otherwise healthy 22 year old to have zero sexual interest.

Started on Metoprolol about two months ago for a sudden onset of heart irregularity, mostly skipped beats. I'm already experiencing some of same problems described on this site. Because of that, I was looking for information and ended up on this site. My symptoms include daily headaches, inertia and lack of motivation, feel like sleeping all day long, wt gain, foggy headed, bloating and stomach discomfort. These symptoms have either started or intensified since I started on this medication. I plan to wean off this as soon as possible, with or without the doctor's cooperation. I've had a cardiac workup since I started the medication and no problems were detected.

I recently posted on July 20th under Toprol XL side effects (45-yr old Male, USAF) and at the time was scheduled for a Cardio-version procedure for Chronic Atrial Fibrillation.
The procedure was successful and I am now on Betapace 160mg twice a day to maintain sinus rhythm. The drug took a little getting used to for the first few doses, but now has settled into my system pretty well. I did experience extreme fatigue, some light-headedness, a little blurry vision (Not bad, just when trying to read really small print in magazines and stuff) and general "weak" feeling for about two days. Now (4-days after Cardio-version) I am feeling very decent and have my energy level back.
I have one of those, Homedics Wrist based Heart/B.P. monitor cuffs and I've been crusing in normal beats with great B.P. on the Betapace. In my previous posting I explained that I'm pretty drug intolerant, but so far the Betapace has been amazing! I am not on Betapace AF, just Betapace Regular. Hopefully, I can stay in normal rhythm for a long time, but we'll see I guess.
I would recommend folks with Heart Rhythm issues like A-fib try Betapace, if their Doctor says it is an option. Oh, I have also been sleeping like a baby on this stuff, which is wonderful.

I needed Metoprolol Tartrate for a very high heart rate for graves desease, I was in the 115's+ lowered too 8o beats per min. Which is great!
BUT, having some horrid side effects.
BAD night chills, intolerance to cold. Shake for 3+ hours then sweat. Feels like I was hit by a train after then I get very nauseasous and light headed
Sleep is bad, toss and turn all night and have a greater fear of the dark
ALSO, my bones hurt all the time!! Never did before, had tests done nothing there.
This is the only drug I could find that didn't make my heart flutter and feel all funky. Its a great drug for just that. All the side effects suck..bad

My BP had been slightly elevated for over a year and my doctor felt it was time for medication. He started me on 25mgs and continued to increase it till I reached 100mgs. I started having anxiety attacks, lightheadedness, dizziness and finally ended up so sick that I was in bed for three days. It was the toprol. I was only on toprol for 3months but found out that trying to come off the drug was the hardest thing I have done. I never had BP spikes before but at the end of the first 24 hrs. without Toprol my BP was hitting 200/104. I went to ER. Matter of fact, the spikes continued and I was in and out of ER until I was finally admitted for tests. The spikes were also accompanied by flushing, rapid pulse(122 beats per minute), lightheadedness and diarrhea.Many times I thought I was having a heart attack. I have seen two cardiologists, an internist and now an endocrinologist for these "BP spikes". All tests come back normal. No matter what the new medication is, nor how low my BP might stay for up to three days....the episodes still happen. My BP can go from a normal range too 200 systolic in a matter of less than 1/2 hr..........Has anyone else had spikes in their BP when coming off toprol. It has been 11 months since stopping this awful drug and I still I no answers....but I have a pile of medical bills.

I too had HORRIBLE experiences on Toprol-XL. I was put on it after I walked into a doctor's office and my BP was 235/152. Yep..you read that right! Scary times. I started taking the med, and I too gained 35 pounds with no change in diet. I was tired, weak, groggy - I honestly felt like I was slowly dying. At that point, I decided that high blood pressure was far better than the experience I had on Toprol. It ruined my marriage. Can you say ZERO libido? I decided that I would try a different form of metroprolol - metroprolol tartrate versus succinate. I did this when I went out of town - I honestly thought my heart was going to pound out of my chest - coming off this medication was horrible, and if the other posts are true about this being worse to come off than opiates, I REALLY feel for addicts now. I have been off the Toprol now for about 9 months, and I feel so much better. I've lost what I call the Toprol weight, and I made some life changes. I did the following: (A) I purchased a rebounder (mini-trampoline) and have built up from 5 minutes per day to 15 minutes per day (goal = 40 minutes per day) - there are HUGE health benefits in rebounding and it's really easy on my joints (google the benefits - I promise you won't be disappointed). I turn on the TV or turn on my Ipod and bounce away. (B) I joined Freelife International, and began drinking Go Chi juice (www.pbowen.freelife.com) because it has three scientific studies proving its effectiveness. (C) I stopped drinking caffeinated soda and began drinking a homemade blend of green (matcha) & darjeeling teas (if you want the recipe, e-mail me and I'll send it pamela.bowen@gmail.com), and (D) I bought a device called RESPERATE (www.resperate.com). I HAVE MY LIFE BACK!!! Don't think you have to live the way you are forever!

I was on Prednisone for just over two weeks for a bad skin rash (allergic reaction). I went to the ER they gave me an injection on Prednisone. The next day my Doctor puts me on 40mg a day for 10 days then down to 20mg, and then 10mg. The side effects were (and are) crazy. Blood sugar and Blood pressure are through the roof. My heart pounds,races, skips beats. Hands shaking, nervous, and panic attacks. Yeah, sure, the rash is gone, but I feel like a train wreck. I took my last dose 2 days ago, and have been told it can take 2 to 4 weeks for this to get completely out of my system and end the side effects. Can anybody else verify this?? Good god, what a mess!!

Im not wanting to scare any of you, but my reaction to this family of antibiotics happened in Spring 2002. I took one dose of this quinolone antibiotic for a sinus infection and was in the ER four hours later. After taking the medication, I felt very fatigued and lay down on the couch, I woke up a few minutes later feeling like I was falling, and my heart sustained 170+ beats per minute heart palpitations for several hours. The last thing I remember was calling 911 because I was home alone and knew something awful was happening. The ENT's said that they had never seen anything like it. I experienced horrific anxiety attacks for weeks afterward. Keep in mind I had been a very healthy gal before and had never experienced any type of health problems. I now see a rheumatologist, a neurologist and a gastroenterologist. I have been diagnosed with MCTD (Multiple connective tissue disorder) a Lupus like illness. My neurologist says that my central nervous system was damaged in the reaction as well. He also says that physicians are grossly misinformed about this family of antibiotics, and in his opinion, anyone who prescribes them for anything less than a life threatening condition is committing medical malpractice. I agree wholeheartedly since my life will never be the same.

Hello, I have been on NuvaRing for about 2 months now. I have no sex drive at all. I don't want to be touched let alone even have sex. I feel dizzy all the time, get bad headaches, my heard will beat a million beats, I get very moody and mean to my boyfriend who has been so understanding. I hate being on it and I am taking it out tonight. I hope to get my sex drive back and be my normal self. oh also since using NuvaRing i have developed acne! i have never had it before ever and now I do!! There is nothing good about this ring....I guess one positive is you don't have to remember to take a pill once a day. I am going back to condoms. forget the ring.

i am 26 years old .

I am a female, 55 years old, and have taken Toprol XL 100mg. for the past 5 years for an irregular heartbeat. The symptoms of the premature beats caused an annoying sensation in my chest that I could not tolerate. My cardiologist prescribed several beta blockers before I finally found that Toprol worked the best for me. I have suffered with leg cramps for years....even before taking the Toprol. A nurse who worked for my internist suggested that I try a calcium supplement called "Calcet". This triple calcium supplement is a life saver. I only have to take half of the recommended dosage to have excellent results.....no more being awakened at night by severe leg cramps! The product is sold "over the counter" and can be purchased in any pharmacy or grocery store. As for the side effects of the Toprol; I am sure that I suffer from some adverse reaction as a result of taking the medicine. In any case, as with all medications, the outcome is a trade-off.....one must determine if the harm outweighs the good that the medicine offers.

Weight gain, general bodily aches and pains , anxiety/panic attacks/general depression, difficulty in concentration, loss of general interest.

November 25, 2007 - I am a 42 year old woman, tall very thin, and always in good health. I was prescribed Singular for mild asthma symptoms, ie.. asthmatic cough-very mild, heavy feeling in the chest, constant sore throat (my work requires me to use my voice a lot). Initally my symptoms improved, I was thrilled! But, after about a month I got up one morning and thought I was having a stroke - my head was killing me, and my heart was pounding so hard! I took my blood pressure only to find that my normally low pressure was now 144/105! My pulse ws nearly 100 beats/min. That's just while I was sleeping! I was shocked! The only meds I was on was the Singular. I decided to do a little experiment on myself. I immediately stopped taking the Singular and kept a record of my blood pressure. It took about 3 days for my blood pressure to come back down to normal levels. I have noticed some weight gain as well. I will not take this drug again!

Here’s a little update from my last post, I hope it may be useful. The reference to snake venom set me thinking, as around six years ago I suffered anaphylaxis after being stung by a wasp on the end of my tongue. I was rushed to casualty as my head and ears swelled up. I was coved in a red spotty rash and although the major symptoms subsided after a day or so after treatment , it after several weeks before I was back to normal. I now carry adrenaline in case of a similar incident. Many of the symptoms were similar to what I have experienced over the last month, the shortness of breath, the red spotty rash ( forgot to put that in the last post. I still have the spots on my arm and back!) , painful joints, blurred vision etc….

So it got me thinking, is there a connection? It would be interesting to note if any of those posting here have similar intolerance to insect venom.

A quick Google brought up a reference to a paper by Janice L Stumpf, Nadine Shehab and Anish Patel in the Annals of Pharmacotherapy Vol 40 No 4 p699-703 titled ‘Safety of Angiotensin-Converting Enzyme Inhibitors in Patients with Insect Venom Allergies’

In the conclusions it states ‘….it seems prudent that patients with document allergic reactions to insect venom avoid ACE inhibitor therapy, if possible..’

I’m convinced that I was slowly going into a form of anaphylaxis brought on due to allergic reaction to linisopril, I now know what I will be telling my GP, as I’m sure many doctors will be unaware of this link. Make sure that if you suffer from the same intolerance that your doctor is made aware.

Hope this helps.

I went onto Topamax last year and almost died. Following the graduated increase schedule, every time my body came close to acclimating to the drug, the new dose would hit it like a ton of bricks. By the time I had reached the target dose, I was scarcely able to think, had difficulty getting out of my chair, and couldn't focus my eyes.
The schedules do not work for everybody. I was an idiot. My (former) doctor was too difficult to communicate with.

When I finally got it right, it was a tiny dose. Beats the daylights out of Depakote.

WOW I can not believe all the complaints about the mirena ...... I had one placed about 7 years ago ...NO PROBLEMS ..... Had it removed because I wanted another child back Nov 2005 and got pregnant in July 2006 !
After I had my second child in April 2007 Had another Mirena Place in June ! Love it ! It sure beats having a tubal , since I am not sure if I want to have anymore children . I had thought about having a tubal done and decided against it ! Mirena was a great option for me ! I have had 2 children I am small framed and have not gained any weight ! It may not be the right choice for all but I have have 2 placed and have had no problems !

I'm diabetic, have underactive thryroid, hypertension. On several meds including 20mg Lisinopril. I was put on 40mg twice a day beta-blocker last week after my umpteenth time complaining about exactly the same stuff as I see on this website. Have been in the hospital twice in the past year for these problems (they said I was dehydrated)...wore the heart monitor, all that. Heart is fine they say. Just beats weird now and then. I'm now goung to have to talk to Dr. about this drug. Sounds like it may be my problem. I, too, have wondered, "Am I trying to have a heart attack".

i have been taking Yamine for about a month and a half, after being on a generic pill for a couple years. I didnt know if these symptons i was having was caused by yasmine, but now i think it may be. I have been getting lightheaded, blurry eyes, shakiness, hot flashes..almost like a panic attack, and i have become very dehydrated, even though i have been drinking alot of water. I even went to the doctors for these symptons and they still don't have an answer, so i think it may be yasmine.my newest sympton as of yesterday is chest pain. also i feel like my heart is beating fast all the time, and i feel fatigued way too often, which is causing me to eat more, becauase i am starving way to often, and if i don't eat i feel like i am going to collapse. Also my sex drive has gone to non-existant- is that common? I workout all the time, and eat pretty healthy, so i don't know what else these symptons could be coming from. Is anyone else experiencing these sympons?

I am on my last shot and I am so Glad.I have had night sweats,hot flashes,sleeping diffuculties,no energy,achey and a little weightgain.I am curious to see how I feel once I am off this for good.If anyone has any ideas or any comments about Lupron let me know.

I took 500mg of Levaquin once a day for two days. I stopped taking it because of the frightening side effects that I experienced. The doctor prescribed the antibiotic for a mild case of campylobacter. I normally never take medicine for anything, but the doctor assured me that this antibiotic was very strong and would take care of my problem. However, after a few hours after the first dose I began to experience a rapid heart beat, tightness of the chest, and about once every fifteen minutes I could feel my heart skip a beat. Unfortunately, I took another dose the following day, but I experienced much of the same. I stopped taking it after that because I thought that no treatment was worth these effects. It has been 3 days since I took my last dose and my heart is still racing and skipping beats. I told my doctor and he told me that this was just a common side effect of levaquin when caffiene is mixed with levaquin. But I have avoided caffiene for days. It's very scary to have something wrong with your heart when you are otherwise very healthy. I hope these symptoms leave because it's driving me crazy!!!!