Kicker symptoms and conditions

I have been on Yaz for 3 years. I am now 39- I took it to help with Pre menstrual tension and moodiness, and mild acne. I have done nothing but shed like a DOG since I have been on it, I have no sex drive, I have gained 5 pounds, which is a lot since I am only 5ft.4 in. I just found out the real kicker... I have signs of kidney disease now, high creatinine levels, and can only link it to the use of YAZ. There is a class action law suit forming against Bayer Co., and anyone using this should check it out. They are talking about the possible RECALL of this medicine, and I would hate to think of any young girls out there ending up with kidney damage like me. Please be informed before you continue to take it.

My experience with Mirena has been awful. I had it inserted a little over a year ago (2 months after the birth of my younger son). Since then I had cramping ALL the time, significant hair loss, periods every three weeks, then every two, then every week and a half. They only last three days on average, but I go through a heavy tampon an hour. I lost a lot of weight while on Mirena, but I don't know if that can be attributed to it-just diet and exercise. I had severe bloating, depression and mood swings, complete lack of sex drive (very much unlike me), here's the kicker. When I went to get it out (last week), they couldn't find it. So after 3 ultrasounds, 2 xrays, and a CT scan, they found it. It's perforated my uterus and is floating around in my abdomen. The evil thing has gone rogue!!! I'm scheduled for a laproscopic surgery next week to find the damn thing, followed by a more in-depth surgery to remove the evil.

If you're thinking about getting it---DON'T!!!

This post is for the ladies who wonder will they feel better or notice any change after having the mirena removed. This is my own personal experience . I've had it out for about 2 weeks now after having it in for 3 1/2 years. I feel Great! I couldn't have a panic attack if I wanted to. I have had more energy, haven't had a headache. I have a returned sex drive. Sadly my hair is still very thin and patchy. The big kicker is I've lost 4 lbs as of today. My stomach now looks like I'm 3 months pregnant as opposed to 5 months. The big difference is noticed in my face and waistline. I don't feel so hungry all the time now and feel motivated to keep this going. I haven't had one heart palpitation since either. Yes I still yell sometimes, but not out of anger or rage. It's now to be heard over the yelling and screaming of my happy kids who used to cower because of my yelling that was so mean spirited and full of frustration from being so tired and feeling ill most all the time. I just worked last night 13 hrs got 5 hours of sleep today picked the kids up from school, played with them and cooked dinner to boot. I would have been in bed 2 weeks ago waiting for my husband to come home and rescue me. This has been my experience thus far and I keep posting to give those ladies hope that they can feel better once they get mirena removed. I hope others will have a positive experience with removal like I have had. Good Luck and Happy Recovery.

I got the Mirena inserted in Aug of 2008. what a horrible experience,it hurt so bad i almost passed out from the pain . at first I thought it was a great thing to have and who wouldn't when they tell you, you might not have a period. I'm 33yrs old and was on Depro-Provera before and loved it.

Since I've had this put in I have lost my sex-drive, gained 25lb, have horrible cramps, spot here and there never knowing when I might start bleeding. Then to add to it in the past month I have been having dizzy spells.

I have set it up to have this thing removed on May 12th. The biggest kicker of it all is that after talking with my uncle who is a gyno out of state, he told me the Mirena never should have been put in since I have never had children and have had a LEEP before. Needless to say I'm counting down the days until i get this stupid thing out.

I have tried the NuvaRing off and on over the past year. My journey started because every pill I tried gave me mild to severe headaches for 3 to 10 days a month. I have not had headache issues with NuvaRing -- yeah!!

BUT -- here is the kicker. I take Zoloft too. When on the pill and taking Zoloft, my anxiety was under control. When I use the NuvaRing and Zoloft I spin into anxiety mode again, almost as if the Zoloft doesn't work at all.

I am 39 and my spouse won't do something permanent. I feel really trapped.
Does anyone have any suggestions?

I took Levaquin 3 times for 10 days each time over 2 or 3 years. I am not exactly sure as I'd have to backtrack my records. It was for a stubborn sinus infection. (BTW, it didn't help) Is it possible that now, 2 years after taking it, that my tendons are 'tight' and sore from the drug? I have been complaining that they feel like tight springs for months, totally inflexible. I didn't know about this, so I decided to really stretch them. I did 4 squats and the next day, my R knee was blown up. I got an MRI which showed a torn meniscus from doing the squats. Since then, I've discovered what Levaquin does. Could it be that my tendons were so tight, that they didn't give, but the pressure from them being so tight could have put so much pressure on the meniscus, that it tore?

This is unbelievable... i thought everything that's been wrong with me, has been in 'my head', sex drive, weight gain, fuzzy vision, mood swings...

I honestly think this should be taken off the market. I cannot believe everyone's comments about this contraception. I have taken the pill over the years, depo provera, and thought my mood swings were bad then, but what really is the kicker, is the sex drive, hot flashes and weight gain/bloating.

At 29 years old, i have never felt the way i've felt on this, i've been trying to explain to my boyfriend 'it's just me' !, now i realize why.
as for the weight gain, i have always been conscious of my diet and exercise. for the past two weeks i have especially been trying to lose weight, but to no avail. hot flashes, it's insane. Please after reading this, look for another form of birth control. This should never have been approved. I took it out immediately after reading other's comments.

I am actually very relieved and excited to see that there is a connection between erythromycin and depression. I had taken erythromycin for years for acne. I found a strange correlation between taking the drug and feeling depressed. I asked both my doctor and pharmacist about this, and they both responded as if I were both crazy and stupid. "Of course not," was the reply. So I continued to take it.
I began taking it again about a week ago, and have found that I've been slipping into a very dark depressive state. This time I am very aware of what is going on around me, since I stopped taking my anti-depression medication last February (under the care of a physician and a psychiatrist) I am noting the same 'darkness' that I felt in previous times with erythromycin. A general 'nothing matters, might as well die' sort of attitude, as well as irritability and a strong desire to isolate. I started researching this morning on the internet, and I have found several links now. There have been studies that have shown a direct correlation between erythromycin use and depression.
Okay, now, here's the kicker: the erythromycin I've been taking is topical. It's a 2% solution, suspended in alcohol. I've been slathering it on my face three or four times a day. Apparently it doesn't matter if it is absorbed through the skin or through the stomach/intestines. Erythromycin causes depression in me. I don't care what my face looks like. I'm going to stop taking it.

I took Cipro many times but in November I took it with a prednisone dose pack, this seems to make the tendon issue worse according to todays report.

I have had severe achiles tendon pain for 7 months now. I can't bend my ankle when I walk. I also had surgery for a torn rotator cuff in December, no injury to my shoulder, it just tore.

I have wide spread tendinitis an now I know why. Is this a temporary situation? I hope!!!
ksquared

My mom took Levaquin for a sinus infection and within three days of starting the medicine her kidneys began to fail. Her heart rate and blood pressure were elevated. After 6 months of going to doctor after doctor, she was diagnosed with chronic kidney disease and high blood pressure. Now she is on dialysis three times a week. The kicker...she had just had a complete physical with a blood work up three weeks prior to taking Levaquin and she was absolutely fine. Now, she's dying of chronic kidney disease.

Read my symptoms first; at the bottom it will tell you how long I had the IUD and the time line of the symptoms.

constant pelvic discomfort
(sometimes to the point where Advil usage doesn't even help)
("zaps" or "pings" of pain...light lightening bolts)
almost constant bleeding
(sometimes with clots - in differing sizes)
(coloring can be bright red to burgundy and brown)
(odor from the bleeding is very noticeable)
immediate weight gain
(this includes severe abdominal protrusion)
(I belly dance, & the costume I had just worn 2 weeks prior to insertion no longer fit)
severe swelling of the extremities
(hands usually do swell in hot weather, however, I've never had my feet and lower legs swell up like this - I had elephant feet/legs)
immediate acne issues
(my skin is always clear except for a few during my period)
moodiness
brain fog
(I'm a bookkeeper, & I noticed an immediate problem with my making stupid mistakes or taking longer than normal to resolve usual issues in this regard)
clumsiness
(could be attributed to the brain fog)
breast tenderness
(feels like someone's constantly squeezing/poking them)
movement of the IUD
(I could feel that it was out of position; it was more on my right side and caused ALOT of discomfort)

Here's the kicker, ladies. This was all within 1 WEEK of USE.

I demanded removal of this nasty thing & the GYN office refused.
After two more weeks of hell, I insisted, & they finally removed it.

This is what I experienced AFTER the removal:
Immediate relief in my pelvic area, BUT, still having pelvic pain.
INTENSE bleeding & clotting. To the point where I bled through my clothing at work (yes, I was using tampons & heavy pads).
The GYN's office didn't seem concerned; they said this was my body's "normal" reaction. (yeah, right). I finally stopped bleeding a good 5+ days later.
Even more breast tenderness.
Weight gain/bloat has not gone away. (I'm quite active)
Still experiencing brain fog.
Acne is starting to dissipate.

I have a ****** Group set up to shout to the world about this horrid device; look for: mirenajustsayno

Report your experience directly to Mirena; they have a contact # to report an "Adverse Reaction". From there, file a report with the varying health organizations.

On another note, I also had several ultrasounds done at the GYN's office prior to the insertion. The DR stated I had no ovarian cysts, no fibroids, BUT, my uterus was overly large. I sounded at a 10 as opposed to the usual 8. I was told it didn't matter, that I was a good candidate. He also stated that I had "a little endo".
(The reason for my use was to control the heavy bleeding during my period, along with the severe cramps.)

Well, I had some ultrasounds done at the hospital late last week, about 10 days after the removal of the Mirena. This is the result:
irregular complex cyst on my left ovary
unusually thickened uterine wall (no other explanation other than it was thicker than average)
It was noted that the series needs to be repeated.
(I'm assuming they want to look deeper)
Note that I have not resolved whether or not there was any perforation from the IUD moving out of place; the GYN never ran an ultrasound to verify it - they just did a regular exam & told me "it was still in my uterus". (that exam initiated severe bleeding for several days as well)

Good luck and let me know how you're doing!

And, yes, I do have several friends that LOVE their Mirena.

I was put in this med about 6 mos ago in order to protect my Kidney, I had a transplant years ago. My BP was already low in the mid 120s/85-90 and this has dropped it to 120/80.

However on starting this med, I suffered many of the flu-like symptoms to the point where I was out of work for a couple of days. Since then, I have, in retrospect had malaise, depression symptoms, occasional shortness of breath and a general lack of energy.

And last night, the kicker, I was with my new girlfriend for the first time....yep, no work, at all, which led me to checking out the net for symptoms of the meds I was on.

I took 300 mg. wellbutrin about 1 1/2 years ago and did not react well to it.
I just quit taking cymbalta after about 3 months because of sexual side effects, but here is the kicker. I started on a lower dose of wellbutrin about a week ago (175 mg xl) after only 3 days I was so screwed up it was a no brainer that I could not take it. It has been 4 days since I quit and I am still getting waves of disorientation and mild panic. How long will this last. Damn I only took it for 3 days and the side effect have lasted 7

I am reading this thread and will, as a male, caution everyone about the possible effects of Ortho Tri-Cyclen Lo. I am 41, have been married 19 years and have two children. I believe I occasionally suffer from bouts of mild depression which I have treated through therapy (about every 18 to 24 months). My wife had been on OT Lo for a long time until 6 months ago when she finally went off about 6 months after I had a vasectomy.

I cannot do justice to the transformation, at least from my perspective, that resulted after about 30 days of being off OT Lo. Sex drive went from very low to higher than anything I have ever seen. Call me a typical male if you want, but I can tell you the emotional impact of feeling like your wife really wants to be with you versus having almost no interest in sex.

Also, the way she approached problems changed dramatically. Therefore, the way I participated in those problems was able to change. No more highly emotional responses that were very difficult for me to understand while managing my own emotions and our level of conflict. The way way we were able to resolve problems became a partnership, not me bending to emotions I suspected neither she nor I could control.

Biggest problem: Irregeular periods. So, she goes back on the OT Lo and 1 week later we have a huge meltdown because she thinks I am ignoring her and the kids while away on a business trip. I am not for a minute going to tell you I am perfect, but this is precisely the type of issue that hurt our marriage for 18 years (in part because I am not great at handling emotional issues like this, particularly when I don't believe they are true) and went totally away during the 5 months she was OT Lo-free.

Kicker: She doesn't recognize how much differently she is processing her emotions and I have not found a way to address the issue without going through another major emotional battle that historically wouldn't have worked anyway.

Sidenote: I never wanted to get a vas. until I read an article that referenced depression as a possible side-effect of the Pill. I was willing to do anything to help change the emotional equation of our marriage because I didn't know how long I could last managing my bouts of depression in our environment.

So, probably not everyone had or will have the same effects. But please make sure you are paying attention to yourself, your level of happiness and how you handle things. FWIW.

I just got an injection yesterday in my shoulder. The injection had the following in it: 1ml of 40mg per milliliter of kenalog solution along with 1ml of 1% lidocaine solution without epinephrine and 1ml of .5% marcaine solution.

Here is what happened after the injection... Within 30 minutes I was experiencing nausea and a headache on the left side of my head, behind my eye, and to the outer side of the eye. Within an hour I had pain radiating throughout my entire body! It has not been almost 24 hours and I am still in pain. My head is splitting, I'm still experiencing nausea, and the pain is all over in my bones and joints, and my hips hurt really bad. I'm also experiencing a terrible dizziness, and light headed feeling, and confussion.

Here is the real kicker... I have severe drug and food allergies! There is virtually NOTHING I can take without having a reaction. I can only eat fish, fruits, and veggies, otherwise I get very sick, and have severe stomach cramps to a point I cannot even stand or walk! My doctor knows all of this, and he still told me this was perfectly safe, never been a reaction, and I would be okay. Only problem that may arise is infection, but that is extreamly rare!

Does anyone here have any idea what is happening to my body, and how long it might last?

I am 20 years old I have had an irregular period since I first got it at 12 and extremely bad problems with cramps, so my doctor prescribed Ortho Tri Cyclen .. I think its great .. I have mood swings here and there causing me to get a little more emotional then usual at times and my breasts have become a lot bigger but other than that its great

I was given Metoprolol, a generic for Toprol-XL several months ago, for high blood pressure. It was prescribed after I was determined to be allergic to Lisinopril. ( It caused a cough that lasted 3 months; I sounded like a TB patient.) Anyway, I have been taking Effexor for years, for anxiety attacks. Now that I take Metoprolol along with the Effexor, I am so tired and drained all the time, that I am contemplating quiting work. I go to the grocery, come home and lie down. I can't seem to have energy to breath correctly. My Dr. won't believe that this has anything to do with meds. I have now developed blood and mucous in my stools, diarrhea, and very urgent BMs. This all started after taking these two meds in combination for about 4 months.

Hello,

I have 3 friends who have liked the Mirena, so on their testimony and after talking to my OB/GYN, I decided to give it a try. I have a history of a J Pouch surgery when I was 19, and I'll be 37 in June. My husband and I luckily have one little girl, but it's doubtful we'll have more due to multiple reasons, and I was doing this so that we could finally have spontaneity. We've been together for nearly 18 years.

I had it in for only 5 days. I suffered things I've NEVER suffered: raging hormone headache, bloating like I couldn't believe, anxiety, a panic attack, not just crying jags - SOBBING jags that would come on in a panic, a "doom" feeling and this horrible feeling of loneliness. I was jittery... I don't drink caffeine, but this felt like I'd just had 15 espressos... I had all this nervous energy, but no focus.

After just 5 days, I went in and had it removed. After removal, I continued with the headache for 4 days, these were headaches unTOUCHED by any pain meds, bloating that finally abated and fatigue like you couldn't believe. I never nap, and I spent one full day on the couch without any motivation to do anything, and I also napped everyday and slept at night for 10 hours three nights in a row.

My doctor and nurse were understanding. They said I might have been "Hormone Naive," as I've not been on any kind of birth control, but whatever... it was a horrid experience and I'm so glad it's out. My doctor said I was in the minority of people with this kind of experience to birth control, but she didn't deny its existence, nor did she persuade me to try to "give it more time," and for that I was thankful.

After suffering from terrible skin from about junior high, I finally got a good enough job so that I had insurance to pay for a dermatologist. After heavy antibiotics and Retin A, I was given Accutane. In the next 3 months I suffered through: Severe dry skin and chapping, my hair fell out in clumps, my fingernails curled like parrot beaks, terrible muscle pain, severe depression (even though I didn't realize it until I was off of it), and of course the scarlet leather facial skin that "showed the drug was working".

Then after all that, shortly afterward my grandfather's Type 1 diabetes appeared in me (at age 40!). This warning about getting diabetes was NOT in the warnings that I had to sign off on then, but it IS now (funny, huh?). The kicker is, that after all that, I didn't even have acne. A better doctor correctly diagnosed me with Rosacea, gave me a simply lotion (Metrolotion), and my face has been fine ever since.

Stay AWAY from this drug!!!

Stay away from Prednisone

My prayers to all of you who take these destructive "medications". here's my short story.

I had been diagnosed with Sarcoidosis back in 2003. My doctor gave me 60MG per day (three 20 MG tabs) for over six months, with the weening off period lasting another six. To make a long story shorter. I went through many of the same problems like, bloating in the face and body, rashes, a bump that looks like a wart--that still won't go away, and a continuing state of memory loss. I get baffled easy now. I also continue to go through mood swings.

But here's the kicker, I haven't taken Prednisone for over 3 years and I was trying to begin lifting weights. I thought I popped something in my arm, but the doctor says that I have "aseptic necrosis", that has developed in my left shoulder and soon to start in both sides of my hips. For those who don't want to "google" the term, basically parts of my shoulder and hip bones are not getting blood flow and are dying (necrosis).

With my memory loss, I am having difficulties performing at work and doing routine tasks at home. I did not think this "medication" would have affected me this much.

Prednisone needs to be on the banned list of medicines.

I have asthmatic bronchitis. In June 2006 I came down with an infection in my lungs, which also set off my asthma. Between the two I was hospitalized and put on 240 mg of intravenous Prednisone and the antibiotic Levaquin. I was cured of the infection and was able breathe normally again but it took a great toll on my body It took me 3 months to taper off of the Prednisone and almost a whole year to feel myself. I was a strong, physically active person before this happened to me and I have not gotten my energy level and endurance back to what I was before I was sick. When I was released from the hospital I went from 160 mg of intravenous Prednisone to 80 mg of pill Prednisone. That step down was too severe and I went through intense joint and muscle pain in my body that it woke me from a sound sleep in the middle of the night. I luckily had an old Vicodin that I took which only made the pain bearable. I should have upped the Prednisone to make it go away but I wanted off. This pain lasted one week with each day getting less. The side effects I experienced from then on were so plentiful that I almost can't remember them all. The physical problems were, thin skin that bruised or ripped and bled profusely with the slightest bump, blurred vision, sensitivity to light, muscle cramps in my legs and hands, sleeplessness, dry mouth and frequent urination. My stomach bloated and got stretch marks. I didn't have any before that. The muscles in my thighs and upper arms atrophied so bad that I could not walk up stairs w/o using my arms to help. My arms were also very weak and I got hemorrhoids; another muscle that was affected. I had a bad case of the drops. I couldn't hold on to anything and broke many glasses. I got moon face that took a couple of weeks to go away after I was off the Prednisone. Because I was on such high doses, my hair died and stopped growing. About 40% of it fell out in one month. It took 6 months to grow back and it all grew back curly. On January 30, 2008 my bronchial tubes closed again due to a sinus infection. Again I was hospitalized with 240 mg of intravenous Prednisone and Levaquin. This time I responded much better, because I jumped on the infection/asthma instead of waiting. I stepped down from 240 to 180 to 90 to 60 and decrease 5 mg a day until I was off. This time I did no lose my hair land did not get hemorrhoids. The other physical effects were pretty much the same but much less severe. However, this time the emotional effects of Prednisone were much worse than last time. I was not a nice person. I was short tempered and argumentative and even had to stop myself from resorting to violence a couple of times. That is definitely not who I am. Prednisone stops your adrenal glands from working and adrenaline is you chemical way of coping with stress. I have been off of the Prednisone for one week and still find it hard to cope with the slightest controversy. My brain is still in a fog and I get confused easily. I cannot handle too many questions at once and forget things. My face is still round. Both times, I have found it the hardest dealing with the Prednisone at the very end and even after I finished taking it. I think it builds up and even though the chemical is suppose to be out of your body in 24 hours, it's effects stay a lot longer. I thought I knew what to expect but the second time was different again. It is a horrible drug but my trade off was breathing. Sometimes I think, that if I have to go through this a few more times, the side effects will kill me before the asthma. I wish all you Prednisone users loads of luck and stay positive.

I started taking Toprol XL after being diagnosed with SVT back in May of 2003. I was only in my late 20's & was very trusting, at the time. I was recently sent to a cardiologist because I was having horrible chest pain & the Toprol XL 50 MG wasn't working at keeping the heart rate down. The GP put me on a double dose as well as Cardizem to help with the chest pain & rapid heart rate. I was already on Lanoxin 0.5MG, the highest dose allowed. The cardiologist took me off of the Cardizem right away because he said that is was too stressful for the heart to be on that much heart medicine. I went though several tests & was told by the cardiologist that I didn't have SVT & that this was actually Postural Tachycardia (POTS) & Neurocardiogenic Syncope. I was taken off of Lanoxin, but kept on Toprol XL 100 MG. He put me on lots of salt & water to increase my blood volume which would help my blood pressure when standing. That was in June of 2007. All went pretty good, I thought, until January 18, 2008 when I was working. My heart rate went up to 136 just standing or walking across a room. I called the doctor & talked to a nurse who suggested that I take another 1/2 of a Toprol. I did that & felt better for awhile, but it was short lived. I had been having chest pain, rapid heart rate, fatigue, muscle pain, joint pain, headaches, nausea, vomiting, short term memory problems, rapid weight gain, hair loss, cold extremities, & other things I can't think of right now for what seemed like forever. My gynecologist & my cardiologist first thought that I had thyroid problems, but all tests have come back negative. They then thought that maybe it was from the birth control pills that I had been on for the ovarian cysts. I was changed from one medicine to another & at first I thought that was what was wrong. I am now certain that all of the problems that I have been having were & are a result of the Toprol XL. I was even told that all the problems were "psychiatric in nature". I know that that isn't it at all! I have never had anxiety problems & the GP now thinks that's all that is wrong with me & wants me to go on Zoloft. I tried it, but became so ill that after one pill, I quit. I now plan on weaning myself off of the Toprol XL without the GP's knowledge or consent. The cardiologist was planning on weaning me off at some time in the future, but I am starting without him knowing it at the time. I'll just tell him when I see him next month. Thanks everyone for alerting me to the facts about this medicine. If I had known then what I do now, I'd have never consented to starting it in the first place. My only question is, are some of the "side effects" going to be a permanent thing for me or will they eventually go away? Any advice would be welcome! Thanks again!

I only took Levoxyl for 5 days then stopped. The first couple of days were just headaches and extreme nausea. At night I would have sweats and during the day chills. I was going to live with these side effects but then on the fourth day I started being nervous, my face was flushing and one of the veins in my leg swelled. Then on the fifth day - along with everything else I began feeling a little weakness in my muscles - but the kicker was my toes and fingers were so sore and hurt so bad I couldn't stand it. My fingers felt as if I had been typing non stop all day - first thing in the morning and all day long. I called my physician who said that Levoxyl couldn't give any of those symptoms and I was imagining it all. I WAS NOT imagining any of it! I didn't wake up and say,"oh, i want my fingers and toes to hurt all day long for no reason". He didn't like me questioning him, but I wasn't questioning him, I was questioning Levoxyl. I asked him if there were any withdrawal symptoms and he said no. So I stopped taking it. Of course, I am not symptom free yet, as I figure it will take a couple days to get out of my system. My thyroid is slow and I know I am going to need to take something - I just wonder what suggestions other people with Levoxyl have done. And if anyone who has gone off it, actually had worse problems in the withdrawal phase. I know five days isn't that much, but I think my body is very medicine sensitive and responds very well. Thanks so much for anyones comments or advice!
Tammy in Florida

Dr. put me on Loestrin 24 on Dec 9, 2007. Immediately my period stopped (after a non-stop episode for 14 days) but then I started gaining weight (15 lbs), rapid heart rate after climbing 5 steps, extreme irritability to almost psycho stage and the kicker, my blood pressure kept shooting up. Today, it was at 154/99.

At the time I saw my OB/GYN a week ago, my BP was at 150/99 and she said she wasn't concerned. She doesn't feel that the pills have anything to do with my BP, weight gain or increased irritability. All my life, I've never had high BP until I got on these pills. I know my body.

Funny thing, my general practitioner was very concerned about my BP and told me to bring it down in 2 weeks or he's putting me on pills.

I've spotted for 5 days and am now on full-blown period (day 3) and it's heavy and my cramps are very painful. I have decided I will not to take the Loestrin starting tomorrow even though I risk the chance of having on-going periods.

I don't feel comfortable putting my heart at risk because of some pill supposedly regulating my period. Doesn't seem regulated with 5 days of minor spotting/clotting then full-on period. I have no clue how long it will last but at my age (45) guess that's just part of the cycle of being a woman.

Started coreg in 2000. 2-3 Months into taking Coreg I noticed my back beginning to ache. I questioned my Dr. about possible side effects and he looked at me like I was nuts. I have been scanned and examined in all possible ways and nothing interesting was found that could be causing my back pain. Jump ahead many years to the present and again I have been scanned even more than before to try to find the cause of my pain. Like before nothing interesting has been found. I still feel coreg was the cause originally and is now continuing my pain. 7.5mg vicadins won't even dent the pain. Any related comments would be appreciated.

Greg