Extremities symptoms and conditions

I am a 51 year old woman and I have been on Lisinopril for about 12 months. At first it was 20mg, then increased to 40mg per day. I started having shortness of breath and decided to cut back to the 20mg after a month or so. I am a nurse so I often adjust meds that I am on. I found this board about two months ago. I am so glad I did! I have BP of about 126/82 on meds. I have just stopped the 20mg two days ago, after developing more chest pain. I have lost all the weight that I needed to and eat a low salt diet now. I already feel better today. Chest pain is almost gone. I see my DR. tomorrow about all of this. I am going to try to stay off all HTN meds if I can! I had so many side effects that I never realized were being caused by this horrible drug. Some of them included: chest pain, shortness of breath, rib pain, extreme hair loss, tingling in all extremities, joint pain, muscle pain, headache, loss of appetite, loss of sex drive, difficulty thinking and comprehension, memory loss. I just wanted to let others know that I also know this drug is very dangerous. I am hopeful that I will continue to feel better as the weeks go by.

Since July 12, 2009 (Saturday) my life has been altered by a cure for a UTI that caused me to be taken by ambulance to the E.R. with a 105.6 fever. The horrible feeling of waking up shaking from the fever and not being able to stop it was scary. That was quickly followed by an ambulance ride to the local E.R. It was explained to me that the cause of my fever was a UTI that became a kidney infection. The E.R. doctor prescribed Levaquin 500 mgs for 10 days and Lori-tab for the ache very typical of a kidney infection. I am a 42yo woman who owns a motorcycle, swims, dances with a group and loves to wear beautiful heels. My life has changed since that night in the E.R. July 14 (Tuesday) , I was in my doctor's office complaining about bad headaches and feeling achy. I asked if this should be a concern since headaches were part of the warning label. The response was to remain on the antibiotic since the benefit far outweighed the side effects. The rest of the week was full of aches, pains, swelling, and a cloudy mental state. By Friday, the 17th of July I was laying in bed after noticing I no longer had ankles and I hurt all over. Thinking maybe this would pass I rested for an hour and my partner came to check on me. My jaw was tight and felt like it was locking down, every part of my body, every joint was hurting including my head. I called my doctor's office and asked if this was an allergic reaction and should I go to the hospital. The on-call said she was at the E.R. and maybe I should come in to be seen although it would be a long wait time because they were busy. I was seen, they talked about finishing with Cipro and then decided they would give me Bactrim. I asked how long I could expect to feel the effect of the Levaquin, the answer was 3 to 4 days. Since then, I have been in and out of the E.R. with acute and chronic pain. Walking has become almost impossible on some days. All of a sudden I have a back and hip problem. I am getting lumbar epidurals now and have sold the motorcycle. Oh, Dr. Higgins said, "Levaquin is a great drug". This was a E.R. doctor that was angry that I asked if this seemed to be an on-going issue from taking Levaquin. I am desperate to be pain free for even one 24 hour period. A storm of depression and clouds have set in...the thunder is my pain....

I've taken prinzide for about seven months and have suffered dizziness, severe heartburn/acid indigestion, confusion, irregular heartbeat, numbness/tingling in my extremities, a general feeling of malaise, and tachycardia. The dizziness and heartburn were irritating; the tachycardia was downright scary.

I would wake up from a dead sleep and my blood pressure would be around 117/60 and my heart rate would be 105 bpm! I've been off Prinzide for five days and my heart rate is in the 70-80 bpm range -- still not great, but much better.

I have taken 40mg of protonix for two weeks and I get severe foot and leg cramps, particularly at night. I stop taking the protonix and the cramps go away. Due to severe GERD. I need to take something. Is there any alternative medication or some treatment to offset the cramps? My arms and fingers hurt, my extremities seen to be losing feeling,

I conducted a search for "long term effects of Topamax" and discovered this site, and am so glad to have done so. I have been on Topamax for around 2 years now, at the 200mg level, for chronic, sustained migraines. I have figured out, through tracking, that I will get a migraine lasting 3-4 days during ovulation and again on my period. The Topamax has helped considerably with the headaches, although I do still get at least one per month. It is generally not of the same duration, though, and is fairly easily controlled with pain meds.

I've been a bit worried, though, about continuing the drug for life, as it seems I need to do to control these headaches--thus the search. I, too, have experienced the "mental fog," and general decreased cognitive abilities. I am an extremely intelligent person, a writer, a former English teacher. Why am I unable to pluck words from my brain when I need them?

I've also experienced the tingling and numbness in various extremities, sensitivity to cold, blurred vision, fatigue, and loss of taste sensation. I've also become a royal bitch to my husband and children--although I had no idea that this could be related to this medication. I feel relieved to know this now...to know that I can change and be the person I once was. I don't like myself very much right now, but it's like trying to stop a runaway train. I can no sooner prevent or alter my knee-jerk reaction to things than I can stop that train.

I've been off of the Topamax for approximately two weeks now, and have already gained 5 pounds, although I work out 2-3 hours daily and play competitive volleyball 2-3 times per week for several additional hours. I had initially lost around 18 pounds and kept it off, even when my appetite returned. I'm uncertain, though, why I'm gaining the weight back so rapidly. I'm eating fewer than 1500 calories/day and exercising like crazy. It doesn't make sense.

I don't care about the weight, though. My chief concern is the return of my cognitive function. Has anyone experienced a return to their prior cognitive state after getting off of this medication?

My daughter is a 4 year old child started on Singulair after she was unable to tolerate Zyrtec. For the first few days her allergies seemed better and we were encouraged by her improved allergy symptoms (allergies to poplar trees, grass, and lambs weed manifest as headaches, itching (usually of the extremities), and stomach aches). However, after 2 days her behavior became increasingly erratic. She was emotional, tantrum prone, irritable, anxious, and had difficulty sleeping although she appeared and said she was exhausted/tired. After several weeks on Singulair, we stopped the medication to determine if it was causing the behavioral and sleep problems. The symptoms stopped after discontinuing Singulair and she went back to her usual happy, well behaved self. After being off of it for several weeks we decided to try it again due to her allergies flaring up and wanting to be sure it was the Singulair causing the behavioral problems (because for all of its negatives, the greatest positive about Singulair is that it definitely helps her allergy symptoms). Unfortunately, the irritability, anxiousness, tiredness, tantrums and insomnia returned. We tried giving it to her at different times during the day but the symptoms were still present (although she slept a little better when we gave it to her in the morning). We also tried cutting the dose in half and giving it to her around noon. Decreasing the dose did help with the symptoms to some degree, but they were still bad enough to outweigh the benefits of taking the drug. As a nurse, I love Singulair for the relief it provides allergy sufferers...unfortunately for my daughter, the side effects outweigh the benefits. Given the rates of ADD, ADHD, and other behavioral problems diagnosed in children nowadays, I thought it pertinent to report these symptoms present in my daughter that are solely caused taking this medication.

I am 47 year old female with 5 days of headache and high diastolic bp. Doctor prescribed lisinopril. It made me want to sit for hours without moving. I was sleepy but could not sleep, cloudy thinking, anxious, thought I was going to die, had pangs all over my body and in extremities, racing heart with difficulty catching breath, etc to all the above symptoms. I stopped it after two weeks. I had bronchitis for four weeks. Then I developed dizziness/nausea and burning in the hands and feet. After researching that, I took a B12 and that tingling symptom cleared in a few hours. I don't know if the drug changes the metabolism in your system. I still am fatigued, occasionally have racing heart, and problems with sleep. Don't know how long it may linger in the system. Can't seem to find an answer. It has been 2 months since I took it and 6 weeks since being off it. By the way, my BP is now typically 117/82 with loss of 15 pounds. I prefer to treat naturally. Look up Taurine, CoQ10 and Hawthorne and see which may be best for you.

ok, so I am 28yrs old just had my second lap for endo and my doctor has recommended lupron, after reading this I am soooooooooo scared to even get near this med. Its like you either take this with the hope of saving fertility and no pain..or not and have endo ravage your body and you will live with unbearable pain!!! I have no idea what to do, my post-op surgery appt is this week, and i am so scared after reading this. Is there anyone that did not have weight gain, headaches etc...anyone that can testify that lupron actually worked for them? Cause right now its my health on the line, my ability to have children, my ability to have a normal life free of endo pain or these crazy, horrible side effects...please help me!!!

I began taking januvia and within a few day the joint pain began. it seemed
to be worse while sleeping and by morning i felt like i was hit by a mack
truck. joint pain,muscle stiffness and restless in all extremities and neck
including shoulder pain. i did not realize at first it maybe related to the
januvia. now i stopped taking it and expect the pain will stop.

I am a 48 year old female who had just recovered from pneumonia and was prescribed avelox for a lingering sinus infection. Within hours after taking just 1 400 mg pill, I began experiencing a severe reaction. First there was a rash all over my body, with swelling and flushing all over. Then I became nauseated to the point of dry heaves and my temp went to 104 digress. My body then had neurological shakes, I could not control them -- just like Parkinson. I had no energy to move. My husband rushed me to the ER where I was treated with steroids, liquid benadryl, nausea medicine and IV fluids. After a few hours, I was released. Two days later, after another trip to the ER because of tingling, rash and no blood flow to extremities the same treatment was given. It has now been two weeks and I am just now feeling like I am coming out of this and getting back to normal. I have just spent over 10 days in bed, untold amount of money at ER and lost two weeks of my life.. BTW, the ER Doc said he would never prescribe Avelox to anyone due to the numerous reactions he has seen. If there is a class action suit, count me in.. Never let anyone take this drug..

Lithium Carbonate nearly killed me. My doctor knew I was bulimic and he prescribed it any way, in combination with Geodon and Lamictal, even though I've been medication intolerant of 34 psychiatric drugs since I was 15. I am now 23. One year ago my boyfriend said he didn't like how I was changing in personality, that I was "different". I couldn't conceive his perspective. After only 2 weeks exactly of taking the Lithium at 900mg a day, I landed in the ICU where I was fighting for my life for 5 days. I had what looked like seizures but they were not. I had a dystonic reaction to the drug. It all began with a hand tremor on my left side. Ever since then, I get "episodes" where my ENTIRE right side goes dead and my left side extremities jerk and twitch and it hurts like hell. My neck snaps to the left and my lungs freeze long enough to where my lips turn blue. I live back home now. I cannot live alone. These episodes come out of nowhere. I have not been the same since that April Fool's day (how ironic right?)...I am to go to Johns Hopkins to find out what happened. They believe it may be a drug induced movement disorder. I also lose speech during these episodes or at random on its own while in class or talking with a friend. It's scaring the living hell out of me. To think that my central nervous system very well may have been POISONED makes me sick to my stomach...this doctor was reckless and used me as a lab rat. And now I pay the price. He went to med school at age 17 and did 4 years brain research on monkeys post graduation....I trusted him...if HE could do this to me, imagine what a D.O. or typical M.D. with little training could do with this toxic stuff?! I almost died. And I fear that I eventually will...The symptoms of muscle spasms and cognitive impairment have only worsened. I get annoyed with outer stimuli very easily at times, followed by hours of confusion and I cannot understand what people are saying to me nor can I finish a thought or even identify an object (nominal aphasia). If you ask me, stay AWAY from this unnatural form of help, you're better off with homeopathic medicine and breathing techniques. I learned the hard way. I just hope this helps at least one of you from starting this horrible drug. It can have PERMANENT side effects on WHO you ARE, i.e. your personality. My perception of reality has forever changed and I cannot go back. Do your research. And REALLY think about the risks before you begin taking this drug....or any of them for that matter....
On youtube you should watch this eye opening documentary that my friend found for me about big pharma. It's...jaw dropping. search "big pharma big bucks" on youtube.com and you will see what I mean.
Hope this helps. I will post the outcome of a final diagnosis, because as of right now, I cannot go to the ER when these episodes occur because they AUTOMATICALLY assume it's "in my head" simply because of a history of depression and PTSD. So all they do is give me NO pain meds for the muscle pain or even any tests ordered to find an answer, and call for a psych consult...HELLO?! talk about breaking the Hippocratic oath "FIRST do no harm". I'm a responsible, smart, and determined young woman who's been in in-patient treatment before and is very aware on how to handle my day to day strives. But these doctors...sigh....they just don't listen...it's ALL about liability for them. And it angers me. So I wait at home crying because I can't talk to anyone, in agonizing pain, and await for the moment my lung muscles freeze and I cannot breathe...it frightens me to my very core. NO ONE should have to go through with this...NO ONE. So, do your homework. Please. For you and your loved one's sake.
-H.

Wow! I can't believe what I'm reading. I started YAZ three years ago at the age of 21. My gyn prescribed it for me for mild acne and pretty bad cramps. I was super excited about having clear skin. This is my only positive experience I have with YAZ and almost to no periods. In the beginning, I was a healthy 21 year old female who was active, was in a stable relationship and loved life. All of that changed. I turned into a miserable person, someone I couldn't even stand. I would yell at anyone; it didn't matter if I didn't even know you. If you looked at me wrong I made a comment, so my doctor put me on Prozac for depression and OCD (obsessive compulsive disorder). One of the side effects of Prozac and Yaz is fatigue, headaches and decreased sex drive. I began experiencing horrible migraines to the point where I would throw up, have unbearable pain behind my right eye and photophobia. So, my doctor put my on Topamax as well. One of the side effects of this is tingling in the extremities. So now on a daily basis I have: nausea (I throw up every morning from YAZ), I sleep all the time ( I go to bed around 6 pm), zero sex drive (my fiancee thinks I'm not attracted to him anymore. I tell him that the hottest man in the world could walk in and I wouldn't care), mood swings, tingling in my arms and feet (like they're asleep). I was HEALTHY UNTIL I STARTED YAZ!!!!!!!!!!!!!! Oh, I was also rushed to the ER 2 summers ago to rule out a PE in my lungs (severe chest pain with a heart rate in the 130's). The doctors diagnosed me with low potassium (another side effect of Yaz).

Like most of you all I am on Topamax 100mg. I am a 27 year old female that has suffered from severe migraines for over 20 years that would last up to 2-3 days and completely debilitated me. I would bleed from my tear ducts from the extreme pressure and I would need to be in a quiet, cold, closed off room to be left alone until the migraine was gone to continue on with my life. It was ruining my life and taking over my day to day routine. I could never really commit to anything without the constant worry in the back of my mind about a possible migraine until I found Topamax. Now on Topamax I went from 4-5 migraines weekly to 1-2 monthly, it is truly amazing, however there is a catch. Although the medication is wonderful and I will never get off of it at the rate of success that I am at, I do have side effects. I have extreme tingling in my extremities, (hands, feet) along with my face. It feels like they are constantly asleep. I also have noticed the poor tasting carbonating drinks along with my taste buds changing with certain foods that I use to be so fond of. I also have a very smokey haze where it almost feels euphoric if I wake up in the middle of the night. I have horrible nightmares of people that I have not seen in or thought of in years, memory loss and spelling issues-all goes away after 3-4 months of uses. I had shortness of breath, however that subsides as well with the use of the medications along with several other side effects. I have lost over 30lbs that is along with diet, so I can't say it is all Topamax. I have noticed little nodules that have been showing up on my hands since I stared taking the medication that I am in ? about I have a call in to my neurologist to see if he has heard of any such thing. Other than that I love the medication, because if not having migraines is one of the side effects-lol I can handle the side effects. I hope that this will help anyone that might have anything similar to what I am going through. If you can shed some light on my nodule situation please let me know. Thanks

The side effects are: ******

Everyone has explained the exact symptoms as listed on these two websites. The Mirena website will not list these and the IUD is not marketed as such because let's face it, no one would use it, but if you study actual drug websites and the scientific facts of what the drug does , then you would not be surprised that your hair is falling out , your butt is getting big and you have no sex drive. These are "less serious side effects". But when we were all approached with the device, no one ever said "hey, it makes you cramp up and have strange tingling sensations in your extremities, accompanied by joint pain, but what the heck, it’s good for 5 years!" Pretty sure you would have said ..."huh? That doesn’t sound good to me”.

The hormone released in the IUD is levonorgestrel a synthetic, biologically active progestin. Progestins are hormones, an imbalance in hormones cause the same crappy side effects that you are having. This is why people feel better then they have the device removed, because you body goes back to making the correct hormone balance customized for YOU. Progestin is prescribed for male and female alike, guess what I’m not male!

I'm pretty sure that this "synthetic progestin”, is messing with my normal hormone creation. Although Dr's may disagree, I’m seeing a connection here.

So mine was inserted due to irregular periods , I had no other complaints and yes, now I have the weight gain , depression , join pain , etc ... but, I did go to a hormone specialist 1 year later , who did a hormone panel and found out that my hormones are out of whack ...due to the device?, or pre-device insertion? I have no idea, but now I am on hormone replacement therapy and guess what, symptoms are gone.

So my advice is this, if you just had a baby, had sudden period changes, or any medical reason why this evil thing was prescribed, or maybe, you were just fine and had this IUD inserted for birth control purposes and now all of a sudden you could care less about sex and taking this thing out for a test drive. PLEASE demand that your doctor due a blood test to determine your hormone or thyroid level to see if it is out of balance.

If you young, they won’t believe you, if your older or just had a baby, you have a better chance. But please explain , hey it’s just a simple blood test , if it comes back normal , hey the Dr is right, your crazy ,so move on to plan B which is taking the thing out, or If your right then 5 years of birth control is a great thing WITH corrected hormone levels.

HRT makes this uterine parasitic device much more manageable for me. The IUD did stop my heaving bleeding , abnormal periods and sever cramps for which I suffered for years , and I don’t want to take it out because I do not want to endure that same pain , so try a little estrogen , progesterone, testosterone , DHEA cocktail it worked for me and I hope it will work for someone who is have the same issue.

I started taking Lipitor in 2004 and by 2008 was taking 40mg daily. I'm not sure exactly when certain symptoms manifested themselves, as looking back they now seem insidious, but I do know they became bad enough in 2008 I went off the drug myself, especially after reading postings like those at this website. After being off the drug for a month, it was clear to me the most of the symptoms dissipated, but it did have a residual affect. I realized I had suffered a loss of range of motion (ROM) in my left arm (frozen shoulder) and have been in physical therapy for over a month to restored 80% of it. I could not have done this while staying on Lipitor as I was experiencing “deep” muscle pain and weakness. I still have some weakness and pain in my left arm and shoulder and don’t know if it is permanent.

I am Hypothyroid and take Synthroid and am currently going through menopause and am on partial HRT. I took no other meds other than the Lipitor. At one point, I thought my symptoms were stress related, but realized my symptoms were causing the stress. Aside from the muscle pain, spasms, tingling and numbness experienced in my left extremities, I experienced gastro intestinal disturbances, occasional vertigo, some lower back problems and other aching in other extremities (like that of flu symptoms). I also suffered recurrent mental fogs, which I initially attributed to some lack of regular exercise (although I lead a relatively an active life), but that was not the case, as even after aerobic activity the tingling and pain would resume.

When I told my physician I had stopped taking the Lipitor (at that time for nearly a month), he didn't blink an eye. I agree with previous blog; the idea of statins are to lengthen your life, but what kind of life is it when you are in misery and nothing short of ceasing the medication brings relief?

I'm not advocating everyone "doctor themselves. Listen to your physician, but most importantly listen to your body and trust your instincts when it comes to these types of medications. Symptoms listed about scripts described as "rare" are usually not that rare at all. You are not crazy.

I am so miserable. I had the mirena inserted at 6 wks post partem in June 2008. My doctor told me I'd bleed for about 3-6 months initially until my body "stabilized". I spotted on and off for 4 mths, and had my first yeast infection ever within that 4 months! I also began to become very moody, weepy, tired all the time, experienced terrible constipation, bad headaches and had the most irritating acne. I even went to my regular doc about being tired to get my thyroid levels checked and they were fine. I didn't even think that it could be the mirena b/c I didn't do the research on it before hand! I wish I would have! I have also experienced another yeast infection-and think I may have another now! That makes 3 since I've had this thing-in a 6 month period! Then in early October I began having hives on my extremities, and since have it on and off all over-no change in soaps or lotions or anything like that. I have no reason for them...except for the mirena. This past week I've had terrible abdominal cramps and painful intercourse. So I went to check for the placement of my strings...and...they're not hanging out anymore! So I will definately be calling my OB in the morning and having this thing removed...hopefully no damage has occured!

I am so thankful for this site. I thought maybe it was just me. For one, I am allergic to Sulfa. My doctor knows this, as does my pharmacy. Still, they give me Lisinopril with Hydrochlorothiazide which you should NOT take if you have a sulfa allergy. From day one, I started with anxiety, agitation, nausea and what felt like a racing heart - though my pulse was normal. Day three I called the doctor and they said this was normal as my body "adjusted" to the medication. It has been over two weeks and the same thing keeps happening. I tried taking the meds at night to hopefully sleep through the side effects but no - it just kept me awake. I put another call in today and have yet to receive a return call from my doctor. I hope the doctor calls me and NOT the front desk girl because I have a lot of questions and concerns. Other symptoms I have been experiencing since I started Lisinopril are sever muscle cramping last for over 24 hours, dizziness, heavy chest/racing heart beat, restlessness and less frequent urination. For a 37 yo female who has to "potty" constantly, even throughout the night, going once in an 8+ hour period is not normal! The worst side effect though is definitely the anger and agitation. I feel like I am going to burst out of my skin or die banging my head against the wall. Last night I tossed and turned for 2 hours in agitation. I thought I would surely have a heart attack from the stress. Oh yeah my BP has NOT dropped at all (tho it fluctuates on or off the meds) on the 20 mg dose. Go figure.

Knew about the sun sensitivity of many drugs so that didn't bother me so much, HOWEVER, the rash is gonna kill me! I itch everywhere! Ok, maybe not _everywhere_ but the joint areas and my back are the worse. My ears itch too. Called the nurse, line, took two Benadryl waiting on them to call back, will probably just OD on the cough syrup and pass out for the night. Crap! I was only one dose from done tonight. I had/have pneumonia and a wicked sinus infection. Maybe it'll be enough to pull me through. I hate taking anything if I can avoid it.. hate it more when I have a reaction. My last drug reaction was Penicillin when I was a kid .Cut foot, got blood poisoning, and ended up with raspberry type of rash all over my extremities from the drugs.

I recently lost about 25 lbs and decided after about 8 years of 10 mg of lipitor, to go off of it, cold turkey. I consulted both my MD and my pharmacist about whether or not I should wean, and both declined.

I now feel that my sweats, hot flashes are out of control. I am so hot and tired. I feel as though I cannot do the daily functions that I am responsible for.

I truly had NO side effects that I know of ON the drug. I just figured I'd see how I do now that I lost some weight. I wonder if going OFF lipitor is dangerous?

If anyone knows, please reply!

Thank you!

I started taking REGLAN for gastropoesis 5 months ago. Since I have been tested for MS due to my side effects from REGLAN. Thousands of dollars in medical bills. Symptoms included, numbness and tingling in the extremities and face, forgetfulness, muscle weakness, fatigue, depression, anxiety, insomnia, loss of fine motor skills, confusion, muscle rigidity, etc. I quit taking REGLAN last night hoping that there is no permanent damage. Anyone have any hopeful conclusions?

I find it very interesting about the possible link between Singulair and visual disturbances. My daughter had been told (about one year after being on Singulair) that she had damage to a nerve in one eye. She had never received any type of head trauma and the Doctor could not figure out how this happened. He told us that eventually her headaches would get so bad that she would have to have her eye removed while they tried to repair the nerve, and then they would replace her eye. I would be interested to hear if there are any other stories similar to this.

My daughter went for her yearly physical with our pediatrician. That morning we went in and the doctor insisted that she get immunized. Of course that immunization was Gardasil. My daughter felt fine and she was okay that day. After the doctors appointment she went on to school, and I went on to work to complete what I thought was to be a normal day. That afternoon I picked her up from school and she told me that she thought she may be getting sick. She complained of a stomach ache, and a mild headache. We went home and she ate very little, but told me and her dad that she felt better.
That evening she was to cheer at her first football game of the season in a neighboring town. She left with her best friend and her mother around 6 pm. at 8:44 that night her best friends mom called and told us that she had passed out at the game.
By the time that we had gotten there EMT's had taken her to the local ER, at that time she had barely regained consciousness, and her temperature was 103 degrees. Her extremities were cold, and her body was burning up. Her breathing was shallow, fast and irradic. Her pulse and blood pressure was extremely high. About an hour later the convulsions started.
After what seemed like eternity, the physician narrowed this down to the side effects of Gardasil. They started IV fluids, and meds, but still to no avail she kept convulsing. After a few days of heavily sedated sleep, she awoke to blurred vision, fever and nausea.
We were not told of any adverse reactions to this drug or we would have never given it to her!

Hey all,
Just had the Mirena put in last Wednesday. Did not hurt at all (I was SOOOO scared that it was going to!). In fact, I literally didn't realize that she had already put it in. I had a TINY bit of cramping after. Nothing like pmsing or anything. And that was for like 20 minutes a little after I got home. I took some IBProfin and had not had any cramps since. Very minimal bleeding. I am breastfeeding so I am not sure if that plays a role with the bleeding.

So this leaves me with one question (well, just one that I want to post and get responses to)....

For all that had problems with the Mirena, did they start from the beginning? From the moment that it was inserted? I wonder if there is a link...well, honestly I am kinda hoping there is a link. It would ease my mind a bit and it would let all of the women who have problems from the get go know that it isn't for them and it could be removed right then.

Oh, and for those that had a problem with the acne, how long after the Mirena was inserted did the acne come into play?

Thanks in advance!

I have been taking Singulair for 5 weeks and stopped after developing high blood pressure, numbness and tingling all over my body, flushing, anxiety, memory loss/difficulty concentrating, skin burning sensations, fatigue, "heavy legs" feeling, heart palpitations. I have been off of this drug for 3 days. I still have the side effects and hope that they will go away ASAP. I am also a very well-controlled 28 year old diabetic and when I had neuropathy-like tingling sensations in my extremities (from Singulair) I became worried and angry. I am seeing a doctor tomorrow for a full exam. If this drug has caused me permanent nerve damage I intend on filing a lawsuit against the drug company.

I started taking YAZ about a year ago. The first three months especially I noticed that I could cry and wanted to cry about everything from the phone ringing to dropping a paperclip. I screamed at my then bf for hours about everything and nothing. I snapped at everything, I couldn't control anything. After three months when my body slightly adjusted other side effects took over. I had vision blurriness randomly, migraines almost every three days that overtook my life and barely went away with sever migraine meds, appetite off the charts, depression, face heaviness when sleeping which was incredibly painful, numbness in my extremities.. its been a nightmare. I got off for a few months because I wanted to be free of it, and i was. Unfortunately because of my medical condition I need to be on b/c for life. I started taking it again and have been on it for several weeks and ALL of the side effects are back with a vengeance including crazy acne and bloating. Someone shoot me. I hate this drug.