Severe pain symptoms and conditions

I am a 44 year old female with diabetes. I have high blood pressure and as a precaution was prescribed simvastian(zocor). I have only been on it for about 3 weeks...I have been feeling tired and very moody lately...but yesterday I woke up with my right leg swollen from the calf down my foot with severe burning pain and numbness. Now I have experienced Neuropathy in my left foot for years and somehow thought maybe this pain and numbness and swelling had to do with that...until this morning when I woke up to a severe pain in my right calf ( I immediately thought blood clot).. well I have a doctor's appt tomorrow to see what this is....right now Im sitting at work in so much pain and discomfort I want to cry...my feet are burning, my right leg and right shoulder are in burning pain...and my hands are numb and burning and in pain. I have to sit for hours at a time and cant just take a break when I need too...Ive only been taking this medication for 3 weeks and can not believe that all this pain and burning is from one little pill. Has anyone else had severe swelling from this medicine. Any other diabetics taking this medicine and having the same side effects? Im certain they are going to want me to stay on this medication and at this point after reading all these wonderful post, Im going to stop...Im even having difficulty in typing this post my hands hurt so bad. Im so angry that when I asked my Doctor about side effects he never mentioned these. he told me about being nauseated, constipated and so one...Ohh and I have also gained about 10 pounds in 3 weeks without changing my eating habits...anyone else have that? Thank you for letting me vent here. I was scared to death until I found this site. I was seriously considering leaving work and going to the ER room...Now Im just going to stop taking it and waiting this out till tomorrow....

I'm so glad I found this web site because I did think there was something seriously wrong with me, I took Prevacid for years without any side effects, switched to Nexium because it was cheaper and never had any problems with it, I was just at my doctors in Dec. 08 asked the doctor if there was a generic brand for Nexium because the cost has risen on that also so he prescribed 40mg of Omeprazole, took my 1st dose on Dec 31st, I thought I was having a heart attack, had severe pain between my shoulder blades, alot of burping, sick to my stomach, when I would eat it felt like my food was stuck in my chest, and also had a very nervous feeling, my husband suggested, that I stop taking the Omeprazole until I could talk with the dr. I only took it for 4 days and had these effects, I can only imagine what long term would do, I am feeling better still slight effects, but nothing like before, I will never take this drug again, I guess I will go back to forking out more money for the Nexium, it is just crazy the price we have to pay for meds.

When my daughter was 15 her dr suggested she get the vaccine. Trusting the doctors advice, i ok'd it. The first two injections were fine. Immediately after receiving her 3rd, her arm, neck, and shoulder got really sore and then about two weeks later she developed severe pain in her upper abdomen causing her to pass out. That was on November 22, 2007 and she hasn't been the same since. She has suffered severe pain, nausea, dizziness, fatigue, IBS, anxiety attacks and depression brought on by the sickness. Our life for the past year has consisted of going to doctor after doctor trying to figure out what is wrong with her. She has been diagnosed with mono, UTI's, had her gal bladder removed, etc. Funny, they diagnose her with all these things but no treatments have worked. She went from being a very beautiful, active 15 year old girl with lots of friends and activities to barely being able to get out of bed in the morning. My question is, does anybody know how to help or what to do ?

I took Levaquin 500 milligrams once a day for 5 days for a sore throat. Before I completed the fifth pill, I began to have severe pain in my right knee. It hurts so bad I can hardly walk up and down the stairs. It is even hard to get up from a sitting position 0r to get out of the bathtub. I wish I had never taken this drug. The sore throat was a lot more bearable!!!

I hate Mirena. I am on Lexapro and hate that too. (Not a negative person, I promise...just trying to be brief). Have gained about 20 lbs and I was already about 20 lbs overweight to begin with...

That said, I want to be drug free - no lexapro, no mirena and those hormones! Am trying to wean from lexapro right now. YUCK. This is a nightmare. DIZZY and NAUSEOUS.

Also, just wondering if anyone else had severe pain in the abdomen after getting Mirena inserted? I experienced a sharp pain in my abdomen for quite some time and assumed it had to do with the foreign object in me. I asked my doctor, but he didn't think one had anything to do wtih the other. When I say sharp pain, I mean, it felt like someone was taking a sharp object and cutting me from the inside out...

That eventually subsided, but the weight gain, the depression, and ALL of the other stuff mentioned happened to me too. I just want my life back!!! I'm SO tired...

Sigh....

I was diagnosed with Diverticulitis and put on the usual regime of Levaquin (500mg a day) and Flagel. The case turned worse and was admitted to the hospital (they thought I had a blockage but turned out did not) and was put on IV of the same medication. Released from the hospital 4 days later and stayed on the Levaquin as prescribed. When I ran out, I called my regular doctor who sent in the renewal prescription. However the his aide made an error and the bottle read 500mg 4 times a day…nobody including the pharmacy caught it. So for 3 days I was taking 2000mg a day of Levaquin. When I started getting worse (truly thought I was dying), I got to the doctor and he said I had taken turn for the worse and could not figure out why. He asked if I was taking the meds and I said yes 4 times a day…his face when white. I had the bottle with me and he panicked. They apologized for the error and I was told to stay off my feet, no heels, they ran ekg’s that day and the following Monday, blood work to check the kidneys etc.

Subsequently, I have had extreme pain in my joints and muscles – everyday, all day. Some days I just cry it hurts so bad. If I bend down I can hardly get back up because of my right knee. I have talked with a doctor I happened to run into about this and she said that Levaquin dosage has saturated my body and gotten into the joint and muscles and takes a long time to work it out. I can hardly lift my arms above my shoulder without severe pain. Stabbing pains in my knees, shoulders, arms and hands.

I have not gone back to the doctor because when I mentioned the pain the when I was in that last time…he just wanted to give me more meds! I have been seeing a massage therapist who specializes in deep tissue restoration and repair. It helps some, but he as well says this is going to take a lot to time to work out.

I have depression to the point of feeling like I am a nothing and what good am I to anyone feeling like this. So like snoop45...that is exactly what i feel like!

dawn62

J.

Hi everyone.I just finished my 2nd round of levaquin 500 mil the 750 mil was given to me after my pneumonia and hospitalization I was terrified.I had never been hospitalized for anything.I'm 42 quit smoking 6 yrs ago.No other health issues,well could stand to lose some pounds.
5 days ago my knee began to hurt which I never thought twice about since I have knee issues but, then my right knee, then my hands now my entire body is sore and hurting so bad I cannot walk up the stairs to our home now due to the severe pain in my knees.I have had no other side effects.I have been on STD from my job since 11 24 due to the pneumonia.I am suppose to see my doctor today and go back to work tomorrow ha that a joke the pin I'm in.He has been my doctor since I was 19 yrs old.He is a good doctor and I am scared to death to find out what he has to say about my symptoms and the crazy bad side effects. I do not want to go back in the hospital or be told what I have is permanent.At first I thought I had the Flu.My immune system is shot due to the pneumonia so I just thought well this is great I've got the flu .Then I began reading online the side effects of this drug and was horrified.

I would implore any and all who may be prescribed this drug to talk it over with there Dr.or ask for another drug.Yes the drug kicked the pneumonia out of me which 6 other drugs could not but,the side effects are terrible for some.
I will pray for us all here today.God help us to heal.I UNDERSTAND WHAT EVERYONE IS GOING THROUGH.Hang in there. Don't give up hope or faith.

After reading all of these posts, I realize I'm not alone. Mirena was the perfect option for me because I'm very forgetful when it comes to medications. What sold me was when I was told it has a 99.9% effectiveness against getting pregnant. I was only told of the good things. After it was inserted i was in SEVERE pain from the cramping, it reminded me of labor contractions. I took 600mg of ibuprofen then layed down and cried myself to sleep. I got it July 28th, 2008. Since then I've been bleeding on and off but more bleeding than not. I get sharp, cramp-like pains in my lower stomach and sometimes vaginal area. I also suffer severe lower back pain. I was bleeding so bad at one point and it was very different from any period I'd ever had so I thought maybe I was miscarrying. I called the doctor and it was rather blown off and I actually got kind of laughed at, saying it's just your body adjusting. I have restless nights and wake up exhausted. I have those far out dreams like you do when you're pregnant, except I'm not. I also get bloated and uncomfortable at times. I've been bleeding now for almost a month straight. It comes and goes, which is very aggravating. I'd almost just thought about getting it taken out and just going with oral birth control that way I'd have a normal period but I love not having the boundaries in the bedroom. I'm giving it the 6months, like they told me it'd take and if all my symptoms are still present I'm considering removal.

This is painful for me to type due to the pain in my hands & fingers. I had ankle surgery to fix a torn ligament and an ankle scope on Oct. 30, 2008. I was put on 500 mg of Levaquin to prevent infection. On Nov 4th, my entire body felt like it was beat up. I could barely get up off of the couch. I also developed severe pain and burning in my foot. I couldn’t support my weight on crutches due to pain in my arms & wrists. I took this dose for 10 days. On Nov 24th, I couldn’t take the pain anymore. I ended up being hospitalized for 10 days. I had severe swelling in my ankle and bruising up to & including my toes. The doc thought it was an infection so I was started on 2 types of IV antibiotics. Didn’t get any better. On Nov 26th, the doc tried to aspirate it and only dried blood came out. It was sent for a culture and came back negative. He asked me how my pain was and I told him the back of my ankle hurt really bad. He said “the MRI that was done on Nov 25th showed I developed tendinitis in the Achilles tendon. I asked him how that happened since I haven’t walked on that foot since my injury date of August 23rd. He said he wasn’t sure. I had 2 previous MRIs (Sept & Oct) which did not show tendinitis at all! On Dec. 1st I went back to the operating room so the doctor could cut open the golf ball size hematoma on the outside of my ankle. He got a lot of jelly-like blood from the back part of my ankle. He left the drain in overnight and then removed it. I was released on Dec 3rd with a script for 750 mg of Levaquin for 7 days (which I finished yesterday). The swelling is down about 25% and I have been out of the hospital for 8 days now. The pain in my body was so horrible today that I went to my family doctor. She did a thorough exam of my joints-which was complete agony!!!! She explained that she was going to run some tests to see what is wrong. She explained to me that she thinks this is a reaction to the Levaquin & she has had patients who have had ruptured tendons from this medication. She sent me for bloodwork and gave me a script for morphine (Avinza) to control the pain, which 750 mg of ES Vicodin and 800 mg of Ibuprofen didn’t make it any better. I feel helpless as my 9 year old has to do everything for me because I simply cannot get up. I hope my doctor figures this out real soon! This is unreal to have to suffer like this. I will keep everyone on this page in my prayers! Good Luck to everyone!

I had my Mirena put in April 2007 - wasn't that painful at all, didn't have any real side effect (so I thought anyway). I has spotting for first couple weeks then nothing. No periods at since May 2007!! But I noticed after the first of this year that my hair was falling out, I always have abdominal pain and cramps. I ended up in the ER this week with severe pain thinking I had appendicitis or something - turns out its an ovarian cyst the size of almost a baseball! The doctor explained it would go away with my "cycle" but since I have NO PERIOD that isn't going to happen and it's to large to reabsorb so I now have to have a surgery to get the cyst removed. THE IUD IS COMING OUT ASAP. Have an appointment Friday.....I'm in so much pain from the cyst though I doubt I'll be able to handle it being removed....if not then right after that surgery it's going, going, GONE! I'd rather have another baby!

I have posted here before when suffering the severe leg pain. I took pain meds for 2 months and it seemed to have subsided. Then, 10 days ago, right beneath my achilles tendon pain, on the side of my foot, under my ankle bone., started giving me severe pain. I could not understand what happened, it hurt as if it was bruised. When I looked at the area hurting me, there was no bruising but was swollen so badly I looked like I had a baseball under my skin! I am having difficulty walking now. I have an awful feeling that I may have a ruptured tendon! I am seeing an orthopedist on Monday afternoon. Has anyone here had a tendon rupture? How would you describe it to be? I'd appreciate if anyone with experience like my own would email me asap!!!

I AM ON MY SECOND DOSE OF AVELOX. I AM GETTING SEVERE PAIN IN MY HEAD. WHAT DOCTOR IN HIS RIGHT MIND WOULD PRESCRIBE THIS MEDICINE. I AM NOT GOING TO TAKE ANY MORE. STAY AWAY FROM AVELOX. K. INCE

DRUG: CIPRO FOR UTI. NOV 08. FEMALE AGE 52.

STARTED ON CIPRO FOR UTI ON 11/15/08. I TOLD MY DOCTOR THAT CIPRO IS A EVIL ANTIBIOTIC. I STOPPED TAKING CIPRO ON 11/18/08 WHEN I WOKE IN THE MIDDLE OF THE NIGHT BECAUSE OF THE SEVERE PAIN IN MY JOINTS AND THE RIPPING AND BURNING IN MY CALFS. I FINALLY GOT OUT OF BED AND COULD HARDLY WALK. I DISCOVERED THAT MY TOES, FINGERS, ELBOWS, BOTH KNEES WERE SEVERELY SWOLLEN. AT THIS POINT I HAVE NOW EXPERIENCED ALMOST ALL OF THE SIDE EFFECTS AS LISTED IN THE "PACKAGE INSERT" THAT CAME WITH CIPRO.

BEGINNING MY FIRST DOSE ON SAT. AFTERNOON (11/15) I THOUGHT I HAD THE FLU ALONG WITH THE UTI AND THAT WAS WHAT WAS CAUSING MY FEVERS OF 102.9 WHICH I KEEP DOWN THRU IBUPROFIN. THE BLOATED STOMACH AND TENDERNESS WAS EXPLAINED FROM MY FRIEND WHO WORKS IN THE PHARMACEUTICAL INDUSTRY AS PROBABLY CAUSED FROM THE INGREDIENTS IN THE ANTIBIOTIC THAT DESTROY OUR OWN BODIES "NATURAL ENYSEMS"
I ALSO WAS CONSTIPATED FOR 4 DAYS. (I HAVE BEEN DAILY ALL MY LIFE). EXTREME FATIGUE KEPT ME EITHER ON THE COUCH OR IN BED, I NEVER SLEPT SO MUCH IN MY LIFE. I LOSSED ALL MY APPETITE, WAS DIZZY, AND VERY SICK OF BEING SICK. I ALSO HAD PERIODS WHERE I WOULD JUST START CRYING (ONE TIME I REMEMBER OVER THE DOG AND NOT WALKING IT) EMOTIONALLY, I WOULD BEST DESCRIBE MYSELF AS HAVING SEVERE MOOD SWINGS. ALSO HAD HEART PALPITATIONS. , SHORTNESS OF BREATH, ODD TASTE IN MOUTH WAS ANOTHER "EXPERIENCE" WHILE ON MY JOY RIDE WITH CIPRO.

TODAY IS SATURDAY, 1 WEEK LATER - ANTIBIOTIC FREE FOR 4 DAYS. I STILL HAVE EXTREME SWOLLEN JOINTS AND FIND IT DIFFICULT TO MOVE AROUND ALTHOUGHT ITS BETTER. TODAY I CAME DOWN IN THE BASEMENT TO LAUNDRY FOR THE FIRST TIME SINCE LAST SATURDAY. (I DIDN'T CARE ABOUT MY HOUSEHOLD CHORES ALL THIS TIME). RIGHT NOW, MY HIPS AND BUTT ARE SORE FROM SITTING - MAYBE BECAUSE LAST Night I WENT TO BED AT 7:00 pm AND WOKE UP AGAIN AT 6:00 AM OR IS IT BECAUSE OF THE SWOLLEN JOINTS SIDE EFFECT. I DO FEEL BETTER AND AM HOPEFUL THAT ALL OF MY ACHES AND PAINS WILL GO AWAY. I STILL AM NOT 100%, I STILL AM EXPERIENCING PERIODS OF WANTING TO PUKE, AND HEADACHES COME AND GO.

I WILL NEVER TAKE CIPRO AGAIN. WHAT I REALLY WOULD LIKE IS TO TAKE THE COMPANY DOWN THAT PRODUCES THIS DRUG. THIS DRUG SEEMS TO ATTACK A INDIVIDUALS "WEAK SPOTS" AND MAGNIFY THE SYMPTOMS. I AM PRAYING THAT ALL OF THESE SYMPTOMS ARE TEMPORARY.

THANK YOU FOR YOUR WEBSITE AND BLESS EACH ONE US WHO HAVE BEEN A VICTIM OF THE EVIL ANTIBIOTIC "CIPRO".

Doctor prescribed Lisinopril along with Metformin about a year ago , he told me the lisinopril will help protect my kidneys from the diabetes along with reducing my high blood pressure. I started with cramping and shaking which left me bed ridden for days! I blamed the metformin, thinking it was reducing my bodys sugar level. In this time I started having these pulsating, center of chest, waves of severe hot pain, I went to his office and he put me on an EKG machiene. Everything was fine. I have these bouts every so often, along with lip numbness and severe pain that feels like my right arm is caving in with muscle spasms, my veins stick out in the effected arm along with a numb cold feeling!(goose bumps too?). My physician told me it may be GERD.He put me on protonics which helped for a while, but it is back! I also get edgy,have trouble staying asleep and walk around like a zombie in a fog all day long. I started getting strobe light migraines without the pain recently, wondering if anyone else has had these symptoms from Lisinopril? By the way my blood sugar is in control. Also on allopurinol with no problems.

I've had all these same symptoms at one point during the two years I've been taking Advair. I've had exercise induced asthma since I was 18 but I can still work out at age 38 regularly with the help of Albuterol/Proventil. I stopped taking Advair after I completed my last disk in Sept, 08. It all makes sense now after the fact from reading here. Firstly, I cant tell you how severe the muscle cramps were. No words can describe upper body cramping in every muscle that I endured for weeks (it felt like knives all over)!!! The same happened with my legs...the muscles became so tight they contorted! My Dr. gave me an m.r.i. took x-rays and several blood tests...even gave me an h.i.v. test because he had no idea what would cause all these symptoms. He said it was "complicated". The test results found nothing. All lof my symptoms are gone now that I've stopped taking it (mouth sores, bleeding gums, strange skin lumps, hair loss, dry eyes, swollen tongue feeling, lump in throat feeling, severe cramping all over my body for 3 weeks). The Dr. noted that I had gained 10lbs since my last visit. I told him, "I've barely been able to MOVE with this cramping much less exercise with my regular weekly routine!" "It even hurts to breath deeply!" I still have a dry cough that hasn't gone away and normally I clear up after the seasonal rag weed season is over. We have had two hard frosts already...that usually clears my allergies.

On September 9th, 2008, I had the mirena inserted and it was horrible. My right ovary felt like it had exploded and a burst of burning pain radiated down my leg. I broke out into a sweat, felt dizzy, and nauseated. The doctor said they never had that reaction before and had me lay down until I felt better. The doctor wanted to do an ultrasound, right then, but the doctors that did the ultrasounds were not available, so she gave me a Motrin and told me to go to the emergency room if I had severe pain or bleeding. She sent me home. This THING is constantly on my mind since I had it put in. I hate it!! I am tired all the time, headaches, bloating, dry eyes, back pain, hair loss, constant feeling of being in a fog, cramps everyday, and the burning pain I experienced during insertion comes back more and more frequently. My ovary and leg hurt me so bad that I feel like I'm going to pass out. Two weeks after insertion I went in to have the strings trimmed and let the doctor know my symptoms-she looked puzzled and made me feel like I was crazy, but suggested that we have an ultrasound done, so she scheduled me an appointment for it-two weeks later. I had a follow up with the doctor one week after that and she said everything looked fine and to take ibuprofen for the pain. I went back three weeks later to have my strings trimmed-again. She was amazed that they seemed longer than they were the first time she trimmed them. She said that it was either "settling" lower, or it was falling out. She did an internal exam, but did not feel it, so she suggested that I at least give it another month before I consider taking it out. I agreed because I paid a lot of money for it and my options are limited. Since my last visit, I've been researching mirena a bit and was surprised to hear that so many women have been experiencing these side effects. I plan on having the mirena removed, but have been researching tubal ligation as my next step. Then I ran into something called tubal ligation syndrome, which has side effects that I am currently experiencing. I talked to my boyfriend about all of this last night and he has agreed to have a vasectomy. The bad thing about that is I have to wait for him to have it done and wait until his sperm count is at zero. That could take a month or more! The good thing is that I won't have to think or worry about getting pregnant anymore and I won't have some foreign piece of hormonal plastic in my body any longer. I will never recommend the mirena to anyone-ever!

I am a 65 year old female taking 20mlg of lipitor for almost 10 years. All of a sudden I started having severe pain, shaking and weakness in the calf muscle. The pain is unbearable. Doctors after doctors including a cardiologist, rhoumatologist and internist don't know the reason. I have stopped lipitor for 3 days. I cry and pray to god to help me everyday. I cannot exercise which is my passion for many years. I am hoping the lipitor is the reason and not something else. I have to wait and see. But I suspect it is.
SR
I do have nausea, depression and low back pain and arthritis and frequent headaches.

I havent tried Nuvaring yet.... I just got back from the doctor with some free samples. I'm on the Ortho Evra patch currently and I have side effects that made me concerned enough to try something different. I was on the Depo shot for 4 years. I decided to get off of it after I had cycts removed from my ovaries and had pre cancerous cells removed. Which the doctors said would lower my chances of having children. I decided to take a whole year off of birth control. To give my body a chance to "recover". The only problem I had was my periods kept getting longer and longer and more frequent. Next thing I know the doctors tell me I have Polycystic Ovarian Disease. Which also lowers the chance of having children because of the irregular bleeding. The pill makes me so nautious I couldn't stand it so I thought I'd try the patch. Now I have menstrual cramps when I'm not ovulating, I'm so moody its not even funny, I'm eating all the time and tired 24/7. The only thing it did do was regulate my period. Which is what I wanted... But I've only been on it for two months. My doctor told me you cant even feel the Nuvaring and it has a low dose of estrogen so I wont be moody. But reading all of the comments and stories.... I think I'm just going to not be on any birth control and see if my body naturally regulates itself. If I was using the birth control just to avoid pregnancy it would be different, I would want to be on at least something. But I'm glad to know I'm not the only one that thinks birth control is evil and causes alot more problems than doctors tell you. So I think I'm just gonna toss my free samples of Nuvaring, get off the patch and see what my body does naturally.

Only on it for 1 month so far and already having issues. I apparently have the worst case of endometriosis all my doctors have seen, including a cancer specialist that had to do all my surgeries because of the severity. Granted, I am only 31 years old and have had a full hysterectomy. So, after 3 surgeries I am still having severe abdominal pain and bleeding (don't know where that is coming from since I don't have a uterus anymore) so they said try Lupron and I finally gave in. Now I started getting such severe pain in my lower back that I can't stand for longer than 15 minutes and terrible side aches. I started getting headaches (which I already take pills for for years now),and have gotten the hot flashes as well. What are we to do ladies? I am so sick of complaining to the doctors about pain. You feel as if you are a big cry baby. What are my options here and does this ever stop?

I have extreme thumb spasms, often both thumbs at the same time. i had an episode a few weeks ago of a severe pain in my hip running down my leg. I was in bed all weekend as a result and needed a cortisone shot to help relieve the pain. I forgot a name right after they tell me and I am only 50 years old. I lose my balance and sometimes almost fall and have vertigo every now and then. I wonder if all these symptoms are from lipitor. I have been on it for at least 3 years.

I, too, am lactose intolerant and have been taking Lactaid. Just three days ago, I had another attack of severe abdominal pain, constipation, then diarrhea, and the feeling that I needed to vomit. The severe pain lasted for two hours. I still have some discomfort. I nearly called 911. This episode is the third that I have had. I was hospitalized for four days last May. That time and the one previous to it, I was diagnosed with ischemic colitis. No firm explanation was given for the cause other than constipation could cause it. However, the first time that I experienced ischemic colitis, I was not constipated. I now suspect that Lactaid may have brought on all three episodes and will stop taking it. I would much rather have the side effects of milk then those of ischemic colitis!

I am 53 years old and was advised to switch my BP med from Hyzaar
to lisinopril by the insurance company to save money. I took
20/25 Lisinopril/HCZT for about 6 months. My BP was so
low, I was getting lightheaded, so we reduced it to 10/12.5.
My BP stabilized at a reasonable level. Eventually, I started
to get chest pain around the sternum and ribs but it felt deep
inside. Also, I had wandering upper back pains -
stabbing pains - that would move around, but most often
would be felt in the middle of the upper back. I also started
to get occasional bloating where my abdomen would swell and
even be very rigid to the touch. Antacids had no effect. It
would eventually subside on it's own. I also developed painful
pericarditis 3 different times (swelling of the pericardium
sac around the heart and fluid buildup). The sensation is severe
pain with each heartbeat. I went to a clinic the first time and
received anti-inflammatory drugs and the second time I had to go
to the ER. The 3rd time, I self medicated with leftover drugs from
the previous episodes. I thought I was a dead man living on
borrowed time. I finally started doing research and found this site.
I stopped lisiniprol on a Friday and all symptoms of the chest pain
and back pain subsided within one day. In addition, I haven't had
any recurrence of pericarditis or bloating. Needless to say, the
associated anxiety of impending death is gone as well. I am now back
on Hyzaar and feel like a new person.

I've been on Loestrin for almost 5 months now, but I'm still not so sure how I feel about it. Before I took the pill, I had 7 day long, heavy periods, headaches, cramps, vomiting- the whole nine yards. The first month I took the pill, I got my period as usual, but for about 5 days ( the 5 days I happened to be on vacation, fun). The next month, my period lasted about 4 days, the next month three days, and this past month I didn't get it at all. I have to admit, I was quite relieved when I read some of other comments with women also having missed periods, or no periods altogether, as I'm not ready for a mini-me quite yet. The only major problems I've had with this pill so far are severe mood swings, which my boyfriend doesn't appreciate very much, and the last few days I've had severe pain in my lower abdomen, which, if it persists, will force me to visit my gyno. Overall, I do like this pill, it's really toned down my migraines, which I've had for years, and seems to be quite effective at lessening my heavy blood flow and severe cramps.

I was prescribed this medication on Thursday, 10/23. Ater taking my first dose, I immediately threw up. I read that this was a common side effect and thought nothing of it. I was fine after the 2,3, and 4th dose. Then I took the 5th dose on Monday night and woke up around 1:30 A.M. with severe burning and tingling in my feet. I put some muscle rub on it, and figured it was unrelated. I stand on my feet all day as a teacher and just thought my feet were tired. After taking the 6th dose, I once again woke up around 1:30 AM with very severe pain in my knees. I was in tears over the severity of this pain. Even now, my knees and feet are still hurting and tingling. I called the doctor today to see about getting my prescription changed, even though I only had 4 pills left to take, and she asked me to come in and be evaluated. Another co-pay, when they shouldn't have given me this poison to begin with! I am 24 years old, and have to take care of an 8 month old baby. My husband is scared out of his mind and so am I. I am way to young to have to deal with joint pain, and am praying that this isn't permanent damage!

Had a heart attack in July and had a stent put in blocked artery. Prior to that I was taking Cartia for blood pressure. Cardiologist switched me to Lisinopril.
I've been having severe pain in my lower back on both sides and also around my rib cage. I'm in cardiac rehab and today my nurse/therapist told me they are increasing Lisinopril from 10 mg to 20 mg. After reading posts on this site, I'm a bit concerned.