Vengance symptoms and conditions

Hi, i'm 24 and i've had my mirena coil fitted now for over a year. I have been experiencing cramps, bleeding, headaches, tiredness, dizziness and aches in my legs but never thought anything of it. Until now when my cramps are severe in my tummy and lower back. I can describe them as a few things, labor pains, severe period pains and also appendicitis pain. its not my appendix, as I had it taken out years ago. I recently went to my GP who advised that I have a pregnancy test just to rule out an ectopic pregnancy, which came back negative. She advised that I should take regular paracetamol for the pain and see how I go. But they don't seem to disappear. I now have the same cramps but now also my bum area as well as my tummy area and lower back when I go to toilet whether for a number 1 or number 2, and it is excruciating which makes me cry. I also recently had intercourse with my partner, and the cramps came back with a vengeance, and i was in so much pain, i almost called an ambulance. I have no idea as to what I think it is until I started writing my symptoms into the internet and came back that it may be my mirena coil. I never thought anything of it at first, but after reading other peoples side effects of the coil i'm beginning to wonder. Some people are saying that the coil had pierced there uterus and infected their ovaries, and they suffered with the same side effects that I am experiencing. I am scared as to what I think it may be, in case my coil has done the same. I have also noticed that i cannot feel my coil strings but at the same time I have not experienced any bleeding. Could anyone give me advice. Thank you N.

They think that I have either crohns or ulcerative colitis. I have tried antibiotics, lialda, mesalamine enemas, with no improvement. After another colonoscopy they put me on prednisone at 40mgs, 30, 20, 10, then 5 decreasing weekly. Well the first week was okay. I had some of the side affects, insomnia, extreme hunger, and crazy. I could deal with that. But then when I decreased down to 30mg, my body flipped. I awoke from the middle of the night with burning pain in the knees. So bad I took 4 ibuprofen and threw myself in the tub with epsom salt. I thought okay that was weird because I have never had a joint pain in my life. I saw the gastroenterologist that day bc I was still having abdominal pain. He totally blew off the knee pain and said he had no idea what that was. I thought okay maybe it will go away. A few days went by and nothing. 3 days later and I awoke one morning crying in pain because of my legs. I called the on call doctor who also said he had no idea and go to the er. So I went crying hysterically for 4 hours. Even after 3 rounds of dilaudid I was still in pain. They suggested a Rheumatologist. So I went to one a week later who said I was going through steroid withdrawals. And there is nothing we can do but treat the symptoms of pain. I am now down to 10mgs have been out of work for 2 weeks and am absolutely miserable with severe leg pain, muscle weakness and fatigue. He also adjusted the drop down increments to 5 instead of 10. Anyway I will never take this drug again and I think they rushed to this one. Just wanted to share. I am glad I found this website because I went from a fully functioning physically fit 28 year old to a crippled crying crazy person. I think I was scaring my husband, honestly, until we both read some of your postings which were similar.

Im reading these stories and crying... So many lights keep going off the more I read... Im 30 and had my first child last June. They put the "thing" in 6 weeks post-pardum and it made me dizzy and sick to my stomach instantly, hut like hell, and I spent a couple days in bed on pain pills. But I figured a week or so was worth five years of freedom... HA!!! I had barely stopped bleeding and getting energy back for a couple weeks since before from having the baby, but this started that back up with a vengeance. I have been walking around like a b*tchy zombie for almost a year now. I actually went to the doctors in November to ask them if a pain I was having in my pelvis and my grumpy, irritable mood could be from the Mirena. I was told I probably had post pardum depression and possible a cyst, instructed to wait until after 6 or 7 months post pardum to see if my mood improved and get a follow up ultrasound if the pain in my pelvis got worse. Well that particular pain did go away, so I figured they were right, I let the "thing" do it's job and tried to forget about it as I was instructed to do. But the moodiness NEVER went away! I forgot who I was altogether, could not go to work any more, and attributed it to being a new mother, things change! Another 6 weeks later I actually split up from my fiance as I had driven him crazy... I spent Dec-Feb alone with a tiny baby, depressed out of my mind, and TOTALLY out of it everyday. Zero energy, but I figured I was just depressed. My fiance and I have since gotten back together after I practically had to tear him out of the arms of another woman, and convince him I could change. Still in all that time I never thought about the IUC. I still feel sooo freaking tired all the time, which has progressively gotten worse, and would have kept on except that about two months ago my back started hurting. I thought I pulled a muscle, so I stayed layed up resting. I thought I needed a new mattress so I went out and got another one, no change... Then I started thinking I might have some sort of infection, because Ive never had any muscle pain that lasted 6 weeks for no reason. I remembered the Mirena having PID warnings about people with multiple sex partners. Even though I have only had one, he had another, so I'm thinking I must have an infection and set up an appt to see the OB and get tested... In the meantime I came to this site after my mother sent me link of side effects... I read a few more each evening and have become more and more convinced that this is the problem, not only with my debilitating back pain (which has progressed into abdominal pain shooting down my legs as well), which has now progressed from irritable to severe, and not being able to function day-to-day. But also the moodiness, angriness, depression, foggy headedness, dizziness, headaches, lack of sexual desire, bloated feeling, insomnia - big time, I can be tired all day and it takes me two hours to fall asleep at night, then I sleep 10 hours and spend the next day tired all day - its not any way to live and I'm fed UP!!! - And then the hair thing... this topped it off for me, just too weird that all these people have the same problems, convinced me that I was fixable! It would have never occurred to me before I read this, but one day about 5 months ago I woke up with a weird new layer of very short hairs at the front of my scalp, not noticing severe hair loss, but my hair is VERY thick, so I cant really tell, but I did notice the short ones popping up. I actually thought my fiance cut my hair to use for voo-doo or something, I also thought my mother in law gave me something to dry up my breast milk, because shortly after having the "thing" installed my milk inexplicably dried up while we happened to be staying a week with them, now I think it was the Mirena. I have an appointment Thursday to take the "thing" out, and I am nervous about the pain, disappointed because the "thing" was so expensive, and I'm unsure what else to do about BC. But REALLY looking forward to finding myself again, I miss me, I know my fiance does, and I think my child would like to meet me too ;)
... Even if it isn't doing all these things, the paranoia and psychological trauma Im feeling just thinking about it is enough to convince me that this IS NOT for me! Wish me luck - I will follow up in a few weeks

My husband was recently prescribed Bactrim from his family doctor for a case of the ful. We thought it strange, since flu is normally not treated with antibiotics, viral we thought. Anyway, we felt Doc knew best, so he took three doses. His original symptoms of the flue were simply nausea, vomiting and a bit of diarrhea. After taking the bactrim, he developed a very high fever, headache, pain in legs and feet, burning eyes, chills so severe his whole body shook with a vengeance. He was sent home from the ER and told this was "worsening flu symptoms" and to continue the medication. We didn't follow the advise, and thought it might be the bactrim. He still continued to get worse, and went back to ER next night, bad stomach pain and all other symptoms worse. We found out it was all due to the bactrim, which shouldn't have been given in the first place for a mild case of the flu. He also suffered decreased kidney function, which has taken some time to come back to normal (luckily). His heart rate is still increased after several days, and may remain so permanently, requiring him to take beta blockers for the rest of his life. The doctors won't admit this is from the bactrim, but i have found medical literature stating otherwise. His doctor said it was his fault for not reading or understanding the little insert that came with his medication from the pharmacy. A lot of this information wasn't even on it. There are so many other choices of antibiotics to use, which do not chance a horrible reaction, permanent medical problem, or a fatality, which seems to be the case more often than it should from the medication, bactrim.

I have been on Cymbalta for about 6 months now and I have had to learn to live with at least 7 days a month of yeast infection symptoms. I know this is a side effect of Cymbalta, as I advocate against using medication whenever possible. I have only had this condition since starting this med, and over the counter creams and suppositories don't affect it or help at all.

Has anyone else had this? My doctor does not believe there is a link but I know this to be my truth.

I just discovered this after 3 months of total misery, 7 different doctors, multiple tests, 1 hospitalization, 16 pound weight loss, almost lost my job, etc., etc., etc.. I want to know if this will have permanent effects on my body and heart and will I ever be the same again. I have been back on the brand TOPROL XL for 9 days now. Keep in mind I didn't know what was happening to me, I never thought twice about the switch to generic, it was cheaper and I also had a lot of stress going on in my life at the time.

My pharmacy switched my "Toprol XL 50 mg" to a Generic one called "Metoprolol Succinate ER 50 mg" (manufactured by Sandoz) in December 2007. I have been on some form of Beta Blockers for years due to PVC's, AVNRT, Bigeminy, Trigeminy and Couplets. NOT High Blood Pressure. In my case I get very symptomatic from the arrhythmias: very low blood pressure, chest pain, fatigue, blacking out. I've had EP studies and attempted ablations in the past, but they were unsuccessful. For the last 2 years I had been under control on this med. Within a week of starting the new generic, I was at my eye doctor because my left eye went from 20/20 to 20/60 and was so blurry that I felt like I had suntan lotion or something in it. The new symptoms just kept coming. Since Dec 07, I have been to a Neurologist, Neuro-Ophthalmologist, Endocrinologist, Gastrointerologist, Ear Nose and Throat Doctor, Cardiologist, and many more. The generic form caused my arrhythmias to come back with a vengeance, I got depression, I couldn't sleep, my chest hurt, my BP was like 85/45, I lost 16 pounds and couldn't eat. I was almost passing out, seeing stars, I had bigeminy/trigeminy day and night for days on end, I was crying for nothing, very moody, I was coughing and wheezing, I had tingling in my arms and hands, loud ringing in my ears, I couldn't concentrate let alone think. I had tons of blood work that the doctors said, "just didn't look right". Upper GI test discovered a hiatal hernia, MRI discovered brain lesions, I had a high red blood cell count (but not anemic), my ferritin was high, my blood sugar was high, I was tested for MS, Lupus, thyroid, everything under the sun and was borderline for these diseases! I thought I was going to die, I had never been depressed in my life and this was the worst. I was beginning to think I was a hypochondriac. But, it was all there on paper, all the tests showed something wrong, but they didn't know what.

I googled Toprol brand versus generic and found out that it wasn't just me, thousands of people have had these same reactions since they started making Generic Toprol. Please read up on it, everyone who writes their story can't be wrong (there is at least one from every state complaining of the same thing). I've been taking the old TOPROL XL BRAND for the last 9 days and my arrhythmias have completely stopped, I have an appetite again and the depression has lifted. I hope it didn't cause any permanent damage.

I know this is probably happening to people everywhere who don't have access to the internet or maybe don't get out much. If you ask the pharmacist, they will tell you that they are exactly the same and they are NOT. The generic may work perfectly for you, but it doesn't work for all. In trying to figure out why I was so symptomatic, the doctors in the hospital took me off the beta blocker completely....I could have had a stroke or heart attack. I started back up on the brand name when after I googled it and realized that you can't just "go off" Toprol. I just wish I would have discovered it about 3 months ago. They thought for sure I had either MS or Lupus and were trying to rule out all the mimics of these very serious diseases. I'm going back to my doctors and have them repeat all the blood tests, etc. to make sure everything is back to normal.

I'm trying to get the word out.

I had a Kenalog shot march 07, and it seemed to work wonders. In September, my allergies came back with a vengeance, so I returned to the same doctor. I was given another shot, in the same spot on my buttocks. I started having my period every two weeks. Normally very skinny, I have gained about 10-15 pounds. I started to notice facial hair. I went to an OBGYN and was tested for PCOS. A weeks ago, my boyfriend noticed a large indentation in my buttocks, with some bruising at the site of the injections. One of our friends mentioned a similar side effect from allergy shots. After researching and reading all this... I believe both of these to be side effects from the shot. I was never warned of any side effects, only told it would be better than taking a pill every day. I am so terrified and so depressed about this, I wish I would have been warned. I am not sure what to do!

I started taking Lisinopril in October of last year and at first I thought it was great. It reduced my blood pressure significantly and stopped my migraines and stopped my ankles and hands swelling. However, in January of this year I started to experience very painful, itchy swollen eyelids and a general feeling of itichiness all over my face and neck. As I have suffered from eczema on and off for years, though never on my face, I put it down to that. The itching and redness does respond to steroid creams and antihistamines a little and it clears up for a while, but then is back with a vengance a few days later. It's very embarrassing and I have to stop wearing make-up when it's bad. I've only just realised after six months of this that it could be the Lisinopril. I've also had a bit of a dry cough but not enough to really bother me. However, whilst making breakfast one morning this week I nearly fainted so now after reading everyone's experiences on this website I really think I need to visit my doctor and have my medication changed. Thanks to everyone who has contributed to this site - it's really helped me to know about the side effects of Lisinopril.

Take large doesage of Lamictal. 400MG in the AM and now 400MG in the PM. 7 months pregnant and the level keeps falling. It does work I think to help control seizures some. Still have a few cp seizures but not too bad.
Do have racing heart beat once or twice a week and when the dose in increased the dizziness does come with a vengance. Usually after a day or so the dizziness does go away.

i have been on yasmin for three years. the first side effect i noticed was the dizziness. i used to have awesome balance (i was a gymnast), but now can barely stand on one leg with my eyes closed. the week after i started taking yasmin, i got in TWO car accidents and messed up my perfect driving record. i attribute it all to the dizziness.

i have PCOS...severely. my doctor perscribed yasmin to help control the disease and slow the facial hair i was slowly but steadily accumulating. PCOS also caused a me to develop muscles incredibly fast. i had a very boyish phsyique...broad shoulders, square waste, lots of muscle definition. i hated that so much that i felt the yasmin was my savior. he also put me on aldactone (spironolatone - the drug they say not to take with yasmin), but this caused me to become so exhausted and my hair to totally dry out. i went of the medication, but stayed on yasmin.

suddenly, i am experiencing horrible nausea and stomach problems. i can barely stand to eat anything other than yogurt. this has been going on for about a month, and i am so sick of being sick! i am also experiencing fluid retention to a severe degree. i am trying to flush it out by drinking tons of water, but i dont' think it's working. i have water in my ears as well. no one has been able to determine a reason that my ears hold water constantly. it's the worst pressure headache you'll ever experience. i believe yasmin is responsible for my nausea because when i had my period last week the nausea went away. sunday came around and I am back on the pill, and the nausea is back with a vengance. last night i dryheaved until i couldn't stand it anymore and just gave up and went to bed. i didn't sleep very well because of the numbness in my arms and legs. it's been keeping me up all night lately.

i scheduled a doctor's appointment tomorrow. i asked if they thought yasmin could be responsible for everything i've been experiencing, and they said not if i've been on it for 3 years. i'm so happy to have found this website. it makes me think i am NOT crazy and the pill is really messing me up.

i went of the pill for a week and lost five pounds previously. i'm hoping that going off for a while will be the right thing for me to do and i'll have relief from all of these horrible symptoms!