Gp symptoms and conditions

I've been on Omeprazole for about 8 weeks now for acid reflux and for the last six weeks or so I've suffered from a very dry mouth (constantly drinking water!!), sore throat, occasional headaches and insomnia in that I'm finding it increasingly hard to get off to sleep. When I do get to sleep and I wake up I feel like death, my mouth, throat and nose feel like they're full of mucus that won't shift.

For the last week or so I've felt like my mouth and lips are swollen up - I've only just read the side effects on the leaflet with the tablets and several of my symptoms are listed on there so I'm thinking it's not psychological, has anyone else had a similar allergic-type reaction?

My GP has advised me to come off the Omeprazole when I finish my current box, but having read the side effects I'm coming off them tomorrow.

I had my Mirena removed over a year ago. No period at all whilst it was fitted nor since its removal- until last night. I have, at the moment, what I recognize to be a normal period (am seeing a GP to make sure) but would be really worried if I had not read so many other Mirena 'horror stories'.

Thank goodness it is not all in my head. For the past year, I have been feeling as strange as the comments I have just read. Life is hard in the first place, but since having this IUD, life has been hard and very overwhelming. I have had constant mood swings, at least 3-4 days out of the week. Not only do I feel extremely nauseated 10 days before my period, even after it has come and gone, I feel nauseated again a week later. I had hoped that this new method of birth control would give me new freedom to have relations with my husband without being overly concerned about getting pregnant due to the less likelihood of the device failing. Boy was I wrong. I don't even think about sex. Nothing for the most part that he does turns me on. I can't even concentrate on feeling sexual when we are having sex. I just want to hit him or flip out on everyone. I feel a flush of anger go through my body that makes me think of very dangerous ideas, such as harming myself or others that are not really doing anything to deserve my anger. I have been very paranoid about everything and feel that I can not trust anyone, especially when I am telling them how I feel. I think that they just think that I am crazy. I have had extreme pain in my back near my spine, which I had thought before reading your comments was perhaps a side effect from the epidural I received during my child birth. I also have extreme pain in my sacral and hip areas that I never had before. My stomach is bloated with more stretch marks than I had when I was pregnant, my feet hurt. And I have an uncontrollable hunger at times. My short term memory is passe'. In fact, I took off my engagement and wedding rings in the house and can not for the life of me remember where I might have put my engagement ring. I am going to have this thing removed as soon as I get on my husband's insurance, before I go completely mad and hurt myself or my family. In closing, who cares if our doctor doesn't believe these things are not side effects. The truth is that God created all of us with common sense to know if something is blatantly wrong with us. We need to be wise and take care of our bodies and minds. This is something that God expects us to do. We have to live up to our obligations and commitments to our families like we promised we would when we got married.zfcII.

It was such a relief to read side effects experienced by so many ladies, i was begining to believe i was loosing the plot!!! what with mood swings, nausia,headaches,stabbing pains,and much more.... I had the mirena fitted about 8 months ago for heavy painful periods which i have had for as long as i can remember so the thought of normality and freedom was heaven. also not having to go through anymore trial and error medication taking seemed to good to be true. I really thought mirena was my answer...(Oh How Wrong)..... Iv had enough of all these horrible feelings and was about to go to my GP for a prescription for something to treat depression, im normally quite a level headed person but i couldn't explain the feelings i was having. I decided to look on the internet for side effects of mirena and hey presto here i am!!!! what a relief i actually did because instead of taking another prescription away with me i hope to be getting this foriegn body removed ASAP... before Mirena my specialist told me my other option was a hysterectomy im not sure what this procedure involves for me but at this moment my priority is getting this thing out!.

The doctor was observing me for very low globulin G levels and had me on 500 mg Keflex for a month trying to make my body "respond"? I took a bad sinus infection, went to my ENT, and he took me off the Keflex and put me on Cipro (500 mg) twice a day. I had taken this almost two weeks when my ongoing appt. with the first doctor came due. I called her office and they said I must come on in to get my lab work done. I did and she saw how sick I really was. She took me off Cipro and put me on Levaquin which I had never taken. During the first three days, I got sicker and sicker.
I thought it was just the "sickness" getting worse. One day I sat staring into space for over an hour without realizing what I was doing. Also, that day I noticed large knots in various places (under the skin). I live alone and became increasingly concerned. May I say, during that space in time,
I lost 25 lbs almost immediately. Nassau, sinus worse, felt terrible, and
hurt like the dickens. I could not sleep (and still have problems with it) and thought it all me, having never read anything about side effects. That night at 2a.m. I found the sheets that came with it, read, and identified with
everything written on the paper. I had to take one hand and put it under the opposite arm at the shoulder to help move it from my side. The muscles in the upper arms were like - separated. I found large knots under
my arms as on my body in various places. I could not raise my arms away from my sides. At 8 am I phoned the doc's office. They said, oh! it couldn't be that bad. I faxed the underlined, highlighted sheet to them and fifteen minutes later they called. The doctor said not to take any more
and it should be out of my body in 48 hours, if not see my primary phys.
She knew my GP had retired to help with her son, and had talked to me about taking her place until I got someone. A lot of it was out of my body in approx. 48 hours but my right arm (upper) and upper right leg was a mess. It is some better after April - Oct. taking medicine, therapy, and exercise but I still limp, especially when I get tired. There had been no strength for a long time. It was like the muscles separated and tendons enlarged, strutted, are very painful. The challenges are great up and down steps, etc. Can't lay on that side at night, put pillows under and between legs and when the doctor examining did a "frog-leg" with the right one, it didn't want to hold me up for several days. When I walk it gets to hurting very badly. Can't cross my legs when I sit. Wiggle and turn when sitting.
The very bad thing is this: The doctor never tried to help me get over this. When I went to other doctors for help, most of them looked the other way completely. For example, I tried to tell my new primary about the problems and pain from the muscles and tendons - he suggested lab work and a colonostomy. A rheumatologist kept saying I had "hip" pain. He did sent me for therapy though with a diagnosis of tendinitis in the upper arm.
He never addressed the case and cause. I would like to know if this is something to last the rest of my life. What can be done? You can only have therapy so long. An assistant told me to look this up on the internet.
I did not know this existed but I'm glad to know it has not all been my
imagination or "in my mind". My symptoms: dropped 25# in about three weeks, nausea, depression, sleepless, severe pain, taunt stretched tendons, droopy separated muscles,dizzy, and more. If anyone has any answers of who to contact and what to expect, please tell me. I've had anyone I talked with or saw to make note to never give this to me again.
God bless all experiencing these bad side-effects and make us well
again. --By ******

I was prescribed Metronidazole for an abscess in my gum, I only managed to take them up to day 2. I had terrible dizziness and basically felt very drunk, (if only I was). By the end of the day I was unable to drive back from work and was instructed by my gp to stop taking the pills immediately as these side effects are very common. Never again will I take them!!!!

I have had two mirenas, the first was fantastic. I never had any side effects and it was the best thing since chocolate!!! However the second one appears to have only lasted two years. This last month I have had stomach cramps and mood swings but no bleeding, the GP suggested I have it removed which was done today to see if this was what was causing my problems. I need to go back in one month. Will keep you posted!!

hi there i have been on simvastatin about a year now and have felt so ill since taking them i am now due to have several blood test to see what they can find " as i suffer with nausea, pains in my legs and body /and terrible depression and i cant remember me feeling like this before i started taking these tablets i really don't feel like me no more / and i can easily sit down and cry because off feeling like i do / now i have been told to take double dose because my cholesterol is higher / i have spoke to others of these tablets and they have had same reaction so i have decided on my own thoughts to stop i will tell my doctor.and i am hoping i will get back to my old self i will try and keep my cholesterol in control and i think its well worth a try than to have all these side affects B.

After reading the comments posted here I was rather alarmed to say the least. I've never heard of this site before, but I'm really glad that I'm doing some research for my not have book project, otherwise I would not have stumbled across this site.
I had been prescribed Yasmin by my GP at the time, I remember asking about any side effects and was simply told nothing out of the ordinary to worry about. Now that I think back to that appointment what an absolute idiot I feel. I had been taking Yasmin for 5-6 months. I started noticing that something wasn't quite right coming into the third month.

I was experiencing being extremely insecure, suicidal thoughts, crying for no particular reason, extreme mood swings, irritable, anxiety, depression. head aches, socially withdrawn, lack of interest in sports and keeping fit, weight gain, lack of interest in life and violent behavioral outburst.

I had under gone several blood and urine test only to be told that everything was normal, and that I need a holiday - I was just stressed out. My poor Boyfriend, the crap that I would dump on him became unbearable. I couldn't help myself, I had no control over what was happening to me. I started to loathe my work environment and the work colleagues.

It was until my boyfriend and I had an all mighty king disagreement of all disagreements with me venting like Mt Versuvies and physically attacked one of my best friends that I had convinced myself there and then that I was having a nervous breakdown. My boyfriend and I where we were working decided to leave and for me to get medical attention once and for all. We both knew that something was wrong with me big time, but had no idea that this little pill would prove to be so deadly. That day was Monday the 1st of Sept. The day we decided that enough was enough and seek out medical attention.
First I got rid of my usual GP and found a much better switched on intoned female GP. My mother had first planted the suggestion in my head after hearing what I was experiencing. She said to me I think you have been poisoned and I want you to take along all the medication including women's multi vitamins along to your new GP and show her.

On consulting my new GP she too asked what the matter was, I therefore relayed my symptoms again and showed her all my medications and bingo she simply said it's the Yasmin pill that you have been taking that has been causing you all this grief. Just like that, but to be on the safe side she sends me off to more tests and she's right. So what to do about the poison in my body. I undertook a drastic change in lifestyle and dietary intake. Made a commitment with myself no working away in the bush until I have detoxed the toxic chemicals out of my body. Total vegetarian, fruit and vegetable juices 3 times a day, over 2 litres of water, 2 Tblspn castor oil and 2 Tblspn of olive oil daily. Colonic hydrotherapy every second day followed my endermologie sessions also - 3 a week. Daily yoga stretches, reading self help literature and researching this horrid pill. Oh course this isn't for everyone and can be quite costly - but now Sunday the 28th I glowing with improved health and well being. I above mentioned side effects have have most like magic disappeared from within.
The hardest thing accepting that I was doing this to myself and not knowing that I was poisoning myself. I hope everyone else out there that has been experiencing the same horrible side effects can find a solution to getting themselves back on track and finding that they will sparkle again if not brighter.
By MissFreeSpirit

I am 43 year old financial advisor at the second largest bank in the United States. I have always considered myself in very good athletic shape. Three star athlete in baseball, football and basketball in high school. I went on to letter for four years as captain of a division I baseball team. After college I continued to run, work out, and manage/play baseball up until this day. It was at my routine physical that my Dr diagnosed me with hypertension. No surprise I thought as being under plenty of pressure at work. My blood pressure was140/85.
Although I continue to work out three to four time's per week my weigh has spiked from 190lbs to 208 lbs in the year and a half that I have been taking Linsinopril. Until I found this web site I couldn't explain the cough, pain in the left side of my neck or the feelings of emptiness/depression that have followed me around like a cloud. That is when I can get out of bed and function that is. I used to be happy and fun loving. The person that you wanted to be around. I truly believe that this drug( that I have heard contains snake venom) is a big reason why I haven't been myself. I am not the type of person to spend time researching the internet and have always been skeptical of nuts writing or responding to any one or thing over the internet. I consider myself to be fairly rational and sane. However, this drug has made me dull and empty. My lowered sex drive almost ended my marriage. For a year in a a half I have been in a psychotic hell. I never thought about questioning my Dr. until recently when my marriage almost ended as a result of my feelings and anxiety attacks. Although my blood pressure is 115/70 my life has been a mess. I find it hard to believe from the posting here that only 1% of users of Lisinopril have suffered any type of serious psychological reaction to this drug. Perhaps the clinical trals focused on rats or elephants, but certainly not living humans.

I have since stopped taking Linsinopril (two weeks now) and the sun is beginning to come through the clouds again. If you have been taking this drug I plead with you to stop immediately as it seems enough clinical data was ever taken to fully understand the impact of this drug.

I hope that someone else does actually read this post and find it useful enough to impact their life. STOP TAKING THIS POISON

I'm 42 and have 2 children. I had Mirena fitted end April 08 after a recommendation from a friend. A month later I noticed joint pain in my left thumb which over the weeks and months spread to all my fingers, then my hips and finally general stiffness all over. I was training for a 5K at the time and just put this down to post running achiness. I didn't initially connect this to Mirena, I just worried that I was showing signs of arthritis and went to see my GP. No mention of Mirena from her but she just did some tests to see if it could be viral or some form of rheumatism. All results came back negative which was a relief but nothing more was suggested as to why I was having these problems. (which for someone who rarely visits a doctor made me feel as if I was going mad and imagining things) It didn't improve - I was also getting palpitations from time to time so after googling mirena and joint pain I was surprised (and a bit relieved) to find many blogs about this problem, mainly in the US (I live in the UK). Went back to doctor at local family planning clinic who told me yes mirena could cause some arthritic symptoms but she was noticeably reluctant to concede that this was causing my problems. I was urged to keep the Mirena and see a rheumatologist first.

I got the distinct impression that the professionals I spoke to are going to extreme lengths not to say for certain that this device can cause serious and debilitating arthritic pain in many cases.

I have an appointment to see a rheumatologist and I decided to have the mirena removed 5 days ago. I'm hoping the joint pain will go. But am worried this IUS may have triggered something in my system that may not go away.

I'm 34 and my children are 3 and 5 years old. I had my Mirena coil fitted on 12 Sept 2007, so have now had it just over a year. During that time, I've had bouts of intense abdominal pain, almost constant vaginal discharge, bleeding after exercise or sex and a curious sensation in the region of the uterus that feels like when a baby moves inside you. My doctor dismisses all my symptoms as being nothing at all to do with the coil, but having read the other posts on this site I'm not so sure....
I'm also constantly exhausted and get spots. I am a coward though, and having the coil fitted was so excruciatingly painful that I'm not sure I can face having it taken out so (relatively) soon. I'm off to see the female GP at my practice next week so it will be interesting to hear her take on things.

I am 45 and have been taking statins for 5 years since having 3 heart attacks in a 4 day period.At first I was on Atorvastatin 10mg and didn't suffer any side affects,I was put on Simvastatin 40mg 2 years ago due to cost.Since then I suffer with very sore muscle pain down the length of my right arm.My GP keeps on prescribing painkillers and doesn't mention the fact it may be side affects of the Simvastatin.I find it sad that costs of drugs are the reason I am in pain.

I've been on simvastatins for about 2 years after TIAs. I'm 56. I had two small Strokes about year ago despite being on simvastatins. Had brain scan which showed two small areas of scarring and carotid artery scan- arteries fine. Started experiencing dizziness last year and GP diagnosed vertigo and gave me seasickness pills which didn't do much good. Since then I've experienced headaches which last for weeks, increasing fatigue (now struggle to get out of bed in morning) muscle pain which is getting really bad and sore feet (?). Increasing memory loss, confusion, lack of concentration, eye problems (when I first wake in morning my vision is blurred for ab out 30 minutes or so. I've been worried i mmay be developing Alzheimers. I've also piled on weight and the texture of my hair has changed - it has become very soft and silky and become thinner - normally my hair is very thick. Also I've had two perms in last 6 months which won't hold curl - been having perms for years and never had this problem. I've had several blood tests including for under-active thyroid and they have all been clear. I've been really worried about all these problems and did some research and came up with this site. I am beginning to think my problems stemm from taking 40mg Simvastatins so am going to stop them and book appointment with GP. Any comments/advice would be appreciated.

I have been on Coreg for 1 year and switched to Coreg CR(time Release) for the last year. Since then, I have had bronchial inflammation that I have had to use antibiotics to recover from what starts out as a normal cold or flu. I have never had to use anything but over the counter meds in the past, and rarely got sick to begin with. This has occurred 3 times since Feb. My GP told me that this is a common side effect for this class of drugs. I work out 3 times a week and ride about 20 to 30 miles a week on my bike in addition and have had no other problems. Does this sound similar to anyone elses experiences

I have been io Lisinopril for several months, and the only side effect I can say is a VERY ANNOYING rash on the inside of my upper thighs. It comes and goes and gets worse with warmth, like a heat rash. I also have now developed a rash on my butt that is looks to me like shingles. Very itchy, to the point of bleeding from scratching. I treated with diaper rash ointment and triple antibiotic ointment to not much improvement. Reently tried a jock itch ointment which seems to be working. Also took myself off Lisinopril 2 days ago, and things are getting better, but very slowly........

I just came back from my GP and I am off work now until the end of the week and it's all because of Yasmin. I decided to go on the Pill as I started a new relationship and was told by my friends that this was the best pill available on the market. My doctor put me on it as well but from day one it's been a disaster. I am very thirsty, it makes me go to a bathroom every 20 minutes, I became very moody, irritated and almost depressed. And this is only after 6 days of taking it!. My breasts are very sore, I feel completely out of place, hot flashes and mood swings.I feel like a zombie. I cried in a bathroom at work today. I cried in my manager's office today as she wasn't sure what was going on with me. Thank God, she was very supportive and understanding. It was her who encouraged me to stop it straight way. The doctor I went to see today said to me the same thing - to get off it straightway. Hopefully I will become a normal person soon. I will be trying another type of contraception but will never go back on the pill again. In six days it turned me from a happy person into a person that I can hardly recognize as myself. And from reading all the comments which have been posted here, it makes me think that it's not worth it. I will be trying another method of contraception but will not be messing up with my body again. The price to pay is too high.

My 71 year old mother was put on Advair approximately two years ago after she was diagnosed with COPD. She has always been a tiny, petit woman her entire life, and after being placed on Advair she has nearly doubled in weight. This week she has broken out in shingles (herpes zoster) on her back and left breast. For a year she has had psoriasis on her right hand. Never before has she had so many rashes and skin issues since being on Advair. She has also experienced joint pain and numbness since being placed on Advair and began having panic/anxiety attacks as well - something she has never had in her life. Also, the hoarseness, or "lump in her throat" she is always trying to clear is nearly always present. Monday she is suggesting to her GP that she be weaned off of Advair altogether and we'll see what other options are available. Maybe this is the "miracle drug" for some; but for others it has been a nightmare.

I have been taking Yasmin about 12 days. I have experienced some but not all of these symptoms. Sometimes I think Im crazy, that it must just be me but other times Im convinced that it must be this pill. I have only read page 84 of comments but I was wondering if anybody felt like they were just zonked out. Like sometimes I just feel like Im staring into nothing with no particular thoughts or anything. I just feel like Im there zoneing out and like I cant feel or be any other way.

I hope someone can help. I am 42 year old female and I have been on Lisinopril 9 years. I now take 5mg daily, down from 10 when I first started taking it after developing cardiomyopathy. Lately my ever constant post nasal drip is worse, my throat is sore, headaches daily. I clog the sink daily with the hair I lose after the shower. My GP doc has done loads of tests on my head to check causes of headaches but all is normal. Never mentioned maybe 9 years straight on Lisinopril could be the problem. Of course I can't see my cardiologist for weeks. Any one experience the same?

This is my second bout with what my doctor thinks is erlickiosis. The first time I was at the point where I could only move like an old man doing "the nursing home shuffle". Everything was swollen. Feet, hands, knees even my jaw was hurting. I couldn't stand on my own even though two weeks prior I was walking 3-5 miles per day on some good size hills. I was hospitalized and given steroid injections. Within 12 hours I was standing on my own. I was given Perdnisone 30 mg X 3 days 20 mg X 3 days 10 mg X 3 days 5 mg X 4 days. Except for some insomnia and peeing 5 times a night there were no other effects. Within 2 days I was crippled again. Now my GP was in Africa and my Internist was leaving for vacation in India. Internist would not put me back on Prednisone because he wanted me to see a Rhumatologist. I made an appointment but it was SIX WEEKS OFF. Two days later i was admitted to a different hospital. This one was where my Rhumatologist had access. Long story short Prednisone 80 mg 7 days 60 mg 7 days 40,20,10mg 7 days each. Had to start taking insulin again. Glucose never went over 200. Avg glucose last 5 weeks is 120. Gained 5 pounds because I work out every day with free weights and lots of cardio. Hopefully, I won't have to many side effects when weaning is accomplished.

Do any of you take Lisinopril by itself without a diuretic like HCTZ (hydrocortothiazide)? I got dehydrated 2 days ago & doctor has cut my HCTZ in half-- I felt light-headed, dizzy, pounding heartbeat like I was having a panic attack. I've been on this lisinopril/hctz combo for 3 months. I don't have any of the adverse allergic reactions (rash, itchiness, swelling) at all; nor do I have the cough thing at all. But weakness, chest-pounding heart, dizziness, fatigue all coming now daily. I wonder if our problem is the HCTZ, so is anybody on lisinopril WITHOUT HCTZ?

Everyone here PLEASE LISTEN TO ME! Dr. Holtorf in Torrence, California is the only one who tests for REVERSE T-3 and 80% of people are not being treated properly for thyroid function. The Holtorf Medical Clinic is the ONLY way you will find the answers and people are experiencing miracles.

Yes, kenalog has many side effects with SOME people. I'm both a patient that takes kenalog and a third year medical student. I've been receiving kenalog injections twice a year during allergy season for the past 5 years. All I can say is THANK GOD. I can deal with a itchy/running nose, the sneezing, and the itchy eyes. What I cannot deal with are the asthma symptoms that act up whenever my allergies do. I get little enough sleep as is, what I do get doesn't need to be interrupted by waking up not being able to breath.
What must be realized here is that however many posts are on this and like sites, the people who suffer from the side effects are in the minority. For most patients this drug provides great relief with little to no side effects.
For those who said that their doctors did not tell them what they were being given, or warned about the side effects, yes, those physicians should have warned their patients about the possible side effects. HOWEVER, it is also YOUR responsibility as a patient to ASK what you are being given, and what the possible side effects are. Never let anyone just stick a needle in your butt without asking what the heck they're doing first. I'm not defending those physicians that don't tell the patient what they're doing; they are in the wrong. But they see tons of patients very day, most of it route. And many patients lack the knowledge to ask what they are being given, and what might happen from it. Even if the physician took the time to explain, a lot of people wouldn't understand or simply don't care. Don't be one of those patients. Ask your PCP: what is this drug? what does it do? what are the possible side effects? what percentage of patients experience these side effects?. Take some responsibility for yourselves.

I found this site as I want to read on the side effect of this Kenalog which was injected to my face by the doctor to reduce the size of two liquid cists (apparently only one injections). After the injection, I had my period which is only 15 days after my last period, which never happened to me as my cycle is always longer than 30 days and is very regular. Per the doctor, I thought the "cist" would be gone in few days. It did not and instead, I experienced rashes on my entire body and after one week, my ankle and knee was swollen and it was rather painful and I can hardly walk around for two days. Together with the swollen on the leg, the injection on my face is also swollen up and my face looked really in bad shape. I went back to the doctor and I was given one week of antibiotics to drain away the "infection".
Since the cist is still on my face and it really bother me as it is red and very itchy, though my face is not that swollen / puffy anymore. I came back and see the doctor again to have him cheked up on my face. He just gave me one month of antibiotic. I have no idea that having that injection would cause me so much troubles.
It is now more than a month after the injection, my face has a hole as that was injected with kenalog and the other cis on the face is still there. The worse thing is that the cist is is getting very itchy and it was not so before the injection. I am still patiently taking the antibiotic and promised to comeback and see the doctor after one month.
I still having pain on my join and reading your comments, I realized the pain is definitely associated with Kenalog.
I'd love to hear more from you on how things turn out. Thank you.