Fist symptoms and conditions

I am 61 years old. I started taking Lisinopril 10mg, once a day about 6-7 months ago. Because of cough, I switched to Diovan 80mg, once a day (samples from my physician friend). After running out of Diovan samples, I started taking Lisinopril 5 mg, once a day again about three months ago. For better BP control, I ended up again taking Lisinopril 10 mg, once a day about 5-6 weeks ago. I started to simultaneously suffer from having persistent, extensive and progressively worsening joint and muscle pains in my both sides of neck, both shoulders, both upper arms, left elbow, left lower arm, both wrists, both hands, all fingers, both knees and left calf muscles. I had difficulties walking, moving my arms, shoulders, doing anything with my hands at the peak of the pains about 7-8 days ago. In the night, my fingers were very stiff and uncomfortable that I hardly could make a fist and I had difficulties getting up to go to bath room because of pains. I felt like I were a 90 years old man. Even Cataflam and Advil did not work well to relieve the pain. As a retired physician, I started to suspect it was Lisinopril-induced side effects. I searched on Google and found this web site. Now, I realize that I am not alone. I got my Lisinopril from CVS Pharmacy. I immediately stopped taking Lisinopril about one week ago. All my joint and muscle pains have been dramatically subsiding (although not completely disappeared) without taking any NSAID pain killer. Even "cough problem" became much worse during the same time. I am convinced that Lisinopril I got from CVS caused my serious, extensive, multiple joint and muscle pains. Perhaps, FDA should look into this side effect: whether it is common ACE inhibitor related side effect or it is possible manufacturer, country origin of the product related problem (made in a non-USA country and imported by CVS?). I would never take Lisinopril again. Posted by myh810.

I was taking Lisinopril for a month. I am a 38 year old male. My fingers on my right hand and joints began to ache and swell up which is making them weak and painful to grasp anything or make a fist. I never had these symptoms until I started taking this medication. I continue even after stopping Lisinopril for the last 5 weeks. Now my doctor is thinking I might have Rheumatoid Arthritis. It takes 4 weeks for this Lisinopril to work. Which is bringing me to think this medicine caused me to have these problems by triggering something in my system. Has anyone else had these problems with this medicine?

I had my Mirena placed in April 2003 after the birth my second child and by August 2003 I had headaches, nausea, yeast infections, severe fatigue, pain and fever. By September 2003 I was fed up and made an appointment with a specialist, at my fist appointment he found a 8cm cyst in my left ovary and the 4 cm cyst in the right. The Dr. made me come in for an ultrasound every 6 weeks and told me the cyst will go away on there own. 2 years and over $10,000 in out of pocket medical fees asked to have the Mirena removed. The Dr. insisted it was not the cause of the cyst or pain and scheduled exploratory surgery. On September 16th 2005 the Dr. removed my ruptured left ovary and found a mass of scar tissue on the right ovary along with endometriosis lesions in on and around my uterus. The pain was gone for 2 months and quickly returned. I asked again to have it removed and when he declined I made an appointment with planned parenthood and had the Mirena removed. Since the removal of my Mirena I have had 1 miscarriage and 3 additional surgery's, I still have cyst on my right ovary and just had my first abnormal pap.

My eight year old son was diagnosed with mild asthma by our GP and was taking Ventolin for a persistent cough. When this didn't relieve the cough the doctor prescribed Singulair. He started the Singulair in March 2009 and within 2 months we realized that his personality had dramatically changed. It has taken us a while to figure out what was going on because eight year old boys are starting to assert themselves more and I think the side effects have been escalating over the last month. He was angry most of the time, very hateful towards his siblings, saying very dark, nasty, hurtful things. He argued every time we asked him to do something and would snap into a screaming inconsolable emotional wreck at the drop of a hat many times a day over trivial or imagined problems. He was having nightmares and bursts of hyperactivity that were overwhelming. He told us he felt frustrated all the time and hated everything. When we tried to calm him he was unreachable. Just yesterday he had his fist clenched and pulled back ready to punch me when I was trying to help him with a computer problem. He was shaking and his face was contorted with rage and he just wasn't my little boy anymore.
It has been devastating for our family and we were ready to take him to a psychologist. He is normally an incredibly considerate, perceptive, loving child, highly intelligent, helpful and fun loving with a great sense of humor.
He has also complained of leg pains and has been wetting the bed again. It was only yesterday that I began reading about other people's side effects and have taken him off Singulair as of last night. Whilst he has still been argumentative today already the aggressive intensity seems to be easing.
I am absolutely mortified that I allowed this to happen to my son and my family and I am so grateful to others for sharing their experiences.
We still need to address his asthma and will make an appointment with a specialist next week, but given his asthma is so mild he should not have ever had to suffer these side effects.
I only hope now that he has not sustained any long term effects and that his younger brother has not been scarred by the truly horrible things that my son has said to him.

My 14 year old daughter received her fist Gardasil shot in Sept/Oct 08. Soon after she started losing her hair and thinning. Now it is coming out in handfuls. She is so upset and I believe that she is becoming depressed due to the emotional heartache. She has not received any more shots. Anyone who reads this don't give this to your daughter.!

I had tried the ring back in august or September of 2008 for less than a week. I went without a period and a pregnancy till March of 2009. No dr knew why on either. I bled for 3 months. I kid you not. I have finally started to taper off and was diagnosed with bacterial vaginosis, cervicitis, and pelvic inflammatory disease. (PID) Up until the other day, I was still throwing clots. Luckily, they were much smaller than when it all started because those clots were as big as my fist. (About the size of a baseball, maybe a little smaller) But the last few days I was hurting so badly I had to go to the ER today. I was also having horrible depression to the point of wondering why I was even with my husband! I love him with all my heart and our daughter as well, why would I want to leave them?

I have a 2 yr old and I could not function enough for my husband to be able to leave the house because of the pain. I was put on two antibiotics and an anti nausea pill because the antibiotics prescribed are known for that side effect. But better nauseated than sterile since mu husband and I are wanting more kids. I don't suggest the ring for anyone because it's played hell with me especially knowing that the ring has even caused menopause and sterility as well as other worse issues.

54 year old Male, Retired Marine, Very physically active, with Type II Diabetes; 5mg. Thanks for this Website. Started Lisinopril 3/25/09. Took it for 25 days, found this website and stopped taking it immediately. I had severe JOINT PAIN. It started in my hands, then feet, knees were next, then moved into my shoulders. The pain was the worst I've ever felt. Approximately 60 days after stopping the drug I went to see the Dr. after the Pharmacist told me Lisinopril should have been out of my system after 2 weeks. The Dr gave me Steroids (Prednisol) which completely eliminated ALL pain in 2 days . I was tested for Polymyalgia Rheumatica, however the my Sed Rate was normal. The blood tests did reveal that my RHEUMATIOD FACTOR is elevated (34.3 where the normal range is 0.0-20.1 IU/ML). Was told that if the pain returned, then I would be referred to a Rheumatologist. 3 Days after finishing the dosage pack of Prednisol, the pain/swelling in my hands and shoulder has returned. Going back to see the Dr today to discuss next steps.

Although the doctors don't agree, I believe Lisinopril caused this pain, and although out of my system now, triggered something that isn't going away.

The rest of this describes the roving pains I experienced.

Hand pain included swollen fingers, inability to make a fist or type on a keyboard. After light yard work on Sat., shooting burning pain up the inside of both arms. Trying to close your hands into a fist, you can feel the tendons up your arm burn with pain. Motrin did not alleviate the pain. Hot water did not help.

Pain in my knees each morning. The pain worsened over night and frequently causes you to wake up. The pain was like your knees were being squeezed in a vice. No position is comfortable. Motrin sometimes helped, but after awoken, getting back to sleep was impossible.

Feet swollen. Couldn't wear any shoes for extended periods. Loosening the laces helps, but still caused pressure which becomes unbearable and the shoes have to come off.

Shoulders; This is the strangest one. First pain was in the left shoulder, like I had impacted a brick wall at a full run (actually no trauma occurred). The pain felt like someone had stabbed it in my shoulder in the socket. At it's worst, no position is comfortable. Had to put my arm in a sling. 5 Days later, the same type pain moved to the right shoulder.

My girlfriend is 36 she had a kidney infection and got Levaquin IV in the hospital. Her legs were going numb and she could hardly get up to go to the bathroom in the hospital. She thought it was her infection. They sent her home two days later with 5 pill containers. One of them was Levaquin. She called me today and said she is having terrible pains in her hands, wrists, hips, and knees. She says she cant make a fist or hold a bag of groceries and her hands have swollen up so that she cant get her rings off. I told her I would do a search on the net to see if it might be one of the drugs she was taking. Slowly but surely I made it to the Levaquin. The drug maker fairly non chalantly refers to tendon rupture as a side effect effecting mostly people over 60 years old. I dug a little further and found this web site and was amazed at how many people are being poisoned by this drug. I am praying if she stops taking it the pain and debilitating effects will go away quickly. She has two disabled boys she has to take care of, including lifting them into wheel chairs and into beds. This is no joke! I am so angry at this drug maker and these doctors who often times do more harm than good.

I've been on levothyroxine 150mcg for about 3 months before that it was 100mcg and so on. I have gain lots of weight and tired all the time. depression also, headaches. I hate this gaining weight, sleepy all the time and depression is from gaining weight. I thought this med is to up boost my thryiode but it doesn't seem to be working. my dr. said I'm on the highest dose there is. I don't know what to do any more. I was thinking about taking myself off this but not sure what will happen if i do. I hope there is someone out there that might be able to let me know if they are going through the same things what they are doing and how they feel now.

I have been taking Bupropion XL 150mg ("generic" Wellbutrin) once a day as a mood stabilizer everyday for exactly 2 weeks. I suddenly developed severe itching in random different areas on my body. My lower scalp, palms of my hands, and ankles were the first areas that itched but did not have any obvious marks on the skin as to what was causing it. About 3 hours later it became progressively worse and started showing tiny red raised areas in the previously stated places on my body and started to spread to my neck, wrists, mid-chest below my breasts, behind my knees, and upper thighs near the front panty lines, but even worse on my lower back.

I was becoming a bit scared and annoyed by the constant itching and the hives that were forming in those areas. I had never in my life had hives before. The bottoms of my feet were so itchy but they did not have any hives on them, they just itched! I took 2 benadryl and tried to sleep but woke up quite a bit during the night because of itching.

By morning, the hives were worse and especially on the back of my neck where it was swollen and red and I could not even bend my head back. My face was slightly swollen and my eyes were puffy as well. My right palm was so swollen and painful and I could not make a fist.

I called my doctor but he was on vacation, so I had to talk to a message service he had set up in his absence!
I went to the emergency walk-in care center near my home and was evaluated by a physician who concluded that all this was actually due to the Wellbutrin which I myself found hard to believe and wanted to deny it in my mind. He ordered me to stop taking it and prescribed all sorts of drugs to counteract the hives and itching.

I am writing this only about 9 hours after seeing the emergency physician and have had some rest and taken my prescribed medicines, Medrol ( a steroid-type drug) to treat the swelling, Hydroxyz hcl for the itching, Allegra for allergy, and Zantac for the side effects (stomach pain) of all these drugs I now have to take for a while!
The swelling has gone down a bit and itching has subsided somewhat. In conclusion I must note, that it was the pharmacy's decision to substitute the Wellbutrin my doctor had prescribed with a "generic" version (bupropion) that is still so new to the market and is still undergoing studies on human subjects. We are the guinea pigs and did not even know it.

I'm reading everyone's symptoms from the Mirena IUD and now I wish I never had it inserted. I had and IUD in for almost 6 years and had to trade it in for a new one. Not sure if my former one was Mirena because I didn't have bad side effects like now. In December I had the Mirena inserted and it was a very painful insert for me this time around as well. I immediately felt heavy cramping and couldn't stand up from the table it hurt so bad. I kept telling my GYN that maybe it was inserted incorrectly and she looked at me like I had 3 heads. She gave me Advil and told me to let it settle in. Needless to say I had some cramping for the rest of the day. 2 weeks later I got my first period following the procedure. It was normal, lasted about 10 days (longer than usual) and then went away. Yesterday, out of nowhere and only 1 week after it stopped, I experienced extremely red and heavy bleeding and clotting the size of my fist. I almost thought I was having a miscarriage or something. It's crazy how much cramping followed. I have been feeling strange all week, getting bad pimples on my face, gained a lot of weight over the holidays without really going overboard on eating, sex has been a bit painful and leaving pain in my lower abdomen. I've NEVER bled this much in my life. Not even after giving birth to two kids via C-section. It's pretty scary. I'm wondering if I made a big mistake. Never had problems like this with the last IUD. Leaving messages for my doctor but should I be worried???

I was diagnosed with PCOS and my doctor suggested getting on birth control to adjust my hormone levels. She suggested NuvaRing for it's ease of use. The first two months, everything went great... I noticed my daily discharge seemed to increase, but no real big deal. The third month was horrible.. I got my period and had THE worse cramps! I've always had a problem with pain during the first 24hrs, but this was unreal! Pamprin usually does the trick for me, and I only feel a dull pain, but not even Pamprin would rid me of this horrible pain. I few hours, the worst of the pain had past. I went to change my tampon, and I had discharged a section of my lining that was the width/height of my fist! No WONDER I was in pain!! I called my OBGYN and she said this is a side effect of NR, and is natural, no worries. This pain and large tissue discharge continued for 3 more months. I told the OBGYN I needed a different form of BC... she refused. Needless to say, I switched OBGYN's and I'm on YAZ now... since I've switched BC, I've had a light, and painless period. Obviously NR did not agree with my body. I like it for it's ease of use (I don't remember to have to swallow a pill @ the same time everyday), but it's not worth it for the pain I had to go through. I would NEVER recommend NuvaRing to anyone looking to getting on BC.

Hi,

Fist off I'm a fit 38 year old male, not overweight, don't smoke, occasional social drinker.

I've been taking Lisinopril since being diagnosed with high blood pressure in Feb 08, I was started on a dose of 5mg, which was then increased to 10mg and finally 20mg.

The Lisinopril never really got my high blood pressure under control and my Doctor has now switched me to Bendroflumethiazide, only been on those for about a week so have to see how they go.

Lisinopril certainly made me feel terrible:-

Constant Fatigue
Depressed
Foggy
No concentration
Dizzy
Tinnitus
Pounding headaches

if you feel like this then I'd go and see your Doctor and try something else

I've been on Mirena for about 14 months now. For the past 3 months I've experienced this awful allergic reaction on my face. I'm not completely sure it's being caused by the Mirena but it's weird to me that every time I've gotten this rash it's been between the fist and last day of my period. the rash starts with hives on my nose, chin, under my lower lip, and cheeks, and by the next day is blisters that crust over. By the 4th-5th day or so it's just very dry looking skin. It itches and burns so badly though and I don't know if I go through this again. If anyone has any insight PLEASE email me at ******!!!!

I have been on this medication for 3 months now. I am a 28 year old male, 6'2", weigh 211lbs, and in overall good health. My blood pressure average is 144/72 without the medication, but on the medication it seems to stay around 136/66. It took about one week for the blood pressure medicine to start working and when it did I felt very tired (which is normal). Now, in my third month I have started to notice new symptoms like severe headache in the right front lobe, severe tiredness, cold fingers and toes (in warm conditions), severe lower back pain, mood swings, blurred vision in the right eye (same location as headache), and a occasional twitch in my right thumb (probably not related to the medicine). When I first started this medication I did read all of these post and figured that everyone was crazy and/or nuts, but know I am thinking that I would rather stop the medication
and start seeking out for a better medication.. I know medicine has side effects but damn!!! Anyone else have cold fingers and toes while they have been on the medication..thanks

I just recently had the mirena iud inserted. Oct 30 2008. 3 months after having my first child under a normal vaginal delivery. When I have asked my doctor regarding any side affects he stated that women may have heavy bleeding the first 6 months/ and that after those 6 months that your periods will actually disappear.

The first week that I had the mirena in, I began bleeding almost instantly. Blood clots the size of my closed fist came out of my body from the uterine wall I suppose. I went through a super tampon/ and a pad in an hour and a half. ( I am one of those women who normally use a super tampon maybe once in a while/ normally a reg. size does the job) This bleeding has not stopped since the mirena was inserted.

Looking at a computer screen is part of my daily routine at work. It seems as though my eyes feel blurry through out the day as I am working. Towards the end of the day I can barely stand to look at it. This has never happened to me before. It is almost like I want to turn all lights off and sit in the dark, with no noise(headaches).

Of course sex drive is at the all time low. Who is in the mood to go for it when you are bleeding with a terrible headache?

The first few nights I had a horrible time falling asleep and staying asleep.

Well... at this point I have had headaches... all day for a week now. My head hurts like someone is pounding it against a wall. I have not had a headache in years. My stomach has been upset/ feeling as though I may have to throw up.

I am afraid that I may start seeing the other symptoms that ladies have talked about.
When you had the symptoms did they all happen at once or one at a time over different time periods?

Hi everyone....
I just had the Mirena inserted Friday...primary reason was easy birth control and second was because I did not want to take estrogen. I'm 29 and do not have any children so the insertion was pretty uncomfortable to say the least. I'm good with pain but this was intense...if that's anything like childbirth no thanks! Thank goodness its over quick. Anyway, I had some cramps afterwards for that first day and my whole "area" felt like it was clenched in fist...really tight and sore. I took Motrin and used a heating pad for my cramps. The next day I was good as new...no cramps, barely any spotting. So although it's only day 3, I'd say my experience thus far is totally manageable. Everyone's body is different. I've been through the ringer already with my hormones...been put on lots of different forms of progesterones to regulate my cycles and even premarin at one point...I know what hormones can do. If it's not working for you, you're not crazy!!!! Just tell your doctor you don't like it, you won't have it, and get it out! You've gotta be your own advocate in the medical world. No woman should put up with feeling like a lesser version of herself at the hands of birth control.
I'll keep yas posted as time goes on...I see that some women start out feeling great then get issues down the line.

I am a 22 year old, healthy female and received my fist two shots last September. By November, I began to notice my hair falling out, which became more excessive in December, prompting me to receive blood tests for thyroid problems, nutritional imbalances, etc. Everything came back negative and I self diagnosed the problem to be a hormonal imbalance caused by my birth control (which was hard to believe being that I had been on it for two years with no hair loss). I stopped the pill the end of January and my hair loss coincidentally stopped as well. I received my third shot in April, and sure enough the same devastating hair loss began two months later, which is classic with drug induced alopecia (hair loss). I am CONVINCED that Guardasil has caused this devastating reaction that has caused me to loose half my head of hair. It is October and I am still experiencing significant hair loss. This vaccine has caused me nearly a year of emotional turmoil over my thinning hair.

I had the Kenalog shot 3 weeks ago - lumbar region for bulging L5 disk pressing on nerve causing burning pain in my right leg from knee to ankle. 1st shot was DepMedrol - left me worse off than when I started. Next the Kenalog: the fist week afterwards I lost strength in my leg and couldn't walk up the stairs, plus pain worsened and I lived on Percoset. Then into the 2nd week the pain lessened and last week I felt great. Today am feeling some pain again and I've been bleeding since Saturday (I'm post-menopausal). Called my GYN and will need an endometrial biopsy just to make sure it's not something else. Was never told about potential side effects - was told this was a "safe" drug and a safe procedure. I am due for a another shot 9/8 - will cancel it after reading all the posts. I'll probably need surgery - but rather that then some of the horrible side effects I'm reading about. Good luck to all of you.

I've been taking Levaquin for about 3 weeks. Last week, suddenly, every joint in my body started aching. I mean from my neck, hands, hips, knees, ankles, feet, everything. For the past week, when I wake up, I can't even make a fist without experiencing excruciating pain. I've always been very active, running, basketball, soccer, skiing, you name it, so this is scaring the heck out of me. I'm 47 years old, and up until a week ago, I was hiking with my family, running everyday with my dog. Now I feel like I'm 100 years old. It hurts to walk, stand up, etc! I have an appointment with my doctor tomorrow! I'm ticked about this!

Lipitor 20mg
*Muscle deterioration:*
I had to stop taking walks.
*Diarrhea:*
I am sorry to tell my doctor doesn't know how to treat me.
He raised Tenormin to 50 mg a day, and it made a catastrophy. Severe electrical heart problem. Very debilitating. Permanent chest pain. I acted: I reduced it to a minimal level of 12.5 mg a day.
I have stopped Lipitor 20 mg and replaced it with.

Nattokinase
CoQ10 (Ubiquinol)
Cucurma
Lecithin
Omega 3
Magnesium supplements
Very effective!
Above is from science. Lipitor is from business.

Now, all angina symptoms are gone. No more arythmia.
I have also dropped one aspirin a day, and replaced it with Allicin. (Concentred garlic)
I have learn that aspirin is doing the opposite of the expected effect for 40% of people. It is causing a sever eye pathology, macular degeneration, and stomach bleeding. And after many months it has no beneficial effects, only adverse effects.
Garlic has so many positive side effects.

Here are some more side effects that I encountered during my ordeal with Lipitor. A week after I started the medication, I started experiencing blurry and decreased vision, this used to go away and come back sometimes, I could swear I always had 20/20 although I never went to eye doctor, but I never needed glasses all my life, if fact any type of glasses will blurry my vision and make me dizzy. I had my first eyes exam a couple days after I discontinued Lipitor, guess what? I have 20/20 vision.
More details about the back and right arm pain, not only the pain was unbearable, I felt my muscles sagging and they did not have any strength, this thing sucked the life out of my muscles, it made me very tired and easily irritable. My fist victim was my little baby ( my beautiful 4 year old), her daddy couldn’t hold her anymore, I even avoided staying close to her, because anyone who touches that right arm will make it feel like another deep stab to the arm deep into the bone. I have never experienced pain like this. I knew about toothache when I had a cavity at 23, but it was fixed and went away, I even experienced the pain of a broken arm at 16, but this thing was something else. The other victim is my wife, I stopped doing stuff, I used to be a very active dude, I do stuff on weekends with family and even every day after work ( you name it, park, boating, swimming pool, malls etc..). It felt like I was dying one piece at a time, going down the tubes fast with no clue of what was wrong with me.

I am also a victim of having the Kenalog injection administered over 8 months ago to alleviate poison ivy itching symptoms. Prior to having the injection, I was not informed of any side effects. Not only did the injection not alleviate the symptoms, but has resulted in a discolored and uncomfortable indentation in my left buttock area and psychological anguish because of disfigurement of my body. It is 8 months later and the indent appears to continue to deepen and lengthen. The dermatologist who administered the injection stated that there was nothing I could do to reverse such effects. I reported my case to the FDA (Food and Drug Administration) Med Watch. I urge others to report their adverse event to the FDA--just click on this link and complete the form: http://www.fda.gov/medwatch/. The FDA is responsible for assuring safety of medications. Therefore, it is imperative that the FDA recognize the adverse effects to provide any credibility to a class action suit. Please consider forwarding your case to the FDA to force them into action and begin addressing these atrocities. Such documented cases and recognition by the FDA will provide leverage for attorneys in pursuit of a class action suit.

HI, i too have to say i am kind of relieved after reading this website that i am not alone with my experiences of the kenalog injection. I was given kenalog injections to treat hayfever, although i wasn't told the name of the injection. They did help and i probably would of continued this year if it wasn't for the side effects.
I was told that to have one a yr was safe, then just before xmas i noticed a dent on my hip, this started getting larger and looked almost like scare tissue, I too was worried i had some sort of flesh eating disorder. The dent is still there and i will never have that injection again. I also have been experience problems with my hips and pain around my coxis,i am not sure if this too is related to the injection. I was told by my doctor who is very good that the kenalog had eaten my fat tissue causing a dent and that it will get better in time.

i am on my second pack of Yasmin. In the beginning,i got really sick to my stomach, probably because my body was getting used to the pill. As soon as i began the week of sugar pills, i had terrible headaches on one side of my head. the headaches lasted about a week, and by the end of it, i was ready to lose my mind. now, today,i woke up and began feeling very dizzy and numb all over my body.after a few minutes my vision was fading until it got to the point where all i could see was outlines of things. Everything looked like a picture with really high contrast.i looked at my mom and her face was bright white with black detailing. it was really weird. i also noticed a sort of white glow all over everything. i was so terrified. i am not the type of person who ever faints or anything, so this was really odd. it went away after about 5 minutes, but it was so scary that it felt like an hour had passed. I'm not 100% sure if this is caused by Yasmin, but i haven't done anything different that would make this happen to me. i am going to the doctors, but in the mean time, i'm going to stop taking the pill. please let me know if anyone else has had an experience like this