Thumb symptoms and conditions

I'm a 47yo female & sorry for putting this as a reply to another post - new here:

Gosh.. glad I found this place - have been taking Warfarin for AF for about 2 weeks now and have been slowly sliding down hill. Thing is you just never know when to contact a doctor hey.

My symptoms, bloating, weight gain already, light headed, blurred vision, have had numbness & tingling in right arm and leg, and now I'm slowly getting colder and colder, and have a high sensitivity to light. Just started my monthly cycle and it's literally flooding, and I have an awful pain in the left hand side of my neck - it's sharp and unbearable at times. Some days when I'm driving home from work I feel I should pull over, not sure what my body is going to do to me next. I lack concentration, am crabby most of the time (and was picked up on that today at work) - and very emotional.

I don't like this at all - at what point do I mention any of this without seeming like a whinger?
I have a physical job, which has been reduced to 'light duties' due to the risks at the moment, which I'm grateful for. Today I bumped my thumb only slightly and it swelled up in a bloody lump - the blood has disappeared but the swelling is still there together with 'loose' skin where the originally larger swelling was. Everything seems just so weird.. I don't feel like ME any more - I want ME back :((

I am happy that I have come across this website. My son was born in July 2nd, 2009 and I had the Mirena IUD inserted on August 24th, 2009. The insertion wasn't all that painful, but the cramps that followed were. It lasted for approximately 2 weeks following and I had some spotting here and there. I have had serious cramping on my right side and after sexual intercourse, I always bleed and cramp on my right side. I have complained about my right wrist hurting bad and my thumb seemingly being dislocated. After reading these post I see that I could possibly have joint pain as a side effect. I can honestly say that the joint pain didn't start until after the Mirena insertion but I never associated it with that.

I thought that I'd love the Mirena because I wouldn't have to worry with pills or having to remember to take birth control, but the side effects are not worth it. I have also had some weight gain. Serious mood swings. Depressed moods and very emotional. Ive been short tempered about just minor things and I haven't been motivated to do much of anything around the house.

I'm debating on whether or not I should have the Mirena removed. I'd hate for any of my symptoms to get worse.

I am a 48 year old female with a-fib. I am not overweight...just started falling apart since now I am menopausal. I've been on Warfarin for 6 weeks. My INR has hardly moved. I'm now on 8 mg and have my INR test on Monday. I started at a 0.9. Now I'm at 1.20 and have been there for three weeks in spite of upping the warfarin. I've not changed my diet except to exclude greens and green tea when I began the therapy. Everything else is consistent.
I just started exercising again a week ago. Something I haven't done in five years since I lost my sister. I bought a Total Gym and enjoy it. It has helped me get some energy back, has helped alleviate some of the mental fog, and has lowered the incidence of anxiety attacks. (I've been getting anxiety lately...since the mental fog and memory lapses...that bothers me since I love to read and write and the mental fog seems to be taking the joy out of it now.) The reason I decided to start strength training again is because of the joint pain I have been experiencing lately. I didn't have it before warfarin. I do now. Only one joint, though. The strength training does help, but every once in awhile, that sharp pain comes back to visit. It's just a little less now.
I plan to tell the doctor that I have begun strength training again. Not just because it's good for me and my heart, but it seems to help with the side effects of menopause and warfarin...without adding another drug like an antidepressant.
Warfarin...I believe is a life saving drug. BUT, I have to do my part too.

BTW, if I didn't have triple thick hair, I would complain about hair loss. Right now, it's a non issue for me. Just saves money at the hair dresser.

I was prescribed Yasmin to help with ovarian cyst in September of this year. Well everything started off ok, but after a few weeks things started going down hill. Boobs hurt something awful, skin cleared up some but still got cystic pimples that hurt. Well yesterday, I finally had to stop taking them because I suddenly developed numbness in my left thumb and pointer finger. I don't recommend this pill in any way shape or form.

Within 5 hours of first dose, I had "severe body aches" like those with the flu. My joints and muscles hurt so much that night that I had to call my parents to help me take care of my kids the next morning. I told the doctor who prescribed it, and he said to try to stick it out for the week...what horrible advice! Thinking it was crazy advice, I reluctantly took doses 2, 3, and 4 and experienced the joint/muscle pain each time, but I guess I just somehow tolerated it as if I had the flu. My hands became rather puffy as well. After the 5th pill, I woke up in the middle of the night with HORRIBLE joint and muscle pain, which was so awful that I could barely move; I was able to move a little bit, with extreme pain all over my body--particularly my knees, wrists/hands/thumbs, feet, and shoulders. I felt and heard unnusual snapping, cracking, and popping all over my body when I would move around at all. I stopped the med immediately, and noticed some improvement over the next several days. It has since been 9 days since the last dose, and I still have considerable pain in my knee, my thumbs/wrists, and arms. Unable to do my regular exercise, I tried gentle swimming and light water aerobics several days ago, but found even that to be too painful to do. I'm still unable to pick up my young children, drive without pain (mostly in right knee and muscles connecting to it, when pushing the brake) and am still somewhat limited in typical daily activities. Also, for the last 5 days or so, I've had a strange nodule present on a tendon in my thumb which has been hurting since taking the antibiotic. This has been a very frightening experience, to say the least.

I've had severe joint pain in my thumb, hands, wrists, and arm all the way up to my shoulder. One side is worst than the other. My muscles hurt! I stopped Advair two days ago and I hope this pain ceases soon. The only thing that helps is Motrin 800 mg and Zostrix cream. I will NEVER take Advair again! I am a 55 year old woman and the pain makes me feel like I'm 80!

I took a 8 day regiment of 750 mg for pneumonia. I started developing joint pain in my right thumb on day 5 and then my left shoulder on day 6 by day 9 I was unable to raise my left arm over my head. It is now in both hands. I am so stiff in morning I cant turn a door knob with out lots of pain and forget trying to open the dishwasher where you have to squeeze the lever to open the door. In the shower I use my right hand to raise my left arm ober head so the warm water can run on my shoulder blade. warm water also helps relieve the pain. I am hoping this is just a temporary setback cause I never had symptoms like this before. 57 yo male

Been on Wellbutrin for almost 6 weeks now. Last week I started having a really itchy scalp, no flakes, just itchy and then bumps would appear where I had itched. My vaginal area was also itchy and I treated myself for a yeast infection unknowingly. This past weekend I broke out in what I now know was hives (urticaria angioedema). First my left ankle swelled (3 inches) and looked like it was sprained, but instead it was super itchy and then became achy and painful. Within 24 hours that ankle went down but the other side swelled up so badly that I had pitting edema in my ankle and could leave dents in it. The third day, still with constant scalp and ear itching, i developed hives and large welts on my inner thighs as well as a large welt on my shoulder. I have been taking benadryl, which seems to help the itching for a little, but not for long enough. Yesterday I was at work and my butt started to itch so badly I had to leave. I had developed huge welts in the creases between my leg and butt right were one sits on a chair! Huge 3-4 inches. I was so uncomfortable. My thumb also had swelled up and I could not move my left hand without burning itch and pain. I finally called the doctor and set up an appointment.
I was told to take benadryl 25-50mg, zantac 150mg twice a day, and Zyrtec once a day to control the hives. This has helped a bit.
When I saw the doctor today and we went over everything, the ONLY change in months has been the addition of the Wellbutrin. I am going to stop taking it today and since my story sounds much like the ones below hopefully this will improve before my eyes or throat swell! Thanks for all your posts.

I took Levaquin for 20 days for a sinus infection. It wasn't until that last day that my right knee was in tremendous pain; I couldn't straighten it out or really move it. It's been almost 2 weeks since I stopped the Levaquin and my right knee is still painful. It feels really tight and if I turn my leg I get a sharp pain. I have to walk gingerly or I will have a shooting pain in my knee. I also have pain in my elbows and my right thumb, along with sporadic headaches. The pain seems to change daily. Does anyone have any experience as to whether this thing will go away -- every?

I took Levaquin 750 for 10 days for a sinus infection. I took first 5 doses, went to see my doctor again 6 days later because I was still sick. She prescribed again 5 does of Levanquin 750. I am still coughing and I feel very tired. It did not help at all. I am still sick and I have muscle pains in my two calves and stress Achille tendon. I am a runner and I have sometimes problems with my calf: I have been not running too much recently and I was wondering how come suddenly I had those muscle pains in both my calves. I am not sure if it is related to Levaquin, but when I read all those comments, I am worried. Why I have been prescribed this antibiotics if it is obviously dangerous?

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 am as relieved to find this site, after reading this it's like a puzzle where all the pieces have come together. Unfortunatly now I am worried about what this Kenalog has done to my body.

In Aug 2008 I recieved a 40mg Kenalog shot to help stop the swelling in my lips, tongue and throat...which is ironic and funny to me since those happen to be the same symptoms I would have experienced had I had an allergic reaction to the shot. Nice job thinking that one through doc.

The shot did nothing to relieve the swelling (thanks docs!), but apparently has done a number on my body.

Two months later (Oct 2008) I have been left with a visible dent on my right buttocks, where the shot was given. It started as a grey dent about the size of a small thumb, but has now grown to the size of an Ozarka bottle top.

Additionally the non-visible ailments I have been suffering are numbness in the right leg, sometimes it gets so severe that my leg feels tight and paralyzed. I have noticed heart flutters, and about two weeks after the shot I noticed a sudden weight loss of 12lbs in 2 weeks. This might not seem like much, but for a 25 year old who is 5'5'', muscular, and very active my healthy weight is about 125lbs, I am now 111 lbs (I weighed that much in JR. HIGH!! ugh!) it's bothersome. I can't seem to gain weight and instead continue to loose weight. Additionally I get blurred vision randomly and for extended periods of up to 3-4 min.

The dent is bothersome, but it is just a visible ailment. What worries me more than anything else is the fact that the above ailments seem to be related to the Kenalog shot...so what unseen damage has it done to my body??

I called the nurse who gave me the shot and she offered no help what so ever.

I have sent this site to other family and friends so that they can be aware of the side effects of this too commonly used drug. I hope the side effects that we are suffering go away, and that this product is taken off the market.

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 just received my Patient Medical Alert card from the Charcot-Marie-Tooth Association. It is a wallet size card for me to carry with me that list drugs that have or possibly have severe side affects for people with CMT. Seeing MACROBID on it reminded me of my experience with it about 10 years ago.
I am very prone to UTIs. My GYN prescribed MACROBID. After only 1 pill, my right thumb went numb. It spread to my index finger and then my middle finger. I was scared and called my GYN who told me there was no way that the Macrobid was the cause. I didn't stop with that answer. I then called the drug store, where I purchased it from and spoke to the pharmacist. I explained what was happening. He also told me that the Macrobid couldn't be the problem. I didn't take his answer and asked him to please get the contra -indications list and read it. There, in fine print, was possible peripheral numbness that can lead to death. I had 4 small children at the time, so you can imagine my horror. He contacted the pharmaceutical company that makes MACROBID. They called me to record my side effect and told me to NEVER take it again, that I could die if I did. It took several weeks for the feeling to come back in my fingers and hand. They had told me it could have been permanent. I didn't know I had CMT then. And this little card didn't exist then. I am writing this to warn others. If you don't know what CMT is, go to ******. It is a neurological degenerative disease. I am affected worse in my hands. I have a postural tremor in both hands now.
I hope my story helps someone.

Wow....sounds like Kenalog is not a drug to be administered without careful consideration of the pros out- weighing the cons. I had a Kenalog injection in my elbow at an urgent care center while on vacation about 8 mos ago (painful elbow was impacting vacation activities). It took my pain away 100%. Never gave it another thought even until just recently when it began hurting again. Did, however, notice the atrophy at injection site...and a grayish tone to skin. Indentation has not grown, but certainly has remained. My elbow is also super sensitive. Feels like the nerve is right there under a thin layer of skin.....so sensitive. I also have leg shakiness, hip weakness, anxiety, nausea, and increased heart rate....I assume these are related as I did not have these issues prior. These issues bother me way more that the indentation on my elbow. Dont like not feeling well. I guess the learning is that all medications are foreign to your body and thus have potential side effects. One needs to ask questions and or do own research on their own prior to consenting to take a mediation to be sure the benefits are worth it.

I started taking Yaz about a year and a half ago. I'm no longer continuing this pill after this month's pack is finished. I have to say that at first, it was a really great pill. The first month was hell. I bled for a month straight, and I was so irritable, and emotional, and my bf would talk about silly shit, like beached whales and I would start bawling. I spent four months living overseas after starting the pill so I didn't notice the loss of sex drive and sensitivity at first. But when I came back I started to notice all the little things that were becoming huge issues. My sex drive is more or less gone. I actually fell asleep last night while my boyfriend was trying to get me aroused. That's awful. I always feel tired lately. I get a lot of headaches. I read that this pill increase your potassium, and my mother's told me she has a lot of potassium so when she eats bananas she gets splitting headaches, and I'm the same way, so I'm starting to realize where all these headaches are coming from. Sometimes they are so bad that Advil does nothing at all and I end up having to rub between my thumb and forefinger while trying to fell asleep to make the pain stop. I've become extremely moody. My moods change so often now. I'm irritable. I am coming off of two really tough years of my life, and things are really great for me right now, and I don't feel great. I never want to have sex. Foreplay doesn't feel as good as it used to. I don't get aroused quickly, and I have a lot of trouble climaxing. I smoke weed and was smoking mixed spliffs with my bf for some time not even thinking about it, and the reaction the tobacco had with the pill was horrible. I'm certain that if I didn't stop I would have ended up in the ER. I would experience fainting spells, momentary blindness!!, I'd go really pale after getting very hot. I nearly passed out on at least four occasions before discovering the link. After I stopped, I felt much better. But now I can feel all the emotional side effects. I've also been sleepless for a long time, and I think that has to do with the pill, too. Lately I've been getting very nauseated if I eat shortly after taking the pill. And it doesn't matter what I eat. I'm constantly burping like I have a nervous stomach, but I've been calming my mind lately so there's really no reason for it. I've got a lot going on with life and whatnot, but I'm usually able to handle a lot of pressure and stress without breaking down, and this pill has made me almost incapable to dealing with the slightest bit of stress. It's horrible. And I don't want any part in it, or in the pharmaceutical business. I'm going to try tracking my own ovulation. At least I won't have some crazy hormones messing up my system.

Oh. I also had a fibroadenoma (breast cyst) this summer that I had to have a biopsy on (which was really fun, let me tell you...), and I can't say that the pill caused it, but I've never had cysts in my breasts before... The pill did inflate them an extra cup size, and during the third week of pills they are so tender I can't even let my boyfriend touch them or hug me tightly because they hurt so badly. And I live in NYC and there are a lot of stairs to bounce down and it's painful.

I see all the same symptoms with everyone who takes this pill and has a bad experience, and I've decided that it's not for me. The man can wear a condom for a while, while I try to regain my normal self again.

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 was a competitive runner with a number of sub 3 hour marathons under my belt before I was prescribed statins for elevated cholesterol 2 years ago. The first go round was 40mg zocor but muscle soreness and loss of strength started within 2 months. Switched to NIASPAN but couldn't tolerate it. The last 7 months have been on 10mg of Lipitor and now have intense pain in my legs, soreness in my wrist and thumb and swollen feet. I can still run but much less than before and much slower. I regularly go to the gym but have seen a steady decrease in the amount of weight I am able to lift. I have a blood test in a couple of days and will be looking for myalgia again. I have discontinued the statin and don't plan to start again. I was healthier before the DR decided to "help" me with my cholesterol problem.

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!

I started Adoxa (generic form of Doxy) about 2 weeks ago for a cyst. About 5 days after taking the med, I was swimming and my hands had the weirdest sensation... After I got out of the pool, my feet were on fire as were my hands. Thought I just had gotten sunburn, though I don't normally burn. A couple days later, I had a severe tingling/burning in my fingers and toes. Couldn't sleep because of the pain. This lasted 2 night and I stopped taking the Adoxa. Went to Urgent Care because the burning was not subsiding and and my toes and fingers were EXTREMELY sensitive. I couldn't even open a pop can. Dr. said I had Periphrial Neuropathy and it is not a side effect of the Adoxa that I was taking. Told me I had symptoms to a bigger problem. I have been off Adoxa now for 4 days and the tingling/burning/sensitivity has all gone away! I know that it is the Adoxa and will not ever take it again!!! Remember to trust your instincts when you take medications!!!!

Since taking (November 2006) and quitting (Febuary 2008) Lipitor I have had a series of muscle/joint problems. This is an update and recap.
Summer 2007 I had left knee problems which surprised the physical therapists because it did not respond well to ultra sound, nor did the pain increase with mobility. I was surprised when I developed similar but lesser problems in my right knee. Autumn 2007 I was diagnosed with tennis elbow on the left arm. Late 2007 my left shoulder becomes a problem. Within days of quitting Lipitor in early 2008 I had extreme pain in my right thumb along the bone, then the middle of my hand then between my first and second fingers. Pain has also been across my wrist and up both sides of my right arm. I am wondering if I will be diagnosed with carpal tunnel - but surely this does not start with extreme pain along the bone in the right thumb!
I am feeling much better than when I was taking Lipitor, but wonder if I dodged the bullet.

he cortisone worked!). My left knee feels "normal" again, not perfect but nearly like it used to be. Within a couple of days of quitting I had severe pain in my right thumb along the bone, then in the middle of my right hand, then between the first and second fingers in my right hand. I currently have minor pain in my right wrist (this is new) on the pinkie side and minor pain in my left shoulder where the arm joins (this has been intermittent for a couple of months). I am feeling much better - but would not be at all surprised if pain appears in another part of my body before this is all history!

I am a 42 male, I have always been healthy and felt healthy as long I can remember, I never went to the doctor. So this year, 3 months ago to be exact, I decided to do “the right thing”, start taking a physical at least once every years, who know something might be wrong with me and I don’t know it.

Anyway, after I took the physical and some blood tests, my doctors office calls me and they told me that the sugar was a little high (124) and that I am at risk for Diabetes, so they started me on a diabetes medication. Although my Cholesterol wasn’t high, they suggested starting Lipitor (20 ML) just in case because I am at risk and I don’t want to take chances.

A month into it, I started having some back pain, but never suspected medication. I was exercising at least 4 times a week, some cardio and free weights, so I thought, I might have made the wrong move while exercising or maybe sleeping without knowing it ( although I never recall such a thing). Usually it takes a few days for the pain to go away when I did the wrong move, but this pain wouldn’t go away. A month after that (last month), a sharp pain started on my right wrist (shooting pain), that goes up my right arm until my shoulder blade and upper right back. The pain was so sharp and wouldn’t let go, all day, all night and every minute in between. Also, I experienced some numbness on some of my right fingers (especially the thumb and index). I never suspected the medication. Of course the doctors wanted me to take all sorts of tests and MRIs etc..you name it. They also wanted me to go on pain pills (strong ones), I never did, and I used Advil instead, which did not help much. This pain ruined my two week vacations to France (I didn’t not want to forgo the airplane ticket and the hotel, they were already paid for).
I started “googling” the web for “sharp back pain”, just to get some clues, which led me to side effect sites, which led me to this site. I decided to stop all medications immediately 3 days ago, the pain went away, I still have s slight numbness on my thumb, although it is much better, I will keep you posted. Thanks to all the people who shared their story with us, I know that everyone of us could be a different case, what worked for me doesn’t necessarily work for someone else, I know that many here are frustrated about these side effects and whether they are permanent or not, I wish I have the answers. One thing is sure, Lipitor could be poison for some people, I felt going down fast for the last 3 months with no way to stop it, glad I found this site.

This is also a follow up. My daughter 11 was put on Singular 4 years ago. The first symptom we noticed was the rubbing for her thumb abd fingers. We thought that it was anxiety because i had recently been hospitalized. For the past 4 years we have attributed most of her symptoms tp PANDAS. She also found out recently that she has high cholesterol. All of these kids having the same side effects can not be a coincidence. I will file a report with the FDA. We took her off of it about 1&1/2 weeks ago and have seen definite improvement. With everything she's been through I'm sure that she's continue to need support even after this medication gets out of her system.

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 a 57 year old man, who has been suffering from asthma several years. This spring my doctor put me on Singulair as an additional medicine to my cortisone-inhalator. after one month I feel symptoms of depression an mood-changing, severe ups and downs.
AND - as an additional symptom i have partially lost my feeling in some fingertips, and now parts of my left thumb and even a feeling of "cold2, mostly in my left hand.
anyone who share that symptom?
M.