Warfarin Sodium and joint pain

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'm 48 and had a PE 4/2/09. I entered this site looking to see if hair loss was a common side effect to the Warfarin I've been taking and, lo and behold, not only do I now have an explanation for my thinning hair but the acne, the joint pain, WEIGHT GAIN (UGH!) and gas / bloating. The powers that be have decided that the cause of the PE was my Yasmin birth control pills (a huge law suit going on for Bayer now - the producers of Yasmin, Yaz and one other one) and put me on the Warfarin for 6 months to life - we'll see about the 'to life' part on 10/02/09. I think regardless, I'm going with 'Tannabo' and trying the Nattokinase once I'm done with the Warfarin. Thank you for this 'enlightening' website and everyone's input!

After reading these posts I am more confused than before, because my experience is so far very different. I was diagnosed with DVT about two weeks ago and now take Coumadin daily; the Lovenox injections have been discontinued. The reason I'm so confused is I now feel the best I have in 5 (five) years.

Before being placed on the anti-coagulants I had memory and concentration issues that were progressively getting worse and greatly affecting my job, and had daily headaches. I had joint pain that made it difficult to get up after sitting for awhile; they felt constantly inflamed. I felt fatigued all the time and my muscles hurt like I had really pushed them; I just didn't have any strength, and had muscle cramps. I was constantly yawning and found my jaws hurt from clinching my teeth, subconsciously trying not to yawn. I was extremely sensitive to physical touch, even hugs hurt. I also felt extremely depressed and cried almost daily. My lips and left cheek tingled, as well as other parts of my body. Plus I would get the feeling of sudden pressure in my head (different from a headache) like it was going to pop off, and I my eyes didn't seem to track what I looking at and had difficulty in remembering or comprehending what I just read.

About 6 (six) days after starting treatment it completely changed and these symptoms are essentially gone. I have talked with my doctor and pharmacist and they are baffled. I am concerned this change, while welcomed, may indicate an underlying condition that is not yet diagnosed. Has anyone ever heard of such an impact from starting Coumadin treatment?

I had a several small PEs in my right lung 2 weeks after cosmetic surgery. I just turned 37, run every day and in great shape. I was put on both lovenox shots for 5 days and Coumadin for 6 months. After 6 weeks the side effects with Coumadin were so severe (weight gain 14 pounds in 6 weeks, joint pain, tiredness, hair loss) that I took myself off cold turkey and started on NATTOKINASE. I am doing great! I would recommend searching the natural approach like Nattokinase, vitamin E, cayenne pepper, etc. I have stopped gaining the weight and it's starting to come off. All of my other side effects went away too. I've been off 4 weeks now. All of the doctors were mad and scared me when I went off of Coumadin. I had to do my own research and listen to my body.

Ive been on Warfarin for 4 months after being diagnosed with a blood clot in my leg. Cause of clot is really unknown. I was on 13m and last week was told I no longer had to take it because my levels have been high. I stopped taking the warfarin and my side affects since starting it has been the following. Joint pain in my hip and arms, swelling and retaining fluid, sharp pains that jolt thru the leg randomly, experienced some nausea and dizziness the first few days after not taking the drug. since Ive stopped the warfarin 5 days ago it feels like the clot is returning in my leg. Is this possible?

I'm 39 and have been on Coumadin for about a month. Was diagnosed with DVT in right calf after taking Yaz birth control for only about 4-5 months (no other pre-conditions - I'm a non-smoker, fairly active, not overweight, no recent airplane trips or long car rides.) I was on Yaz to treat severe problems with my period which has been the case since I was a teenager, but I was tired of having to call in sick to work every month, and had hoped Yaz would eliminate that problem. I had been on other BCPs when I was in my 20's, and never had any symptoms of clotting, so didn't think that it would be all that risky to try again, despite me being slightly older than the typical woman on BCP. Obviously, I am not taking Yaz anymore, and will not be able to take any other hormonal therapies for the rest of my life. But I guess that's minor compared to the risk of developing PE from an undiagnosed blood clot.

Anyway, I've been noticing I've been getting sudden, severe headaches since starting the Coumadin. I have a history of migraines but I usually only get one or two per year at most. Now I've had what feels a lot like a migraine twice in a matter of a couple weeks. My husband has also commented that I've been irritable and acting "spacy".

My INR has also been all over the place. They've been alternating me between 5 mg and 7.5 mg per day. For the first few weeks I was right where they wanted me - between 2 and 3, but then last Friday my results were 4.6!! Way too high. I go back this afternoon to see if anything's changed over the weekend, after skipping a dose and then doing 5 mg Sat. and Sun. I do hope they can find the right balance and don't have to keep tinkering with the dosage. I'm wondering if that's what's contributing to the headaches. Maybe if they can stabilize how much I'm taking from day to day, my body will adjust.

I wonder if anyone "official" is tracking the number of DVT/PE patients that can trace their onset of symptoms to Yaz. My sense is that this is a much more serious and prevalent side effect than their marketing dept. would like to admit.....

Dealing leg pain and swelling fpr over 6 months - having 2 DVT test and 3 MRI's they finally found that I did have a DVT in my left leg and now I am taking Warfarin as of May 30th 2008. I now have severe joint pain, sore skin/sensitivity, my vision is going I can hardly read anything all of a sudden, so exhausted, sleeplessness - even after taking an ambien and getting some sleep, I can take a shower dry my hair and I am ready to go back and lay down because I am so tired. the doctor says thin blood does not carry oxygen as well so this is why I am tired. I am not anemic as I just had that checked. I can feel my muscles getting weaker. From reading what everyone else says it must be this drug, but I don't think I could live without it since my clot is so massive. I feel like my life will end soon I am getting weaker by the day...is this just my imagination? I know I am depressed but I do think all of the symptoms I am having is from the warfarin(besides the pain from the DVT which is still very painful)

I have been on Warfarin since Sept 2004 when I had multiple blood clots in both lungs. Since then I have had two more PE's (one with a therapeutic INR) and a blood clot in my left arm (INR was also therapeutic). Genetic tests show nothing.

Since starting Warfarin I have had
- dizziness issues,
- eternal extreme fatigue
- hair loss
- short term memory and cognitive issues,
- joint pain and
- head aches all the time. I think the headaches are the worse since I can't take any NSAID's for them.

I have lost weight and push myself to exercise because it is supposed to make you feel better, right? Well not yet. I keep waiting.

I have not been able to return to work and worry about the long term implications of this.

Many times I have wondered about my sanity and if I was imagining all of this, so finding this forum at least lets me know that there is a possibility that it is not all in my mind.

I have been seeing a psychiatrist to help me work through the almost dying 3 times thing, but it is hard to accept since no one knows why I throw the clots. My INR is not stable in spite of close monitoring of Vit K and other drugs, and my INR must be taken twice a week.

I have been on Coumadin for about 2 months now after surviving a cerebral sinus venous thrombosis (blood clot on my brain - akin to a stroke). I am s 34 yo female who races triathlons and leads a very active healthy lifestyle. My side effects seem to be mild compared to what I read of others. I am on 5mg/day, except 1 day a week I take 10mg. My INR has been pretty stable. The side effects I notice are mild forgetfulness which I am hoping goes away as I start my 3rd year of law school next week! I also had some weird skin peeling on my hands, but that has subsided. I seem to urinate more often than normal and soda pop tastes weird to me now. Anyone else experience the frequent urination and/or taste issues?
Thanks!
Dana :)

Hot hands joint pain

My second run in with a blood clot resulted in passing out on my way to pick up my 8 yr old daughter and being rushed to the ER because of a PE (near death), I'm thankful to be alive however (no reason for PE and being on coumadin for the rest of my life) I feel so tired now, I don't want to go to work, I can't concentrate, I suffer from dizzy spells, I'm always hungry (weight gain), nausea sometimes. before passing out I was working out, doing Taebo, the balance ball thing, walking. Now I feel like I'm and old woman. I'm 32 yrs old and taking #5 coumadin and I feel so bad the majority of the time and yes the doctors say "it's shouldn't be the coumadin" but I think it is my whole world has changed and I'm just trying to get back to being the fun, outgoing, active me. I miss myself so much, its like I'm depressed. I MISS MYSELF.

SINCE BEING ON WARFARIN , I HAVE EXPERIENCED MUSCLE CRAMPS , REALLY BAD JOINT PAIN , AND DRY COUGH . YES , IT COULD BE MY AGE ( 79) - - AND THEN AGAIN IT COULD BE WARFARIN . IF I DISCONTINUE THE WARFARIN , IS MY CHOICE BETWEEN A HEART ATTACK , OR THE REST OF MY LIFE AS A CHRONIC INVALID ?? IS THERE A THIRD OPTION ?

My 79 YO father began taking Warfarin following a TIA 2 years ago. It has caused him some fatigue but lately he has been experiencing quite bad swelling of the feet and ankles and also a lot of joint pain not present before the medication. Are there any alternatives to this medication?