Warfarin Sodium and rest of my life

I am 26 years old. I've been on warfarin for almost eight years. I wish I had seen a site like this eight years ago when I started on warfarin (after DVT and P.E) I may have had some insight into the hellish two years that were to follow: hair-loss, depression, weight-gain. But I attributed all this to stress (it was pre-med varsity and I was under a lot of pressure academically).
Anyway, now my life is more settled, I eat right, exercise furiously 5 times a week...but I have digestive problems. Bloating, gas, overall discomfort in my stomach almost every night. I've cut out milk, wheat, coffee...nothing.
But tonight I started thinking...could it be the warfarin?
Does anyone experience or know about possible side-effects of warfarin on the digestive system, and does anyone have some useful advice????

I was diagnosed with Factor V Leiden after suffering from bilateral PEs in February 2004. I am on Warfarin for the rest of my life (I turn 45 in November). Since starting the Warfarin I have gained about 70 pounds. Nothing I do seem to work. I have tried eating better. I would love to exercise but my knees are shot. Probably from lugging around all this extra weight.

Has anybody else had this problem? From what I have read online, doctor will say the drug doesn't cause weight gain but come on.

Can anything be done short of stopping the medication? I am too afraid to do that. It sucks that there is not an alternative rx that would work.

I suffer from depression too (have for almost 15 years). As my weight has climbed, my meds for depression don't work as well. I am at the end of my rope & slowing losing my grip.

I was diagnosed with Factor V Leiden after experiencing bilateral PE's in February 2004. Since then, I have gained A LOT of weight. Not that I needed to but dang. I am at my highest ever & nothing I do will make it go down. I am almost 80 pounds heavier than I was in 2004. Something is not right. I suffer from depression (have for more than 15 years). My medication doesn't seem to have the same effect. My joints are killing me so it's hard to exercise.

A side note, shortly after being hospitalized for the PE's for a week, I noticed my hair thinning. Doctor told me it was because of the "shock" to my system due to having the PE's.

I will have to be on Warfarin for the rest of my life. I turn 45 in November. Ugh.

Has anybody had the same problem with weight gain? Is there anything to do about it? I feel I am at the end of my rope & slowing losing my grip.

The severe headaches EVERY day. that the doctor was sure were not related to the coumadin.. are debilitating. They are usually in the evening or during the night, as I take the medication later in the day. However, I do not know how I will be able to take this med the rest of my life. I am 66 and just spent time losing weight on weight watchers program.. only to see the scales climbing daily. I appreciate the insight on this site to let me know that I am not imagining all this and not alone.

Im 23 years old. One of the youngest people that is on coumadin I got sick when I was 22. I developed blood clots on my liver and stomach. Due to blood deficiency. I was told by the doctor it was inherited by one of my parents. My side affects are very fatigue, tired for no reason, skin blotches, slow memory, I get tired after 10 minutes of running like Im ready to collapse. Im always dizzy. =( I feel very fragile. I do get depressed sometimes because I feel like im very young at my age for this to happen. I found out I have to be on coumadin for the rest of my life. But we all move on....

E-mail me ******

Hopefully someone can share there idea's or another source of help.

Wow - I'm so glad I found this site. I am 43 years old and had a PE last August in both lungs - every test imaginable has been done and still no idea why I got the PE. I should be on Warfarin for the rest of my life but I can't stand it much longer. I have headaches every day, cold sweats, dizziness, can't remember things, can't concentrate at work and the WEIGHT GAIN! My doctor just tells me to eat healthier but watch those leafy greens! I get no support at all from her. She also put me on Cipralex for depression and I'm now considering going off both medications and seeing a Naturopath. I'm sick of feeling like I'm 80.
L.

I had open heart surgery August 23rd 2006 for a conginital heart defeat (Aortic Valve replaced with mechanical St Jude valve). I wanted a bio valve but Drs insisted I should have the mechanical valve because of my age (45 at the time).

Prior to my heart surgery I was a performer, singer/songwriter/actress/comedianne and I loved what I did. It was my life. Now, after 2+ years post-op and on Warfarin (7.5 mg daily for life) I feel like life has ended and I'm just a walking dead person. The effects I feel daily are as follows...

Dizziness
Severe Headaches
Blurred vision
Memory Loss
Fatigue
Weight Gain
Trouble concentating
Fluttering effect in my head/ears- Hard to explain
Hair loss
Unexplained pains in chest & left side of my body
Unable to sleep well
Tiredness- even when I've done nothing to be tired for
Nausea
Gas & Diarrhea off and on
teeth pain- Like I've drank something very cold
feeling in my head similar to a brain freeze- like you ate ice cream too fast
Night bleeds in my month- wake up with a mouth full of blood daily
What do think, is that enough??

I'm going in tomorrow for a cat scan because the headaches have been so bad they feel I need to be checked for brain tumor and/or internal bleeding. When I tell the Drs I think this is due to Wafarin they pratically laugh in my face as if to say, "Silly silly woman, don't be foolish! We know whats best for you. Remember, we saved your life!" Really? Did you?!

I want nothing more than to get off this rat poison and regain my life, but to do so could mean a stroke or heart attack. I would go under the knife again to have the mechanical valve removed and replaced with a biological valve, but do you think my insurance company (Kieser) would pay for a "silly" thing like that? Right!

Welcome to the greatest country in the world!

I'm going to start a website to help people like us. I want your stories, please send me your info, together we might make a change, what can it hurt to try? Email me ******

B.

I experienced a DVT 6 months ago, out of the blue. Did the Lovenox injections for a month, twice daily. Have been taking warfarin sodium since August. My hair was always very thick and healthy. I noticed in November that there was lots of hair in the bathtub whenever I shampooed. My hairdresser has also noticed the change. My hair is getting very thin and it is also getting brittle. Is there something that can be done to correct the hair loss...other than stopping the WS which I apparently be on for the rest of my life.

24 yr female diagnosed with PE and DVT. I have been on Warfarin since may of 08 and it has turned my world upside down. Weight gain (20lbs in 3 months), major hair loss, very bad acne, and memory loss. Not to mention i can't shave my legs or anything else for that matter with out getting major in grown hairs. I NEVER had any of these problems before. I am loosing muscle mass and feel as if I am a 70 year old woman. I don't know what to do but cry. The doctors keep telling me its not the medicine but I feel it is, my body is telling me it is. things are not easy, and it is affecting me I feel for the rest of my life.

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.....

Hi I am a 36 year old female, and have been on warfarin for about six months now, I was also on it back in 2004 for six months I had a blood clot in my left lung in 04, and was off of them after six months. But now i Dec 07 i had a clot in my leg, and several in my lungs. I have to be on it forever now according to my docs. It sucks, I am having very bad memory loss, blurred vision also, I get dizzy a lot, and as of last week my levels are not high. I was on a smaller dosage the first time around, but I am currently on 7.5 mg, and it sucks, I want to be off of these. So I also do experience the same symptoms as the rest of you. Memory loss is really affecting my everyday life. Also depression is a big symptom also, I have always been a happy person, not any longer.

I am 31 years old. I was first on warfarin when I was 15. I was on the BCP and a smoker as well. just 2 months of being on the pill I developed a DVT in my left leg. I was on the warfarin for about 2 years then came off. I reember being tired alot but that was it. Then again when I was 22 I developed yet again another DVT in my L leg.. as well as 3 PE in my lungs. I was prescribed warfarin and I was on that for 2 years .. was taken off due to dizzy spells. Now again I am on warfarin .. for the rest of my life. I have a genetic disorder for clots and had a mini stroke. By the grace of GOD I only have a limp in my right foot... the side effects I experiance now are dizzy spells, headaches, blurred vision, and muscle aches and spasms. If your docot is denieying these side effect they really just dont think its serious enough to take you off. All my doctors over the last 16 years have all told me of these side effects. What you eat and drink has alot to do with it and other meds you may be takeing. I am also on chantex and beleive the two together are to be the cuas se of my syptoms. I also experiance tingling for shor periods. I have been on it now for one week. My doctor told me once it is regulated to a point where I dont have to up my dosage or lower my dosage and I am pretty much at a steady dosage the side effect will cease, until then I think if you dont like your docotor and dont beleive hes looking out for you in your best interrest yo ushould find another one.... Thats important... you must have a docotor you can trrust and one whom will listen to you.

I have been on Warfarin since the end of Aug. 2007 when I had my mitral valve replaced with a mechanical valve. I will be on it for the rest of my life. My doctor.'s all assured me there were no side effects other than the bleeding risks. I now know this is not true. The side effects I am dealing with make me sometimes wish I had chosen a tissue (pig) valve, even though I would be guaranteed another heart surgery within ten years. I am 39 years old and a mother of two young kids. Since being on Warfarin I have experienced various body aches that come on suddenly but don't stay long; extreme hot and cold; itchy hands and feet; dry hair and hair loss; seeing "spots" usually followed by a headache; very thirsty; ongoing bowel troubles, possibly developed colitis; but the worst side effect for me is the fatigue and depression. I feel like I traded in my old self for my mechanical valve. Like I said, I'd have to have a tissue valve replaced eventually, and as bad as heart surgery is, I'd rather have 10 happy years w/out Warfarin than this struggle I deal with almost everyday. My brother is a surgeon and even he buys into the "no side effects" b.s. I work out as much as I can, which used to make me feel great, now I feel like it helps me get by but not the positive effect it used to have on me mentally.

Female, 27, 6 months on Warfarin 7mg daily.

Diagnosed with functional protein c deficiency (congenital) in May of 2007 after suffering a blood clot that travel down into my toes. I’ll have to take warfarin for the rest of my life but I have been extremely lucky with lack of side effects. In the beginning I was tired, depressed, leg cramps, moody and slight weight gain. I’m happy to say that all of those symptoms besides the leg cramps have subsided. Of course after reading some of these posts and seeing that the side effects could occur years later has me a little worried. I’m interested in learning about any kind of herbal remedies if anyone has any suggestions

i am a 33 year old male and i have been taking warfarin for the past nine years. i have had most of the side effects that i have read about here. before i began taking the drug i asked my doctor about side effects and i was told that there were only two; bleeding and bruising.
i have since learned that the research had not been done. that is why they don't know about the side effects.
here are just some of the effects that i have had in my nine years on this drug. memory loss, hair loss, itchy feet, blurred vision, headache, brittle/crumbling teeth, stomach pain, non healing wounds.
i have began to do more research on my own lately, since it has been almost 10 years since i first began taking warfarin. the only new side effect that i have learned about is calcification of cartilage. i have been lucky not to have had this problem yet.
i have had no trouble yet with bleeding, although i do get some pretty bad bruises. i usually have three or four bad ones on my legs or arms at all times.
i am sure i will develop more side effects as the years go by. i am 33 years old now and will be taking warfarin for the rest of my life.

p.s. i have a titanium st.jude mitral valve

I am so glad to read all of this information. I am a 40 year old female. I have suffered 2 PEs. I have varied from being on 10 mg of warfarin to 25 mg a day. This is the first time I got to go 1 month between INR checks. I'm on 11 mg/day with INR of 2.1. I am having SEVERE recurrent headaches, sleepless nights, feeling tired all the time, and problems with my memory. Drs tell me they don't know what this is from and there are no side effects to warfarin. I have a vena cava filter in and I'm on the medicine for the rest of my life. Glad to hear I'm not losing my mind (just having horrible side effects regardless of what the doctors say!)

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 ?

I just started taking Warfarin on December 11, 2006 due to blood clots from surgery. My protime numbers won't go over 2.0, so I'm taking 12 mg and will probably start Lovenox injections. All my life I have rejected taking pharmaceuticals of any kind, and now this. I've told my doctor to get me off these meds asap, but now I have to see a hemotologist. If he says warfarin for life, I'll tell him no thank you. I will not live the rest of my life poisoned. As for side effects, the only thing I've noticed is a fitful night's sleep. I really haven't been that tired. I do get achy, but figure that's from physical therapy from surgery.

I have been diagnosed as a homozygous Factor V Leiden mutation and will have to be on warfarin for the rest of my life. I feel really dragged out and tired and need a couple hours of sleep midday. Sometimes though I wake up at 4 am and am wide awake. It is not dependent on my nap. In general, since going on warfarin I feel generally weak and tired. I sunburn more easily and it takes longer to heal. They do not say these are side effects but it sure seems odd that it has happened since warfarin 8 months ago.