Swollen ankles symptoms and conditions

I had the Mirena fitted in May 08, and boy did I see hell before heaven, I wished I had seen this website befork agreeing to the Mirena. It was very painful on insertion with lower back pain that I almost passed out. I began to notice a slight tingling in my breasts, this increased as time went on and felt like a thousand hot needles attacking my breast with terrible pains and sweating. .I have restless nights and gets moody very quickly, my joints aches and pain tremendously, I move at the pace of a 100 year person, my movements are slowed down and its an effort to get out of bed on mornings. I haven't even got the energy to play with my grandson.I saw the practice nurse and told her I want this out of me ASAP, I can't wait for the two weeks to come.I had the Mirena implanted in me because I became anaemic with heavy periods and not for contraception-- Ladies BEWARE, read and think carefully about the harm you might be putting your body through, the Mirena might not be for every on, I think there should be more research carried out on new products, who knows the manufacturers are only interested in selling their products to earn a quick buck. I sympathize with all of you who had the Mirena coil.

Day 29 of Norvasc generic 10MG. I have swollen ankles and at the end of the day they a little painful. I cannot stay up past 10:30 P.M. I just feel so tired. Periodically my legs will turn red and are hot up to my knees-looks like a sun burn. I have been in a really bad mood lately. Everything annoys me...is this the meds or just me? I was on Linsinopril for about 3.5 months and coughed the entire time until I thought I was going to die. Doctor changed me to this. Swollen ankles much better then coughing all day and night. I'm just wondering if my bad mood is a side affect. Anyone have the same?

So I made an appointment to have my mirena removed on Monday. However, i am scared now that my post symptoms are going to be far more worse than they are now but, it needs to be done. So, if you have had it removed can you please reply to this posting so i can have some idea as to what i could be facing?

I've never responded to a site like this, but now feel compelled to. I had my Mirena fitted 13months ago, after a friend recommended it on the strength of her excellent experience with it. I was on anti-depressants already, so haven't felt an overwhelming sense of depression, but have been thinking for the past 10 months or so, that I get way more tired, have an overall achy body often, painful joints and swollen ankles. All stuff I never experienced before. But the thing that really did it for me was the weight gain. I was only slightly over normal weight at the time of insertion but have been gaining weight steadily. Initially I thought it was just a bit over over-indulgence, but after weighing myself last week, I've made the horrifying discovery that I've gained 13kg in 13 months!!!!!!!! I've never fluctuated more than about 4 kg in my whole life, eat healthily and am normally active. Nothing has changed to what I was eating/doing before. I specifically searched the internet today to see if weight-gain is a problem. It's not listed as a major side-effect on the 'official' sites, yet I see it on many of the postings on this one.
And for those of you who are into alternative therapies, I had myself checked with a kinesiologist for dietary intolerances/allergies that could have caused this weight issue, and what came up is that the problem is progesterone. When she checked if my Mirena was a problem for me, it came up VERY positive. When checked if I should have it removed, the response was equally positive.
It's a pity, as I had none of the other problems mentioned and it's such a convenient method of bc. But in my case it's coming out, before I have to come out as a seriously obese 41 yr old!!!!!

Started using Caduet in 2005. Found I got the usual side effects plus swollen ankles. Doctor changed my PX to Lisinopril about a year ago.Seemed to work well, lower BP and no side effects. About 2 months ago started getting lightheaded,nausea,and a few other side effects. Is it common to use this drug for that long and then get the side effects? How long will it take for these effects to go away if use is stopped?

Thank you so much for your website. I cannot begin to tell you what this drug has done to ruin my life.

I had been on it for over 4 years on a misdiagnoses (Never should have been on it) and was told
“It was no worse than Tylenol.” Ok I thought as I was suffering from a few swollen joints every
now and then but was fine otherwise.

Then one day I was working and someone noticed my face was swelling. I looked in the mirror and
low and behold my face was rubbing my glasses. I asked my doctor and he said “it will go away soon.”
I am very athletic so I continued to run and work out as I slowly went from a 30” waist to a 50” inch waist!!
People at my office thought I was on a food binge like no other. My wife was stunned on how fast this
happened as was my family. Now the problem had gotten much worse. Constant body aches and swollen ankles.
After a year I went from jogging, to walking, to using a cane to using a walker…how sad my family felt
for me and no friends insight. my company then laid me off as I used the walls as a walker and simply could
“perform up to par.”

Next came the extremely high sugar, blood pressure, Glaucoma and I suddenly noticed I was having problems
seeing. Went to the eye doctor and was told I was getting cataracts but it would take a couple of years to form.
90 days later I could not drive and could barely see in both eyes, now I was almost blind.
Now 80lbs overweight almost blind with Glaucoma, high blood pressure, diabetes and cataracts. not to mention severe depression and mood swings that were unbearable, and yes still using a walker from severe muscle pain.

Well the time came where I lost my health insurance and was unemployed. I was out of Prednisone
one day and called my doctor. He said come in for $320.00. I said I didn’t have it and pleaded for them to call
in a 30 day supply, I was told that they “weren’t a charity” and “go to the emergency room” click!! My wonderful
doc was gone. Well I went to the emergency room the next day and was told “they don’t give refills.” I had been
off prednisone for a day and as some people know if you stop that high of dose for that long you may die from
adrenal crisis. So I stood in the emergency room for 12 hours waiting to go into this crisis! Finally a nurse convinced
a doctor to see me for 30 seconds, gave me a refill and a list of welfare clinics and booted me out the door. They
hated my appearance and hated me for no cash.

One day I decided to end this nonsense and tread everything I could from sources I hadn’t read that were very old
regarding what was wrong with me. I went on self imposed diet of 1000 calories a day and lost 60 lbs…yes!!
I stated weaning from the Prednisone and took a ton of supplements I had read about. I got down to 7.5mg every
other day. Yes, suffering tremendous total body aches, severe mood swings, dizziness, severe hunger and
confusion but I plowed though. By the way I don’t recommend this but I couldn’t get a refill for a prescription from anyone
because I ‘had made to much money.” So I turned to the Internet for everything. I bought 500 5mgs for $23.00 screw the doctors I don’t need their prescriptions. I am now totally off for 6 weeks I do have some bad stiffness, muscle aches and mood swings but after 4 years of pure hell I am truly thankful to be off this dangerous drug, it ruined my life.

So I went to a new Doctor finally and my diagnoses was a food allergy and simply had a small stint of bursitis a total mis- diagnoses from my first Doctor! Doctors aren’t gods so take it from me trust yourself first and do your research.

My prayers to all who suffer from this drug. Damn the incompetent doctors who wrongly prescribe it!

Dan

PS Does anyone know how long these severe body aches last after completely stopping. Its been 6 weeks and its just a little better. My doctor told me to fight it out or get back on pred. NO WAY!!

Thank you so much for your website. I cannot begin to tell you what this drug has done to ruin my life.

I had been on it for over 4 years on a misdiagnoses (Never should have been on it) and was told
“It was no worse than Tylenol.” Ok I thought as I was suffering from a few swollen joints every
now and then but was fine otherwise.

Then one day I was working and someone noticed my face was swelling. I looked in the mirror and
low and behold my face was rubbing my glasses. I asked my doctor and he said “it will go away soon.”
I am very athletic so I continued to run and work out as I slowly went from a 30” waist to a 50” inch waist!!
People at my office thought I was on a food binge like no other. My wife was stunned on how fast this
happened as was my family. Now the problem had gotten much worse. Constant body aches and swollen ankles.
After a year I went from jogging, to walking, to using a cane to using a walker…how sad my family felt
for me and no friends insight. my company then laid me off as I used the walls as a walker and simply could
“perform up to par.”

Next came the extremely high sugar, blood pressure, Glaucoma and I suddenly noticed I was having problems
seeing. Went to the eye doctor and was told I was getting cataracts but it would take a couple of years to form.
90 days later I could not drive and could barely see in both eyes, now I was almost blind.
Now 80lbs overweight almost blind with Glaucoma, high blood pressure, diabetes and cataracts. not to mention severe depression and mood swings that were unbearable, and yes still using a walker from severe muscle pain.

Well the time came where I lost my health insurance and was unemployed. I was out of Prednisone
one day and called my doctor. He said come in for $320.00. I said I didn’t have it and pleaded for them to call
in a 30 day supply, I was told that they “weren’t a charity” and “go to the emergency room” click!! My wonderful
doc was gone. Well I went to the emergency room the next day and was told “they don’t give refills.” I had been
off prednisone for a day and as some people know if you stop that high of dose for that long you may die from
adrenal crisis. So I stood in the emergency room for 12 hours waiting to go into this crisis! Finally a nurse convinced
a doctor to see me for 30 seconds, gave me a refill and a list of welfare clinics and booted me out the door. They
hated my appearance and hated me for no cash.

One day I decided to end this nonsense and tread everything I could from sources I hadn’t read that were very old
regarding what was wrong with me. I went on self imposed diet of 1000 calories a day and lost 60 lbs…yes!!
I stated weaning from the Prednisone and took a ton of supplements I had read about. I got down to 7.5mg every
other day. Yes, suffering tremendous total body aches, severe mood swings, dizziness, severe hunger and
confusion but I plowed though. By the way I don’t recommend this but I couldn’t get a refill for a prescription from anyone
because I ‘had made to much money.” So I turned to the Internet for everything. I bought 500 5mgs for $23.00 screw the doctors I don’t need their prescriptions. I am now totally off for 6 weeks I do have some bad stiffness, muscle aches and mood swings but after 4 years of pure hell I am truly thankful to be off this dangerous drug, it ruined my life.

So I went to a new Doctor finally and my diagnoses was a food allergy and simply had a small stint of bursitis a total mis- diagnoses from my first Doctor! Doctors aren’t gods so take it from me trust yourself first and do your research.

My prayers to all who suffer from this drug. Damn the incompetent doctors who wrongly prescribe it!

Dan V

I've had my Mirena in for about 2.5 years. To start with all seemed fine. Now I experience very long periods of discharge - not pleasant - brown clotty stuff - that can go one for three weeks or so. Worst of all, I have over the past 6 months or so experienced increasingly bad edema in my legs and ankles - I have some beautiful skirt suits but have been in trousers all summer because my ankles look like old ladies'.

Having said which, I am nearly 50. But even though my ankles have never been my best feature, they certainly don't need any extra help. I am convinced it is connected to these extended 'periods'. My doctor said if my intuition is that the swollen ankles is connected to the coil/menstruation, I should have it removed. I'm looking forward to it.

Mary, London, UK

My experience with Yasmin was decreased aggression, mood stability and increased breast size. when I stopped taking the drug, I had an increase in aggression, less fatigue and no weight loss.

My T-3 levels are fine. My blood work is fine. Not many headaches. My mood became more depressed when I stopped taking Yasmin.

Not sure if I am suited to take the drug. So, I am starting Yasmin again to see if I notice side-effects. My estrogen levels were low prior to starting Yasmin the first time. So, I am wondering if my testosterone is a bit too high, and if Yasmin levels me out so to speak.

I think those with normal estrogen levels, prior to taking Yasmin, are badly affected by Yasmin. I wonder if those of us, with lower natural estrogen levels are as badly affected by Yasmin.

Will let this site know in a few months.

ALSO get this pill from Canada - ******
It costs $22 and it is the exact same packaging, etc.

Hope this helps

I had the Mirena inserted on June 3rd, 2008. Does anyone have anything positive to say about the Mirena. This site really scared me. The only symptoms that I have are swollen ankles and spotting.

Thank you

OK guys, I have been reading all your side effects for a couple of weeks now, and finally decided to jump into this pot! You will not believe this, but I have been on Diovan 80 mg twice a day along with a couple of other blood pressure medications. It's been about 2 years, maybe a little less, and for the past 10-12 months, I have complained to my doctor that my joints and muscles ache so much that I feel like a 100 year old person. I also have has every side effect mentioned on the 9 pages listed here with all of you. I have had every test imaginable for artery's/veins/muscles/joints/sleeplessness/hair loss/weight gain/swollen ankles...you name it, I've been tested for it. They can find nothing wrong with me at all. NOTHING! I'm sure they feel that it's all in my head, since I've been quite sensitive to a lot of meds. in the past!

I am usually very active and run around like a crazy woman most of the time, but I was absolutely walking like I'd been hit by a truck. I went to my doctor with all of the complaints listed under Diovan printed out, and believe me, she took notice. We stopped Diovan that night and I started on a couple of new meds. that have absolutely no side effects. It will be two weeks this coming Wednesday (June 4) and I am almost a new person. I'd say, about 98% pain free. I actually felt relief after being off for about 5 days. It's getting better day by day. I actually feel that this stuff was killing me slowly. Get off asap!
By the way, I tried to look up the new meds, and they are so new that I can't find anything. For me, they are an answer to prayer.

I have been on Wellbutrin for a couple of years & it has been a life saver. But it is very possible my hair loss is due to it. I have always had a full head of hair & no hair loss in my family at all. I'm also experiencing hearing loss but don't know if this is due to the Wellbutrin as my Father & sister have had hearing loss. My doctor intends to lower my dosage next month & I am going to ask him if air loss is a side effect.

Hi,

I just found this site, as I am looking for an explanation for the extreme joint pain that I am having, along with swollen ankles/feet. I have been dealing with some type of chronic contact dermatitis that no one has been able to solve, since last July. I have been on numerous steroids, then on Cyclosporine, for several months, which can play havoc with your kidneys. I also started taking Singulair for the itching, which is one of the few things that has really helped. Since November, I was taking Singulair on and off. But, as I recall, I began taking it daily since around late January. Around late February, I began having joint pain, which still continues, and lately, is becoming excruciating! When it first began, I blamed it on the Cyclosporine and kidney breakdown. But, since I have been off that, the pain has continued to worsen. Then I thought it may have something to do with the Doxepin, which I also take at night for the itching. I stopped taking that two nights ago, but the pain continues to worsen.

Now, from what I am reading, these blogs make me believe it could be the Singulair. Can anyone tell me how long it takes for the pain to go away once you stop taking the Singulair????? I will gladly stop taking it if this pain will go away. In fact I will be thrilled, because I was suppose to begin testing next weak for possible Lupus, because it doesn't seem that the Physicians who prescribe Singulair, are well aware of these issues.

I would appreciate anyone who can give information as to how long it takes for the side effects to subside. Thank you!!!
(In pain in Boca Raton, FL)

OMG! I am so glad I came across this web site. The posts are amazing! I never would have connected all of my side effects with the Mirena. I thought only my bizarre bleeding was due to Mirena and now all my other problems make sense. First of all, I had the Mirena installed in June 2007. I thought it was awesome and even recommended it to my friends (just like the other person--SORRY!) Anyway, for about the last 4 months I don't bleed red, only brown. Yes, only brown! At first I didn't really care but now it is to the point that whenever I have sex (which like the others I don't really want) I bleed brown. Right now it has been 3 weeks of brown bleeding! So, by the time this stops, I will get my period. So, my husband and I are averaging sex about 1 times a month. I also have the rash under my wedding ring, which I never would have associated with Mirena, but a previous post did. I have been getting dizzy and lightheaded lately and figured it was either my sugar or BP, but both of those are fine. I also have the worst hip pain ever--hip pain?? What, am I 90 years old! I sure feel like it. I am always tired- I even take naps with my kids! My mother, who is 60 runs circles around me. She helps me so much that I can't even use the excuse that I am tired because of running a household. At least I am not depressed, however, I do go through some pretty tough mood swings. I also have a weird smell coming off of me, not a bad smell, just weird. It is coming out of my skin. I have swollen ankles and my fingernails look like crap. I used to grow such long beautiful nails and now they break and split. I don't want to blame everything on Mirena. I am sure that the way I eat and lack of exercise have a lot to do with it. I am overweight and until now I have blamed my symptoms on my extra 50 pounds. However, the bleeding I am sure, is due to Mirena and that is reason enough for me to have it removed. I am going to call my doctor today and have it removed..I am done with it. I will post back in a few months and let you know if there have been any changes. Thank you everyone for letting me know that I am not crazy!

I'm feeling really scared now because I've had the Mirena, well 2 of them, in for around 8 years. In all that time I've experienced really debilitating back problems and I thought at one point i would end up in a wheelchair. I just didn't connect it to the mirena even though my back problems worsened after having it fitted. I've also developed swollen ankles and fluid retention generally. Over the last three years I've had migraines and throughout I've been irrational and impossible for two weeks around my period.
My skin is awful now and seems to have lost most of it's elasticity.

I am finally booked to have this thing removed but I fear it could be too late to reverse much of the damage. I'm sure that skeletally my back is just too messed up. My skin hangs now like a 60 year olds because of the excess weight I'm carrying but if I could just get some energy back I'd be so happy.

I am 56 year old New Zealander, had stent inserted 1 year ago.
Was first put on Lipex, after 6 months on that would have welcomed departure. Came off it voluntarily and problems went away.
NZ is too mean to provide Lipitor with out a fight, so after much cajoling my doctor finally got permission to provide me with it.

At first it was fine, but slowly the same symptoms as with Lipex returned.
I have every single symptom I have read about here.
Joint pain, short term memory loss, nausea, swollen ankles and by association I am getting pretty depressed.

I had to come off beta blockers for similar reasons.

Finally this week I have developed kidney pain and have decided that that is it.
Lipids are out for the duration, I am told that half an onion a day will reduce your cholesterol naturally, so that is where I am going.

Thank you all for providing me with proof that these drugs do not work for all of us.

I have been on Lipitor for several years, but switched to generic Zocor (Simvastatin) for 3-4 weeks because of the high co-pay. I didn't seem to have any bad side effects with Lipitor (or not as bad as Zocor), but have had swollen ankles, sore knees, and difficulty walking for the past couple of weeks--that's why I'm here--to see what others are experiencing.

I've been on Predisone for about 5 months for severe allergies. I now have excessive acne on my cheeks. I never had a single acne outbreak in my entire life. I stopped the meds for 3 weeks and my face cleared up. As soon as I started the meds again the acne came back. I also, have experienced swollen ankles but that was very temporary.

Today i was proscribed with 50 mh prednisone ,5 tablets .4 times a day so that is 1000mg of prednisone a day has anyone had same thing .i was dyagnosed with optic nuritiritis.i am really scared to take this medicine and so many mg a day. please help!

My question is: Does anyone knows if Propranolol is a good substitute for Toprol-XL?
I read that there isn't any weight gain reported with Propranolol.
I'd love to hear your experiences with it.

I've been on synthroid since October 1996. My ankles are always swollen. That didn't start til I started the medication. My Endocrinologist keeps telling me that it has nothing to do with the meds. My TSH levels are constantly being taken. He says to cut down on salt. I don't eat much salt and besides, I know people that practically eat whole pigs and they don't have swollen ankles. Has anyone experienced this? Any suggestions, I'm desperate!!!

I have had thyroid disease for 6 years. I just had my medicine increase less than one week ago from 125 mcg to 150 mcg. The endocrinologist did this with a lab result from over 6 months ago and I was never retested before he upped my dose. 2 days after my new dose I broke out in a rash head to toe. The next day I started itching and went to my doctor and she said I have no idea what is going on with you. Then I went to the Pharmasist and he said you are having an allergic reaction to the dye in the 150 mcg blue tablets (125 mcg are white). The following day I got new medication I now am taking 3 50 mcg tablets. But I now am swollen ankles to feet and elbows to hands. My hands are like balloons. When I go to bed at night my hands are completely numb. Has anyone else had any symptoms like this?? Help I cannot figure this out. I am thinking that I may be over medicated. Thank you Heidi

I was diagnosed with Colitis just over two years ago. At the time, I was having severe symptoms and my doctor put me on 40 mg of Prednisone for 3 days, 30 mg for 3 days, 20 mg for 7 and 10mg indefinitely. The 40mg dosage caused me to not sleep at night, severe nevousness and basically feeling like I was on drugs. I felt this way until I got down to 20mg. Initially, I had swollen ankles and overall swollen feeling in my body. After I had been on this drug for more than a few months, I began to notice my hair falling out, my finger nails breaking and a severe tooth sensitivity to cold (never had this before). Over the last two years, I have been on and off of Prednisone and have had the exact same side effects each time. Right now I have been on 20mg for the last 6 months. I am meeting with my doctor this week to discuss some naturopathic solutions to get off of this horrid drug. Any one heard of using ingestible aloe vera as an alternative to Prednisone?

wow. i am a 36 year old female that started taking 50mg of toprol about 1 month ago for frequent pvc's. all these side effects i am reading about are just blowing me away. i have several...foggy, tired, difficulty falling asleep, muscle aches, weakness, tingly legs, weight gain, depression, nightmares, swollen ankles, hopeless feeling, decreased sex drive, cold hands and feet, leg and foot cramping.... NONE of which i had before. THIS MEDICATION IS EVIL!!!!!!!!!!!!!!!!!!!!!!!!!! i will be weening myself off of it starting NOW!!!! i would much rather feel my heart beating funny than feel like this.

My husband was just hospitalized for what we think are Levaquin side effects. He took it for a groin infection and got swollen ankles and stopped taking it. He has had fevers, night sweats, chilling, severe joint pain, swollen ankles and knees, to the point he is incapcitated. He was previously very healthy at 51 yrs. until this drug!
******