Swollen feet symptoms and conditions

I have just started lyrica and read on different sites and its main site before i decided for myself to take it since im in constant pain from multiple accidents i have fbro- and lumbar and disc back problems etc, yo get anyway i have tried a lot of different meds for pain yo name it almost tried it, i found the best thing that worked for me was one vicodin es plus one 75mg lyrica, my pain subsides for hours by at least 50% i can actually do a lot more since i have started it and even lost four pounds since last week. I read a lot of people gain weight, get swollen feet,feel drunkish all that, the only time i feel like that is when i take the lyrica with my xxnax i have anxiety disorder as well very bad. ADHD . If i dint have to take pills believe me i wouldn't..But as all pills narcotic and narcotic they only mask the pain, my brother informed me since i can do more take it a little slow baby steps cause if you over exert your self your pain is 6 times worst.I have lost 89 pounds so far HOORAH! Just 40 more to go, baby steps..lol..anyhow i could talk all day, i try to keep a positive attitude which helps, god and prayer help, and try to walk around without a chip on my shoulder because i don't feel because if im miserable everyone else shouldn't be, ya know ..Its not rgt. Cripe if i was rich i would be waited on hand and foot but unfortunately im not rich and could never afford that unless i won and played the lotto.lol..i had to even get samples from a different doctor other than my regular doctor cause he girls were messing up in the office or Michigan State was, which lately they are changing all there systems and messing alot of low income people up, and that blows too..I will continue will lyrica...It works better than neurontin which gave me headaches, and weigh gain and nausea. I actually on neutrontin gained 10 pounds in 5 days, i quit NEURONTIN! Lyrica is really good, everyones body chemistry is different so, give it a try it might just work as good as it does for me. Thanks for listening and feel free to write me anytime here, thanks! Skully725

I believe that the biggest key to success with loestrin 24 is to wait it out! you have to give it at the very least 3 months to get in your system and really regulate and for your body to adjust!! i say this only because i have been on it going on 9 months and i love it! the first 6 weeks were horrible! headaches, spotting, back aches, chest pains, swollen feet, acid reflex, my face broke out, dry skin, i even found more hair in the shower than normal for about the first 3 weeks, but you name it, and its a proven side effect, i had it! i have a fever for about 11 days of between 101-103!!! but my obygn just kept telling me this was the pill for me and i though the had lost his ****** mind!! but i did stick it out! all the side effects started to disappear around the beginning of the 3rd month. and so did all the spotting and my period completely!! wow! im 21 and no mood swings, no average side effects of a periods, nothing.. nadda!! its amazing! this is the only bcp i have been on! and i wouldn't change it for anything! but let me remind you, im not on the pill to prevent me from getting pregnant, i have endometriosis!! this is extremely common in white females!! my obgyn said i developed it between the age of 11-14 ( i started my periods when i was 10! and it went totally undetected for 11years! now, my mom always thought i was just a totally baby! but the pain and the blood clots i would pass when i was that young was so scary. but i never went to a obgyn til i was 20 and i had insurance, lived on my own and could afford to go. so now im so happy on the pill! there were times when i was younger that i would give anything to be punched in the lower back cause the pain was so bad! i couldn't stand, i would be walking and just fall to my knees cause the cramps would just take over. this happened at school a lot, but the day it happened at work i knew i had to do something! so they did a few months of blood test, 6 peps smears in about 2 months.. and a few other test and determined it had to be endometriosis!!! if you ever feel like your insides are tearing appart.. you need to ask your obgyn about testing you for endometriosis!!! *google it!!** anyways, back to the bcp, after the fifth month i was happy again, no pain, no more side effects, no moody-ness or random out breaks of tears!!! its amazing. i dating this one guy! and not having a cycle is sooooo wonderful. he loves that i don't have a cycle!! which means no "time of the month" crap to deal with!!! lol!!! i cant tell you how much i love being on this pill. OHHH i almost forget! you can now get your script with or with out insurance for just 24$ a month!!! no matter what! just to buy the pills like like 80 a month, with full coverage insurance ( which i have ) its still 60 a month. well i found this website and i called, answered a few questions and now i get it for just 24 a month!!! ask your obgyn for the info!!! amazing!!

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 son Emmett was put on Omnicef for pneumonia and ear infection. On the second day of being on this drug he had terrible diarrhea, black and watery and he would scream every time he was pooping. He wouldn't sit and would cry if you tried to lay him down to change him-this made me think his stomach hurt pretty bad. Sometimes he would stand there and look at his stomach and just scream. On day 10 of Omnicef he had something on his stomach develop that looked like a heat rash that started off as white bumps then turned red. Two days later (2 days after the drug was all taken) the bumps became bright red and were everywhere. He also had swollen knees that were hot to the touch and wouldn't walk around. We went to the doctor and he said it was a reaction to something he ingested. He said we should give him Benadryl and just watch him. The Benadryl worked for a couple days then stopped working all together. New red spots would come back as soon as the others went away. Three days later we were headed to the ER because of swollen feet, all of his toes connected and his feet were so puffy he wouldn't stand on them, they were also hot to the touch. Luckily we saw a different doctor and he did some blood tests. It turned out he had mycoplasma infection which is also knows as walking pneumonia. He was given Zithromax and was better within 12 hours. The red spots and bumps and swollen extremities were all cleared up. I don't know if he was allergic to Omnicef because he is allergic to Penicillin or if he was just given the wrong drug for the walking pneumonia and it wasn't getting any better. It is definitely worth getting a second opinion in the same day after going through this last week.

I am switching from Lyrics to Neurontin. I have always had a weight problem and lost 50 lbs.on Weight Watchers and have gained about 10 of it back. I am switching from Lyrics to Neurontin, hoping to stem the weight gain. Opinions and experiences please . . . am I jumping from the frying pan into the fire? I CANNOT ALLOW THIS WEIGHT TO COME BACK ANY FURTHER !!!! HELP !!!!!!

LC - Ohio

I am being treated for ulcertive colitis. I have been on prednisone since Sept of 08. I started out on 40 mg. In late Oct. my doctor started tapering me off 5mg per month. Each month following the tapering date, I would get sick. As I look back, all the signs of withdrawal were there. This Jan. I tapered once again, but the window was only 3 weeks. I hit rock bottom. If there was a symptom, I have it. Nausea, burning in my digestive tract, diarrhea every time I eat, muscle ache, numbness in my legs, swollen feet, sore bones and joints. ( The worst was in my feet. I ended up seeing a podiatrist. He thought plantar faciaitis until I told him about being on prednisone. The small bones in my foot were swelling, The muscles in my calf were buning they were so sore. That was last week. Today my other foot started. I can hardly walk. In addition to that, I am lightheaded, have elevated blood pressure, and fatigue. I also had some vision problems that sent me to the doctor. I went through a ton of testing which all were negative. It seems that pseudotumor is another symptom of withdrawal. I have a history of that. It would have been nice to know that. As I look back each month, I had different muscle and joint pain that lasted about a week. I was put on an acid reducer in Dec. to help my stomach, but in all of this time, I was not told that these all may be withdrawal symptoms. I have been off work for two weeks now in addition to the days I missed each month. My physician is now controlling the tapering procedure. They up the dose to 10 mg again. They plan on weaning me by 1mg doses. This has been a terrible experience for me. I have only been severely sick one other time in my life. This pain is awful. It is chronic. This drug may be beneficial, but it is like poison too. Anyone who takes this should really ask a lot of questions, and be careful..

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.

This is my second bout with what my doctor thinks is erlickiosis. The first time I was at the point where I could only move like an old man doing "the nursing home shuffle". Everything was swollen. Feet, hands, knees even my jaw was hurting. I couldn't stand on my own even though two weeks prior I was walking 3-5 miles per day on some good size hills. I was hospitalized and given steroid injections. Within 12 hours I was standing on my own. I was given Perdnisone 30 mg X 3 days 20 mg X 3 days 10 mg X 3 days 5 mg X 4 days. Except for some insomnia and peeing 5 times a night there were no other effects. Within 2 days I was crippled again. Now my GP was in Africa and my Internist was leaving for vacation in India. Internist would not put me back on Prednisone because he wanted me to see a Rhumatologist. I made an appointment but it was SIX WEEKS OFF. Two days later i was admitted to a different hospital. This one was where my Rhumatologist had access. Long story short Prednisone 80 mg 7 days 60 mg 7 days 40,20,10mg 7 days each. Had to start taking insulin again. Glucose never went over 200. Avg glucose last 5 weeks is 120. Gained 5 pounds because I work out every day with free weights and lots of cardio. Hopefully, I won't have to many side effects when weaning is accomplished.

memory loss, panic attack, vision, speech, chest pain, tiredness, loss of sex, headache 3-4 days, loss of food, weight gain, acine, leg pain, swollen feet, muscle problem, hair fall out, hair gets thinner, stomach ach,, double vision, staring.

I had Mirena inserted after the birth of my 2nd daughter - November 07. Things were going ok (at least that was what I thought) until about two months ago. I really did not think about the Mirena much. Maybe that was because my sex drive has been soooo gone that I have only used the benefit of the Mirena about 3 times. The problems I guess really started when my period disappeared. That happened 3 months after I got in inserted. I thought that was going to be great because my periods usually last 7 days from start to fully finished. But with this thing, I did not bleed but I definitely was still having a period. Bach aches, mood swings, headaches, bloating, etc. I started to think something was really wrong when I got a headache that lasted about a week, and I don't normally get headaches that last longer than a few hours. I could not figure out what was wrong with me. I even went to the emergency room to have them tell me that there was nothing wrong and it was probably just stress. I started to think that maybe it is the Mirena. I started doing searches on the adverse side effects of the Mirena and thank God I found you guys. I have most of the symptoms described here and other Mirena side effect pages. I will be having this awful thing removed in about two weeks. I don't know what my husband and I are going to do about birth control. We both do not want anymore kids but I am only 28 and do not want to have my tubes tied.
Headaches
Joint Pains
Low Back Pain
Mood Swings
No Sex Drive
Massive weight Gain (I have not lost any of my baby weight plus i put on a few more pounds)
Breasts Double in Size
Fatigue
Dizziness
Depression (low self-esteem)
My feet have even grown (probably because of the weight gain)

Kidney stones pain,swollen feet and lower legs,joint aches. taking 200 units a day
100 am and 100 pm

60 yr old/young female: I started generic toprol (metoprolol 50mg xr) yesterday (11/22/07). Took about 3:00 PM. The next morning around 6:00 AM, I had a hot flash that equated to one you would have if you had taken niacin. Body was burning and I was sweating. Looked in the mirror to see if I was flushed, because of the severity of the hot flash I thought my body would be totally red. It wasn't. I called my pharmacist to report this event. He researched and found no evidence of such. He did say that it did not rule out the possibility that it was caused by the Toprol. Asked me to keep him posted as his customers were the ones that helped him be able to report side effects to other. Well I found this site and low and behold I have read of the hot flashes and all of the other problems. I will not be taking this medication. I am not a pro medication person anyway and related that to my dr, but at some point you feel you have to have trust in someone. I don't trust medications. I know at some point in my life I will probably have to take something, but not Toprol. Sounds as though it will cause more problems than it will cure. Thanks so much for your input. It will prevent me from having to wean myself off this mess. Oh yeah, I was also feeling the depressed, anxiety mentioned. Not at a high level , but just knew I wasn't myself. That was after just one dose. I can't imagine how it would have progress. I feel very blessed.

I've been on Prednisone after and allergic reaction to penicillin (Amoxicillin) (bullous pemphigold - large blister on my arms and legs, some on the back and very little on the stomach) I've been on the medication for three days (40mg/day) I cannot standup or move my hands, my entire leg hurts and the foot is swollen (it could be from the penicillin). I'm hoping it will go away after I come off prednisone but has anyone experienced long term pain from this drug?

I'm pretty sure my pain is from the allergic reaction. Has anyone had long term pain from any type of bullous reaction?

I HAVE BEEN ON THIS PILL FOR 2 MONTHS SINCE MY LAST MISCARRIAGE AND AFTER READING THESE POSTS I AM REALIZING HOW BAD IT IS. I BLEED EVERY 2 WEEKS EXCEPT WHEN MY PERIOD IS DUE..MAKING ME FEAR PREGNANCY.. I AM BLOATED. I HAVE PURPLE VEINS IN MY BOOBS..SEVERE SWELLING SWOLLEN FEET AT NIGHT, NIGHTMARES, CHILLS, BACKACHES, MOOD SWINGS, LARGE NIPPLES AND I HAVE LOST 10 LBS IN 2 MONTHS WHICH I DIDN'T NEED TO LOSE. I AM NEVER HUNGARY EXCEPT AT 3 AM AND I PEE ALL NIGHT LONG. I TAKE THE PILL IN THE AM..NEVER AT THE SAME TIME.. ANYONE ELSE FEEL LIKE THEY ARE PREGNANT THE WHOLE TIME THEY ARE ON THIS PILL? WAS ALWAYS ON ORTHO...THIS IS THE FIRT TIME I HAVE EVER BEEN ON A DIFFERENT BUT MY DR GAVE ME 6 MONTHS WORTH OF SAMPLES... NOW I SEE WHY.. THANKS GUYS.. I AM SWITCHING BACK ASAP.. THIS BLOWS....
D.M.B. FROM NY

Summary of what I've read so far...

On emotional level:
1. Anxiety/Depression
2. Fear of having throat/lung cancer
3. Fear of having a heart attack/failure/angina
4. Short temperedness
5. Vivid dreams/nightmares
6. Thoughts of suicide
7. Feel like we're going to die soon

On physical level:
1. Tingling/ pins and needles, on arms and fingers
2. Leg pains (cramp, etc...)
3. Chest pains ( various description...)
4. Shortness of breath
5. Back/neck pain
6. Trouble sleeping
7. Coughing, itchy/scratchy throat
8. Loss of sex drive
9. Dizziness
10. Lack of energy / feeling exhausted / fatigue
11. Muscle/joint aches
12. Night sweats / cold sweats
13. Hair loss
14. Nausea
15. Abdominal pain
16. Swollen feet/ankle
17. Palpitations

Alternative medicine without or minimal side effects...
so far, DIOVAN has been recommended.
I'm calling my doc tomorrow and will insist on DIOVAN...lol.

Feel free to add to this list.

Better health to you all.

God bless!!

I am having tingling burning sensation in my feet, legs and hands and arms. My blood pressure was not improving on 5 mg so I upped it to 10 and those symptoms are much worse. The tingling sensation goes all the way up my left arm and up above my knees on my legs.

I have tried to take the Lisinipril before and stopped for these same reasons. My doctor does not seem to think that it is due to the Lisinipril. so I tried it again and the burning, burning sensation is driving me crazy and keeping me awake. I have to get up and stand in cold water for a while to get some relief.

I have not read about anyone with the same symptoms. Does anyone out there have these symptoms??

painful breast and nipples, rib cage front and back pain more so when lying down, weight gain, aching legs, swollen feet,spots on chest and back, 4 months after insertion and after depo injection have got continuos brown discharge, and not much sleep so tired all the time.

Flowerbabies-

Posted to the site you created as well to see if others would like to weigh in on this:

lowerbabies-

so heres is what I wonder. If the chest pain we are both experiencing is in fact due to the loss of magnesium as part of taking this pill, than how many other women that are experiencing that are having direct heart damage and being told that instead, to cover it up, that it is anxiety and stress? I mean seriously? Afterall, if magnesium prevents the heart muscles from spasming-and Yasmin causes a deficiency in magnesium ......then what, I am wondering is the link to the week before our menstrual cycles that this chest pain shows up?

There is an article in Health magazine I read called A Woman's Heart. Basically cites/talks about the fact that the public nor most doctors are taking the time to understand the single largest killer of women in America-Betsy Berne was the example they provided and that often women do not take themselves and doctors do not take women seriously enough. She ignores her chest pain for a week. Then is encouraged to see an internist who detects a murmur. This is true in my case as well...., then they did an electrocardiogram, and a chest Xray to discover that her heart was enlarged. An transeophageal echocardiogram (a more invasive test) that required she undergo open heart immediately.

This article goes on to state how many women are often not taken seriously who complain of chest pain and are often misdiagnosed with panic attacks while what's actually occuring is a misfunctioning valve between the left ventricle and atrium-with severe leakage and improper blood flow. Ordinary MVP is nothing to worrry about . They say it effects between 5 and 20 percent of population-mostly women.

In this article she also mentions that classic symptoms for women are: chronic fatigue, shortness of breath, nausea, abdominal pain, dizziness, and swollen feet. Also advises that for women, who have smaller arteries than men, when they have a heart attack there is usually no plaque in their arteries-a heart attack is when one of the vessels occludes-and they're more prone to artery spasms.

Other symptoms/warning signs: uncomfortable pressure, squeezing, or pain in the chest that last more than a few minutes, or pain that spreads to the shoulders, neck and arms. Chest discomfort with lightheadedness, fainting, sweating or nausea. Unexplained anxiety or weakness, palpitations, cold sweat, paleness. Shortness of breath, chronic fatigue, jaw pain. Isn't this alot of what many women are describing experiencing?

Chronic dry eyes, increase weight gain (face & stomach), irratibility, highly emotional outbursts, swollen feet & hands, poor circulation in feet, hands & legs followed by severe cramps, increased appetite, poor sleep habits, & whatever else I forgot to list.

I have been taking Doxycycline 100mg twice a day for about 10 days now. It has for some reason effected my joints. It started in my knees and seems to be moving to other joints like my wrist. I did see other posting with the same problems, but not a lot. I also had one day of being a little light headed early on but it didn't last more that a few hours. I do a lot of sports, so having knees that hurt and I have trouble using sucks! I am done taking the drug and hope to see improvement shortly, but really have no idea how long before my knees may feel normal.

well the first time i took doxycycline i got swollen feet, so my girlfriend massaged them and it made it so bad i felt like i was walking on bruises. now i took it again about 2 years later and my feet have swollen again and i have terrible back pain. but the doctor said that's not a side effect of the medicine. ok.

hello everyone,
My wife has been on prednisone since 4 weekas ago.She started with three tablets which is 60 mg.After a week they decresed the dosage to 2 1/2 tablets 50 mg and it went down to two tablets 40 mg a week later and so on.Here is her side effects: at first she experienced blurred vision but only for 10-30 minutes but they went away as the dose decresed,moon face(rounded and chubby) week joints in elbows, wrists, knees and feet.She eats a lot more than she used to,anxiety,
her eyes pulsate , irregular heart beats,sharp poking pains in neck legs head feet chest.Mood changes,gets mad at me over little things,back pains , neck pains,back muscle soreness ,cant sleep much,her head feels very big,walks very slow,gets tired fast,swollen feet,sensitive to light sometimes,headiques,feels pulsating through most of her veins,sensitive to noise,dizziness.She has about two more weeks on this medicine which she had to take due to narrowing of her blood vessels on brain(postpartum cerebral angiopathy) very rare complication after she gave birth to a healthy boy.My wife thinks it all happened because the anesthisyologist messed up on the epidural shot which he had to perform it three times on her.If anyone one out there knows how long does it take for her to get better please let me know it will be very appreciated. Thank you all
God Bless

Since taking Actos I have had swelling in feet and legs, shortness of breath and weight gain. I quit taking it for a week and some of the swelling went down and I lost about five lbs. I don't want my diabetes to get out of control but neither can I afford to gain weght.

When I took this medication I experienced hives, high fever, a red swollen face, NIGHTMARES, HORRIBLE HORRIBLE HEADACHES horrible pain in my arms and legs, swollen feet........and all this for a mild uti........thanks alot DOCTOR IDIOT

I just wanted to add that I have experienced shoulder pain (couldn't lift my right arm), back pain and thigh pain, plus swollen feet and right eye vision disturbances. Been off about 2 weeks and finally think I am getting some slight improvement. I hope it continues to improve.