Podiatrist symptoms and conditions

januvia has helped bring my sugar down and my weight, but the problems i have been experiencing are constipation, the podiatrist told me i had slight neuropathy, my joints in my feet would swell and i stay buying alka seltzer and Tylenol pain pm. i do at times get high anxiety which he gave me the generic xanax for and that does help a lot. so my stress is better, but really has helped me is eating special k cereal in the morning and drinking lots of water and eating 3 meals a day. - J., Texas

Wow, who should I believe? Placebo controlled studies which suggest Avelox is a perfectly safe drug or a bunch of crazy people who like to TYPE every OTHER word IN all CAPS who are probably all middle aged women with psychological problems and/or fibromyalgia, irritable bowel syndrome, or other made up diagnoses.

Here's a hint morons: The reason why every drug in existence now lists every possible side effect is because of crazies like you. This way, the drug company can protect themselves from litigious idiots like the poster below who wants to join a class action lawsuit. This only compounds the problem, though, because then more crazies look at the side effect profile and when they see that "Oh my gosh, it says right here it causes x, y, and z" it just validates in there mind that this is somehow a dangerous drug.

I swear, if all of the pampered babies in this country were put to work in a rice field in Cambodia, there would be a lot less nonsense in the world. You would see what true pain and suffering is about.

It has been almost two years since I took one tablet of 500 mg levaquin for a throat infection. I immediately felt lightheaded, then came the hot prickly skin, rapid heartbeat, insomnia and just a feeling of doom. I did not take another pill. Right after this my ankles started to hurt and podiatrist said had a torn posterier tibial tendon. To this day, I cannot walk without a limp, and can only wear athletic shoes with orthotics. If I stand for or walk for a small period of time I am in a lot of pain and have to sit. I was diagnosed with rheumatoid arthritis from the inflammatory markers in blood tests and rf factor, even though mri of my hands and wrists are normal. My right shoulder and arm hurt, my wrists and fingers hurt, my knees, neck. It is better, but I will never be the same as I was - no more running, walking my dog, going camping with my daughters girl scout troop - can't go hiking. I am 50 and I feel like I am 90. Would like to sue someone.

I have only been on Nuvaring for about 9 months now, but I can not handle this any more. Since I have been on the ring, my periods have actually become more regular and shorter - yay - my problem is that since I started using it, I have been experiencing cyclic emotions, severe leg and foot cramps, almost constant sinus infections, and severe headaches.
The week before I remove the ring, I am a complete and total basketcase, thinking everyone hates me (including family and friends) and I almost constantly cry for no reason at all. The rest of the time, I am fine. I talked to the doctor and he told me it is not the ring and put me on an anti-depressant. Two months later, I talk to him again and he ups the dose on the anti-depressant and tells me I need professional counseling. I went, an was told these cyclic symptoms seem to be more hormonally related since it is at the same time every month.
After about the first month of use, I started getting HORRIBLE leg and foot cramps at night. I have had my potassium tested, it's fine, I was sent to a podiatrist who put me in leg and foot braces to sleep (which cost a bundle and did not help!) I have added additional potassium to vitamins and started drinking 64 oz of water a day (even put a bar of soap at the foot of the bed and a knife under the bed!!! I was willing to try anything). Still having problems.
As for the sinus infections, they have been almost constant, which previously I rarely got, but since starting the ring I am almost constantly have. Same with headaches!!! I REALLY don't get it.
Oh, and did I forget to mention that EVERY time my fiancee and I have intercourse I have to check to make sure it is still there?!? The first time I lost it, I got a call from him later in the day telling me I had lost my "braclet" (he had no idea about the ring). I didn't worry because it was the day to remove it anyway. As time has progressed, the ring will either end up in the bed or on him (!?!). I could understand if we were doing something odd, but we are pretty "normal."

I have now changed to a different doctor who told me I am not crazy, he has had other similar complaints about the ring, and is putting me on Depo, which I used several years ago with no problem). Three days and counting...

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..

After 3 weeks on Fosamax, I had an attack of back pain that put me in bed for a couple of days. I wondered if it might be the Fosamax. I quit taking it for 2 weeks. I thought I would give it another try to see if it came back. This time after taking Fosamax for 3 weeks, my ankle is swollen and I am having gout like symptoms and feel achy like I have the flu. My podiatrist did some blood tests for gout. The results came back fine. Low uric acid levels. I do not have gout. He took a lot of fluid off of my ankle joint. The pain has been horrible. I am in athletic shape, working out at the gym 5 days a week, and bicycling. This has been torture. I am stopping the Fosamax. I had a horrible reaction to Lipitor a few years ago with pain from my knee into my back. I could hardly walk. I am the one that figured out what was up then and stopped the med.

I am wondering if the plantar foot pain that my husband is suffering for 6 months could be from lipitor that he is taking for several years now. Has anyone have this problem?

I was “poisoned” by Levaquin -- resulting in acute tendinitis in both Achilles tendons.

Background:
I am a healthy, athletic male in his mid-50s who has never had an Achilles tendon problem. In early July 2008, my doctor (general practitioner) prescribed Levaquin for an infection. I took the medication for 14 days, as prescribed.
Sudden onset of acute tendinitis in my Achilles tendons occurred near the end of the medication period. The tendinitis occurred in both Achilles tendons simultaneously. Nothing related to my lifestyle would have caused the tendinitis.

Symptoms:
Symptoms included the following at one time or another:
1. aching
2. sharp pain
3. feeling of heat/burning
4. tightness
5. pins and needles in small areas (micro tears?)
6. weakness at rear/base of each heal.
7. When I woke-up each morning my tendons and the back of my heal pads felt sore, weak and tight.
At the height of the problems, I had extreme difficultly walking and negotiating stairs, and I thought there was a risk that my tendons would detach from my heal bone.

Doctors’ Advice:

My general practitioner’s and my podiatrist’s advice was to: (a) not run, cycle, hike or otherwise exercise my legs in any manner other than easy walking and swimming, (b) gently stretch, (c) take ibuprofen, (d) ice regularly, and (e) use heal lift shoe inserts made by my podiatrist. Their advice was based on the view that the damage that was done is more like damage cause by an injury than damage caused by an insidious drug. My readings on the subject indicate that little is known about the mechanisms behind this fluoroquinolone-specific toxicity. It is believed that the tendon’s collagen fibers become disorganized and infiltrated with small blood vessels -- resulting in weakness. And there are no specific treatment plans for this problem.

After 2 months of living with these symptoms, I decided to change course.

My Approach to Healing:

Because I never believed my pain was the result of inflammation, I stopped icing and taking ibuprofen. Because stretching seemed to further weaken the tendon and set me back, I stopped stretching. Because I believe that the body heals itself best when used, I started cycling at an easy pace. I then worked-my-way-up to cycling more aggressively, and to walking in the neighborhood. That’s where I am today. Two days ago I had my first day without discomfort in 3 months. Yet, I have a long way to go. I am not yet hiking or running. It’s a slow healing process with occasional setbacks when I push my tendons a bit harder than I should, Given the progress I have made, I am hopeful for a full or nearly-full recovery in another few months.

Other things I have done in the past month:

1. Taken L-Lysine (1000mg daily), which is believed to aid collagen formation.

2. Taken Magnesium (250mg daily), which some believe may help leech the fluoroquinolone molecules from the tissues because of the affinity of these antibiotics for minerals.

3. Taken Fish oil pills (3000mg daily), which improves circulation

4. Used a heating pad, which improves circulation

5. Started regular Acupuncture (first time for me), which improves circulation

What you can do:

1, Be easy on your tendons until you get a handle on the problem. Don’t over-use tendons when they are in a weakened state.

2. “Listen” to your body and take steps you think best to help the healing process.

3. Tell your friends to beware of potential side effects from fluoroquinolones.

4. File a MedWatch report with the FDA at fda.gov.

5. Share your findings/advice on this forum.

Good Luck

I was prescribed this medication by my podiatrist for mosaic style plantar warts. Began applying Lazerformaldehyde nightly. No discomfort upon application at first, but experienced severe burning of my foot upon application as applications continued. Caused my foot to dry so bad it began bleeding in places. Very uncomfortable. I think I am going to drop back on its use, my foot is so swollen that I can't even tell if the medication is doing anything for my wart problem.

my husband had never been one to go to G.P.s or have reason to take prescription medication( not even an aspirin ) . Finally had a medical test- Cholesterol was high- was not given a chance to change his eating habits- and was placed on LIPITOR ( this was 18 months ago ) and since- everything has gone downhill from there. He has suffered nausea, blacked out, had headaches/tingling sensation,chest pains, aching/fatigue to legs/feet and arms. - shoulder pain- has problems getting up from bed or from sitting position- has generally lost power in his arms and legs. His doctor was advised over the past several months of his pains- but had no idea what caused them and changed the script to Crestor. ( still a Statin drug ). Have ( on good avice from chemist assistant ) now got him on daily dose of Q10- and he ( 2 weeks ago ) decided to stop taking the Lipitor or any other cholesterol lowering statin drug- of his own choosing. He has had several visits to podiatrist to help alleviate the pain to his feet - which are sore and swollen. His liver levels were also high at on stage. All this has happened to him sine he started the Lipitor statin. Prior to this- He has never had previous medical conditions or medication. Seems to point the finger at one reason- LIPITOR !!!!!- THEY CANT BLAME IT ON ANYTHING ELSE. Just want him to get back some energy. He is 56. One more story to add to the thousands of complaints, Why isn't anyone in the medical field / lawyers commenced a full investigation to all these complaints? thousands of people cant be wrong. Bring on Erin B.

I was put on Lipitor in 2004 and didn't realize what was happening to me-I thought I was just getting old. (I'm now 66) I went from a very active person to one who struggled to get out of the car and my entire body ached. I was constantly tired, I had trouble putting thoughts together. I would sit at the kitchen table and cry because I felt so awful. I started losing my balance and falling down. In one of my falls in December 2006 I injured my left hip. I went to a chiropractor to see if he could help relieve the pain in my hip. While going over my symptoms and medications he pointed out that the Lipitor I'm taking could cause most of my symptoms. He suggested I call my doctor and talk to her. I did and she said that Lipitor could cause severe muscle aches-she wanted to do a blood test and said that I could just go off the Lipitor. My blood test was normal. That was in March 2007 and I have been off the Lipitor since. The fatigue and muscle aches have gone away. I still have the hip pain (bursitis) and have been going to physical therapy for that. My memory is improving but I still have to concentrate, repeat names and write things down trying to remember. I'm trying to lose weight (most of it gained around my middle). I go to the gym and exercise to try to build my muscle strength. I'm not tired all the time, I've read that the symptoms can last a long time and sometimes may never go away. I've been told by the doctor that if my cholesterol is up at my next visit that she wants me to go back on Lipitor. She also said that if it had been the Lipitor, the symptoms would have gone away right after I went off the Lipitor. I will absolutely refuse to go on any Statin-I cannot take the chance of feeling so badly again.

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??

I am a heathy 63 year old male. Completed a half marathon last year. Run 15-20 miles a week and bike 20-35 miles a week. I've never had any medical problems except to be on blood pressure medicine for 20 years. It is controlled.

Last April I had a bout of plantar fasciitis in my right foot. The podiatrist recommended and I purchased orthotics.

The heel pain did not subside, in fact the whole foot became sore all the time. The other foot joined the party and within a couple of months I could not run because of pain.

I used stretching exercises recommended. Purchased two foot splints to hold the foot at 90 degrees at night to reduce tearing of the tendon. I mixed Aleve and Iboprophin to help with the pain. No relief.

The discomfort in both my feet was at a level it hurt to get out of bed and walk. I did not wish to walk to the mail box or go shopping with my wife. I hold national computer workshops. I could not stand all day. I had to use a bar stool. When I finished for the day, I'd go to my hotel room and order from room service. I had no interest in walking.

I was wondering if it was the orthoditics. Tried it without them. No change. It was now into the 8th month. I was thinking I was just an old man who had worn out his feet running.

Then I did research on the Interent and discovered Lipitor side effects. I had gone on Vytorin (Lipitor/Zetia combo drug) a couple of weeks before the plantar fasciitis started.

I slowly reduced my Vytorin until it was zero. Within 3 weeks 95% of pain was GONE! Within 2 months it was completely gone including the heel pain.

I now run again, walk and have my quality of life back.

When I went for my annual physical I explained what happened. The doctor did not say wow, that is common. He was kind enough not to make a judgement call. He said well, you must have had a side effect not well known. I told him it was muscle pain in my feet rather than large musle groups as is usual with this side effect of Lipitor.

My lipids are not over the hill bad but he is aggressive in treating carcio vascular issues. So we are going to try Zetia by itself and then possibly Niacin.

Let me say, I am not an extremist about statins nor do I believe there is a conspiracy wiht drug companies. Statins do work for most people.

I have a strong opinion that we must have a equal relationship with our doctor to determine our treatment. The Internet gives us that opportunuity to get the knowledge we need to talk to our doctor. Without the info on boards like this I would been a broken down old man with bad feet using the electric cart at Sams and selling my RV.

Best wishes in your search for satisfactory health.

Started Fosamax February, 2006. By April 2006 I had hip, back and foot pain. Hair loss became very apparent. I checked this site and saw hair loss as a side effect. I had never realized this before - these sites are a big help. Before Fosamax I had been on Actonel for a year (no pain, but mild hair loss) but was told to switch to Fosamax by my insurance company). Stopped taking Fosamax in April 2006. Pain slowly subsided but left foot was still so swollen by July 2006 that I saw a podiatrist for suggestions to ease discomfort. She suggested metatarsal pads until swelling and pain subsided (about another month). Seem to have no lasting side effects by January 2007. Will never take Fosamax again.

I was referred to a podiatrist on March 1st 06 for a growth on the bottom of my foot. I was given an injection of Kenalog and have experienced severe pain at the injection site. I have broken out in hives all over my ankles, lower and upper legs.My thighs are covered in horrible bruises after the hives went away, but the hive an severe itching returns every evening. I have had severe fatigue, my tongue is raw, I can not eat. I know it is a reaction to the kenalog. I am in menapause, but am having slight bleeding since the injections, I didn't connect it to the kenalog until I read these posting. I have an appt. with my primary care phsycian in the morning, I will never, never have another one of these injections again. Thank you so much for taking the time to post this helpfull info.

Hi everyone!

This is the first time I have been on here, but I have read a couple of pages so far.

The main reason I am here is to do some research regarding some changes I have been experiencing. I have been getting horrible cramps in my feet and toes for months now to the point that I fall to the floor crying. I recently went to a Podiatrist who told me that it was my birth control. I have a doctor's appt. on the 13th so I am desperate to see what she says. Please let me know if anyone else has experienced this.

I have also been extremely tired for the past year and only in the last 5 months have I been getting nauseous for no reason. I never thought twice about it being a side effect of Yasmin, which I have been taking for over 3 years now.

I definitely feel like I need to get off of this and I am also curious to see what everyone else is taking now post-yasmin?? Please let me know!

Thanks!

I am not sure if the steroid shot I received in my foot in February 2005 was Kenalog or not. However, In the past 3 weeks I have a light color streak halfway down my foot from the toe almost to my leg. Near the 2 & 2rd toe there is a deep indention. I saw my primary care doctor today and she basically was taking up for the podiatrist who shot this steroid in my foot. I told her he never told me I would have this type of side effect or damage to my foot as a result of getting the steroid shot to relieve pain. This happened at a VA Hospital. Does anyone know if I can sue the government or that doctor?

Podiatrist gave me a total of 2 injections containing Kenalog into the top of my forefoot for an injury (I banged my foot, but no broken bones). About 2 months after the 2nd injection, I noticed an indentation and skin discoloration directly beneith an injection site. Now many months later, I have lost a significant amount of the fat pad on the ball of my foot. I have chronic pain in the ball of my foot. I wonder how the Kenalog has affected the muscles or bones in my foot, since it destroyed the fat pad.

This podiatrist NEVER mentioned that there are possible side effects of steroid injections. He only stated positive things about the shots, and I didn't know any better. If he had told me that there were side effects like fat pad atrophy, I would NEVER have let him inject my foot. My foot would have been fully healed today had I not received those injections, but instead ended up with a chronic condition!