Spite symptoms and conditions

I am a 48 year old female with a-fib. I am not overweight...just started falling apart since now I am menopausal. I've been on Warfarin for 6 weeks. My INR has hardly moved. I'm now on 8 mg and have my INR test on Monday. I started at a 0.9. Now I'm at 1.20 and have been there for three weeks in spite of upping the warfarin. I've not changed my diet except to exclude greens and green tea when I began the therapy. Everything else is consistent.
I just started exercising again a week ago. Something I haven't done in five years since I lost my sister. I bought a Total Gym and enjoy it. It has helped me get some energy back, has helped alleviate some of the mental fog, and has lowered the incidence of anxiety attacks. (I've been getting anxiety lately...since the mental fog and memory lapses...that bothers me since I love to read and write and the mental fog seems to be taking the joy out of it now.) The reason I decided to start strength training again is because of the joint pain I have been experiencing lately. I didn't have it before warfarin. I do now. Only one joint, though. The strength training does help, but every once in awhile, that sharp pain comes back to visit. It's just a little less now.
I plan to tell the doctor that I have begun strength training again. Not just because it's good for me and my heart, but it seems to help with the side effects of menopause and warfarin...without adding another drug like an antidepressant.
Warfarin...I believe is a life saving drug. BUT, I have to do my part too.

BTW, if I didn't have triple thick hair, I would complain about hair loss. Right now, it's a non issue for me. Just saves money at the hair dresser.

This is not a new side effect, but the same day I started taking Levaquin for sinusitis, I suspected something was wrong. Within hours, ears were roaring. First night, NO sleep, and that's WITH Ambien CR. Day 2.....depression! Immediate. This is in spite of having a severe depression under control for over a year. Sudden. I really started suspecting Levaquin then, but thought it was a coincidence. Took it this morning. Deep, dark depression. After reading these posts, I knew my suspicions were correct. The depression is getting better after 10-12 hours after the dose. This is really scary stuff. Really scary. Oh, yes, and I had the stomach pains, also. Told my husband it was just hurting like a bruise, not like indigestion or gas. I will report it to my doctor so they will no it's a "no-no" for me....in spite of all the websites that said how safe it was. Glad I found this website. Thank God.

I don't know if I can blame Zocor on my weak thighs--my doctor says that muscle weakness as a result of the drug should include all of my muscles. I've also developed an extremely itchy neck-also not sure if this is related. Weight keeps going up in spite of increased exercise and limiting daily caloric intake to below 1500 calories.

I am a generally active and fairly healthy 77 yr old who had been taking 10 mg of Lipitor for over 12 years with no obvious adverse effects. Recently I started having pain in my right leg, severe enough to wake me at night. This was followed by a significant weakness in both legs, and for a while, accompanied by a lightheartedness. The doctor had me take a series of lumbar and leg x-rays which didn't show much of significance. He wrote a prescription for physical therapy, which I did not follow.
I did internet research on my own which made me aware that Lipitor could be the cause, in spite of the fact that I had tolerating the drug for so many years. I told the Doctor of my suspicions and we agree to stop the Lipitor for at least 6 weeks to see. A few days later, all my symptoms were gone. So be cautious, adverse effects from Lipitor can occur anytime.

confusion, dizziness, clumsiness, slow thinking, fuzzy-headed feeling, nausea, stomach pain, severe cramps, constipation, aching joints, swelling fingers.

Was in the hospital receiving IV and inhaled steroids for breathing problems. Sent home with 10mg prednisone twice a day. It was even worse. ---puffy face, no sleep,and extreme weakness in my thighs--hard to even walk up stairs. Had a CAT scan of my lungs and my dr. was alarmed---said for a 112 pound woman,my stomach was the size of an obese person! now I'm going to have a stomach emptying test to see if that or the steroids is the problem.

Been taking this for the past ten years and it is the only thing that allows my skin to quickly recover from eczema. Eczema started at age 22. After my first injection I felt more powerful than Darth Vader and noticed an increase in energy and stamina. A few weeks later, a crash begins and I feel the side effect of lethargy. Consistently, after each Kenalog shot, my skin will develop several pimples around my buttocks area and sometimes on my back after a month or two. I would prefer never to use Kenalog, but it has been the only thing that relieves the patches of skin that become red and flaky due to stress, lack of sleep, and a poor diet. Ultimately, I did develop 'hypercutia' which is a skin condition which allows my dermis to bleed more easily. After stopping the Kenalog injections for a few years, my entire dermis still remains thin and more vulnerable to bleeding. I make my living as an actor and it is part of the reason i still rely on Kenalog whenever an audition comes up and I need to show my body. The pimples eventually become little scars, which eventually become little darker spots on my body. I still believe that in spite of all the side effects, it is worth it if you make your living as an actor or model.

feeling some relief to have validation to why i have been feeling this way.

i thought i was going the way of father (heart attack in his 40s) due to many symptoms over the past month similar to heart issues, except the leg cramps. i thought of my mother in-law, her diabetes, poor circulation.

i knew i had just had a thorough heart evaluation with my doctor last spring and everything was fine, except my hereditary cholesterol. frustrating. he had prescribed lipitor at that time. last week while driving to my office Christmas party i thought about driving straight to emergency.

food always seemed to help, as well lots of water. I think because i had liquids when eating, dehydration is what was being addressed.

on my own, i stopped lipitor (only prescribed medication i take) four days ago. no more nausea, no more light headiness (briefly early morning yesterday), no more weakness, leg pain decreased; these were my main symptoms.

I also experienced occasional foot cramps, general aches, heaviness in my esophagus immediately upon eating (thought of my mom with her hiatal hernia) indigestion maybe.

I had one episode a month ago (about the time all this started) where out of the blue i thought my legs were going to fall from under me, they became tingly like they were going to sleep, i was light headed as if i could faint. i had just finished a relaxing picnic by a natural stream, on a beautiful sunny day.

doctors who prescribe this medication should be more aware of these side affects. seems they are either not listening to their patients, or do not have the knowledge of these side affects, and in result, should not be allowed to prescribe.

My concern now is how long the discomfort in my legs will last, though they have improved. to make sure no serious damage has occurred,
i will see my cardiologist in two weeks to have blood work.

I would suggest to anyone who has not contacted their physician since stopping the statin, to do so. print a copy of this site and bring it with you!

T. - 47 years - trying to stay healthy!

I am a pediatrician and my and I take care of my one year granddaughter is with allergic rhinitis and bronchial asthma. In her past history other than her usual problems she developed an episode of ketotic hypoglycemia after a viral syndrome.
I started her in Singular as she was having nocturnal episodes of cough in spite of having Pulmicort twice daily. As soon as she was started in Singulair she developed restless episodes of irritability. She never behaved that way before. She is now sleeping well all night after she had discontinued Singular.

I posted several months ago on this string and wanted to update. I had bloodwork done for the 1st time since I quit the 20mg of Lipitor in August. LDL went from 123 to 210. Total Chol went from 191 to 285. HOWEVER all shooting pains I had been experiencing in legs, feet, and chst are GONE! Went back to my Dr. today, told her that same result and my serious objection to taking any kind of statin and she prescribed CRESTOR while telling me it was more potent than Lipitor! WTF!!!

I refuse this course, am drinking 30 - 40 ozs. of water each day now like I should have been, doubled my CoQ10 to 200mg/day, finally getting back into the gym to lose weight and get the HDL up from the level of 36 it is now. also started to drink the new yogurt type "shot" of Promise for cholesterol that provides 2 grams of plant sterols per day.

I will not take statins ever. I WILL find a natural way to keep my Chol under control. I've also been convinced that you don't have to be at or under the 200mlg of total chol to be healthy. Look at your C Reactive Protein and Homosiytes (sp?) If they are in range you should be good.

I know Lipitor was the cause of my rupturing each of my Achiller tendons a year apart while playing tennis in my late 40's Muscle pain soon followed.

Last night I woke up burning all over and about to explode from the firey heat. Made it to the bathroom where my husband found me, eyes fixed and unresponsive...I was worse than comatose...I was dying. He talked to me and keep me "with him" and was telling me he was going to call EMS when finally I began to comer out of it. My eyes were fixed and I could respond to him. I had turned a gray color.I will never take it again. I, in reality nearly died, not from discomfort, but from a whole system shut down. I had only taken 500Mg at bedtime for about a week. No More for me...ever!!! jcw in San Antonio

Hi,

I have two boys and my second son is now 2 months old. I had Mirena inserted at the end of May (it is now June 21) and I have had terrible cramps, non-stop bleeding and things that I have never experienced before like terrible mood swings, I am extremely emotional, feel depressive and dizzy whilst driving up the mountains, etc. AGAIN, I HAD NEVER EXPERIENCED ALL THESE BEFORE MIRENA. Additionally, I had no problems losing weight in my first pregnancy and I am naturally active and slim. This time around, since inserting Mirena, I have not lost any weight in spite of watching what I eat and exercising regularly.

It is Saturday today, just got back from a trip, and I am having Mirena removed next week.

I had my left lung fill with fluid and collapse after radiation treatment for Breast Cancer. The lung was drained with Thorocentesis and I was hospitalized for a week and put on prednisone - 40 mg reduced to zero in 1 week. I experienced symptoms of heart attack as reaction to reduction from prednisone. When it was determined by enzyme testing in hospital that heart not damaged I was sent home with prescription of prednisone starting at 60 -10 days, to 40- 5 days, to 30 - 10 days, to 20-10 days. The cumulative effect of these doses was all the side effects mentioned by others, loss of emotional and physical balance, stability, swelling, moon face, insomnia, depression, crying, stomach pain, constipation, etc. I dropped myself to 20mg for 9 days but on the 8th day had recurrence of lung pain and feared possible fluid build up through tissues damage/leak caused by radiation - they are calling it pleurisy or pleural effusion. (It was also determined that I must be on constant oxygen and sleep on oxygen as my breathing capacity is below 88 off of oxygen.) Dr. found not enough fluid to drain without risk to damaging my diaphragm so upped the prednisone again to 30 for 14 days. Using pain and shortness of breath as a measure of lung condition I must not dampen pain now but suffer it to monitor my lung so as to avoid trips for constant X-rays. I continue to suffer from prednisone and it has disabled me so that my normal life cannot be resumed in any way. I want to get off of it, but after reading these reports, I am very worried - supposedly the steroid is allowing my radiated lung to heal, but if that is not happening I think the steroids are possibly more life threatening than the lung - in any case, what life? What other choices do I have to survive the damage done to me by radiation?

I am a 49 year old male and took a 14 day course of Cipro for a UTI. By day four the souls of my feet were very sore, especially first thing in the morning but no other side effects. Mentioned sore feet to Dr after 7 days of Cipro but he did not believe it was from Cipro and had me complete the course. After 14 day course of Cipro feet were now so painful that I could barely walk on them especially after resting or getting out of bed. Also burning sensation on skin of feet and hands and some minor tremor. Saw a specialist and he immediately confirmed Cipro as the culprit and advised never to take that drug family again. Have since done the whole web search thing and discovered the whole saga of these drugs. Other symptoms have also appeared, some pain in middle of back, sharp pain in middle of back of both knees, hot and cold flushes, pain in left bicep, fingers that are very susceptible to joint injury and feelings of weakness and anxiety. Has been over three weeks now since I stopped Cipro and condition shows no improvement, may even be slightly worse. About to try a shotgun approach with treatment as there appears little documented evidence of anything conclusive on line. Starting course of anti-inflams (Voltaren) and these have already reduced the pain in my feet. Also magnesium and calcium supplements (theory goes that it may mop up any remaining Cipro and there is plenty of reports from sufferers saying that symptoms continue to appear for some months after stopping Cipro), Vitamin B6 (can apparently help with some types of nerve pain and tingling) and Fish Oil (omega 3's can help reduce inflammation). Not very scientific I know and can't be sure that all these are compatible with each other but am a bit desperate at this stage. Bracing myself for a three to six month recovery (just based on experience of many others). At this stage I am just hoping that damage is not irreversible as this appears to be a real risk. As everyone here will agree it is amazing how this situation is being allowed to continue. I could have stopped my Cipro on day two or three if I had been made fully aware of the risks and what to look out for. I am no expert by any means on this but from what I can gather Cipro and its relatives do nerve damage by the very way they work. It appears that anyone taking these drugs will inflict some nerve damage but for many it will not manifest to a degree that is a problem or at least a noticeable problem. So in some ways we are all sufferers, just to varying degrees. Another point mentioned often is that the symptoms may not appear for some months after the Cipro is stopped and therefore is not always associated with the drug. Also some say there is an accumulative affect with using the drug a second or third time. Symptoms may appear only after multiple use or symptoms may get much worse and more likely irreversible with multiple use. It's all scary reading. At this stage I am just hoping I can make a full recovery. Do damaged nerves repair themselves, does the Cipro eventually leech out of our systems .... I don't know. I will post in this forum again in a few months or sooner if I make a recovery.

I've had my Mirena out for a week now and I'm very irritable and tired! I do feel relieved to have it out thought b/c all the bleeding, cramping, cysts and weight gain had been enough! I was wondering if anyone else has had the Mirena out and if you could email me and tell me what to expect for the next couple of weeks that would be great!! ******
Good luck to everyone!

My doctor put me on prednisone for pain and inflammation and I have never felt better in my life. It's a miracle for me right now and I'll take my chances with the side effects for being pain free. I'm a happy lady for now.

I am 43 and have never used the birth control pill. My doctor prescribed NuvaRing to help with symptoms of perimenopause. After 1 month my blood pressure went from 100 over 60 to 180 over 110 and has remained above normal in spite of medication. Has anyone had this side effect or heard of this side effect?

I have been on NuvaRing for about 9 months now. I really love the convenience of it. I have had no complaints until now. About two months ago I was having some issues with insomnia. I tried a prescription sleeping pill (rozerem, I'm not sure how to spell it) for about a week and after I got off of it I was back to my usual sleeping habits. It didn't even cross my mind that it could be the ring. I thought it was just stress from school. I might have been that and not the ring.

I have put on about 15 pounds but again I attribute that to my eating habits, not the ring. However, the past month and a half I have been on a strict diet and meeting with a personal trainer 2-3 times a week. On top of meeting with the trainer I go to the gym for a least an hour everyday. In spite of all this, I gained 3 pounds (on top of the 15). My doctor said it could be my thyroid but I just got the results of my blood test and my thyroid is normal. So I think it must be the ring.

The problem is that I really like the ring and I don’t want to get off it. Has anyone gained weight from the ring but been able to lose it while staying on the ring?

When I first started taking lisinopril, I had several episodes of dizziness and almost fainted. That was when I looked up the side effects and was alarmed to find out that it is made from the venom of a poisonous snake from Brazil. I stopped taking it for several months, but my blood pressure kept climbing, so finally decided to give it another try. It didn't give me any problems at first. Just before Christmas last year, I had a bad cough and congestion, for which the doctor prescribed antibiotics and cough syrup with codeine. The antibiotics did nothing for it, but the cough syrup finally gave me some relief. Since then, the congestion got a little better, then worse, with the good spells lasting only a few days, compared to the coughing getting worse and worse. Finally when my throat was very wheezy with every breath, I decided to check the symptoms of lisinopril again. I called my doctor and told her I wanted to go off of it and see if it helped. That was 10 days ago. My throat is clear now, but I still have a lot of lung congestion. The crazy thing is that my blood pressure kept going up in spite of taking lisinopril. I've been taking atenolol for years, and now the dr put me on lovaza, which brought my blood pressure down to normal within a day.
Another thing when I was taking lisinopril, I began to wonder if I had fibromyalgia because I had so much pain all over my body. I don't know it the lisinopril caused that, but I don't feel nearly as much pain since I quit taking it.

I started taking Lamictal about six weeks ago for epilepsy. Now keep in mind, I was on Dilantin which worked great for 17 years and then suddenly stopped working. I have been in medication hell since then. First Topamax made me dumb as a rock. I would space out all the time. Worst drug ever. Then Keppra which was better in that my memory/ability to speak came back but I had these intense ups and down. I had rages constantly. Now I'm on Lamictal. So far, it's better than the Topamax and the Keppra, however the dreams are very intense as are the night sweats. I'm also experiencing much hair loss. Fortunately I have a full head of hair but I'm afraid I will eventually lose it all.

As a prime candidate for osteoporosis I was prescribed Fosamax at least 12 years ago if not longer. At the time I started taking it, my mother was very ill and did pass. That was when I noticed small 'jumps' in my legs at night which I attributed to the stress of the time.

Over the years, the 'jumps' increased in intensity to almost convulsive movements of not only my legs - but my arms - head - neck - torso. There were times when I thought I would be flung from my bed or dislocate my joints so strong were the muscle contractions. It was impossible to get to sleep and I was often woken from sleep by a convulsive movement.

I went to the Seattle Sleep Clinic for help (around 2000/01) after 5+ years of progressive worsening of these symptoms. Unfortunately, the doctor only wanted to fit me into the 'restless leg syndrome' in spite of my constant statement that I had NO feeling of 'creepy crawly, etc' before the convulsion. None. They just whipped me about out of the blue. No resolution.

About two months ago I ran out of Fosamax (actually taking a generic here in Mexico) and (for whatever reason) I did not refill. Since then I have noticed a HUGE lessening in these god-awful, annoying, scary convulsive movements. I have made no other changes in medications nor can I think of anything else that would cause this reprieve. A "milagro" isn't likely.

I haven't seen this side affect listed and am wondering if any other people have experienced this 'convulsive' problem?

Gracias,
Jillian

I started taking Yasmin 2 years ago, and after about the first 2-3 months of taking Yasmin, I started experiencing horrendous pains after sex. Once my doctor figured out what was going on, I was diagnosed with Endometriosis. Not long after that, I was diagnosed with Polycystic Ovarian Syndrome. Now I am more than likely unable to have children, and am at risk for cervical cancer, cardiovascular disease, and Diabetes.
If anyone else has recently been diagnosed with Endometriosis, or PCOS after taking Yasmin....PLEASE reply or contact me!!!!!!!!!!!