Chemotherapy symptoms and conditions

I'm sorry if someone has covered this already... my grandmother is actually the one on Prednisone because she was diagnosed with peripheral neuropathy about a year and a half ago and I believe they recommended it to help her strengthen her muscles so she could walk. It has really taken a terrible toll as she is now unable to walk, and even using a walker can be stressful and difficult. Once she was put on Prednisone they continued to increase her dosage and because of it she now has terrible tremors. It kills me to watch her go through this and wish that I could fight the illness for her. I just want her to be able to eat without feeling so stressed out because her hands aren't steady. The doctor did say that the medication is causing her tremors, and we were relieved to find out that it wasn't Parkinson's, and now they are beginning to wean her off of the medication but she is still taking it at the moment. If anyone has finally tapered off from the medication, who originally had tremors, did you find that your tremors did go away once you were off the medication? How long before the shaking stopped and you felt better? I just want to give her hope that after she is off the medication there will be some relief. I feel awful knowing there is nothing I can really do but support and be there for her, and do some research. If anyone could help me with my questions it would be greatly appreciated. I'm sad to hear other people's terrible issues with this medication and as far as I know I have only heard negative responses to this drug, so it's unfortunate that in this day and age they haven't found something safer that has the same effect that doctors are looking for in a medication. I wish everyone a safe and happy recovery.

I took Zocor for 9 months after I had a heart attack. After about 8 months I began having sever muscle spasm in my legs. I had a couple of episodes where when walking I couldn't pick up my feet and thought I was having a stroke and had to sit down and rest before walking on. I had to do this several times to get where I was going. I told my cardiologist and he had me stop the Zocor. The spasms stopped but I never regained the strength in my legs. Today I have had to put ramps in at home cannot climb steps. The ramp is difficult because of the incline but it is better than crawling up my steps to get in the house. I can only walk about 50 steps before my legs give out on me. I cannot walk on uneven ground without holding on to something or someone. I have now had 2 back surgeries because I have been told over and over it is my back with no relief for the legs. This last surgery my left foot drags and my big toe hangs down and I cannot pull it up. Now I fall a lot because of that and have to wear an AFO to keep my foot and toe up so it doesn't drag and trip me. The back doctor thinks it another pinched nerve and wants to open back up again. I am so tired of them trying to convenience me it is my back when I know it was the Zocor and the damage apparently is irreversible but no one wants to agree with me. I am sick of it and just wish they would say yes it was the Zocor and get you a scooter and live the best you can. I know I am headed for that road I use a walker and cane when I don't have someone with me to hold on to. Because I am so unstable on my legs.

Except for having high cholesterol (310), I'm a 29 yr old healthy active female, very petite and weigh 98lbs. My mother has had a quadruple bypass and 4 stents at the age of 54, high cholesterol is just hereditary in my family. My doctor put me on 40 mg of zocor. The first week taking zocor I started feeling strange, a little soar here and there and very tired at times, also I have become very forgetful. It's been almost 2 months now and I have severe pain in my legs. First it was the right leg and now both legs, the pain starts at my lower back all the way down to my cav. I have a burning painful feeling sometimes numbing feeling, its driving me crazy!!!! I can't stand for too long cause I feel tons of pressure on my lower back pushing down my legs, It feels like my sciatic nerve. I went to my doctor and he said he is 95% sure that this is from the zocor medication, he told me to stop it right away. This is my first day without it, I know I need to do something to prevent what happen to my mother, I'm on a strict healthy diet, staying away from all fatty cholesterol filled foods, but there has to be a better way then taking statin drugs! If anyone has some ideas of what kind of alternative meds I can take, please help.

I was 54 at the time (2007) and in good physical health, however, after having my first round of chemotherapy as a result of breast cancer, I developed a severe throat yeast infection and my white blood count plummeted. I had ceased taking my many vitamins that have kept me in reasonably good health for the past 25 years because of nausea and generally just not feeling good. The doctors prescribed Levaquin.

Almost immediately, I developed heart palpitations and continued to have fever, nausea, and a rushing feeling throughout my body that was draining me of all energy. I could tell I was fading fast. Upon calling the doctors I said then that I thought it was the Levaquin but they insisted I stay on it otherwise they would put me in the hospital.

After the 4th day on it and with my blood pressure sinking (80/30) my husband called the doctor and they said to go to the ER. I again said to the ER doctor that I thought it was the Levaquin and he scoffed at that. After several hours and many tests, the ER doctor released me and said I could stop taking the Levaquin and he prescribed something to help me to sleep.

By the next day, I already started feeling better and within 3 days I was back taking my vitamins and feeling much better. I never took chemo again after this experience. Unfortunately since then, I have experienced severe ankle and leg cramps in the middle of the night, muscle spasms in my legs. I don't trust my ankles, they feel weak. I assumed it was linked to the chemo and never guessed it could be tied to Levaquin.

I went to my internist doctor who prescribed Flexeril which has helped with the cramps. My massage therapist has noted many times that my tendons and ligaments seem twisted and she has to really work on them which ultimately feels better. I never thought any of these symptoms were tied to Levaquin until last night when I saw the ad on TV regarding Levaquin and tendinitis. I will show this info to my Internist the next time I see him. How does one know if what I am experiencing is linked to Levaquin.

I started taking prednisone along with Cytoxan, a chemotherapy drug 15 years ago when I was diagnosed with an undifferentiated connective tissue disorder that led to symptoms like idiopathic pulmonary fibrosis. After a couple of years, the inflammation cooled off and I no longer had increasing scar tissue in my lungs (IPF is almost always terminal) so I was glad of that. However, sometime in that first year or so I developed hardish lumps under my skin and severe pain that felt like it was "under my skin" but not my muscles, as in fibromyalgia. The lumps are even more painful, and the skin feels as if someone tried to "skin" me and then just llay the skin back down.
I have had to be on timed-release morphine for years in order to function with this pain, as it is especially painful if I brush up against something or sitting or lying down pressure is intense. Also the skin on my tongue gets so tender I have to use kids' toothpaste or it burns terribly.
After 15 years some of the lumps have gone away, but I've recently had to go back on the prednisone for my lung inflammation.
The last time I got a new prescription for prednisone I read the tissue-paper printout (not the short one you get with every Rx, the one written for professionals which includes all the new data, tests, side effects, etc.) What I want to point out, as I've not read one person saying this, is that to avoid a lot of the side effects and the harm to the glands which produce our own natural steroids, is that they are now recommending that it is taken only EVERY OTHER DAY. They say there may be some slight increase in symptoms on the "off" day, but that this keeps the natural cycle in place in bodies subjected to this drug and therefore reduces symptoms.
This is what my last pulmonologist prescribed for me and so far I have had minimal side effects--no ravenous appetite and weight gain, no "moon face" and it has still helped my symptoms.
Please ask your pharmacist for the flyer that comes with the new package and read this for yourself and then take it to your doctor. It may not work for those in dire need of the prednisone but could perhaps be tapered to this once the first lethal symptoms die down. ASK YOUR DOC--I cannot believe I have not heard more about this as it's right on the flyer--but docs are so busy, it's understandable. I'm grateful my doctor is up on the new research because I don't mind taking the prednisone this time, and I used to HATE it!
Good living to all and I wish you all the healthiest life possible.

I have cancer, and am on chemo, my doctor prescribed budeprion xl 300mg (not my oncologist) I am completely dehydrated and just horrible !! should I discontinue the budeprion. I have had fluid infusions each of the last to days. I have a dry mouth and no appetite

How long does it take to go back to working out?I had a DVT in my right calf a month ago.I am a 33yr old male.I am on 17 1/2 grams of warfarin they say my liver is good processing it.I now walk a mile and have shortness of breath and have to elevate my leg because the blood pools to my foot even when I just got the support stockings.I've used to run five mile a week and work out with free weights.I was advised to swim but I was wondering when I could got back to the gym or run outside?Does this last a while......? or for life? I usually bounce back from things I had cancer 5 yrs ago.I have the pressure stockings 30-40 pressure and they help a lot.The symptoms of baldness remind me of the chemotherapy.I am naturally bald any ways.So to all the DVT suffers keep your heads up there are always worse medical conditions that I see a lot....because I work in a medical feild.

hya everyone,my partner has been on prednisone for over 6months while having chemotherapy 4 bone cancer.He is being weaned off the drug slowly and is now on half dose and is experiencing very bad joint pain,headaches,sweating along with depression and lower back pain.Hopefully after coming off the drug completely these symptoms will eventually go away.We sympathize with all who has to go through similar situations.

I have corrected my typing error I am not on 400mg it should have read 40mg. Thanks to the reader of my experience who very kindly pointed out my error!!!!
Despite having a brush with the big C last year (I finished chemotherapy in January) I have been very fit and healthy during my 61 years! A few weeks ago I started having palpitations, hence a visit to the doctor revealed high blood pressure and cholesterol reading of 9.9!!! Shock, horror. He informed me that it was genetic and prescribed Simvastatin 40mg and Bendroflumethiazide 2.5 mg daily. Not being satisfied with the enclosed leaflets I have looked up more info. on the net. Should I have done this!!! After reading some of the posting on the site I am feeling a bit apprehensive. Last night I had a terrible night couldn't sleep for the pains in my legs and a bit nausea this morning. But I need to be sensible, I really don't have any choice but to take these drugs just hoping that I won't have to stay on them for the rest of my life and I don't get any of the side effects that some of you have suffered. I also wonder if the chemotherapy could have caused by raised cholesterol? Hope to keep you posted and would welcome any comments!

Despite having a brush with the big C last year (I finished chemotherapy in January) I have been very fit and healthy during my 61 years! A few weeks ago I started having palpitations, hence a visit to the doctor revealed high blood pressure and cholesterol reading of 9.9!!! Shock, horror. He informed me that it was genetic and prescribed Simvastatin 400mg and Bendroflumethiazide 2.5 mg daily.
Not being satisfied with the enclosed leaflets I have looked up more info. on the net. Should I have done this!!! After reading some of the posting on the site I am feeling a bit apprehensive. Last night I had a terrible night couldn't sleep for the pains in my legs and a bit nausea this morning.
But I need to be sensible, I really don't have any choice but to take these drugs just hoping that I won't have to stay on them for the rest of my life and I don't get any of the side effects that some of you have suffered. I also wonder if the chemotherapy could have caused by raised cholesterol?
Hope to keep you posted and would welcome any comments!

I am a healthy female with little to no history of adverse reactions to medications. I was prescribed a 10 day dose of Levequin (500 mg) for a minor but stubborn skin abscess. After the third day, I woke up with significant joint soreness in my fingers. Progressively the soreness spread daily to my wrists, elbows, ankles, knees, hips, etc. I did not suspect the antibiotic at first, but I know my body, and I know something was WRONG.
After my 8th dose I decided to look online...it is at least good to know that what I'm experiencing is definitely from Levequin. Thank you all for sharing your stories.

I especially found MERCEDESLANE posting on April 15th interesting. I guess this person works in the health care system. Considering this uncompassionate individual, who apparently wants everythone to know he has a Mercedes, can't spell (whine), and does not have basic grammar skills. Wow...my faith in the our health care system is stronger than ever. But what do I know, I'm just an "IDIOT" with shingles that needs to have a couple of glasses of whine while I pop my remaining Levequin.

Sadly, I am just another case among many it seems. I am a 26 year old female who was prescribed ciprofloxacin for a UTI at my urgent care center. I have health problems to begin with and did not want any more. You know, I’ve had to take all kinds of meds over the years, including harsh ones, but it was never so bad as to prompt me to write comments on the internet about it. What does that say about Cipro? When I got home from the doctor I read the paper before swallowing the pill, which included the description of side effects. Unfortunately, it did not include the truth about what could happen to you while even taking this drug for a short time. If there had been some kind of warning about the strength and potential risk of taking this drug, I most likely would have steered clear from it since I am sensitive to medications and already suffering. The paper led me to believe false information, listing some common antibiotic side effects, and I ended up starting treatment. Some of the negative effects I experienced while on this medication for only 2 days were: severe muscle/overall body weakness, difficulty breathing, fatigue, mental confusion, difficulty concentrating, anxiety/nervousness, restlessness, mild carpal tunnel pain, slight vision change, stiffness, pain, an overall feeling of terrible heaviness, including of the chest, and possible heart palpitations. It felt like the medication was damaging my body; like it was eating away at my muscles or something. I've never had chemotherapy before, but some how that's how I would imagine it. It felt like it was doing damage to every cell in my body. The worst part is the weakness and altered thinking right now. I hope these symptoms go away completely. I felt better after quitting the drug, but not completely. I am just thankful for my hope in Jesus Christ. Even if things don't improve, I am comforted that He cares for me. I am going to be praying for this terrible situation where doctors are just handing this out for common problems without giving proper warning. May fewer and fewer people have to suffer because of Cipro and this class of drugs. I am also going to report this to the FDA and hopefully to my doctor’s office. I would like to see clear and extensive warnings on this drug, if not for it to be taken off the market. My personal advice to any one who is currently on this medicine and experiencing side effects would be to: drink milk or eat other dairy products to lessen the symptoms. It seemed to temporarily help me.

I was prescribed 750 mg. Levaquin, one a day for 14 days for a severe sinus infection. We left to visit my son and family in Texas two days after starting the medicine. The entire time we were there I could not sleep. The second day we were there I was walking down the stairs when a pain hit me in my left calf that was so bad I thought I had surely torn a muscle or something worse. It continued to be painful for several days. We returned in four days and I noticed that I was aching all over. I have arthritis and some other problems, so didn't think too much about it. However, it continued to get much worse. My feet hurt so badly that I could hardly bear to walk. My heels are especially painful. I cannot bend my toes without terrible pain and my feet have been swollen. I have sharp tingling pain in my toes as well. My hips and knees are very painful. I am shuffling around just trying to walk and get up and down. I started having a strange pain in my right shoulder area. Am still having insomnia. This is very scary and after reading all the posts it is even more frightening since you don't know what to expect even further down the road. I have an appointment in the morning with a neurologist. I don't know what they can do and I don't want to be put on a bunch of other drugs. I just hope he acknowledges that the Leviquan caused this and doesn't try to come up with some excuse. I have absolutely no doubt the Leviquan caused this as it was immediate and continued to get worse as I took it. I stopped after 11 days and only wish I had stopped sooner, but you just keep making excuses for the weird things that are happening until you finally realize there is something very wrong. I have experienced a lot of pain in my life, but nothing like this. My brother has acute leukemia and has horrible neuropathy in his hands/arms, feet/legs caused by a clinical trial with two chemotherapy drugs. Now I am afraid I may have it in my feet, or something as bad. If the doctor has anything worth reporting I will let you know. Good luck to everyone and thanks for listening.

My daughter who just turn 7 has been on and off Zyrtec for the past 6 months. This last time it finally clicked... She was on it for about 3-4 weeks and I notice her mood changed and she was now very angry at anything and started hitting her sibblings and throwing things at me out of anger. She also was waking up at night either with bad dreams, or couldn't sleep. My husband and I realized that this all started about the time we put her back on Zyrtec. Two days ago, I took her off it and the next day she was an "Angel" compared to before. WOW what a difference. I did notice today (day two) she was sneezing more and didn't feel as well physically. So we are not out woods yet.

She also has been taking Singular for several years and I have been reading more about that medicine as well. I am not sure if needs to be taken off that yet, and will do an experiment. The timing isn't the best since school starts in just two weeks, but it might be worth it to have a happy child again.

On a side note, last year in school, they diagnosed her as having social anxiety. She is "extremely" shy and closed off in school. It would take her hours to do her homework which should have taken about 30 min. I am curious if stopping singular would help clear her head and make her less anxious. (She was on Zyrtec as well during that time).

This would be such an answer to prayer if it works. My two sons are so much happier than my daughter and I always wondered why. This may be the answer!

I took Zolpidem (Ambien) last night for the first time. It was prescribed to me by my oncologist as I have been having trouble sleeping ever since I have started chemotherapy for breast cancer one week ago. I fell asleep quickly and slept well for 5 hours, but awoke at 2am with a headache. I took 1 gram of Tylenol at 2am but was unable to go back to sleep because the headache became increasingly worse and did not go away until I drank some coffee at 5am. It was the worse headache I have ever had. The caffeine made it go away finally.

I took Lipitor for 2 years with all the pain in my shoulder, hand and arm as well as fuzzy memory. I had a friend over for Lunch an have no memory of anything that happened including his arriving and leaving on his Harley and we all know how loud they are. I ended up in the hospital with all kins of tests including an MRI all of which I have no memory of to this date. My hospital bills are still coming in as well as all the Doctors that saw me. I just received my Divorce and then this happened , I was out of work for a week , the Doctors thought I had had a heart attack, stroke or aneurysm.I also had all the foot pain making it impossible to stand up , leg cramps, sleeplessness, sheer exhaustion, depression, headache and nausea. The Doctor at the Hospital took me off of the Lipitor and said to take a 325mg. aspirin daily . This happened on March 23, 2008 . I am felling better but I still pain in my shoulder , neck , stomach , and feet and legs but is nothing like it was. Here I am left with a few thousand dollars of Doctor and Hospital bills. Why can`t something be done about all of this we are all going thru? I called the FDA to report it and got no where. Did I really expect anything to happen ! I hope someone gets something done for us . I would be one of the first to sign up to take Lipitor off the market and get what is due us.

I have been taking singulair for a little over two years now 10mg once a day everyday for allergies. A year ago I began have a lot of suicidal tendencies. I was actually locked in a hospital psych ward after slicing my wrist wide open. They kept me for three days saying I was a danger to myself. I had to have my husband, friends,neighbors,etc to actually testify that this was very unusual behavior for me to be allowed to go home. Since then paramedics and the police have been called to my home by either my husband or a suicide hot line for fear of suicide. Three years ago I was on Chemotherapy for 8 months it was one of the hardest things I've ever had to go through in my life, but, I did it in order to live. So this type of behavior had my whole family, husband, and myself baffled. Today my husband was watching the news and called me to come see what they were saying about singulair! I was shocked, but, also relieved! I'm seriously thinking of suing. I'm really glad this came out in the open.

I cannot believe this. I just sat here and cried. Timing is impeccable on this. I had just unplugged my 8 year-old sons tv, and yelled at him for misbehaving. He has gotten several notices over the last few months from school about disrespectful, violent and aggressive behavior. I didn't know what was going on with him. That just wasn't like him at all. Now, I know. He had been taking Singulair since he was about three years old for allergies and asthma caused my allergies. He really only took it seasonally, but this year, he's taking it for about five months without a break, and I would have never linked the terrible behavior to the medication because I was NEVER warned of these types of side effects. Why was this never put out there for people? This is my child, whom I love more than life itself, and I have punished him, yelled at him, grounded him, all for something that he possibly could not control, and I cannot take any of that back. How can this be happening? And to hear that the drug maker wants nine months before pulling off the shelves for testing? Seriously? I am just so shocked, and he will never take another Singulair again, regardless of what those greedy bastards say can be proven or not proven. My child's health and mental stability are more important that they seem to think it is. What kind of long term effects can this have? I just feel so uninformed, and when it comes to drugs ESPECIALLY for children, why has this not been addressed? I am so glad that people are posting their experiences, because to know that we are not the only ones who have been going through this, and to know that we can now correct the situation makes this just a little easier to deal with.

My son was prescribed Strattera for ADD. 25 mg for three days,
but when the dosage increased to 40 mgs, it was a nightmare.

This was the worst medicine I have ever had my 12 yr old son take. He lost his appetite, had insomnia for several weeks and behaved like he was in a stupor when he was awake.
I would NEVER EVER have him take this drug again and I do not
recommend it to anyone else.

I am a 62 year old widow. Have insulin-dependent stage 2 diabetes. Was put on Lipitor 20 mg 2 years ago. I am astonished by this web site which lists every one of my concerns: short term memory loss, severe hip pain, shooting pain (especially in my eyes) foggy vision, fatigue as though I'm on chemotherapy, nausea, hair loss and, no surprise, recurrent depression with weepiness. What's motivating me to write is I've recently met a kindly, attentive gentleman, and now I discover I also have zero libido! I've been married more than once; I know what's missing. More than all the other aches and pains, I would love to sue for "loss of pleasure in life"

I had the Mirena inserted before starting chemotherapy in August 2007. I thought all of the side effects were related to chemo and steroids, but I've been off of those for 5 months now. I'm beginning to think all of my symptoms are being caused by the Mirena. I have horrible, painful acne. The worst I've ever had in my entire life and I'm 34yrs old. I had weight gain with the steroids, but have only been able to lose 10 lbs since I stopped taking them. I have headaches, dizziness, fatigue, acne, dry skin, dry mouth, itchy scalp, seem to be loosing a lot of hair in the shower, no sex drive, no orgasm, insomnia, nightmares, lack of concentration... and the list goes on. I went to see a dermatologist who told me the acne was mostly likely being cause by the hormones from the Mirena. I'm calling my Ob first think on Monday to have it removed. I can't wait to feel like myself again.

I have been taking Levoxyl for 1 1/2 yrs, I had my thyroid removed due to severe hyperthyroid. In the past year, I have been getting pains and weakness in my hands. It is so bad now, I can't open a jar or lift a frying pan. It hurts sooo bad. My legs hurt and my knees have real bad joint pain.
The funny thing is, it's not every day and not always both knees. It is however all the time in my hands. Last week I went to an Arthritis specialist in San Antonio. He ran every blood test avail. Tested for Rhum. arthritis, Lyme disease, AA, and all kinds of stuff. He x-rayed my knees and injected cortisone in my knees and hands. - that hurt -
He found nothing wrong!
I searched on line tonight for "Levoxyl and joint pain" and this site came up. Boy am I glad I am not the only one who is questioning this horribly possible side effect. Oh, I also have memory loss. I feel like I am 80 yrs old. Just to make sure you know what type of person I am, here goes: I am fit, active, 37 yrs old and 115 lbs, I eat well and take vitamins, non smoker, non drinker.
On Monday, I am calling my doctor. I am printing this web site and all of the postings like mine. There must be something I can be put on that will fix this. Can anyone tell me if they have no Thyroid and have gotten off this stuff; does the hand pain stop? Does it get better or is this permanent damage?

Kerrville TX

i have been on prednisone for over a year now for ITP. i started taking 150mg then 140 then 130 etc. i hate it so badly. i am not the same person. the doctors are trying to wean me off it but then something happens and i get bumped up to taking more again. at first my face swelled up like a balloon and i put on weight. i now go to the gym almost everyday and have lost it. i could not drive at night because i couldnt see properly. i had just given birth to my first child so i was extreemly emotional and cranky. i used to be a happy person now im irritable and have no patience. i used to get 'the wobblys' i couldnt walk straight and fell into walls. i experienced so many side effencts i cant remember them all. now they are apart of my life im so used to it. i dont even know whats real with my body and whats the pred. i hate it. but i cant be on it forever so if i dont get better real soon its chemotherapy for me. woo frickin hoo. good luck everyone.

I am 47 year old woman who was diagnosed with breast cancer in January 2003. Following 2 unsuccessful courses of chemotherapy, where the cancer spread to the skin around the site of the original tumor on the right side and then to the lungs, I am now receiving Navelbine.I have completed 1 cycle of treatment and have begun to see a reaction on the skin. The side effects I have felt are numbness and occasional loss of sensation in my right hand and arm. I am interested in hearing about similar side effects.

I'm 18 years old and I have been taking high doses of prednisone for over 3 years for a blood disorder known as hemolytic anemia. At one point I was taking 80mg a day. I am now on 30mg a day. It is unknown whether my body will ever be able to function without the steroids and chemotherapy has even been suggested by one doctor. The difficulty of having massive amounts of weight gain (30 lbs. in 3 months) during high school was virtually unbearable. In addition to that, I now have to take 2 antidepressants to counter the mood swings and depression that the prednisone causes.