Tumor symptoms and conditions

Does anyone have ringing in their ears due to the arimidex? I have just over a year left to take this drug and I CAN'T WAIT to stop. ( I was a stage 0 (.9 cm tumor/0 lymph nodes)....treated with Chemo (adriamycyn, cytoxin and taxotere), then radiation and now arimidex. ) I was almost 41 when this started, I'm 45 now and want my life back. Don't get me wrong, I want to be cured, but sometimes the side effects are disheartening. This sure does sound whinny and I am sorry. I am happy to be cured, but so tired of all the side effects!!!!!!!!! UGH Thanks, dpr

Two years after taking Chantix a tumor was found on my brain. I also have the pain all over every muscle, bone and joint every day. Do not take risks like I did. I trusted the FDA, and Pfizer and now I regret being so trusting.

I am a 49 year old female I took Cymbalta for 3 days and on the 4th morning I woke up with severe blurred vision and roaring in my ears that was April 26,2008. My ears are still ringing. I clenched my teeth so hard in my sleep I traumatized one of my upper molars which resulted in a root canal and crown. I have been to a ENT to have my ears checked, he said I had minimal hearing loss and gave me lipo flavonoid to take for the ringing. I just went to a neurologist today who is requesting an MRI on my brain to rule out a tumor. I don't know if this is a coincidence or not ,I know the clenching caused the damage to my tooth. The neurologist said ringing in the ears is not a side effect of Cymbalta. My life has been a nightmare since I took it.

I was diagnosed with a tumor called a pheochromocytoma after taking this drug- the drug caused this same tumor in animals

After a year of battling effects from an eye injury, an optho-neurologist finally came to the conclusion that I had orbital inflammatory psuedo tumor. I was told to take 60 mg immediately and then take 2-40mg doses (AM and early afternoon). On Friday, July 18th I took 60 mg at 6:30 p.m. and was so nauseous and barely slept. That next day I took 40mg in the morning and another 40mg around 2:30 p.m.. Although I had been, throughout the year, experiencing pain in my left eye and cheek..what I experienced by 4:00p.m. that next day was more severe than ever. I started having shooting pain and a headache so excruciating that I was in tears. (I had two children naturally).
By 10:30 I had several hours of this pain when the worst happened. The left side of my face drooped and I had difficulty speaking. By the time I got to the hospital I could not move my left arm and left leg. After five days in the hospital and every test imaginable (cat scan, MRI, EKG, etc) they ruled out all stroke, MS and anything else that would show up on these tests. During the hospital stay (although they did not cite prednisone for this event), they started tapering me off. I went from 80 to 50 in one of these days and thought I would DIE. There was no pain reliever/narcotic strong enough to take away the headache. I spent ten days tapering and prayed every day for the end. Sweating, no sleep, crying and did I mention...my headache has still NOT gone away. I have a couple of hours here and there without this pain but for the most part I have been in this hell even after my taper. The clincher is that NO ONE at the hospital or afterwards would admit that this was a side effect but they also could not provide a response. It took three weeks for me to work my way back to walking and using the left side of my body. Has anyone heard of this before? Good luck to all of you, it has meant a lot to read your comments.

Strange happening. I have pancreatitis with having a Whipple procedure done 4 years ago tying off a large tumor on my pancreas. Because of this I am now a type 2 diabetic with high blood pressure. both stemming from the surgery. Recently, within the past year, I was put on lisinpril. Because of financial reason's I stopped taking the Lisinipril but just recently seeing a new doctor I started taking the lisinipril again and after two days have experienced severe pancreatic pain. Finding out by way of my son in law going into emergency and finding that he too has the same conditions and is taking lisinpril. Doctor's told him Lisinipril should not be taken by anyone with severe pancreatitis.

Had been given Flonaise perscription by U.S.Army allergist. Worked ok got bloody nose from it once and a while. used over a period of four years. All of a sudden woke up to the smell of what I thought was acetone aka nail polish remover. This was not the case because we had no nail polish remover in the house. Every thing smelled like acetone, for up to two weeks. I went to see a nurology doctor and had an MRI done worrying about a possible tumor. narrowing things down we concluded it was the Flonaise. I discontinued the drug and still four years later can not smell much of anything. Once in a while I can smell a slight smell for a moment then its gone. I have been using a "Netti Pot and flushing my sinus's out three times a day. I have had no more problems with severe symptoms of rhinitus. Wish I could get my smell back.

I've been diagnosed with anxiety and panic attacks since Nov. 15 2007 ended at the hospital emergency room, after using Xopenex been using Advair and Singulair due to my asthma once my Doctor increased my Advair from 250mg to 500mg twice a day on Sept. 5th 2007 noticed fast palpitations and overwhelming. Knew and complained for quite sometime that I wasn't feeling like myself. Since Nov. 26th 2007 I stopped taking Advair, Albuterol inhalers,Nebulizers due to the fact of my new Anxieties that I never had. Continued taking my Singulair medication thinking that it was safe. Only been on Singulair a little over a year. Still continued to experience Anxiety and Panic attacks. Due to this I've been seeing a therapist since Dec. of 07.Has affected myself, my children who have witnessed my episodes of Anxiety attacks and know thats not me.Also has affected my performance at my job and attendance. Just took two MRI's of the brain just last week thinking there maybe something wrong with my brain.My side affects have been Dizzy spells,feeling faint,blurry vision,extremely tired,muscle spasms,loss of concentration, and not being focused. These are my experiences with Singulair and I believe that the FDA should further investigate these allegations. I know for a fact I've been experiencing this for quite sometime and my Doctors tell me I'm just depressed. Ignoring the fact they prescribed me so many medications that trigger Anxiety depression and God knows what. Thank you Cita

Has anyone here ever heard of anemia being associated with Toprol? Since they increased the dosage of my husband's Toprol, he has developed anemia and they cannot find a cause but every time I ask about the possibility that it could be the meds causing it (he is on coumadin, too), no one will firmly say no - always a "could be" - so just wondering if anyone else has had this experience. Thanks!

I was on Prednisone for 8 days because of a sinus headache that wouldn't go away. I was also put on amoxicillin for a possible sinus headache. I started on 60 mg for 2 days and than 40mg for 2 days , 20 mg for days and last 10mg for 2 days. The first day I took my headache became 10 times worse and I considered going to the ER. The second day I was suffering from muscle fatigue in my legs and my thighs burned. It also triggered my sciatica pain and pelvic pain caused by ovarian cysts and ovarian tumor. I believe it was the bloating that put more pressure on the sciatica and the cysts that caused the pain. It took a couple of weeks for the sciatica pain to subside, never really got rid of the pelvic pain. I am never ever taking Prednisone again, it has way too many side effects. Also, I think it caused a yeast infection.

I was doing just fine taking 50 mg of Topamax but I was still having minor headaches. My doctor said to go to a neurologist because there may be a tumor to worry about. He doubled my morning dosage and added an evening dosage so now I am taking 200 mg. a day. I started the insanity on Friday. By Monday i went grocery shopping and couldn't remember what I was shopping for. Thank God i brought my husband with me...when I could remember that he was with me. And then when I remembered to ask him what we came for I needed to remember where it was. Upon returning home I offered to help my 7 year old grand daughter with her spelling homework. Do you how embarrassing it is to not remember how to spell first grade spelling words? Tuesday was Mardi Gras and we went to the movies so I was saved any further mind questions. Then along comes Wednesday and I returned to work. Well, I tried to get to work. I got lost. Here I was at Walgreen's trying to figure out what I was doing out at 6:00 in the morning. What day was it? The looks on other's faces when you ask them these question is not something funny. So, I get back in my car and aim in the direction I hope is work. Luckily, I remember where I habitually stop for breakfast. My memory comes back again and I make it to work. I am on time and all is well. Now, the day begins.

I haven't had a period since December. Here it is February. And no, I am NOT pregnant. I can't concentrate. I ate 2 chicken nuggets for lunch and am full (now that is a healthy lunch, huh?). I was addicted to Dr. Pepper and now can't even stand the smell of it. I can't walk and chew gum at the same time. I found a note that I wrote sometime yesterday that really scares me because I don't remember writing it. It says, " Headache @ 1:55 no known trigger jut sudden movement to pick up papers from bin over desk. Nausea as well. Need to go to sleep forever." Good feeling to have? Depression is kicking in.

I just called my doctor and he says decrease the medication down to 100 mg. Ummmm...How about I decrease it down to 0 mg and I take a Imitrex or 2 and a hot bath with a nap when I get home and live to see my grandchildren grow old! I think living with a migraine or 50 is far better than what I have been feeling this past week.

If anyone can tell me that it gets better in less than 2 weeks I will stay with it but 1 more week of this and I will be a patient in a mental hospital. I can't even play Nintendo with my grandson...NOW THAT IS DEPRESSING!

I have been on Prednisone for about two weeks now! I hate it!!! I have never liked medicine, i don't even like to take Advil. They gave it to me for something called a idiopathic pseudo-tumor behind my eye, thought that it was an infection at first but the antibiotics didn't work.. I'm on a pretty high dose, i was on 80mg for 9 days and now I'm on 60mg so far has been 3 days. I have had all sorts of bad side effects from it! WAY bad anxiety attacks, heart palps, bad night sweats, dizzy, confused, like everyone else the brain fog feeling, bad knee aches, hungry all the time but i haven't really gained wait but am bloated in the stomach. After taking it for only 4 days i almost went to the ER i felt like i was going to have a stroke or something, my legs felt like they were turning into jello, and i got really light headed, I was about to freak out! I think that it dropped my potassium levels or something, i ate a few bananas and that made me feel better. It is starting to get better now that i dropped to 60mg but i still hate it, and I'm starting to get really bad chest pain (heartburn or gas?!?) not too sure but its starting to become unbearable.. I get to go down to 40mg next week and then 30mg for a week then to 20 for a week and so on! I'm a bit nervous now cuz i thought that depressing would make it better but everyone is saying that it get worse. I hope that it don't get much worse cuz i don't know how much more that i can take! My eye looks great so the meds did the job, but i still don't know if i would ever take this again knowing this much about it! I'm glad that I'm only going to be on it just a little over a month but even that seems way too long! good luck everyone take care of your selfs! oh yeah I'm only 23 and this stung really makes you feel old, i feel at least 40 it hurts to get up or sit fast!

Hello fellow sufferers,
Several years ago I had a CT of my face and head due to frequent migraines...They had thought maybe there was a tumor or blocked blood vessels, but to my complete surprise all of that was normal, but I had all the sinuses on the right side of my face completely blocked...The doctor @ that time asked me some questions about my breathing and pain...Of course my breathing through the nose wasn't that great, but I had always taken that as a bonus since I work in the hospital...NO pain really either...Due to the fact that sinus infections have a direct pathway to the brain they decided that I needed Levaquin...On the second day of taking the medication I was in complete tears...The bottom half of my body ached like someone had kicked the %^&* out of me...First off I thought that maybe it was because I had my leg in a full cast and that had just been adjusted so stupidly I continued with the med another 2 days and the symptoms got to the point that I couldn't walk...I called the pharmacy right away and told them of my symptoms and they said they had no documentation of such side effects so I continued thinking it was something else ( they always tell you to complete the full course of an antibiotic so you don't kill off half the "bug" and the other half goes resistant)....Stupid....I finally made an appointment and had my husband literally carry me cast and all down there...The doctor had no explanation for the symptoms I had but did lab work to kinda shut me up and low and behold it reviled that I had full blown arthritis so off to a rheumatoid specialist...We went through my health history and other that the sinus infection, migraines and a broken leg I was fine except for the constant pain from the waist down........It took 7 months to return to "normal" blood test went back to normal too...I had made a second trip to the pharmacy and insisted on filling out a form for side effects and had proof of it with the weird lab tests that had since gone back to normal...This form was supposed to be sent to the drug company (not sure if it ever was).....Thought I would just share my experience with you and hope it helps others...I am an RN with 15 yrs surgical experience and thought I was going nuts when on this stuff...Since then I have always included this as an ALLERGY since it is one of the best and most common drugs used for things like sinus infections and I don't ever want to take this again.
Sincerely,
Debbie

I am so glad that I stumbled on this page so I can warn others so they won't have to go through what I am going through. I began using NuvaRing in August 2007 because I couldn't remember to always take my pill at night. I noticed a change in my mood, I was having major mood swings which was affecting my home life and my work life (I teach middle school), I was having headaches that would last for days. Also, I began having nausea and a stabbing pain in my right side just under my ribs. I went back to my family doctor (who by the way suggested the ring because that is what she is on) and she set me up for gall bladder tests. I went through 2 inconclusive tests on my gall bladder and was still having pain and nausea. I was then sent to a gastroenterologist for stomach issues. I have had an upper GI, CT scan and MRI. The tests showed that the root of my problem was a tumor on my liver. I am now awaiting an appointment with a specialist to discuss the removal of the tumor or what I can do for it. The ring was the cause of the tumor. I am 29 years old and have always been active, working out, I have 2 small children whom I play with often, I used to play bass guitar at my church but I had to stop that because I was too tired to go to practice! The tumors are very fragile and can burst to cause internal bleeding which can be fatal! PLEASE, PLEASE, PLEASE DO NOT START THE RING OR TAKE IT OUT TODAY!!!! There is nothing worse than looking at your children and your husband thinking that you could have internal bleeding that could kill you and you would never be able to see them again because you just didn't want to get pregnant! I didn't read the pamphlet that came with it, I just trusted it because that was what my doctor used. This "rare" incident that happens to like one in a million has happened to me! I took it out the 30th of Dec and have had much more energy and felt better about myself. That doesn't change the fact that I have this tumor that I have to deal with now. I was only on it for 4 months!! Be careful

I am a 39-year-old female who was put on Toprol 25 mg about four years ago due to heart palpitations. The Toprol didn't affect the heart palps at all, but I liked the fact that it kept my heart from racing after I ate, which had been a problem for me since high school. I took it sporadically for a couple years. At some point I started the generic, but I can't remember just when.

About two years ago I noticed that I was hearing noises in my right ear. Gradually the noises prompted me to see my PCP. She thought my BP was a little high (about 138/80) and she doubled my Metoprolol dose right away to 50 mg. She told me the noises were caused by my blood pressure, not the medication.

The noises got much worse right away and I was hearing them almost 24 hours a day. Sometimes it was a whoosh-whoosh noise (which I guess is classic for high BP) and sometimes just like a faucet had been turned on in my ear. At this point I definitely suspect it's the medication itself, not the BP. On days when I don't take the med, the noises are much better or not even present. My heart does tend to race though, and the palps are the same either way.

I'd like to wean myself off the med, and if my BP elevates try a different medication. I can't stand the noises anymore so my priority is to stop them. I am curious if this particular side effect has happened to anybody else here?

Glad to find your site. I have been on Lisiopril for 2 years (ever since my Insurance stopped paying for my Aceon and I had to have a substitute drug for blood pressure control). I have had increasing cough and horseness for the past 12 months to the point that I now have 24 hour symptoms! I also have been having leg cramps at night the past few months.
I will stop Lisinopril TODAY. Plan to monitor my blood pressure and see what happens. Does anyone see any problem with doing this?????

Reply 15 minutes ago on Aug 17, 2007 by kimhammonds, #1261
Oh my goodness. I have had this thing for almost two years now. I feel so much better about myself after reading these reviews. I have went to the eye doctor because I was sure I had a tumor behind my eyes. I have had terrible headaches, blurred vision (he decided to change my contacts that i have worn for 12 years), extremely irregular bleeding, hair loss, acne (that I never had as a teen), and awful mood swings. I have my next yearly exam scheduled and am seriously going to discussing this. A friend of mine talked me into getting it because she loves hers. NOT ME!

Well, I am not the type to post things on line but I'm so angry and disgusted with the whole medical and pharmaceutical industries for promoting this product FALSELY. I got the mirena 5 weeks ago and am having it removed in two days- and counting. I am extremely anxious and depressed. I feel "raw"- like I want to cry for absolutely NO REASON. I just gave birth to a beautiful boy two and a half months ago and have a lovely 15 month old boy as well. I need my mental health for these babies and MIRENA has taken it away. I was told (as most women who are posting about Mirena complaints) by my doc that there would be no side effects despite me telling him that I did not do well on the pill. When I had to go to the psychiatrist because of how MISERABLE I felt, she called the ob-gyn and he said it was "absolutely not" the Mirena- leaving me to feel like a basket case. Fortunately I looked on line and realized I AM NOT CRAZY and I KNOW MY BODY better than all these doctors. I had read about Mirena before getting it inserted but only on their website- obviously heard no horror stories there. I wish I would have read websites like this one before having it inserted. Anyhow, NOBODY is going to tell me that what I feel is NOT because of Mirena- I KNOW IT IS. I am having this awful thing removed and no doctor will persuade me to "try it a little longer." They can say it's not the Mirena but we all know the truth and the truth will prevail eventually.

I am really hoping someone can help me with the side effect issues I am having after taking Prednisone to cure a tumor on my larynx.. I was on the drug for six months.. taking 60 mg a day. It saved my life and at the same time it was just about to kill me, I am not kidding. The horrible effects it had on my body was really worse than the tumor that was taking my life. It would have almost been easy to die.
But today I'm very grateful for the miracle it did on my throat. I did not have a voice for many years.. today I can sing and that makes it's a great gift.
I was wondering, after being on it for so long and coming off nice and slowly, should my joints be in this much pain? My body aches are horrible.. all the muscles hurt and that never seems to go aways. Is this normal?

I am taking 25mg of toprol for SVT/MVP started about 6 months ago. started having mild joint pain while doing yoga, just thought I was getting older (I am 46) joint pain started getting much worse in my hips and spreads down my legs when walking for more than 20-30minutes. I have had breast cancer and am concerned it may be a tumor I am scheduled for a bone scan on Monday but after reading the messages on this site I feel much better that it may not be bone cancer and might be this medication. time will tell.

My doctor prescribed me Prednisone on May 3. I'm on 10 mg. I start out on 3 tabs 2x a day for 4 days, then 2 tabs 2x a day for 3 days, then 1 tab 1x a day for 2 days. I was put on this for a sudden attack of joint pain/stiffness/swelling of my elbows, wrists, hands, knees, ankles and feet. I was in extreme pain. So far this drug has given me no side effects other than needing to urinate a little more often than usual. My pain is gone, as is the swelling. I'm almost scared to go off this b/c of the fear of the pain coming back. My blood tests came back on Friday and my doctor told me that I had Rheumitic (sorry, I know that's spelled wrong) inflammation and if the pain did come back after I stopped the Prednisone that I'd have to do more blood tests. I just turned 30 and I'm scared to death what else might be wrong with me.

I recently got off nuvaring due to finances, after reading these posts I have realized the pains I have had the last four months were probably from the nuvaring, I have had migranes and dizziness and blurriness. But since coming off nuvaring I have suffered a hard pain near my left overy, I also have a rash on my tummy. The pain is all day and gets worse here and there. A cousin told me she had to have her overy removed from a tumor she had because of Nuvaring, yet she has to stay on Nuvaring because she doesn't want to lost the other one.

My sister had been using advair for many years the past 6 to 12 months she had been experiencing unexplained problems. weight gain-mainly in midsection( Dr did ultrasound to check for tumor), increasing dry mouth to the point of mouth and throat sticking together Dr. did tests to rule out serious conditions but came up with no answers, She has been complaining of being tired more easily and getting short of breath unable at times to climb stairs, in the last month she was mentioning problem sleeping, acid reflux getting worse, on September 5th she had a sudden attack and died within minutes. The Dr said the cause was bronchiospasms. I heard something on TV and started doing some checking and advair has been known to be involved in sudden deaths due to bronciospasms. The symptoms she experienced in the months prior sound like they also might of been side affects or adverse reactions and the Dr. never suspected her medication when no other cause could be found. I want to warn people that if they are even possibly having adverse reactions to advair check it out closely befor continuing. My sister was only 58.

I have been taking Yasmin for about 6-7 months due to abnormally long periods after the birth of my second baby at age 37. I also have a tumor in my uterus that might be causing painful intercourse, so the Dr. said to take it for three months straight and then have a period. In the meantime I have noticed severe sotmach cramps and diarriha (how ever you spell it) since October. Funny thing was that the first round I was suppose to take 2 months of Yasmin and at the end of the second month have a period, then do 3 months and have a period, but I noticed that on the 2nd month after I had my period (which I acutally stopped taking Yasmin since the white pill is only a placebo) and then started back on the next round of the 3 month cycle I started having real bad stomach cramps, etc. I am about to have my 2nd period of the 3 month cycle and I won't take the placebo and see if my stomach feels better. If it does, then I am stopping Yasmin. Another note, I take Yasmin at night and wake up at 1 am and 4 am like clockwork with stomach pain. I will keep everyone posted after the "placebo" period to see if my stomach gets better. I anyone has any similar symptoms, please let me kow. Tammy.

Hi Ladies...
How about headaches? Was on Yasmin for 4 years and have been off for about 6 weeks. For the last 3 weeks I have had the worst constant headaches you can imagine. Very migrain like-with lots of pressure in my eyes-sinus area. Anyone else with this...starting to wonder if it's something horrible like a tumor!
Cristy