Narcotics symptoms and conditions

I suffer from severe endometriosis, and occasionally, if something goes awry, I have terrible cramping. The pain is extremely intense and has caused me to pass out. I have tried several medications, some narcotic, some non, and some naturopathic. I would say that Dilaudid is the best I've tried. Not only does it do a wonderful job of getting rid of pain, it also seems to be easier on the stomach than other opiates in its class, and causes less side effects. Of course, highly addictive such as other narcotics, but if taken only when needed it is a lifesaver.

mirena has done wonders for me. i have no complaints. i got mirena in Feb. 08. so about a year and a half ago. i got it because i had the most unbearable periods where they had me on narcotics and it was completely ruining my life to the point where they wanted me to have a hysterectomy at the age of 20. when i got it implanted, i had severe pain or about 2 days, but since then:

-i have not had a period...
-i get occasional cramps once a month around when i would be having my period, but they are no where near as painful as they used to be...
-my boobs have grown a little...
-i haven't gained much weight, expect for the weight that i had lost on all my medication before...
-and i still have just as much sex as i used to...

all in all, mirena literally saved my life.

I have a disk bulg and was prescribed narcotics, and injections in my lower back at about 6 mo intervals. I have abruptly gone off my medications and went on 2 300mg per day working up to pain relief. I just received injections so pain is levels are tolerable. the neurontin is give nuvaring me sever anxiety, raising blood presser to high levels for me, insomnia, nervousness, How long before these side affects go away? Any one else experience this?

I had a lot of trouble from it anyway, the mood swings depression, cramping and discomfort during sex. i had mine for 2 years and 3 days ago i was at work and and i started getting extremely bad cramping. I went to the ER and they did an X-ray..then they TRIED to do a pelvic exam and couldn't because i was screaming in pain. Come to find out the mirena was hard to find cause it went sideways and was poking all sides if my uterus wall! The nurse had to give me narcotics through an IV just so they could remove it. Now i feel normal again in only days time, i don't know what i was thinking getting that man-made device inside something so fragile. I DO NOT recommend the Mirena to ANY woman out there........

I was first prescribed Neurontin in November of 2008 for cervical disc bulge touching my spinal cord causing severe nerve pain in my left extremities. I was prescribed narcotics and eventually prescribed Neurontin. The side effects from Neurontin, at that time, were seemingly intolerable, but as the narcotics were decreased several months later, I found the Neurontin was actually effective and did its purpose. The side effects from the Neurontin were not that great to outway the pain factor I had. I believe this drug does its job!!!!

I had a Mirena put in a month ago and it was AWFUL.. I think it was misplaced, because within 15 minutes I could not walk, was sweating, dizzy, and shaking, and had the sharpest pain you can imagine.. it was expelling itself. So I went back (almost called an ambulance, went with a cab cause I hadn't gotten far down the street anyway) and got it removed immediately. Yesterday I had another one put in, by a different (more trustworthy) Doctor. Extremely painful process, ended up laying in bed all day downing ibuprofen. But today I am fine, just some mild cramping.

What I really wonder is who out there has compared Mirena with other birth control methods.. I had to get one because I had awful experiences with migraines and other side effects from pills. I have spent months researching different methods of birth control and reading reviews on all of them.. honestly, every method has hundreds of postings describing the exact same side effects. The best birth control methods are, by nature, hormonal, so it isn't surprising that people have similar reactions to them. Mirena is supposed to be better in that it acts more locally and does not have estrogens. Can anyone tell me how this worked out compared to other methods, or if they had migraines? I just get so scared reading all of these horror stories, and I cant tell if they are general reactions to hormones or specifically from Mirena. Thanks for your help...

since starting topamax in may 08, 50mg twice daily, i have had constant pain under my right rib, feels like something is eating a hole straight through to my back where the pain wraps around. also have some trouble breathing, constipation. have had gallbladder ultrasound, hida-scan of gallbladder, endoscopy, cat scan of chest and abdomen and chest x-ray, along with a zillion blood tests all showing normal. no one can find the source of my pain, the only thing is how the time corresponds with my pain and when i started the topamax. can anyone tell me of any similar side effects they have had, is it the topamax causing this? and should i stop. i'm feeling as if i'm poisoning myself. i need help. thank you for anything you can tell me.

Very high tolerance for medications incl 60mg morphine, 20mg oxycontin 4x day, however, I just cannot seem to tolerate Fentanyl. Have tried it two times in past, both the 25mcg and 50mcg. The first week or so is great, after that the side effects are more than I can tolerate. All of these side effects were extreme and unbearable not just mild. They affected my ability to function and sent me to bed on more than one occasion. Extreme fatigue, nausea, sweating, anxiety and weakness. I felt as though I had a very bad case of the stomach flu. Both occasions I stuck it out for 2-4 weeks till I finally had to quit using it. Any suggestions as to why would appreciated. Some of my side effects aren't even listed in brochure.

I am taking Adalat XL 60 mg. once a day.. as far as BP went was working fine.. They found I needed a stent in my heart... specialist put me on metropol 12.5... after the operation i went back to him.. BP was 80/53.. wow, no wonder I was feeling tired.. he advised me to stay on it.. NO WAY.. just my Adalat XL is working fine.. BTW.. and for the Gladys1948.. a few days after i started the metropol (lisiopril) I noticed a floater in my right eye... was disconcerting.. but is slowly leaving since stopping the drug.

Hi everyone,
I cannot live without xanax and its terrible, I have been on them for 5 months and have tried to stop them and its a nightmare. I suffer memory loss, have blackouts that I do not remember what I have said after a few drinks. It does help ease the social anxiety. But I have become moody, sleepy. . Does anyone else have these problems?

i took cipro for a UTI over 10 years ago and have had floaters, neuropathy, tingling, and numbness in my hands and feet ever since then. it was not until THIS YEAR that i stumbled upon information on the internet about CIPRO and its side effects. but immediately following my use of the drug i went to a doctor who insisted i had carpal tunnel and i asked then why is it in my feet? then a neurologist who found nothing and patted me on my little college girl head, told me it was "just stress," and prescribed me narcotics to calm me down. i threw the prescription in the garbage on the way out of his office... then was tested for diabetes and briefly thought i might have MS. eventually, after many docs finding nothing and my family thinking i was a total hypochondriac, i just decided to ignore the symptoms. pain in my joints, floaters in my eyes, numbness and tingling in my hands and feet. after years i figured if i wasn't dying from whatever it was and it wasn't getting any worse, then i would just live with it. one day when it was particularly uncomfortable i did an internet search and came up with CIPRO info. there was a class action law suit at one time because right around the time i took CIPRO, it was a new drug and had not been sufficiently clinically tested. there's no recourse for me now, but i feel better having solved the mystery.

i am appalled to see so many people still suffering in 2008 and this drug still being prescribed. i'm sorry you're all going through this. i tell everyone i know not to ever take this drug. i feel lucky to be still functioning. i am very healthy, just have the annoyance of these symptoms that never go away.

46 yr old male and was started on Lip. about a month ago. Overall cholesterol level was 116!! Within 3 weeks I began having soreness move across my legs and hips to begin with, Just a drained feeling. Then leg cramps in my left legs. The drained feeling intensified until I went back to my Dr. last week who immediately ordered me to stop taking any more. I had been off about 4 days when I began have severe pain, lost all color, was not able to get out of bed, could barely talk or walk and was taken to the Doctor's office this past Sat.. I was not able to set up.My wife had to basically talk for me because I was in so much pain, could not communicate, was feeling like I was leaving my body. I do not and have not taken any narcotics or alcohol, but I was given "the field sobriety test", or what I would call it, as I am retired from law enforcement and have given thousands..... But never one for lipitor!!!

I told the Dr. I do not want no drug, I want an answer. I was told to come back on Monday as the Lab. folks wouldn't be in until then. I would not have to wait.

I have used this facility for many years, but I am totally shocked. I feel I have came as close to dying as any situation I have ever been in. I have never hurt to bad. I have never have so many leg cramps. I have never woke up each morning feeling like I have never slept a minute but have been working my butt off chopping wood or digging ditches or climbing mountains all night, simply exhausted.......I will always advise people about this drug....

Wow! I've done a lot of reading post Mirena and wish I had spent the time before instead of just relying on the pamphlet from the Dr's office.

I made it a whole 3 days!

Insertion was fine but it should have raised a flag when the Dr said "oops, it slipped out, hang on one more minute". I felt fine all that day (Wednesday). By Thursday cramping was pretty intense, vomitting, diarrhea, low grade fever, lower back pain, headache, rapid heartbeat. Called Dr "Oops" & told me I had a stomach bug, symptoms not from Mirena. Friday sucked, stomach problems went away but everything else just got worse.

By Saturday I was immobile on the couch, no other way to describe it than to say it just friggen hurt! Dr "Oops" closed on the weekend so I went to the hospital. ER doc couldn't find the threads to take it out and didn't have the "magic tool" required to fish them out. His solution was take antibiotics for possible infection and a narcotic pain reliever (3 mo old little boy at home, narcotics not an option) and have it removed on Monday.

Being stubborn, I insisted on seeing the on-call OBGYN who was upstairs waiting to deliver a baby. He was kind enough to come down and fish the strings out without this "magic tool". The relief was immediate, especially given that the Mirena had turned 90 degrees inside me. I'm lucky it did no damage. This Dr explained that the symptoms should not have been that bad had it been in correctly.

I've been bleeding heavy with clotting since Sunday, cramping is nothing compared to what it was. Think I have a yeast infection brewing from antibiotics, just to add insult to injury. I am just glad to have it out!

I would have to rate Mirena up there in the top 5 most unpleasant experiences of my life. Please do your homework and weigh your options before trying Mirena. The pamphlet from the doctor's office doesn't tell the half of it. And if you do decide to have it, consider having it done on a Monday to give yourself a few days to see how you like it before the weekend arrives. I'm sure having it come out of place is rare, but I'm proof it can happen. Good Luck to all :)

My doctor started me on Lipitor over a year ago. I started having muscle pain in my shoulders but didn't equate it to the meds until I was watching television one day and a Lipitor commercial came on. It said that some people experience muscle pain.....I thought HALLELUEH THAT'S WHAT IT IS.....I stopped talking the meds and went to see my doctor who immediately changed my meds to Zocor.....guess what? The same thing happened. Went to see her again and she switched to Crestor.....same thing happened....so I started doing my own research and was amazed at what I learned and bewildered as to why my doctor was acting like I was some whining baby.

No problem, I say to myself and stopped the meds. That was last November, in January I had my yearly physical and blood tests were ordered for me in December......guess what.....my triglycerides were still high so my doctor orders Antara. It didn't say "cor" anything so I'm thinking it's not the same stuff. No, it wasn't the same stuff it was WORSE!! Within three weeks I was crying I was in so much pain. I called her and got her nurse practitioner who says that my doctor said to stop taking the pills and the pain will go away. I call back and say, "you don't understand, I can't sleep, I can't move, I can't function the pain is so bad." After several calls back and forth, and let me tell you I NEVER call my doctor unless something is incredibly wrong and that is less than rarely. Well, my doctors partner tells the nurse practioner that they will not prescribe narcotics for me. WHAT? Who asked for narcotics? I needed relief from this pain.....I would have gone for amputation!!!

So I change docs...more blood work.....high triglycerides, I refuse to take any statins. She says she has something for me that will not cause muscle pain and hands me samples of Welchol.....this one took less than a week for increased muscle pain...again I wanted to trust, but guess what i learned when I went to the Welchol site? The first side effect listed? Muscle pain.

Called the new doctors office to let them know that I was experiencing pain again and was told to stop the Welchol (which I had already done) and take Red Yeast Rice and have bloodwork done in 3 to 6 months and come back to see her. Oh no! Not without research and guess what? A side effect of Red Yeast Rice? Muscle pain.

It has been 4 months since I stopped taking the Antara and took Welchol for a week in that 4 months. Sometimes my shoulders/neck and arms don't hurt too much. Unfortunately most times they do. Both doctors insist that the pain cannot be from the drugs because the drugs have left my body. The new doctor said I probably have myolgia just because I'm 52 and that it's just a coincidence that it happened while taken the drugs but then goes on to agree that I must be "sensitive" to statins. Both doctors treat me like I'm stupid and nuts all balled up in one. I am frustrated and in pain most of the time. I have been trying to find out how long to expect this pain and am dismayed to learn that it can be years or never go away.

Yes I have high triglycerides (so does my mother and she experiences the same kind of pain so refused to take statins) and I've been warned that not taking statins could cause pancreatitis and/or heart problems. My question to that is - "then my choice is chance the heart stuff or live an incredibly painful life?"

I'll take my chances and pray for the best because right now my quality of life stinks!!

I just started using Singulair a few days ago. I am 54 years old and just started coughing at night only. I would be fine during the day and then never failed, at night I started to cough keeping me awake. I was given antibiotics, narcotic cough syrups but it only helped temporarily and then I went back to coughing nights only again. So as I mentioned, I started taking Singulair a few days ago because my physician thinks I have developed allergies and Singulair is noted to help night coughs. It is helping my night coughs but I still cough a few times at night and now I cough quite a few times in the day when I never use to cough in the daytime. Wondering if Singulair is worth taking as the symptoms are becoming opposite? I hate taking drugs and don't know if I should find a safer alternative? Help, anyone? Thank you

I will never take this drug again - I was prescribed it for bronchitis along with prednisone. I have severe asthma and have been taking prednisone for short periods without problems since childhood. My first and only dose caused hives, itching, dry heaves, and severe chest pain and heart palpitations. Ended up going to the hospital by ambulance - Where I was ignored for 5 hours - apparently they thought I was seeking narcotics (overheard one of the nurses) for the chest pain. Ridiculous, I don't suppose my body covered with hives was faked too - I know that some people abuse medications but I am not one of them!!! I didn't even ask for pain meds. Anyway, I still feel pretty shaky today...but relieved that they gave me a different antibiotic - Hopefully the prednisone will help with the allergic reaction. Good luck to all of you and get well!

Please talk to you doctor before ever stopping a medicine cold turkey, you must ween yourself off of anti-depressants/anti-anxiety medications in order to avoid serious side effects. I've been told that the withdrawal symptoms can be worse than any other drug around (including hard-core narcotics or alcohol).

Here is a new one...I have most of the above mentioned as well, mainly stomach upset..but has anyone else had problems or extreme bloating from IV narcotics or painkillers?? I broke a rib and went to ER..they gave me IV Dilaudid, another time I went to ER for severe strep throat given same IV painkiller..both time after about 10 minutes I bloated up like I was nine months and my lips turned blue and cold..I thought i was having a heart attack. Very painful...I thought it was because I no longer have my gall bladder...ER docs said that is no correlation....is it the YASMIN??? Anyone??

I started having panic attacks while taking Percocet. I am a chronic alcohol user, and I am saying this just in case it rings a bell for anyone. I have since stopped taking Percocet (about 3 days). I was a habitual/recreational user ... meaning that I took them when available, but I did not always have them. Since my last dose, I have been having recurrent panic attacks that are very scary. They include physical symptoms (heart pounding, cold and hot flashes, feeling of difficulty breathing, sweating, shaking) - and the much more scary mental symptoms (fear of death, walls closing in, inability to think or concentrate, vivid dreaming, fear of people, etc.). It appears that some other people have had issues like this, but not everyone. Can someone share their story with me. Has anyone had similar experiences ? Do they go away at some point ? Is it withdraw (I am not sure since they started while I was using them - but continued after I stopped) ? I have heard that it just takes some time, but it is very scary. I get some relief by drinking ... in fact almost complete freedom from most of the symptoms, but I can't just drink all day. Please help.

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

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

So let's do something. This is our life that is slowly being destroyed.
I started with the office Hagens Berman Sobol Shapiro.
I found a bit about them on the link below. *****

I have been on methadone for about 4 years. I have gained about 60 pounds within 2 yrs of being on the program. I never had a weight problem in my whole life until now. Dieting and exersize did nothing.Also have severe constipation.Ive tried about 15 diffirent drugs to help the constipation. Most of them helped the issue but still leaving me with 1 or 2 bowl movements within 8 days.If I dident take anything for it Id wind up in the er with no bowl moement at all in severe pain.Also my stomache is huge, at times I look about 5 months pregnant. If anyone has any advice for the problems I am having please let me know.

I get bronchitis when I use this product. I have had to resort to illegal methods of getting the older inhalers. I can't afford to be down sick for 2 weeks at a time because a government decides for me that my medicine is bad. I'm sorry, me breathing is more important then ANYONE elses opinion. Especially those without asthma who say HFA is exactly the same. It's not. I haven't been able to tell a diffrence between it and primitine mist. Both INFERIOR products.

I believe my son is having complex partial seizures. He went through all the others mentioned here. Still having some issues with anger, diarrea, nightmares, and rash. Its been 3 weeks. I would be interested to hear about anyone having seizures after the meds are discontinued. Thanks all.

I am taking Topomax for migraines. I always start everything at a really LOW dose since I have a lot of probs with side effects. Started at 15 mg and went right away to 30mg (15mg twice daily) the second week because I was dying from headaches. The other antidepressants prescribed for constant daily headache prevention all of a sudden weren't working. I didn't want to take my abortive med for migraines every day (Amerge) so I was curious if Topomax might help my daily headache pain. Possibly my daily headaches had become migraines... so hard to tell one from the other anymore. I teach exercise for a living and so much of my headache pain is exercise induced. I found that while on topomax, all of a sudden 2 Advil would take away a headache I would get after exercising which never happened before. I would take two Advil before doing some of my hardest exercise to prevent a headache and for the most part that worked too... and that never worked before. I had tried all kinds of NSAID's before and after exercise at the advice of my neurologist to no avail. I did have one diffuse headache yesterday that might have been a true migraine and I took Amerge because Advil didn't help. I have been on the 30 mg two week now. But, now the downside. Since on the 30mg I feel like my chest is heavy a lot of time when I do water exercise... I am exhausted a lot doing my usual routines... I feel edgy, can't sleep well at night. I HAVE to have a two hour nap after teaching in the morning or I can't function mentally or physically. I sleep well for that nap time. Seems like I have thermoregulation problems. I teach water exercise and if the water is a little cold it bothers me and it never used to. Then in the pool awhile I feel hot. Same when I sleep.. I need a lot of covers, then I throw them off. Then they are on again. No I am not menopausal yet. My brain is hazy on topomax as well. I take bellydance lessons and sometimes I realize I can't remember what my teacher just told me. Now people reading this, don't think that just because this happens to me, it will happen to you. I know people who LOVE topomax with zero side effects. They don't tend to write in to posting boards. Also, sometimes side effects go away. Be patient if you want to give topomax a shot. I am thinking I am going to go back to 15 mg again... and see how I tolerate that. Because I teach exercise, the hardest thing is to feel the heaviness in the chest and the lack of ambition. This is not me. It is great not to have the headache pain, but I don't know if this is the drug for me. I was excited about the "losing weight " side effect , and I could see how skinny people who lose their appetite easily might be affected, but it takes a lot to stop me from eating LOL darn! I did read in another chat some poor chap had sinisitis for months and took TONS of antibiotics before finding out Topomax gives sinisitis type side effects in a small amount of people. So if you get sinisitis, don't take antibiotics before checking out if topomax is the culprit.

My heart goes out to every person out there trying to find the magic bullet for their headache, siezures, whatever... ADVICE.. .start with SMALL doses... you may be able to get used to side effects if you work up slowly in ALL drugs. In many drugs that didn't come in small doses, I took out 3/4 of what was inside just to get a mini dose. Ask your doc if you can mix one capsule or one pounded up tab of your med with juice and store it in the referigerator. You can drink say 1/8 cup a day of the juice to get 1/8 of a capsule. It is a lot easier than chopping up a tab into eighths. Also ask your doc about childrens doses that come in liquids with droppers. Topomax makes taking smaller doses easy with the sprinkles.. you are encouraged to open the capsule and sprinkle as little as you want on food. Good luck all. L.