Dope symptoms and conditions

I was prescribed this medicine by my back doctor as I have a herniated disk in my lower back. Injections didn't seem to be doing anything and since this medicine which is intended to treat seizures, has the side effect of blocking nerve pulses to the brain. I thought I would give it a try and see if I could get through the day. I had been on Hydrocodone but that stuff made me dizzy and nauseated if I didn't lie down after taking it. I don't remember the exact dose but I don't care to one way or the other. I had auditory hallucinations and a migraine headache for 3 days. I ended up missing two days of work and could barely function. Maybe that was the idea as a seizure medication it would dope them up and they wouldn't need to function.

I'm only 18 and my doctor didn't know exactly what was causing my stomach to bleed so he dope me up on Omeprazole. I have only been taking it for about 4 or 5 days and I feel increased drowsiness, that only benefits me me because I struggle with insomnia. I find it difficult to keep my eyes awake and concentrating in school is a burden. I have very mild headaches and I feel like I am getting sick. I can't stop sneezing, my eyes are watery and blurry, and my saliva and snot are tasting awful like medication. Anyone have answers for me???

I had all of the above side effects when I was on this crap. Topamax is highly dangerous. I now have developed Narcolepsy, have problems with my joints, my memory has trouble here and there for simple things. I am only 29, and haven't taken this stuff for about 4 yrs. I have permanent problems now that I have to live with for the rest of my life. I didn't have a choice in the matter. I was ordered by the court to take a psychological evaluation. They asked some questions and determined that I was Bi polar. Topamax was the drug they put me on, and look where I'm at now. I also have Migraines, which I had way before this poison, and my advice to everyone is that this stuff is dangerous, don't take it!

Let me start by giving you some history.

My sister is a 22 year old girl who worked full time and was never seriously ill until this summer.

During the last full week of June my sister started having headaches. She told me that these headaches were like none she had ever had before. Days later she started complaining that her legs and wrists hurt. She said that her legs were so tired and achy she could barely walk up the stairs. At that time I dismissed what she was saying. My sister constantly wears heels and I chalked up the complaint to a pair of shoes that were not yet broken in.

By July 4th, the headaches were so intense that she went to urgent care. The physician she saw in urgent care gave her an antibiotic and sent her on her way. By July 7th, she was having difficulty standing up and walking was almost impossible. My sister started complaining about severe joint pain. Her ankles began to swell and her stomach appeared distended.

On July 8th, my sister went to her primary care physician. I believe he sent her for an x-ray and said that she had a cyst on her sinus cavity which was causing her to have severe headaches. He then gave her another antibiotic and referred her to a rheumatologist never even thinking that these two symptoms may be related.

On July 10th, my sister saw the rheumatoid arthritis doctor her pcp referred her to. He dismissed her complaints saying that she probably has some form of arthritis, but that there are over 800 forms and it would takes months to pin point exactly which one she has. He then gave her a prescription for Celebrex and sent her on her way. She spent the entire week in bed because her joints were so swollen and achy that she could not move. She actually crawled to go to the bathroom.

By the middle of the following week, my sister's stomach began to burn. She contributed it to being a side effect of the Celebrex and stopped taking it on July 21st. We had no idea that the pain was so bad. My sister's last normal meal was on July 22. By the 23 she had no appetite and could not go to the bathroom. On July 24, the stomach pain was so bad that she could not work, or sit, or function. All she did was cry. She went back to her primary care physician who then prescribed her prevacid to help with the so called indigestion. He told her if the pain continues she could call him. On July 25th the pain became unbearable. My sister called her PCP as directed and he told her to go to the ER. Never once did he say he would meet her there! I brought my sister to the ER where they did an x-ray and cat scan of her stomach. They found nothing. At that time my sister had not gone to the bathroom or had anything to eat since the 22nd. The physician in the ER said that she was literally "full of shit" and needed to go home and take a liquid laxative. My sister is only 22 and my parents were away on vacation. We were stupid and didn't know any better and were so happy that they didn't find anything that we accepted his findings and got out of there.

My sister took the liquid laxative prescribed by the ER physician as soon as we got home. We waited anxiously for it to relieve her stomach pain. After many hours the laxative did not work and my sister ended up back in the ER. This time she was screaming in pain. One of the doctors there told her that if she couldn't calm down she needed to leave her ER. My sister did just that. At this point my parents (back from vacation) took my sister home and called Digestive Disease. A doctor there told my mom to give my sister 2 Enemas. He said that should relieve her pain. My mother followed the doctor's orders, but the pain did not stop. Sunday, July 27th my sister was right back in the ER - this time at another hospital. This time my sister was admitted to the hospital for severe stomach pain. After 5 days and numerous tests my sister was discharged. The doctors found nothing in her cat scans, x-rays or ultra sounds. The pain was more manageable (she was on morphine every 2 hours) and they said she was ok to go home.

August 1st my sister had a great day. She was sitting up in bed and seemed to be in good spirits. The following day she couldn't get out of bed. This time it was neck pain. My sister said the pain in the back of her neck was so severe that she could not lift her head up or move it side to side. By August 4th she was admitted to the hospital again. This time we brought her to University Hospital in Syracuse, NY. We were sure to get some answers there...or so we thought. As soon as my sister arrived in the ER they started treating her with antibiotics. They were certain she had an infection. They then told us they would have to do a lumbar puncture to check her spinal fluid for infection. We thought we would finally have an answer to what was wrong with my sister, so we agreed. The spinal fluid came back fine - no infection. At that time they admitted her to the hospital. While at University Hospital my sister was treated by a team of doctors. They tested my sister for lyme disease, west nile, lupus, leukemia etc. They performed a spinal tap, cat scans, x-rays, ultra sounds, blood smears, etc. All of these tests came back negative. The doctors could find nothing abnormal except for an elevated white blood count -22,000 (it was also very high during her last hospitalization), an elevated C reactor and a very high SED rate. After 4 days of numerous tests and pain killers (first morphine, then Dilaudid, then Dilaudid with a fentanol pain patch) they discharged my sister. The head doctor told her that he believed she had viral meningitis and that it would eventually work its way out of her system. By this point my mother and I were skeptical. We did the research and viral meningitis should only last approximately 10 days. Mig had been sick since the last week in June. No one was putting all these symptoms together. On the day of her discharge my sister started getting her stomach pain back. The pain was mostly on the left side of her lower stomach - under her belly button. Again she was told the pain was due to constipation and she should buy some Miralax when she got home.

My sister was home for a mere 2 days before she would be hospitalized again...for the 4th time. Her stomach pain was back and worse then before. My family could not believe this was happening. My sisters spirits were down and the excruciating pain was making her mentally unstable. This time the ER physician recommended a hematologist come in to see my sister. We just wanted answers so we agreed. This hematologist, Dr. R stated that she believed my sister had drug induced lupus. We were shocked as my sister was tested for lupus twice before and both times the test came back negative. Dr. R explained that she believed my sister got drug induced lupus from the Gardasil shot. My entire family was shocked. We had never heard of any severe side effects like this from the Gardasil shot. Dr. R asked my sister for her permission to test her again. My sister agreed and a week later my sister learned that she was positive for drug induced lupus. My entire family was so happy that my sister finally had a diagnosis and could begin treatment. We were told that after a 6 week steroid treatment (Prednisone) my sister would be back to her old self. We were ecstatic!

My sister was home from the hospital and on the steriod treatment for 10 days when things started to go wrong again. The doctors were very concerned with the dosage of Prednisone that my sister was taking (80mg. I'm not sure how many times a day). They cut the dosage down in half over the course of a few days to prevent kidney damage and other side effects. Once the Prednisone was decreased, my sister started getting sick immediately. Her forearms were very weak - she could not put any pressure on them. Her shoulders would tingle and she would get shooting pains down her right arm. One of her doctors believed she was developing fibromyalgia and prescribed her lyrica. Shortly after my sister began taking lyrica she started seeing stars. She had double vision and a migraine that would not go away. My mother called her doctor and told him about this. His answer was for my sister to stop taking the Lyrica. She did immediately.

On August 29th, my sister still had a migraine. This was day 3 without a break. She woke up early Saturday morning and began vomiting every 30 minutes. After a few hours of non stop vomiting my mother called her doctor. His nurse practitioner was on call and she told my mother to take my sister to the ER immediately. My mother went back into my sister's room to tell her they had to go back to the hospital and she found my sister having a seizure. My sister has no history of seizures. My mother called 911 and the ambulance came to bring my sister back to the ER...her 5th hospitalization.

Shortly after arriving at the ER, my sister had another seizure. Immediately after the seizure the ER doctor ordered my sister to have an MRI. My sister had one during her last hospitalization only 2 weeks before. That MRI was normal. This one was not. There are lesions all over my sister's brain. The neurologist told us that he cannot believe she does not have permanent damage. According to him there is no oxygen going to her brain.The neurologist also explained to us that her brain looks as though she has been poisoned. He said that her MRI is very similar to an MRI of a patient who has been poisoned with antifreeze. Later I learned that Gardasil has both aluminum and sodium borate (which is in both rat poison and cockroach killer). However, according to the doctor once your brain looks like my sister's all the poison is out of your body. My sister's team of doctors started debating as to whether this could all still be from the Gardasil shot...my sister's last shot was on 02/22/08. Some believe that the side effects started off as mild, but since they were left untreated for so long they've turned into a serious neurological problem. They told my family the only way to truly know what is going on is to do a brain biopsy.

Yesterday, my sister was transferred to Mass General in Boston. We were hoping for a bigger hospital, better technology, more seasoned doctors. So far my sister has been treated badly. When my mother told the doctors' about the Gardasil shot and the devastating effects it has had on my sister they dismissed it. When my mom asked the doctors to test my sister for heavy metal toxicity they completely ignored her. I fear that she will never get the proper care.

It is so funny to read all of the negativity but nothing positive! I came here looking for side effects and get a bashing about how horrid Yasmin/Yaz is! Let me first start off by listing my side effects that I wanted to know about:

breast tenderness
change in appetite
tiredness
red spot in eye

Next, let me tell you that I researched BEFORE taking this medicine because 1. I have MS 2. I suffer from migraines and seizures and 3. I take a whole boat load of medications! My doc recommended Yasmin for PMDD coupled with Sarafem to help my mood right before and during my time of the month. I must say that I have only been on it for about 10 days so I do not know anything of how it works with my period.

I am APPALLED at the fact that there are few, if any, positive comments about this pill! I know for a FACT that it works because I know 7 people personally that are on it that have NO PROBLEMS! So, I ask you all that have negative comments, what is wrong with you, other than you HATE the pill? What OTHER meds were you on while taking it? I read a few comments about stopping for a month and then starting again and then wondering why they felt like crap?? Well HELLO?! You are effing with your body's hormones! And there is a difference between Yaz and Yasmin hormones. If you had a bad experience with Yaz, make sure you are not confusing it with Yasmin! Yaz is a 24 day hormone pill where Yasmin is only 21 days.

I am not a doctor, but like I said, I have done my research. I have suffered with adult acne and PMDD for years. It sucks. If Yasmin helps, I want to know. I don't want to read a bunch of bull about people who mess up their cycles by taking the pill and smoking or taking the pill with meds they shouldn't be taking them with. I know what I can and cannot take. Most of what I take is natural and what is not, well, it CAN be taken with Yasmin. Like the website for Yasmin says and like most of the informational, non-biased websites say, Yasmin and Yaz is not for everyone. Some people cannot handle this type of hormone.

I can guarantee you that some doctor or pharm company can tell you that whatever symptom you are having is from something completely unrelated to the BC you are taking. Warnings are clearly marked...read them and obey!

Folks, Lipitor is the most widely prescribed drug. People are blaming their various problems on lipitor. They should see the appropriate specialist to address their specific symptoms vs self-diagnosing and blaming it on lipitor.

I was given this for bee stings. I wish I had more stings and no prednisone!! I shoke, Sweated from feet and hands, thought i was on the virge of a heart attack, insomnia for 9 days, quit my job of 7 years, drove my truck 2,000 miles over the coarse of a week, almost beat up my finance and my dad, (I'm never a violent person!), went to E.R. twice and given sleeping pills that didn't work, CRAZY STUFF TO SAY THE LEAST!! I lost my job, got a battery charge that my public defender thinks we cant beat, and almost lost the love of my life. Now over the past couple months I have had sever depression and have had to put my whole life back together. I'm grateful I didn't die though! THIS SHOULD NOT HAPPEN TO ANYONE, BUT IT DOES TO A LOT OF PEOPLE!! Please call me or email If there is a lawyer who could help stop this! ******
God bless America!

I dont know if it has anything to do with Topamax but i think i may be doing some weird stuff in my sleep or not sleeping as much as i think i am. i would call it cat napping. other than that, the first 2 months were horrible. i had the numbness in the hands and feet and i could never find what i wanted to say and i would stutter and feel like a dope. the doctor told me to wait it out for awhile and sure enough, the worst of the side effects went away. I still have problems finding things to say and im a bit more spacier but my seizures and my headaches and everything that was wrong is gone. Overall. its all good. I would just like to know what the heck im doing in my sleep and if its ever happened to anyone else. Maybe i should call my doctor. hah.

I work in a health care system and we have used levaquin for this last cough, cold and flu season. It has worked wonders for the various upper respiratory infections.

No one has developed rashes, boils, or bone/muscle pain. After reading the first response, her abnormal reaction sounds more like a bad case of shingles.

Then, I read the last post where the person drank two glasses of whine to help with the blah blah blah. Mixing alcohol with any type of medication will not help with Your sypmtoms were a "full fledged panic attack" as you stated from the beginning.

Nothing but idiots posting here!

Well what more can be said really ? most all of us have suffered a great deal for a long time with going to a bunch of quack dr.'s listening to drug reps (Pushers) sell their dope and we all want to believe there is hope but there is none .these problems we have know one knows the actual cause so therefore there won't be a cure . sure there are a few success stories but for the majority these side effects are only the beginning I really don't want to bear children anymore due to i am afraid of what I put in my body and are my plumbing problems hereditary? I couldn't live with myself knowing that I passed on all theese problems to my child. I have been off lupron now for well I can't remember what year it was I think it was 2005or 2006 and I am still having issues.....................
Bone/Joint pain , MEMORY , G I problems , Weight gain , Depression , Tired all the time , Dizzyness , I can't walk straight , heart palpatations , upset stomach , impatient , the hair thinning has got better , but the dandreff hasn't , i'm irritable , moody , and my fave acne the night sweats went away after they gave me the northindrone it really helped and the prozac really helped with the sever mood swings . But I am not myself I haven't been in a long time . the worst side effect is a broken spirit. the con's FAR outweigh the pro's

pain killers and muscle relaxers with a laporoscopy with a briliant surgeon like a endocrinoligist not a plain GYN Along with a great diet and exercise and maybe throw some metformin in for kicks and that my friends is a great start . we do have alternitives . we just have to search for them sometimes .

My 44 year old, otherwise very healthy husband has been taking Lipitor (10mg) for several years. Currently been showing ALS-like symptoms. Left foot dragging, muscle cramps, twitches, etc. We are headed to Duke University to find out of he has ALS. He is off of Lipitor for 3 weeks now, taking CoQ10 and lots of vitamin C. If anyone else has had these symptoms and they've been rectified, could you share how long it took and how soon you began to feel the initial improvement? Thanks KCC>

I'm a 26 year old female and I've been on Topamax since March 2007. It has completely gotten rid of the debilitating headaches I experienced 3-6 times a week. It also got rid of my anxiety. I got my life back, my antidepressant kicked in at the same time. I experienced all the usual side-effects, tingling hands and feet, forgetting words, memory problems, loss of appetite, but was COMPLETELY pain-free. I still am. However, I never remember anything now, forget whether or not I did something, paid my bills, etc, lose things constantly, and I have lost about 20 lbs. Not good. I look anorexic. I have bones sticking out. Eating is hard. I forget to eat and drink all day and food is just unappealing. I feel fuzzy and stupid and slow. Not sharp like I used to be. It has killed my confidence and self-esteem. But I was wondering if any women out there got yeast infections while they were on Topamax. I've had one monthly since I started it, and my doc said it's a rare side effect. Oh yeah, I've had mild hair loss and mild to moderate acne now. This drug, it is such a 50-50. Living with chronic pain, those headaches were awful. But doubting yourself is awful too. Anyone have similar experiences?

I stoped taking effexor 13 days ago due to financial difficultys and couldnt afford to re-up. before that however i was on effexor for a year, 150 mg. I logged online yesterday to read other forums on withdrawls if any that others may be experiencing, I was amazed to see that the physical conditions I was experiencing trouble with were widley experienced by others as well, I was just relived, i didnt know what to make of all the horrable withdrawls i was going through, not knowing they were just that. so day 13 and I am feeling much better, I am exited to get back to my self 100%. I started taking effexor to begin with to help with depression and ADD. It didnt help that i was also abusing meth, so i probably needed it more then as far as depression goes and getting off the dope. Im clean now, and im such good spirits, Effexor worked for me in so many ways and i am greatfull for that. But one thing I wont miss is the lazyness that i felt most of the time, I hard a hard time sleeping, and never slept through the night, then id want to sleep the next day, I couldnt drive for fear of falling asleep on the road, which did happen plenty of times to cause the fear. I was in a good mood but motovation was low. Well thanks for letting me share with all of you, reading the poasts here really helped me to understand what it was i was going through. Best wishes!

i have been prescribed med for anxiety. i have been up for 2 going on 3 days now. i cannot sleep. it makes me "on edge", abusive, and hostile towards everyone. my family thinks i am on "dope"