Knowledgable symptoms and conditions

PREDNISONE.... a word that is unknown to the naive and despised by the the knowledgeable. Before i begin i want to tell you that prednisone for lack of better word F***ed me up. So heres my story with the pill. About a year ago i was officially diagnosed with Minimal Change Disease, now remember i am eighteen at the time, and was prescribed prednisone to cure the disease. Now being unaware of the severity of the drug and disease i casually continued life while taking 80mg per day of prednisone. Well this was good and all because it did in fact put me in remission, but the side effects were starting go surface. My face ballooned up "moon face", started experiencing random series of depression, became insomniatic, and unfortunately gained several pounds. Well this was not the end of side effects as for me. I continued with the medication and after 6 weeks of 80 mg i began my 5 week course of 60mg. Then after that i started 4 weeks on 40 mg and began tapering 5 mg every 2-3 weeks afterwards. Toward the middle of 60 mg the drug started taking its toll on my body as my skin lost its elasticity so i started getting gruesome strecht marks all over my body. I also became constipated for whatever reason most probably prednisone was at fault. I became very frightened actually terrified so i started to research about the drug in hopes of finding ways to avoid some side effects. In doing my research i found out very disturbing information regarding prednisone. Along with all the side effects that i mentioned above, prednisone also causes cateracts, glacoma, diabetes via insulin resistance, and osteoporosis. Now these i consider as the more severe permanent side effects as the list unfortunately is much longer. Finding out about the side effects i became extremely paranoid and started a very strict diet to hopefully avoid some permenat side effects. I admit reading about the information on prednisone created my paranoia and/or possible phycosis which ultimately led to my stress which led to my severe depression. Now this wasn't any old type of depression, i was sersiouly in need of some help. Everyone around me could tell something was wrong and really i dont blame then for in fact i felt as if my soul had died, the very essence of my being. Now magin if you can someone taking away your youth from you, sucking the very life out of you... thats exactly how i felt. To add along with the depression my grades became a wreck in college as i dropped several classes, lost a friend, developed problems with my parents as they tired to help me, and disrespected family relatives with my uncontrollable mood swings. A few weeks in of dieting and exercising i lost a lot of weight (15-20 pounds). As far as side effects non had changed i still had to deal with all that was mentioned above especially with the fragile skin that was a real burden as i had even a few stretch marks on my face from sleeping on my side. At this point of my long and what seemed to be a never ending journey i become exteremly weak. My body had no energy to run on as i refused to eat and when i did eat it was either foods that are considered free foods or protein nothing else. Everything at this time had been taken away from me including smoking marijuana (marijuana drops blood sugar as this would cause me to start feeling faint and lightheaded), alcohol (same as marijuana drops blood sugar), and the fact that i was not comfortable in my own skin (literally). I was driving myself insane. Everyday i was behind the computer searching for more and more. I was obsessed and became my worst nightmare. Oh by the way half in the medication therapy i showed 1+ grams of protein in my urine which my doctor possibly thought it could have been a relapse. This news i did not take lightly i had lost it and was prepared of comiting suicide. I cant lie, i really did not want to live anymore i just wanted to end this and suicide seemed like a very real and convienent possibility. If it had not been for my parents talking to me giving me a 3 hour speech and lecture i do not know what i would have done. Suicide at that point became out of the question because i could not do this to my family. So i went and purchased urine dip sticks to monitor the protein. The doctor had given me a 2 week window or chance to get back into remission or else he was going to prescribe me cytotoxic agents aka chemo therapy drugs. This was horrible news to me. So as i monitored my protein i found out of a very interesting trend. I noticed that my protein levels in the afternoon were in fact positive for protein and were usually up and down as far as how much but in the mornings i noticed i was always negative. Now this give me a huge bit of hope because when in researching about MCD months earlier i found out that there is a coniditon called orthostatic proteinuria which affects mostly young adolecent males and is a condition described as for some unknown reason there is protein loss in the afternoon when the person is upright and active then when they are supine or laying down the kidneys do not allow any portein loss. This condition is in fact harmless. I was very happy from then news and i told my doctor, he was somewhat doubting, but i don't blame him he is looking out for my best interest, but sure enough after the 2 weeks had past i went in again for my appointment after testing and i was negative for protein as i had expected. We began tapering after that point and i continusouly monitored my own tests at home and eventually i got off the steroid, actually today is that day after a 9 month period of heartache and distress. You know people say that they went to hell and back in a hard moment in life, well i went to hell stayed there for 9 months then came back. I feel so everyone who as ever needed to take steroids for long periods of time, i know its tough but believe it as it is indeed a potent drug and in most cases a miracle drug. It gave me a second chance at life and no matter how hard it was or how much pain it put me through i cannot complain for it did in fact cure me and thats why i can never hold any grudges. So thats my story i kno its not pretty but what can i say it is indeed mine whether i like it or not.

Two days ago, I needed to drink two doses of gastrographin one hour apart two hours before an abdominal CT. Not more than 20 minutes after drinking the first does with 12 oz. of cranberry juice I felt a burning sensation in my eyes and they started to water. I also felt disoriented for a moment or two, similar to what one might feel when they are driving tired and they have a hard time keeping their eyes open. By the time I had started drinking the second dose, I had diarrhea and visited the bathroom three times before setting off for my CT appointment.

Once reaching the medical facility, I used the restroom twice more within 40 minutes time before my scan. I feel like I am telling you way more than I would tell anyone else however it was remarkable to me to have to visit the toilet five times in less than three hours! I was made to drink a third dose just prior to my scan and given an IV dose of contrast. Throughout the remainder of the day I felt out of sorts: loss of appetite, lethargic, thirsty, and although less frequent visits to the toilet were necessary, I continued to have diarrhea.

The next morning I awoke with the most enormous headache. I have never had a hangover but what I felt was what I imagine a hangover would feel like . . . I felt crummy! I still had the diarrhea and I was drinking water like a mermaid out of water.

Today, two days later, I feel like I am back to normal. I attribute the crummy side effects I experienced to the gastrofrafin but not being knowledgeable about such things, I decided to research possible side effects on the web. So that's how I got here.

As I write this, I'm on my fourth day taking Levaquin 500 mg. prescribed by my doctor for severe nasal congestion, sore throat, difficult cough. I have bouts like this on a yearly basis that start around Thanksgiving till late spring. I do remember taking Levaquin before though didn't notice anything bad (yet). As I read through different messages, I now come to realize that maybe I should go back and check the time I took Levaquin because I've been suffering from so much muscle aches and pains for a quite a very long time now. Since I started taking Lipitor 3 years ago, I'm inclined to think my pains were due to side effects of Lipitor. That's just another issue.

As of yesterday afternoon, on the third day of taking Levaquin, I was informed by my pharmacist that I OVERDOSED since Friday and Saturday by 2000 mg. I was prescribed 500 mg. one tablet per day. Whoever typed "Take one tablet every day by mouth after meals" in the pharmacy must have too many "ssss" in their pockets. "After a meal or after meals" are definitely not the same, don't you all agree? I didn't just read the label and followed instructions as I understood it. The pharmacist confirmed what I read back to him as typed. I thought pharmacists know how a certain drug should be taken. But that's another story to tell. I'm too concerned learning about the bad effects of Levaquin for me to find time and question a pharmacist integrity.

I called my doctor first thing today and told them of this oversight (should it be mine or the pharmacist?). I was told to continue with the medication and call them how I'd feel in a couple of days. So I took just one tablet today. That was easy.

Now after reading all these different bad things happening to people taking Levaquin, I am thinking of the future. Should I be worried about the bad side effects of Levaquin taken exactly as prescribed? What about those 2 days of overdose? I guess, I have to find that out myself in due time as I will not stop from finding out more about this drug.

I don't think I will continue taking this drug tomorrow. I don't know what will happen but I'm sure my doctor will find a way to fix my upper respiratory problems. He must have heard about other patients complaining about Levaquin. I will make sure he will take my opinion seriously.

To all of your valuable inputs and opinions and warnings about the harsh effects of Levaquin, thank you very much and may you continue on passing to one and all your valuable insights. Count me in!!!!!

Tomorrow will be a new day and I will be on my toes making sure I will fight the harsh side effects as early as I could. I know it will be worth the fight if I kick these damaging effects at its early stage, hoping I will be lucky to do so.

God Bless to all!

All you are Hypochondriacs. If one person says this medicine is causing this, then of course; you all have the same problem "some how." Isn't this weird? It is called the "placebo effect." Normally all the people involved in the testing are given "Lisinopril" (or some other drug), then the placebo group is given a vitamin supplement, the group receving the vitamin supplement is being told they are receving "Lisinopril." Mysteriously?, the "placebo group" is all feeling better and their symptoms are gone. This is due to the fact that all these people in the "placebo group" have interacted with eachother and have told eachother "I feel better" than of course everybody feels better. So WEIRD!! So, my point is this forum is all your peoples "placebo group." If you guys never heard of these side effects from this forum you would have never experinced them. Hypochondriacs all of you are. This is a very good medicine that is helping all of you make up for your peoples lack of self-disipline to control your diet or exercise enough to lower your blood pressure naturally. So be thankful. Lets not complain about false side effects because John has them. I wonder what the side-effects of that cheese burger are that caused high blood pressure. It is funny, I don't see a forum for that. So deal with your so called "side-effects" that are associsted with "Lisinopril" or go on a diet people. Get over it!!

I want to reiterate that I am simply stating my personal experience with Yasmin how I felt on it what concrete factors I discovered with my hormonal balance with both salivary and blood tests, which both stated I had low testosterone. There is indeed a lot of controversy over salivary testing for hormones, one website will tell you it is the most accurate reading, while another will tell you it is unreliable. The same can be said for blood testing. As for bioidentical hormone replacement the same goes for this issue. Some will praise it others state it will do nothing for you. I think all of the women on this website are well aware of how adversely a drug can react in your body and are cautious of anything they will continue to put into their bodies, myself included. I am simply trying to give some insight into the root of the problems we are experiencing having experienced them myself, so that they may find knowledgable medical professionals who can help them make informed decisions regarding their health. Note that I do not encourage anyone to take anything without the direct supervision of a skilled physician, as is the same route I am following with my doctor.
Thanks, BitterRN