Personal experience symptoms and conditions

I am on 75mg in the morning and 50mg in the evening (125mg/day total), for my seizure disorder. If I could get off of it I would because I know how bad psychiatric drugs are. I used to be on various antidepressants for about 4 or so years, until I learned that "mood disorders" are all a crock, and drug companies are making a killing off of all the psychiatric drugs. Did you know that it has never been proven that depression or bipolar or whatever is caused by chemical imbalances?? It has been proven, however, that psychiatric drugs mess up the brain. Do some research on this. Go to the sight ****** I am so thankful I am off antidepressants but my life will never be as good as it was before I ever put the first one in my mouth. I would encourage everybody who has been diagnosed with "bipolar" to slowly and gradually withdraw from your medication and don't give up until 6 months have past. It takes a very long time for the drugs to get out of your system and you will feel like you are going through hell as you withdraw but in the end it is all worth it. Back to the Lamictal, I have now been on it for about 4 years. It does not control my myoclonic jerks completely (I have Juvenile Myoclonic Epilepsy) but controls my grand mal seizures as long as I take care of myself. I have pretty much no side effects, except for possibly poor memory/forgetfullness/can't find the word I'm looking for/etc, and possibly some slight "ocd" tendencies. It is hard to distinguish from the leftover effects of being on antidepressants (which caused me a lot of anxiety, panic attacks, depression, etc), because I do have some mild anxiety left over from them, but has drastically improved. The man problem I am suffering now from the Lamictal is feeling the effects of it wearing off in the evenings. In the last few months I have been feeling that feeling on and off throughout the whole day!! And my myoclonic jerks are increasing. I really don't want to go up on my dosage due to the brain damage psychiatric drugs cause and all the bad side effects I could experience, but neither do I want to change medications because I am at a very stressful time in my life where I am already going through a lot of changes. No idea what to do. Just wish that God would heal me of my seizure disorder!!! (it is a kind I am told I will never grow out of) Even if I had to go through the withdrawal from the Lamictal it would be worth it! If only...

I have been on this for 6 days for a UTI. I personally am not allergic to sulfa drugs and have had absolutely no problem while on it so I can't speak to specific side effects but I do have something to say about it. I'm a little confused as to why so many of you believe that this drug should be taken off the market. Surprise, a lot of people are allergic to sulfa drugs which accounts for the vast majority of adverse events described by nearly everyone on this post. And guess what, every single drug comes with side effects (Tylenol, Advil, Tums, etc. are no exception) and you accept the risk of those side effects when you put it in your body and weigh that risk against the possible benefits. It's not your doctor's or the drug company's fault you're allergic! Antibiotics, including this one, have saved millions upon millions of lives. It seems intuitive but it evidently must be said: if you're allergic to it STOP TAKING IT and call your doctor so he can prescribe a different antibiotic. Seriously people, it's not rocket science. Hives are a pretty straight- forward symptom of an allergy and one that can be diagnosed by the lay person. I am a medical professional, but even if I wasn't, you don't need an MD behind your name to figure that one out. Why would you continue to take it after having an obvious reaction? (a reaction that, by the way, is a well documented, clearly stated possible side effect of this particular medication if you'd taken the time to ask any questions whatsoever regarding your own health, not a surprise adverse event of a bad drug) It's not rocket science, it's common sense people. When I'm prescribed something I'm not familiar with, my first question is, "What do I need to know about this." Even after a satisfactory explanation, I look it up before taking it. In fact, that's how I found this post. Which brings me to my last point, why is it that people blindly put things into their bodies that they know nothing about. If the pharmacist doesn't explain drug information to you in person, that's what the little drug safety pamphlet attached to your Rx is for. Read it, that's why it's there. OR, there's always the option of using this wonderful resource called the internet. Use your brains for god sake and take a more active, responsible, and informed role in your own healthcare process. You are ultimately responsible for your own health, and to be completely honest, you're one of the only people who actually cares about it (guess what, your doctor probably isn't one of them because he has a hundred other pain in the ass patients with no common sense to keep track of). Think people...

Today, I completed 10 days of taking 100 mg twice a day. It was prescribed to me by my dentist to prevent infection (took a tooth out). I had severe depression, nausea, dizziness, anxiety. I got to a point that I believed I needed psychological help. This is not me, so I begun research. Thanks to this site, I called my dentist and kaiser to told me to stop taking it since 10 is the maximum. The doctors do not believe it causes depression, but what do they know in my own personal experience with doctors with prescriptions they have put me through hell. I WANT TO THANK YOU ALL...YOU WERE MY HELP...MY SANITY. GOD BLESS EVERYONE...I AM JUST HOPING NO MORE SIDE EFFECTS ON THE LONG RUN...AND TO BE BACK TO MY NORMAL POSITIVE, OPTIMISTIC AND FUNNY SELF. HAPPY 4TH OF JULY!

My 4 year old Son has had diarrhea from about the last 4 weeks... we have started some tests for Celiac disease but today it only occurred to me today that he has been on Singulair for about that time frame... after all the worry and reading these other storied Im even more convinced that it maybe the Singulair..
Im just hoping that someone might read this sometime today or the next couple of days to tell me if when they come off the singulair how long did it take for the diarrhea to pass. My son had is last tablet 2 nights ago ( so he has only been off it so far for one night. But he still has the diarrhea.. should it have started to come out of his system already.

This post is for the ladies who wonder will they feel better or notice any change after having the mirena removed. This is my own personal experience . I've had it out for about 2 weeks now after having it in for 3 1/2 years. I feel Great! I couldn't have a panic attack if I wanted to. I have had more energy, haven't had a headache. I have a returned sex drive. Sadly my hair is still very thin and patchy. The big kicker is I've lost 4 lbs as of today. My stomach now looks like I'm 3 months pregnant as opposed to 5 months. The big difference is noticed in my face and waistline. I don't feel so hungry all the time now and feel motivated to keep this going. I haven't had one heart palpitation since either. Yes I still yell sometimes, but not out of anger or rage. It's now to be heard over the yelling and screaming of my happy kids who used to cower because of my yelling that was so mean spirited and full of frustration from being so tired and feeling ill most all the time. I just worked last night 13 hrs got 5 hours of sleep today picked the kids up from school, played with them and cooked dinner to boot. I would have been in bed 2 weeks ago waiting for my husband to come home and rescue me. This has been my experience thus far and I keep posting to give those ladies hope that they can feel better once they get mirena removed. I hope others will have a positive experience with removal like I have had. Good Luck and Happy Recovery.

Hello I am clinically depressed. They doctors said I was "severely depressed." I haven't done these post ever so I apologize if I can't make my side effects clear and easy to understand.

Well to the point I am taking Lamactil and Wellbutrin for over a year now. The side effects I have are acne, laziness, always tired. But the side effect I hate the most is really perverted thoughts. Every waking moment I am always thinking about sex of some sort. I can't enjoy a movie because I am always thinking of sex with the person I am with, be female or male. I am straight but I just can't shake thoughts and hate it to no end. PLEASE let me know if anyone is experiencing these side effects.

I had Mirena inserted in 2007 due to a lack of tolerance to birth control pills. The experience was very painful for me. However, the doctor explained that the initial insertion process is different for every woman as we are not all designed the same. My cervix/uterus is oddly positioned. According to the doctor they are "crooked". As a result, the doctor had a difficult time properly inserting the mirena, which in turn resulted in major pain! But, this was just my personal experience. Not every woman will encounter this difficulty. However, I would recommend taking at least 2 ibuprofen before the procedure. Throughout the past 2 years, I have experienced a range of symptoms. Major depression, severe mood swings, acne, lack of energy, excruciating lower back pain which mocked mild labor pains, and the overall inability to function normally. I begged the Doctor to remove the Mirena 6 months ago, but she convinced me otherwise considering I cannot tolerate birth control pills either. Nevertheless, I am 35 years old, have one child already, and do not plan on having more. Well, last week, I was basically confined to my bed due to excruciating lower back pain, and severe bleeding. I called the Doctor, and they finally saw me today. I insisted on having the Mirena removed once and for all, and already feel 100% better just 12 hours later! The purpose of my message is not to discourage anyone, as we all have different levels of tolerance when it comes to pain, medications, etc.....Yet, I felt compelled to share my personal experience as it was not a positive one for me! The only "positive" symptom I obtained from the Mirena was a lack of periods. Unfortunately, there was a downfall to that as well. Due to a lack of a regular menstrual cycle, I felt extremely bloated, and had difficulty losing weight despite working out 5 days a week, and eating a proper diet. I sympathize with each and every one of you, and appreciate your efforts in sharing your experiences. Upon stumbling upon this website a few days ago, I finally found the courage to have this thing removed so I can once again "feel normal!" Good luck to all of you!

I am 71 years old, I have been taking 80mg of ZOCOR ( Simvastatin ) for the past 16 years. five months ago I started to hurt in my lower back, hips,Knees,thighs, for two months then it traveled to my shoulders, wrist, hands, fingers. the Dr. gave me a round of prednisone (one shot and 11 pills) the pain stopped and everything was wonderful for two weeks,the Dr. stated that I had avused my body in the years gone by now the pain has started back in my shoulders, wrist, hands the pain is very strong,and my legs are starting to get weak again, I am taking Naproxen 500 mg two times a day and also taking Hydrocodne10mg every four hours also have Oxycodone 10mg to take every four to six hours, I have mentioned the results that I have read about the Statins in this forum but the doctor, does not act like it has any significance. does anyone have any suggestions??? if so please let me know, this pain is killing me, if you have any info. please email me at. ******

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I've been noticing that you as well as bobby are continuously replying to many of the posting. I stopped taking lipitor in December after having chest pains for 10 months which included being hospitalized for 2 days of testing. I'm still having the chest pain although I believe it's getting better. There was a week in the beginning of this month that I had no pain at all but now it's back. My question to you and bobby is you keep saying you still have some side affects for months but fail to list them. What are they and with your experience, why does Lipitor cause chest pain? What have you found out in your research? Is this drug causing damage to the interior lining of the arteries? Is this why many people are getting the pains from?

I was prescribed Reglan to increase my breast milk. I have no history of depression or anxiety. After a month or so having taken Reglan I got extreme anxiety and insomnia. I knew I was experiencing something that was NOT normal for me. It was a terrible experience. I had to move in with my mother so she could help me with my baby. I was diagnosed with post-pardum depression/ anxiety and put on antidepressants. Something I never would have believed would happened in my life. I am now weening myself off of them. Although my Ob/Gyn says that this experience was not due to the Reglan I was on. I am not convinced. I was taking it three times a day. I will never take Reglan again.

so far, ive been on Yasmin for almost 3 wks. the first week i had no side effects but as time progressed i started getting abdominal craps with a watery vaginal discharge; it sorta feels like i'm having my period except ther's no blood. i'm constantly nauseous and i have no appetite. my legs can feel numb at times and i get these really sharp pains in my chest. my body practically feels tender all over. i'm really depressed lately and my moods change drastically. Is this normal?

I had my second Lupron shot this last mid October that lasts, supposedly, 3 months. So I will be 5 months in this mid December and I have to say I was one of the people who was fine with Lupron...up until now. I had and have all of the typical side effects of hot flashes, headaches, memory loss, mental fog, etc. Then I had my first ever migraine a week ago that knocked me on my butt for 2 days. My memory loss and depression are by far, by far, the worst side effect I have experienced. At this point I am concerned my memory problems and mind fog will not go back to normal, which has already adversely affected by daily life. I was one of the people who spoke positive of this injection even after reading all the horror stories but now I am beginning to wonder if they were right on some levels. When reading all the different experiences I would get confused and wouldn't know what to believe. I am not saying I would change things, the jury is still out as to whether the benefits will outweigh the difficulties, but my personal experience and symptoms have been getting worse just in the last few weeks, so that would be between month 4 and 5 on it. I could lead a pretty normal life up until recently and I'm a pretty tough person, I clean houses for a living and work hard with a packed schedule so I am not just stating little symptoms I experience but ones that actually have affected my daily life. Just being honest so you know what to possibly expect, depending on your body's reaction. That is a point to keep in mind, everyone's body reacts differently but if the majority of people are saying the SAME side effects, makes you wonder if there is a consistent pattern.

One thing I will tell you that has helped me is B vitamins regularly in your system and staying as active as possible. Write things down to remind you for the memory issues, don't over-commit to things because of the mental affects-it hits you hard when you can't follow through, and try to watch your sugar intake, which messes with your emotions. Hope this is helpful.
I would love to know from someone who has the same symptoms (which looks like almost everyone who is on it) and who is now off of Lupron for at least a few months, if the symptoms of memory loss and mind fog go away. Is my memory permanently damaged?

I'm 31 years old, in a stable relationship and had the Mirena inserted in April in order to lessen the amount of synthetic hormones going into my body. I'd also never really found an oral contraceptive that didn't have some major side effect (nausea every night 2 hours after taking the pill). My doctor told me that the chances of side effects I'd read about on the internet (acne, weight gain, loss of sex drive, depression, etc.) were statistically extremely unlikely.

The side effects didn't appear immediately, but after about 3-4 months, I got everything but the depression. I'm a yogi and practice vigorously 5-6 times a week but was gaining weight around the middle, I broke out in large, deep, incredibly angry pimples all over my chest, back and chin (places I've never had pimples). I hardly wanted to touch my boyfriend. The thing is, it wasn't until I went to see an acupuncturist for my acne that she pointed out that my change in birth control might be the source of some of my symptoms. Once I really started researching side effects of Mirena, I realized that my experience was not as rare as my doctor had made it sound.

I had it taken out today and a Paragard IUD (cooper, without hormones) put in. Even then, the doctor was extremely resistant to even the idea that Mirena had anything to do with any of my symptoms. He was actually rather condescending and aggressive towards me. He did point out that when I had my Mirena put in, I stopped taking Oral Contraceptives and that loss of those hormones could be the cause of my acne. I admit that it could be a possibility, but my acne is worse than when I was a teenager (when I wasn't taking birth control) and in places that I've never had a problem with before. And the loss of hormones don't explain weight gain, vaginal dryness or loss of sex drive. I'm open to the possibility that the Mirena isn't the source of all of my problems. It probably works very well for a lot of people. However, my personal experience along with the other women on this site should be taken seriously by the medical community instead of cast off as "unscientific." I know my own body and I think that often, our gut feelings are dismissed because there isn't a readily available scientific explanation. As we've seen through history, medical opinions change and known effects of drugs/hormones/chemicals are slowly discovered. Doctors should be open to the possibility that we actually know our own bodies.

Almost everyone is affected differently by different types of birth control pills. They are not all the same, please talk with your doctor about what is best for you. Sometimes is DOES take a few tries with different pills to find the best one for YOU.
This is my personal experience with Yaz... I have been on it for 1 year and 1 month exactly. I am 22. I was on Ortho-Cyclen (not tri-cyclen mind you) for a full year previous to Yaz. My periods without birth control were usually very heavy and lasted a week plus a day or two without birth control. My doctor suggested birth control to help with those problem. Ortho-Cyclen helped somewhat shortening my periods to about 5-6 days and made them a "normal-like" flow. After taking it for a year, she suggested Yaz to me help make them even shorter and lighter. Well I switched immediately after the last pill of my Ortho-Cyclen and things proceeded very nicely since I had already been using a method to regulate my cycle.
Yaz has helped me tremendously, my periods are only 3-4 days now and much lighter. I start them after 2 days of placebo and usually have a little bleeding into the first 2 active pills of my next pack.
The only side effects I have noticed are;
1) Weight gain: (I have gained about 8 lbs on this pill) and I even get more exercise than I used to when I was on Ortho-Cyclen. I eat healthy as well.
2) Breast tenderness: I have more noticeable breast tenderness while taking this pill. (But it is not every single day)
3) Cramps: I get cramps now on the first day of bleeding, but they are well taken care of with an aspirin or ibuprofen.
4) Slight depression: I cannot directly link this to Yaz as I am not a professional. However, I do find that a week to a few days before my pill period, there may be a day or two when I find myself crying over some nonsensical thing. (I never noticed this with Ortho-Cyclen.)

Another thing I have noticed though, and it's pretty nice, while I have gained a little weight on this pill, I do not get bloating before/during my period as I used to before I started using birth control pills. And yes, I used to get bloated using Ortho-Cyclen. So I can say that I have to thank Yaz for this "desired effect."
Also, I never suffered from any bad acne problems before using birth control, just the occasional breakout before getting my period, and Yaz actually did away with even that little issue.

I have been on Prednisolone about 4 times in recent years. the highest dose was last year when i was on 80mg reducing weekly by 5mg. I have had most of the side affects you all talk about above. I have severe colitis so the side-effects of this drug are something i have to put up with. at the moment i have all the classic side-effects i usually get, rapid hunger, swelling to my face (moon face), neck has layer of fat, swollen back (buffalo hump), bruising easily, horrible taste in my mouth, swollen stomach. the one good side effect is it gives me lovely smooth skin lol. anyway the point of my post isn't to rip this drug appart as i have to say for me its a wonder drug and this time has prevented me from having my bowel removed! from personal experience once you finish the steroid treatment after a few weeks you'll notice the swelling go, my hunger usually fizzles out quite quickly (altho i have a large appetite in the first place!!) none of the side effects are permanent, so please all rest assured you will go back to normal just try not to put on too much weight while on the drug.

My personal experience with Zyrtec was so awful that I decided to document it in a blog in great detail to try and help other people: http://zyrtecsideeffects.blogspot.com/

I suffered severe depression, menstrual problems and other health issues whilst on Zyrtec. The depression literally disappeared overnight when I stopped taking Zyrtec. I suffered horrific withdrawal symptoms for 6-7 weeks after stopping Zyrtec which I have documented in my blog.

I've been on topamax at 400mg 2x a day for about 8 years now. It is a great drug but it has HORRIBLE side effects! It ( along with lamictal) gives me WONDERFUL seizure control. And it is safe for pregnancy. BUT it has destroyed my memory. short term and long term I cant remember much of anything! The sexual side effects is just awful. It makes reaching an orgasm almost impossible! I am very scared that I may have full blown alzheimers by the time I am 30!

Has anyone gained they're memory back after stopping topamax?

As of last night, I was so excited about my choice to use Mirena. The informational piece of art they gave me sounded wonderful. No period. No Cramps. No babies for 5 years at MY CHOICE. As a 19 year old woman, having the ability to decide when I'M READY and not become a statistic, I was SOLD.
Well, I had Mirena inserted this morning! It was the worst pain I have ever felt. I have never given birth, so they alerted me that they were going to give me 4 shots to numb my cervix... first the nurse practitioner who promised me she would be doing the procedure.. DIDN'T. She let the " doctor" do it. Who i had assumed would be knowledgable and would have years of experience. Not kidding here ladies, she sat there and said " did I do it right?" " did I give her enough numbing medication?" " should I cut the strings more?" I was ASTONISHED. but when your laying on the table, feet in the air and your cervix dilated, you just want the whole thing to be over.. but I sarcastically said " have you ever done this before" and i got " of course, I'm so sorry it was more painful than we had described." I wanted to burst into tears. I got extremely hot and felt dizzy, I told the nurse, and she started to fan me down. Afterwards I sat up, and saw the surgical tools, I wanted to vomit. Once they left the room, I stood up and blood just gushed. As they told me to come in on my period at my heaviest peak of flow, it was just 3x worse.
Apparently I didn't do enough research, I read all of these ladies opinions and concerns and I'm starting to question if it's the best choice for me. My aunt, and cousin had them NO PROBLEMS. And my soon to be mother- in - had hers surgically removed in the 70's for perforating her uterus. I figured it was new technology and Mirena would be better.
And now I'm just worried sick. 20 lbs in months... I'm 5'4 and weigh 107 pounds, 20 lbs would be OBESITY. Acne? Hair Loss, dry itchy scalp?? A FOREIGN OBJECT GETTING LOST INSIDE MY BODY?
The thing is, my OBGYN cant even take in appointments when I have an emergency UTI, yeast infection or need to make my annual pap.. but they " squeezed me in" for the following day to insert something that is causing so much pain for other women. I asked the valid questions, I did my research by reading allllll of the information. I asked about weight, they said it wouldn't affect me. Acne- they said " if it does cause acne, use this topical" and prescribed me cream. I asked about the expulsion, and they said " it never happens, we do this all day, everyday. We highly recommend it, we use it ourselves and have no problems" I also asked about discomfort that it would cause for my fiance... " he wont feel a thaaang, don't worry about it sweetie, those strings will wear down as your body's natural acids break them down, they'll become soft and he wont notice it unless you tell him." I'm just wondering, If some many women have these problems over the last several years, why isn't anything being done, and why is it so silent. Problems with Mirena seemed impossible to the doctors, in fact when I asked the doctor about acne, she seemed shocked and said " well, I have had some acne on my back, but I dont believe it's cause by Mirena" almost as if she hadn't done any research herself.
Well, this site has officially freaked me out. I don't need any more acne than I already have. Nor do i need to have any problems in my relationship.
The only thing I have noticed so far, besides the MAJOR pain during placement, is mild to heavy cramps throughout the day, which I have used 2 Vicodins to ease. I felt tingliness in my feet and ankles, but wasn't sure if it could have been caused by other random things. I've always had SOME joint pain, and I believe it's too early to see any new changes. I will keep posting.
*Also, have any of you women that have had problems been smokers" I occasionally smoke and wonder if this could cause any EXTRA problems?

My personal experience with Cipro is what they say is a mild case. To me I felt I would die. I've documented everything blow by blow on a new website ****** I was so angry with the medical profession for crippling me, so I took the time and channeled it into the only thing I could. My daily report. 6 weeks and I'm well on the road to recovery. To all of you who say it can't be done, it can. To all of those who say it will recur, perhaps, but I have great faith in the power of natural supplements to heal and support the body in it's repair. If you are suffering and reading this, make sure you visit my site and make your own decisions on what course of action you will take.

The experience has changed me forever, I will no longer have blind faith in the medical profession. We can't fight in the courts, but people have power in numbers. Share your experience, share your pain and help warn others about the toxic substances doctors hand out like candy.

YOU call the shots with YOUR healthcare.

I am a 54 year old male who started taking Lipitor about 4 years ago. It seemed OK at first, but over the next several years I began to have increasing amounts of joint pain after exercise. Nor muscle pain, joint pain. And it seemed to be a result of exercise. By the time I stopped it, I was hurting after everything, not just exercise. I felt better within the first two weeks, but it took about 4 months for me to be able to exercise vigorously again. Over the years I seemed to have forgotten how much vitality I used to have. I am a physician, and because of the long lag time until I felt better, I wondered whether improvement might have related to other factors, so after about 5 months I decided to restart Lipitor. It surprised me that after just one dose, I got back all of the joint pain and fatigue when I was at my worst on Lipitor. I was really hurting. Needless to say, I didn't take any more.

Coincidentally, a physician friend of mine who had statin induced polyneuropathy had a similar experience. After his symptoms went away he found that after only one dose the entire polyneuropathy came back.

Stopping and restarting the drug is a way to test the correlation between the drug and the side effect. For such a large spectrum of side effects to recur after only a single dose, it argues that the problems that my friend and I had was due to some sort of immune memory response. I have not seen this in the medical literature.

I am off it now for about 8 months and am able to comfortably play singles tennis and jog - much more energy (and I took 200 mg of CoQ10 a day with the Lipitor).

okinawak so sorry to hear about your daughter. All I can relate to you guys is my personal experience. I was on Norimin for a couple of years from the age of 19. For the last year (up until a couple of months ago) I was on Yasmin. I experienced anxiety whilst taking these pills which I attributed to stress, but since I have been off the pills I am feeling fantastic. I stopped taking Yasmin because I was experiencing other things like pains in my calves, hair loss and getting spider veins, loss of libido (I'm only 23). :-( I decided upon reading other experiences on this page to stop taking Yasmin. I am happy to report back that I am feeling great... Fantastic in fact. I won't say that its directly related to Yasmin as I have no way of proving that. All I can say is how I felt during and after. And for the last three months I have felt greater confidence in my ability to deal with what life throws at me. I am feeling happier all the time, and I think my libido is improving. All the best to you guys, and all those out there worried about symptoms, please go see your doctor!

I was given 40mg Lipitor for elevated cholesterol. I took it until I started having muscle weakness .I am a retired nurse of twenty five years, and knew this symptom was not correct. So I stopped taking the medication and told my doctor of this.He did not protest in any way.My symptoms now include;two torn ligaments, sob,mental deficits, muscle wasting, night sweats, weakness,h/a's, and more. I have not taken Lipitor for two years now. Damage is done.My doctor said it should be out of my system by now. Is this a cover up?

I have no personal experience of Levaquin or the other quinolone antibiotics (Cipro etc.)

A very dear friend was prescribed Ciprofloxacin during the summer of 2004. I am sure that was the reason for his sudden confusion among other things.

His suffering made me look for information on the Internet and I read a lot of books by Peter R. Breggin and Stephen Fried.

Today I just received another one - Medicine Madness ( Peter R. Breggin) and I am happy to say that he has also included a chapter about ordinary prescribed drugs that can cause psychiatric symptoms.

He, for instance, writes about "Antibiotic Madness".

It`s about this very group of antibiotics.

Here are some lines from his text:

"Hardly anyone thinks of antibiotics as potentially dangerous psychoactive drugs but many of them are".

"Levaquin is a member of the quinolones family of antibiotics, a group that is known to cause severe emotional reactions".

The best thing you can do for yourself and the people around you is to inform your self!

I was prescribed a 6 day pack of 4mg Methylprednisolone (Medrol) at the ER for an allergic reaction I was having to a gel that I used on my sking. The Medrol worked great at stopping the allergic reaction. My swelling, pain, and rash began to rapidly clear up. Unfortunately I began to have many side effects. On day 5 I was unable to get out of bed I was so tired and dizzy. I had a headache and mental confusion and unclear thinking. I called my primary care provider on a Sunday to ask if it is okay to stop taking the steroid. She said it was and that it was unlikely the medrol was causing my symptoms. She told me I had a virus. I told her the symptoms I was having were listed as side effects on the drug info sheet but she did not believe me. IA few days later I made an appointment to see a doctor, not the same one who took my phone call. This doctor said all of my symptoms were from the Medrol. She knew because of personal experience she saw in her mother who was also taking steroids. She told me medrol can cause a manic response or a depressive, the latter is what I was having. As part of my exam she wanted me to have blood work but said I should wait at least 2 weeks to allow the drug to get out of my system. It is now 19 days since my appointment and I am still having side effects: nausea, complete lack of appetite, dizzy, and tired all the time. I put a call in to my doctor today and am waiting to hear back. I am sorry that I took this medication, will never take again. How long will it take for this med to get completely out of my system so that I feel normal again?
A friend told me her mother had a manic episode on steroids. When I was younger I took steroids for a brief period and had much milder side effects.

Im a Spanish 22 year old girl who just had my first dose today. I had side effects such as dizziness, nausea, vomiting and sweating.

Can I still take the second dose??Will I have side effects again?Will they be worse?