Pharmaceutical company symptoms and conditions

A brief note about "Adderall": this is the trade name of an amphetamines product. It consists of four different amphetamines, such as amphetamine sulfate and amphetamine lactate. However, the "sulfate" and the "lactate" parts are NOT important. The only thing that is important is AMPHETAMINE, regardless of which form. 100% of the effects of Adderall are because of its content of amphetamine, NOT the specific forms of the amphetamine (called, chemically, "salts"). You can get the same effects from generic amphetamine (typically dextroamphetamine sulfate) as from Adderall. The company that makes it claims that Adderall works quicker and lasts longer, but this is mostly bullshit. It is really not significant, and in fact plain old generic dextroamphetamine is generally considered superior to the other forms, including the forms in Adderall. (See the en.wikipedia.org writeup on Adderall for details.)

Incidentally, the Adderall company, facing patent expiration on Adderall and thus more generic competition, is now heavily pushing its new "Vyvanse" -- another amphetamine product with very dubious if any advantages, and indeed probably MORE side effects than Adderall or other amphetamines, and, of course, a much higher price. More pharmaceutical company bullshit! Don't buy it.

Anyway, to return to the main point: Adderall or generic amphetamine makes no difference, except this one big one: The PRICE! Adderall is ridiculously expensive -- typically $1-4 per pill, sometimes even more. This is a total ripoff, since amphetamine is a CHEAP old drug, and the actual cost of 10 or 20 or 30 mgs of it (as in one typical tablet) is negligible, well under a penny. In other words, they ought to sell for, say, $10 or $15 per hundred -- enough to cover the cost of the drug itself (perhaps 10 cents or so) plus all the costs of tableting, bottling, distribution and so forth, with room for the pharmacy's markup. The idea of paying $100 or $200 or even $400 for a dime worth of a cheap old drug is outrageous -- but it happens. It is the greed of the pharmaceutical company combined with the greed of the individual pharmacist that causes this. Pharmacies vary a great deal in pricing, but the producing company also grossly overcharges.

Bottom line: INSIST ON THE GENERIC. Even if insurance covers it and you only have a $5 co-pay. Why? Because the health care system of the U.S. is driving the country bankrupt, and super-high drug costs is one of the reasons. This is one way you can make a contribution, however small, to solving the problem of a medical-academic-industrial-pharmaceutical complex that costs the U.S. well over $2 trillion per year (far larger than the military-industrial complex, and far more per capita than any other developed country). Part of the problem is prescriptions that cost $300 for 50-cents worth of a drug. Be part of the solution.

End of rant. Be well!

Hello Ladies,
I have had my Mirena in for about three weeks now and have had severe migraines since it was place. My doctor prescribed Migraine medication to resolve the issue and as soon as the medication wears off BAM it’s back again not to mention the heart palpitations I been having as well. I never have had any of these issues before in my life. I called the Dr to have it removed and his nurse went on about how wonderful this IUD is and the expense in which mu insurance company paid for. I explained, that I don’t care what the cost is or was and I cannot function with this headaches and taking medication to mask the problem is not the solution either… This morning I couldn’t even get out of bed because of the pain my husband picked up the phone and called the Dr Office he said either remove the IUD or I’m taking her to the emergency room… Hmmmmmmm….. Low and behold it came out this morning and I’m feeling better already.. Ladies, listen to your bodies and if something doesn’t sit well with you on this IUD then I suggest having it removed. For the bloggers on here that say it’s a God send that’s wonderful and I hope you continue to well with it for those of suffering each and every day it has not been a God send for us. I have to also say I wonder if these bloggers saying it wonderful are from Dr’s offices or the pharmaceutical company itself. Just a thought!!!!!

I have received a Kenalog injection (40 milligrams) in my right hip. After a few weeks passed I noticed my hip starting to "cave" or "dent" in. It is dented in so much now you can feel the bone. I appreciate the other posts regarding this drug because I was starting to think there might be something terribly wrong with me. I would love to hear any more updates on the side effect of this drug and what is being done to remedy them. Will the pharmaceutical company be liable?

The experience is not with me, but my daughter, who is a sufferer of PCOS and experienced acne problems She's been on Ortho Tri-Cyclen Lo since January 2007, and received positive results for acne and regulating menstrual cycle, with minimal side effects. Since being switched to generic tri-lo sprintec (July 29), she's experiencing lethargy, some headaches, moodiness, acne, and slight depression, which is very unlike her. What I recommend to everyone on this website is to submit adverse event to the pharmaceutical company, Teva. They should have a website and or a call line for presenting your concerns. I will be doing this because this drug definitely needs to be reported and possibly pulled from the market.

I'm so glad I found this site, I only wish I'd found it 2 weeks ago before I had this wretched thing fitted. I had my Mirena put in 10 weeks after my little girl was born as I was told it was safe to use whilst breastfeeding. That was on Friday 28th August '09, it's now Tuesday 8th September and so far I've experienced:
head aches, I don't normally get headaches
fuzzy vision and tension right across the front of my head, eyes and upper face,
severe cramping
constant bleeding, not particularly heavy but still
extreme fatigue when I was getting back to stage after a difficult birth where I felt like I had enough energy to resume my otherwise vigorous exercise regime
constant lower back pain
swelling in my hands and feet so I cannot remove my rings, they were loose before.
bloating in my stomach so I can't even get my maternity trousers fastened!
feeling of anxiety and can't be bothered to do anything which is very uncharacteristic
depression to the point of crying ALL DAY yesterday, I never cry, not even when Bambi's mum got shot!
no libido whatsoever, what's the point in this thing if you don't want to have sex anyway?!?
falling hair and bleeding, sensitive gums
a dull ache over my whole body
and last but not least I've put on 9lbs in 10 days, I'm supposed to be trying wedding dresses on in just over a week, that wont be happening now!!!
If I can't get this thing out myself this afternoon I'm going to the doctors to have it taken out tomorrow!!!
I feel like I'm going mad, I've felt like this before (though never to this extreme) on the pill and the depo injection all of which contain levonorgestrel, coincidence, I don't think so! how on earth did this drug get licensed?!?
My fiance is a chemist and works for a big pharmaceutical company and said that although the dosage of the drug is much smaller, because it's absorbed locally it has a much more potent effect on the body than the pill because a great deal of the hormone in the pill will be broken down in the stomach before it's absorbed into your system, they don't tell you that on the leaflet do they! I'll be switching to condoms until I'm no longer breastfeeding and then back to a non levonorgestrel pill. I CAN'T WAIT TO BE BACK TO NORMAL and it's only been in there for 10 days!!!

Love Levaquin. I am allergic to Erythrymicin and Penicillin. Levaquin is the best thing for me. One of the only antibiotics I can take. I thank god for it all the time.

My teenage daughter was taking generic Wellbutrin (manufactured by Watson pharmaceuticals) 150 mg. daily for about 3 weeks or so and started having serious hair loss on the top of her head. The prescribing psychiatrist told her to stop the medication and after about 2 weeks, the hair loss has stopped almost completely. I have read a number of blogs including this one that indicate that hair loss is a side effect yet the Wellbutrin trials only listed hair loss as a side effect for less than 1% of patients. Given the U.S. Supreme court ruling today that says that even if the FDA has approved a medication, a pharmaceutical company is still responsible for fully reporting side effects and can in fact be sued in individual states if they do not provide sufficient warning, I would be interested in hearing ideas of how we can put more pressure on the manufacturers of Wellbutrin and its generic equivalent so that they give better warning of this side effect.

March 3, 2009
I returned to the doctor today to get a different antibiotic because Avelox made me worse off than the sinus infection I had. I stopped taking it about two weeks ago and still have side effects from the drug. My doctor had given it to me about two other times. The last time I recall was in November. I didn't finish taking my prescription then either.
I thought maybe I was having flu symptoms also, but it was the drug making me more ill. RASH, HIVES, RED HANDS, SWOLLEN TONGUE THRUSH, BUMPS ON MY TONGUE, TINGLING IN MY BACK, VOMITING,HEADACHES, PAIN IN MY STOMACH NOT LONG AFTER TAKING A DOSAGE. FREEZING HANDS, THROAT FEELS LIKE IT'S CLOSING UP AND DIFFICULTY SWALLOWING, COULDN'T GET OUT OF BED, MUSCLE FATIGUE, ACHES WEAKNESS, JOINTS HURT, TINGLING IN HANDS, ANXIETY,CRYING SPELLS, NIGHTMARES, SKIN SENSITIVITY, INSOMNIA, THEN EXTREME FATIGUE, DIZZINESS AND LIGHT HEADED UPON STANDING AND/OR GETTING UP FROM A SITTING OR SQUATING POSITION. EVERYTHING HURTS ALL THE TIME IN EVERY MUSCLE...... I BASICALLY FEEL LIKE I AM DYING.
My fiance thought I was totally losing my mind. I was moody, aggressive, irritable, depressed etc... I felt like like a different person.. My fiance of course got sick also and his doctor prescribed it to him. His side effects included muscle aches and pains and extreme fatigue and mood swings. I looked up some side effects when I was started taking it a few weeks ago, but didn't pursue the research until the side effects got worse. I took it for 7 days this time. My fiance took it for three days. I called him at work after seeing this website and told him to stop taking the medication immediately. I am still sick with a sinus infection, and a whole slew of other crap going on. I called the doctors office and went in right away to get a different medication. To no avail, when I went to my doctors office there was a rep from Avelox there. I said don't give that Avelox to anyone sarcastically. I then saw his tag on his shirt and his bag full of Avelox samples. He asked what type of symptoms I had and I told him.. He said he would report it to the company.... What do you think they will do about it? MOST LIKELY NOTHING. I am an educated person with the capability and time to research anything I need to and I will do my best to dig up the most dirt I possibly can about this horrible medication. They need to stop pushing these meds on doctors to give us and make us more ill than we were to begin with. I JUST HOPE MY AILMENTS AREN'T PERMANENT. People try to make light of the situation because they don't want to be sued. I think the FDA needs to be revamped and the Government should stop letting these pharmaceutical companies poison us. I AM NOT EXAGGERATING EITHER! DO NOT TAKE IT.
I have been going to my doctor for about fifteen years and she never gave me any medication that had made me this ill. I get samples a lot because I have no insurance. Sometimes she gives me scripts. Today I got Zithromax which always worked well for me in the past. Very little side effects. I realize that everyone reacts differently to certain meds, but come on now! It isn't just a coincidence that all of us commenting and complaining here are imagining these horrible side effects! Today I got Zithromax which always worked well for me in the past. (Very little side effects).Then why did I ever have to take Avelox if there are other antibiotics that will make me better not worse. They push these meds on doctors to give to us that's why! I always trusted and admired my doctor. She always treats me well and does right by me. What is going on with these medical companies?! SOMETHING HAS TO BE DONE ABOUT THIS!

16 days ago on Jan 17, 2009 by chris555, #16131
Sorry to disappoint you, but I have no vested interest in Merck or any other pharmaceutical company for that matter. What I have a vested interest in is providing some balance to those parents who come to this blog site and are scared to death. That is what happened to a very good friend of mine. After reading the posts here, she was so panicked she took her 12 year old off Singulair. A kid who had no problems on it by the way. A few days later my friends kid was rushed to the ER and almost died from an asthma attack. That is what I have a problem with. People here telling others the side effects will creep up, that kids should stop their medication right away, etc.

Reply 8 minutes ago on Feb 03, 2009 by concernedcitizen, #16701
To chris555:

Merck warns on it's Singulair website that Singulair is not an effective replacement for fast acting inhalers in the event of sudden symptoms. Originally when Singulair was developed it's purpose was to prevent damage and inflammation that is caused by excessive number of eosinophils in respiratory tissue. There is no evidence at all that Singulair is effective as the only treatment for asthma to prevent or treat acute asthma attacks. And, Merck makes this very clear in the warning notice.

The efficacy and safety of Singulair has a genetic component. That means that it is entirely possible that some people are not compatible with the way in which Singulair works. Adverse side effects are very possibly the result of compatibility problems.

Sadly, Merck has succumbed to the disease of "corporate greed." Meaning that they care more about profitability and the shareholders than they do about the patients. For this callousness, some day this corporation will suffer the punishment. Merck has always known that the cysLT1 receptor is a gene with more than several variations. If they told doctors to watch out for side effects due to genetic variations, then they wouldn't be able to sell this drug like it's harmless - cherry chewable - candy. The adverse side effects are real. Patients started reporting them immediately when the drug was released. Singulair is dangerous to people with gene variations and it causes unnatural biochemical events to take place.

IMPORTANT SAFETY INFORMATION
SINGULAIR will NOT replace fast-acting inhalers for sudden symptoms. You should still have rescue medication available and continue to take your other asthma medications unless your doctor tells you to stop.

I take the Lisonopril and HCTZ and within a few days, I started experiencing dizziness (bad case of Vertigo), fatigue. My doctor took me off. It has been a week now, and I am still suffering from the side effects. Crappy I tell ya! I won't take that stuff anymore. God will just have to take me, because I am done. A co-worker told me her doctor prescribed it, but her grandmother said take Ordorless Garlic tablets. That was a year ago. No more High BP. I am trying that. Won't hurt.

To get the real information in regards to what level of research that is going into this investigation is.go to the Institute for Safe medicine practices click on Quarter watch.
To people like chris555, I believe you are engaging people for sport and say very hurtful things,your day will come and it may just be in the unemployment line.I can only imagine that you must work for Merck or you would not feel so threatened by the good that has come from Parents advocating for their childrens safety.I want you to know, that all who knew our family and our child understand what took place and our reasons for trying to get the proper information where it should have been," on the label". When our child died no one knew about all the added side effects from post marketing reports,which is "a reliable way to track a drugs adverse events".Maybe you should do more research on the legitimate information of causal relationship. Don't be so afraid of a possible drop in revenue for the drug company that I believe you might be an employee of.K. M.

I am 34 years old. I am a pharmacy tech. I have asthma and allergies. I have taken singulair pretty much every day since it came out on the market. I've had asthma since i was about 10 years old. I took theophylline as a kid. Steriods on and off especially during times when my allergies are bad. I still use Advair during the fall and spring. Every drug has a side effect. However breathing is pretty good damn thing. Do I have days when I feel low? Yeah. Do I sometimes have nightmares? Yup. Are "natural" products the answer. Not always. The fish oil that some of the posters are touting can also cause GI problems. Some of the natural products contain herbs and other plant derivatives that can be harmful for a child that suffers from allergies. Not proactively treating asthma can be deadly. Some of the parents are suggesting steriods as the answer - those can cause weight gain, growth suppression and can lead to a worsening of asthma.

Singulair has never made me feel like I've wanted to kill myself. I was more depressed and angry as kid when my asthma did not allow me to partipate in normal childhood things. I was sad and hated life when I couldn't keep up with friends at recces because I was having trouble breathing. You have to outweigh the costs with the benefits. I am more irritable when I have asthma flareup then I am on a normal day. For me, I choose to breathe. And singulair has been helping me for almost a decade.

I'm not saying the medication isn't causing these symptoms but maybe there is an underlying cause to your child's depression.

Any drug has a side effect. But without medical research and the medications that come with them - people would still be dying of simple diseases and we wouldn't have vaccinations. As a society, as a whole, we are a culture that looks to someone else to fix things and then blames the people who try to fix it. We need to stop being the "hot McDonald's coffee'" society.

The medical professional is particularly unhelpful in this matter. Talking with medical personnel about fluoroquinolone poisoning is a go-nowhere exercise. In an era when Monsanto genetically-modifies our seed stock you might think medical caregivers would advise us in advance that their prescription antibiotics mess around with their patients' DNA. (IT's that deregulation thing, yes?)

I experienced painful calves and a strange dream, possibly a nightmare, immediately, e.g., on the very same night, after having injested one Levaquin dosage for a prostate condition and maybe a year after separately having taken cipro for a week to combat traveler's diarrhea. The post-Levaquin early evening dream was strange insofar as I rarely drempt, and I never recall having been roused to wakefulness by a dream shortly after having gone to bed. Early on I did NOT associate Levaquin with the really terrible symptoms that I experienced within 60 days of having injested Levaquin.

My wheels fell off when I entered a period of insomnia. I thought my sleeplessness was stress-related because my health history includes a major depressive episode 11 years ago. I presented myself for help to a psychiatrist who prescribed a small dose of an atypical antipsychotic as a sleeping aid. My drug-induced sleep felt like a coma that lasted each night for a couple of hours. There were heart palpitations, agitation, panic attacks, racing heart, racing thoughts, insomnia, depression, paranoia, poor cognition, body shuddering, muscle twitching, night sweats, and pain in both Achilles heals. The symptoms filled a note book page. I felt like Jean D'Arc who was being burned chemically at the stake from the inside out. I would rise in the morning and then minutes later fall back into bed. I could stare off into space and completely lose track of time. I could not even find the right words in mid-sentence. I could not fill-in the registration papers when I presented myself for a second opinion at Mayo Clinic. I became a full babbling idiot. My wife said that I had retreated or devolved into some kind of primate or ape who communicated solely his emotional states by means of eye contact only.

I asked my doctors if the sum of levaquin and cipro had pushed me over my peak quinolone tolerance level. Or was it the medicine that the psychiatrist had prescribed to make me sleep? . I was no stranger to depression and I knew my symptoms were not merely emotional or psychological in nature. Why did I always feel as if I had been poisoned? The psychiatrist decided my paranoia warranted higher med levels. I declined the advice and stopped taking the meds altogether. My anxiety today is lower, my sleep is improved but fitfull. My neck aches. My head feels as if it were in a vise. It's not a headache and it's not painful, but there is a tingling, crawling, scorching sensation at my forehead and behind my eyes as if someone had beat me with a pillow and then filled my head with novocaine.

I'm not sure there's a moral to the story. It might sound a tad over-the-top, but I think we're faced by a pharmaceutical plague. There's really no excuse for the absence of informed consent. There is nowhere above ground, e.g., nowhere on main street, and no-one with whom you can speak in order to take the full measure of fluoroquinolone poisoning. If you are at this URL merely to find out about the FDA's recent black box warning re: Levaquin's link to ruptured tendons, you are in for peep into hell. Read the other thousands of postings on this site, and decide for yourself who bears the ring of truth.

I am a male 55. Started taking Altace 15 years ago. BP kept creeping up. I work outside for a living. Sometimes work is very hard, climbing mountains, carrying land surveying equipment ect. Dr started me on lisinopril 40 mg, dropped altace which I had been taking with HCT 25mg. Started getting numbness in left hand and charley horse in elbow after playing mandolin for 10 minutes. I thought this strange. Now I have muscle cramps in legs and I am wiped out when I get home. (thought must be getting old) Then other joints, shoulders, and knees stared hurting and lower back. Started thinking what has happen to me?! I am completely falling apart! That's how I found this web site. Now I wonder, snake venom sounds about right. I had started thinking I had been poisoned. Guess I'll make a DR appointment or move to an "old folks home". At least I won't have a stroke.......right?

Hi All,

I was diagnosed with dermatologists when I was 14 years old and put on very high dosage of prednisone to get my disease under control (40 mg a day at the beginning). My muscle enzymes were out of control (CPK was almost 8,500 when it should be less than 215) and I was barely mobile, huge amounts of weight loss, alopecia, Raynaud's, etc. That was 11 years ago and I am now almost 100% better. Prednisone saved my life, but the side-effects were TERRIBLE! Especially for a girl going through puberty. Kids at school don't understand you're sick, and they can be extremely cruel. Luckily for me a large number of my family members are in the medical profession all over the world and my parents were able to pool knowledge to find the best treatment for me without all the horrible side effects. An uncle in Germany suggested I take a Prednisone alternative widely available in Europe called Diflazacort. This medicine is not available in the states apparently because the FDA thought it was exactly like Prednisone so was unnecessary. I'm sure this is some pharmaceutical company lobbying to preserve Prednisone's monopoly on inflammatory diseases, but regardless it makes finding Diflazacort difficult for Americans. This is a HUGE shame since this medicine gave me ALL of the benefits of Prednisone with NONE of the side effects. My mood swings, water retention, increased appetite, hazy brain, thinning skin, etc etc etc ALL stopped with Diflazacort. This wasn't only true for me either. A family friend had been diagnosed with Crohn's at the time and he was put on Diflazacort from the beginning of his treatment after seeing how I reacted to it and NEVER had any of the negative side effects I had to deal with. Really this drug was like a miracle for me. Prednisone prevented my sure death, but Diflazacort gave me my life back in its entirety. I've now been off of any steroid for 7 years and my muscles are fully back to normal. Some of the fat deposits Predinose caused still linger, but to most people's eyes I'm totally back to normal. I wish I could find everyone having problems with Prednisone side-effects and tell them about Diflazacort. Even though it isn't available in the states (although I heard recently they are trying to get it approved again since a number of studies showed Diflazacort is much more effective treating Crohn's than Prednisone is) you can get it on the internet or if you have doctor friends abroad as I did. I'm always wary of buying drugs over the internet since there's no control so I would suggest contacting doctors in Europe or Asia directly or through your doctor here in the states. Anyways, I wanted everyone to know that some people do get better and I wish you all the best of luck!

Hi All,

I was diagnosed with dermatologists when I was 14 years old and put on very high dosage of prednisone to get my disease under control (40 mg a day at the beginning). My muscle enzymes were out of control (CPK was almost 8,500 when it should be s no control so I would suggest contacting doctors in Europe or Asia directly or through your doctor here in the states. Anyways, I wanted everyone to know that some people do get better and I wish you all the best of luck!

I already had my side effects written here and I wanna thank to the person that started this web-site.
AND
If anyone decides that there is something we can do against the pharmaceutical company that is keep making this pill - let me know because I'M IN!!!!!
Let's see if we can stop this one way or another.
Yasmin is on of the most prescribed birth control pills. In Europe, 14 GIRLS DIED BECAUSE OF YASMIN, one last week, a 22 years old from Croatia. Imagine how many others could have died and no one knows the reason!

Hi Ladies- I promised I would post to let you know how I am doing WITHOUT Aviene. I posted the Sept. 10 comment entitled Thanks ladies because I felt your posts have helped me.

I stopped taking the Aviene on a Thursday and all side effects stopped and no new ones occurred. All is well, I enjoy life without being a freak show.

In a DAY AND A HALF WITHOUT AVIANE MY HEALTH RESTORED.

I mentioned the 20 pound weight gain within a few weeks, by the following Tuesday I lost 9 pounds and today is the 26th and I lost 15 pounds. No anxiety, no irritation, no face issues (in a week it cleared up), no mood or energy issues, no excessive thirst, burning of eyes, chills, fever, rashes, itchy -nothing. I was allergic to it and my body wasn't breaking down the coloring agents etc whatever the hell is in there b/c it's not like you get a box or product descriptions. This isn't personal comments, I spoke with pharmacists, doctors, doctor friends, nurses etc. I work at a hospital I have great resources to share with you.

Whatever your side effects are, let's do this. Let's listen to our bodies, listen to experiences and draw your own conclusions.

I know my body, I know myself, and I know my life changes, mood changes, physical changes were due to this pill.

Please consider when being worried about what will happen if you quickly go off it that the consequences of staying on it are more severe. For me, and for many of us, the side effects didn't stop but kept adding and if you are reading this and are just curious or feel something is off with you do not take it any further. I am sharing that I am not a sensitive person and do not experience side effects... and I completely broke down physically and mentally from the amount of side effects and had to self defend.

Many of your comments helped and let's face it if you read that some ladies lost their hair... come on... obviously something is wrong with this pill.

Take care ladies, my sincere hope is that my post will help you, as you have helped me.

So you know, I went back on Alesse and all is well. My drug company didn't cover Alesse but ALESSE HAS A PATIENT CARD FOR THOSE WHO DO NOT HAVE INSURANCE AND FOR THOSE WHO DO BUT THE COMPANY DOESN'T COVER ALESSE RATHER THE GENERIC AVIANE. Your patient Alesse card you get will cover the difference that your insurance company may not. I paid $ 2.89 for my monthly prescription which is less than if the insurance company covered it. Check with your pharmacy location site if they participate in the program and it is not hard to find one that does.

You may not like Alesse, I can only share my experience with Aviane that did make my life a living hell. Happy to be OFF it!

Please take care and self defend your situation and reach out to those around you.

My 6 y/o daughter has been taking Singular for approx. 2 years. She began to have regular stomach pains shortly there after. She was sent to Children's hospital where they put her on a laxitive which made things worse. Then we began testing for food allergies only to find out that she tested positive for a 3 page list of foods. We eliminated those food and had her tested again. She was subsequently allergic to the foods we eliminated. She was recently down to rice, a few meats and some vegetables. Guess what, she is now allergic to those foods.

All this time she has been complaining of severe leg pain, eye pain, throat pain, numbness and tingling in her hands a feet, all of which come an go. I have reported this to all the doctors and specialists we have seen. She had undergone countless blood tests to rule out autoimmune disorders and all come up negative.

She began to develop severe anxiety and just had the blues most of the time. She would be crying and saying off the wall things like, "I don't think my fish is happy". She couldn't stand to be away from me and would stress out about even weather or not she would sit by me at a restaurant. I mentioned this to all of the doctors. They said to not make too much of it. One suggested she see a psychologist. NOT ONE DOCTOR EVER LOOKED AT THE SINGULAR.

Finally about 4 weeks ago my neighbor who is a scientist at a pharmaceutical company called me and told me about the "black box" warning that had just come out on Singular. I took both of my children off of it immediately. My daughter went through about a 10 day period where her anxiety got worse and then it was just gone. We are adding foods back into her diet and at this point she has not had any severe allergic reactions.

The last 2 years have been a complete nightmare for her and for us. I am a medical professional and I have had doctors treat me like a hypocondriac, hypersensitive, attention seeking mother. I feel so justified and saddened by the recent findings all at the same time. Most of all I am so grateful that we figured this out before things go even worse.

Please let me know if anyone else is suffering food related reactions as a side effect.

Just had mine inserted..it wasn't a pleasant experience at all as my cervix kept tightening up. I didn't feel well the rest of the day, cramping, bleeding, and fatigue. Better today. I hope I don't develop further problems/
What surprises me about this site is that many of the things you are describing are listed by the pharmaceutical company and the FDA as warnings and precautions as well as possible side effects. My doctor went through all of these step by step with me. I have a follow up appointment in 4 weeks and then another at 12 weeks then annually...all to check the device.
Yes, it is terrible that you had to go through these things, but this is a foreign device that is inserted in your body to deliver progesterone...if you are breast feeding, this will get to your infant; you are at risk for an infection; you are at risk for it to move/dislodge; it is a hormone and you may have adverse effects; it shouldn't be used if you have fibroids; immediate postpartum use is cautioned.
I am glad you are sharing your experiences, but I think it would be even more useful to report them to the FDA. Thanks.

I have been reading all of these posts and have another question. I hope that someone can help. My daughter, 8 years old, has been on Singulair since she was 4. She is normally a very happy girl with a wonderful disposition. For the last year or so, she has been having trouble getting herself to sleep at night. She says that she hears things in her head such as ringing or "noises". A few hours before she knows it's bedtime, she cries and when we ask her why she's crying, she can't give us a reason. We initially thought that she was crying for no reason because she didn't want to go to sleep. I remember reading about the side effects of Singulair causing mood swings, etc., but her's are not violent mood swings. Just very emotional and has a hard time coming down from the "episode". I'm at a loss...I have not talked to her doctor yet about it, but have told her that we will make an appointment this week to discuss it with him. My husband suggested that maybe it sounded like she was having a panic attack or anxiety attack. I hate to label her as that at such a young age. My mind now goes back to the side effects of Singulair and maybe this is to blame. Any help or suggestions would be greatly appreciated. Thank you! Concerned Mom

Please contact me if you would like to help by sharing your story with the media,I am looking for stories of recovery after stopping the medication.Please use my private email under kate2 or just reply under this posting.Kate M.

I am a 47year old male.I,ve been on simvastatin for about 10 weeks now and have been experiencing mild short term memory loss for a few weeks. I put this down to the onset of old age?. I,ve also been getting spurious pains to elbow and finger joints? could these problems be associated with the medication?.

In my previous message I was wondering why the same medication has to have so many different names.

I haven´t had a reply to that, but I found some information on Wikipedia that migth be helpful when looking for more information.

Zocor (=Simvastatin) can have many different names as you can see below.

"Brand names: Zocor, Zocor Heart Pro, marketed by the pharmaceutical company Merck & Co. and Denan (Germany), Liponorm, Sinvacor, Sivastin (Italy), Lipovas (Japan), Lodales (France), Zocord (Austria and Sweden), Zimstat, Simvahexal (Australia), Lipex (Australia and New Zealand), Simvastatin-Teva, Simvacor, Simvaxon, Simovil (Israel), Simvotin (India) and other."

I don't think that anyone can predict a time frame for getting over an adverse drug reaction. Below is my opinion but I see a lot of evidence that it is basically shared by other people maybe not exactly as I state it.

Adverse drug reactions deplete many essential nutrients from our systems. Inflammatory response is very stressful on the body. It is sometimes a very big effort to work on the diet to put back what has been taken away. It can take a long time.

Quinolines particularly deplete B-vitamins, folic acid (B-9), calcium/magnesium/zinc and omega-3 fatty acid. Sometimes the blood-lab work shows elevated homocysteine which proves that the body has suffered inflammation. Cardiologists now use homocysteine levels to show whether someone is at risk for heart disease due to inflammation. Deficiencies of B-6, B-9, and B-12 are known to cause elevated homocysteine.

Here is the pharmaceutical company ZINGER. Now companies such as Merck and Pfizer are going to offer niacin products to lower cholesterol. Well, yeh, duh !. All of these drug reactions are causing depleted B vitamins which elevate cholesterol. Then after they have tried to kill us by depleting our B - vitamins, they want to sell us another pill to give the B vitamins back to us. How many people out there are on some kind of a pill with side effects that cause inflammation? What a business? It is win, win, win.