Garbage symptoms and conditions

Boy, after reading all the negative testimonials on Lipitor, I will throw mine in the garbage. That is what they are meant for. I have severe headache, and muscle pain, and foggy head, and I have only been on the crap for 2 months. I believe a lot of people's health is being ruined, and a lot of deaths are happening as well because of Lipitor and other statins. Mark my word, one day this drug will be withdrawn from the market, and the poor Pharmacutial companies will be in huge trouble.. They have the world convinced that we all need statins to bring cholesterol down.. The era when my parents lived , and lived long lives, and on farms, with butter, bacon, lots of fats, and never heard the word STATIN. I think every one that is writing to this forum and complaining about LIPITOR, should make a phone call to PYzier and tell them your side effects, that is the only way anything positive will come from this forum.. thank you for listening... I have called Pyzier and told them as well.

If you are taking this medicine, STOP! I took this medicine for about three months. I started to feel like I had a congestion. I cough lightly at first then into a hard cough which progressed into a hacking. My wife thought I was critically ill. I was spitting up clear congestion at work into my garbage can. This stuff is bad, I found this site and stopped taking the medicine. It took 3 week for the cough to subside. It’s been about 4 months, and I would say I am only about 98 percent back to where I started . About every 3 weeks I out of the blue start to slightly hack. I know one thing this is not a good medicine. When I started my BP was 138/109. My doctor told me to try this. Because of this medicine I could not do my job and my doctor never told me it was the medicine. When I told him he told me he didn’t think it was the medicine and prescribe some cold medicine

I'm 25, and I have never used bc. I was given this from my gyno. because my bf kept taking off his thingy. So the first day, the very first day my hair started to come out. I gave it two weeks, and threw it in the garbage. I had hair falling out everywhere, I had EVERY side effect listed. My vision was also screwed up. I didn't know what the hell was going on with me. My bf broke up with me, my moods were crazy, my boobs hurt, i had cramps, heavy bleeding, nausea, all i wanted to do was eat food, stomach pains, depression, anxiety, a headache, I was dizzy to the point were I just wanted to start crying, I even had the shits...This pill is a joke. I can deal with minor things like spotting, and I realize it takes 3 months for your body to adjust, but I couldn't even take it for 2 weeks. I did notice that if you take vitamins, the side effects were better.. but still my heart hurt so much I thought, holy crap, I'm going to have a mini-stroke at the age of 25. I am so thankful to god that I found this site and I could read other people's stories. I really think the idea of bc is wonderful, but until they make a pill that my body will accept- I'll stick with condoms, they have worked so far, I would even go on to say, I rather never have sex again then to go through the toll of this pill. This should have never been put on the market.

Most of the "side effects" are die off responses (sometimes referred to as a herxheimer response similar to that which occurs when treating syphillis) from bartonella or borrelia. Levaquin is a potent intracellular antibiotic...where these and other organisms can hide. These can be subclinical infections where (at this time) you are not even aware you are infected. If your "side effects" start around the 3rd day into your prescription...rejoice...and suffer for a while, you are killing something really bad.

I am finally writing after reading these posts since the end of April. That is when I took my 11 year old son off singulair, in an act of desperation. He has been on singulair on and off for about five years for seasonal allergies. He started again in mid-March so it could get into his system, before the allergies started. Immediately thereafter his behavior changed. He was arguing on a daily basis. He would hit, kick or trip me when he was angry. He was starting to destroy things in anger. He seemed to be fueled by anger. It was affecting the whole family. He was starting fights with his younger brother, my husband's heart was palpitating and I was crying every day. I heard about Singulair side effects and looked it up. I saw that it caused behavioral changes and out of desperation, took him off, not knowing what to expect. We had three days of total peace, then on the fourth day another outburst. Then my son told me he had taken a singulair the night before. That was it. I threw every pill in the garbage. He no longers acts like that. It's been almost two months so I am convinced it was the Singulair. By the way, he always complained of headaches, stomach aches and would scream in his sleep. Who knew - it was the singulair all along.

My doctor prescribed seroquel to me for my severe anxiety. I took one b/f bed and woke up feeling horrible. I could barely get myself out of bed, I was foggy brained and lethargic. I thought it would pass so I went about my morning routine, when finally it hit me I couldn't take it any longer. And it resulted in a Full blown panic attack!!!! I took my clonazepam and eventually after sleeping for a bit, felt better.
I threw the pills in the garbage, I will NEVER take them again. I'm so scared to try anything new, b/c of what happened after taking seroquel. However I'm running out of options:(

PRAISE GOD for all of the stories shared on this site. And I've only read page one. My husband called me back today to say that he "googled" Singulair and found some interesting things (to say the least). While we were on the phone, my three-year-old was in the throes of another meltdown, kicking me, hitting me, throwing whatever he could get his hands on. My older two boys, 8 and 12, were ordered, once again, to lock themselves in their rooms to avoid being hurt by him. He will throw stuff, bite, hit, kick, and, at times, spit on us. This disturbing behavior is rather constant lately. He is like a mad man. Very scary.

Caleb has been on Singulair since about age 1, when he was diagnosed with chronic sinusitis and allergic rhinitis. Unfortunately, we initially equated his rages with the onset of "terrible two's" and dismissed his behavior to a chorus of "oh, he's just a boy!" My husband felt, at times, that I was just not disciplining him properly. I intuitively knew, having raised two other boys, that this behavior was abnormal, even for severe tantrums. We received a variety of suggestions from his pediatrician, caregivers, and grandparents, all to no avail. We have several calm days but things always deteriorate back to insanity. He is VERY unpredictable.

Last Thanksgiving, Caleb (age 3) was kicked out of his daycare setting for biting and hitting. Once I witnessed him run as fast as he could into a group of playing children, falling on them, kicking them. He would walk up to sweet little girls half his size and push them down as hard as he could. It was a nightmare. My husband had to take 3 weeks of leave to stay home with him while we prayed and searched for new care. We had him evaluated and he was staffed into the "developmentally delayed" program in our school district (for poor adaptive skills and personal/social behaviors). We recently had his tonsils removed, hoping that some of the sinusitis symptoms and behaviors would improve. They really haven't. This past week we have been looking into the Feingold diet. We have been PRAYING for answers. The last time we spoke with his developmental neurologist, he recommended a trial of Risperdol (sp?). We feel like more meds would be like a band-aid, not a solution. But his rage is becoming unbearable.

So, that brings us to today. I was so moved by your accounts. Unlike so many of you, we don't have much of a "before" to go by. But his "after" sounds VERY much like what you have all described. It's probably the pure rage that I see on his face that is the scariest part. And at the same time he seems desperate and vulnerable. He truly seems to snap. If we had pool chairs, I can just picture him throwing them (citing another post :).

We are going to throw the Singulair away. He will never, ever have it again. Even if this isn't the cause of his problems, I certainly don't want to exacerbate any behaviors with this toxic medicine. I will post again just to let anyone who's interested know if this changes his behavior. I am praying that my entry will help someone else, just as all the other postings have helped me. I have renewed hope.

I have copied many of your comments to a Word document. I will be sharing it with a high ranking officer at the medical clinic/hospital on Keesler Air Force Base. I hope that he will discuss this with his staff and that perhaps we can at least make a difference here. I, too, will be filing a report with the FDA. I can only pray that this medicine has not permanently altered his developing brain.

Hi Everybody, I wrote back in April about my horrible Yasmin experience, and just wanted to update. I've been off Yasmin for almost three cycles now, and although I'm still on blood pressure medication, I've had no headaches, no heart-pounding anxiety attacks, etc. I feel much better all around. Still, it makes me very angry that there are so many women who've had really bad experiences, and this garbage is STILL on the market. I checked the Yaz website, and in the fine print it says you can report your side effects to the FDA by logging on to www.fda.gov/medwatch, or calling 1-800-FDA-1088, SO LET'S DO IT!!!

I'm a 44 year old female, and I have been taking 40mg. of lisinopril for over a year now. I also take omeprazole 20 mg. (a sub for prilosec) every day. Before taking lisinopril, I did have high blood pressure, but since taking this medication, I have had more problems than that. I have an irritating cough all the time and phlegm in my throat so thick that I feel as if I am chocking to death. I also have a severe rash all over my body and on the bottoms of my feet, and on my hands. I am depressed all the time, have no interest in sex whatsoever, and basically feel like crap all the time. I have a very bad pain in the left side of my neck that I know is not a result of sleeping the wrong way. I have to say, I never felt this way before taking this medication, but today I got to the point that I wanted to look up side effects to see if what I'm taking is hurting me. After reading some of these posts, I believe I know what my problem is. My husband was also on lisinopril, but 20mg and had such a terrible cough that we thought he had pneumonia. He is off the medication now, and his cough had disappeared. For me, the rash, and depression is the biggest thing. I have decided to take myself off this medication on my own, and try to find another way to deal with my high blood pressure. If you know of any herbs, and/or foods that help with blood pressure, I would love to hear about them. Thank you all for the information you have posted here. I'm sure it will help others think about what the doctors and pharmaceutical companies are trying to do to us. Seems the more medications they prescribe, the worse side effects we endure. Thanks again everyone!

Oh thank god - I thought I was the only one! I'm on my 4th month of Femcon and am about to throw it in the garbage mid-pack. I bled the entire first month I was on it and now I barely get a period between packs - never mind the breakthrough bleeding that happens consistently in week 2 and 3 of the active pills. . .so annoying. But the worst part is the mood swings - I feel like I'm becoming a crazy person. I have a horrible temper and am normally quite mellow. I can't wait to feel like myself again (and I'm sure my husband and kids feel the same)

I am 33 years old and after a blood test about 6 months ago showed my cholesterol levels high my doctor prescribed me 40MG Zocor (actually generic Simvastatin). Since then I've started to forget things and just cognitively I'm slower and less capable. I also had more aches and pains and a weird creak in my knee showed up, but I really didn't key in on that stuff. I went back to my doctor and told him about the cognitive issues and he said "that shouldn't be a side effect of this drug".Well I am very glad I found this website because at least now I know I am not crazy. I stopped taking that garbage about 4 weeks ago and ever since that fog has been lifting.
I have also made a new commitment to myself to include more "heart healthy" foods into my diet and to completely eliminate all red meats as well. I realize there may be some validity to the studies done remarking that high cholesterol is an indication of something bad, but I am not convinced the medical community actually has a comprehensive understanding of cholesterol in the body. I will still go into the doctor to get my levels checked, but I will probably not go back to my old doctor. I'll probably find a doctor who is a little more open to other options. I hate to say it, but I have lost my confidence in my doctor. If I tried to pull something like that in my job as a computer network engineer my customers would simply say "it wasn't like this before you started". Jedi mind trick doesn't work buddy. My body wasn't like this before you gave me that stuff.

I am a 47 year old male who took 3 days of 10mg singulair ending April the 16th. On the 4th day, I was walking around in a national chain store and started getting severe numbness and tingling in my arms and legs.
According to the info. pamphlet that comes with the drug, this can be a serious adverse reaction.
About 13 days later, I still get episodes of tingling and numbness in different areas of my arms and legs, and now, some areas on my face. My family doctor says there is nothing to be done about it, and my allergist says I may need to see a neurologist. I think the doctors need to go see a neurologist and have their heads examined for giving us this garbage to take in the first place!
Never had any of these problems until a took singulair! Hope these side effects aren't permanent!
Good Luck to you all, and may all of us get healthy again real soon!

My name is Charles and I had a major heart attack in 1998 after suffering through great stress. I now have 4 stents that work pretty well for me although each day without pain is a blessing and I am just not as energetic as I was BHA. My doctor recently told me I needed to increase the good cholesterol HDL and prescribed Niaspan to help. While trying to find a cheap alternative to Niaspan and even where to buy Niaspan at a reasonable cost, I came across this page and found out WHY my back was absolutely killing me. I took my office chair down to the garage blaming it for this pain. At Sunday School this morning I hurt so much I had to roll over on the floor and get up like from my hands and knees. Niaspan I conclude is causing all of the lower back pain. Niaspan's lower back pain I discovered is widespread. This crap should be taken off the market. Niaspan is total garbage and should be taken off the market.

For only three days I have been taking 2 squirts of Nasonex in each nostril once a day. At the end of day 3, I have developed terrible hand tremors (like Parkinson's) whenever I pick up a glass of water or something heavy.
I know it's from the Nasonex because I didn't have this ever before!
It's very scary. Also, I have had really confusing, freaky dreams at night.
It's going in the garbage!!!

Can Statins Cause Chronic Low-Grade Myopathy?
Statins (hydroxymethyl glutaryl coenzyme A reductase
inhibitors) are highly effective drugs for reducing serum
cholesterol and low-density lipoprotein cholesterol levels.
Clinical trials have shown that they also reduce risk for
coronary heart disease events, coronary procedures, and
stroke by about one third (1). Millions of people in the
United States and worldwide are being treated with statins.
In clinical trials and in clinical practice, statins have proved
to be remarkably safe.
The one notable side effect of statin therapy is myopathy.
A small fraction of patients who are treated with
statins will develop severe myopathy (2). In the worst cases,
severe myoglobinuria, acute renal failure, and even death
can occur. The incidence of severe myopathy is low, perhaps
1 in 1000 patients (2). Predisposing factors for severe
myopathy appear to include advanced age, relatively low
body weight, female sex, certain medications, use of multiple
medications, multisystem disease, and acute illnesses
or major surgery (3). If statins were avoided or used in low
doses in these circumstances, it is likely that the incidence
of severe myopathy could be greatly reduced.
Less severe forms of myopathy undoubtedly occur. In
some patients, fatigue and muscle pain and weakness develop
with moderately high serum creatine kinase levels
but not acute renal failure. In these cases, the myopathy
resolves when statin therapy is discontinued.
Still more patients report various muscle symptoms—
fatigue, pain, and muscle weakness—but have normal creatine
kinase levels. These symptoms probably are unrelated
to statin therapy in many patients. In middle-aged and
older people, muscle, joint, and tendon symptoms are very
common. Naturally, if a patient takes a medication that is
believed to produce muscle problems, symptoms are often
attributed to the medication. On the other hand, the major
controlled clinical trials have not detected a higher prevalence
of muscle symptoms during statin therapy versus placebo
(1). This failure of detection has generally led clinical
trialists to conclude that statin-associated myopathy with
normal creatine kinase levels essentially does not exist or
that, if it does exist, it cannot be detected above the “background
noise” of muscle symptoms in the general clinicaltrial
population.
Many physicians in clinical practice nonetheless believe
that they can identify a subset of statin-treated patients
who have a unique set of statin-related muscle symptoms.
Some patients clearly relate the onset of muscle
symptoms to initiation of statin therapy. These symptoms
may abate after discontinuation of therapy, only to reappear
when statin therapy is restarted. The number of such
patients is not large, and thus it may have been impossible
to identify them in large clinical trials.
In this issue, Phillips and colleagues (4) report on a set
of studies in four patients who had muscle symptoms during
statin therapy that resolved during placebo use. Quantitatively
measured muscle weakness also resolved during
placebo use. Muscle biopsies were performed in three patients
during statin therapy and then during placebo use.
Several pathologic changes were seen on biopsy specimens
obtained during statin therapy: increased lipid content of
mitochondria, fibers that did not stain for cytochrome oxidase
activity, and ragged red fibers. The authors suggest
that these patients had statin-associated myopathy with
normal serum creatine kinase levels.
Despite the study’s small size, we cannot dismiss these
observations as random variation in muscle structure.
However, these highly suggestive results are clearly preliminary.
The number of patients was small, and all appropriate
controls were not used. Nonetheless, this study is novel
because it used quantitative measures of muscle strength
and muscle biopsy to address the question of myopathy
with normal creatine kinase levels during statin therapy.
To be confirmed, the current data would have to be
extended to many more patients in whom muscle symptoms
are closely correlated with statin use. Reproducibility
of symptoms during therapy and symptom resolution after
discontinuation of statin therapy would be necessary. A
definitive study would have to be carefully designed and
executed. It would need to be double-blinded and placebocontrolled
and include sufficient numbers of patients to
provide a valid statistical comparison. In addition, investigators
would have to carefully consider the appropriate
selection of patients. The development of a registry of candidate
patients at multiple sites could facilitate a multicenter
study.
Is a carefully controlled, sizable study of this type
worth the investment of time and effort? To date, no evidence
indicates that prolonged statin therapy leads to permanent
muscle damage or progressive myopathy in patients
with normal creatine kinase levels. Controlled
clinical trials attest to the general safety of statins, and
symptomatic side effects appear to be limited to a relatively
small proportion of treated patients. In addition, no therapy
prevents or treats statin-induced myopathy, short of
withholding the drug. On the other hand, statins are being
prescribed to millions of people, and are usually continued
throughout the patient’s lifetime. It is certain that statins
cause myopathy in some patients. For these reasons, a valid
argument can be made for a more extensive study of lowgrade
myopathy in patients treated with statins.
In the meantime, physicians should recognize the great
benefit of statin therapy in high-risk patients and their
documented safety for most patients. For high-risk persons,
the proven efficacy for preventing cardiovascular disease
outweighs the unlikely possibility of permanent muscle
damage. Phillips and colleagues’ preliminary results
certainly do not provide adequate information on the spec-
Editorial
www.annals.org 1 October 2002 Annals of Internal Medicine Volume 137 • Number 7 617
trum, scope, or prognosis of myopathy with normal creatine
kinase levels during statin therapy. For these reasons,
prescription of statins for eligible patients should continue
despite the current results. Moreover, before discontinuing
therapy, physicians should carefully evaluate any patient
receiving statins who reports muscle symptoms. In most
cases, the symptoms will be found not to be consistent
with chronic myopathy, and often they will not be related
temporally to statin treatment. High-risk patients in particular
should not be deprived of major cardiovascular risk
reduction just because they display symptoms not clearly
documented to be closely related to statin therapy.
Despite these comments, the actions of statin on muscle
metabolism and structure deserve further investigation
to clarify the confusing area of low-grade myopathy apparently
associated with statin use in a few patients.
Scott M. Grundy, MD, PhD
University of Texas Southwestern Medical Center at Dallas
Dallas, TX 75390-9052
Current Author Address: Scott M. Grundy, MD, PhD, Center for
Human Nutrition and the Departments of Clinical Nutrition and Internal
Medicine, University of Texas Southwestern Medical Center at Dallas,
5323 Harry Hines Boulevard, Y3.206, Dallas, TX 75390-9052.
Potential Financial Conflicts of Interest: Honoraria (from Merck &
Co.; Pfizer, Inc.; Bristol-Myers Squibb; and Bayer); Grants (from Merck
& Co. and Pfizer, Inc.)
Ann Intern Med. 2002;137:617-618.
References
1. Executive Summary of The Third Report of The National Cholesterol Education
Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment
of High Blood Cholesterol In Adults (Adult Treatment Panel III). JAMA. 2001;
285:2486-97.
2. Staffa JA, Chang J, Green L. Cerivastatin and reports of fatal rhabdomyolysis
. N Engl J Med. 2002;346:539-40.
3. Pasternak RC, Smith SC, Bairey-Merz CN, Grundy SM, Cleeman JI, Lenfant
C. ACC/AHA/NHLBI clinical advisory on the use and safety of statins (1)
(2). J Am Coll Cardiol. 2002;40:567-72.
4. Phillips PS, Haas RH, Bannykh S, Hathaway S, Gray NL, Kimura BJ, et al.
Statin-associated myopathy with normal creatine kinase levels. The Scripps Mercy
Clinical Research Center. Ann Intern Med. 2002;137:581-5.
© 2002 American College of Physicians–American Society of Internal
Medicine
Editorial Statins and Low-Grade Myopathy
618 1 October 2002 Annals of Internal Medicine Volume 137 • Number 7 www.annals.org

I started on Singulair about 7 months ago and I tell you I've been sick all winter with asthma. I've had respiratory infections, bronchitis, etc. I don't smoke at all nor am I around smokers. I've found myself depressed and having suicidal thoughts. My mood swings have been off the charts. I get mad about the most insignificant events and sometimes I even get violent. I've broken dishes and even kicked the garbage can into pieces. I am by no means ever violent but after reading everyone's testimony about Singulair, can my symptoms be a result of taking this drug for 6 months now. If so, Merck needs to be held responsible. I lost out on a 5 year relationship because of my behavior.

READ THIS:
I'm posting this again for the sanity of the concerned parents on this board to let you know you're not alone:

My 5 year old son was diagnosed with mild asthma and put on Singulair. Within a few months he began having uncontrollable fits of rage, displayed self-loathing behavior, had night terrors, and was inconsolable during these episodes. He became very destructive and was a danger to himself and our family. He even talked about killing himself and would say things like "I don''t want to be in this life anymore" and "I want to kill myself". He would threaten my wife and his siblings and told them he wanted to kill them. It was a truly terrifying experience. Our pediatrician was clueless to these side affects and recommended we have our child go through a psychological evaluation. I knew this was not my child''s normal behavior so I searched the internet for Singulair side affects and found some message boards where parents just like myself were telling their stories of their children''s aggressive behavior. I immediately took my son off the drug and within a couple days he was back to his normal self. He told us that he no longer has "that feeling inside of him". Five year old children don''t even know what suicide is and to see my son talk like this was extremely frightening. He is a sweet, intelligent, loving boy who had never exhibited behavior like this until he went on Singulair. We have not seen this behavior after taking him off the drug.

I was prescribed Biaxin for a sinus infection and I was only able to take it for 3 days (out of a 10 day prescription) because of the ungodly taste it left in my mouth. I couldn't sleep at night because the taste of hot garbage in my mouth would wake me up. I tried chugging water, gargling with Listerine - NOTHING helped. It was so disgusting! I will NEVER take this nasty med again!

Okay...I'm really freaked out!!! Just got back from the pharmacy with Singulair only to find my tv bombarded with news on the suicide risks. I'm an adult asthmatic with severe allergies and have always been on Allegra and various inhalers, nebulizer etc.... For the first time, even after requesting allegra, the doctor (specialist) told me to try this new plan instead it consists of daily dosages of atarax, asmanex, xyzol, singulair, and maxair...I feel over prescribed and don't know what to do. All day today I felt groggy and irritated...and at this point want to thor everything in the garbage because I'm scared.

I have been taking this crap for a bacterial infection for 4 days now. I have a history of depression and the dr. never warned me that horrible depression was a possible side effect. I have been horribly and scarily depressed since the second day on this garbage. I have been heaving, had the worst stomach pains- like heartburn mixed with a kick in the gut, dizziness, etc. I was advised to stay the course since I only have 3 days left but I will never take this stuff again.

Well, I am not posting a side effect. I actually stumbled upon this website while trying to look up whether hypoglycemia is a side effect of Levaquin. I am a physician assistant and routinely prescribe this medication. Unfortunately ALL medications have the potential for causing many many many different side effects. Obviously one has to weigh the benefits of using the medication with the risk of side effects. And certain side effects are obviously more common than others. While I appreciate the point of a website like this, it is very frustrating for me, as a clinician, to read someone posting things that are absolutely untrue which can potentially cause undue distress or worry for everyone who may read it. I am referring to the person who wanted "to let everyone know of the relationship between levaquin and vancomycin." Her only source for this WRONG information is a nurse who told her daughter. Did she ever think that the nurse could be wrong and that maybe before posting something like that she should ask a pharmacist or a physician. Vancomycin and floroquinolones are not related pharmacologically!!!!

I've been on this garbage for about 2 months and today will be my last day. Just a bad feeling deep within my body since I've been on it. It's really hard to explain, along with all the other SE's, the terrible soda taste, tingles in feet and hands...I find, for me, stay away from ALL forms of alcohol and no headaches...forget this med!

I have read most of the postings on Yasmin but I haven't seen one where women pointed out experiencing terrible amounts of clots and incredible amounts of actual mensing... So it makes me wonder if I have another underlying condition? I have been taking Yasmin for about18 days now, started on my first day of mensing, and 18 days later, still mensing like there is no tomorrow and passing clots the size of the palm of my hands at times!!! It's unreal! And I went and bought 3 packages, I wanted to finish one and see but I think it's all gonna go to garbage now!! And to say I use to have a 30 day cycle with 2 days of pre-spotting followed by 3 days of actual mensing... some clots but not half as big and certainly not as many!!! Very disappointed with Yasmin. I am done with it.

Very Bad Experience.
I didn't want to take a BCP since I try to not put any medications in my body if I don't have to...now I remember why. This medication has had a very negative impact on my quality of life. I have extreme tenderness of my breasts, I am exhausted all the time, my periods are longer and fairly irregular, the cramping is very painful and more regular than before I took Yaz...but the worst thing is my moods. I'm irritable and anxious and crabby. I am critical of everything my boyfriend does even though he's a great guy. I am impatient and seem to find fault and negativity in everything around me where before it was 'glass half full'. The headaches and blurred vision doesn't help either. I'm going back to my old ways and would not recommend taking this bcp to anyone.