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200 Side Effects posted for aol

April 7th
2009
2:57 PM

You Can Now Boost Your Thyroid Function,

Eliminating Your Most Troubling Symptoms…

Without A Prescription and Without

Begging Your Doctor!

How? By adding a simple but vital supplement to your diet: Iodine.

Just how important is iodine? Consider this… about 25¢ worth is all that stands between an infant developing normally and one that’ll be severely mentally handicapped the rest of its life.

Iodine is essential to a proper functioning thyroid. But as we grow older, our thyroid starts slowing down. It just can’t metabolize the iodine it needs as efficiently, and that means the hormone produced (also known as thyroid) goes down as well.

There are 2 other reasons why most of us are iodine deficient:

Inadequate dietary intake, and
Exposure to toxic substances that displace iodine.

Iodine is a mineral, but one that is not abundant in the food we eat. Primarily found in very small quantities in seawater, soils are naturally deficient in iodine, especially the further away you get from the ocean.

Iodine is also fairly easily displaced from your body by toxins called toxic halides… fluoride, bromine and chloride.

Fluoride is by far the worst culprit. Found in toothpaste and in your water supply, every time you take a shower, brush your teeth or drink from the tap, your body gets a little exposure to fluoride, leeching out good iodine. And contrary to popular belief, fluoridated water is actually rather poor at preventing tooth decay.

Why is it in our water supply then? Poor science combined with corporate greed and political ignorance paved the way. Basically a toxic by-product of aluminum production, fluoridation was sold as a way to prevent cavities because some areas with natural fluoride in the water also had lower instances of tooth decay. Based upon that spurious observation, fluoridation began.

If You’re Human, You’re Most Certainly Iodine Deficient!

Because of these factors, 96% of all people tested are iodine deficient! This according to a study of 4000 patients conducted by Dr. David Brownstein, Medical Director for The Center of Holistic Medicine, and renowned author of several books on hormones, iodine and hypothyroidism.

The World Health Organization also concurs, estimating that 72% of the world’s population is being affected by iodine deficiency.

This trend is worsening. Over the last 30 years, the NHANES (National Health and Nutrition Examination Survey I) shows iodine levels have dropped 50% in the U.S.A. alone.

-- By fernando111 | Reply | (2) replies | Private Message me

January 13th
2009
10:36 PM

I was on Loestrin 24 for 9 months and thought it was wonderful....until I was recently hospitalized for 2 weeks with blood clots in both lungs. The doctors determined that it was the Loestrin. If anyone knows of a class action lawsuit against them, please let me know.

-- By ksearcy | Reply | (14) replies | Private Message me

December 13th
2008
10:37 AM

My 7 year old female Siberian Husky, Niceah is suffering with her second serious flare-up of IBD. She was taking 20 mgs. of prednisone every 12 hours for several days. We are now down to 12 mgs. daily and working towards 12mgs. every other day. She is lethargic and her body and belly have swollen frightfully to the point where it is difficult for her to lie down without grunting and sighing. She pants heavily. She drinks and eats constantly. Her nose is dry. Her tummy grumbles all day and night. I have been boiling chicken breast and mixing it with sweet potato and Enzymes & Probiotics. I am currently working with a holistic advisor concerning Niceah's diet once she has weened off the prednisone. The side effects of this drug are frightening and I am so worried that something more permanent and damaging will occur. Has anybody experienced this?? If so, I would appreciate any advise. Robin. copher370@aol.com

-- By copher | Reply | (13) replies | Private Message me

November 6th
2008
8:18 AM

I have been diagnosed with a pericardial cyst and thought that the problems I have been having were related to this.....until I found this site! I have been taking omerprazole for over a year now and have had several disturbing symptoms. Heart palputations, racing heart, night sweats and hot flashes, sudden onset of nausea that lasts for about 5 to 10 minutes then goes away and horrible chest, back and rib cramping, which is the same feeling as having a severe gall bladder attack. Recently the worst has happened. In the past I have had the sweats thinking it was only menopause and chest pain thinking it was the acid refllux. We shall see....as of today I am stopping the drug to see what happens. In the past week the most severe problems have occured. I started with bronchitis and the antibiotics and prednisone the doctor put me on seemed to be having side effects which I have never had before with them. The only other medication...omerprazole. (haven't had bronchitis since BEFORE I started taking the omerprazole) After the first day I began having severe chest, back and rib cramping which seemed to worsen by the day, more so that ever before. Then came the swelling in the hands and feet until they looked like I had elephantitis. There is aching somewhat in my arms with a strange weakness. And...the heartburn became so bad that I feel like it's coming out of my mouth. So..the doctor increased the omerprazole to 40mg or up to 80mg if needed. I have been taking 40mg and it didn't seem to really cure the reflux! So I was going to increase it. Not now! I believe after reading all the posted side effects everyone has been having, most of my problems are being caused by one thing....omerprazole! I was truely believing I was having a heart attack, but since I just had ALL the tests done and was given a clean bill of health and better with the exception of the pericardial cyst, I couldn't believe this to be the problem, so back to the doctor I went. She has put me on motrin for the pain and skelaxin for the cramping which seems to be helping. But, and this is the big but, I am going to come off the omerprazole and see if this will begin to eleviate the symptoms completely. Will update this in a couple of weeks when the drug is totally out of my system. Thank-you for this site and keep posting.

-- By lynnsvoice | Reply | (2) replies | Private Message me

May 26th
2008
7:51 PM

My doctor failed to catch pneumonia in time when I was 13. It cause irreversible lung damage in left lung. I have had to take prednisone for 41 years now. I now have a cortisol insufficiency, hypothyroidism, and IGA, IGG immune deficiency. Although prednisone saved my life; it has now damaged master glands. I have heard it can kill you if taken over a long period of time because of it's immunosuppresive properties. People need to know this and the drug companies still push it as an anti inflammatory.
I use natural cortef for replacement of cortisol insufficiency.
Who makes prednisone? Be knowledgeable about alternatives and don't be afraid to ask the doctor for something that is more natural to what your body makes!!

Sincerely,

Nancy L.
***

-- By nleer | Reply | Private Message me

May 15th
2008
11:34 AM

Hi. I am so sorry to read your story. My 17 year old daughter’s story is similar. She had her second Gardasil vaccination during the end of January 2008. During the month of February and March, she had abdominal problems. Beginning on March 30th, she had seizures. She had a CT of the head, MRI of the brain, EEG, 24 hour EEG and as I type this note, she are in the epilepsy center at Jefferson Hospital in Philadelphia and the doctor just came in to tell me that every test is coming back normal and that my daughter is having “stress” seizures. My daughter has no more stress than any other 17 year old girl does.

I related to the doctor my thoughts pertaining to Gardasil and I feel as though he has dismissed my idea.

I have found some many stories similar to yours and my daughter’s but I believe because Gardasil is so new, nothing is coming out yet about it.

If anyone has any other information, please advise!! We are desperate here in Philadelphia.

Jodi
***

-- By jodispeaks | Reply | (6) replies | Private Message me

May 12th
2008
3:26 PM

Hi Everyone,
I just spoke to Sarah Sellers from the FDA ,she seems to be working hard on the review of Singulair.She has received a lot of good information from all who contacted her.She now needs reports on completed suicides or thoughts and attempts, to further her investigation.The email address is sarah.sellers@fda.hhs.gov Please if this drug has had these effects on you or a family member report this as promptly as possible.Thank You Kate Miller

-- By kate2 | Reply | (3) replies | Private Message me

April 10th
2008
6:43 PM

had a sinus infection after a cold- z pack did not work - was given prednisone and 21 days of avelox - after 7 days had a lot of dizziness and lightheadedness - feeling hot and warm - tongue feels hot and inflamed and worst headaches - no more sinus infection - stopped the drug - anyone know how long it might take for headache to abate after stopping this drug.?? please email me at marlenie1955@yahoo.com. thanks.

-- By marlenie1955 | Reply | (3) replies | Private Message me

April 6th
2008
5:45 PM

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

-- By maxinep | Reply | (3) replies | Private Message me

April 2th
2008
5:38 PM

I can hardly believe what I have read on this board. It is my son's story repeated over and over again and the sad fact is that I never put 2 and 2 together until I saw the news stories last week. My son has been on Singulair for years (he is now 7 years old) along with other drugs for asthma. We recently started taking him to a therapist because of his extreme unhappiness, violent temper tantrums, bad nightmares, many tics, and overall negative attitude. I took him off the singulair 5 days ago and cannot believe the results so far. My son is not affectionate in any way, does not even like a simple pat on the back, no hugs or kisses for sure. Two days ago he came over and gave me a kiss and a hug out of the clear blue. I cannot express enough what this meant to me. I have 3 other children that can't get enough of hugs and kisses, but coming from my 7 year old it just brought me to tears. The hugs have continued and he even told me that he loved me. The therapist had me convinced that he had a sensory deprivation disorder... until now. I cannot believe that until now I have not heard anything metioned in the news and that the medical professionals are so quick to dismiss claims against Singulair.
I am so thankful that I have found this website and for all of the people that have taken the time to include their experiences as it is evidence that there are serious problems when it comes to prescribing Singulair to children. I cannot help but to be saddened when I think of all the years I have lost to this with my son. All the time spent in frustration and tears over what I thought were serious behavior issues on his part. Not to say that I never expect any negative behavior out of a child, but certainly not like I have had to endure in the last years. The last few days have been amazing...I pray it continues. Shame on Merck for not being forthcoming and only keeping their bottom line in mind.

-- By momtoboys4 | Reply | (1) replies | Private Message me

November 9th
2007
10:11 PM

I had a CT scan with Isovue 370. About one week to ten days later, I abruptly started with severe pain, burning and tingling in both legs from about 2 inches above my knees to my toes. Had 2 bouts of cystitis symptoms five days apart. Was checked for infection- had none but had blood in my urine. I have had an EMG, x-rays and an MRI and the doctors find no reason for all this. I have been on Neurontin for 7 mos for this condition and am getting no help from the medical profession. My GP says it couldn't be the Isovue 370 but a neurologist says- probably was but doesn't know any treatment. Please help- it is so painful and I am having trouble walking now.

-- By betsyl | Reply | (1) replies | Private Message me

November 5th
2007
11:43 AM

I have pain in my left hip flexor when taking Lipitor. I was on 40mg/day and went on a daily walk with my wife after her back surgery. My left hip flexor would cramp. Sometimes it would cramp so bad, I had to quit walking and catch a ride home.

I had a month holiday off of Lipitor and could run after a week with no pain.

I started back on 10mg/day and the pain has returned, but not as bad.

I did an experiment- Laying flat on my back, I could lift my left leg one foot off of the floor. I stopped the Lipitor for seven days and could lift my left leg two feet off of the floor.
Can anyone help me?

-- By doylehigh | Reply | (1) replies | Private Message me

October 25th
2007
7:24 PM

Hello, I was put on Prednisone for 12 days and made it through 11. It's been about 11 days since I've taken it and I'm still having symptoms. I have such bad anxiety and depression, mostly after dinner. My heart rate and blood pressure shoot up, and I have to pee every 15 mins. I had gone to the ER on the last day I was on it because I was having evil thoughts and crying uncontrollably. They told me it was probably steroidal psychosis and sent me to a shrink who now has me on Ativan until the Paxil she also prescribed me kicks in. Does ANYONE know how long this drug will be in my system? I took a tappered 12-day dose starting at 60mg. This drug may save lives, but it's really put hard times in mine. Any response is*****

-- By joegibralter | Reply | (3) replies | Private Message me

October 18th
2007
12:23 AM

UPDATE FROM MORE4SURE :) .... i have been off Lisonopril now for one week, and i feel so much better i can hardly believe it! i occasionally get a little pain when i breath, and still an upset stomach alot but im hoping those issues will go away eventually. as for all the other problems i was experiencing during the 4 months i took Lisinopril, non stop coughing, constant headaches, blurred vision, shortness of breath, fever/chills/body aches etc, etc.. pretty much all gone. i no longer wake up every day tired, weak and unable to function normally. FEELING GREAT!! life is good again :) i hope my situation will help someone else who is having problems with this med. please feel free to email me ****** good luck and good health to all...

-- By more4sure | Reply | Private Message me

October 12th
2007
6:54 PM

I went on levaquin-2 rounds of it, due to pneumonia. I felt very out of sorts and discombobulated. Dizzyness, word recall problems, insomnia, diahrrea. My tongue was coated with a thick white film. One night my tongue and my hand felt very disconnected to me, and I had a strange but familiar taste or sensation in my mouth but I couldn't name it. It lasted 3 or 4 minutes. I think I may have had a petit mal seizure. I have been having trouble with my vision, things I read are blurry now, and I have never worn glasses, or had vision problems before. I have been off of this medication for 6 days now, and I am still feeling some of these side effects. I rarely have any side effects from medications. I will never take this again.

-- By lwalter | Reply | (5) replies | Private Message me

October 5th
2007
10:02 AM

I can't believe all of these posts, wow. I was starting to feel as though I was alone with all of the symptoms I was experiencing. I started this drug 2 1/2 weeks ago at 25mg am/pm and am currently up to 75mg am/am. I have really bad chest pain/tightness and mild shortness of breath. As someone else had mentioned, pop is enhanced not dulled, seems as though its like pins on my tongue. I have been forgetting words but not too bad, just for a couple of seconds. The anxiety is the worst, sometimes I lay in bed and the chest pain will increase and I get so axious it feels as though I'm going to die. I went to the ER last night but they did an EKG and told me my heart was fine that the chest pain most likely was not related to my heart. (I'm a 22 year old male and have never had problems with my heart) These chest pains only started after starting this drug. I'm ready to try something else. This was the first drug I was put on for my seizures, my doctor said it could possibly help the seizures/headaches/weight. These side effects are just too much.

-- By czambrano | Reply | (2) replies | Private Message me

September 25th
2007
6:06 PM

45 year old male took lipitor back in Nov 2006 started getting skipped heart beats which i never had before. Now i stopped taking lipitor and a still get the skipped beats.. anyone get anything like that please respond..

-- By frankg | Reply | (1) replies | Private Message me

August 23th
2007
10:09 AM

Femcon Fe gave me a pulmonary embolism (blood clot in my lung) when I was barely on it for 3 months. I spent four days in the hospital and went home on coumadin for about a month.

-- By lilbabyswts | Reply | (1) replies | Private Message me

August 1th
2007
9:47 AM

extreme weight gain... has anyone else experienced this?

-- By mellson1 | Reply | Private Message me

July 25th
2007
9:30 AM

Hi I was a nuvaring user. I am 18 and my gyno told me that nuvaring would be better than any other birth control on the market. I really wanted to start on the patch but my gyno insisted on nuvaring.....yea that was the biggest mistake ever!! I had it for only 15 days because a 15 day period wasnt exactly what I wanted... I had no smile on my face for 13 days and I hated it! My back felt like I was constantly carrying boulders on it and I felt tired all the time. My coworkers had to constantly crack my back for me because I was almost in tears from the pain. I stopped using it and within a few days I was fine. I felt better, my freakin back felt better, and I finally felt clean for sex! But now im experiencing a problem that I hope someone out there can help me with... I stopped nuvaring about 3 weeks ago and ever since I have had gross brown discharge come out of me... Yea lost alot of nice underwear due to that. and now I have my period but its like alot!! minimal cramps but the blood sucks but im assuming that its normal? but does anyone have any advice??? maybe been through it???

-- By orlistarlett | Reply | Private Message me

July 18th
2007
10:56 AM

hi guys! about four months ago my doctor switched me from ortho tri cyclen lo(which I had been on for two years) to yasmin. It was the worst experience I have ever had in my entire life. About a week into the medicine I started getting horrible headaches, terrible anxiety and suicidal thoughts. I was sooo scared from this medicine that I stopped taking it thinking that everything was going to get better! Well wasnt I wrong. I developed OCD really bad to a point where I would sit and worry that I would hurt someone I loved or that I would hurt myself. and I had disturbing thoughts in my head that made my anxiety worse. I have been off the medicine for like 4 months and I am now taking 50 mgs of zoloft for my OCD, anxiety, and depression. I am unsure that it is working yet it's only been two weeks! I hope and pray eveyday that I finally start feeling myself! It's been horrible! Has anyone had this experience from this medicine? and if so do you think that I should get a hormone test, because I am almost convinced from reading other posts that my hormones are wacky! Well thanks for reading! and I hope everyone feels better! :)

-- By jtyre1 | Reply | (5) replies | Private Message me

July 13th
2007
4:41 PM

I need to add more side effects I experienced with Januvia, I would wake up at the same time every morning with a "Strange headache at exactly 3:00 A.M. It was so bad it would wake me up. Pain and numbness running down my right leg and left arm. Also I was suffering from Depression because all of this pain. Now it's like I am a new person.. I've been off Januvia almost a week.

Kathy

-- By highlandergirl61 | Reply | Private Message me

July 5th
2007
5:38 PM

Hi I am a 22 year old who started taking yasmine in march 2007 by the end of my 3rd month i began to realize that i was having savere side affects to my BC thanks to my mother! I was having really bad migraines in the first months but they went away, having forgot they were giving me migraines i continued to take it since they went away. My last week of the white pills in the 3rd month i had 3 random panic attacks for no reason. I went to see my Dr who prescirbed me zoloft. I have not been known to be anxious or depressed before. from sun to thurs i was on zoloft and a nervous wreck. I was anxious, emotional, depressed, and having horrible thoughts. I discontinued the zoloft but started my next pack of BC and was still having an emotional crisis. I then spoke to a pharmacist who said to go off and if i feel better within a week my feelings could be attributed to the BC. It has now been since saturday that i took my last pill. It has definetely been a roller coaster but i do think i am getting better! The thoughts are much less, i am able to experience joy, but i do get a little anxious at time. I think the anxiousness is from going through such a traumatic experience. I haven't spoken to an OBGYN about my problem because im afraid they will just say its just me, and BC couldnt have these affects! I think We woman know our bodies and im just looking forward to feeling 100% better althought i think it may take some time. I would love to talk to someone else about there expeirences if you would like to contact me my e-mail is ******* Thanks for sharing your stories and hopefully mine will be of some help to you.. oh yeah and i dont want sex, i dont know which side affect is worse!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

-- By tburns109 | Reply | (2) replies | Private Message me

June 27th
2007
8:29 PM

Has anyone experienced chronic loose stools while on this medication? If so when you stopped it, for those who did , was there a noticable change in your bowels, as far as not loose anymore? My grandfather is taking this medication and I'm not sure for how long ...but he is taking many others....and has been experience loose bowels for about 4 months now. The docs cant seem to figure it out , I feel like the medications and the mixing of medications is causing this and possibly already done some major damage. My grandfather is 86 years old and just recently had a massive heart attack.
Thanks ,
Maggie

-- By maggierosebud | Reply | Private Message me


 

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