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50 Side Effects posted for philadelphia

June 7th
2008
12:17 AM

My baby (1 yr) was just prescribed Singulair from a CHOP doctor. I am so thankful that I found this website. I certainly will not fill the prescription. I was hesitant at first anyway because he only had one fluke "asthmatic" insident that sent him to the ER (but has many food allergies and dog allergy). Anyone have any advice on where I should go from here? Honestly, I am afraid to go back to that doctor and they told me it would be very difficult to switch doctors at CHOP. Everyone knows CHOP is one of the best. It is so hard to get honest advice. Every doctor thinks you will sue. Or they're out to use you for their research. He thinks this was the beginning of asthma and it will get worse. It was a scary episode...first time I ever called 911 for one of my children. Breathing is obviously very important, but he never has any problems breathing otherwise (running, laughing, playing) Just got a cold that turned bad quickly. Should I prevent with meds.? My thought is to just keep the neb. and Albuterol handy. I hate giving daily meds. to a developing baby. My gut says to let God develops his immune system naturally. (Not against periodic meds. - So thankful for Benadryl!) Please help! Mommy of 4

-- By mommy4thelord | Reply | (3) replies | 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

April 25th
2008
1:36 PM

Hopefully this will prove to the doubters that there are genetic reasons for the variation of efficacy and adverse side effective when taking Montelukast.

I have several areas of concern (concerned citizen is concerned). One of the main areas is the reliability of Montelukast due to differences in genetics among populations. The cysLT1 (Singulair) receptor is a GENE. As I said before, it would be possible to predict those patients for which Montelukast would and would not be effective and those patients whose gene expression profile would cause them to have unwanted side effectives.

I have been looking for a way to give reasonable proof of that which could be used to convince your doctors that Montelukast is not for everybody. I happened to locate a researcher who had invented and patented methods for predicting drug sensitivity and efficacy in inflammatory disease. I have quoted below from his patent application. He intended to provide a method for determining efficacy and drug sensitivity for pharmaceuticals which include leukotriene antagonists - Montelukast.

Quoted from:

Methods for predicting drug sensitivity in patients afflicted with an inflammatory disease
US Patent Issued on December 12, 2006

Methods are disclosed for predicting the efficacy of a drug for treating an inflammatory disease in a human patient, including: obtaining a sample of cells from the patient; obtaining a gene expression profile of the sample in the absence and presence of in vitro modulation of the cells with specific cytokines and/or mediators; and comparing the gene expression profile of the sample with a reference gene expression profile, wherein similarities between the sample expression profile and the reference expression profile predicts the efficacy of the drug for treating the inflammatory disease in the patient.

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The field of pharmacogenomics measures differences in the effect of medications that are caused by genetic variations. Such differences are manifested by differences in the therapeutic effects or adverse events of drugs. For most drugs, the genetic variations that potentially characterize drug-responsive patients from non-responders remain unknown.
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In another embodiment, the invention is directed to a method for predicting the efficacy in a human asthma patient of leukotriene antagonists including, but not limited to, montelukast (a.k.a., SINGULAIR™; Merck, Whitehouse Station, N.J.), zafirlukast (a.k.a., ACCOLATE™, AstraZeneca, Wilmington, Del.), and zileuton (a.k.a., ZYFLO™; Abbott Laboratories, Chicago, Ill.), comprising: obtaining a sample of cells from the patient; obtaining a gene expression profile from the sample in the absence and presence of in vitro modulation of the cells with specific mediators; and comparing the gene expression profile of the sample with a reference gene expression profile, wherein similarity in expression profiles between the sample and reference profiles predicts the efficacy in the human asthmatic patient of leukotriene antagonists.

Many of the cells involved in causing airway inflammation are known to produce signaling molecules within the body called "leukotrienes." Leukotrienes are responsible for causing the contraction of the airway smooth muscle, increasing leakage of fluid from blood vessels in the lung, and further promoting inflammation by attracting other inflammatory cells into the airways. Oral anti-leukotriene medications have been introduced to fight the inflammatory response typical of allergic disease. These drugs are used in the treatment of chronic asthma. Recent data demonstrates that prescribed anti-leukotriene medications can be beneficial for many patients with asthma, however, a significant number of patients do not respond to anti-leukotriene drugs.

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The genes selected are those that have been determined to be differentially expressed in either a disease, drug-responsiveness, or drug-sensitive cell relative to a normal cell and confer power to predict the response to the drug. By comparing tissue samples from patients with these reference expression profiles, the patient's susceptibility to a particular disease, drug-responsiveness, or drug-resistance can be determined.

http://www.patentstorm.us/patents/7148008-description.html

The inventor's website: Hakon Hakonarson M.D. The Children's Hospital of Philadelphia

http://stokes.chop.edu/research/profiles/?ID=251

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

July 26th
2007
9:04 PM

I am totally shocked at what I have learned about Lipitor. My physician prescribed 10mg for me over 4 years ago. No major problems until recently. Severe neck/shoulder pain for about 3 months. Dr said it was a pulled muscle. Gave me Skelaxin. No help. Went to Chiropractor--yanked, cracked, beat, etc--no help. In the past 2 weeks or so I have developed pain in my hips, back and legs. Blamed it on being 52 years old. As I read some of the experiences on here I could relate to each one. I also have gained about 30 pounds in the past 4 years, short term memory is terrible. NO ENERGY> 3 years ago-Dr started me on Wellbutrin for depression, then added Zoloft. I am to the point now I want to get off of all this and see how I could really feel. Not sure about withdrawals. Any comments on stopping the meds?

-- By sissy1954 | Reply | (8) replies | Private Message me


 

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