MommaBee
02-20-2006, 03:49 PM
I just don't know what is going on with my skin...it is painful and tender to the touch, starting on my scalp and down my neck and face. It is only on the right side and abruptly stops in the middle of my scalp. To brush my hair is painful or to put my face cream on. I have just started taking Tricor and Avapro (I have taken the Avapro before with no problems) for my high blood pressure and cholesterol and told my doctor about this. He is perplexed and couldn't find anywhere in the literature on the drugs about the side effects that could cause skin sensitivity. There isn't any reddening of the skin or rash, so I am really curious what this is...??? I also have a couple of patches on my arms and back. If you have any ideas or know that this is a side affect of the Tricor, I'd be glad to hear from you.
Thanks!
Thanks!
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NHone
02-21-2006, 12:45 AM
[QUOTE=MommaBee]I just don't know what is going on with my skin...it is painful and tender to the touch, starting on my scalp and down my neck and face. It is only on the right side and abruptly stops in the middle of my scalp. To brush my hair is painful or to put my face cream on. I have just started taking Tricor and Avapro (I have taken the Avapro before with no problems) for my high blood pressure and cholesterol and told my doctor about this. He is perplexed and couldn't find anywhere in the literature on the drugs about the side effects that could cause skin sensitivity. There isn't any reddening of the skin or rash, so I am really curious what this is...??? I also have a couple of patches on my arms and back. If you have any ideas or know that this is a side affect of the Tricor, I'd be glad to hear from you.
Thanks![/QUO
Tricor has some harsh side effects as do all cholestoerol lowering medications. Among them, contact dermatitis, fungal dermatitis, skin ulcer, toxic epidermal necrolysis. Also herpes zoster, and herpes simples (shingles). I would bet that it is a reaction to the tricor if you hadn't had it before. You might tell your doctor about these. As he will know shingles is an inflamation of the nerve endings. Sounds like somthing on that order. I had shingles but never did break out in a rash. Did you ever have shingles before... could be a less severe cause this time or just hypersensitivty caused by the tricor. Watch what you have closely, and if you notice ANY swelling of your lips or tongue...get to the emergency room.....!!!!!
Thanks![/QUO
Tricor has some harsh side effects as do all cholestoerol lowering medications. Among them, contact dermatitis, fungal dermatitis, skin ulcer, toxic epidermal necrolysis. Also herpes zoster, and herpes simples (shingles). I would bet that it is a reaction to the tricor if you hadn't had it before. You might tell your doctor about these. As he will know shingles is an inflamation of the nerve endings. Sounds like somthing on that order. I had shingles but never did break out in a rash. Did you ever have shingles before... could be a less severe cause this time or just hypersensitivty caused by the tricor. Watch what you have closely, and if you notice ANY swelling of your lips or tongue...get to the emergency room.....!!!!!
MommaBee
02-21-2006, 02:45 PM
Thank you for your reply!
I find it strange that this doctor (new) didn't know these things. I also couldn't find anything online about it. My first thought was shingles (no I haven't had it before) as I remember reading that it made your skin painful. I will be seeing him again in a month. If this isn't better by then, I am off this medication. I took Lipitor with no side affects. My tryglisorides (sp?) are at 760. BAD! Total cholesteral is at 256. This is the reason for the Tricor. Anyway, you have given me more information than he did! Thanks!
I find it strange that this doctor (new) didn't know these things. I also couldn't find anything online about it. My first thought was shingles (no I haven't had it before) as I remember reading that it made your skin painful. I will be seeing him again in a month. If this isn't better by then, I am off this medication. I took Lipitor with no side affects. My tryglisorides (sp?) are at 760. BAD! Total cholesteral is at 256. This is the reason for the Tricor. Anyway, you have given me more information than he did! Thanks!
NHone
02-21-2006, 02:57 PM
Thank you for your reply!
I find it strange that this doctor (new) didn't know these things. I also couldn't find anything online about it. My first thought was shingles (no I haven't had it before) as I remember reading that it made your skin painful. I will be seeing him again in a month. If this isn't better by then, I am off this medication. I took Lipitor with no side affects. My tryglisorides (sp?) are at 760. BAD! Total cholesteral is at 256. This is the reason for the Tricor. Anyway, you have given me more information than he did! Thanks!
Momma: you can tell you doctor that they information i gave you is from Lexicomp online. It is a service that is used by major medical centers, pharmacologists, doctors etc.
I find it strange that this doctor (new) didn't know these things. I also couldn't find anything online about it. My first thought was shingles (no I haven't had it before) as I remember reading that it made your skin painful. I will be seeing him again in a month. If this isn't better by then, I am off this medication. I took Lipitor with no side affects. My tryglisorides (sp?) are at 760. BAD! Total cholesteral is at 256. This is the reason for the Tricor. Anyway, you have given me more information than he did! Thanks!
Momma: you can tell you doctor that they information i gave you is from Lexicomp online. It is a service that is used by major medical centers, pharmacologists, doctors etc.
vipergg22
02-21-2006, 06:44 PM
This is a list of possible side effects for tricor. Usually statins are worse than fenofibrates though.
SIDE EFFECTS
CLINICAL
Adverse events reported by 2% or more of patients treated with fenofibrate during the double-blind, placebo-controlled trials, regardless of causality, are listed in the table below. Adverse events led to discontinuation of treatment in 5.0% of patients treated with fenofibrate and in 3.0% treated with placebo. Increases in liver function tests were the most frequent events, causing discontinuation of fenofibrate treatment in 1.6% of patients in double-blind trials.
BODY AS A WHOLE: Chest pain, pain (unspecified), infection, malaise, allergic reaction, cyst, hernia, fever, photosensitivity reaction, and accidental injury.
CARDIOVASCULAR SYSTEM: Angina pectoris, hypertension, vasodilatation, coronary artery disorder, electrocardiogram abnormal, ventricular extrasystoles, myocardial infarct, peripheral vascular disorder, migraine, varicose vein, cardiovascular disorder, hypotension, palpitation, vascular disorder, arrhythmia, phlebitis, tachycardia, extrasystoles, and atrial fibrillation.
DIGESTIVE SYSTEM: Dyspepsia, flatulence, nausea, increased appetite, gastroenteritis, cholelithiasis, rectal disorder, esophagitis, gastritis, colitis, tooth disorder, vomiting, anorexia, gastrointestinal disorder, duodenal ulcer, nausea and vomiting, peptic ulcer, rectal hemorrhage, liver fatty deposit, cholecystitis, eructation, gamma glutamyl transpeptidase, and diarrhea.
ENDOCRINE SYSTEM: Diabetes mellitus
HEMIC AND LYMPHATIC SYSTEM: Anemia, leukopenia, ecchymosis, eosinophilia, lymphadenopathy, and thrombocytopenia.
METABOLIC AND NUTRITIONAL DISORDERS: Creatinine increased, weight gain, hypoglycemia, gout, weight loss, edema, hyperuricemia, and peripheral edema.
MUSCULOSKELETAL SYSTEM: Myositis, myalgia, arthralgia, arthritis, tenosynovitis, joint disorder, arthrosis, leg cramps, bursitis, and myasthenia.
NERVOUS SYSTEM: Dizziness, insomnia, depression, vertigo, libido decreased, anxiety, paresthesia, dry mouth, hypertonia, nervousness, neuralgia, and somnolence.
RESPIRATORY SYSTEM: Pharyngitis, bronchitis, cough increased, dyspnea, asthma, allergic pulmonary alveolitis, pneumonia, laryngitis, and sinusitis.
SKIN AND APPENDAGES: Rash, pruritus, eczema, herpes zoster, urticaria, acne, sweating, fungal dermatitis, skin disorder, alopecia, contact dermatitis, herpes simplex, maculopapular rash, nail disorder, and skin ulcer.
SPECIAL SENSES: Conjunctivitis, eye disorder, amblyopia, ear pain, otitis media, abnormal vision, cataract specified, and refraction disorder.
UROGENITAL SYSTEM: Urinary frequency, prostatic disorder, dysuria, abnormal kidney function, urolithiasis, gynecomastia, unintended pregnancy, vaginal moniliasis, and cystitis.
SIDE EFFECTS
CLINICAL
Adverse events reported by 2% or more of patients treated with fenofibrate during the double-blind, placebo-controlled trials, regardless of causality, are listed in the table below. Adverse events led to discontinuation of treatment in 5.0% of patients treated with fenofibrate and in 3.0% treated with placebo. Increases in liver function tests were the most frequent events, causing discontinuation of fenofibrate treatment in 1.6% of patients in double-blind trials.
BODY AS A WHOLE: Chest pain, pain (unspecified), infection, malaise, allergic reaction, cyst, hernia, fever, photosensitivity reaction, and accidental injury.
CARDIOVASCULAR SYSTEM: Angina pectoris, hypertension, vasodilatation, coronary artery disorder, electrocardiogram abnormal, ventricular extrasystoles, myocardial infarct, peripheral vascular disorder, migraine, varicose vein, cardiovascular disorder, hypotension, palpitation, vascular disorder, arrhythmia, phlebitis, tachycardia, extrasystoles, and atrial fibrillation.
DIGESTIVE SYSTEM: Dyspepsia, flatulence, nausea, increased appetite, gastroenteritis, cholelithiasis, rectal disorder, esophagitis, gastritis, colitis, tooth disorder, vomiting, anorexia, gastrointestinal disorder, duodenal ulcer, nausea and vomiting, peptic ulcer, rectal hemorrhage, liver fatty deposit, cholecystitis, eructation, gamma glutamyl transpeptidase, and diarrhea.
ENDOCRINE SYSTEM: Diabetes mellitus
HEMIC AND LYMPHATIC SYSTEM: Anemia, leukopenia, ecchymosis, eosinophilia, lymphadenopathy, and thrombocytopenia.
METABOLIC AND NUTRITIONAL DISORDERS: Creatinine increased, weight gain, hypoglycemia, gout, weight loss, edema, hyperuricemia, and peripheral edema.
MUSCULOSKELETAL SYSTEM: Myositis, myalgia, arthralgia, arthritis, tenosynovitis, joint disorder, arthrosis, leg cramps, bursitis, and myasthenia.
NERVOUS SYSTEM: Dizziness, insomnia, depression, vertigo, libido decreased, anxiety, paresthesia, dry mouth, hypertonia, nervousness, neuralgia, and somnolence.
RESPIRATORY SYSTEM: Pharyngitis, bronchitis, cough increased, dyspnea, asthma, allergic pulmonary alveolitis, pneumonia, laryngitis, and sinusitis.
SKIN AND APPENDAGES: Rash, pruritus, eczema, herpes zoster, urticaria, acne, sweating, fungal dermatitis, skin disorder, alopecia, contact dermatitis, herpes simplex, maculopapular rash, nail disorder, and skin ulcer.
SPECIAL SENSES: Conjunctivitis, eye disorder, amblyopia, ear pain, otitis media, abnormal vision, cataract specified, and refraction disorder.
UROGENITAL SYSTEM: Urinary frequency, prostatic disorder, dysuria, abnormal kidney function, urolithiasis, gynecomastia, unintended pregnancy, vaginal moniliasis, and cystitis.
MommaBee
02-21-2006, 10:20 PM
WOW! Thank you for that info, vipergg22!
And you too, finres!
I knew it was the Tricor, but couldn't seem to find the info I needed. Thanks!
And you too, finres!
I knew it was the Tricor, but couldn't seem to find the info I needed. Thanks!
Lenin
02-22-2006, 10:11 AM
Two conditions come to mind, momma; shingles (a friend had it across her face at eye level...great pain) and tic doloreaux, an inflammation of a facial nerve.
CobaltBlue
03-12-2006, 11:07 PM
Interesting....tricor, a fenofibrate has herpes zoster and simplex listed as side effects....
Just defies all logic
I knew it was the Tricor, but couldn't seem to find the info I needed. Thanks!
Not so sure on that one mommabee, it is way outside the norm as far as side effects from this med go...I could be wrong though (and that certainly would not be the first time)
Just defies all logic
I knew it was the Tricor, but couldn't seem to find the info I needed. Thanks!
Not so sure on that one mommabee, it is way outside the norm as far as side effects from this med go...I could be wrong though (and that certainly would not be the first time)
NHone
03-13-2006, 07:09 PM
Interesting....tricor, a fenofibrate has herpes zoster and simplex listed as side effects....
Just defies all logic
Not so sure on that one mommabee, it is way outside the norm as far as side effects from this med go...I could be wrong though (and that certainly would not be the first time)
Sorry Cobalt...You'll have to argue with the people that make tricor... it came out on their product information sheet...and is also listed on lexicomp online....This time we're just the messenger
Just defies all logic
Not so sure on that one mommabee, it is way outside the norm as far as side effects from this med go...I could be wrong though (and that certainly would not be the first time)
Sorry Cobalt...You'll have to argue with the people that make tricor... it came out on their product information sheet...and is also listed on lexicomp online....This time we're just the messenger
Stumper
03-13-2006, 07:24 PM
Momma,
It CAN'T be the Tricor that is next to impossible. Only 2 out of 100 show any type of side affects whatsoever. Or 20 out of 1000 and THAT is debatable as to what the side affect is...probably just a sore muscle.
My guess is that you have shingles. Typically shingles is another form of Chicken pox in adulthood. Have you ever had it as a child?
It CAN'T be the Tricor that is next to impossible. Only 2 out of 100 show any type of side affects whatsoever. Or 20 out of 1000 and THAT is debatable as to what the side affect is...probably just a sore muscle.
My guess is that you have shingles. Typically shingles is another form of Chicken pox in adulthood. Have you ever had it as a child?
CobaltBlue
03-13-2006, 08:15 PM
Sorry Cobalt...You'll have to argue with the people that make tricor... it came out on their product information sheet...and is also listed on lexicomp online....This time we're just the messenger
Don't be sorry :) Sometimes it helps to realize what has to be reported, and why some weird associations result.
Here is a better explanation of why I worded my response that way....
I have a protocol for a drug study (lets say Brand X chewable vitamins) and purport it to be an appetite supressant. I submit the human use protocol to the institutional review board. It comes back approved. Suppose I solicit and sign up 200 participants. Let's suppose that in this unheard of case, zero paricipants fail to complete the study. However, during the course of taking this experimental vitamin to supress the hunger, four of my participants (who just happen to be roommates and heard of the study as a way to supplement their income) develop chicken pox. Now I report that 4/200 or 2% may develop chicken pox as a side effect to Brand X chewable vitamins.
Don't be sorry :) Sometimes it helps to realize what has to be reported, and why some weird associations result.
Here is a better explanation of why I worded my response that way....
I have a protocol for a drug study (lets say Brand X chewable vitamins) and purport it to be an appetite supressant. I submit the human use protocol to the institutional review board. It comes back approved. Suppose I solicit and sign up 200 participants. Let's suppose that in this unheard of case, zero paricipants fail to complete the study. However, during the course of taking this experimental vitamin to supress the hunger, four of my participants (who just happen to be roommates and heard of the study as a way to supplement their income) develop chicken pox. Now I report that 4/200 or 2% may develop chicken pox as a side effect to Brand X chewable vitamins.
MommaBee
03-13-2006, 10:31 PM
I am still not sure it was the Tricor. It seems to have gone away by itself now. I don't believe it was Shingles either. Just don't know. I am also in perimenopause and concedered that that could have caused it too.
Thank you to all that replied!
Thank you to all that replied!
NHone
03-13-2006, 11:20 PM
Don't be sorry :) Sometimes it helps to realize what has to be reported, and why some weird associations result.
Here is a better explanation of why I worded my response that way....
I have a protocol for a drug study (lets say Brand X chewable vitamins) and purport it to be an appetite supressant. I submit the human use protocol to the institutional review board. It comes back approved. Suppose I solicit and sign up 200 participants. Let's suppose that in this unheard of case, zero paricipants fail to complete the study. However, during the course of taking this experimental vitamin to supress the hunger, four of my participants (who just happen to be roommates and heard of the study as a way to supplement their income) develop chicken pox. Now I report that 4/200 or 2% may develop chicken pox as a side effect to Brand X chewable vitamins.
Good explanation...but one of the participants could have gotten chicken pox due to the appetite supressant causing causing an immune problem in his body.... the room mates could have contracted it form him because of an immune problem in their body because they were in such close closed quarters.... But that is highly unlikely.... I appreciate what you said because it does make you question things (which should be done) and it made me think. However...you know drug companies, they would have pulled out the eye teeth with a pair of rusty pliers before they ever let anything go into the side effects that could possibly make them look bad...Unless it was unaviodable. My opinion is just that the tricor reduced the immune system ( as statins are known to do) and the latent chicken pox virus produced the shingles (herpes).
Here is a better explanation of why I worded my response that way....
I have a protocol for a drug study (lets say Brand X chewable vitamins) and purport it to be an appetite supressant. I submit the human use protocol to the institutional review board. It comes back approved. Suppose I solicit and sign up 200 participants. Let's suppose that in this unheard of case, zero paricipants fail to complete the study. However, during the course of taking this experimental vitamin to supress the hunger, four of my participants (who just happen to be roommates and heard of the study as a way to supplement their income) develop chicken pox. Now I report that 4/200 or 2% may develop chicken pox as a side effect to Brand X chewable vitamins.
Good explanation...but one of the participants could have gotten chicken pox due to the appetite supressant causing causing an immune problem in his body.... the room mates could have contracted it form him because of an immune problem in their body because they were in such close closed quarters.... But that is highly unlikely.... I appreciate what you said because it does make you question things (which should be done) and it made me think. However...you know drug companies, they would have pulled out the eye teeth with a pair of rusty pliers before they ever let anything go into the side effects that could possibly make them look bad...Unless it was unaviodable. My opinion is just that the tricor reduced the immune system ( as statins are known to do) and the latent chicken pox virus produced the shingles (herpes).
CobaltBlue
03-14-2006, 07:51 AM
My opinion is just that the tricor reduced the immune system ( as statins are known to do) and the latent chicken pox virus produced the shingles (herpes).
Good point there and I can't argue with that ;)
Good point there and I can't argue with that ;)
Lenin
03-14-2006, 10:13 AM
I think almost EVERYONE who has ever had chicken pox will develop shingles in the 4-5 decade window after the initial infection. The acquired immunity to the always present herpes zoster virus seems to last about that long. My bout with shingles was, to the year, 40 years after I had chicken pox (at age 6.)