Review: could Arthrotec cause Fibromyalgia syndrome (Fibromyalgia)?
Summary: Fibromyalgia syndrome is found among people who take Arthrotec, especially for people who are female, 40-49 old, have been taking the drug for 1 - 6 months, also take medication Lipitor, and have Pain.
We study 5,530 people who have side effects while taking Arthrotec from FDA and social media. Among them, 27 have Fibromyalgia syndrome. Find out below who they are, when they have Fibromyalgia syndrome and more.
You are not alone: join a mobile support group for people who take Arthrotec and have Fibromyalgia syndrome >>>
Arthrotec has active ingredients of diclofenac sodium; misoprostol. It is often used in arthritis. (latest outcomes from Arthrotec 5,782 users)
Fibromyalgia syndrome (constant pain in their muscles and soft tissues) has been reported by people with osteoporosis, pain, depression, high blood cholesterol, high blood pressure.(latest reports from Fibromyalgia syndrome 24,073 patients)
On Nov, 29, 2014: 5,530 people reported to have side effects when taking Arthrotec. Among them, 27 people (0.49%) have Fibromyalgia Syndrome.
Time on Arthrotec when people have Fibromyalgia syndrome * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
|Fibromyalgia syndrome||16.67%||50.00%||16.67%||0.00%||0.00%||16.67%||0.00% |
Gender of people who have Fibromyalgia syndrome when taking Arthrotec * :
|Fibromyalgia syndrome||96.30%||3.70% |
Age of people who have Fibromyalgia syndrome when taking Arthrotec * :
|Fibromyalgia syndrome||0.00%||0.00%||0.00%||0.00%||4.55%||50.00%||13.64%||31.82% |
Severity of Fibromyalgia syndrome when taking Arthrotec ** :
|least||moderate||severe||most severe |
|Fibromyalgia syndrome||0.00%||0.00%||100.00%||0.00% |
How people recovered from Fibromyalgia syndrome ** :
Top conditions involved for these people * :
- Pain (7 people, 25.93%)
- Fibromyalgia (5 people, 18.52%)
- Hypercholesterolaemia (4 people, 14.81%)
- Neck pain (4 people, 14.81%)
- Arthritis (4 people, 14.81%)
Top co-used drugs for these people * :
- Lipitor (8 people, 29.63%)
- Neurontin (6 people, 22.22%)
- Vioxx (5 people, 18.52%)
- Trazodone hcl (5 people, 18.52%)
- Claritin (4 people, 14.81%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
Do you have Fibromyalgia Syndrome while taking Arthrotec?
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- support group for people who take Arthrotec and have Fibromyalgia Syndrome
- support group for people who take Arthrotec
- support group for people who have Fibromyalgia Syndrome
Drugs in real world that are associated with:
Could your condition cause:
Can you answer these questions (Ask a question):
- Does anyone experience heart palpitations causedby their acid reflux ?
I have had acid reflux/Gerd for 4 years + Was not believed that symptoms were real for a while as had no heartburn and a diagnosis of Fibromyalgia which even now some medics think is imaginary...it's NOT!!! Following a demeester score of 45 ( very high confirmation of acid reflux) and discovery of a large hiatal hernia, ( a classic physical cause of acid reflux) I had hernia repair operation and LINX anti reflux surgery. Throughout the four years a major symptom of my acid reflux were heart palpatations. They started at the same time I started with reflux and cleared up after the surgery. I have been reflux free palpitation free and antacid free for four months. then I was put on Gabapentin for back spasm and the reflux returned along with the palpitations. Medics keep insisting this is just anxiety yet eat a food that gives me reflux also starts the palps which is the indicator of the reflux as I do not have heartburn. Comes on when relaxing and eating watching tv ( no anxiety present) and when I am sleeping peacefully ( no anxiety present) my heart wakes me up and fires off into tachycardia. Recently a doctor has said it is now known that acid reflux irritates the nerves in the solar plexus area and that triggers the palps. Anyone else experienced this? Are there any studies on it at all? Thanks all.
- Can mrsa cause chronic intestinal pseudo obstruction?
I had a small bowel obstruction caused by adhesions from an appendectomy carried out 20yrs previously and had grumbling pain ever since but been labelled a malingerer by my family GP until one day at work when I started with terrible tummy ache and sickness like I'd never known, fetching up bile with force. I hated going to hospital after yrs of being called a moaner but after a day of rolling round in pain, temperature of 103 an dehydration, my Mammy insisted we go and I was seen straight away - to my shock I was in theatre within 3hrs with a serious obstruction.
I never really recovered... The obstruction returned after 2 days and a portion of necrotic bowel was removed, then further fever and cellulitis then MRSA and deaths door.... Isolation in high dependency (intensive care) wound break down, ventilated and all related issues that come with that - chest infection, pneumonia, bed sores. Total time in hospital 8 months. Negative pressure dressing on laparotomy wound, colostomy, picc, 4 rounds of vancomycin, minor flirt with heart failure (just water related) an eventually everything healed. Had a large incisional hernia to repair and some corrective work to the horrific scarring but then the neuropathy started plus problems eating, spewing up after any solid food, more than a few forks, diarrhoea and sickness or constipation nausea and pain driving me mad, tried all manner of drugs, nerve blocks, physio, floating tank, acupuncture, opiates, non opiates, spinal cord stimulation, an now a consultant just had a 'eureka' moment and said were you treated with vancomycin when you had MRSA? If so I'm pretty sure you have chronic intestinal pseudo obstruction and is 90% sure but wants to take a muscle biopsy to be certain. I've had so much surgery and bad news in the last 10yrs I'm terrified of germs, hospital acquired bugs and anaesthetics, is there any other way? Or can I have this test done awake - conscious sedation? I had it before during spinal cord surgery so I know what's involved and it's better than GA as I know what's going on, who is doing what to me etc...
Does anyone with a medical background know about this ailment/disease? Does it sound feasible that MRSA or it's treatment could have caused this? I was surgically debrided up to every other day when the vac pac/negative pressure machine and dressings were changed and the doctors told me I lost a great deal of tissue and had a lot of nerve damage due to the infection.
Any patient perspectives on this illness would also be very much valued in helping me make a decision, moving forward. If all this is going to accomplish is to attach a label to the pain but not actually change anything, after fighting it for 10yrs now, avoiding hospital as much as I can, I really can't see the point of exploratory surgerys and biopsys now when it is known that I have this propensity towards adhesions and a new wound means a potentially new adhesion growth site.
If it helps, the appendectomy happened when I was 10yrs old, the MRSA when I was 30 and I am now 40.
- Has abilify affected your ability to make good decisions?
My husband and I are 73. We had a paid off home and money in the bank until the past 3 years. We have made some terrible decisions and now we are practically penniless. We couldn't understand why we had made such bad decisions and let someone talk us into losing our money. We have also been on Abilify about the same amoount of time and I noticed that the commercials say a side affect can be lack of judgement or something to that effect. Has anyone else had this happen?
- Does mucinex guaifenesin help treat fibromyalgia? (3 answers)
I have tried so many treatments for fibromyalgia. I am going to try guaifenesin next . Any advice would be appreciated.
- Is it my thyroid or am i mentally ill? diagnosed w/ hashimoto's thyroiditis but untreated - chronic pain unmanaged also (2 answers)
I moved to OR from HI and brought all my records, signed releases, and had many diagnoses, all but the thyroid, was being treated and long-term. I also took Oxycontin & Oxycodone for severe chronic pain from bilateral SI joint fusion (right screw protrudes & leg also becomes numb and weak with activity) & lumbar and cervical degeneration & facet arthropathy. I had volunteered reducing dosage as I'm always trying to reduce Rx intake to alleviate side effects (I am tiny, even for a youth & adult dosages seem to drug me). Next month, it was known that I could not function well because pain was not managed, but needed to resolve it in OR, as moving. OR Drs. refused to return me to higher dosage (taking minimalist Oxycontin 10 mg CR & Oxycodone/Acet 5mg). After being unable to get up to go to bathroom, walk, contacted adult services to see about in home services & possible foster care placement for young son since I was losing independence & failing in general health & cognitive functioning. I was forced to take bottles of OTC Tylenol to function, with Dr's knowledge, & knowing I had past lesions on liver to follow. Several months later had follow up liver ultrasound, & new small lesions found on liver. After emailing dr about from DHS questioning failure to manage my pain vs. conditions that were disabiling, 6 months later, dr told me I was experiencing withdrawals every morning & finally agreed to increase Oxycontin to 15 mg, which has enabled me to tolerate the pain & function. I have been treated as a drug-seeking patient since attempting to transfer my care.
I have multiple autoimmune conditions, most of which I no longer treat with Rx as I have been overmedicated & side effects are too numerous. So I actually am opposite in many ways. I stopped Lyrica, Silenor (sleep), Elmiron, Bentyl, Dexilant. Stress affects me seriously since I had a TBI and experience anxiety stress disorder, which seems to contribute to auto immune responses. But still knew triggers & familiar with self - this thyroid diagnosis & symptoms experienced new & too destabilizing to live.
Diagnosed w/ Hashimoto's thyroiditis after 1/2 thyroid removed Nov 2011; my antibodies are unbelievably high. I declined in thinking, memory, anxiety-unable to think/track, losing most,getting lost driving, sleep very dysfunctional, too emotional, crying easily & often (unusual for me). I feared losing ability to live independently. My maintenance Rx (Silenor, Lyrica) seemed to drug me. I tried to explain to drs. that I needed thyroid replacement hormones that I never had these problems before.
They referred me to a psychiatrist for medicine management consultation, who gave me mental health diagnoses (histrionic personality disorder, somatoform (hypochondria) that discredited me & ruined my medical records for future validity. Is it thyroid symptoms? Was unmanaged pain contributing? Too much Tylenol? What does a dysfunctional thyroid do to a person? How do I get my medical record addressed to reflect accuracy?
More questions for: Arthrotec, Fibromyalgia syndrome
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- Not a great experience
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