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Review: could Evening primrose oil cause Fibromyalgia?





Summary: there is no Fibromyalgia reported by people who take Evening primrose oil yet.

We study 183 people who have side effects while taking Evening primrose oil from FDA and social media. Find out below who they are, when they have Fibromyalgia and more.

You are not alone: join a mobile support group for people who take Evening primrose oil and have Fibromyalgia >>>

Evening primrose oil

Evening primrose oil has active ingredients of evening primrose oil. It is often used in premenstrual syndrome. (latest outcomes from Evening primrose oil 235 users)

Fibromyalgia

Fibromyalgia (a long-term condition which causes pain all over the body) has been reported by people with osteoporosis, pain, depression, high blood cholesterol, high blood pressure.(view latest reports from 24,072 patients)

On Nov, 25, 2014: No report is found

Do you have Fibromyalgia while taking Evening Primrose Oil?

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  • 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.
    Reply
  • 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?
    Reply
  • 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.
    Reply
  • 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?
    Reply
  • Does anyone else continue to have all over body pain 3 years after taking lupron depot for endometriosis (1 answer)
    I had 9 injections of lupron after a partial hysterectomy. Ever since then my body has never been the same. I continue, 3 years later suffering from weakness. I had to quit my job as a registered nurse and after 2 and 1/2 years I was forced to file for disability.
    Reply

More questions for: Evening primrose oil, Fibromyalgia

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  • Had nms in 2005, will trileptal increase chance of recurrence?
    In 2005 I had NMS, which was not detected by my drs for 4 months. I'd been on Lexapro & Seroquel for 2 yrs, but was weaned from Lexapro & placed on Lamictal 3/05. Began getting low-grade fevers, which I was told were not caused by the Lamictal. I quit taking it anyway, fevers (along with uncontrollable shivering) continued & got higher. By 5/05 my temps were reaching 105 deg F. Husband said I became combative, refused to go to hospital. Early June/05 he came home to find me wrapped in blankets, with a temp over 105 F. He tried to place me in a tub of cold water, said I was rigid & screamed when he tried to move me. I was in the tub, speaking "in tongues" (his description, I have no memory of this). He called 911, took me to hospital. I woke, no idea where I was or why. After a lumbar puncture & 2 days in ICU I went home. The fevers continued...2 weeks later he came home to find me wrapped in sheets, towels, blankets, with the heat on full (it was in the 90's outside) he called ambulance again. I awoke to find myself under an ice blanket with nurses pushing large vials of dantrolene into both arms, several liters. Another LP, a stint in ICU...this time they told me it was NMS. The dr who dxd me said he was surprised I was alive, & not a vegetable, as my temp had peaked at 109 deg F. I suffered brain damage; short-term memory loss, brain can't control my body temp, my blood pressure went up. An arteriogram showed completely healthy heart & arteries, no plaque at all. I lost all body fat as well as some muscle mass. The fevers continued even after stopping the Seroquel. I visited my PCP for a checkup in 9/05, temp was normal. I started shuddering, my temp went up a full degree every 5 minutes. PCP admitted me to ER, my heart rate was over 272 B/M; they stopped my heart 3 times to "reset" it, which didn't work. I spent 3 days in hospital. Several months later my P doc tried me on Lamictal alone; I got Stevens-Johnson syndrome. I stopped the drug as soon as the signs appeared. I've been untreated, except for Neurontin & Primidone, until my manic episodes became unlivable. 3 weeks ago I went 8 days with no sleep, became psychotic. My P doc gave me Trileptal, which has evened my moods, but I've been getting low-grade fevers (highest was 103.6). Would having had NMS in the past make me more prone to falling to it again with the Trileptal? It's the only new med I've taken in over a year.
    Reply
  • Not a great experience
    I was on norvasc for two months and had to go off because of severe swelling of feet and legs. Also rapid heart beat and very profuse sweating. it was horrible. It also raised my blood pressure. after going off BP dropped by @least 10 points both diastolic and systolic.
    Reply
  • So sleepy with savella
    I am just finishing the starter pack of Savella and I am so sleepy I can't hold my head up. My pain and other Fibromyalgia symptoms are tremendously better but I am sleeping like crazy. Hopefully I can have both doses at night and this will help. I am so glad to not be in pain but I need to be awake also. I am going to talk to my doctor about perhaps another medication to help curb the sleepiness. I can't use caffeine or stimulants due to anxiety but need something to take this sleepiness away.
    Reply
  • Lyrica photosensitivity
    Spent several hours outside in partly sunny conditions on Sat. Swelling started a little on Sun. But by Monday my face was ver swollen and red with small bumps most noticeable across the cheeks, nose and area of the forehead where bangs did not cover.
    I have only been using for (6) months.
    Unknown whether to continue this drug or not. It was helping; so I am torn.
    Reply
  • Wheezing stopped after topamax sessesion
    Wheezing noted by primary physician in this non-smoker. Stopped Topamax per doctor's instruction. 48 hours later was examined by physician and noted that wheezing stopped.
    Reply

More reviews for: Evening primrose oil, Fibromyalgia

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  • I have had chronic fatigue since 5 May 2012 - nearly 2 and a half years. Recently stopped Lexapro for depression which I was on for a year and slowly reduced before cessation. Old back problem bulging disk L5/S1 pain left thigh, hip, buttock worst at night. Recently went on tramadol and immediate sl ...
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  • I have been on trazodone for about 4 months and it is working well to treat insomnia, and anxiety. I started taking evening primrose oil less than a month ago to help with menopausal symptoms and it has been very effective. About a month ago or maybe longer, I started to have increased muscle pa ...
    Reply
  • I went to a Rheumatologist and he said I have Hashimoto disease and said its not serious enough to take meds for. The test is - Thyroid Peroxidase Antiboties - my number is 363. It says that is should be
    Reply
  • Following moderate whiplash injury in a road traffic accident three years ago, symptoms of pain, exhaustion, IBS, headache, nausea have continued and my quality of life consists of work and recovering.
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More related studies for: Evening primrose oil, Fibromyalgia

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