Review: Fan xie ye side effects
In this review, we analyze Fan xie ye side effects by the time on the drug, gender and age (0-60+) of the people who have side effects while taking Fan xie ye. The review is based on reports from FDA and social media, and is updated regularly.
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What is Fan xie ye
Fan xie ye (latest outcomes) has active ingredients of senna.
It can also be called: Senna, Alexandrian Senna, Alexandrinische Senna, Casse, Cassia acutifolia, Cassia angustifolia, Cassia lanceolata, Cassia senna, Indian Senna, Khartoum Senna, Sena Alejandrina, Séné d'Egypte, Senna alexandrina, Sennae Folium, Sennae Fructus, Sennosides, Tinnevelly Senna, True Senna.
On Nov, 26, 2014: 0 people who reported to have side effects when taking Fan xie ye is studied. Please check back later.
Most common side effects over time * :
Most common side effects by gender * :
Most common side effects by age * :
* Some reports may have incomplete information.
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Are you taking Fan xie ye?
Comments from related studies:
From this study (2 months ago):
I am also on another oxycodone a slow releasing one every 12 hours please can you help with this copper taste and how I can get rid of it
From this study (3 months ago):
NOTE: TOOK BRAND NAME(ELI LILLY)CYMBALTA JUL 2013-APR 2014; APR-SEP 2014 TEVA Duloxetine HCL DR, same strength. TEVA has had several recalls of Duloxetine HCL DR, but not this lot, at least not yet.
ACUTE ONSET CYANOSIS with no underlying cause; no history of cardiovascular disease/other related diagnoses. Read that cyanosis and tricyclic antidepressants have been linked/relationship established, therefore discontinued Cymbalta to rule in/out drug as underlying cause. There is no doubt, in this case, it was an adverse effect of Generic Cymbalta 60mg daily. Will submit report to FDA-Medwatch.
From this study (7 months ago):
I noticed the small light brown blotches on my lower legs the beginning of April. No itching or raised skin. The Amantadine is the newest medication. I think it has been approximately 6+ months.
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Can you answer these questions (Ask a question):
- Can long-term methadone use cause or increase the risk of colon cancer?
I had a two-level spinal fusion at L4-S1 in 2000 after being injuried at work in Sept. 24, 1997. I lost everything after...the unjury, ability to do my job, my wife and family (couldn't take the strain) my home, my sense of self and purpose, direction and belonging...credit rating and ability to pay my bills.
After a long period of waiting to settle my workmens' comp. case, I returned home, from the Bat Area back to Arizona to take of my mother with a yet un dianosed case of moderate dementia.
Then, in 2011 I had a 2nd surgery to relieve spinal stenosis btwn. L2-L4, just above the fusion site.
I've been taking methadone since early 2004, a little over ten years, now. I've had high blood pressure since my injury.
Now, I waiting to be scheduled for a colonoscopy, with my father having had polyps and the way I've been feeling..drained, tired all the time, and stomach pains ( in addition to my chronic low back pain), I...
find myself wondering if there is any relationtionship between the methadone and other meds and cancer?
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You may be interested at these reviews (Write a review):
- Understanding and living with cancer
After having one treatment of Gemzar, I had a severe reaction, which caused me to have many seizures. This caused me to developed PRES, which in turn has caused me to have brain damage.When I came out of my induced coma I did not know where I was, nor did I know who my family members were. I could not bathe myself, drive, my speech was broken, I could not add two plus two. I was not the woman I was before Gemzar treatment.Now I am unable to work, I am unable to live on my own, I must always be in the company of another person. I have lost my home and car and job due to this condition. I am currently in speech therapy and soon will start occupational therapy (which is VERY costly) This month marks the one year anniversary of this condition for me. I am making progress. I am able to bathe myself, I can do a little cooking, (although the first time I tried I caught the kitchen on fire a little), I am still living with my Mother , as she is my care taker, my nurse, my driver, my chef, my house cleaner. I currently receive disability. My student loans have gone into default. I could go on but I am depressing myself. I am, followed by my Oncologist every two months now.I want to share this information to anyone and everyone who can benefit from this information.
Thank you, Chelette Williams, BA,MBA.
- Off label use of drugs for peripheral neuropathy causing memory loss (1 response)
I have peripheral neuropathy with standard symptoms of burning, tingling, stabbing pain on the tops of my feet. I have had this condition for over 15 years getting worse over time. The last 5 years I have seen a couple of doctors and through trial and error we settled on a combination of Savella and Methadone to dampen the pain which can go from a nuisance constant 2 to "I'm ready to cut off my feet" constant 8. Taking Savella and Methadone keeps me at a 2 or below except in the evenings when it can get to 5 or 6 and keep me awake. Over a period of a year or so, and I can't remember when it started, I was given Tizanidine, Pramipexole, Oxcarbazpine, Gabapentin and Lyrica (at separate times). I do not remember which of these I was on for the longest or at what point I noticed I was unable to remember what happened the day before, conversations I had with co-workers, decisions and agreements with my manager and things I had done earlier in the week or month. I'm sure a timeline could be put together but since I had lost short term memory I could not do it even now. When I finally figured out what was happening, I was close to losing my job as a Computer Hardware Engineer, which requires extreme concentration and memory. I stopped taking whatever I was on at the time and looked for anything to help me regain my memory and ability to concentrate. I am now taking herbal supplements and using iPhone apps to help me regain concentration and memory. After over 6 months of being off of these drugs I am close to having my previous facilities back. I cannot stress enough the importance of a doctor talking with their patients about memory loss and the ability to concentrate when taking these types of drugs. One of my doctors just gave me Topiramate to try and help with the evening pain and after reading the side effects I will not even try it. Better to be in pain and keep my job.
What really bothers me is I think simply taking one additional pill of Savella will solve my pain issue, but my doctors scoff whenever I make a suggestion and try to put me on something else. After making a medication suggestion one doctor threatened to take me off all medication. I guess he showed me who's the boss. All this is causing me to trust doctors less and less.
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NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.
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