Review: could Testosterone cause Mvp (Mitral valve prolapse)?
Summary: there is no Mvp reported by people who take Testosterone yet.
We study 186 people who have side effects while taking Testosterone from FDA and social media. Find out below who they are, when they have Mvp and more.
You are not alone: join a mobile support group for people who take Testosterone and have Mvp >>>
Testosterone has active ingredients of testosterone. It is often used in testosterone. (latest outcomes from 390 Testosterone users)
Mvp (mitral valve prolapse) has been reported by people with osteoporosis, osteopenia, depression, multiple myeloma, high blood pressure. (latest reports from 3,349 Mvp patients)
On Jan, 4, 2015: No report is found
Do you have Mvp while taking Testosterone?
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- support group for people who take Testosterone
- support group for people who have Mvp
Drugs in real world that are associated with:
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Can you answer these questions (Ask a question):
- What's the cause of heart palpitations
E-fib or irregular heart beat, more noticeable at night. Have been on hormone replacement since 1995. Started on the patch that caused irritations then switch to 1% Androgel packets. Used 1/2 a packet per day for years, then libido dropped and started using full packet. Everything going good until I started using 25mgs of zinc some months later I started having heart palpitations.
Stopped androgel and zinc, heart palpitations stopped after 2 weeks, almost afraid to start up again!
- What are the side effects of axiron
What are the Axiron withdraw symptoms when you go cold turkey and stop taking it?
- What is the effect of taking testosterone while having sciliosis?
For transgenders, do you know what is the effect of taking testosterone while having scoliosis?
For specialist of endocrine/orthopedic/basta specialists:
(gender therapists)- what effects are you expecting when your patient is taking testosterone while having scoliosis? Will you let them still to take hrt just to achieve what they need and want?
- Do you have issues snoring from testosterone
I was in an IED explosion in Afghanistan, had a TRAUMATIC BRAIN INJURY, 2005.JULY 28THlevels were extremely low. my V.A. doctor put me on testesterone 2011 BREAST CANCER, AUG 11TH 2012 HIT AND RUN ON MY MOTORCYCLE. DUE TO all the pain meds chemo, etcetera. MY testosterone. At first it was the best thing that had happened to me since I woke up in the hospital now I snore like a drunk Marined. and the culprit is the testosterone. I need to save my marriage and do something aboot this. any ideas what I can do
- I cannot get a direct answer from any of my drs.,is my sciatic pain caused by my interstitail cystitus? (1 answer)
I have had interstitail cystitus for almost four years now.I have been on every kind of drug,other than pain pills.I will not take them,I don't believe in them they only mask the problem and cause addiction.of course,just my belief.I have had d.s.m.o. repetitively for first year and a half twice a week.I have tried physical therapy .I have had five hydrodistention.I just recently had my first hydrodistention with botox injections.nothing has kept me out of pain .even when I am doing good I can only seem to reach a six in my pain level.my frequency average is and has been 30-40Times a day.I am,or,was a chef kitchen manager.could not perform and lost two jobs because of this disease.my flanks,my lower back ,my legs,my arms all ways in pain.pelvic pain is constant.I'd rather not go into further details way too personal.but this has taken my life.I am 35.I have led a fairly healthy life.I have no life now.I am seeking disability .Every Dr. I go to has a different option about the sciatic part of my problem some Dr.s are very sure and as a matter of fact about how it is in conjunction with I.c..others look at me like I'm nuts?why do I limp?why can't I get in and out of a car,or bend down and touch my toes,pick heavy stuff up.just to laugh at times hurts.this is my life ,I gotta wonder ,is there any one else out there going through the same symptoms and no relief?
More questions for: Testosterone, Mvp
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Fibromyalgia dx after pregnancy of only child at 42/other dx followed and seem to be in conjunction. heart issues did not appear until after the use of fibro meds- cymbalta, lyrica, neurontin, and more. had 1 seizure believed to be related to seretonin syndrome/years and years of mistreatment by doctors. unable to recall how many docs and meds through the years. one other very significant issue- after tooth extraction had puncture to left maxillary sinus-after YEARS of neglect by docs, found max. & ethmoid sinus completely opaque on CAT scan. Had surgery. Now, years later, have mucous plug that sporadically comes out upon sneezing. Fairly recent CAT scan shows sinuses again completely opaque. Certain needs further attention, but basically afraid to go through surgery again. Also- may have had heart attack. ER visit said no, but shortly after, had abnormal ekg. Again, neglect from docs. Am now active advocate for fm/chronic pain patients. Disgusted by the whole lack of interest of medical community. Looking for answers through my own research to try to find a way to improve quality of life...
- 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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