My daughter has been fainting and it appears due to low blood pressure. This seems like an intense drug to help raise her blood pressure. Is anyone out there taking this drug for fainting/low blood pressure?
My daughter is 13 and started having issues in February after two significant viruses. She has passed out MANY times since then. Her pediatrician put her on Fludrocortisone and we didn't see good results. We followed up with a pediatric cardiologist who took her off the meds b/c she says she doesnt see good results and started her on Theromtabs. This is an over the counter salt replacement tablet you get from drugstore.com. Very cheap and incredible results. (well... for two weeks anyways). We are now back to passing out, multiple times per week. The cardiologist states that anytime her body is "insulted" (ie: virus, bacteria or her period) she will have setbacks. She had her period and it most certainly got worse.
I am frustrated, aggravated, tired, worried and all other feelings one can have when something is wrong with a child. At times, I wonder if its partially psychological (makes me feel like a bad mom when I admit it), she is an honors student, places very high demands on herself to keep grades stellar, is a people-pleaser, etc...
Any insight anyone else may have would be greatly appreciated. My "normal" daughter is no longer "normal". She is missing her 8th grade trip to Washington D.C., 8th grade formal dance, National Jr Honor Society events and just being a normal kid.
I don't know what to do for her. The cardiologist says "it will take time", but she has missed 2 months of school. How much time???
I started taking Fludrocortisone because I have been diagnosed with syncope (fainting) to stop my blood pressure from dropping low and having me pass out. It has helped as I haven't had a fainting spell since taking it. I have been extremely tired and can fall asleep. I don't know if this is a side effect but will discuss with my MD.
I have been on this med for two weeks beginning 9 oct 11, and I have not noticed any benefits. After reading the side effects, I am informing my Dr. that I no longer want to be on this med. I'm going to try and increase may salt intake instead. For the last three years I've had dizzy spells accompanied by vision loss. What I have bee doing to treat the symptoms is laying down or walking in order to increase my blood pressure, or get blood to my head. Please let me know if you discover any natural treatments. jpw46atyahoodotcom
Yes I too take fludrocrotison. Took it for 2 months. Than I started passing out again. Now I take .1 twice a day. Gives me headaches. I am 50 yrs Now my bp. stays a round 80/50. I wish ur daughter the best. Is this something we will have to take the rest of our lives ? My concern is when I feel stressed my bp jumps to 158/98. I also had a cardiac cath. Had a small blood clot.. but it seem to make me feel better for a while ..good luck.
I've been on and off fludrocortisone for 18 months. When I first started taking it I was having severe syncopal episodes and diagnosed via tilt table (et al) as neurocardiogenic syncope. The fludrocortisone does raise my average BP but has not entirely resolved near-syncopal issues. I also ate lots of salty foods and drank 96oz of water/day.
Curiously I also had two surgeries (fundoplications where the stomach is wrapped around the esophagus to prevent GERD) during these same 18 months. After the 1st surgery I was pain free from GERD and syncope free without the fludrocortisone; my BP stayed 100/60 and my pulse about 60-64. As each surgery "failed" (due to a too-short esophagus) the syncope and bradycardia returned. Back on the fludrocortisone, salt and water.
However I also have started having "benign" ventricular heartbeats (no ischemia) which cause significant chest pain and cause enormous fatigue to where I am nearly totally sedentary. I have just started adding salt tablets to the fludrocortisone/salty foods/water regimine.
Does this sound familiar to anyone?
I have been taking Fludrocortisone for neurocardiogenic syncope since December 2011 and have had no more collapses. I still have what I call episodes and take Midodrine as needed to combat them. The dizziness and extreme fatigue continue to be an issue and have made a normal life difficult. I work around it as best I can but find the smallest cold knocks me around and I seem to get sick all the time. Living in Australia means the extreme temperatures take an enormous toll on me.
To date I have found limited understanding of the disorder and it is hard to explain to people the impact it has. Currently going through tests re: gastrointestinal pain and worried it may be the Fludrocortisone - also dreadful insomnia.
Really interested to hear others stories and experiences - would be nice not to feel so alone.
I took fludrocortisone (florenef) for almost a year. I ended up in the hospital with pvcs due to hypokalemia so make sure to keep an eye on your potassium levels. I don't wish potassium via iv on my worst enemies. I must say though it is the only drug I've found that helps which stinks because I can no longer take it.
- Fludrocortisone Information for Consumers
- Fludrocortisone Information for Healthcare Professionals (includes dosage details)
- Side Effects of Fludrocortisone (detailed)
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