Had to go to the ER a couple of nights ago, spent most of yesterday in doctors' offices, all from these horrible leg cramps! Electrolytes are fine, calcium and potassium levels fine, no deep vein blood clots - the doctors don't know what is causing them.
Here's my beef: It used to be that all you had to do for leg cramps was take quinine ( the malaria medicine) - cramps gone in about 10 minutes. But you can't get quinine anymore for leg cramps ( I don't think America has an FDA approved drug for leg cramps at this time). It is so frustrating to know there is a drug that will stop the horrible pain, but you can't have it. Plus to have a doctor standing there telling you, " I wish I could prescribe some quinine for you, used to prescribe it all the time, but you can't get it anymore."
I haven't been this flustered with the FDA since they banned Vioxx. I'm sorry about the 100,000 or so heart attacks/strokes related to the drug, but most of those folks were taking Vioxx everyday for chronic pain. I only had to take it a couple of times, and only then for a day or so. It worked great for me, now I can't get it anymore.
Why can't they (FDA) just put warnings on the bottles and let the consumer decide if they want to take the risk?
Yet another case of a few people having a problem and the rest of us paying the price. Let's throw out the baby with the bathwater!
Here's my beef: It used to be that all you had to do for leg cramps was take quinine ( the malaria medicine) - cramps gone in about 10 minutes. But you can't get quinine anymore for leg cramps ( I don't think America has an FDA approved drug for leg cramps at this time). It is so frustrating to know there is a drug that will stop the horrible pain, but you can't have it. Plus to have a doctor standing there telling you, " I wish I could prescribe some quinine for you, used to prescribe it all the time, but you can't get it anymore."
I haven't been this flustered with the FDA since they banned Vioxx. I'm sorry about the 100,000 or so heart attacks/strokes related to the drug, but most of those folks were taking Vioxx everyday for chronic pain. I only had to take it a couple of times, and only then for a day or so. It worked great for me, now I can't get it anymore.
Why can't they (FDA) just put warnings on the bottles and let the consumer decide if they want to take the risk?
Yet another case of a few people having a problem and the rest of us paying the price. Let's throw out the baby with the bathwater!