I took my first dose of Alendronate and then experience significant muscle pain for the next 4 days. Does anyone know if I should expect this to happen each time I take it or is it something to happen for the first few times until my body adjusts to the medicine?
Do you mean Fosamax (alendronate)? If you do, its for treating bone problems like Osteoperosis by adding bone mass and slows bone loss. I use it for Osteopenia.
The prescription drug Fosamax (the generic is alendronate sodium) is a medication which has been prescribed to hundreds of thousands of postmenopausal women to treat osteoporosis and help increase bone mass thereby reducing the chance of spinal or non-spinal fractures. Fosamax has also been prescribed to increase bone mass in men with osteoporosis. Brand name Fosamax is manufactured in the United States by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.
The authors examined the effects of high-dose oral alendronate (40 mg daily) for 6 months on 3 adult patients with intractable headache due to fibrous dysplasia of the skull. Each patient had disease processes not amenable to surgery. The patients underwent clinical follow-up at 1, 3, and 6 months. Their pain levels were documented at each visit by using a visual analog scale. All 3 patients demonstrated a significant decrease in pain levels and became independent of scheduled analgesics.
I am also taking Aromasin for bc. Stopped alendronate (I am osteopenic due to 30 yrs of prednisolone and Arimidex) in case this caused the oesophagitis. Would appreciate your advice.
thankyou,i am with contact of my doctor ,he said there is no solution for damaged vertibras,but calcium and vitiman d and alendronate sodium/cholecaiciferol tablets will help spine and bones from further damages but what to do with prednisones i cant stop them because of asthma and taking of them will damage other bones isnt there any other solution instead of prednisones, i know there is nothing accept these because my doctor told me:(
The authors examined the effects of high-dose oral alendronate (40 mg daily) for 6 months on 3 adult patients with intractable headache due to fibrous dysplasia of the skull. Each patient had disease processes not amenable to surgery. The patients underwent clinical follow-up at 1, 3, and 6 months. Their pain levels were documented at each visit by using a visual analog scale. All 3 patients demonstrated a significant decrease in pain levels and became independent of scheduled analgesics.
Osteoporosis medications like Raloxifene (Evista), alendronate (Fosomax), risendronate (Actonel) and ibandronate (Boniva) all can cause flu like symptoms in individuals that are taking them. I am not sure what medications you are on, but this could be your problem.
s hard to miss the vein unless they are very bad at it. Drink a lot of water so your veins swell and are easy to feel. Usually they put iv in the crook of my arm, like a blood test, because I have a very good vein there. They don't hurt me anymore unless the person is inexperienced and ends up digging around in my arm with the needle to find the vein.
I also have recurrant Ovarian Cancer, and Crohn's Disease. What medications are you on other than B12 injections? I have found many of the other medications I take other than chemo make my hair fall out. I am currently not taking IV chemo, but still losing hair. I guess I've gotten used to hats, but look forward to the day I don't need them!
Also, would it perhaps be possible to add some alendronate, or something else to help her bone density and still be able to benefit from the thyroid medication? Thank you so much!
When the breathing spazaming was under
Control i could no longer walk days later and a one iv steriod drio down 2 to go i have my fingers crossed for miracles.
Anyone had iv steriods?
How have you noticed its helped?.
I had an IV inserted for contrast dye for an MRI. Now the area is a lump, swollen,red , and itchy. Any ideas what to do?
I had a baby more than 2 months ago, when I was in the hospital the nurse was trying to put an IV on my left wrist but then after 3 unsuccessful painful try, it end up on my right wrist. a day after I went home, i started to have this very painful on my left wrist with a bluish bruises and the bruises was gone but the pain still there, even just to lift a glass or move it or anything is sooo painful.
I had a contrast IV for a Chest CT. It infiltrated, causing pain and swelling. I need a follow-up scan (a 6-month check). What are the chances this will happen again. I have tiny veins and am nervous.
I have been told I am going to get started on a 3 day course of IV steroids. I would like to ask those of you that have had this what they felt like during and after they had it? Did anyone have any adverse side effects? Did you feel they helped reduce the flare up?
I've been using heroin and cocaine together through IV for the last year every day and recently i've been experiencing extreme pain after doing a shot the same size i've done in the past, it feels like i may be having mini heart attacks, but sometimes i can relieve the pain by burping.. after the pain dies down, i feel a burning sensation for a while after, and feel as if i cannot move my arm too much or it will cause a sharp pain in my heart.
i had a stress test the end of may. they put an iv in my arm where it bends. it has never healed the injection site. it is about the size of a dime. does not hurt at all, but am concerned about it.
So, yes you can get a sore arm from an IV but most of the time it is from trauma to the area or a badly inserted IV etc. You can get an infection at an IV site but they do use Betadine Iodine and other antiseptics to clean the area well. Usually, the infection comes from an IV or catheter tip left in for several days or longer. A well known source of infection is by Staphylococcus epidermidis (usually) but there are other organisms that can infect a catheter site.
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