March 24th
2008
9:53 PM
I am a 25 year old, who was perfectly healthy prior to recently when I was diagnosed with Nephritic Syndrome and Minimal Change Disease and possibly FSGS (kidney diseases) I was put on 60 mg of Prednisone for 1 month then I was lowered to 40 mg for one month and I am then dropping to 30 mg. I am also taking Fosamax for my bones and a Vitamin D pill because my last lab test showed low vitamin D levels.
I am dizzy constantly and can not live a normal life, I can not drive or do any activities that I had previously done. My chest is so tight and constricted all of the time, my heart rate is so fast and pounds at my chest. I have no energy to do anything, I can barely open a door at times. I am beginning to grow unwanted hair on my face. My abdomen is always bloated. I have pain in my rib cage, and shoulders. I feel very sore throughout my entire body. I do not really sleep at night, so I look very tired all the time.
I have actually lost weight, I have no appetite at all. I am down 10-15lbs.
Now for the Pro- my Kidney Diseases are currently in remission and this has happened much faster than the Nephrologist had thought.
I am very anxious to getting my life back to normal and getting off the Prednisone.
Has any one else experienced increased heart rate, chest tightness, or rib pain?
I wish everyone the best in their roads to recovery!!
-- By nicipp | Reply | (9) replies | Private Message me
September 6th
2007
3:40 AM
I am a 27 y/o male in good physical condition (i did a triathlon 2 months ago) I was prescribed levaquin 750mg a week ago for an throat infection and fever. After the first dose I had sever abdominal pain (like someone was stabbing me). After the 3rd dose my back started to hurting and my calf's cramped up. I stopped the medication immediately. It has been 5 days since I stopped the medication and I have a burning sensation on my back. It is on both sides and stretches around toward my stomach. It feels like I have bad sunburn but there is no redness, swelling or discoloration. I also still have fever and muscle spasms all over my body (mostly in my legs). I went to my doctor yesterday and he is running a bunch of blood testes and I hope he can find a way to treat the symptoms. Does anyone know how long this should last? I just want it to go away so I can get on with my life. Any help or suggestions are appreciated.
-- By agolsen1 | Reply | (4) replies | Private Message me
July 25th
2007
1:38 PM
Well.....I've had two good bone density tests (the proper test)...the last i had was in 2002, and showed an actual increase of density of 7.5% in one hip, and 4% somewhere else....I was THEN put on Fosamax by my dr. because I am "white, thin, hysterectomy and smoke...." and said he wanted to keep my bones healthy. Hence, I've been on this since. I'm now wondering.....I had alopecia (hair loss) 2 years ago, just patchy, it's back in fine, no recurrence. I'm seeing a chiropractor now, as I feel constantly "pretzeled" My head feels like it weighs 100lbs on a wobbly neck, my fingers are often sore, one of my knees is dodgy, ....we have no athritis, osteoporosis in my family, I cannot remember a female breaking a bone! I just don't feel great all vague feelings. I exercise every evening 20mins on a glider, I'm 105lbs, I eat a sensible diet, I do everything at 100mph, so not sedentary! I go for my Bone density the end of this month, and I have a feeling this is the end of my Fosamax!
-- By camberwell | Reply | (1) replies | Private Message me
July 11th
2007
2:25 PM
Acne, decreased libido, depression, inability to lose weight (even with exercise and dieting), among other side effects. I have never had an acne problem but not a week went by without major pimple outbreaks on my chin. Sex is totally unappealing and my decreased sex drive has really effected our marriage. Mood swings have not been fun. Also had some backpain that I can't understand. Had it removed today and it was a nightmare - the IUD had migrated and was way up high in my cervix, had to have a hysteroscopy to have it removed. I have had two vaginal deliveries and this was far worse than either of those. Painful, terrible cramping, thought I was going to pass out and I normally have a high pain tolerance. Would never recommend the Mirena IUD to a single person!
-- By amie_milton | Reply | Private Message me
July 7th
2005
8:50 PM
After 3 weeks of taking tapazloe I developed Very severe joint pain. It felt like I was paralized. Then after 2 days it would attach a different joint. Scarest thing I ever had to experience and I have had 2 children via c section. Worst part is that the dr said that it wasn't the meds so I continued taking them!
-- By gshopkins | Reply | (3) replies | Private Message me
May 24th
2005
11:18 AM
I had severe, debilitating pain in my legs after taking three days worth of pills. I had noticed fairly bad pain in my legs the day before, but thought it was just the flu (I had been given the Levaquin for a chest infection). By the fourth morning, I could no longer straighten my legs or walk properly. I have a very high pain tolerance, but thought I would go insane from the pain. Due the medication I am on for blood pressure, my doctor could not offer me any pain relief except Advil and Skelaxin, which does not work.
I had read the insert that came with the Levaquin, but it only mentioned "leg pain" which did not sound at all serious, so I took it and paid a huge price. I had been walking two miles a day and now am not able to walk 1/4 mile without causing severe pain, and it has been three months since I took it!
Levaquin should be taken off the market!
Levaquin (2) Mirena (1) PredniSONE (1) Fosamax (1) Tapazole (1) Neurontin (1)
July 26th
2008
6:51 PM
I am my husbands caregiver. He is on many medications the last 26 years due to chemical poisoning thanks to our government not protecting their civilian painters at the Army Depot where he worked.
-- By charking | Reply | (1) replies | Private Message meHe has permanent brain damage, CRS damage, memory loss and short term memory, CHF and Bollis Emphysema. Now he also has Type II diabetes a severe case as he was not diagnosed for 7+ years of testing.
To make this short. He has been on many drugs for pain, diabetes, blood pressure, the brain damage, ( he is a recovering, not drinking alcoholic)
Recently the doctor took him off the Codeine # 3 that he had been taking for almost 15 years, 8 per day. and gave him time release Morphine Sulfate.15 MG. They also gave him Gabapentin for the neuropathy which is severe in his feet and starting to go up his legs. He is over weight, above the waist, and has not had a problem with High Blood Pressure, for many years since taking 60 mg daily of Inderal. His Blood Sugars have been between 98-140 without medication. When he was first diagnosed he was put on glyberide and it worked so good he was off it in 6 months and totally diet controlled since then but about every 3 years he would go on it for about 6 months and then he was ok again.
He has not needed it for the last 7 years. Since starting the gabapentin he went from 300 to 600 to 900 and slowly increased the dose to 1600 mg. The 300's are caps, the 600's are tablets.
All the sudden he has pounding headaches, I took his BP which we had not been watching and it was 198/115 with a 98 pulse. The only change was the gabapentin and Morphine. The morphine does not seem to be causing any side effects, once he was used to getting sleepy.. but once the gabapentin was added, all he does is sleep. The blood sugars also went up with the blood pressure. His were 358 higher than they have ever been except when he was first diagnosed. I was able to get the glyberide and that is bring down the sugar levels only taking 1/4 tab 2 x a day, and the blood pressure is also coming down, it was 139/85 with a pluse of 76 which is still too fast. I talked to some pharmancy friends and they said " Its the gabapentin " so I told the doc I wanted to stop it and he said to start leveling off, one 300 mg cap every 4 days. We were down to 2 a day till Friday and saw the doctor. Due to his taking Cymbalta they did not want to give him any of the other anti depressants so they want him to back on the gabapentin up to 1200 a day instead of the 1600 a day.
Taking into consideration his medical issues and meds, I don't believe this is a safe or sound decision, but I know how much pain he was in before the gabapentin.
I wish they would be more forthright about the side effects of this medication. They said it only causes blood sugar issues in 1 % and they did not even address the high blood pressure etc.
His pupils are also different, he has the kidney pain, but his biggest problem is sleepy.. hopefully it's not his kidneys or his heart. They did blood tests on Friday and I am asking for a EKG.. in the mean time we are monitoring both blood pressure and blood sugar 6 or more times a day. Thank you so much for sharing. It really helps to know we are not alone.