Morphine sulfate symptoms and conditions

When taking morphine sulfate SR for lower back pain, taking urine tests will show traces of methadone. Try explaining you don't to your doctor!

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.
He 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.

Initially I was fine when taking Kadian w/several morphine sulfate tabs for breakthrough pain. Was also taking 5 MG Valium since being treated for chronic nerve neuralgia I've had for over 20 years. Felt wonderful until my prescription for Valium ran out and I did not get refilled. I did not know the Valium was counteracting the negative side effects. When off Valium, horrendous headaches returned with extensive negative side effects,such as tremors, nervousness, voice quivering--that persisted over 1 month off of Valium; well past stage of withdrawal from Valium!

I do get the difficulty in swallowing... not on a regular basis... but at night... as I am falling asleep... I also experience... spikes in appetite and horrible sleeping habits.. but... my main concern is numbness in my hands... I am taking Morphine Sulfate.... 100mg every 12 hours... and 10mg... (for severe spikes in pain) 1-2 every 4 hours, as required. I have stuck to the every 12 hour pill diligently... and I take the 10 mg as required ~ approximately 6-8 every 24 hours.

I have be on several different pain meds the past year or so and approximately 1 week maybe sooner after starting the Morphine I starting experiencing numbness in both hands... It is driving me insane. My Dr. has prescribed arm braces for when I sleep... to keep my wrists straight... Hence... Carpul Tunnel.. Is this Morphine related???

And... is rehab in my future after surgery and recovery... ???

My Daughter is on morphine sulfate. she is 18 and has has RSD for 4 years. She has been on the morphine for 3 months now, but is losing her hair. Dose anyone know if this is a side affect? She is really getting upset over the loss of her hair.

Morphine sulfate causes me to have difficulty swallowing. Instead of being an automatic process, one I normally do without thinking, I have to consciously force the muscles in my mouth and throat to perform the swallowing action. I do not notice other side effects.

I am the person who posted the above message about kidney pain as a bad side-effect of N. use for fibromyalgia -- I use the drug for muscle pain, and to get to sleep at night -- and am at the point of trying to lower the dose, as well as wean myself off of it, before permanent damage can happen to my kidneys (and I hate the brain-fog).

Some research into the chemical and physical effects of the med lead me to believe that it works by helping the kidneys take a certain substance out of the blood stream -- the same way that dialysis works for kidney-failure, so definately Neurontin will affect the operation of the kidneys (see posting on "husband taking it for prostate problems" -- is this because of problems urinating?).

There have NOT been any studies on how Neurontin works -- or dangers/side-effects of the drug --for any other use besides epileptic seizures. If a person is experiencing bad side-effects he or she should immediately contact the doctor who prescibed it and ask for a different med, or for the dosage to be reduced (don't just stop taking it, which is what a lot of people do about bad side-effects -- that could be dangerous.). Such use makes a patient a guiney-pig for research, and the makers of Neurontin have been under attack for aggressively pushing it for what are called "off-label" uses.

If the doctor won't listen to you about this, find another one. IT'S YOUR BODY and no one knows better how you feel inside of it. Also you could experiment with withdrawing yourselve from high levels of the dosage, or asking that the amount of the med in the rx be reduced...fast- withdrawal sometimes causes seizures (as I understand it) and of course you have the complete right to ask a doctor to listen to your symptoms and needs.

Also if you're a person who notices bad effects in a child or a spouse you should make it an urgent project to point the bad effects out to the doctor, to become an advocate for the person who cannot do it. Good luck. JanK in Portland OR (and I am not a doctor, just a person with a lot of experience in surviving the American health system.)