Guest guest Posted February 5, 2000 Report Share Posted February 5, 2000 Hi, everyone! Karyn, I believe you are correct about all pancreatic enzymes being alike. As far as I know, the ingredients are the same in the various products, but the amounts of each ingredient differ. Common brand names are: Creon, Ilozyme, Ku-Zyme, Pancrease. They all contain lipase, protease, & amylase in varying amounts; Cotazym also contains calcium carbonate. There are also some enzyme drugs that contain pancreatin; I don't know anything about these drugs. Does anyone know about pancreatin? (Some brand names are:Panazyme, Dizymes, Entozyme, Pancrezyme.) Hope everyone is having a comfortable weekend. jang Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 8, 2000 Report Share Posted February 8, 2000 , Sorry to take so long to respond to your question about enzymes. I have been extremely ill over the past several days. I am finally and officially out on medical leave until further notice. This was forced upon me by both my physician (GI) and employer. I only hope it will last a short time. I'm counting on getting myself back to work before the end of this month, if I can help it. If only the Pain Clinic would get my pain meds back to where they were before they began tampering with it 2 months ago. My GI doctor is supposed to call the pain clinic so that by the time I go for my next visit on Friday they will know to increase my levels. To get back to the point of this message, " what enzymes do I take and in what quantities? " I am on Creon 20 mg tabs. I take 2 (40 mg) with meals and at bedtime. What are you taking, if anything? Andre' Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 2, 2000 Report Share Posted March 2, 2000 <> Hi , Are you taking your enzymes while you are on TPN? Karyn <A HREF= " http://hometown.aol.com/karynwms/myhomepage/business.html " >Pancreatit is Support Network</A> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2000 Report Share Posted March 3, 2000 Karyn, Hi, I am not on TPN, I haven't taken any enzymes in 4 years, I tried them but they made terrible mouth ulcers and I didn't want to deal with that too. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2000 Report Share Posted March 3, 2000 In a message dated 3/3/00 12:51:07 PM Central Standard Time, LR96@... writes: << I am not so sure that by not taking your enzymes that you are doing the right thing. Those enzymes help your pancreas, by not having to work so hard. If your pancreas is damaged it may not be able to produce enough of the enzymes. This may help the pancreas to not have to work as hard. Taking the enzymes may help to reduce or limit the amount of acute attacks. >> I was under the impression that pancreatic enzymes which are amulase, lipase, and pancrease are necessary for food digestion. Under normal circumstances a healthy pancreas would not produce these enzymes unless there was the presence of food in the GI tract. It seems as though there would be a risk of autodigestion to introduce enzymes into the gut without the prior consumption of food. I'll ask my GI what he thinks, too. Karyn <A HREF= " http://hometown.aol.com/karynwms/myhomepage/business.html " >Pancreatit is Support Network</A> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2000 Report Share Posted March 4, 2000 Sorry I think this has been misunderstood. To be more specific I am meaning those who are to take the enzymes that are not npo ( those on tpn are usually npo?)I was referring to those that have choosen to discontinue without physician knowledge. Sorry for the confusion. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 6, 2000 Report Share Posted March 6, 2000 In a message dated 3/3/2000 2:19:38 PM Eastern Standard Time, LR96@... writes: << I tried them but they made terrible mouth ulcers and I didn't want to deal with that too. >> , What sort of enzymes were you taking? I take Creon (40 mg per meal) and have never heard of this side effect. Andre' Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 7, 2000 Report Share Posted March 7, 2000 I think the name of the enzymes were pancrease it has been a while about 4 years ago. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 7, 2000 Report Share Posted March 7, 2000 I STARTED TAKING MY ENZYMES AGAIN ODAY. i HOUGH ABOUT WHAT ANDRE SAID ABOUT THEM HELPING THE PANCREAS WORK PROPERLY AND THAT MIGHT KEEP IT WORKING LONGER. ALSO I READ HAT THEY HELP KEEP THE FAT OU OF THE LIVER AND KIDNEYS. bU THE NAUSEA STILL COMES IN WAVES. bUT AFTER LISTEN9ING O ALL OF YOU, I AM NEVER GOING TO COMPLAIN AGAIN WELL AT LEAS NOT FOR HIS WEEK. THANKS LYNNEAR Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 8, 2000 Report Share Posted March 8, 2000 hi my name is jim, i am dodie's husband. i am sorry that i forgot the name of the person who wrote about the pancreatic enzymes causing ulcers in their mouth. this also happened to me. when i was in the hospital and first started taking viokase. i started off by chewing them and after a few days and the start of ulcers,i asked the doctor why this was happenening and he told right off i had been chewing them and i needed to swallow them whole to have the enzymes work properly through my system. i hope this work for you Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 8, 2000 Report Share Posted March 8, 2000 Jim, I know longer take them I have not for 4 years. I am a nurse and I knew to swallow them, for me they caused terrible mouth ulcers and the Dr. said no more Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 10, 2000 Report Share Posted March 10, 2000 i SARED TAKING THE ENZYMES AGAIN BE AUSE ONE OF YOU WROTE THT IT MIGHT JUST HELP THE PANCREAS WORK LESS HARD THEREBY KEEPING IT MORE HELAHY LONGER. lYNNNEAR Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 10, 2000 Report Share Posted March 10, 2000 Hi Lynn and all, I really support you in doing this. Anything that we can do to help our frail pancreas' the better. That was interesting what the others said about them causing mouth ulcers. Before I went on TPN and I was taking them, I had no problem. I found that the Viokase went down easier than the Creon capsules. Karyn <A HREF= " http://hometown.aol.com/karynwms/myhomepage/business.html " >Pancreatit is Support Network</A> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 18, 2000 Report Share Posted March 18, 2000 In a message dated 3/7/2000 9:22:34 PM Eastern Standard Time, LynneAR@... writes: << I STARTED TAKING MY ENZYMES AGAIN TODAY. >> Linnear, That is truly wonderful news. While you may still feel miserable, it would become much worse without them. Like you, I too tried to do without my enzymes for a period of 4 years. I found I got progressively worse over time and may have been instrumental in my most recent surgery. Andre' Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 21, 2000 Report Share Posted March 21, 2000 aNDRE, tHANK YOU FOR ANSWERING. SOMETIMES i JUST READ HE MAIL AND DON' SAY ANYTHING BUT WHEN i DO IT IS NICE TO BE ANSWERED. lYNNEAR Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 28, 2000 Report Share Posted April 28, 2000 -- On Thu, 27 Apr 2000 16:11:01 Crystal, & Jillian Pratt wrote: >This last time i was in the hospital my enzymes did not go up at all >everything was normal. And my gp was not suprised he told me eventually >this would happen has anyone else experinced this? > Hi Crystal. Glad to hear you are back home. After about 2 or 3 years of chronic pancreatitis I also stopped having elevated amylase & lipase levels. My doc said my pancreas was no longer able to secrete these enzymes in amounts large enough to give abnormal lab results. Sometimes my liver function tests are abnormal during flare-ups, but usually they are " normal " also. My doctor feels that in chronic pancreatitis, after a while lab results don't give an accurate picture. jang --== Sent via Deja.com http://www.deja.com/ ==-- Before you buy. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 29, 2000 Report Share Posted April 29, 2000 In a message dated 4/27/00 4:11:45 PM Central Daylight Time, grayman@... writes: << This last time I was in the hospital my enzymes did not go up at all everything was normal. And my GP was not surprised he told me eventually this would happen has anyone else experienced this? >> When I presented to the ER 8-4-99 with excruciating pain, my enzymes were also not elevated. They did admit me with my persistence. Four days later they were going to dismiss me with a diagnosis of " abdominal pain " of unknown origin. They said I couldn't have Pancreatitis because my enzymes were not elevated, as a matter of fact they were almost gone. I finally had to demand a CT scan and my pancreas was shriveled up rock. One of the symptoms of Chronic Pancreatitis is the loss of exocrine Pancreatic function. The primary enzymes that are found to be deficient are Lipase, Amylase, and Trypsin. With ongoing, and even intermittent inflammation or the deposition of calcifications within the pancreas, the exocrine cells become damaged. The enzymatic process in which they become activated is also damaged. Therefore, the traditional Lipase or Amylase test to determine the presence of Pancreatitis is inappropriate for patients with chronic Pancreatitis. It is disappointing that the doctor's do not receive adequate training regarding pancreatic pathophysiology. Karyn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 29, 2000 Report Share Posted April 29, 2000 Hi everyone... My name is Suzanne....but just call me suz... :-) I'm new here, and so glad I found you :-) I was brought to the ER on Easter and home on Thursday...with pancreatitis....I have been having attacks since July of 99, and have been tested for gallbladder problems since Oct....and with negative results :-( I have pain on the right side all of the time, and I just don't ever feel like myself. I'm afraid to go anywhere, for fear of an attack...yet I can usually tell when one is coming. My blood count, I think was 185 in the ER...but I'm not sure if that's the exact number..I was trying to look at my papers when the Dr. came in....Is that really high?? I'm having another endoscopy done, but not the same one...I think it's MMKP?? I'm a bit nervous, because every test has come back negative, but I live in pain, and fear...I just want to get better :-( Any adivice would be appreciated...especially on what to and no to eat...the Dr. told me a low fat diet, but I thought I was doing that already....no fat yogurt, Lean Cuisines and the such.... Thanks for listening...and any help would be deeply appreciated....I just want answers and to feel better :-( God Bless, suz... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 29, 2000 Report Share Posted April 29, 2000 In a message dated 04/29/2000 9:10:47 AM Pacific Daylight Time, KarynWms@... writes: << The primary enzymes that are found to be deficient are Lipase, Amylase, and Trypsin. >> Has anyone had an elevated trypsin? My doctors can not figure out what it means, althought they say it is probably due to the inflammation. Any thoughts? -Malisa Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 29, 2000 Report Share Posted April 29, 2000 In a message dated 4/27/2000 5:11:43 PM Eastern Daylight Time, grayman@... writes: << This last time I was in the hospital my enzymes did not go up at all everything was normal. And my GP was not suprised he told me eventually this would happen has anyone else experienced this? >> Yes, my levels always register within normal ranges. They are never elevated any longer. I was told that this was normal in my case since most of my Pancrease has been removed in my Whipple surgery. Andre' Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 29, 2000 Report Share Posted April 29, 2000 Hi Suz:) First of all welcome I know you've come to the right place for support. We have suffered and continue to suffer with the pain, nausea, and frustration of this illness. Second make sure your Dr. is a GI specialist and not just a basic family practitioner. You will need a Dr. who truly knows the ins and outs of pancreatitis. IT is more than just the alcoholics disease. Some of us have never drank, but we have the disease. We have all at one time or another dealt with various Drs. until we have gotten one that we are comfortable with. IT is very hard to get frustrated and impatient, especially when you know you're not yourself. Stay positive and as far as a diet goes, you should avoid foods that are high in fat. However, I have had pancreatitis since 93, and as of 2000 I don't tolerate anything anymore, that's anything. I got sick yesterday from eating some carrots. I don't tolerate raw fruits and vegetables, go figure. You get use to knowing what you can and cannot tolerate. GOOD LUCK and GOD BLESS. Marie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 1, 2000 Report Share Posted May 1, 2000 By the way, last year when I went into the hospital for the first time with Pancreatitis, my gall bladder tested negative for problems, too. When they removed it last Wed., the anesthesiologist said it was so diseased and horrible looking and so full of stones and a gall bladder doesn't just get that way in a matter of months. The fact that my gall bladder had gotten so bad had to have occurred over YEARS and they have even attributed my " IBS " that I have dealt with for over 9 years to my horrible gall bladder. Get someone to check and make certain it isn't your gall bladder. Better yet, find someone who will say it HAS to come OUT! A lot of times the gall bladder has nothing to do with Pancreatitis, however, I am one of the ones whom it did affect. I would want to be sure if I were you. Shari - Singing Pampered Chef Queen *Jesus Loves You* Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 1, 2000 Report Share Posted May 1, 2000 When attempting to lower your fat intake think of things like lean meats, fish, chicken,( I hate chicken) I even buy lite (Not NO fat) hot dogs as long as it is a good name brand they are fine, I also buy lowered fat smoked sausage. I do not tolerated cheese well except for white cheeses, swiss, montery jack, ramono, parmasean, be careful of highly processed foods they can be trickey in their advertising, it is best to do your own cooking if you possibly can, I would be thrilled to give you some recipes for easy things both main dishes and of course sweets also just let me know and I will send them to you. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 2, 2000 Report Share Posted May 2, 2000 In a message dated 04/29/2000 11:10:39 AM Central Daylight Time, KarynWms@... writes: << One of the symptoms of Chronic Pancreatitis is the loss of exocrine Pancreatic function. The primary enzymes that are found to be deficient are Lipase, Amylase, and Trypsin. With ongoing, and even intermittent inflammation or the deposition of calcifications within the pancreas, the exocrine cells become damaged. The enzymatic process in which they become activated is also damaged. Therefore, the traditional Lipase or Amylase test to determine the presence of Pancreatitis is inappropriate for patients with chronic Pancreatitis. It is disappointing that the doctor's do not receive adequate training regarding pancreatic pathophysiology. Karyn >> I've had multiple hospitalizations where the enzyme levels were normal, however it is not everytime that I have an acute attack. In some research I had found it says that the Amylase levels are only elevated for the first 24 to 48 hours, which is one of the reasons it is difficult for doctors to diagnose this disease. From the information I've gathered from this group there are other reasons that make more sense for this to occur. I think sometimes I try to just tolerate the pain as long as I can before finally giving into it. I know this isn't the best thing to do, but I just don't want to give it up I guess. Sandy In a message dated 4/27/00 4:11:45 PM Central Daylight Time, grayman@... writes: << This last time I was in the hospital my enzymes did not go up at all everything was normal. And my GP was not surprised he told me eventually this would happen has anyone else experienced this? >> When I presented to the ER 8-4-99 with excruciating pain, my enzymes were also not elevated. They did admit me with my persistence. Four days later they were going to dismiss me with a diagnosis of " abdominal pain " of unknown origin. They said I couldn't have Pancreatitis because my enzymes were not elevated, as a matter of fact they were almost gone. I finally had to demand a CT scan and my pancreas was shriveled up rock. One of the symptoms of Chronic Pancreatitis is the loss of exocrine Pancreatic function. The primary enzymes that are found to be deficient are Lipase, Amylase, and Trypsin. With ongoing, and even intermittent inflammation or the deposition of calcifications within the pancreas, the exocrine cells become damaged. The enzymatic process in which they become activated is also damaged. Therefore, the traditional Lipase or Amylase test to determine the presence of Pancreatitis is inappropriate for patients with chronic Pancreatitis. It is disappointing that the doctor's do not receive adequate training regarding pancreatic pathophysiology. Karyn ------------------------------------------------------------------------ Was the salesman clueless? Productopia has the answers. http://click./1/3019/0/_/593940/_/957024590/ ------------------------------------------------------------------------ PANCREATITIS SUPPORT NETWORK Online e-mail group To reply to this message hit " reply " or send an e-mail to: Pancreatitisegroups To subscribe to this e-mail group, simply send an e-mail to: Pancreatitis-subscribeegroups Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 4, 2000 Report Share Posted May 4, 2000 In a message dated 05/01/2000 10:40:58 AM Central Daylight Time, FRETZRICE@... writes: << By the way, last year when I went into the hospital for the first time with Pancreatitis, my gall bladder tested negative for problems, too. When they removed it last Wed., the anesthesiologist said it was so diseased and horrible looking and so full of stones and a gall bladder doesn't just get that way in a matter of months. The fact that my gall bladder had gotten so bad had to have occurred over YEARS and they have even attributed my " IBS " that I have dealt with for over 9 years to my horrible gall bladder. Get someone to check and make certain it isn't your gall bladder. Better yet, find someone who will say it HAS to come OUT! A lot of times the gall bladder has nothing to do with Pancreatitis, however, I am one of the ones whom it did affect. I would want to be sure if I were you. >> About 2 years ago now I was in the hospital again with pancreatitis. My doctor did several tests and even though I did not have gallstones it was determined that I had a diseased gallbladder. Even after a week in the hospital on mega antibiotics the gallbladder was still inflamed. The surgeon did not want to do surgery unless there were gallstones, however my internist felt that there was still something causing the inflammation and that it was more than just my pancreas. Well, once the surgeon did remove my gallbladder and I did get much better. I do still have problems with my pancreas, but I do believe I would have had many more problems with the gallbladder, especially since there are so many problems already. Sandy By the way, last year when I went into the hospital for the first time with Pancreatitis, my gall bladder tested negative for problems, too. When they removed it last Wed., the anesthesiologist said it was so diseased and horrible looking and so full of stones and a gall bladder doesn't just get that way in a matter of months. The fact that my gall bladder had gotten so bad had to have occurred over YEARS and they have even attributed my " IBS " that I have dealt with for over 9 years to my horrible gall bladder. Get someone to check and make certain it isn't your gall bladder. Better yet, find someone who will say it HAS to come OUT! A lot of times the gall bladder has nothing to do with Pancreatitis, however, I am one of the ones whom it did affect. I would want to be sure if I were you. Shari - Singing Pampered Chef Queen *Jesus Loves You* ------------------------------------------------------------------------ Get paid for the stuff you know! Get answers for the stuff you don’t. And get $10 to spend on the site! http://click./1/2200/0/_/593940/_/957195574/ ------------------------------------------------------------------------ PANCREATITIS SUPPORT NETWORK Online e-mail group To reply to this message hit " reply " or send an e-mail to: Pancreatitisegroups To subscribe to this e-mail group, simply send an e-mail to: Pancreatitis-subscribeegroups Quote Link to comment Share on other sites More sharing options...
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