Protonix patient assistance

Common Questions and Answers about Protonix patient assistance

protonix

Avatar m tn could anyone give me ideas as to where or who i would contact to get some patient assistance for acute hep c treatment? I am not working, cannot wait on s.s. disability. I try to do some construction work when available, but it is really rough.
199177 tn?1490498534 I was reading the post about suboxone prices ,someone wanted to know if the was any assistance for the cost . I did some research this is what I found RECKITT BENCKISER suboxone patient assistance programs 1-866-512-2216 I don't know what are the guidelines but its worth a call . Any little bit I am sure would be very helpful. If I find anything else I will post it.
Avatar n tn Since I have been taking Protonix for GERD, my heart seems to be pounding in my throat. This has never happened to me before and is alarming. My blood pressure has always been low. Is this normal? Is there anything else I can take beside Protonix?
2121656 tn?1395674749 Hi there! not sure if you remember me or not. We exchanged postings awhile ago & I shared my bad experience with you I had with a ENT performing a negligent sinus surgery, as well as being told I had a hiatal hernia. I had asked your advice about discontinuing protonix if I don't have a hiatal hernia. Your advice was to ween off protonix by switching to pepcid or Zantac. Well, I visited my gastro/hepatologist for a issue with high liver enzymes. He asked why I was taking protonix.
1622229 tn?1299050798 I wanted to share some encouraging news for people who have Chronic Hep B and have financial difficulty affording Baraclude. I contacted Brystol Myers Squibb and applied for the Patient Assistance Program. The website and application is here: http://www.bms.com/products/Pages/programs.aspx It took about a week and they have approved me to receive the medication and are shipping it to my home.
Avatar f tn This is my understanding of the patient assistance programs for Incivek. The list price, which no patient will have to end up paying, is $49,200 for 12 weeks. HOWEVER, the patient assistance programs, are more than generous. Typical Co-pay for the three prescriptions that will be needed will be between $50 and $250 each.
Avatar n tn old and have tried all the different perscription medications. I have been taking protonix for about 5 years now and I'm concerned about long term use of protonix and all the other heartburn medications I have been taking for 30 years. I still suffer from heartburn daily. I have had 4 Endoscopy's done at different times and my Dr. say's it does show some inflammation but no Barrett's Desease, thank God.
Avatar f tn Anyone out there on Protonix? I was diagnosed with acid reflux and was put on Nexium which helped slightly with my burping but I was still getting stomach aches. I went for an abdominal ultrasound, endescopy and CT scan with IV contrast and all came back fine. My Dr just switched me to Protonix.
Avatar f tn The Dr gave me Nexium, but I was still getting upper stomach pain and pressure in the chest an back. I was switched to Protonix and it seemed to help with the upper stomach pain right under the breastbone. I'm taking two pills a day. Does anyone know how long Protonix takes to work? I was told that some PPI's could take 4 to six weeks to take affect.
1713494 tn?1327519682 Would your local mental health service have access to that information? Maybe whereever you go for governement assistance (financially) they may have some info. Have you tried a google search?
Avatar m tn First, I've been to the doctor and they prescribed Nexium, because of my stomach acidity. I used to wake up in the middle of the night choking because of the acid reflux was so bad. I raised my pillows and have alleviated this issue. That being said, after a regular meal, my stomach is extremely full (today it was just soup and two Grands biscuits) and it feels like I have to throw up. Sometimes I'll start coughing because of this and actually throw up.
Avatar f tn Without the patient assistance program I probably wouldn't be SVR - when my insurance refused to let me extend, they coudln't have made it easier and didn't even make me feel bad about needing them to help.
Avatar n tn I am also on Copaxone - can I suggest that you talk with them again at Shared Solutions and ask what criteria they use for patient assistance? They fund for people without insurance or underinsured through NORD - national organization of rare disease. Unfortunately it sometimes takes more than one phone call to connect with the right people at SS to get help. If you can't work it out with SS you might talk to your neurologist about other options.
Avatar m tn If in need, call the Schering-Plough Patient Assistance Program at 1-800-521-7157 and/or the Roche Patient Assistance Program at 1-877-757-6243. November 10, 2008 http://www.hepatitis-central.com/mt/archives/2008/11/choosing_and_af.
572651 tn?1530999357 There are so many drug assistance programs out there for us in the US who are not on medicare/medicaid or live in Massachussetts. I'm thinking it might be helpful to start a thread of some of these so everyone is taking full advantage of the drug companies' generosity. Ok, you know I'm being facetious with that comment - they want us to take their drug and are bribing us to do so by helping with the copay.
Avatar f tn If you go on tysabri, or any other drugs, be sure and get on their patient assistance program. It is great help with the co-pays.