When Will Opana Er Be Resumed (Page 2)

Has anyone heard when novartis plant will start making opana ER again? This was my best pain med.

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Cactus Arizona, I am still at this time getting Opana ER well at least last month I take 40mg every 12 hrs. & Dilaudid for break through pain. I don't feel like listing my many ailments, except my new one if frozen shoulder which came from Levaquin (never take this medication again) my pain doc feels it is not painful yet my Ortho said it is extremely painful which I'm duh I already know it is. The PT is excruciating because they stretch you until you scream & the next day all I can do is cry. At this point I am still able to get my Opana ER but when I ask him about what I will be changed to I don't get an answer. I'm very frustrated he is not tapering me & just says oh we will deal with it then? I too am frustrated with the people who misuse and post on here and answer questions. It is annoying and has destroyed many of us who need it. For those that are disabled & need this medication, who don't abuse or trade with people because that also hurts us as well, it matters if you're in pain or not, there is a petition on change.org right now that needs many signatures from the disabled to fight to keep our pain meds. In 2018 they will be cutting even more meds out. Please I don't know if I'm allowed to post it on here the link go there and sign it. It needs tons of signatures. Thank you for the information you posted, if there's anything I can do to help let me know. I've talked to the makers also more than 3x already. I might be hunting for a new doctor at this point.

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