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What is Potiga
Approved as Treatment by the FDA
Ezogabine, otherwise called Potiga, is approved by the FDA for 1 uses including Refractory Partial Onset Seizures .Effectiveness
When to interrupt dosage
The advised measure of Potiga hinges on the acknowledged disorder. The dosage amount can be found in the table below, subject to the method of administration (e.g. Tablet, film coated - Oral or Oral).Warnings
There are 20 known major drug interactions with Potiga.Potiga Novel Uses: Which Conditions Have a Clinical Trial Featuring Potiga?
At present, there are no active trials examining the potential of Potiga to ameliorate Refractory Partial Onset Seizures.Potiga Reviews: What are patients saying about Potiga?
Patient Q&A Section about potiga
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.Is ezogabine a controlled substance?
"Ezogabine will be classified as a Schedule IV drug under the Controlled Substances Act, due to the potential for abuse leading to physical or psychological dependence."
Why was potiga discontinued?
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The company has stated that the withdrawal is for commercial reasons due to limited use of the drug and declining numbers of patients who start therapy with the drug."
What kind of drug is potiga?
"Potiga is a drug used to treat partial onset seizures. It may be used alone or with other medications. Potiga belongs to a class of drugs called anticonvulsants or neuronal potassium channel openers."
Why was retigabine withdrawn?
"This product is no longer being manufactured because it is not being used as often and the demand for it is declining. The letter from the company says that healthcare providers should start seeking other options for treatment for patients who are currently taking this product and to do so gradually over the course of at least 3 weeks by reducing the dose. New patients should not start taking this product."