trigonometry1972@gmail.com |
2009-02-28 07:56:49 UTC
The FDA has recently announced that drugs containing metoclopramide
must carry a boxed warning about the risk of tardive dyskinesia. Risk
of this condition is much higher with long-term usage and currently
the existing labels already carry an unboxed warning. The FDA
recommends that treatment last no longer than three months.
Often tardive dyskinesia will continue after stopping the drug and
rarely reverses. The FDA has said that manufacturers of the drugs that
contain metoclopramide are to also implement a risk mitigation
strategy that is to ensure patients will receive a medication guide
with each prescription which details the
adverse effects.
Metoclopramide-containing drugs include tablets, syrups and injections
which are used for short-term treatment of gastroesophageal reflux
disease in patients who haven't responded to other therapies.
must carry a boxed warning about the risk of tardive dyskinesia. Risk
of this condition is much higher with long-term usage and currently
the existing labels already carry an unboxed warning. The FDA
recommends that treatment last no longer than three months.
Often tardive dyskinesia will continue after stopping the drug and
rarely reverses. The FDA has said that manufacturers of the drugs that
contain metoclopramide are to also implement a risk mitigation
strategy that is to ensure patients will receive a medication guide
with each prescription which details the
adverse effects.
Metoclopramide-containing drugs include tablets, syrups and injections
which are used for short-term treatment of gastroesophageal reflux
disease in patients who haven't responded to other therapies.