This medication may cause a condition known as tardive dyskinesia. In some cases, this condition may be permanent. Tardive dyskinesia is more likely to occur when metoclopramide is used for longer than 3 months, in high doses, or when used in the elderly (especially elderly women). Contact your doctor immediately if you develop any unusual uncontrolled movements (especially of the face, mouth, tongue, arms or legs)....
Read moreThe FDA has issued a new warning about the use of Reglan or Metaclopramide, a medication that may be used to treat Gastroesophageal Reflux... Read more »
As most of you know the FDA just released a new "Black Box Warning" for metaclopramide or Reglan. In my opinion this warning is long... Read more »
I recently received an e-mail, asking about a herbal preparation that the reader had found on the Internet. Paraphrased, it read:"I... Read more »
Most of us only think about adverse drug reactions when we hear about a celebrity who has died from a lethal mix of narcotic medications. ... Read more »
The FDA Safety Information and Adverse Event Reporting Program “Your FDA gateway for finding clinically important safety... Read more »
A reader asks Joe and Teresa Graedon of The People's Pharmacy if the reflux drug Reglan could be used to enhance breast-milk production. The Graedons... Read more »
An adverse drug reaction (ADR) occurs when a drug, supplement or food interferes with or interacts negatively with another drug. While ADRs may be... Read more »
A reader who recently had joint surgery asks Joe Graedon of The People's Pharmacy if the naproxen he was taking for pain could be the cause of his... Read more »
The U.S. Food and Drug Administration (FDA) is requiring a black box warning be added the label for the heartburn drug Reglan. The FDA says the drug... Read more »
The following is a copy of a letter sent to healthcare professionals following an FDA MedWatch warning about decreased sweating as a potentially... Read more »