However, in November 2010, the US Food and Drug Administration (FDA) removed Darvocet from the market due to concerns about its potential for heart rhythm abnormalities that could lead to serious and even fatal events.
Common side effects of Darvocet use can include dizziness, drowsiness, nausea, vomiting, and constipation. More serious side effects can include heart rhythm abnormalities, seizures, and liver damage. Darvocet is no longer available for use and patients who were previously prescribed Darvocet should consult with their healthcare provider for alternative pain management options.
Before being withdrawn from the market, Darvocet was classified as a Schedule IV controlled substance by the US Drug Enforcement Administration (DEA) due to its potential for abuse and dependence.
Darvocet is a brand name for a prescription pain medication that contains the active ingredients propoxyphene and acetaminophen. It was used to manage mild to moderate pain.