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Pronunciation |
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(proe
POKS i feen & a seet a MIN
oh fen) |

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U.S. Brand
Names |
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Darvocet-N®; Darvocet-N® 100;
Propacet®; Wygesic® |

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Generic
Available |
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Yes |

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Synonyms |
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Propoxyphene Hydrochloride and Acetaminophen; Propoxyphene Napsylate and
Acetaminophen |

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Pharmacological Index |
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Analgesic, Narcotic |

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Use |
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Dental: Management of postoperative pain
Medical: Management of mild to moderate pain |

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Restrictions |
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C-IV |

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Pregnancy Risk
Factor |
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C |

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Contraindications |
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Hypersensitivity to propoxyphene, acetaminophen, or any component; patients
with known G-6-PD deficiency |

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Warnings/Precautions |
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When given in excessive doses, either alone or in combination with other CNS
depressants, propoxyphene is a major cause of drug-related deaths; do not exceed
recommended dosage; give with caution in patients dependent on opiates,
substitution may result in acute opiate withdrawal symptoms |

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Adverse
Reactions |
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1% to 10%:
Gastrointestinal: Nausea, vomiting
Neuromuscular & skeletal: Weakness
Miscellaneous: Psychologic and physical dependence |

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Drug
Interactions |
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Decreased effect with charcoal, cigarette smoking; increased toxicity with
cimetidine, CNS depressants; increased toxicity/effect of carbamazepine,
phenobarbital, TCAs, MAO inhibitors, benzodiazepines |

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Mechanism of
Action |
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Propoxyphene is a weak narcotic analgesic which acts through binding to
opiate receptors to inhibit ascending pain pathways
Propoxyphene, as with other narcotic (opiate) analgesics, blocks pain
perception in the cerebral cortex by binding to specific receptor molecules
(opiate receptors) within the neuronal membranes of synapses. This binding
results in a decreased synaptic chemical transmission throughout the CNS thus
inhibiting the flow of pain sensations into the higher centers. Mu and kappa are
the two subtypes of the opiate receptor which propoxyphene binds to cause
analgesia.
Acetaminophen inhibits the synthesis of prostaglandins in the CNS and
peripherally blocks pain impulse generation; produces antipyresis from
inhibition of hypothalamic heat-regulating center |

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Pharmacodynamics/Kinetics |
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Onset of action: 15-60 minutes
Time to peak serum concentration: 2-2.5 hours
Duration: 4-6 hours
Serum half-life:
Propoxyphene: 6-12 hours
Norpropoxyphene: 30-36 hours |

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Usual Dosage |
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Adults: Oral:
Darvocet-N® 100: 1 tablet every 4 hours as needed;
maximum: 600 mg propoxyphene napsylate/day |

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Dietary
Considerations |
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Should be taken with water on an empty stomach |

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Mental Health: Effects
on Mental Status |
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Dizziness, drowsiness, insomnia, and paradoxical excitement are common; may
cause nervousness, restlessness, confusion; may rarely cause depression or
hallucinations |

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Mental Health:
Effects on Psychiatric
Treatment |
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Concurrent use with psychotropics may produce additive sedation as well as
increase their serum levels; monitor for altered clinical response or
preferably, use a different analgesic |

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Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
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No information available to require special precautions |

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Dental Health:
Effects on Dental Treatment |
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No effects or complications reported |

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Patient
Information |
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See individual agents. Pregnancy precautions: Inform prescriber if
you are or intend to get pregnant. |

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Nursing
Implications |
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Monitor pain relief, respiratory and mental status, blood pressure, excessive
sedation |

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Dosage Forms |
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Tablet:
Darvocet-N® 100: Propoxyphene napsylate 100 mg and
acetaminophen 650 mg
Genagesic®, Wygesic®:
Propoxyphene hydrochloride 65 mg and acetaminophen 650 mg
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