Dihydrocodeine: Difference between revisions

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===Treatment of Adverse Effects===
===Treatment of Adverse Effects===
Abdominal pain, hyperthermia, pancreatitis Euphoria, nausea and vomiting, respiratory depression, constipation and cough suppression.
Abdominal pain, hyperthermia, pancreatitis Euphoria, nausea and vomiting, respiratory depression, constipation and cough suppression.
==Pharmacokinetics==
{|class="wikitable"
!Oral bioavailability
|Oral bioavailability is only about 20%, probably because of substantial first-pass metabolism in the gut wall or liver.
|-
!Onset of action
|peak concentrations of dihydrocodeine occur about 1.2 to 1.8 hours after oral doses.
|-
!Metabolism
|Dihydrocodeine is metabolized in the liver, and is excreted in urine.
|-
!Elimination half-life
|Elimination half-life is reported to range from about 3.5 to 5 hours.
|}

Revision as of 23:28, 4 October 2020

Dihydrocodeine is an opioid analgesic . It is used for the relief of moderate to severe pain, often in combination preparations with paracetamol. It has also been used as a cough suppressant.

Generic Name 藥名 HA Code 藥物代碼 Classification藥物分類
Dihydrocoedine DIHY01 DD

Mechanism of Action

Equivalent doses of opioid analgesics

Analgesic/Route Dose
Codeine: PO 100 mg
Diamorphine: IM, IV, SC 3 mg
Dihydrocodeine: PO 100 mg
Morphine: PO 10 mg
Morphine: IM, IV, SC 5 mg
Oxycodone: PO 6.6 mg
Tramadol: PO 100 mg
Route of Administration PO (tablet form)

Dosage

Moderate to severe pain:

Oral 30mg after food every 4 to 6 hours; up to 240mg daily.
Modified-release preparations are taken twice daily.
Subcutaneous or intramuscular 50 mg every 4 to 6 hours.

Doses in children:

  • may be given orally, or by deep subcutaneous or intramuscular injection;

1 to 3 years: 500 micrograms/kg every 4 to 6 hours

4 to 12 years: 0.5 to 1 mg/kg every 4 to 6 hours

Older children may be given the usual adult dose.

Side Effects

As for Opioid Analgesic in general

The commonest adverse effects are nausea, vomiting, constipation, drowsiness and confusion.

Large doses of opioids produce respiratory depression and hypotension, with circulatory failure and deepening coma. Death may occur from respiratory failure.

Treatment of Adverse Effects

Abdominal pain, hyperthermia, pancreatitis Euphoria, nausea and vomiting, respiratory depression, constipation and cough suppression.

Pharmacokinetics

Oral bioavailability Oral bioavailability is only about 20%, probably because of substantial first-pass metabolism in the gut wall or liver.
Onset of action peak concentrations of dihydrocodeine occur about 1.2 to 1.8 hours after oral doses.
Metabolism Dihydrocodeine is metabolized in the liver, and is excreted in urine.
Elimination half-life Elimination half-life is reported to range from about 3.5 to 5 hours.