nts with hepatic insufficiency.
Since dihydrocodeine is metabolized by the liver the effects of this combination product should be
monitored closely in such patients.
Renal Impariment: This product should be used with caution and at reduced dosage in the presence of
impaired renal function.
Pancreatic/biliary Tract Disease: Opioids may cause spasms of the spinchter of Oddi and should be
used with caution in patients with biliary tract disease, including pancreatitis.
ADVERSE REACTIONS
The most frequently observed adverse reactions with dihydrocodeine include light-headedness,
dizziness, drowsiness, headache, fatigue, sedation, sweating, nausea, vomiting, constipation,
pruritus, and skin reactions. With the exception of constipation, tolerance develops to most of
these effects. Other reactions that have been observed with dihydrocodeine or opioids include
respiratory depression, orthostatic hypotension, cough suppression, confusion, diarrhea, miosis,
abdominal pain, dry mouth, indigestion, anorexia, spasm of biliary tract, and urinary retention.
Physical and psychological dependence are possibilities. Hypersensitivity reactions (include
anaphylactoid reactions), hallucinations, vivid dreams, granulomatous interstitial nephritis, severe
narcosis and acute renal failure have been reported rarely during dihydrocodeine administration.
Other reactions observed with the ingredients of this product include lassitude, nausea, giddiness,
dryness of mouth, blurred vision, cardiac palpitations, flushing, increased irritability or excitement
(especially in children).
DRUG ABUSE AND DEPENDENCE
This combination product is subject to the provisions of the Controlled Substances Act and
has been placed in Schedule III. Dihydrocodeine can produce drug dependence of the codeine
type and therefore has the potential of being abused. Psychological dependence, physical
dependence, and tolerance may develop upon repeat administration of dihydrocodeine, and it
should be prescribed and administered with the same degree of caution appropriate to the use
of other opioid medications. Symptoms of dihydrocodeine withdrawal consist of irritability,
restlessness, insomnia, diaphoresis, anxiety, and palpitations.
OVERDOSAGE
An overdose of this product is a potentially lethal poly-drug overdose situation, and
consultation with a regional Poison Control Center is recommended. A listing of the
Poison Control Centers can be found in a standard reference such as the Physician's
Desk Reference.
Signs and Symptoms:
Symptoms of an overdose include pinpoint pupils, respiratory depression, extreme
somnolence progressing to stupor, loss of consciousness or coma, skeletal muscle
flaccidity, cold and clammy skin and other symptoms common with narcotic overdosage.
Convulsions, cardiovascular collapse, and death may occur. A single case of acute
rhabdomyolysis associated with an overdose of dihydrocodeine has been reported.
Recommended Treatment:
Immediate treatment of an overdose of this product includes support of cardiovascular
function and measure to reduce further drug absorption. Vomiting should be induced with
syrup of ipecac. If the patient is alert and has adequate laryngeal reflexes, oral activated
charcoal should follow. The first dose should be accompanied by a