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Opium Tincture
Pronunciation
Generic Available
Synonyms
Pharmacological Index
Use
Restrictions
Pregnancy Risk Factor
Contraindications
Warnings/Precautions
Adverse Reactions
Overdosage/Toxicology
Drug Interactions
Stability
Mechanism of Action
Pharmacodynamics/Kinetics
Usual Dosage
Dietary Considerations
Monitoring Parameters
Test Interactions
Mental Health: Effects on Mental Status
Mental Health: Effects on Psychiatric Treatment
Dental Health: Local Anesthetic/Vasoconstrictor Precautions
Dental Health: Effects on Dental Treatment
Patient Information
Nursing Implications
Dosage Forms
References

Pronunciation
(OH pee um TING chur)

Generic Available

No


Synonyms
Deodorized Opium Tincture; DTO

Pharmacological Index

Analgesic, Narcotic; Antidiarrheal


Use

Treatment of diarrhea or relief of pain


Restrictions

C-II


Pregnancy Risk Factor

B/D (if used for prolonged periods or in high doses at term)


Contraindications

Increased intracranial pressure, severe respiratory depression, severe liver or renal insufficiency, known hypersensitivity to morphine sulfate


Warnings/Precautions

Opium shares the toxic potential of opiate agonists, and usual precautions of opiate agonist therapy should be observed; some preparations contain sulfites which may cause allergic reactions; infants <3 months of age are more susceptible to respiratory depression, use with caution and generally in reduced doses in this age group; this is not paregoric, dose accordingly


Adverse Reactions

>10%:

Cardiovascular: Palpitations, hypotension, bradycardia

Central nervous system: Drowsiness, dizziness

Neuromuscular & skeletal: Weakness

1% to 10%:

Central nervous system: Restlessness, headache, malaise

Genitourinary: Decreased urination

Miscellaneous: Histamine release

<1%: Peripheral vasodilation, CNS depression, increased intracranial pressure, insomnia, mental depression, nausea, vomiting, constipation, anorexia, stomach cramps, biliary tract spasm, urinary tract spasm, miosis, respiratory depression, physical and psychological dependence


Overdosage/Toxicology

Primary attention should be directed to ensuring adequate respiratory exchange; opiate agonist-induced respiratory depression may be reversed with parenteral naloxone hydrochloride


Drug Interactions

Decreased effect: Phenothiazines may antagonize the analgesic effect of opiate agonists

Increased toxicity: CNS depressants, MAO inhibitors, tricyclic antidepressants may potentiate the effects of opiate agonists; dextroamphetamine may enhance the analgesic effect of opiate agonists


Stability

Protect from light


Mechanism of Action

Contains many narcotic alkaloids including morphine; its mechanism for gastric motility inhibition is primarily due to this morphine content; it results in a decrease in digestive secretions, an increase in GI muscle tone, and therefore a reduction in GI propulsion


Pharmacodynamics/Kinetics

Duration of effect: 4-5 hours

Absorption: Variable from GI tract

Metabolism: In the liver

Elimination: Urine


Usual Dosage

Oral:

Diarrhea: 0.005-0.01 mL/kg/dose every 3-4 hours for a maximum of 6 doses/24 hours

Analgesia: 0.01-0.02 mL/kg/dose every 3-4 hours

Adults:

Diarrhea: 0.3-1 mL/dose every 2-6 hours to maximum of 6 mL/24 hours

Analgesia: 0.6-1.5 mL/dose every 3-4 hours


Dietary Considerations

Alcohol: Additive CNS effect, avoid use


Monitoring Parameters

Observe patient for excessive sedation, respiratory depression, implement safety measures, assist with ambulation


Test Interactions

aminotransferase [ALT (SGPT)/AST (SGOT)] (S)


Mental Health: Effects on Mental Status

Dizziness and drowsiness are common; may cause restlessness; may rarely cause insomnia or depression


Mental Health: Effects on Psychiatric Treatment

Concurrent use with psychotropics may alter the analgesic effects of opioids; monitor for altered response


Dental Health: Local Anesthetic/Vasoconstrictor Precautions

No information available to require special precautions


Dental Health: Effects on Dental Treatment

No effects or complications reported


Patient Information

If self-administered, use exactly as directed (do not increase dose or frequency); may cause physical and/or psychological dependence. While using this medication, do not use alcohol and other prescription or OTC medications (especially sedatives, tranquilizers, antihistamines, or pain medications) without consulting prescriber. Maintain adequate hydration (2-3 L/day of fluids unless instructed to restrict fluid intake). May cause hypotension, dizziness, drowsiness, impaired coordination, or blurred vision (use caution when driving, climbing stairs, or changing position - rising from sitting or lying to standing, or when engaging in tasks requiring alertness until response to drug is known); dry mouth (frequent mouth care, small frequent meals, chewing gum, or sucking lozenges may help). Report slow or rapid heartbeat, acute dizziness, or persistent headache; changes in mental status; swelling of extremities or unusual weight gain; changes in urinary elimination or pain on urination; acute headache; trembling or muscle spasms; blurred vision; skin rash; or shortness of breath. Pregnancy/breast-feeding precautions: Inform prescriber if you are or intend to be pregnant. If you are breast-feeding, take medication immediately after breast-feeding or 3-4 hours prior to next feeding.


Nursing Implications

Monitor patient for excessive sedation, respiratory depression, implement safety measures, assist with ambulation


Dosage Forms

Liquid: 10% [0.6 mL equivalent to morphine 6 mg]


References

Kraus DM and Hatzopoulos FK, "Neonatal Therapy," Applied Therapeutics: The Clinical Use of Drugs, 6th ed, Young LY and Koda-Kimble MA, eds, Vancouver, WA: Applied Therapeutics, Inc, 1995.

Levy M and Spino M, "Neonatal Withdrawal Syndrome: Associated Drugs and Pharmacologic Management," Pharmacotherapy, 1993, 13(3):202-11.


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