PENTAZOCINE HYDROCHLORIDe  (pen-taz'oh-seen)  Talwin Classifications: narcotic (opiate) agonist-antagonist; analgesic; Therapeutic: narcotic; analgesic Pregnancy Category: C Controlled Substance: Schedule IV
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Availability
30 mg/mL injection
Action
Synthetic analgesic with analgesic potency approximately one-third that of morphine. Opiates exert their analgesic effects
by stimulating specific opiate receptors that produce analgesia, respiratory depression, and euphoria as well as physical
dependence.
Therapeutic Effect
Effective for moderate to severe pain relief. Acts as weak narcotic antagonist and has sedative properties.
Uses
Relief of moderate to severe pain; also used for preoperative analgesia or sedation, and as supplement to surgical anesthesia.
Contraindications
Hypersensitivity to sulfite; head injury, increased intracranial pressure; seizures; emotionally unstable patients, or history
of drug abuse; pregnancy (other than labor) (category C), lactation. Safe use in children <12 y is not established.
Cautious Use
Impaired kidney or liver function; cardiac disease; COPD, asthmas, respiratory depression; GI obstruction; biliary surgery;
patients with MI who have nausea and vomiting.
Route & Dosage
Moderate to Severe Pain (Excluding Patients in Labor) Adult: IM/IV/SC 3060 mg q34h (max: 360 mg/d) Child: IM 1530 mg
Women in Labor Adult: IM 2030 mg; 20 mg may be repeated 1 or 2 times at 23 h intervals
Renal Impairment Clcr 1050 mL/min: give 75% of dose; <10 mL/min: give 50% of dose
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Administration
Subcutaneous/Intramuscular
- IM is preferred to SC route when frequent injections over an extended period are required.
- Observe injection sites daily for signs of irritation or inflammation.
Intravenous PREPARE: Direct: Give undiluted or diluted with 1 mL sterile water for injection for each 5 mg.
ADMINISTER: Direct: Give slowly at a rate of 5 mg over 60 sec.
INCOMPATIBILITIES Solution/additive: Aminophylline, barbiturates, sodium bicarbonate, glycopyrrolate, heparin, nafcillin. Y-site: Nafcillin.
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Adverse Effects (≥1%)
Body as a Whole: Flushing, allergic reactions,
shock. CNS: Drowsiness, sweating,
dizziness, light-headedness, euphoria, psychotomimetic effects, confusion, anxiety, hallucinations, disturbed dreams, bizarre thoughts, euphoria and other mood
alterations.
CV: Hypertension, palpitation, tachycardia.
GI: Nausea, vomiting, constipation, dry mouth, alterations of taste.
Urogenital: Urinary retention.
Respiratory: Respiratory depression. Skin: Injection-site reactions (induration, nodule formation, sloughing, sclerosis, cutaneous depression), rash, pruritus.
Special Senses: Visual disturbances.
Interactions
Drug: Alcohol and other
cns depressants add to CNS depression;
narcotic analgesics may precipitate narcotic withdrawal syndrome.
Pharmacokinetics
Onset: 15 min IM, SC; 23 min IV.
Peak: 1 h IM, 15 min IV.
Duration: 3 h IM, 1 h IV.
Distribution: Crosses placenta.
Metabolism: Extensively in liver.
Elimination: Primarily in urine; small amount in feces.
Half-Life: 23 h.
Nursing Implications
Assessment & Drug Effects
- Monitor therapeutic effect. Tolerance to analgesic effect sometimes occurs. Psychologic and physical dependence have been
reported in patients with history of drug abuse, but rarely in patients without such history. Addiction liability matches
that of codeine.
- Monitor vital signs and assess for respiratory depression. Keep supine to minimize adverse efffects.
- Monitor drug-induced CNS depression.
- Be aware that pentazocine may produce acute withdrawal symptoms in some patients who have been receiving opioids on a regular
basis.
- Monitor I&O as drug may cause urinary retention.
Patient & Family Education
- Avoid driving and other potentially hazardous activities until response to drug is known.
- Do not discontinue drug abruptly following extended use; may result in chills, abdominal and muscle cramps, yawning, runny
nose, tearing, itching, restlessness, anxiety, drug-seeking behavior.