Talwin (Pentazocine) - Uses, Dose, Side effects

Pentazocine (Talwin) is an opioid pain medicine that is used to treat patients with moderate to severe pain.

Indications of Pentazocine:

  • Injection:

    • Anesthesia:

      • It is used as a complement to surgical anaesthetic for sedation prior to surgery.
    • Pain management:

      • It works well to manage severe pain that cannot be treated with other methods and necessitates the use of an opioid analgesic.
  • Oral [Canadian product]:

    • Pain management:

      • It is prescribed for moderate to severe chronic or acute pain.
    • Limitations of use:

      • Pentazocine should only be used on patients for whom existing treatment choices (such as nonopioid analgesics and opioid combination medications) are ineffective, poorly tolerated, or would otherwise fall short of providing acceptable pain control.

Pentazocine (Talwin) dose in adults:

Note: Injections of pentazocine have been banned in the US for more than a year.

Pentazocine (Talwin) Injection:

  • Dose in the Anesthesia for pain management:

    • IM, SubQ:
      • 30 mg every three to four hours with a maximum dose of 60 mg
      • 360 mg  per day is maximum dose 
    • IV:
      • 30 mg every 3 to 4 hours, with a dosage cap of 30 mg.
      • 360 mg per day is maximum dose
  • Dose in the Labor pain:

    • IM:
      • 30 mg one time
    • IV:
      • 20 mg as needed every two to three hours
      • 60 mg is maximum dose

Pentazocin Oral:

Dose in the management of Pain:

  • Not receiving opioids at the time of initiation:

    • 50 mg every four hours at first; increasing the dose in accordance with response and tolerability to 50 to 100 mg every three to four hours.
    • The daily maximum is 600 mg.
  • Receiving opioids at the time of initiation:

    • For a thorough dosage conversion, consult the information provided by the manufacturer.
  • Discontinuation of therapy:

    • When stopping a long-term opioid medication regimen, the dose is decreased gradually.
    • There isn't yet a tapering schedule that is ideal for all patients.
    • The suggested timetables range from gradual (10% reductions weekly, for example) to abrupt (25–50% reductions every few days).
      Individualized tapering schedules should be used to reduce opioid withdrawal while taking into account the aims and issues unique to the patient as well as the pharmacokinetics of the opioid being reduced.
    • Slow tapering is required in patients receiving opioids for years, whereas more rapid tapers may be appropriate in patients experiencing severe adverse effects.
    • Signs/symptoms of withdrawal should be carefully monitored.
    • Slow tapering should be done in patients displaying withdrawal symptoms, alterations may include increasing the interval between dose reductions, decreasing amount of daily dose reduction, pausing the taper and restarting when the patient is ready, and/or coadministration of an alpha-2 agonist (eg, clonidine) to blunt withdrawal symptoms.
    • Nonopioid analgesics should be given for pain management during the taper; consider nonopioid adjunctive treatments for withdrawal symptoms (eg, GI complaints, muscle spasm) as required.

Pentazocine (Talwin) dose in children:

Talwin dose in the treatment of perioperative Analgesia: 

  • Children 5 to 9 years:

    • Initial: 0.5 mg/kg intravenous given with an anaesthetic; if the process takes longer than expected, tiny incremental doses may be repeated as needed every 30 to 45 minutes.
    • 1.5 mg/kg maximum total dosage per operation.
    • Based on a study of 50 paediatric surgical patients (n=50), the recommended dosage.

Pentazocine dose in the treatment of postoperative Analgesia:

  • Children 5 to 8 years:

    • 15 mg one IM dose
  • Children ≥9 years and Adolescents <15 years:

    • 30 mg one IM dose

Pentazocine dose in the treatment of preoperative Sedation:

  • Children and Adolescents ≤16 years:

    • 0.8 to 1.9 mg/kg/dose may offer a gentler induction, according to clinical research; 0.5 mg/kg intramuscular as a single dosage.
    • Note: The typical dose for adults is 30 mg.

Pentazocine pregnancy Risk Category: C

  • Studies on animal reproduction showed that there were adverse events.
  • Pentazocine can be used to relieve pain during labor. However, opioids can temporarily alter the heart rate of the foetus.
  • [US Boxed Warning]
    • Neonatal withdrawal syndrome may happen if long-term opiate use is sustained while pregnant. This may pose a life-threatening situation. It's crucial to keep a watchful eye on the newborn.
    • The prescribing physician should only prescribe the lowest possible dosage of opioids if necessary.
    • Neonatal withdrawal syndrome is characterized by fever, temperature instability and vomiting, diarrhea, vomiting or poor nutrition/weight gain, high pitched crying, increased muscle tone, irritability and seizure.
    • Long-term therapy can help with secondary hypogonadism, which is a condition that causes sexual dysfunction.

Pentazocine use during breastfeeding:

  • Whether pentazocine is secreted in breast milk is unknown.
  • Opioids given during labor can disrupt a newborn's natural instinct to breastfeed.
  • Pentazocine therapy for breast-feeding mothers should be monitored for psychotomimetic reactions.
  • Monitoring is important because large doses of opioids can cause sedation and apnea.
  • According to the manufacturer's instructions, breast-feeding is a decision that depends on the risks and benefits to the infant and the benefits to the mother.

Pentazocine Dose adjustment in renal disease:

  • The manufacturer's labelling does not mention dosage modifications.
  • Take care when using.
  • Some therapists have utilised the suggestions below..
    • GFR ≥50 mL/minute:

      • Dosage adjustment is not required
    • GFR 10 to 50 mL/minute:

      • Administer 75% of the normal dose.
    • GFR <10 mL/minute:

      • Administer 50% of normal dose.

Pentazocine Dose adjustment in liver disease:

There are no dosage adjustments provided in the manufacturer’s labeling. However decreased metabolism and predisposition to adverse effect might need dose reduction.

Side effects of Pentazocine (Talwin):

  • Cardiovascular:

    • Circulatory Depression
    • Facial Edema
    • Flushing
    • Hypertension
    • Hypotension
    • Increased Peripheral Vascular Resistance
    • Shock
    • Syncope
    • Tachycardia
  • Central Nervous System:

    • Central Nervous System Depression
    • Chills
    • Confusion
    • Disorientation
    • Dizziness
    • Drowsiness
    • Drug Dependence (Physical And Psychological)
    • Euphoria
    • Excitement
    • Hallucination
    • Headache
    • Insomnia
    • Irritability
    • Malaise
    • Nightmares
    • Paresthesia
    • Sedation
  • Dermatologic:

    • Dermatitis
    • Diaphoresis
    • Erythema Multiforme
    • Pruritus
    • Skin Rash
    • Stevens-Johnson Syndrome
    • Toxic Epidermal Necrolysis
    • Urticaria
  • Gastrointestinal:

    • Abdominal Distress
    • Anorexia
    • Constipation
    • Diarrhea
    • Dysgeusia
    • Nausea
    • Vomiting
    • Xerostomia
  • Genitourinary:

    • Urinary Retention
  • Hematologic & Oncologic:

    • Agranulocytosis (Rare)
    • Decreased White Blood Cell Count
    • Eosinophilia
  • Hypersensitivity:

    • Anaphylaxis
  • Local:

    • Injection Site Reaction (Tissue Damage And Irritation)
  • Neuromuscular & Skeletal:

    • Tremor
    • Weakness
  • Ophthalmic:

    • Blurred Vision
    • Diplopia
    • Miosis
    • Nystagmus
  • Otic:

    • Tinnitus
  • Respiratory:

    • Dyspnea
    • Respiratory Depression (Rare)

Contraindication to Pentazocine (Talwin):

  • Hypersensitivity to pentazocine and any component of the formulation (eg, anaphylaxis).
  • GI obstruction/ paralytic ileus
  • In a setting that does not have resuscitative equipment, severe bronchial asthma
  • Grave respiratory depression

Canadian labeling: Additional contraindications not in US labeling

  • Hypersensitivity to other opioids
  • Alcoholism
  • Delirium tremens
  • Acute appendicitis/pancreatitis
  • Hypercapnia and COPD are symptoms of status asthmaticus.
  • Convulsive disorders, severe CNS depression, head injury, and increased ICP
  • Breastfeeding/pregnancy
  • Combine within 14 days of monoamine-oxidase inhibitors.

Warnings and precautions

  • Cardiovascular effects

    • It is important to avoid it in MI because of its potential for increasing systemic and pulmonary arterial pressures and systemic resistance.
  • CNS depression:

    • CNS depression can cause impairments in mental or physical abilities. Patients should be cautious about driving or operating machinery.
  • Hypotension

    • Patients with hypovolemia, heart disease, or medications that can exaggerate hypotensive effects (e.g. phenothiazines and general anesthetics), should not take pentazocine.
    • It may cause severe hypotension. Avoid it if you have circulatory shock.
  • Injection-site reactions:

    • The epidermis, subcutaneous tissues, and underlying muscles may have severe sclerosis as a result of subcutaneous injections.
  • Respiratory depression [US Boxed Warning]

    • Respiratory depression should be closely monitored as carbon dioxide retention may exacerbate the sedating effects associated with opioids.
  • Conditions abdominales:

    • Patients with acute abdominal conditions may not be diagnosed or treated appropriately.
  • Adrenocortical Insufficiency

    • Patients with adrenal insufficiency (Addison disease) should be cautious.
    • Long-term therapy can lead to mood disorder, osteoporosis and sexual dysfunction caused by secondary hypogonadism.
  • Insufficiency of the biliary tract:

    • Patients with acute pancreatitis or biliary dysfunction should be cautious. Opioids may cause constriction in the sphincter.
  • CNS depression/coma:

    • Patients who are unconscious or comatose are more susceptible to the intracranial effects CO retention. It should therefore not be used.
  • Delirium tremens:

    • Patients with delirium-tremens should be taken with caution
  • Head trauma

    • If intracranial pressure is increased due to head injury or intracranial lesions, intracranial pressure can rise.
  • Hepatic impairment

    • Patients with hepatic impairment should be cautious.
  • Obesity:

    • Patients who are severely obese should be taken with caution
  • Prostatic hyperplasia/Urinary stricture:

    • Patients with prostatic hyperplasia or urinary stricture should be cautious.
  • Psychosis:

    • Patients with toxic psychosis should be treated with caution.
  • Renal impairment

    • Patients with impaired renal function should be cautious.
  • Respiratory disease

    • It should not be used in COPD, cor pulmonale hypercapnia or preexisting respiratory depression. It is recommended to use alternative non-opioid pain relievers.
  • Seizures:

    • Preexisting seizures may be exacerbated or caused by it. Use caution.
  • Thyroid dysfunction:

    • Patients with thyroid dysfunction should be cautious.

Pentazocine: Drug Interaction

Risk Factor C (Monitor therapy)

Alizapride

May enhance the CNS depressant effect of CNS Depressants.

Amphetamines

May enhance the analgesic effect of Opioid Agonists.

Anticholinergic Agents

May enhance the adverse/toxic effect of Opioid Agonists. Specifically, the risk for constipation and urinary retention may be increased with this combination.

Brimonidine (Topical)

May enhance the CNS depressant effect of CNS Depressants.

Bromopride

May enhance the CNS depressant effect of CNS Depressants.

Cannabidiol

May enhance the CNS depressant effect of CNS Depressants.

Cannabis

May enhance the CNS depressant effect of CNS Depressants.

Chlorphenesin Carbamate

May enhance the adverse/toxic effect of CNS Depressants.

Desmopressin

Opioid Agonists may enhance the adverse/toxic effect of Desmopressin.

Dimethindene (Topical)

May enhance the CNS depressant effect of CNS Depressants.

Diuretics

Opioid Agonists may enhance the adverse/toxic effect of Diuretics. Opioid Agonists may diminish the therapeutic effect of Diuretics.

Dronabinol

May enhance the CNS depressant effect of CNS Depressants.

Gastrointestinal Agents (Prokinetic)

Opioid Agonists may diminish the therapeutic effect of Gastrointestinal Agents (Prokinetic).

Kava Kava

May enhance the adverse/toxic effect of CNS Depressants.

Lofexidine

May enhance the CNS depressant effect of CNS Depressants. Management: Drugs listed as exceptions to this monograph are discussed in further detail in separate drug interaction monographs.

Magnesium Sulfate

May enhance the CNS depressant effect of CNS Depressants.

MetyroSINE

CNS Depressants may enhance the sedative effect of MetyroSINE.

Minocycline

May enhance the CNS depressant effect of CNS Depressants.

Nabilone

May enhance the CNS depressant effect of CNS Depressants.

Pegvisomant

Opioid Agonists may diminish the therapeutic effect of Pegvisomant.

Piribedil

CNS Depressants may enhance the CNS depressant effect of Piribedil.

Pramipexole

CNS Depressants may enhance the sedative effect of Pramipexole.

Ramosetron

Opioid Agonists may enhance the constipating effect of Ramosetron.

ROPINIRole

CNS Depressants may enhance the sedative effect of ROPINIRole.

Rotigotine

CNS Depressants may enhance the sedative effect of Rotigotine.

Rufinamide

May enhance the adverse/toxic effect of CNS Depressants. Specifically, sleepiness and dizziness may be enhanced.

Selective Serotonin Reuptake Inhibitors

CNS Depressants may enhance the adverse/toxic effect of Selective Serotonin Reuptake Inhibitors. Specifically, the risk of psychomotor impairment may be enhanced.

Serotonin Modulators

Opioid Agonists may enhance the serotonergic effect of Serotonin Modulators. This could result in serotonin syndrome. Exceptions: Nicergoline.

Succinylcholine

May enhance the bradycardic effect of Opioid Agonists.

Tetrahydrocannabinol

May enhance the CNS depressant effect of CNS Depressants.

Tetrahydrocannabinol and Cannabidiol

May enhance the CNS depressant effect of CNS Depressants.

Tobacco (Smoked)

May lower the level of pentazocine in the serum.

Risk Factor D (Consider therapy modification)

Alvimopan

Opioid Agonists may enhance the adverse/toxic effect of Alvimopan. This is most notable for patients receiving long-term (i.e., more than 7 days) opiates prior to alvimopan initiation. Management: Alvimopan is contraindicated in patients receiving therapeutic doses of opioids for more than 7 consecutive days immediately prior to alvimopan initiation.

Blonanserin

CNS Depressants may enhance the CNS depressant effect of Blonanserin.

Chlormethiazole

May enhance the CNS depressant effect of CNS Depressants. Management: Monitor closely for evidence of excessive CNS depression. The chlormethiazole labeling states that an appropriately reduced dose should be used if such a combination must be used.

CNS Depressants

May enhance the CNS depressant effect of Opioid Agonists. Management: Avoid concomitant use of opioid agonists and benzodiazepines or other CNS depressants when possible. These agents should only be combined if alternative treatment options are inadequate. If combined, limit the dosages and duration of each drug.

Droperidol

May enhance the CNS depressant effect of CNS Depressants. Management: Consider dose reductions of droperidol or of other CNS agents (eg, opioids, barbiturates) with concomitant use. Exceptions to this monograph are discussed in further detail in separate drug interaction monographs.

Flunitrazepam

CNS Depressants may enhance the CNS depressant effect of Flunitrazepam.

Methotrimeprazine

CNS Depressants may enhance the CNS depressant effect of Methotrimeprazine. Methotrimeprazine may enhance the CNS depressant effect of CNS Depressants. Management: Reduce adult dose of CNS depressant agents by 50% with initiation of concomitant methotrimeprazine therapy. Further CNS depressant dosage adjustments should be initiated only after clinically effective methotrimeprazine dose is established.

Nalmefene

May diminish the therapeutic effect of Opioid Agonists. Management: Avoid the concomitant use of nalmefene and opioid agonists. Discontinue nalmefene 1 week prior to any anticipated use of opioid agonistss. If combined, larger doses of opioid agonists will likely be required.

Naltrexone

May diminish the therapeutic effect of Opioid Agonists. Management: Seek therapeutic alternatives to opioids. See full drug interaction monograph for detailed recommendations.

Perampanel

May enhance the CNS depressant effect of CNS Depressants. Management: Patients taking perampanel with any other drug that has CNS depressant activities should avoid complex and high-risk activities, particularly those such as driving that require alertness and coordination, until they have experience using the combination.

Sincalide

Drugs that Affect Gallbladder Function may diminish the therapeutic effect of Sincalide. Management: Consider discontinuing drugs that may affect gallbladder motility prior to the use of sincalide to stimulate gallbladder contraction.

Sodium Oxybate

May enhance the CNS depressant effect of CNS Depressants. Management: Consider alternatives to combined use. When combined use is needed, consider minimizing doses of one or more drugs. Use of sodium oxybate with alcohol or sedative hypnotics is contraindicated.

Suvorexant

CNS Depressants may enhance the CNS depressant effect of Suvorexant. Management: Dose reduction of suvorexant and/or any other CNS depressant may be necessary. Use of suvorexant with alcohol is not recommended, and the use of suvorexant with any other drug to treat insomnia is not recommended.

Zolpidem

CNS Depressants may enhance the CNS depressant effect of Zolpidem. Management: Reduce the Intermezzo brand sublingual zolpidem adult dose to 1.75 mg for men who are also receiving other CNS depressants. No such dose change is recommended for women. Avoid use with other CNS depressants at bedtime; avoid use with alcohol.

Risk Factor X (Avoid combination)

Azelastine (Nasal)

CNS Depressants may enhance the CNS depressant effect of Azelastine (Nasal).

Bromperidol

May enhance the CNS depressant effect of CNS Depressants.

Buprenorphine

Opioids (Mixed Agonist / Antagonist) may diminish the therapeutic effect of Buprenorphine. This combination may also induce opioid withdrawal.

Eluxadoline

Opioid Agonists may enhance the constipating effect of Eluxadoline.

Opioid Agonists

Opioids (Mixed Agonist / Antagonist) may diminish the analgesic effect of Opioid Agonists. Management: Seek alternatives to mixed agonist/antagonist opioids in patients receiving pure opioid agonists, and monitor for symptoms of therapeutic failure/high dose requirements (or withdrawal in opioid-dependent patients) if patients receive these combinations. Exceptions: Buprenorphine; Butorphanol; Meptazinol; Nalbuphine; Pentazocine.

Orphenadrine

CNS Depressants may enhance the CNS depressant effect of Orphenadrine.

Oxomemazine

May enhance the CNS depressant effect of CNS Depressants.

Paraldehyde

CNS Depressants may enhance the CNS depressant effect of Paraldehyde.

Thalidomide

CNS Depressants may enhance the CNS depressant effect of Thalidomide.

Monitoring parameters:

  • BP
  • Respiratory and mental status,
  • bowel function
  • Pain relief
  • signs/symptoms of misuse, abuse, and addiction
  • signs or symptoms of hypogonadism or hypoadrenalism.

How to administer Pentazocine (Talwin)?

Injection:

  • IM, IV, or SubQ usage only. IM injection locations should be alternated (eg, the upper outer quadrants of the buttocks, mid-lateral aspects of the thighs, and the deltoid areas).
  • There should be no intraarterial injection. Only use subcutaneous injections if absolutely essential (may cause tissue damage).

Oral: Tablet [Canadian product]:

  • Only for oral usage. After meals, give the entire dose without crushing, chewing, blending, or breaking.

Mechanism of action of Pentazocine (Talwin):

  • In the central nervous system (CNS), pentazocine functions as a kappa agonist and a partial agonist for mu opiate.
  • It modifies how pain is perceived, how the body reacts to pain, and it blocks the ascending pain pathways.
  • Similar to opioids, this causes analgesia, respiratory depression, and drowsiness.

Absorption:

  • Oral: [Canadian Product]: Well absorbed; low bioavailability due to the extensive first-pass effect

The onset of action:

  • IM, SubQ: 15 to 20 minutes.
  • IV: 2 to 3 minutes
  • Oral [Canadian product]: 15 to 30 minutes

Duration:

  • Injection: 2 to 3 hours
  • Oral [Canadian product]: ≥3 hours

Protein binding:

  • 60%

Time to peak (serum):

  • Oral [Canadian product]: 1 to 3 hours

Metabolism: Hepatic via oxidative and glucuronide conjugation pathways; extensive first-pass effect

Half-life elimination: Prolonged with hepatic impairment

  • Neonates: 8 to 12 hours
  • Children 4 to 8 years (mean ± SD): 3 ± 1.5 hours
  • Adults: 2 to 5 hours

Excretion:

  • Urine (small amounts as unchanged drug)

International Brands of Pentazocin (Talwin):

  • Talwin
  • Dolapent
  • Fortal
  • Fortalgesic[inj.]
  • Fortalgesic[Suppos.]
  • Fortalgesic[Tab.]
  • Fortral
  • Fortralin
  • Fortralin[inj./rect.]
  • Fortralin[inj.]
  • Fortwin
  • Ospronim
  • Pellpenta
  • Peltazon
  • Pentagin
  • Pentajin
  • Pental
  • Pentawin
  • Pentazocinum
  • Sosegon
  • Sosegon[inj./rect.]
  • Stopain
  • Talwin
  • Talwin Lactate

Pentazocine Brands in Pakistan:

Pentazocine Injection 30 mg/ml

Entapin Brookes Pharmaceutical Laboratories (Pak.) Ltd.
Pentacin Medicaids Pakistan (Pvt) Ltd.
Pentazowan Swan Pharmaceuticals (Pvt) Ltd

 

Pentazocine Injection 30 mg/ml

Elcigon Elko Organization (Pvt) Ltd.
Iscigon Isis Pharmaceutical
Mentazocine Medicraft Pharmaceuticals (Pvt) Ltd.
Omsis Sami Pharmaceuticals (Pvt) Ltd.
P-Zoc Fynk Pharmaceuticals
Paingon Mediceena Pharma (Pvt) Ltd.
Pantonil Tabros Pharma
Pentafen Tread Pharmaceuticals Pvt Ltd
Pentagesic Lahore Chemical & Pharmaceutical Works (Pvt) Ltd
Pentagon The Schazoo Laboratories Ltd.
Pentazogon Indus Pharma (Pvt) Ltd.
Pentazogon Indus Pharma (Pvt) Ltd.
Penzocine Amson Vaccines & Pharma (Pvt) Ltd.
Shasogon Shifa Laboratories.(Pvt) Ltd.
Sosegon Sanofi Aventis (Pakistan) Ltd.
Soseno Dosaco Laboratories
Vesegon Venus Pharma

 

Pentazocine 25 mg Tablets

Eroflex Eros Pharmaceuticals
Gosegon Gray`S Pharmaceuticals
Mentazocine Medicraft Pharmaceuticals (Pvt) Ltd.
Opidan Danas Pharmaceuticals (Pvt) Ltd
Panatik Panacea Pharmaceuticals
Pantonil Tabros Pharma
Pentacin Medicaids Pakistan (Pvt) Ltd.
Pentanor Global Pharmaceuticals
Pentaz Universal Pharmaceuticals (Pvt) Ltd
Pocin Rakaposhi Pharmaceutical (Pvt) Ltd.
Segon Saydon Pharmaceutical Industries (Pvt) Ltd.
Sosegon Sanofi Aventis (Pakistan) Ltd.
Zocin Valor Pharmaceuticals
Zocinitt Lowitt Pharmaceuticals (Pvt) Ltd
Zomiten Pliva Pakistan (Pvt) Limited