Penzyl
Penzyl Uses, Dosage, Side Effects, Food Interaction and all others data.
Penzyl is a benzomorphan derivative with mixed opioid agonist and antagonist actions. It alters perception of and response to pain and produces generalised CNS depression by binding to opiate receptors in the CNS and acting as a partial agonist/antagonist.
Penzyl is a potent analgesic which when administered orally in a 50 mg dose appears equivalent in analgesic effect to 60 mg (1 grain) of codeine. Onset of significant analgesia usually occurs between 15 and 30 minutes after oral administration, and duration of action is usually three hours or longer. Onset and duration of action and the degree of pain relief are related both to dose and the severity of pretreatment pain. Penzyl weakly antagonizes the analgesic effects of morphine and meperidine; in addition, it produces incomplete reversal of cardiovascular, respiratory, and behavioral depression induced by morphine and meperidine. Penzyl has about 1/50 the antagonistic activity of nalorphine. It also has sedative activity.
Trade Name | Penzyl |
Availability | Discontinued |
Generic | Pentazocine |
Pentazocine Other Names | Pentazocin, Pentazocina, Pentazocine, Pentazocinum |
Related Drugs | Buprenex, aspirin, acetaminophen, tramadol, trazodone, hydroxyzine, naproxen, Tylenol, lorazepam, oxycodone |
Type | Injection |
Formula | C19H27NO |
Weight | Average: 285.4238 Monoisotopic: 285.209264491 |
Groups | Approved, Vet approved |
Therapeutic Class | Opioid analgesics |
Manufacturer | Maneesh Pharmaceuticals Ltd |
Available Country | India |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
For the relief of moderate to severe pain. Penzyl may also be used for preoperativeor preanesthetic medication and as a supplement to surgical anesthesia.
Penzyl is also used to associated treatment for these conditions: Mild pain, Severe Pain, Moderate Pain, Preanesthetic medication therapy
How Penzyl works
The preponderance of evidence suggests that pentazocine antagonizes the opioid effects by competing for the same receptor sites, especially the opioid mu receptor.
Dosage
Penzyl dosage
Tablet:
Adults: The usual initial adult dose is 1 tablet every three or four hours. This may be increased to 2 tablets when needed. Total daily dosage should not exceed 12 tablets.
Injection:
Adults, Excluding Patients in Labor: The recommended singleparenteraldose is 30 mg byintramuscular, subcutaneous, or intravenous route. This may be repeated every 3 to 4 hours. Doses in excess of 30 mg intravenously or 60 mg intramuscularly or subcutaneously are not recommended. Total daily dosage should not exceed 360 mg. Elderly patients may be more sensitive to theanalgesiceffects of Penzyl than younger patients. Elderly patients generally should be started on low doses of Penzyl and observed closely.The subcutaneous route of administration should be used only when necessary because of possible severe tissue damage at injection sites. When frequent injections are needed, the drug should be administered intramuscularly. In addition, constant rotation of injection sites (e.g., the upper outer quadrants of the buttocks, mid-lateralaspects of the thighs, and thedeltoidareas) isessential.
Patients in Labor: A single, intramuscular 30 mg dose has been most commonly administered. An intravenous 20 mg dose has given adequate pain relief to some patients in labor when contractions become regular, and this dose may be given two or three times at two- to three-hour intervals, as needed.
Pediatric Patients Excluding Patients Less Than One-Year-Old: The recommended single parenteral dose as premedication for sedation is 0.5 mg/kg by intramuscular route.
Side Effects
Physical dependence; sedation, dizziness, euphoria, lightheadedness, alterations of mood; respiratory depression; visual hallucinations, disorientation, confusion; hypertension, tachycardia, circulatory depression; shock; hypotension; nausea, vomiting, constipation; seizures, diaphoresis; rash; blood dyscrasias; local tissue damages (SC), muscle fibrosis (IM).
Precaution
May precipitate withdrawal in narcotic addicts. Impaired respiratory, renal and hepatic function; morbidly obese patients; thyroid dysfunction; prostatic hyperplasia or urinary stricture; biliary tract impairment; adrenal insufficiency (including Addison's disease); abdominal conditions. Elderly or debilitated patients; seizure-prone patients; children and infants (safety and efficacy not established in less than 1 yr); lactation. May impair ability to drive or operate machinery. Administer IM rather than SC (when frequent inj are needed) and inj sites should be varied.
Interaction
Depressant affects potentiated by alcohol, CNS depressants; concurrent use with fluoxetine may lead to diaphoresis, ataxia flushing and tremor associated with serotonin syndrome.
Food Interaction
- Avoid alcohol.
- Take with or without food. Food does not significantly affect absorption.
[Moderate] MONITOR: Smoking tobacco may decrease the plasma concentrations and effects of pentazocine by enhancing its metabolic clearance.
MANAGEMENT: The possibility of reduced therapeutic effects of pentazocine should be considered in smokers.
Penzyl Alcohol interaction
[Moderate] GENERALLY AVOID:
Ethanol may potentiate the central nervous system (CNS) depressant effects of opioid analgesics.
Concomitant use may result in additive CNS depression and impairment of judgment, thinking, and psychomotor skills.
In more severe cases, hypotension, respiratory depression, profound sedation, coma, or even death may occur.
Concomitant use of opioid analgesics with ethanol should be avoided.
Penzyl Drug Interaction
Major: duloxetine, meperidine, fentanyl, acetaminophen / hydrocodoneModerate: furosemide, metoprolol, promethazineUnknown: naproxen, thyroid desiccated, aspirin, multivitamin with minerals, sulfamethoxazole / trimethoprim, glucose, heparin, sodium iodide, atorvastatin, acetaminophen, montelukast, cyanocobalamin, cholecalciferol
Penzyl Disease Interaction
Major: impaired GI motility, infectious diarrhea, liver disease, prematurity, gastrointestinal obstruction, acute MI, drug dependence, intracranial pressure, respiratory depressionModerate: adrenal insufficiency, biliary spasm, hypothyroidism, renal dysfunction, seizure disorders, urinary retention
Elimination Route
Well absorbed from the gastro-intestinal tract.
Half Life
2 to 3 hours
Pregnancy & Breastfeeding use
Safe use of Penzyl during pregnancy (other than labor) has not been established. Animal reproduction studies have not demonstrated teratogenic or embryotoxic effects. However, Penzyl should be administered to pregnant patients (other than labor) only when, in the judgment of the physician, the potential benefits outweigh the possible hazards. Patients receiving Penzyl during labor have experienced no adverse effects other than those that occur with commonly used analgesics. Penzyl should be used with caution in women delivering premature infants.
Contraindication
Penzyl should not be administered to patients who are hypersensitive to it.
Special Warning
Pediatric Use: The safety and efficacy of Penzyl as preoperative or preanesthetic medication have been established in pediatric patients 1 to 16 years of age. Use of Penzyl in these age groups is supported by evidence from adequate and controlled studies in adults with additional data from published controlled trials in pediatric patients. The safety and efficacy of Penzyl as a premedication for sedation have not been established in pediatric patients less than one year old. Information on the safety profile of Penzyl as a postoperative analgesic in children less than 16 years is limited.
Geriatric Use: Elderly patients may be more sensitive to the analgesic effects of Penzyl than younger patients. Clinical data indicate that differences in various pharmacokinetic parameters of Penzyl may exist between elderly and younger patients. Sedating drugs may cause confusion and oversedation in the elderly; elderly patients generally should be started on low doses of Penzyl and observed closely.
This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.
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