Product image of Oxycodonhydrochlorid 1 A Pharma (Oxycodone Hydrochloride) supplied by GNH India

Oxycodonhydrochlorid 1 A Pharma

Active Ingredient:
Oxycodone Hydrochloride
Origin:
EU

Oxycodonhydrochlorid 1 A Pharma (Oxycodone Hydrochloride)

Oxycodone Hydrochloride, the active ingredient in Oxycodonhydrochlorid 1 A Pharma, is an opioid analgesic presented as a 1 mg oral tablet for oral use. It is prescribed for moderate to severe pain management in adult patients. GNH India supplies Oxycodonhydrochlorid 1 A Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

GNH India supplies Oxycodonhydrochlorid 1 A Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

1 A Pharma Gmbh

1
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Indications & Clinical Uses

Oxycodone Hydrochloride is used within the opioid analgesic pathway to treat pain of varying intensity.

  • Acute postoperative pain: provides rapid relief of pain following surgical procedures.
  • Cancer‑related pain: helps control persistent pain associated with malignant disease.
  • Chronic non‑cancer pain: used when other analgesics are insufficient for long‑term pain management.
  • Severe traumatic injury pain: reduces intense pain resulting from major injuries.
  • Palliative care pain: alleviates pain in end‑of‑life care settings.

How It Works

  • Oxycodone Hydrochloride acts as a full agonist at the μ‑opioid receptors in the central nervous system. By binding to these receptors, it inhibits the transmission of nociceptive signals and modifies pain perception, producing analgesia. The drug also influences δ‑receptor activity, contributing to its overall analgesic effect while producing typical opioid‑related central nervous system effects.

Side Effects

Adverse reactions to oxycodone may vary in frequency and severity.

Common Side Effects

  • Nausea and vomiting: mild to moderate gastrointestinal upset.
  • Constipation: reduced bowel motility leading to hard stools.
  • Drowsiness or sedation: increased sleepiness or reduced alertness.
  • Dizziness: sensation of light‑headedness or imbalance.
  • Dry mouth: reduced salivary flow causing oral discomfort.
  • Pruritus: mild itching without rash.

Serious or Rare Side Effects

  • Respiratory depression: slowed or shallow breathing that can be life‑threatening.
  • Severe hypotension: marked drop in blood pressure causing faintness.
  • Opioid use disorder: risk of dependence, tolerance, and addiction.
  • Seizures: rare occurrence of convulsive episodes.
  • Anaphylaxis: acute allergic reaction with airway compromise.
  • adrenal insufficiency: rare hormonal imbalance affecting stress response.

Precautions & Warnings

When prescribing oxycodone, clinicians should consider several safety measures.

  • Assess pain severity and treatment goals: ensure opioid therapy is appropriate for the patient’s condition.
  • Evaluate risk of respiratory depression: monitor breathing, especially after dose initiation or escalation.
  • Review patient history for substance use disorder: identify potential for misuse or dependence.
  • Adjust dose in renal or hepatic impairment: consider reduced clearance in organ dysfunction.
  • Avoid concomitant CNS depressants: limit use with benzodiazepines or alcohol.
  • Store at below 25°C: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Oxycodone may interact with a range of medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Combined use with other strong opioids: increases risk of respiratory depression and profound sedation.
  • Concurrent benzodiazepines or barbiturates: synergistic CNS depression can be fatal.
  • CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): elevate oxy‑hydrochloride plasma levels, raising toxicity risk.

Moderate Interactions (Monitor Closely)

  • CYP2D6 inhibitors (e.g., fluoxetine, quinidine): may reduce conversion to active metabolites, affecting analgesia.
  • Anticholinergic agents: can worsen constipation and urinary retention.
  • Diuretics: may enhance hypotensive effects, requiring blood pressure monitoring.

Frequently Asked Questions

Oxycodonhydrochlorid 1 A Pharma contains oxycodone hydrochloride, an opioid analgesic indicated for the management of moderate to severe pain, including postoperative pain, cancer‑related pain, and chronic non‑cancer pain when other analgesics are insufficient.

Oxycodone hydrochloride binds as a full agonist to μ‑opioid receptors in the central nervous system, inhibiting the transmission of pain signals and altering pain perception. This receptor activation also produces typical opioid‑related central effects such as sedation and euphoria.

The appropriate dose of oxycodone hydrochloride is individualized by the prescribing clinician based on pain severity, patient tolerance, prior opioid exposure, and clinical condition. Dosage regimens are not standardized and must be determined by a qualified healthcare professional.

Oxycodone hydrochloride is classified as a pregnancy‑category drug with potential risks to the fetus, including neonatal withdrawal syndrome. It is generally contraindicated unless the benefit outweighs the risk. Breastfeeding while using oxycodone is discouraged because the drug can pass into milk and affect the infant.

To place an order, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Oxycodone provides strong μ‑opioid receptor agonism similar to morphine but has a higher oral bioavailability, allowing effective pain control with fewer doses. Compared with weaker opioids such as codeine, oxycodone offers more potent analgesia, though it also carries a higher risk of dependence and respiratory depression.

Store the tablets at temperatures below 25 °C in the original container, protected from moisture and direct light. Ensure the packaging remains intact to maintain product stability throughout its shelf life.

The product is supplied as oral tablets intended for swallowing with water. It should be taken exactly as prescribed, typically at regular intervals, and may be taken with or without food according to the prescriber’s guidance.

The most serious risks include respiratory depression, severe hypotension, opioid use disorder, and rare but life‑threatening reactions such as anaphylaxis. Patients should be monitored closely, especially during dose initiation or when combined with other central nervous system depressants.

Oxycodone is contraindicated in individuals with known hypersensitivity to the drug, those with severe respiratory insufficiency, acute or severe asthma, and patients currently misusing opioids. Caution is also advised for patients with significant hepatic or renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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