Product image of Oxycodon-Hcl 1 × Täglich Beta (Oxycodone Hydrochloride) supplied by GNH India

Oxycodon-Hcl 1 × Täglich Beta

Active Ingredient:
Oxycodone Hydrochloride
Origin:
EU

Oxycodon-Hcl 1 × Täglich Beta (Oxycodone Hydrochloride)

Oxycodone Hydrochloride, the active ingredient in Oxycodon-Hcl 1 × Täglich Beta, is an opioid analgesic presented as a tablet for oral use. It treats moderate to severe pain in adult patients when other analgesics are insufficient.

GNH India supplies Oxycodon-Hcl 1 × Daily Beta as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Betapharm Arzneimittel Gmbh

1
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Indications & Clinical Uses

Oxycodone Hydrochloride is an opioid analgesic used in the management of pain across several clinical contexts.

  • 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: Reduces pain intensity in conditions such as severe osteoarthritis when other treatments have failed.

How It Works

  • Oxycodone binds selectively to μ‑opioid receptors in the central nervous system, activating inhibitory G‑protein pathways that decrease neuronal excitability and reduce the transmission of nociceptive signals, thereby producing analgesia.

Side Effects

Adverse reactions to oxycodone vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Constipation: reduced bowel motility leading to hard stools.
  • Drowsiness: increased sleepiness or fatigue.
  • Dizziness: light‑headed sensation, especially when standing.
  • Dry mouth: reduced salivation causing a parched feeling.
  • Sweating: excessive perspiration without exertion.

Serious or Rare Side Effects

  • Respiratory depression: slowed or shallow breathing that can be life‑threatening.
  • Severe hypotension: marked drop in blood pressure leading to fainting.
  • Seizures: uncontrolled electrical activity in the brain.
  • Allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Dependence and addiction: psychological or physical reliance on the drug.
  • Adrenal insufficiency: impaired cortisol production causing fatigue and weakness.

Precautions & Warnings

When prescribing oxycodone, clinicians should consider several safety measures.

  • Assess pain severity and prior opioid exposure: ensure appropriate indication before initiating therapy.
  • Evaluate respiratory function: monitor for signs of depression, especially in opioid‑naïve patients.
  • Review concomitant medications: avoid combinations that increase sedation or respiratory risk.
  • Counsel on constipation management: recommend dietary fiber, fluids, and laxatives as needed.
  • Educate on misuse potential: discuss risks of dependence, diversion, and proper storage.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Benzodiazepines: combined use can cause profound respiratory depression and excessive sedation.
  • Central nervous system depressants: other opioids, barbiturates, or alcohol markedly increase overdose risk.
  • CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): can raise oxycodone plasma levels, heightening toxicity.

Moderate Interactions (Monitor Closely)

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

Frequently Asked Questions

Oxycodon-Hcl 1 × Täglich Beta contains oxycodone hydrochloride, an opioid analgesic prescribed to manage moderate to severe pain when other analgesics are insufficient. It is used in acute postoperative settings, cancer‑related pain, and selected chronic pain conditions under close medical supervision.

Oxycodone binds to μ‑opioid receptors in the brain and spinal cord, activating inhibitory G‑protein pathways that reduce neuronal firing and block the transmission of pain signals. This central action diminishes the perception of pain and increases pain tolerance.

The appropriate dose is individualized by the prescribing clinician based on the patient’s pain severity, prior opioid exposure, age, renal and hepatic function, and other clinical factors. Dosage adjustments follow local prescribing guidelines and the product’s labeling.

Oxycodone crosses the placenta and is excreted in breast milk, potentially causing respiratory depression or withdrawal in the newborn. Use during pregnancy or lactation is only considered when the benefit to the mother outweighs the potential risk to the fetus or infant, and under strict medical supervision.

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, confirming trade or institutional credentials before providing pricing, availability, shipping details and any required import documentation.

Oxycodone is a semi‑synthetic opioid with strong μ‑receptor affinity, offering potent analgesia comparable to morphine but with a slightly faster onset when administered orally. Compared with weaker opioids such as codeine, oxycodone provides more reliable pain control for severe pain, though it carries a similar risk profile for dependence and respiratory depression.

Store the tablets at or below 25 °C in a dry environment, protected from moisture, light and heat. Keep the medication in its original container with the label intact until use, and ensure it is out of reach of children.

The product is supplied as oral tablets intended for swallowing with water. It is taken once daily as directed by the prescriber, and may be taken with or without food, depending on individual tolerance and gastrointestinal comfort.

The most critical risks include respiratory depression, severe hypotension, profound sedation, dependence, and the potential for overdose. Patients should be monitored closely for signs of breathing difficulties, excessive drowsiness, or any sudden changes in blood pressure.

Contra‑indications include patients with known hypersensitivity to oxycodone or other opioids, those with severe respiratory insufficiency, acute or severe bronchial asthma, and individuals who have taken monoamine oxidase inhibitors within the past 14 days. Caution is also advised for patients with uncontrolled psychiatric disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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