Registered Rwanda · Rwanda FDA

INDICONTIN 1.5 MG TABLETS

Indicontin controlled release Tablets 1.5mg

Rwanda FDA-HMP-MA-0733 Film coated tablets 1.5mg

What it does

Indicontin is used to help manage certain medical conditions.

Commonly used for: pain relief, chronic pain management

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Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Registration & product details

Registration no.
Rwanda FDA-HMP-MA-0733
Registration date
15/01/2024
Expiry date
14/01/2029
Status
Registered
Active ingredient
Indicontin controlled release Tablets 1.5mg
Dosage form
Film coated tablets
Strength
1.5mg
Pack size
10 x 10 Tablets
Therapeutic class
-
Manufacturer / MAH
Modi-mundipharma
Country of origin
INDIA

Source: Rwanda Food and Drugs Authority · fetched 2026-03-11 22:07:23 · updated 2026-09-21 02:30:20

Disclaimer: This information is sourced from Rwanda Food and Drugs Authority (Rwanda). Always consult a qualified healthcare professional before using any medication.

About this medicine

Indicontin is used to help manage certain medical conditions.

What it treats

  • pain relief
  • chronic pain management

How it works

Indicontin works by affecting how your body responds to pain.

Who it's for

This medication is suitable for adults who need help managing pain.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: indicontin

Indicontin is a brand name for the drug oxycodone, an opioid analgesic used to manage moderate to severe pain. It works by binding to specific opioid receptors in the brain and spinal cord, altering the perception and emotional response to pain. Indicontin is often prescribed for pain relief after surgery, injury, or in chronic pain conditions.

Indications

  • Moderate to severe pain
  • Postoperative pain management
  • Chronic pain conditions such as cancer pain

Dosage

Children: Refer to the BNF for Children for appropriate dosing information based on age and weight.

Adults: Refer to the BNF or relevant clinical guidelines for specific dosage recommendations based on individual patient considerations.

Mechanism of action

Oxycodone primarily acts as a mu-opioid receptor agonist, leading to the inhibition of pain pathways in the central nervous system. It also has some activity at kappa and delta opioid receptors, contributing to its analgesic effects. This binding results in decreased neuronal excitability and altered neurotransmitter release, which reduces the sensation of pain.

Pharmacodynamics

The analgesic effects of oxycodone can be attributed to its action on the central nervous system, where it modulates pain perception and response. It can produce effects such as sedation, euphoria, and even respiratory depression, reflecting its potential for misuse and the need for careful monitoring.

Pharmacokinetics

Oxycodone is well absorbed after oral administration, with a bioavailability of approximately 60-87%. It undergoes extensive hepatic metabolism, primarily through CYP3A4 and CYP2D6 enzymes, leading to its active metabolites. The elimination half-life ranges from 3 to 5 hours, although this can vary based on individual metabolism and dosing. Oxycodone is excreted primarily in urine, mostly as metabolites.

Contra-indications

  • Hypersensitivity to any component of the formulation
  • Severe asthma or respiratory depression
  • Acute or severe bronchial asthma
  • Known or suspected gastrointestinal obstruction
  • Concurrent use of monoamine oxidase inhibitors (MAOIs)

Adverse effects

  • Constipation
  • Nausea
  • Vomiting
  • Drowsiness
  • Dry mouth
  • Sweating
  • Dizziness
  • Euphoria
  • Dependence and withdrawal symptoms

Interactions

  • CNS depressants (e.g., benzodiazepines, alcohol) may enhance sedative effects
  • MAOIs can increase the risk of serotonin syndrome
  • Anticholinergic drugs may increase the risk of constipation and urinary retention
  • Certain antihistamines can enhance drowsiness

Precautions

  • Use with caution in patients with a history of substance use disorder
  • Monitor for respiratory depression, especially in elderly patients
  • Caution in patients with biliary tract disease or liver impairment
  • Ensure proper dosing in patients with renal impairment

Pregnancy

There are no adequate and well-controlled studies in pregnant women. Use only if the potential benefit justifies the potential risk to the fetus.

Breast-feeding

It is not known whether this drug is excreted in human milk. Caution should be exercised when administered to a nursing woman.

Storage

Store at room temperature, away from moisture and heat. Keep out of reach of children.

Formulations

  • Tablets
  • Extended-release capsules
  • Syrup

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.