Product image of Morfinesulfaat Retard Teva (Morphine Sulfate) supplied by GNH India

Morfinesulfaat Retard Teva

Active Ingredient:
Morphine Sulfate
Origin:
EU

Morfinesulfaat Retard Teva (Morphine Sulfate)

Morphine Sulfate, the active ingredient in Morfinesulfaat Retard Teva, is an opioid analgesic presented as an extended‑release oral tablet for oral use. It treats moderate to severe acute pain, chronic cancer pain, post‑operative pain, and chronic non‑cancer pain requiring opioid therapy in appropriate patients.

GNH India supplies Morfinesulfaat Retard Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva Nederland B.V.

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Indications & Clinical Uses

Morphine Sulfate is an opioid analgesic used to manage pain through central nervous system pathways.

  • Moderate to severe acute pain: provides rapid analgesia for short‑term severe pain episodes.
  • Chronic cancer pain: offers sustained pain control for patients with malignant disease.
  • Post‑operative pain: reduces pain following surgical procedures.
  • Chronic non‑cancer pain requiring opioid therapy: maintains long‑term analgesia when other treatments are insufficient.

How It Works

  • Morphine Sulfate acts as a full agonist at mu‑opioid receptors in the central nervous system. Binding inhibits adenylate cyclase activity, reduces calcium influx, and increases potassium efflux, which suppresses the release of excitatory neurotransmitters. This modulation diminishes the perception of pain and produces sedation, while also affecting the brain's reward pathways.

Side Effects

Morphine Sulfate may cause a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Constipation: reduced gastrointestinal motility.
  • Nausea: sensation of queasiness.
  • Vomiting: expulsion of stomach contents.
  • Drowsiness: increased sleepiness.
  • Dizziness: light‑headed sensation.
  • Dry mouth: reduced salivation.
  • Sweating: excessive perspiration.

Serious or Rare Side Effects

  • Respiratory depression: slowed or shallow breathing.
  • Severe hypotension: marked drop in blood pressure.
  • Anaphylaxis: life‑threatening allergic reaction.
  • Adrenal insufficiency: impaired cortisol production.
  • Dependence or addiction: potential for misuse.
  • Seizures: rare convulsive episodes.

Precautions & Warnings

Before prescribing Morfinesulfaat Retard Teva, clinicians should evaluate patient‑specific factors and monitor for safety concerns.

  • Assess pain level and opioid tolerance: determine baseline analgesic needs.
  • Monitor for respiratory depression: especially in opioid‑naïve individuals or when combined with CNS depressants.
  • Evaluate renal and hepatic function: adjust therapy if organ impairment is present.
  • Avoid use in patients with significant respiratory compromise: contraindicated in severe asthma or COPD exacerbations.
  • Use caution in the elderly: increased sensitivity to sedative effects.
  • Store at ambient temperature: keep below 25 °C, retain original packaging, and protect from moisture.

Avoid Interactions

Morphine Sulfate can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Concomitant CNS depressants (e.g., benzodiazepines, barbiturates): risk of profound respiratory depression.
  • Monoamine oxidase inhibitors (MAOIs): potential for serotonin syndrome.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): increased morphine plasma concentrations.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, carbamazepine): reduced analgesic effect.
  • Diuretics: may exacerbate hypotension.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): heightened risk of gastrointestinal bleeding.

Frequently Asked Questions

Morfinesulfaat Retard Teva is an extended‑release oral tablet containing morphine sulfate. It is prescribed for moderate to severe acute pain, chronic cancer‑related pain, post‑operative pain, and chronic non‑cancer pain that requires opioid therapy when other analgesics are insufficient.

Morphine sulfate binds to mu‑opioid receptors in the brain and spinal cord. This activation inhibits neuronal excitability, reduces the release of pain‑transmitting neurotransmitters, and alters pain perception, providing both analgesia and sedation.

The specific dose and dosing schedule are determined by the prescribing clinician based on the patient’s pain severity, prior opioid exposure, renal and hepatic function, and other individual factors. No fixed regimen is provided here.

Safety data for morphine sulfate in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. Use only if the potential benefit justifies the potential risk to the fetus or infant, and consult a healthcare professional.

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.

Morfinesulfaat Retard Teva provides extended‑release morphine, offering prolonged pain control with once‑ or twice‑daily dosing. Compared with immediate‑release morphine or other opioids such as oxycodone, it may reduce dosing frequency but shares similar efficacy, side‑effect profile, and risk of dependence.

Store the tablets at ambient temperature, below 25 °C, in the original blister pack or container. Protect them from moisture, direct sunlight, and excessive heat to maintain product stability.

The medication is taken orally as a whole tablet. It should be swallowed with water and not chewed, crushed, or broken, as altering the tablet can affect the extended‑release properties and increase the risk of overdose.

The most critical risks include respiratory depression, especially in opioid‑naïve patients or when combined with other depressants; severe hypotension; potential for dependence, addiction, and overdose; and rare but serious allergic reactions such as anaphylaxis.

Patients with known hypersensitivity to morphine or any component of the tablet, those with severe respiratory depression, acute asthma attacks, paralytic ileus, or significant head injury should avoid this medication. Contraindications are determined by the prescribing clinician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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