Product image of Mst 1 (Morphine Sulfate) supplied by GNH India

Mst 1

Active Ingredient:
Morphine Sulfate
Origin:
EU

Mst 1 (Morphine Sulfate)

Morphine Sulfate, the active ingredient in Mst 1, is an opioid analgesic presented as an oral formulation for systemic use. Classified as a Schedule II controlled substance in the EU, it provides analgesia for moderate to severe acute pain, cancer‑related pain, and post‑operative pain in adult patients requiring strong pain control.

GNH India supplies Mst 1 as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, and pharmacies worldwide, with a focus on quality assurance, regulatory adherence, and reliable cold‑chain logistics where required.

Manufacturer / TM Owner

Mundipharma Farmacêutica, Lda.

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Indications & Clinical Uses

  • Morphine Sulfate is an opioid analgesic used to manage pain through central µ‑opioid receptor activation.
  • Acute pain: provides rapid relief for severe injuries or medical procedures.
  • Cancer pain: reduces tumor‑related nociceptive and neuropathic pain.
  • Post‑operative pain: controls pain after surgical interventions.
  • Severe chronic pain: offers long‑term relief when other analgesics are insufficient.

How It Works

  • Morphine Sulfate acts as a full agonist at µ‑opioid receptors in the central nervous system, inhibiting the transmission of nociceptive signals and altering pain perception. By binding to these G‑protein‑coupled receptors, it reduces neuronal excitability, decreases neurotransmitter release, and produces profound analgesia while also affecting respiratory and gastrointestinal motility.

Side Effects

Morphine Sulfate may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Nausea and vomiting: gastrointestinal upset common after initiation.
  • Constipation: reduced bowel motility leading to hard stools.
  • Drowsiness or sedation: central nervous system depression.
  • Dizziness or light‑headedness: especially when standing.
  • Sweating: increased perspiration.
  • Dry mouth: reduced salivation.

Serious or Rare Side Effects

  • Respiratory depression: potentially life‑threatening reduction in breathing.
  • Severe hypotension: marked drop in blood pressure.
  • Anaphylactic reaction: rare but possible allergic response.
  • Dependence or addiction: risk of physical and psychological dependence.
  • Adrenal insufficiency: rare endocrine disturbance.
  • Seizures: uncommon but reported in overdose.

Precautions & Warnings

  • When prescribing Morphine Sulfate, clinicians should consider several safety measures.
  • Assess pain severity: ensure opioid therapy is appropriate for the level of pain.
  • Monitor respiratory function: watch for signs of hypoventilation, especially in opioid‑naïve patients.
  • Evaluate opioid tolerance: adjust dose based on prior exposure to opioids.
  • Avoid concurrent CNS depressants: limit use with benzodiazepines, alcohol, or sedatives.
  • Adjust dose in renal or hepatic impairment: reduce dosage or increase monitoring.
  • Store at ambient temperature: keep in the original container, protect from moisture and heat.

Avoid Interactions

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

Major Interactions (Avoid)

  • Benzodiazepines or other CNS depressants: may cause profound sedation or respiratory depression.
  • Monoamine oxidase inhibitors (MAOIs): increase risk of serotonin syndrome and hypertensive crisis.
  • Alcohol: potentiates central nervous system depression.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole): may raise morphine plasma levels.
  • Diuretics: can enhance hypotensive effects.
  • Antihistamines or anticholinergics: may increase sedation or anticholinergic burden.

Frequently Asked Questions

Mst 1 contains morphine sulfate, an opioid analgesic indicated for the management of moderate to severe acute pain, cancer‑related pain, and post‑operative pain in adult patients when non‑opioid therapies are insufficient.

Morphine sulfate binds to µ‑opioid receptors in the brain and spinal cord, inhibiting the transmission of pain signals and altering the perception of pain, which results in strong analgesic effects.

The appropriate dose of Mst 1 is determined by the prescribing clinician based on the patient’s pain severity, prior opioid exposure, age, renal and hepatic function, and other individual factors.

Safety data for morphine sulfate in pregnancy and lactation are limited. Use only if the potential benefit justifies the potential risk to the fetus or infant, and discuss options with a healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com with 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.

Morphine sulfate is considered a benchmark opioid with well‑characterized efficacy and safety. Compared with newer synthetic opioids, it has a longer history of use, predictable pharmacokinetics, and is often less expensive, though individual response and side‑effect profiles may vary.

Store Mst 1 at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture, direct sunlight and excessive heat to maintain potency.

Mst 1 is intended for oral administration. The tablet or oral solution should be taken exactly as prescribed, usually with a full glass of water, and may be taken with or without food depending on the prescriber’s instructions.

The most serious risks include respiratory depression, severe hypotension, potential for dependence or addiction, and rare allergic reactions such as anaphylaxis. Patients should be monitored closely, especially during dose initiation or when combined with other depressant agents.

Mst 1 should be avoided in patients with known hypersensitivity to morphine or other opioids, those with severe respiratory insufficiency, acute or severe bronchial asthma, and individuals taking MAO inhibitors within the past 14 days.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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