- Approval Id
- 204ed57a2147f8f5
- Drug Name
- MORPHUS MORPHINE SULFATE ORAL SOLUTION BP 1MG/ML
- Product Name
- MORPHUS MORPHINE SULFATE ORAL SOLUTION BP 1MG/ML
- Approval Number
- SIN17362P
- Approval Date
- 2025-10-14
- Registrant
- ICM PHARMA PTE. LTD.
- Licence Holder
- ICM PHARMA PTE. LTD.
- Drug Type
- Therapeutic
- Forensic Classification
- PRESCRIPTION ONLY MEDICINES
- Dosage Form
- SOLUTION
- Dosage
- <p><strong>4.2 Posology and method of administration</strong></p>
<p>Posology<br>
The Morphus oral solution dose is adjusted by the physician depending on the severity of pain and with regards to the individual sensitivity of the patient.<br>
Under medical control the dose can be increased depending on the severity of pain and depending on the use of analgesics so far.</p>
<p>For oral use only and as directed by the physician<br>
The solution is to be administered neat (without dilution) followed by some liquid (water or juice) if needed.</p>
<p>The recommended dose shall be advised by the physician and depends on the individual pain condition and is for</p>
<p>Adults: initial dose usually 10–30mg morphine sulfate (corresponding to 10–30 mL Morphus oral solution 1mg per mL) every 4–6 hours.</p>
<p>Immediately prior to administration the prescribed Morphus oral solution dose is measured with the aid of the provided graduated measuring cup.</p>
<p><em>Elderly patients:</em><br>
In elderly patients or in patients that should not experience sedation the dosage should be reduced. Older patients (usually 75 years and older) and patients with poor overall physical condition may be sensitive to morphine. Therefore, the adjustment of dose has to be done more carefully and / or the dosage intervals have to be extended. As appropriate, lower dosage strengths have to be given instead.</p>
<p><em>Patients with impaired liver and/or kidney function:</em><br>
In patients with liver and/or kidney dysfunction and if a delayed gastrointestinal passage is suspected Morphus oral solution should be dosed especially carefully.</p>
<p><em>Discontinuation of therapy:</em><br>
An abstinence syndrome may be precipitated if opioid administration is suddenly discontinued. Therefore, the dose should be gradually reduced prior to discontinuation.</p>
- Route Of Administration
- ORAL
- Indication Info
- <p><strong>4.1 Therapeutic indications</strong></p>
<p>Morphus oral solution is indicated for the symptomatic relief of severe pain.</p>
- Contraindications
- <p><strong>4.3 Contraindications</strong></p>
<ul class="dash">
<li>Hypersensitivity to the active substance or to any of the excipients listed in section 6.1 – <em>please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information</em>.</li>
<li>Diarrhoea caused by poisoning.</li>
<li>Acute respiratory insufficiency or respiratory depression, obstructive airways disease.</li>
<li>Concurrent administration with monoamine oxidase (MAO) inhibitors or within 2 weeks of discontinuation of treatment with MAO (see section 4.5 – <em>please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information</em>).</li>
</ul>
<p>The risk-benefit of morphine use should be evaluated when the following medical problems are present:</p>
<ul class="dash">
<li>Acute abdomen.</li>
<li>Asthma attacks and acute and severe bronchial obstruction.</li>
<li>Cardiac arrhythmias.</li>
<li>History of convulsions (see Sect. 4.4 – <em>please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information</em>).</li>
<li>Acute alcohol intoxication.</li>
<li>Agitation in patients secondary to use of alcohol or hypnotics, emotional instability, suicidal ideation.</li>
<li>Head injury and conditions with increased intracranial pressure.</li>
<li>Acute liver disorders (hepatitis, hepatic porphyria).</li>
<li>Paralytic ileus.</li>
<li>Coma.</li>
<li>Patients with phaeochromocytoma. Morphine and some other opioids can induce the release of endogenous histamine and thereby stimulate catecholamine release.</li>
<li>Pregnancy and lactation (see section 4.6 – <em>please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information</em>).</li>
</ul>
