Product image of Morphinum Hydrochloricum Teva (Morphine Hydrochloride) supplied by GNH India

Morphinum Hydrochloricum Teva

Active Ingredient:
Morphine Hydrochloride
Origin:
EU

Morphinum Hydrochloricum Teva (Morphine Hydrochloride)

Morphine Hydrochloride, the active ingredient in Morphinum Hydrochloricum Teva, is an opioid analgesic presented as a sterile injectable solution for intra‑articular, intravenous, and peri‑articular use. It is employed to manage severe acute pain and post‑operative pain in adult patients requiring rapid, potent analgesia.

GNH India supplies Morphinum Hydrochloricum Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation for global distribution.

Manufacturer / TM Owner

Teva Gyógyszergyár Zrt

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Indications & Clinical Uses

Morphine Hydrochloride is an opioid analgesic used in the management of pain conditions that require strong, rapid relief.

  • Severe acute pain: provides rapid, potent analgesia for patients experiencing intense, sudden pain.
  • Post‑operative pain: reduces pain intensity after surgical procedures, facilitating recovery.
  • Intra‑articular or peri‑articular administration: delivers targeted analgesia for joint or tissue procedures where local pain control is needed.

How It Works

  • Morphine Hydrochloride acts as a full agonist at the μ‑opioid receptors in the central nervous system. Binding to these G‑protein‑coupled receptors inhibits adenylate cyclase activity, reduces neuronal excitability, and decreases the release of neurotransmitters involved in pain transmission, resulting in analgesia and sedation.

Side Effects

Morphine Hydrochloride may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nausea: feeling of sickness often leading to vomiting.
  • Constipation: reduced bowel movements and hard stools.
  • Drowsiness: increased sleepiness or reduced alertness.
  • Sweating: excessive perspiration unrelated to temperature.

Serious or Rare Side Effects

  • Respiratory depression: slowed or shallow breathing that can be life‑threatening.
  • Severe hypotension: marked drop in blood pressure causing dizziness or fainting.
  • Anaphylaxis: a rare allergic reaction with hives, swelling, and airway compromise.

Precautions & Warnings

When using Morphine Hydrochloride, clinicians should observe several safety measures to minimize risks.

  • Assess pain level: determine severity before initiating therapy.
  • Monitor respiratory function: observe breathing rate and oxygen saturation regularly.
  • Avoid use in severe respiratory depression: contraindicated in patients with compromised breathing.
  • Use caution in renal or hepatic impairment: dose adjustments may be required.
  • Consider opioid tolerance: patients with prior opioid exposure may need higher doses.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Morphine Hydrochloride can interact with other medicines, altering its effects or increasing adverse reactions.

Major Interactions (Avoid)

  • Central nervous system depressants: concurrent use with benzodiazepines or barbiturates may cause profound sedation and respiratory depression.
  • Monoamine oxidase inhibitors (MAOIs): combined therapy can precipitate severe hypertension or serotonin syndrome.
  • Other opioids: additive opioid effects increase risk of respiratory depression.

Moderate Interactions (Monitor Closely)

  • Selective serotonin reuptake inhibitors (SSRIs): may raise serotonin levels and risk serotonin syndrome.
  • CYP3A4 inhibitors (e.g., ketoconazole): can increase morphine plasma concentrations.
  • Diuretics: may enhance hypotensive effects when used together.

Frequently Asked Questions

Morphinum Hydrochloricum Teva contains morphine hydrochloride, an opioid analgesic indicated for the treatment of severe acute pain, post‑operative pain, and pain that benefits from intra‑articular or peri‑articular administration, such as after joint surgery or tissue procedures.

Morphine hydrochloride works by binding to μ‑opioid receptors in the brain and spinal cord. This activation inhibits the release of excitatory neurotransmitters, reduces neuronal firing, and diminishes the perception of pain, providing both analgesic and sedative effects.

The appropriate dose of Morphinum Hydrochloricum Teva is determined by the prescribing clinician based on the patient’s pain severity, route of administration, prior opioid exposure, and individual clinical factors. Dosage regimens are not standardized and must follow the prescriber’s order.

Safety data for morphine hydrochloride in pregnancy and lactation are limited. The drug is generally classified as contraindicated or used only when the potential benefit justifies the risk. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives with their healthcare provider.

To 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 (including cold‑chain if needed), and import documentation.

Morphine hydrochloride is a prototypical opioid with strong μ‑receptor activity, offering rapid and potent analgesia. Compared with weaker opioids, it provides more reliable pain control for severe pain but carries a higher risk of respiratory depression and other opioid‑related adverse effects, requiring careful monitoring.

The product should be stored at ambient temperature, below 25 °C, in its original packaging. Protect it from moisture, direct sunlight, and extreme temperature fluctuations. Follow standard aseptic handling procedures for injectable medications.

Morphinum Hydrochloricum Teva is supplied as a sterile injectable solution and may be given intravenously, intra‑articularly, or peri‑articularly by a qualified healthcare professional. Administration technique, site preparation, and dosing volume follow the prescriber’s instructions and institutional protocols.

The most serious risks include respiratory depression, severe hypotension, and rare but life‑threatening reactions such as anaphylaxis. These events require immediate medical attention and close monitoring, especially in opioid‑naïve patients or those with compromised respiratory function.

Patients with known hypersensitivity to morphine or any component of the formulation, those with severe uncontrolled respiratory depression, or individuals taking monoamine oxidase inhibitors should not receive this medication. Clinicians must also evaluate contraindications related to renal, hepatic, or gastrointestinal disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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