Product image of Monocrixo L.P. (Une Prise Quotidienne) (Tramadol Hydrochloride) supplied by GNH India

Monocrixo L.P. (Une Prise Quotidienne)

Active Ingredient:
Tramadol Hydrochloride
Origin:
EU

Monocrixo L.P. (Une Prise Quotidienne) (Tramadol Hydrochloride)

Tramadol Hydrochloride, the active ingredient in Monocrixo L.P. (Une Prise Quotidienne), is an opioid analgesic presented as an oral tablet for oral use. It is indicated for the management of moderate to severe pain in adult patients when other analgesics are insufficient.

GNH India supplies Monocrixo L.P. (Une Prise Quotidienne) as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable sourcing for regulated markets. Our distribution network ensures timely delivery and compliance with local regulatory requirements.

Manufacturer / TM Owner

Therabel Lucien Pharma S.A.

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Indications & Clinical Uses

Tramadol Hydrochloride is used to treat pain conditions that involve the central nervous system.

  • Acute postoperative pain: provides analgesia to reduce pain after surgical procedures.
  • Chronic musculoskeletal pain: helps control persistent pain associated with conditions such as osteoarthritis.
  • Cancer‑related pain: contributes to moderate to severe pain relief in oncology patients.

How It Works

  • Tramadol Hydrochloride acts as a weak μ‑opioid receptor agonist while simultaneously inhibiting the reuptake of serotonin and norepinephrine in the central nervous system. This dual mechanism enhances descending inhibitory pain pathways and reduces the perception of nociceptive signals, resulting in analgesic effects without the potency of stronger opioids. The opioid component contributes to analgesia at higher doses, whereas the monoaminergic activity provides additional pain modulation, especially in neuropathic components.

Side Effects

Tramadol Hydrochloride may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Nausea: mild to moderate feeling of sickness.
  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Constipation: reduced bowel movements.
  • Headache: mild to moderate cranial pain.
  • Somnolence: increased sleepiness or fatigue.

Serious or Rare Side Effects

  • Seizures: risk of convulsive episodes, especially at high doses.
  • Respiratory depression: reduced breathing effort that may be life‑threatening.
  • Serotonin syndrome: symptoms such as agitation, hyperthermia, and muscle rigidity when combined with serotonergic agents.
  • Allergic reactions: rash, itching, or anaphylaxis.
  • Dependence or abuse potential: risk of developing physical or psychological dependence with prolonged use.

Precautions & Warnings

When prescribing Tramadol Hydrochloride, clinicians should consider several safety measures to minimize risk.

  • Assess renal and hepatic function: adjust use in patients with impaired clearance.
  • Evaluate seizure history: avoid or monitor in individuals with epilepsy.
  • Review concomitant serotonergic drugs: risk of serotonin syndrome.
  • Monitor for signs of respiratory depression: especially in opioid‑naïve patients.
  • Counsel on driving and operating machinery: impairment may occur.
  • Store at ambient temperature: keep in original container, protect from moisture and heat.

Avoid Interactions

Tramadol Hydrochloride interacts with several medication classes; awareness of these interactions helps prevent adverse events.

Major Interactions (Avoid)

  • MAO inhibitors: can precipitate severe serotonin syndrome.
  • CNS depressants (e.g., benzodiazepines, alcohol): increase risk of respiratory depression and sedation.
  • Selective serotonin reuptake inhibitors (SSRIs) and SNRIs: may heighten serotonin toxicity.

Moderate Interactions (Monitor Closely)

  • CYP2D6 inhibitors (e.g., fluoxetine, quinidine): reduce conversion to active metabolite, decreasing analgesic effect.
  • Anticonvulsants (e.g., carbamazepine): may lower tramadol levels.
  • Diuretics: may enhance risk of hyponatremia.

Frequently Asked Questions

Monocrixo L.P. (Une Prise Quotidienne) contains tramadol hydrochloride and is prescribed for the relief of moderate to severe pain when other analgesics are inadequate. It is commonly used after surgery, for chronic musculoskeletal conditions, and in cancer‑related pain management.

Tramadol Hydrochloride works by weakly stimulating μ‑opioid receptors and by blocking the reuptake of serotonin and norepinephrine in the central nervous system. This combined action enhances the body’s own pain‑inhibiting pathways, reducing the perception of painful stimuli.

The appropriate dose of Monocrixo L.P. is determined by the prescribing healthcare professional based on the individual’s pain severity, medical history, and response to therapy. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety of tramadol during pregnancy or lactation has not been fully established. Healthcare providers should weigh potential benefits against risks and discuss alternative options. Women who are pregnant, planning to become pregnant, or breastfeeding should consult their physician before using this medication.

To order Monocrixo L.P., submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

Compared with stronger opioids such as morphine, tramadol offers a milder μ‑opioid effect and adds serotonin‑norepinephrine reuptake inhibition, which can be advantageous for certain pain types. However, it still carries risks of dependence, serotonin syndrome, and seizure, so selection should be individualized.

Store Monocrixo L.P. tablets at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed to maintain stability.

Monocrixo L.P. is taken orally, usually with a full glass of water. It may be taken with or without food, but patients should follow the prescriber’s guidance regarding timing relative to meals to minimize gastrointestinal discomfort.

The most serious risks include respiratory depression, especially in opioid‑naïve individuals or when combined with other depressants; seizures, which can be precipitated by high doses or interacting medications; and serotonin syndrome when used with serotonergic drugs. Immediate medical attention is required if any of these occur.

Tramadol should be avoided in patients with a known hypersensitivity to tramadol or any component of the formulation, those taking monoamine oxidase inhibitors, individuals with uncontrolled epilepsy, and patients with severe respiratory insufficiency. Contra‑indications may also include certain psychiatric conditions; a clinician should evaluate each case.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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