Product image of Guttroff Promed Lox (Oxygen) supplied by GNH India

Guttroff Promed Lox

Active Ingredient:
Oxygen
Origin:
EU

Guttroff Promed Lox (Oxygen)

Guttroff Promed Lox is a medical‑gas product that delivers oxygen for inhalation therapy. It is supplied as a pressurised gas cylinder intended for supplemental oxygen administration. The product contains pharmaceutical‑grade oxygen, with no additional active compounds, and conforms to European Union standards for medical gases. It is used under clinical supervision to raise the partial pressure of oxygen in inspired air in clinical settings for patients.

Manufacturer / TM Owner

Sauerstoffwerk Friedrich Guttroff Gmbh

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Indications & Clinical Uses

Guttroff Promed Lox is indicated for supplemental oxygen therapy in patients who exhibit low blood oxygen levels (hypoxemia).

  • Acute respiratory distress requiring short‑term oxygen support.
  • Chronic obstructive pulmonary disease (COPD) with documented desaturation.
  • Post‑operative recovery where supplemental oxygen improves tissue healing.
  • Carbon monoxide poisoning after initial emergency measures.
  • High‑altitude exposure causing altitude‑related hypoxemia.

Side Effects

Oxygen delivered by Guttroff Promed Lox can produce a range of physiological responses, most of which are related to the level and duration of exposure.

Common

  • Mild headache or light‑headedness.
  • Nasal dryness or irritation from the delivery device.
  • Cough when administered via mask or nasal cannula.
  • Transient visual changes such as blurred vision.

Serious

  • Pulmonary oxygen toxicity with prolonged high‑concentration exposure.
  • Fire hazard due to high oxygen concentration in the environment.
  • Central nervous system effects including seizures in extreme cases.

Precautions & Warnings

Use of Guttroff Promed Lox requires careful assessment of patient condition and adherence to safety guidelines to minimise risks.

  • Verify prescription and target oxygen saturation before initiating therapy.
  • Adjust flow rate to maintain prescribed SpO₂, avoiding hyperoxia.
  • Monitor patients regularly for signs of carbon dioxide retention, especially in COPD.
  • Store cylinders upright, away from heat sources and open flames.
  • Ensure proper ventilation in the treatment area to prevent accumulation of oxygen‑rich atmosphere.
  • Use compatible delivery equipment to prevent leaks.
  • Document oxygen administration in the patient’s medical record.

Avoid Interactions

Oxygen therapy can influence the effectiveness or safety of other treatments, and certain agents may require dose adjustments when used together.

Avoid

  • Smoking or open flames in the treatment area due to increased fire risk.
  • Nitrous oxide anesthesia without proper monitoring, as combined high oxygen levels can enhance toxicity.
  • High‑concentration oxygen with certain chemotherapeutic agents that generate free radicals.

Use with caution

  • Sedatives or opioids that depress respiration; monitor respiratory status closely.
  • Inhaled bronchodilators; assess for additive effects on airway irritation.
  • Antioxidant supplements; high oxygen may alter oxidative balance.

Frequently Asked Questions

Guttroff Promed Lox is a medical‑gas product that provides pharmaceutical‑grade oxygen for inhalation therapy.

It is prescribed for patients with hypoxemia, such as those with acute respiratory distress, COPD, post‑operative needs, carbon monoxide poisoning, or altitude‑related low oxygen levels.

The oxygen increases the partial pressure of oxygen in the inspired air, which enhances diffusion of oxygen into the bloodstream and improves tissue oxygen delivery.

Common side effects include mild headache, nasal dryness or irritation, cough from the delivery device, and temporary visual changes such as blurred vision.

Serious risks include pulmonary oxygen toxicity, increased fire hazard in the treatment area, and rare central nervous system effects like seizures.

Precautions include confirming the prescription, setting the correct flow rate, monitoring for carbon dioxide retention, storing cylinders safely, ensuring adequate ventilation, using compatible equipment, and documenting administration.

Sedatives or opioids that depress respiration should be used with caution; patients need close monitoring of respiratory status when both are administered.

No. Smoking or any open flame must be avoided in the treatment area because the high‑oxygen environment greatly increases fire risk.

Cylinders should be stored upright, away from heat sources, direct sunlight, and any ignition sources, and in a well‑ventilated area.

Healthcare providers should record the prescribed oxygen flow rate, target SpO₂, duration of therapy, patient response, and any adverse events in the medical record.

Patients with chronic lung diseases such as COPD, those at risk of carbon dioxide retention, and individuals receiving concurrent respiratory depressants require more frequent monitoring.

Regulatory details are available through the European Medicines Agency (EMA) and national health authority databases that list approved medical gases.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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