Product image of Ondansetrón Teva-Ratio (Ondansetron) supplied by GNH India

Ondansetrón Teva-Ratio

Active Ingredient:
Ondansetron
Origin:
EU

Ondansetrón Teva-Ratio (Ondansetron)

Ondansetron, the active ingredient in Ondansetrón Teva-Ratio, is a serotonin 5-HT3 receptor antagonist presented as a 4 mg oral tablet for oral use. It is used to prevent nausea and vomiting associated with chemotherapy, radiotherapy and postoperative recovery in adult and pediatric patients.

GNH India supplies Ondansetrón Teva-Ratio as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Teva Pharma S.L.U.,

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Indications & Clinical Uses

Ondansetron is employed across several clinical pathways that involve emesis control.

  • Chemotherapy‑induced nausea and vomiting (CINV): reduces the frequency and severity of acute and delayed episodes.
  • Radiotherapy‑induced nausea and vomiting (RINV): helps maintain patient comfort during and after radiation treatment.
  • Post‑operative nausea and vomiting (PONV): lowers the incidence of nausea and vomiting after surgical procedures.
  • Pregnancy‑associated nausea (hyperemesis gravidarum): provides relief when other measures are insufficient.

How It Works

  • Ondansetron selectively blocks the serotonin 5‑HT3 receptors located on vagal afferent nerves in the gastrointestinal tract and in the chemoreceptor trigger zone of the brain. By inhibiting this receptor, it prevents serotonin‑mediated stimulation of the vomiting centre, thereby reducing nausea and vomiting triggered by chemotherapy, radiation, surgery or other emetogenic stimuli.

Side Effects

Side‑effect profiles reflect the drug’s pharmacology and patient variability.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Constipation: occasional bowel habit changes.
  • Diarrhoea: transient loose stools.
  • Fatigue: general tiredness.
  • Dizziness: brief episodes of light‑headedness.

Serious or Rare Side Effects

  • QT‑interval prolongation: may predispose to cardiac arrhythmias.
  • Severe hypersensitivity: rash, itching, swelling or anaphylaxis.
  • Serotonin syndrome: rare when combined with other serotonergic agents.
  • Hepatic enzyme elevation: abnormal liver function tests.
  • Neuroleptic malignant‑like reactions: extremely uncommon but serious.

Precautions & Warnings

When prescribing Ondansetron, clinicians should consider several safety aspects.

  • Cardiac monitoring: assess baseline ECG in patients with known QT prolongation.
  • Electrolyte balance: correct hypokalaemia, hypomagnesaemia or hypocalcaemia before use.
  • Concomitant serotonergic drugs: evaluate risk of serotonin syndrome.
  • Pregnancy: weigh benefits against potential risks; use only if clearly needed.
  • Renal/hepatic impairment: dose adjustment may be required based on clinical judgment.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Ondansetron may interact with several medicines that influence cardiac rhythm or serotonergic pathways.

Major Interactions (Avoid)

  • Anti‑arrhythmic agents (e.g., amiodarone, quinidine): increase risk of QT prolongation.
  • Certain antipsychotics (e.g., haloperidol, ziprasidone): additive effect on cardiac repolarisation.

Moderate Interactions (Monitor Closely)

  • Selective serotonin reuptake inhibitors (SSRIs) and serotonin‑norepinephrine reuptake inhibitors (SNRIs): potential for serotonin syndrome.
  • Tramadol and other opioids: heightened serotonergic activity.
  • CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): may raise ondansetron plasma levels.
  • CYP2D6 substrates (e.g., metoprolol, codeine): altered metabolism may occur.

Frequently Asked Questions

Ondansetrón Teva-Ratio contains ondansetron, a medication used to prevent and treat nausea and vomiting caused by chemotherapy, radiotherapy, surgery and, in some cases, severe pregnancy‑related nausea. It is administered to adults and children under medical supervision.

Ondansetron blocks serotonin 5‑HT3 receptors in the gastrointestinal tract and the brain’s chemoreceptor trigger zone. By preventing serotonin from activating these receptors, the drug reduces the neural signals that trigger the vomiting centre, thereby controlling nausea and vomiting.

The prescribed dose of Ondansetrón Teva-Ratio is determined by the treating clinician based on the patient’s age, weight, the emetogenic potential of the chemotherapy or surgery, and other clinical factors. Only a qualified health professional should set the dosing regimen.

Ondansetron is classified as Pregnancy Category B in many regions, indicating no proven risk in animal studies but limited human data. It may be used during pregnancy only when the potential benefit outweighs any possible risk. Limited data suggest it is excreted in breast milk; use should be discussed with a healthcare provider.

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

Ondansetron belongs to the 5‑HT3 antagonist class, offering rapid onset and effectiveness against both acute and delayed nausea. Compared with dopamine antagonists (e.g., metoclopramide) it has fewer extrapyramidal side effects, and unlike corticosteroids it does not cause hyperglycaemia. Choice of therapy depends on the clinical scenario and patient tolerance.

Store Ondansetrón Teva-Ratio at ambient temperature, below 25 °C. Keep the tablets in their original packaging, protect them from moisture, heat and direct sunlight to maintain potency.

The product is supplied as oral tablets that are swallowed whole with water. It can be taken with or without food, according to the prescribing clinician’s instructions.

Serious risks include QT‑interval prolongation, which can lead to cardiac arrhythmias, and rare cases of severe hypersensitivity reactions such as anaphylaxis. Patients with known cardiac conduction abnormalities or electrolyte disturbances should be monitored closely.

Ondansetron should be avoided in individuals with a known hypersensitivity to the drug or any of its components, and in patients with congenital long QT syndrome or uncontrolled electrolyte imbalances unless benefits clearly outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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