DrugInfoSys

Ondansetron (HCl)

Drug #533

Ondansetron (HCl) is oral and parenteral antiemetic agent. Ondansetron (HCl) is the first selective serotonin blocking agent to be marketed. Ondansetron (HCl) is extremely safe and highly effective antiemetic that has greatly improved the ability to give chemotherapy. The quality of life of patients has been tremendously better with ondansetron than with older, traditional antiemetics. Despite its effectiveness, ondansetron is not recommended for the routine treatment of nausea due to its significant cost. Ondansetron was originally approved for the treatment of chemotherapy-induced nausea/vomiting by the FDA in January 1991 and tablets were approved for the treatment of post-operative nausea/vomiting in April 1995. It may have central and/or peripheral action, selectively blocks the serotonin 5-HT1 receptors. 5-HT 1receptors are found centrally in the chemoreceptor trigger zone and peripherally at vagal nerve terminals in the intestines.

Primary Characteristics

It is of Synthetic origin and belongs to Imidazole.

It is classified in Selective 5-HT3 Receptor Antagonist pharmacological group. It is also classified under Antiemetic/Antivertigo Agents .

Molecular Weight: 365.8 · pKa: 7.4 · Solubility in Water: 1 in 3 · Non-proprietary name: Ondansetron (HCl).

Molecular structure of Ondansetron (HCl)

Pharmacokinetics

Absorption: Ondansetron (HCl) has an oral bioavailability is 29.5% (±29.5%), pre-systemic (first-pass) metabolism accounts for 73% (±2%).

Distribution: Ondansetron (HCl) has a volume of distribution is 163 ± 25 litre. plasma protein binding is 70-76%.

Elimination: it is metabolised via extensive by Liver, plasma half-life is 3.3 ± 0.8 hr, renal excretion is < 10%.

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Indications

Contraindications

Ondansetron (HCl) is contraindicated in conditions like Hypersensitivity.

Dosage

Ondansetron (HCl)'s dosage details are as follows:

DoseSingle DoseFrequencyRouteInstructions
Adult Dosage
8 mg8 mgEvery 12hOral2 hour before treatment
24 mg24 mgEvery 8hPOOral dose is recommended 30 min before start of sinle day chemothrophy.
16 mg16 mgRectally1 to 2 hour before treatment
8 mg8 mgEvery 4hSlow IV/IMMax. Dose =32 mg. Give 30 Min. before emetogenic drugs.
Paediatric Dosage (20kg)
5 mg/m25 mg/m2IV InfusionInitially for 15 Min (Rec. for 5-12 Yrs)
4 mg4 mgEvery 2hOralMaintenance for 5 Days
Neonatal Dosage (3kg)
No data.

Drug Interactions

5 interactions

Always consult your physician for the change of dose regimen or an alternative drug of choice that may strictly be required.

Side Effects

Ondansetron (HCl) in overdosage may give rise to further complications which include Cardiac arrhythmias, Bronchospasm , Cardiac arrhythmias , Bradycardia , Bronchospasm , Angioedema , Angina , Angioedema , Hyperbilirubinemia.

The signs and symptoms that are produced after acute overdosage of Ondansetron (HCl) are Constipation, Dizziness, Headache.

Ondansetron (HCl) is known to cause more or less tolerable side effects which are usually transient. These include Abdominal pain, Chills, Constipation , dizziness, Dyspnea, Fever, Flushing, Headache, Hiccups, Hypotension , Reaction at injection site, Vision disturbances, Warmth sensation, Xerostomia .

Warnings / Precautions

Dosage restriction is advisable in patients with moderate to severe liver impairment. Ondansetron should be used with caution during pregnancy or lactation. Care is required in the patient exhibiting hypersensitivity to other selective 5HT3 receptor antagonists and in patient with signs of subacute intestinal obstruction.

Interference in Pathology

Ondansetron (HCl) may interfere in the diagnosis of No technical interferance have been reported.

Available Brands

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Single Ingredient

Storage Conditions

Ondansetron (HCl) should be stored Inj (reconstituted soln). Tab, Syrup, Suppositories.

Drug Classification

  1. 1.17.2Antiemetics & antinauseants

Manufacturers