Consumer medicine information

Ondansetron AN ODT Orally disintegrating tablets

Ondansetron

BRAND INFORMATION

Brand name

Ondansetron AN ODT Orally disintegrating tablets

Active ingredient

Ondansetron

Schedule

S4

 

Consumer medicine information (CMI) leaflet

Please read this leaflet carefully before you start using Ondansetron AN ODT Orally disintegrating tablets.

What is in this leaflet

Please read this leaflet carefully before you use Ondansetron AN ODT.

This leaflet answers some common questions about Ondansetron AN ODT.

It does not contain all of the available information. It does not take the place of talking to your doctor or pharmacist.

All medicines have benefits and risks. Your doctor has weighed the risks of you taking Ondansetron AN ODT against the benefits they expect it will have for you.

If you have any concerns about taking this medicine, talk to your doctor or pharmacist.

Keep this leaflet with your medicine.

You may need to read it again.

What Ondansetron AN ODT is used for

ONDANSETRON AN contains a medicine called ondansetron. This belongs to a group of medicines called antiemetics.

ONDANSETRON AN ODT works by helping to stop the nausea (sick feeling) and vomiting which can occur after medical treatments.

ONDANSETRON AN ODT should only be used to treat the nausea and vomiting for which they have been prescribed.

Your doctor may have prescribed Ondansetron AN ODT for another reason.

Ask your doctor if you have any questions about why Ondansetron AN ODT has been prescribed for you.

Ondansetron AN ODT is not addictive.

Before You Take Ondansetron AN ODT

When you must not take Ondansetron AN ODT

Do not take Ondansetron AN if:

  • You are taking apomorphine (used to treat Parkinsons disease)
  • You have ever had an allergic reaction to ondansetron or any of the ingredients listed towards the end of this leaflet (see ‘ingredients’)
    Symptoms of an allergic reaction may be mild or severe. They usually include some or all of the following: wheezing, swelling of the lips/mouth, difficulty in breathing, hayfever, lumpy rash ("hives") or fainting.
  • You are pregnant, trying to become pregnant or breastfeeding, unless your doctor says it is safe
    Your doctor will discuss the risks and benefits of using Ondansetron AN ODT if you are pregnant or breastfeeding.
  • The expiry date printed n the pack has passed
    If you take it after the expiry date has passed, it may not work as well.
  • The packaging is torn or shows signs of tampering

If you are not sure whether you should be taking Ondansetron AN ODT, talk to your doctor.

Before you start to take them

Tell your doctor if:

  • You are allergic to foods, dyes, preservatives or any other medicines
  • you have or used to have liver problems.
  • You suffer from severe constipation or have a blockage in your gut.
  • you have had to stop taking another medicine for your nausea or vomiting.
  • you are taking any other medicines, including medicines you buy without a prescription.
  • You are breastfeeding, pregnant or trying to become pregnant.
  • You have phenylketonuria, as Ondansetron AN ODT contains aspartame.

Taking other medicines

Tell your doctor if you are taking any other medicines, including medicines you buy without a prescription from a pharmacy, supermarket or health food shop.

Some medicines may affect the way others work. Your doctor or pharmacist will be able to tell you what to do when taking Ondansetron AN ODT with other medicines.

Use in children

There is limited experience in children. Ondansetron AN ODT can be taken by children over 4 years of age.

How to take Ondansetron AN ODT

The Pharmacist's label on the pack will tell you how to take Ondansetron AN ODT. If there is something you do not understand, ask your doctor or pharmacist.

How much to take

DO NOT take more Ondansetron AN ODT than your doctor or pharmacist tells you.

DO NOT take Ondansetron AN ODT MORE OFTEN than your doctor or pharmacist tells you.

If you vomit within one hour of taking your first Ondansetron AN ODT of each course prescribed for you, you should take the same dose again. If you continue to vomit, tell your doctor.

How to take it

PEEL BACK the foil top of the blister strip and GENTLY remove the Ondansetron AN ODT.

(DO NOT try to push it through the foil top as the tablet is fragile and will break up inside the foil). Place the Ondansetron AN ODT on top of your tongue. It will disperse very quickly, then swallow as normal.

When to take them

Your doctor or pharmacist will be able to tell you when you should take your Ondansetron AN ODT.

How long to take them

Your doctor or pharmacist will be able to tell you how long you should take your Ondansetron AN ODT.

If you forget to take them

If you miss your dose and you do not feel sick, take your next dose when you are meant to.

If you miss your dose and you feel sick, take the missed dose as soon as possible, then go back to taking your Ondansetron AN ODT as you would normally.

If it is almost time for your next dose, skip the dose you missed and take your next dose when you are meant to.

If you take too much (overdose)

Immediately telephone your doctor or the Poisons Information Centre (telephone 13 11 26) for advice, or go to Accident and Emergency at the nearest hospital, if you think you or anyone else may have taken too much Ondansetron AN ODT. Do this even if there are no signs of discomfort or poisoning.

You may need urgent medical attention.

Keep telephone numbers of these places handy.

If you are not sure what to do, contact your doctor or pharmacist.

While you are taking Ondansetron AN ODT

Things you must do

Tell your doctor or pharmacist that you are taking Ondansetron AN ODT if you are about to be started on any new medicines.

Tell your doctor if you become pregnant or are trying to become pregnant.

Tell your doctor if, for any reason, you have not taken your medicine exactly as prescribed.

Otherwise, your doctor may think that it was not effective and change your treatment unnecessarily.

Things you must not do

Do not stop taking Ondansetron AN ODT, or change the dose without first checking with your doctor.

Do not give this medicine to anyone else, even if their symptoms seem similar to yours.

Do not use Ondansetron AN ODT to treat any other complaints unless your doctor says to.

Side Effects

Tell your doctor as soon as possible if you have any problems while taking Ondansetron AN ODT, even if you do not think the problems are connected with the medicine or are not listed in this leaflet.

Like other medicines, Ondansetron AN ODT can cause some side effects. If they occur, they are most likely to be minor and temporary. However, some may be serious and need medical attention.

The most commonly reported side- effects are:

  • headache
  • a sensation of warmth or flushing
  • mild stomach cramps
  • constipation or diarrhoea
  • dry mouth
  • hiccups
  • dizziness or light headed feeling

Ask your doctor or pharmacist to answer any questions you may have if you experience any side effects.

Tell your doctor immediately if you notice any of the following:

  • ‘wheezy’ symptoms
  • Chest pain or tightness of the chest
  • Changes in the way your heart beats, e.g. if you notice it beating faster or slower than normal, or if it beats irregularly or ‘throbs’
  • Low blood pressure
  • Abnormal muscular body movements or shaking, involuntary upward movement of the eyes
  • Unusual muscle tone causing distortion of the body
  • Fits or convulsions

If you think you are having an allergic reaction to Ondansetron AN ODT, TELL YOUR DOCTOR IMMEDIATELY or go to the casualty department at your nearest hospital. Symptoms usually include some or all of the following:

  • Wheezing
  • Swelling of the lips/mouth
  • Difficulty in breathing
  • Hay fever
  • Lumpy rash (‘hives’)
  • fainting

This is not a complete list of all possible side effects. Other may occur in some people and there may be some side effects not yet known.

Do not be alarmed by this list of possible side effects. You may not experience any of them.

If your nausea (feeling of sickness) or vomiting does not go away, ask your doctor what to do.

In certain illnesses and treatments where Ondansetron AN ODT has been used, blood vessel blockage has occurred.

However, it is important to note that blood vessel blockage has also occurred in these illnesses and treatments when Ondansetron AN ODT has NOT been used. Discuss this with your doctor if you have any concerns.

If you feel unwell or have any symptoms, including anything that is not in this list, you should tell your doctor immediately.

Ask your doctor or pharmacist if you don’t understand anything in this list.

After taking Ondansetron AN

Storage

Keep Ondansetron AN where children cannot reach it.

A locked cupboard at least one-and-a-half metres above the ground is a good place to store medicines.

Keep your tablets in the blister pack until it is time to take them.

If you take the tablets out of the blister pack they may not keep well.

Keep your tablets in a cool dry place where the temperature stays below 25 degrees C.

Do not store this medicine or any other medicine in the bathroom or near a sink.

Do not leave in the car or on window sills.

Heat and dampness can destroy some medicines.

Disposal

If your doctor tells you to stop taking Ondansetron AN ODT, or your tablets have passed their expiry date, ask your pharmacist what to do with any that are left over.

Product description

What it looks like

Ondansetron AN ODT 4 mg (AUST R 196807)
Contains 4 mg Ondansetron White to off white, round tablets debossed with ‘5’ on one side and ‘E’ on one side with an embossed circular edge.

Available in blister packs of 4, 11, or 20 tablets.

Ondansetron AN ODT 8 mg (AUST R 196805)
Contains 8 mg Ondansetron White to off-white round tablets, debossed with ‘7’ on one side and ‘E’ on the other side with an embossed circular edge.

Available in blister packs of 4, 10, or 20 tablets.

Ingredients

Active Ingredient:

Ondansetron

Other Ingredients:

  • mannitol
  • crospovidone
  • lactose monohydrate
  • microcrystalline cellulose
  • aspartame
  • colloidal anhydrous silica
  • magnesium stearate
  • strawberry guarana 586997 AP0551

Please read this leaflet carefully before you start taking Ondansetron AN. ODT You may wish to keep it to read again.

Name and Address of the Sponsor

Amneal Pharma Pty Ltd
12 River Street
South Yarra,
VIC – 3141
Australia

Date of Preparation

May 2017

BRAND INFORMATION

Brand name

Ondansetron AN ODT Orally disintegrating tablets

Active ingredient

Ondansetron

Schedule

S4

 

Name of the medicine

Ondansetron.

Excipients.

Mannitol, crospovidone, lactose monohydrate, microcrystalline cellulose, aspartame, colloidal anhydrous silica, magnesium stearate and strawberry guarana 586997 AP0551.

Description

Chemical name: 3RS-1,2,3,9-tetrahydro-9-methyl-3- [(2-methyl-1H-imidazol-1-yl) methyl]-4H-carbazol-4-one. Molecular formula: C18H19N3O. Molecular weight: 293.4. CAS registry number: 99614-02-5.
It is a white to off-white powder. Ondansetron is very soluble in acid solution, practically insoluble in water.
Ondansetron AN ODT is available as orally disintegrating tablets containing 4 mg and 8 mg ondansetron.
Ondansetron AN ODT tablets contain the following inactive ingredients: mannitol, crospovidone, lactose monohydrate, microcrystalline cellulose, aspartame, colloidal anhydrous silica, magnesium stearate and strawberry guarana 586997 AP0551.

Pharmacology

Mode of action.

Ondansetron is a potent, highly selective 5HT3 receptor antagonist. Its precise mode of action in the control of nausea and vomiting is not known. Chemotherapeutic agents and radiotherapy may cause release of 5HT in the small intestine initiating a vomiting reflex by activating vagal afferents via 5HT3 receptors. Ondansetron blocks the initiation of this reflex. Activation of vagal afferents may also cause a release of 5HT in the area postrema, located on the floor of the fourth ventricle, and this may also promote emesis through a central mechanism. Thus, the effect of ondansetron in the management of the nausea and vomiting induced by cytotoxic chemotherapy and radiotherapy is due to antagonism of 5HT3 receptors on neurones located both in the peripheral and central nervous system. The mechanisms of action in postoperative nausea and vomiting are not known but there may be common pathways with cytotoxic induced nausea and vomiting. In psychomotor testing ondansetron does not impair performance nor cause sedation. Ondansetron does not alter plasma prolactin concentrations.
A study in cloned human cardiac ion channels has shown ondansetron has the potential to affect cardiac repolarisation via blockade of HERG potassium channels. The clinical relevance of this finding is uncertain.

Pharmacokinetics.

Absorption.

Following oral dosing with ondansetron, peak plasma concentrations are achieved in approximately 1.5 hours. For doses above 8 mg the increase in ondansetron systemic exposure with dose is greater than proportional; this may reflect some reduction in first pass metabolism at higher doses. The absolute bioavailability of the ondansetron tablet is approximately 60% (range 36-112%).

Distribution.

The plasma protein binding is 70-76%. The volume of distribution is 1.8 L/kg.

Metabolism.

Ondansetron is extensively metabolised in humans, with approximately 5% of a radiolabelled dose recovered as the parent compound from the urine. The primary metabolic pathway is hydroxylation on the indole ring followed by glucuronide or sulphate conjugation. Although some nonconjugated metabolites have pharmaceutical activity, these are not found in plasma concentrations likely to significantly contribute to the biological activity of ondansetron. Ondansetron is a substrate for multiple human hepatic cytochrome P-450 enzymes including CYP1A2, CYP2D6 and CYP3A4. This multiplicity of metabolic enzymes capable of metabolising ondansetron means that inhibition or loss of one enzyme (eg. CYP2D6 genetic deficiency) results in little change in overall rates of ondansetron elimination.

Excretion.

The terminal elimination half-life of ondansetron after oral dosing is 4.1 to 11.6 hours and after intravenous dosing 2.5 to 6.1 hours. The half-life may be prolonged in the elderly. In patients with severe hepatic impairment, systemic clearance is markedly reduced with prolonged elimination half-lives (15-32 h) and an oral bioavailability approaching 100% because of reduced presystemic metabolism.

Children.

In a study of 21 children aged 3-12 years receiving elective surgery with general anaesthesia, the clearance and volume of distribution of ondansetron following a single intravenous dose of 2 mg (3-7 years old) or 4 mg (8-12 years old) were reduced. The size of the change was age related with clearance falling from about 300 mL/min at 12 years of age to 100 mL/min at 3 years. Volume of distribution fell from about 75 L at 12 years to 17 L at 3 years.
The clinical safety of ondansetron in children under 2 years has not been established. Increased incidence of mortality with no specific target organ toxicity has been observed in young rats with immature drug metabolising enzymes.

Clinical Trials

Chemotherapy and radiotherapy induced nausea and vomiting.

Adult studies.

Highly emetogenic chemotherapy.

In a double blind, randomised study 152 patients were given ondansetron 8 mg i.v. single dose and 173 patients were given 32 mg i.v. single dose 30 minutes prior to cisplatin (≥ 50 mg/m2). No significant difference in terms of emesis control or grade of nausea was demonstrated between 8 mg or 32 mg. However, in some studies conducted in patients receiving medium (50-90 mg/m2) or high doses (≥ 100 mg/m2) of cisplatin chemotherapy, the 32 mg single dose has demonstrated a statistically significant superiority over the 8 mg single dose with regard to control of emesis.
In a double blind, randomised, crossover trial, 103 chemotherapy naive patients scheduled to receive cisplatin (50-120 mg/m2) chemotherapy were recruited. 91 patients completed both courses of ondansetron 0.15 mg/kg (8 mg) i.v. x 3 with or without dexamethasone 20 mg i.v. The combination of ondansetron and dexamethasone was shown to be significantly superior to ondansetron alone.
In a randomised, double blind parallel group study, 420 patients were randomised to receive either ondansetron 16 mg suppository prior to cisplatin chemotherapy (≥ 50 mg/m2) on day 1 followed by ondansetron 16 mg suppository once daily for a further 2 days, or ondansetron 8 mg i.v. prior to cisplatin chemotherapy followed by ondansetron 8 mg orally twice daily for a further 2 days. Results from the primary efficacy analysis (i.e. ≤ 2 emetic episodes on day 1) show that the ondansetron suppository and ondansetron i.v. and oral combined regimens are equivalent. However, results from the secondary efficacy analyses (e.g. number of emetic episodes on day 1, the worst day of days 1-3 and over all of days 1-3) showed that the ondansetron suppository was less effective. Patients on ondansetron i.v. and oral combined regimen remained free of emesis for significantly longer than patients receiving ondansetron suppository.
In a randomised, double blind, parallel group study 542 patients were randomised to receive either ondansetron tablets (3 x 8 mg) plus dexamethasone capsules (2 x 6 mg), or i.v. ondansetron 8 mg plus i.v. dexamethasone 20 mg, prior to cisplatin infusion. 24 mg of ondansetron administered orally was as effective as ondansetron 8 mg given i.v. in controlling acute emesis and nausea induced by cisplatin chemotherapy. One ondansetron 24 mg tablet has been shown to be bioequivalent to three ondansetron 8 mg tablets.
There are no studies on the use of suppositories in radiation induced nausea and vomiting.

Emetogenic chemotherapy.

In a double blind, parallel group study 82 patients were randomised to either ondansetron 8 mg i.v. prior to cyclophosphamide (> 500 mg/m2) based chemotherapy (doxorubicin or epirubicin ≥ 40 mg/m2) followed by 8 mg orally three times a day for 3-5 days or metoclopramide 60 mg i.v. prior to chemotherapy followed by 20 mg orally three times a day for 3-5 days. Ondansetron was shown to be significantly superior to metoclopramide.
In a randomised, single blind study, ondansetron 8 mg orally twice daily in 155 patients was compared with ondansetron 8 mg orally three times daily in 153 patients for 3-5 days following chemotherapy. Ondansetron 8 mg i.v. was given prior to cyclophosphamide (≥ 500 mg/m2) based chemotherapy (doxorubicin or epirubicin > 40 mg/m2) on day 1. Ondansetron 8 mg given orally twice daily was as effective as ondansetron 8 mg given orally three times daily.
In a randomised, double blind parallel group study, 406 patients were randomised to receive either ondansetron 16 mg suppository once daily for 3 days or ondansetron 8 mg orally twice daily for 3 days. The first administration of suppository and tablet began 2 hours and 1-2 hours respectively prior to cyclophosphamide chemotherapy (≥ 500 mg/m2) on day 1. Results from the primary efficacy analysis (≤ 2 emetic episodes on the worst day of days 1-3) show that the ondansetron suppository treatment is equivalent to the ondansetron oral treatment. The ondansetron suppository was less effective than ondansetron oral treatment for a number of other secondary efficacy criteria (complete control of emesis on the worst day of days 1-3, total number of emetic episodes days 1-3 and number of emetic episodes on worst day of days 1-3).

Paediatric studies.

Three open label, uncontrolled, noncomparative studies have been performed with 182 patients, aged 4-18 years old with cancer who were given a variety of cisplatin or noncisplatin regimens. In these trials an initial i.v. dose of ondansetron was followed by oral administration of ondansetron. In these studies, 58% of the 170 evaluable patients had 0 emetic episodes on day 1.

Postoperative nausea and vomiting (PONV). Prevention of PONV.

Adult studies*.

Surgical patients received ondansetron immediately before the induction of general balanced anaesthesia. In a double blind, placebo controlled study 136 patients given ondansetron 4 mg i.v. immediately prior to general anaesthesia was significantly more effective than placebo. In a double blind, placebo controlled study, 207 patients were given a single oral dose of ondansetron 16 mg and 204 patients were given placebo one hour prior to induction of anaesthesia. A significantly greater proportion of surgical patients had no emesis during the 0-24 hour postrecovery period compared with placebo.
*The majority of patients included in the prevention of PONV studies using ondansetron have been adult women receiving balanced anaesthesia for gynaecological surgery.

Paediatric studies.

Three, large, double blind, placebo controlled studies have been performed in 1,049 male and female patients (2 to 12 years of age) undergoing general anaesthesia with nitrous oxide. The surgical procedures included tonsillectomy with or without adenoidectomy, strabismus surgery, herniorrhaphy, and orchidopexy. Patients were randomised to either single i.v. doses of ondansetron (0.1 mg/kg for children weighing 40 kg or less, a single 4 mg dose for children weighing more than 40 kg) or placebo. Study drug was administered over at least 30 seconds, immediately prior to or following anaesthesia induction. Ondansetron showed significant statistical superiority over placebo in preventing postoperative nausea and vomiting. Repeat dosing was not undertaken in these studies. Children at greater risk of postoperative nausea and vomiting are more likely to benefit from prophylaxis; this includes children with a history of motion sickness or previous postoperative nausea and vomiting. No comparisons with other drugs for the prevention of nausea and/or vomiting are available.

Treatment of PONV.

Adults*.

221 adult surgical patients receiving general balanced anaesthesia, who received no prophylactic antiemetics and who experienced nausea and/or vomiting within 2 hours postoperatively were evaluated in a double blind study. Patients who experienced an episode of postoperative nausea and/or vomiting were given ondansetron 4 mg i.v. over 2-5 minutes, and this was significantly more effective than placebo.
*The majority of patients treated for PONV in studies using ondansetron have been adult women receiving balanced anaesthesia for gynaecological surgery.

Paediatric study.

One, large, double blind, placebo controlled study was performed in 351 male and female outpatients (2 to 12 years of age) who received general anaesthesia with nitrous oxide and no prophylactic antiemetics. Surgical procedures were restricted. Patients who experienced two or more emetic episodes within 2 hours following discontinuation of nitrous oxide were randomised to a single i.v. dose of (0.1 mg/kg for children weighing 40 kg or less, a single 4 mg dose for children weighing more than 40 kg) or placebo administered over at least 30 seconds. Ondansetron demonstrated statistically significant superiority over placebo in preventing further episodes of nausea and vomiting. Repeat dosing was not a feature of this study. No data, involving comparisons with active treatments, have been evaluated.

Indications

Ondansetron is indicated for the prevention and treatment of nausea and vomiting induced by cytotoxic therapy and radiotherapy.

Contraindications

Based on reports of profound hypotension and loss of consciousness when ondansetron was administered with apomorphine hydrochloride, concomitant use with apomorphine is contraindicated.
Hypersensitivity to any component of the preparation. (See Precautions).

Precautions

Hypersensitivity reactions have been reported in patients who have exhibited hypersensitivity to other selective 5HT3 receptor antagonists.
Ondansetron prolongs the QT interval in a dose dependent manner. In addition, postmarketing cases of torsade de pointes have been reported in patients using ondansetron. Avoid ondansetron in patients with congenital long QT syndrome. Ondansetron should be administered with caution to patients who have or may develop prolongation of QTc, including patients with electrolyte abnormalities, congestive heart failure, bradyarrhythmias or patients taking other medicinal products that lead to QT prolongation or electrolyte abnormalities.
Hypokalemia and hypomagnesemia should be corrected prior to ondansetron administration.
As ondansetron is known to increase large bowel transit time, patients with signs of subacute intestinal obstruction should be monitored following administration.
Auro-Ondansetron ODT tablets contain aspartame and therefore should be taken with caution in patients with phenylketonuria.
Repeat dosing has not been studied in paediatric patients who experience nausea and/or vomiting despite receiving ondansetron prophylaxis or who continue to experience symptoms after ondansetron treatment.

Use in pregnancy.

(Category B1)
Category B1. Defined as “drugs which have been taken by only a limited number of pregnant women and women of childbearing age, without an increase in the frequency of malformation or other direct or indirect harmful effects on the human foetus having been observed. Studies in animals have not shown evidence of an increased occurrence of foetal damage.
The safety of ondansetron for use in human pregnancy has not been established. Evaluation of experimental animal studies does not indicate direct or indirect harmful effects with respect to the development of the embryo, or foetus, the course of gestation and perinatal and postnatal development. However as animal studies are not always predictive of human response the use of ondansetron in pregnancy is not recommended.

Use in lactation.

Tests have shown that ondansetron is excreted in the breast milk of rats. It is therefore recommended that mothers receiving ondansetron should not breastfeed their babies.

Carcinogenicity.

No evidence for carcinogenic activity was found in two year studies at ondansetron doses up to 10 mg/kg/day by gavage in rats or up to 30 mg/kg/day via drinking water in mice.

Genotoxicity.

Ondansetron did not induce mutations in Salmonella typhimurium, Escherichia coli or Chinese Hamster Ovary cells in the presence or absence of metabolic activation, and showed no potential for causing chromosomal damage in vitro in peripheral human lymphocytes or in vivo in a mouse micronucleus assay. No evidence for DNA damage was observed with ondansetron in a yeast mitotic gene conversion assay.

Effects of fertility.

Oral doses of ondansetron up to 15 mg/kg/day in rats had no effect on male or female fertility.

Interactions

There is no evidence that ondansetron either induces or inhibits the metabolism of other drugs commonly coadministered with it; specific studies have been limited to alcohol, temazepam, and alfentanil to date.
Ondansetron is metabolised by multiple hepatic cytochrome P-450 enzymes: CYP3A4, CYP2D6 and CYP1A2. Due to the multiplicity of metabolic enzymes capable of metabolising ondansetron, enzyme inhibition or reduced activity of one enzyme (e.g. CYP2D6 genetic deficiency) is normally compensated by other enzymes and should result in little or no significant change in overall ondansetron clearance or dose requirement.
Caution should be exercised when ondansetron is coadministered with drugs that prolong the QT interval and/or cause electrolyte abnormalities (see Precautions).
Based on reports of profound hypotension and loss of consciousness when ondansetron was administered with apomorphine hydrochloride, concominant use with apomorphine is contraindicated.
In patients treated with potent inducers of CYP3A4 (i.e. phenytoin, carbamazepine, and rifampicin), the oral clearance of ondansetron was increased and ondansetron blood concentrations were decreased.
Following a single 8 mg tablet dose of ondansetron, a threefold to fourfold decrease in the systemic exposure has been seen in adult epileptic subjects maintained on chronic doses of carbamazepine (n = 8) or phenytoin (n = 8) and not receiving chemotherapy. The effect of these enzyme inducing agents on intravenous ondansetron has not been assessed, but the absence of any first pass effects would be expected to result in a smaller change in exposure than seen following oral dosing. Due to the limited efficacy data in subjects on antiepileptics and the many variables that may influence exposure and response, the clinical significance of this drug interaction in cancer patients receiving chemotherapy is not known.
Data from small studies indicate that ondansetron may reduce the analgesic effect of tramadol.

Adverse Effects

Adverse events are listed below by system organ class and frequency. Frequencies are defined as: very common (≥ 1/10), common (≥ 1/100 and < 1/10), uncommon (≥ 1/1000 and < 1/100), rare (≥ 1/10,000 and < 1/1000) and very rare (< 1/10,000), including isolated reports. Very common, common and uncommon events were generally determined from clinical trial data. The incidence in placebo was taken into account. Rare and very rare events were generally determined from postmarketing spontaneous data.
The following frequencies are estimated at the standard recommended doses of ondansetron according to indication and formulation.

Immune system disorders.

Rare: immediate hypersensitivity reactions, sometimes severe, including anaphylaxis.

Nervous system disorders.

Very common: headache.
Uncommon: seizures, movement disorders (including extrapyramidal reactions such as oculogyric crisis, dystonic reactions and dyskinesia have been observed without definitive evidence of persistent clinical sequelae).
Rare: dizziness during rapid i.v. administration.

Eye disorders.

Rare: transient visual disturbances (e.g. blurred vision) predominantly during i.v. administration.
Very rare: transient blindness predominantly during i.v. administration.
The majority of the blindness cases reported resolved within 20 minutes. Most patients had received chemotherapeutic agents, which included cisplatin. Some cases of transient blindness were reported as cortical in origin.

Cardiac disorders.

Uncommon: arrhythmias, chest pain with or without ST segment depression, bradycardia.
Rare: QTc prolongation (including torsades de pointes).

Vascular disorders.

Common: sensation of warmth or flushing.
Uncommon: hypotension.

Respiratory, thoracic and mediastinal disorders.

Uncommon: hiccups.

Gastrointestinal disorders.

Common: constipation, xerostomia.

Hepatobiliary disorders.

Uncommon: Asymptomatic increases in liver function tests#.
#These events were observed commonly in patients receiving chemotherapy with cisplatin.
To date there has been limited safety experience in controlled trials following intramuscular administration.
Of 7,400 patients who have received intravenous ondansetron during clinical trials, 11 experienced major cardiovascular events, including 3 fatalities, which were considered to be drug related by the investigators (1 probable, 10 possible). It is well known that cardiovascular events, especially of a vascular occlusive nature are not uncommon among patients with cancer, and these events are further increased with cytotoxic chemotherapy, particularly cisplatin.
Table 1 shows adverse events occurring in ≥ 5% of paediatric patients (either group) in three pivotal clinical trials for prevention of postoperative nausea and vomiting. Ondansetron appears to be as well tolerated as placebo.
The overall incidence of adverse events was similar for ondansetron (53%) and placebo (56%). The most commonly reported adverse events were eye disorder(s) as a result of ophthalmic operations, wound problems at the surgical site, nausea and/or vomiting, drowsiness/ sedation, anxiety/ agitation and headache. These events are not unexpected in patients undergoing surgery and there was little difference of these between treatment groups. However the incidence of nausea and/or vomiting reported as an adverse event was significantly higher in patients who had received placebo (11%) compared to those who had received ondansetron (6%). See Table 2.
Fewer adverse events were reported with ondansetron (36%) than with placebo (47%). The most common adverse events were similar to those reported in clinical trials for the prevention of postoperative nausea and vomiting.
Occasionally local reactions at the site of intravenous injection have been reported. See Table 3.
The overall incidence rate was 45% in the placebo group and 47% in the IV ondansetron group.
The neurological body system was associated with the highest incidence of adverse events (placebo approximately 23%; ondansetron 24%). These events were predominantly headache, dizziness and drowsiness.
Cardiovascular adverse events (bradycardia and hypotension) occurred in approximately 4% in both placebo and ondansetron groups; gastrointestinal adverse events (constipation, nausea/ vomiting, flatulence and abdominal pain) occurred in approximately 7% of patients both receiving placebo and IV ondansetron.
The incidence rates were generally similar in both treatment groups for all body systems.

Dosage and Administration

The emetogenic potential of cancer treatment varies according to the doses and combinations of chemotherapy and radiotherapy regimens used. The route of administration and dose of ondansetron should be flexible in the range of 8-32 mg a day and selected as shown below. The lowest effective dose should be used.
The Ondansetron AN ODT tablet is administered by placing on top of the tongue where it will rapidly disperse, then should be swallowed.

Note.

Ondansetron AN ODT may take about 60 seconds to disintegrate on the tongue. This may be longer than time required for other similar orally disintegrating products containing ondansetron. We have however demonstrated that the rate and extent of absorption is not compromised due to longer disintegration time of our product.)

Adults.

Emetogenic chemotherapy and radiotherapy.

For the control of chemotherapy or radiotherapy induced emesis or nausea in adults, two oral doses of 8 mg each at 12 hourly intervals may be given (tablets or orally disintegrating tablets), the first dose being administered 2 hours prior to chemotherapy or radiotherapy. To protect against delayed emesis after the first 24 hours, ondansetron should be continued orally at a dosage of 8 mg twice daily for up to 5 days after a course of treatment.

Children.

Emetogenic chemotherapy and radiotherapy.

Experience is currently limited but ondansetron was effective and well tolerated in children over the age of 4 years, when given intravenously at a dose of 5 mg/m2 over 15 minutes, immediately before chemotherapy, followed by oral therapy at doses of 4 mg twice daily for up to 5 days. The dose of 5 mg/m2 is based on limited data.

Elderly patients.

Emetogenic chemotherapy and radiotherapy.

Efficacy and tolerance in patients aged over 65 years was similar to that seen in younger adults indicating no need to alter dosage or route of administration in the elderly.

Patients with renal impairment.

No alteration of daily dosage or frequency of dosing, or route of administration are required.

Patients with hepatic impairment.

A study which investigated the effect of hepatic impairment on the pharmacokinetics of ondansetron in 24 subjects showed that the plasma clearance of ondansetron is reduced to about 20% of normal, and the serum half-life is significantly prolonged in subjects with severe impairment of hepatic function.
The results in patients with only mildly or moderately impaired hepatic function were less clear. The study showed that in this group the plasma clearance of ondansetron fell to about 50% of that seen in healthy volunteers. Subjects with mild and moderate impairment were not distinguishable from each other for any parameter. This was believed to be partly due to the lack of sensitivity of the Pugh classification system in distinguishing between patients with mild or moderate impairment.
It is recommended that a total daily dose of 8 mg should not be exceeded for patients with moderate or severe hepatic dysfunction. For optimum clinical effect it is recommended that this total daily dose be administered before chemotherapy or radiotherapy.
The severity of the liver disease was assessed according to Pugh's modification of Child's classification (Pugh et al, Brit J. Surg. 1973, 60 (8), 646-649). Patients with a Pugh score of 5 or less were considered to have good hepatic function. A patient with a score of 6 was graded as having mild hepatic impairment, 7 to 9 as moderate hepatic impairment and 10 or more as severe hepatic impairment. The clinical features used in the grading and the weighting system applied are shown in Table 4.

Overdosage

Little is at present known about overdosage with ondansetron, however, a limited number of patients received overdoses. Manifestations that have been reported include visual disturbances, severe constipation, hypotension and a vasovagal episode with transient second degree AV block. In all instances, the events resolved completely. There is no specific antidote for ondansetron, therefore in cases of suspected overdose, symptomatic and supportive therapy should be given as appropriate.
Ondansetron prolongs QT interval in a dose dependent fashion. ECG monitoring is recommended in cases of overdose.
Contact the Poisons Information Centre on 131 126 (Australia) for advice on the management of overdosage.

Presentation

Ondansetron AN ODT orally disintegrating tablets (4 and 8 mg ondansetron) are supplied in pack sizes of 4, 10 and 20* tablets in PVC/PA/Alu/PVC-Peelable lidding foil blister strips.

Ondansetron AN ODT 4 mg.

White to off-white, round tablets debossed with ‘5’ on one side and ‘E’ on the other side with an embossed circular edge.

Ondansetron AN ODT 8 mg.

White to off-white, round tablets debossed with ‘7’ on one side and ‘E’ on the other side with an embossed circular edge.
*Not all pack sizes may be marketed.

Storage

Store below 25°C. Protect from light.

Poison Schedule

S4.