Consumer medicine information

Palonosetron Dr Reddy's

Palonosetron

BRAND INFORMATION

Brand name

Palonosetron Dr Reddy's

Active ingredient

Palonosetron

Schedule

S4

 

Consumer medicine information (CMI) leaflet

Please read this leaflet carefully before you start using Palonosetron Dr Reddy's.

What is in this leaflet

This leaflet answers some common questions about Palonosetron. It does not contain all the available information.

It does not take the place of talking to your doctor or pharmacist.

All medicines have risks and benefits. Your doctor has weighed the risks of you using this medicine against the benefits it is expected to have for you.

If you have any concerns about being given this medicine, ask your doctor or pharmacist.

Keep this leaflet. You may need to read it again.

What Palonosetron is used for

This medicine belongs to a group of medicines known as serotonin (5-HT3) antagonists and is a colourless solution for injection into a vein.

It is used for the prevention of nausea and vomiting associated with cancer chemotherapy.

Your doctor, however, may prescribe this medicine for another purpose.

Ask your doctor if you have any questions about why this medicine has been prescribed for you.

Before you are given Palonosetron

When you must not be given it

Do not use this medicine if you have an allergy to palonosetron or any of the ingredients listed at the end of this leaflet.

Some of the symptoms of an allergic reaction may include:

  • shortness of breath, wheezing, difficulty breathing or a tight feeling in your chest
  • swelling of the face, lips, tongue or other parts of the body
  • rash, itching, hives or flushed, red skin

It should not be used to prevent or treat nausea and vomiting in the days following chemotherapy if not associated with another chemotherapy administration.

Before you are given it

Your doctor must know about all of the following before you are given this medicine.

Tell your doctor or pharmacist if you have allergies to:

  • any medicines
  • any other substances, such as foods, preservatives or dyes

If you are pregnant or think you might be, your doctor will not use this medicine unless it is clearly necessary as it is not known whether it will cause any harmful effects when used during pregnancy. You should always ask your doctor or pharmacist for advice before using any medicine if you are pregnant or think you might be.

It is not known if this medicine is found in breast milk. You should ask your doctor or pharmacist for advice before using it if you are breast-feeding.

If you have not told your doctor about any of the above, tell them before you are given this medicine.

Taking or Being Given Other Medicines

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

Some medicines may affect the way other medicines work. Your doctor or pharmacist will be able to tell you what to do when being given this medicine with other medicines.

How Palonosetron is given

This medicine is given as an injection into a vein. A doctor or nurse will normally inject it about 30 minutes before the start of chemotherapy.

Your doctor will decide how much of this medicine you will be given and for how long.

Overdose

As this medicine is given to you under the supervision of your doctor, it is very unlikely that you will receive too much. However, if you experience any side effects after being given it, tell your doctor immediately.

While you are using Palonoseton

Things you must do

If the medicine starts to upset you or your symptoms become worse, tell your doctor.

Tell any other doctors, dentists, and pharmacists who are treating you that you are being treated with this medicine.

Tell your doctor, if you become pregnant during treatment with this medicine.

Things to be careful of

It is not known if this medicine has any effect on your ability to drive or use machines. You should be certain that you are able to drive and operate machines safely before you try.

Side Effects

Tell your doctor, nurse, or pharmacist as soon as possible if you do not feel well while you are being given this medicine.

All medicines can have side effects. Sometimes they are serious, most of the time they are not. You may need medical treatment if you get some of the side effects.

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

Ask your doctor or pharmacist to answer any questions you may have.

The following common side effects may occur.

  • Headache
  • Dizziness
  • Constipation
  • Diarrhoea

Tell your doctor, nurse or pharmacist if you notice any of the above reactions and they worry you.

The following uncommon side effects may also occur:

  • Loss of appetite
  • Anxiety or euphoria
  • Sleep disturbances
  • Change of sensation in your limbs
  • Visual or hearing disturbances
  • Motion sickness
  • Change in heart rate
  • Prominent or discoloured veins
  • Hiccups, flatulence or dry mouth
  • Upset stomach or stomach pain
  • Rash
  • Joint pain
  • Difficulty passing water
  • Weakness or tiredness
  • Fever or a flu-like illness

You should tell your doctor if you notice any of the above effects.

Your doctor will tell you if the following uncommon side effects occur.

  • Changes in the amounts of certain substances in your blood or urine
  • Changes in your blood pressure

Other side effects not listed above may also occur in some patients.

Tell your doctor if you notice any other effects.

Storage

Keep out of the reach and sight of children

Store Below 25°C

Store in the original container

Keep the container in the outer carton in order to protect from light

Do not use this medicine if the expiry date printed on the pack has passed.

Product Description

What it looks like

This medicine is a colourless solution. It is supplied in a pack of one glass vial, which contains 5 mL of the solution. Each vial contains enough for one dose.

Ingredients

Active ingredient:

Palonosetron (as the hydrochloride)

Inactive ingredients:

  • Mannitol
  • Disodium edetate
  • Sodium citrate
  • Citric acid monohydrate
  • Sodium hydroxide
  • Hydrochloric acid
  • Water for injections

Supplier

In Australia: Dr Reddy's Laboratories Australia Pty Ltd
Level 3, 390 St Kilda Road, Melbourne VIC 3004 AUSTRALIA

Australian Registration Number

Palonosetron Dr Reddy’s Aust R 237484

Prepared on June 2022

Published by MIMS September 2022

BRAND INFORMATION

Brand name

Palonosetron Dr Reddy's

Active ingredient

Palonosetron

Schedule

S4

 

1 Name of Medicine

Palonosetron hydrochloride.

2 Qualitative and Quantitative Composition

Palonosetron Dr Reddy's injection is a sterile, clear, colourless, non-pyrogenic, isotonic, buffered solution for intravenous administration.
Palonosetron Dr Reddy's Injection 250 microgram/5 mL solution for injection is sold as a single pack of 1 vial.
Each 5 mL vial of Palonosetron Dr Reddy's injection contains 250 microgram equivalent palonosetron base as hydrochloride.
The inactive ingredients are mannitol, sodium acetate trihydrate, sodium hydroxide and hydrochloric acid in water for injections. The pH of the solution is 4.5 to 5.5.

3 Pharmaceutical Form

Palonosetron Dr Reddy's solution for injection is a clear, essentially colourless solution in a clear glass vial.

4 Clinical Particulars

4.1 Therapeutic Indications

Palonosetron injection is indicated for prevention of nausea and vomiting induced by cytotoxic chemotherapy.

4.2 Dose and Method of Administration

Dosage for adults.

The recommended dosage of palonosetron injection is 250 microgram administered as a single dose approximately 30 minutes before the start of chemotherapy.
Drug accumulation was observed in subjects administered palonosetron injection on consecutive days or once every two days for three doses (see Section 5.2 Pharmacokinetic Properties). Safety and efficacy data available regarding repeated dosing of palonosetron injection within a course of multi-day chemotherapy are limited (see Section 5.1 Pharmacodynamic Properties, Clinical trials).

Use in geriatric patients and in patients with impaired renal or hepatic function.

No dosage adjustment is recommended.

Dosage for paediatric patients.

A recommended intravenous dosage has not been established for paediatric patients.

Administration.

Palonosetron injection should only be used before chemotherapy administration. Palonosetron injection is to be infused intravenously over 30 seconds.

Instructions for use/handling.

This medicinal product must not be mixed with other medicinal products.
Flush the infusion line with normal saline before and after administration of palonosetron injection.
Contains no antimicrobial agent. Palonosetron injection is for single use in one patient only. Discard any residue.

4.3 Contraindications

Palonosetron injection is contraindicated in patients known to have hypersensitivity to the drug or any of its components.

4.4 Special Warnings and Precautions for Use

General.

Hypersensitivity reactions may occur in patients who have exhibited hypersensitivity to other selective 5-HT3 receptor antagonists. Palonosetron injection should not be used to prevent or treat nausea and vomiting in the days following chemotherapy if not associated with another chemotherapy administration.
There have been reports of serotonin syndrome with the use of 5-HT3 antagonists either alone or in combination with other serotonergic drugs including selective serotonin reuptake inhibitors (SSRI) and serotonin noradrenaline reuptake inhibitors (SNRIs).
As palonosetron may increase large bowel transit time, patients with a history of constipation or signs of subacute intestinal obstruction should be monitored following administration.

Cardiac conduction.

At all dose levels tested, palonosetron did not induce clinically relevant prolongation of the QTc interval. A specific thorough QT/QTc study was conducted in healthy volunteers for definitive data demonstrating the effect of palonosetron on QT/QTc (see Section 5.1 Pharmacodynamic Properties). However, as for the other 5-HT3 antagonists, caution should be exercised in the concomitant use of palonosetron with medicinal products that increase the QT interval or in patients who have or are likely to develop prolongation of the QT interval.

Special populations.

Intravenous palonosetron pharmacokinetics was characterized in twenty-four healthy Japanese subjects over the dose range of 3-90 microgram/kg. Total body clearance was 25% higher in Japanese subjects compared to Whites; however, no dose adjustment is required. The pharmacokinetics of palonosetron in Blacks has not been adequately characterized.

Use in hepatic impairment.

Hepatic impairment does not significantly affect total body clearance of palonosetron compared to the healthy subjects. Dosage adjustment is not necessary in patients with any degree of hepatic impairment.

Use in renal impairment.

Mild to moderate renal impairment does not significantly affect palonosetron pharmacokinetic parameters. Total systemic exposure increased by approximately 28% in severe renal impairment relative to healthy subjects. Dosage adjustment is not necessary in patients with any degree of renal impairment.

Use in the elderly.

Population pharmacokinetic analysis and clinical safety and efficacy data did not reveal any differences between cancer patients ≥ 65 years of age and younger patients (18 to 64 years). No dose adjustment is required for these patients.

Paediatric use.

There are no data on efficacy and safety in patients below 18 years.

Effects on laboratory tests.

No data available.

4.5 Interactions with Other Medicines and Other Forms of Interactions

Palonosetron is eliminated from the body through both renal excretion and metabolic pathways with the latter mediated via multiple CYP enzymes. Further in vitro studies indicated that palonosetron is not an inhibitor of CYP1A2, CYP2A6, CYP2B6, CYP2C9, CPY2D6, CYP2E1 and CYP3A4/5 (CYP2C19 was not investigated) nor does it induce the activity of CYP1A2, CYP2D6, or CYP3A4/5. Therefore, the potential for clinically significant drug interactions with palonosetron appears to be low.
A study in healthy volunteers involving single-dose IV palonosetron (0.75 mg) and steady state oral metoclopramide (10 mg four times daily) demonstrated no significant pharmacokinetic interaction.
In controlled clinical trials, palonosetron injection has been safely administered with corticosteroids, analgesics, antiemetics/antinauseants, antispasmodics and anticholinergic agents.
Palonosetron did not inhibit the antitumor activity of the five chemotherapeutic agents tested (cisplatin, cyclophosphamide, cytarabine, doxorubicin and mitomycin C) in murine tumor models.
There have been reports of serotonin syndrome following concomitant use of 5-HT3 antagonists and other serotonergic drugs (including SSRIs and SNRIs).

4.6 Fertility, Pregnancy and Lactation

Effects on fertility.

Palonosetron at oral doses of up to 60 mg/kg/day (> 170 times the recommended human intravenous dose based on estimated plasma AUC) was found to have no effect on fertility and reproductive performance of male and female rats. Oral doses of 60 and 120 mg/kg/day given to male rats for 2 months prior to mating associated with complete infertility at the 120 mg/kg/day dose. Testicular degeneration was confirmed in a 3-month general toxicity study at oral doses of 60 and 120 mg/kg/day. An IV dose of up to 10 mg/kg/day (> 250 times the recommended human intravenous dose based on plasma AUC) had no effect on male fertility and reproductive performance.
(Category B1)
Palonosetron had no effect on foetal development at oral doses of up to 18 mg/kg/day in rats and 90 mg/kg/day in rabbits. At 60 and 120 mg/kg/day in rats, foetal weight was reduced. Palonosetron did not cause foetal abnormalities at these dose levels. However, palonosetron had toxic effects on the dams at 120 mg/kg in rats and 90 mg/kg/day in rabbits.
Because animal reproduction studies are not always predictive of human response, palonosetron should not be used during pregnancy unless it is considered essential.
 It is not known whether palonosetron is excreted in human milk, but some other drugs of the same class are known to be excreted in rat milk. Because of the potential for serious adverse reactions in nursing infants, a decision should be made whether to discontinue breastfeeding or to discontinue the drug, taking into account the importance of the drug to the mother.

4.7 Effects on Ability to Drive and Use Machines

No studies on the effects on the ability to drive and use machines have been performed. Since palonosetron may induce dizziness, somnolence or fatigue, patients should be cautioned when driving or operating machines.

4.8 Adverse Effects (Undesirable Effects)

In clinical trials for the prevention of nausea and vomiting induced by moderately or highly emetogenic chemotherapy, 1374 adult patients received palonosetron. Adverse reactions were similar in frequency and severity with palonosetron injection and ondansetron or dolasetron. Following is a listing of all adverse reactions reported by ≥ 2% of patients in these trials (Table 1).
In other studies, 2 subjects experienced severe constipation following a single palonosetron dose of approximately 0.75 mg, three times the recommended dose. One patient received a 10 microgram/kg oral dose in a post-operative nausea and vomiting study and one healthy subject received a 0.75 mg IV dose in a pharmacokinetic study.
In clinical trials, the following infrequently reported adverse reactions, assessed by investigators as treatment-related or causality unknown, occurred following administration of palonosetron injection to adult patients receiving concomitant cancer chemotherapy:

Cardiovascular.

1%: non-sustained tachycardia, bradycardia, hypotension; < 1%: hypertension, myocardial ischemia, extrasystoles, sinus tachycardia, sinus arrhythmia, supraventricular extrasystoles and QT prolongation. In many cases, the relationship to palonosetron injection was unclear.

Dermatological.

< 1%: allergic dermatitis, pruritic rash.

Hearing and vision.

< 1% motion sickness, tinnitus, eye irritation and amblyopia.

Gastrointestinal system.

1%: diarrhoea; < 1%: dyspepsia, upper abdominal pain, dry mouth, hiccups and flatulence.

General.

1%: weakness, asthenia; < 1%: fatigue, fever, hot flash, flu-like syndrome.

Liver.

< 1%: transient, asymptomatic increases in AST and/or ALT and bilirubin. These changes occurred predominantly in patients receiving highly emetogenic chemotherapy.

Metabolic.

1%: hyperkalemia; < 1%: electrolyte fluctuations, hypocalcemia, hyperglycemia, metabolic acidosis, glycosuria, appetite decrease, anorexia.

Musculoskeletal.

< 1%: arthralgia.

Nervous system.

1%: dizziness; < 1%: somnolence, insomnia, hypersomnia, paresthesia, and peripheral sensory neuropathy.

Psychiatric.

1%: anxiety; < 1%: euphoric mood.

Urinary system.

< 1%: urinary retention.

Vascular.

< 1%: vein discoloration, vein distention.

Post-marketing experience.

In post-marketing reports there have been very rare cases of:
Hypersensitivity reactions including anaphylaxis and shock; and
Injection site reactions such as burning, induration, discomfort and pain.

Reporting suspected adverse effects.

Reporting suspected adverse reactions after registration of the medicinal product is important. It allows continued monitoring of the benefit-risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions at www.tga.gov.au/reporting-problems.

4.9 Overdose

There is no known antidote to palonosetron injection. Overdose should be managed with supportive care. Fifty adult cancer patients were administered palonosetron at a dose of 90 microgram/kg (equivalent to 6 mg fixed dose) as part of a dose ranging study. This is approximately 25 times the recommended dose of 250 microgram. This dose group had a similar incidence of adverse events compared to the other dose groups and no dose response effects were observed. Dialysis studies have not been performed; however, due to the large volume of distribution, dialysis is unlikely to be an effective treatment for palonosetron overdose. A single intravenous dose of palonosetron at 30 mg/kg (947 and 474 times the human dose for rats and mice, respectively, based on body surface area) was lethal to rats and mice. The major signs of toxicity were convulsions, gasping, pallor, cyanosis and collapse.
For information on the management of overdose, contact the Poisons Information Centre on 13 11 26 (Australia).

5 Pharmacological Properties

5.1 Pharmacodynamic Properties

Mechanism of action.

Palonosetron hydrochloride is an antiemetic and antinauseant agent. It is a selective serotonin subtype 3 (5-HT3) receptor antagonist with a strong binding affinity for this receptor.

Pharmacodynamics.

Cancer chemotherapy may be associated with a high incidence of nausea and vomiting, particularly when certain agents, such as cisplatin, are used. 5-HT3 receptors are located on the nerve terminals of the vagus in the periphery and centrally in the chemoreceptor trigger zone of the area postrema. It is thought that chemotherapeutic agents produce nausea and vomiting by releasing serotonin from the enterochromaffin cells of the small intestine and that the released serotonin then activates 5-HT3 receptors located on vagal afferents to initiate the vomiting reflex.
The effect of palonosetron on blood pressure, heart rate, and ECG parameters including QTc were comparable to ondansetron and dolasetron in clinical trials. In non-clinical studies palonosetron possesses the ability to block ion channels involved in ventricular de- and repolarization and to prolong action potential duration. The effect of palonosetron on QTc interval was evaluated in a double blind, randomized, parallel, placebo and positive (moxifloxacin) controlled trial in adult men and women. The objective was to evaluate the ECG effects of IV administered palonosetron at single doses of 0.25, 0.75 or 2.25 mg in 221 healthy subjects. The study demonstrated no effect on QT/QTc interval duration as well as any other ECG interval at doses up to 2.25 mg. No clinically significant changes were shown on heart rate, atrioventricular (AV) conduction and cardiac repolarisation.

Clinical trials single-dose palonosetron administration.

Efficacy of single-dose palonosetron injection in preventing nausea and vomiting induced by moderately and highly emetogenic chemotherapy was studied in a phase 2 dose-ranging trial and three phase 3 trials. In the phase 3 trials, the primary efficacy endpoint was complete response rate (no emetic episodes and no rescue medication). Prevention of nausea was assessed as a secondary efficacy endpoint. The safety and efficacy of palonosetron in repeated courses of chemotherapy was also studied.

Moderately emetogenic chemotherapy.

Two Phase 3, double-blind trials involving 1132 patients compared single-dose IV palonosetron with either single-dose IV ondansetron (study 1) or dolasetron (study 2) given 30 minutes prior to moderately emetogenic chemotherapy including carboplatin, cisplatin ≤ 50 mg/m2, cyclophosphamide < 1500 mg/m2, doxorubicin > 25 mg/m2, epirubicin, irinotecan, and methotrexate > 250 mg/m2. Concomitant corticosteroids were not administered prophylactically in study 1 and were only used by 4-6% of patients in study 2. The majority of patients in these studies were women (77%), White (65%) and naïve to previous chemotherapy (54%). The mean age was 55 years, (age range 18-97).

Highly emetogenic chemotherapy.

A Phase 2, double-blind, dose-ranging study evaluated the efficacy of single-dose IV palonosetron from 0.3 to 90 microgram/kg (equivalent to < 0.1 mg to 6 mg fixed dose) in 161 chemotherapy-naïve adult cancer patients receiving highly-emetogenic chemotherapy (either cisplatin ≥ 70 mg/m2 or cyclophosphamide > 1100 mg/m2). Concomitant corticosteroids were not administered prophylactically. Analysis of data from this trial indicates that 250 microgram is the lowest effective dose in preventing acute nausea and vomiting induced by highly emetogenic chemotherapy.
A Phase 3, double-blind trial involving 667 patients compared single-dose IV palonosetron with single-dose IV ondansetron (study 3) given 30 minutes prior to highly emetogenic chemotherapy including cisplatin ≥ 60 mg/m2, cyclophosphamide > 1500 mg/m2, and dacarbazine. Highly emetogenic chemotherapy was given only for the first day of the chemotherapy cycle. For the remainder of the cycle, low to moderately (max grade 3 of Hesketh scale) emetogenic chemotherapy was allowed. Corticosteroids were co-administered prophylactically before chemotherapy in 67% of patients. Of the 667 patients, 51% were women, 60% White, and 59% naïve to previous chemotherapy. The mean age was 52 years; (age range 18-86).

Efficacy results.

Intent-to-treat analyses are presented. The conclusions of the per protocol analyses were similar.
Palonosetron was non-inferior to the comparators in the prevention of acute vomiting (within 24h) after moderately and highly emetogenic chemotherapy and comparable in the prevention of nausea (Tables 1-3). Efficacy was greater when corticosteroids were administered concomitantly in the highly emetogenic setting. The secondary efficacy endpoint of the study assessed delayed onset (24-120 h) nausea and vomiting, the results are shown below (Tables 2-4). The comparative efficacy of palonosetron 250 microgram in multiple cycles of chemotherapy has not been demonstrated.

Multiple-dose palonosetron administration.

Published randomised, controlled studies have not been designed to show, or have not shown, improvement in primary efficacy endpoints related to nausea and vomiting in patient arms given palonosetron injection daily or on alternate days, relative to single dose use, in the context of multiple day chemotherapy. It has not been clearly established that such repeated dosing provides significant additional benefit compared to a single dose.

5.2 Pharmacokinetic Properties

After intravenous dosing of palonosetron in healthy subjects and cancer patients, an initial decline in plasma concentrations is followed by a slow elimination from the body. Mean maximum plasma concentration (Cmax) and area under the concentration-time curve (AUC0-∞) are generally dose-proportional over the dose range of 0.3-90 microgram/kg in healthy subjects and in cancer patients. Following single IV dose of palonosetron at 3 microgram/kg (or 0.21 mg/70 kg) to six cancer patients, mean (± SD) maximum plasma concentration was estimated to be 5.6 ± 5.5 nanogram/mL and mean AUC was 35.8 ± 20.9 nanogram.hr/mL.
Following intravenous administration of palonosetron 0.25 mg once every other day for 3 doses in 11 testicular cancer patients, the mean (± SD) increase in the initial phase of the plasma concentration-time curve (AUC0-2.5hr) from Day 1 to Day 5 was 42 ± 34%; how this finding relates to more conventional measures of systemic exposure is not known.
After intravenous administration of palonosetron 0.25 mg once daily for 3 days in 12 healthy subjects, the mean (± SD) increase in systemic exposure over 24 hours (AUC0-24hr) from Day 1 to Day 3 was 110 ± 45%.
Drug accumulation may be greater in the 10% of patients with prolonged elimination half-life.

Distribution.

Palonosetron has a volume of distribution of approximately 8.3 ± 2.5 L/kg. Approximately 62% of palonosetron is bound to plasma proteins.

Metabolism.

Palonosetron is eliminated by multiple routes with approximately 50% metabolized to form two primary metabolites: N-oxide-palonosetron and 6-S-hydroxy-palonosetron. These metabolites each have less than 1% of the 5-HT3 receptor antagonist activity of palonosetron. In vitro metabolism studies have suggested that CYP2D6 and to a lesser extent, CYP3A and CYP1A2 are involved in the metabolism of palonosetron. However, clinical pharmacokinetic parameters are not significantly different between poor and extensive metabolizers of CYP2D6 substrates.

Excretion.

After a single intravenous dose of 10 microgram/kg [14C]-palonosetron, approximately 80% of the dose was recovered within 144 hours in the urine with palonosetron representing approximately 40% of the administered dose. In healthy subjects the total body clearance of palonosetron was 160 ± 35 mL/h/kg and renal clearance was 66.5 ± 18.2 mL/h/kg. Mean terminal elimination half life is approximately 40 hours.

5.3 Preclinical Safety Data

Genotoxicity.

Palonosetron was not genotoxic in the Ames test, the Chinese hamster ovarian cell (CHO/HGPRT) forward mutation test, the ex vivo hepatocyte unscheduled DNA synthesis test or the mouse micronucleus test. It was, however, positive for clastogenic effects in the CHO cell chromosomal aberration test.

Carcinogenicity.

In a 104-week carcinogenicity study in CD-1 mice, animals were treated with oral doses of palonosetron at 10, 30 and 60 mg/kg/day. Treatment with palonosetron was not tumorigenic. The highest tested dose produced a systemic exposure to palonosetron (plasma AUC) of > 600 times the human exposure at the recommended intravenous dose of 250 microgram.
In a 104-week carcinogenicity study in Sprague-Dawley rats, male and female rats were treated with oral doses of 15, 30 and 60 mg/kg/day and 15, 45 and 90 mg/kg/day, respectively. The lowest and highest doses, respectively, produced a systemic exposure to palonosetron (plasma AUC) of > 25 times and > 500 times the human exposure at the recommended dose.
Treatment with palonosetron produced increased incidences of adrenal benign pheochromocytoma and combined benign and malignant pheochromocytoma in both male and female rats, of pancreatic Islet cell adenoma and combined adenoma and carcinoma of pancreatic acinar cell adenoma and combined adenoma and adenocarcinoma and of pituitary adenoma in male rats. Increased incidences of skin keratocanthomas and tail squamous cell papillomas were also observed, mainly in males. In female rats, palonosetron produced hepatocellular adenoma and combined hepatocellular adenoma and carcinoma, and increased the incidences of thyroid C-cell adenoma and combined adenoma and carcinoma, and of mammary gland adrenocarcinoma.

6 Pharmaceutical Particulars

6.1 List of Excipients

See Section 2 Qualitative and Quantitative Composition.

6.2 Incompatibilities

Incompatibilities were either not assessed or not identified as part of the registration of this medicine.

6.3 Shelf Life

In Australia, information on the shelf life can be found on the public summary of the Australian Register of Therapeutic Goods (ARTG). The expiry date can be found on the packaging.

6.4 Special Precautions for Storage

Store below 25°C. Protect from light.

6.5 Nature and Contents of Container

Palonosetron Dr Reddy's injection 250 microgram/5 mL solution for injection is sold as a single pack of 1 vial.

6.6 Special Precautions for Disposal

In Australia, any unused medicine or waste material should be disposed of in accordance with local requirements.

6.7 Physicochemical Properties

Palonosetron hydrochloride is a white to off-white crystalline powder. It is freely soluble in water, soluble in propylene glycol, and slightly soluble in ethanol and 2-propanol.
Chemically, palonosetron hydrochloride is: (3aS)-2-[(S)-1-Azabicyclo[2.2.2]oct-3-yl]-2,3,3a,4,5,6- hexahydro-1-oxo-1Hbenz[de]isoquinoline hydrochloride. The empirical formula is C19H24N2O.HCl, with a molecular weight of 332.87. Palonosetron hydrochloride exists as a single isomer.

Chemical structure.


CAS number.

135729-61-2 Palonosetron.
135729-62-3 Palonosetron hydrochloride.

7 Medicine Schedule (Poisons Standard)

S4 - Prescription Medicine.

Summary Table of Changes