Medication info

Palnon Injection (Palonosetron Hydrochloride)

Prescription medicationIntravenous injectionExpired
Ingredient · strength
Palonosetron Hydrochloride›0.056mg / 1mL
Manufacturer / importer
Aprogen Biologics, Inc.
Appearance
Colorless transparent liquid in a colorless transparent prefilled syringe
Packaging
1.5mL x 5 prefilled syringes, 5mL x 1 prefilled syringe
Approval status
Expired

MFDS item code 202001988 · Approved 2020.03.20

This product's status changed to Expired on 2025.03.20. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Prevention of nausea and vomiting associated with cancer treatment; prevention and treatment of postoperative nausea and vomiting
Who receives it
Adults · Children
Adult administration
1. Adults 1) Prevention of nausea and vomiting induced by antineoplastic chemotherapy: Administer palonosetron 0.25 mg once by intravenous injection over at least 30 seconds, 30 minutes before the start of chemotherapy. 2) Prevention of postoperative nausea and vomiting: Administer 0.075 mg once by intravenous injection over at least 10 seconds, immediately before induction of anesthesia. As with other antiemetics, routine administration is not recommended for patients expected to have a low likelihood of postoperative nausea and vomiting. Administration of this drug is recommended for patients in whom postoperative nausea and vomiting must be avoided, even if the likelihood of postoperative nausea and vomiting is low. 3) Treatment of postoperative nausea and vomiting: Administer 0.075 mg once by intravenous injection over at least 10 seconds as soon as nausea and vomiting occur. 3. No dosage adjustment is required for elderly patients or patients with hepatic or renal impairment. There are no clinical data for patients with end-stage renal disease undergoing dialysis.
Child administration
2. Children (2 months and older) 1) Prevention of acute nausea and vomiting induced by antineoplastic chemotherapy: Administer palonosetron 0.02mg/kg (maximum 1.5mg) once by intravenous infusion over at least 15 minutes, 30 minutes before the start of chemotherapy. The safety and efficacy of this drug in neonates have not been established (no data are available). Data on the use of this drug for the prevention of nausea and vomiting induced by antineoplastic chemotherapy in infants (under 24 months) are limited.

Ingredients

Manufacturer
Aprogen Biologics, Inc.

Efficacy & effects

Prevention of nausea and vomiting associated with cancer treatment; prevention and treatment of postoperative nausea and vomiting

  • Nausea
  • Vomiting
View approved original text

This medication is used to prevent acute and delayed nausea and vomiting caused by moderate to severe vomiting-inducing anticancer chemotherapy in adults. It is also effective in preventing and treating nausea and vomiting occurring within 24 hours after surgery. It is used to prevent acute nausea and vomiting due to moderate to severe vomiting-inducing anticancer chemotherapy in children as well. By effectively managing nausea and vomiting in various situations, it reduces patient discomfort and facilitates the treatment process.

How it is given

Adult administration

1. Adults 1) Prevention of nausea and vomiting induced by antineoplastic chemotherapy: Administer palonosetron 0.25 mg once by intravenous injection over at least 30 seconds, 30 minutes before the start of chemotherapy. 2) Prevention of postoperative nausea and vomiting: Administer 0.075 mg once by intravenous injection over at least 10 seconds, immediately before induction of anesthesia. As with other antiemetics, routine administration is not recommended for patients expected to have a low likelihood of postoperative nausea and vomiting. Administration of this drug is recommended for patients in whom postoperative nausea and vomiting must be avoided, even if the likelihood of postoperative nausea and vomiting is low. 3) Treatment of postoperative nausea and vomiting: Administer 0.075 mg once by intravenous injection over at least 10 seconds as soon as nausea and vomiting occur. 3. No dosage adjustment is required for elderly patients or patients with hepatic or renal impairment. There are no clinical data for patients with end-stage renal disease undergoing dialysis.

Child administration

2. Children (2 months and older) 1) Prevention of acute nausea and vomiting induced by antineoplastic chemotherapy: Administer palonosetron 0.02mg/kg (maximum 1.5mg) once by intravenous infusion over at least 15 minutes, 30 minutes before the start of chemotherapy. The safety and efficacy of this drug in neonates have not been established (no data are available). Data on the use of this drug for the prevention of nausea and vomiting induced by antineoplastic chemotherapy in infants (under 24 months) are limited.

Precautions

This drug should not be used by patients who have allergic reactions to this drug or its components. Patients who have had allergic reactions to similar drugs may also experience allergic reactions when using this drug, so caution is necessary. This drug may slow gut movement; therefore, patients with constipation or symptoms of intestinal obstruction should use it cautiously under medical supervision. Additionally, using this drug with other medications that affect serotonin, a neurotransmitter, may result in a serious side effect known as serotonin syndrome, so patients currently taking such medications need to be particularly careful. When using this drug, side effects such as headaches, constipation, diarrhea, dizziness, fatigue, etc., may occur, so if any unusual symptoms develop, medical consultation should be sought immediately. When engaging in activities requiring alertness such as driving or operating machinery, caution should be exercised as this drug may cause dizziness or drowsiness. Pregnant or breastfeeding women should use this drug only when necessary and must consult a physician before use. The safety and efficacy of this drug in children and the elderly have not been fully established, so consultation with a specialist is required when using it. In the case of overdose, there is no specific antidote, so immediate hospital visit for appropriate treatment is necessary, and caution is required as this drug is not removed by dialysis. This drug should be stored away from direct sunlight and at room temperature, and discoloration or particulate matter must be checked before administration. Remaining medication after use should be disposed of, and while there are relatively few interactions with other medications, it is important to follow a physician's instructions when used in combination with specific drugs.

Side effects

  • Headache
  • constipation
  • diarrhea
  • dizziness
  • fatigue
  • abdominal pain
  • insomnia
  • severe constipation
  • non-sustained tachycardia
  • bradycardia
Show 184 more
  • hypotension
  • hypertension
  • myocardial infarction
  • premature ventricular contractions
  • sinus tachycardia
  • sinus arrhythmia
  • ventricular premature contractions
  • QT prolongation
  • allergic dermatitis
  • rash
  • motion sickness
  • tinnitus
  • burning sensation in the eyes
  • amblyopia
  • dyspepsia
  • dry mouth
  • hiccups
  • abdominal bloating
  • weakness
  • fever
  • systemic warmth
  • flu-like syndrome
  • increased AST
  • increased ALT
  • elevated bilirubin
  • hyperkalemia
  • electrolyte fluctuations
  • hyperglycemia
  • metabolic acidosis
  • diabetes
  • decreased appetite
  • appetite loss
  • arthralgia
  • drowsiness
  • hypersomnia
  • paresthesia
  • anxiety
  • euphoria
  • urinary retention
  • venous discoloration
  • venous dilation
  • neutropenia
  • itching
  • dyskinesia
  • pain at the injection site
  • skin disorders
  • prolonged QTc
  • dehydration
  • ECG QT prolongation
  • bradycardia
  • hypotension
  • arrhythmia
  • generalized edema
  • decreased T wave amplitude on ECG
  • decreased platelet count
  • upper abdominal pain
  • excessive salivation
  • decreased intestinal motility
  • chills
  • increased liver enzyme levels
  • hypokalemia
  • respiratory depression
  • laryngospasm
  • insomnia
  • anemia
  • dehydration
  • electrolyte imbalance
  • hypotension
  • cough
  • wet cough
  • abdominal distension
  • musculoskeletal pain
  • myalgia
  • severe pain
  • bladder distension
  • urethral dysfunction
  • otalgia
  • fatigue
  • fever
  • chest discomfort
  • postoperative pain
  • chills
  • procedural pain
  • postoperative anemia
  • wound exudate
  • hypersensitivity reaction
  • injection site reaction
  • leukopenia
  • systemic weakness
  • death
  • nausea
  • stomatitis
  • muscle weakness
  • acute liver failure
  • cough
  • eye inflammation
  • monocytosis
  • palpitations
  • urticaria
  • numbness
  • back pain
  • increased sweating
  • tremors
  • lymphedema
  • dry cough
  • epigastric discomfort
  • neck/shoulder pain
  • numbness
  • asthenia
  • dysgeusia
  • febrile neutropenia
  • abdominal discomfort
  • unspecified seizure
  • cystitis
  • dysuria
  • boils
  • edema
  • frequent urination
  • limb pain
  • upper respiratory infection
  • pigmentation abnormalities
  • palm/sole erythema sensory disorders
  • nail changes
  • postoperative pain
  • hoarseness
  • blurred vision
  • neurotoxicity
  • neuropathy
  • renal impairment
  • nocturia
  • facial flushing
  • acne
  • female perineal pain
  • dysphagia
  • flank pain
  • sore throat
  • oral opening disorder
  • orofacial pain
  • gingivitis
  • gum bleeding
  • decreased red blood cells
  • generalized edema
  • mucositis
  • vaginitis
  • weight loss
  • weight gain
  • pancreatitis
  • dental damage
  • hemorrhoids
  • toothache
  • nasal cold
  • nasal congestion
  • nosebleed
  • runny nose
  • hair loss
  • migraine
  • pneumonia
  • dry skin
  • skin rash
  • yawning
  • anal bleeding
  • anal pain
  • hematuria
  • melena
  • eosinophilia
  • neutrophilia
  • dyspnea
  • erythema
  • flush
  • pleural effusion
  • acute renal failure
  • shock
  • chest pain
  • nausea
  • palpitations
  • peripheral edema
  • atrioventricular block
  • heart disease
  • increased coagulation time
  • drowsiness
  • tremor
  • prolonged prothrombin time
  • decreased prothrombin activity
  • dyspnea

Not everyone experiences these, and they can vary from person to person.

Storage

This drug should be stored at room temperature between 1 to 30 degrees Celsius in a sealed container to prevent air from entering. Additionally, it is important to store it away from direct sunlight to maintain the drug's effectiveness.

Appearance and packaging

Appearance

Colorless transparent liquid in a colorless transparent prefilled syringe

Package unit

1.5mL x 5 prefilled syringes, 5mL x 1 prefilled syringe

Same-ingredient medicines

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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.