Granisetron Biomendi
Granisetron Biomendi Uses, Dosage, Side Effects, Food Interaction and all others data.
Granisetron Biomendi is a highly selective 5-HT3 receptor antagonist with little or no affinity for other serotonin receptors. It blocks serotonin peripherally on vagal nerve terminals and centrally in the chemoreceptor trigger zone.
Serotonin receptors of the 5-HT3 type are located peripherally on vagal nerve terminals and centrally in the chemoreceptor trigger zone of the area postrema. During chemotherapy that induces vomiting, mucosal enterochromaffin cells release serotonin, which stimulates 5-HT3 receptors. This evokes vagal afferent discharge, inducing vomiting. Animal studies demonstrate that, in binding to 5-HT3 receptors, granisetron blocks serotonin stimulation and subsequent vomiting after emetogenic stimuli such as cisplatin. In the ferret animal model, a single granisetron injection prevented vomiting due to high-dose cisplatin or arrested vomiting within 5 to 30 seconds.
In most human studies, granisetron has had little effect on blood pressure, heart rate or ECG. No evidence of an effect on plasma prolactin or aldosterone concentrations has been found in other studies.
Granisetron Biomendi is a selective inhibitor of type 3 serotonergic (5-HT3) receptors. Granisetron Biomendi has little or no affinity for other serotonin receptors, including 5-HT 1 , 5-HT 1A , 5-HT 1B/C , or 5-HT 2 ; for alpha 1 -, alpha 2 -, or beta-adrenoreceptors; for dopamine D 2 receptors; for histamine H 1 receptors; for benzodiazepine receptors; for picrotoxin receptors; or for opioid receptors. In most human studies, granisetron has had little effect on blood pressure, heart rate, or electrocardiogram (ECG). The drug is structurally and pharmacologically related to ondansetron, another selective inhibitor of 5-HT3 receptors. The serontonin 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. The temporal relationship between the emetogenic action of emetogenic drugs and the release of serotonin, as well as the efficacy of antiemetic agents suggest that chemotherapeutic agents release serotonin from the enterochromaffin cells of the small intestine by causing degenerative changes in the GI tract. The serotonin then stimulates the vagal and splanchnic nerve receptors that project to the medullary vomiting center, as well as the 5-HT3 receptors in the area postrema, thus initiating the vomiting reflex, causing nausea and vomiting.
| Trade Name | Granisetron Biomendi |
| Availability | Prescription only |
| Generic | Granisetron |
| Granisetron Other Names | Granisétron, Granisetrón, Granisetron, Granisetronum |
| Related Drugs | lorazepam, ondansetron, Zofran, dexamethasone, Ativan, metoclopramide, Reglan, amisulpride, droperidol, Zofran ODT |
| Type | |
| Formula | C18H24N4O |
| Weight | Average: 312.417 Monoisotopic: 312.195011409 |
| Protein binding | 65% |
| Groups | Approved, Investigational |
| Therapeutic Class | |
| Manufacturer | |
| Available Country | Spain |
| Last Updated: | September 19, 2023 at 7:00 am |
Uses
Granisetron Biomendi Tablet is used for: Nausea and vomiting associated with initial and repeat course of emetogenic cancer therapy, including high dose of cisplatin. Nausea and vomiting associated with radiation, including total body irradiation and fractionated abdominal radiation.
Granisetron Biomendi Injection is used for: The prevention of nausea and vomitng associated with initial and repeat courses of emetogenic cancer chemotherapy, therapy including high dose cisplatin. The prevention and treatment of post operative nausea and vomiting.
Granisetron Biomendi is also used to associated treatment for these conditions: Nausea and vomiting
How Granisetron Biomendi works
Granisetron Biomendi is a potent, selective antagonist of 5-HT3 receptors. The antiemetic activity of the drug is brought about through the inhibition of 5-HT3 receptors present both centrally (medullary chemoreceptor zone) and peripherally (GI tract). This inhibition of 5-HT3 receptors in turn inhibits the visceral afferent stimulation of the vomiting center, likely indirectly at the level of the area postrema, as well as through direct inhibition of serotonin activity within the area postrema and the chemoreceptor trigger zone.
Dosage
Granisetron Biomendi dosage
Tablet-
Emetogenic Chemotherapy: The recommended adult dosage of oral Granisetron Biomendiis 2 mg once daily or 1 mg twice daily. In the 2 mg once-daily regimen, two 1 mg tablets is given up to 1 hour before chemotherapy. In the 1 mg twice-daily regimen, the first 1 mg tablet is given up to 1 hour before chemotherapy, and the second tabletis given 12 hours after the first. Either regimen is administered only on the day(s) chemotherapy is given. Continued treatment, while not on chemotherapy, has not been found to be useful.
Injection-
Chemotherapy Induced Nausea and Vomiting:
- Adults: The recommended dosage for Granisetron Biomendi Injection is 10 mcg/kg administered intravenously within 30 minutes before initiation of chemotherapy, and only on the day(s) chemotherapy is given. Granisetron Biomendi Injection may be administered intravenously either undiluted over 30 seconds, or diluted with 0.9% Sodium Chloride or 5% Dextrose and infused over 5 minutes. As a general precaution, Granisetron Biomendi Injection should not be mixed in solution with other drugs.
- Paediatric Patients: The recommended dose in paediatric patients 2 to 16 years o f age is 10 mcg/kg. Paediatric patients under 2 years o f age have not beenstudied.
- Geriatric Patients, Renal Failure Patients or Hepatically Impaired Patients: No dosage adjustment is required.
Treatment of Postoperative Nausea and Vomiting:
- Adults: The recommended dosage for prevention of postoperative nausea and vomiting is, a single dose of 1 mg of Granisetron Biomendi should be diluted to 5 ml andadministered as a slow intravenous injection (over 30 seconds). Administration should be completed prior toinduction of anesthesia. The recommended dosage for the treatment of nausea and vomiting after surgery is 1 mg of Granisetron Biomendi undiluted, administered intravenously over 30 seconds.
- Paediatric Patients: Safety and effectiveness of Granisetron Biomendi Injection have not been established in paediatric patients for the prevention or treatment of post operative nausea or vomiting.
- Geriatricpatients, Renal Failure Patients or Hepatically Impaired Patients: No dosage adjustment is required.
Side Effects
Headache, insomnia, constipation, diarrhoea, elevated hepatic transaminases; QT prolongation; bradycardia, palpitations, sick sinus syndrome, chest pain. Application site reactions (transdermal): Rash, pain, erythema, pruritus, irritation, burn, vesicles, urticaria, discolouration; patch non-adhesion.
Toxicity
LD50>2000 mg/kg (rat, oral)
Precaution
Patient with cardiac co-morbidities, on cardiotoxic chemotherapy and/or woth concomitant electrolyte abnormalities. May mask progressive ileus and/or gastric distention. Childn. Pregnancy and lactation.
Interaction
Induced metabolism with phenobarbital. Risk of serotonin syndrome with other serotonergic agents e.g. SSRIs, and serotonin and norepinephrine reuptake inhibitors (SNRIs). Altered clearance with CYP enzyme inducers or inhibitors. Concomitant use with drugs known to prolong QT interval may result in clinical consequences.
Food Interaction
- Take with or without food. The absorption is unaffected by food.
Granisetron Biomendi Drug Interaction
Major: fentanyl, fentanylMinor: sulfamethoxazole / trimethoprim, sulfamethoxazole / trimethoprimUnknown: diphenhydramine, diphenhydramine, pregabalin, pregabalin, acetaminophen, acetaminophen, acetaminophen, acetaminophen, cyanocobalamin, cyanocobalamin, ascorbic acid, ascorbic acid, cholecalciferol, cholecalciferol, ondansetron, ondansetron
Elimination Route
Absorption of is rapid and complete, though oral bioavailability is reduced to about 60% as a result of first pass metabolism.
Half Life
4-6 hours in healthy patients, 9-12 hours in cancer patients
Clearance
- 0.52 L/h/kg [Cancer Patients with 1 mg bid for 7 days]
- 0.41 L/h/kg [Healthy subject with a single 1 mg dose]
Elimination Route
The remainder of the dose is excreted as metabolites, 48% in the urine and 38% in the feces.
Pregnancy & Breastfeeding use
Pregnancy: Category B. No evidence of impaired fertility or harm to the animal fetus have been found. However, this drug may be used in pregnancy only if clearly needed.
Lactation: It is not known whether granisetron is excreted in human milk. So cautions hould be exercised when granisetron is administered to a nursing mother.
Contraindication
Granisetron Biomendi is contraindicated in patients with known hypersensitivity to granisetron.
Special Warning
Pediatric Uses: Safety and effectiveness of granisetron in paediatric patients under 2 years have not been established.
Geriatric use: Efficacy and safety were maintained with increasing age
Acute Overdose
Symptoms: Mild headache.
Management: Symptomatic treatment.
Storage Condition
Store between 15-30°C. Protect from light.
Innovators Monograph
You find simplified version here Granisetron Biomendi
Granisetron Biomendi contains Granisetron see full prescribing information from innovator Granisetron Biomendi Monograph, Granisetron Biomendi MSDS, Granisetron Biomendi FDA label
FAQ
What is Granisetron Biomendi used for?
Granisetron Biomendi is a serotonin 5-HT₃ receptor antagonist used as an antiemetic to treat nausea and vomiting following chemotherapy and radiotherapy. Its main effect is to reduce the activity of the vagus nerve, which is a nerve that activates the vomiting center in the medulla oblongata.
How safe is Granisetron Biomendi?
Granisetron Biomendi appears to be a safe and effective drug for pediatric patients receiving emetogenic chemotherapy.
How does Granisetron Biomendi work?
Granisetron Biomendi works by blocking serotonin, a natural substance in the body that causes nausea and vomiting.
What are the common side effects of Granisetron Biomendi?
Common side effects of Granisetron Biomendi are diarrhea, constipation, stomach pain, weakness, headache, fever, dizziness, drowsiness, trouble sleeping, and anxiety may occur. If any of these effects persist or worsen, notify your doctor or pharmacist promptly.
Is Granisetron Biomendi safe during pregnancy?
Current guidelines suggest that Granisetron Biomendi is an optional treatment for nausea and vomiting in pregnancy (NVP) despite lack of evidence to support fetal safety.
Is Granisetron Biomendi safe during breastfeeding?
No information is available on the use of Granisetron Biomendi during breastfeeding. Until more data become available, Granisetron Biomendi should be used with caution during breastfeeding.
Can I drink alcohol with Granisetron Biomendi?
Your doctor may suggest that you avoid alcohol or reduce the amount of alcohol you drink while you are taking Granisetron Biomendi.
Can I drive after taking Granisetron Biomendi?
Granisetron Biomendi may make you feel dizzy that affects your mental ability. Do not drive or operate machinery if you experience dizziness.
How long does Granisetron Biomendi take to work?
When taken to prevent nausea and vomiting caused by radiation, Granisetron Biomendi is usually taken within 1 hour before treatment.
How long does Granisetron Biomendi stay in my system?
Granisetron Biomendi is a long-acting medication that can stay in your system for a week after just one dose.
When should be taken of Granisetron Biomendi?
Granisetron Biomendi is usually taken 1 hour before chemotherapy is begun. A second dose may be taken 12 hours after the first dose depending on the strength.
How often can I take Granisetron Biomendi?
The recommended adult dosage of oral is 2 mg once daily or 1 mg twice daily.
Who should not take Granisetron Biomendi?
You should not take Granisetron Biomendi if you are allergic to it. To make sure Granisetron Biomendi is safe for you, tell your doctor if you have: heart disease; a heart rhythm disorder; a personal or family history of long QT syndrome; an electrolyte imbalance (such as low levels of potassium or magnesium in your blood); or if you have recently had stomach or intestinal surgery.
What happens if I miss a dose?
Tell your doctor if you forget to take your dose within 1 hour before chemotherapy or radiation. Do not take extra medicine to make up the missed dose.
What happen if I overdose on Granisetron Biomendi?
If you take too much Granisetron Biomendi, call your healthcare provider or local Poison Control Center, or seek emergency medical attention right away.
Does Granisetron Biomendi cause constipation?
The most common side-effects are constipation and headache.
Does Granisetron Biomendi make me sleepy?
This Granisetron Biomendi may make you dizzy or drowsy.
Can I just stop taking Granisetron Biomendi?
Do not exceed the recommended dose. Treatment with Granisetron Biomendi Tablets should not be withdrawn suddenly, particularly if the medicine has been used by the patient for a long time.
Can Granisetron Biomendi affects my heart ?
Granisetron Biomendi can cause a serious heart problem, especially if you use certain medicines at the same time, including antibiotics, antidepressants, heart rhythm medicine, antipsychotic medicines, and medicines to treat cancer, malaria, HIV or AIDS.
Can Granisetron Biomendi increase blood pressure?
In most human studies, Granisetron Biomendi has had little effect on blood pressure, heart rate or ECG.
