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Generic Zofran ( Ondansetron )
Zofran is an antiemetic containing ondansetron that blocks serotonin 5-HT3 receptors to prevent nausea and vomiting. It treats chemotherapy, radiation, and post-operative nausea. Ondansetron comes as 4 mg and 8 mg tablets. The usual adult dose is 8 mg before treatment, then 8 mg every 8 to 12 hours for up to 5 days. Zofran is available in Canada under generic names such as pms-Ondansetron. Follow your doctor or pharmacist's instructions.
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Buy cheap Generic Zofran (Ondansetron) without dr prescription at Canadian Pharmacy
Zofran (Ondansetron 4 mg, 8 mg): Comprehensive Patient Information for Canada
Basic Product Information
| Generic Name (INN) | Ondansetron (as ondansetron hydrochloride dihydrate) |
| Canadian Brand Names / Trade Names | Zofran, Zofran ODT; generic formulations include TEVA-Ondansetron, pms-Ondansetron, MYLAN-Ondansetron, JAMP-Ondansetron, Apo-Ondansetron, Sandoz Ondansetron, and others |
| ATC Code | A04AA01 |
| Available Dosage Forms and Strengths | Film-coated tablets: 4 mg and 8 mg; Orally disintegrating tablets (ODT): 4 mg and 8 mg; Oral solution: 4 mg/5 mL; Injection: 2 mg/mL |
| Manufacturers | Novartis Pharmaceuticals Canada Inc. (Zofran); Teva Canada, Pharmascience, Mylan Pharmaceuticals, Jamp Pharma, Apotex, Sandoz Canada (generics) |
| Prescription Status | Prescription only in Canada |
Mechanism of Action
In simple terms: Ondansetron is an antiemetic medication that prevents and treats nausea and vomiting. It works by blocking serotonin, a natural substance in the body that can trigger the vomiting reflex. Chemotherapy, radiation therapy, and surgery can cause the release of serotonin in the gut and brain, which sends signals that make you feel sick and vomit. Ondansetron blocks these signals, helping to stop nausea and vomiting before they start.
For specialists: Ondansetron is a potent and highly selective antagonist of the 5-HT3 receptor. The precise mode of action in the control of nausea and vomiting is not known. Chemotherapeutic agents and radiotherapy may cause release of 5-HT in the small intestine, initiating the vomiting reflex by activating 5-HT3 receptors on vagal afferents. Ondansetron blocks the initiation of this reflex. Activation of vagal afferents may also cause the release of 5-HT in the area postrema, located on the floor of the fourth ventricle, and this central mechanism may also trigger emesis. Thus, the effect of ondansetron on chemotherapy and radiotherapy-induced nausea and vomiting is likely due to antagonism of 5-HT3 receptors on neurons located in both the peripheral and central nervous systems. The mechanism of action in postoperative nausea and vomiting is not known, but it is possible that common pathways exist with cytotoxic-induced vomiting. Ondansetron does not alter plasma prolactin concentrations. It is not a drug that stimulates gastric or intestinal peristalsis and should not be used instead of nasogastric suction.
Pharmacokinetics
- Absorption: After oral administration, ondansetron is passively and completely absorbed from the gastrointestinal tract, undergoing first-pass metabolism. Peak plasma concentrations are reached approximately 1.5 hours after dosing. For doses above 8 mg, the increase in systemic exposure is greater than dose-proportional. Bioavailability is slightly enhanced by the presence of food but not by antacids.
- Metabolism: Ondansetron is eliminated from the systemic circulation predominantly by hepatic metabolism through multiple enzymatic pathways, including CYP3A4, CYP2D6, and CYP1A2. The primary metabolite is 8-OH-ondansetron, which is rapidly further metabolized to glucuronide and sulfate conjugates. The absence of CYP2D6 enzyme activity has no effect on the pharmacokinetics of ondansetron.
- Elimination: The plasma protein binding of ondansetron is 70–76%. Less than 5% of the absorbed dose is excreted unchanged in the urine. The elimination half-life after intravenous and oral administration is approximately 3 hours, increasing to 3.3–5.4 hours with age.
- Onset of Action: Following oral administration, ondansetron begins to take effect within approximately 30 to 60 minutes. For intravenous use, the antiemetic effect begins within minutes.
- Duration of Action: The antiemetic effect typically lasts for approximately 4 to 8 hours following a single oral dose.
Uses in Daily Life and Best Practice Advice
Ondansetron is prescribed in Canada for the prevention and treatment of nausea and vomiting associated with various medical conditions and treatments. Your physician will determine the appropriate use and dose based on your specific situation.
- Typical Uses: Prevention of nausea and vomiting associated with emetogenic chemotherapy (including high-dose cisplatin) and radiotherapy; prevention and treatment of nausea and vomiting after surgery.
- Administration: Tablets are taken orally with or without food. Orally disintegrating tablets (ODT) should be placed on the tongue and allowed to dissolve; they should not be chewed or swallowed whole. The oral solution should be measured with the provided measuring device.
- Monitoring: If nausea and vomiting do not improve or worsen, consult your physician. Your healthcare provider will monitor your response to treatment, especially during chemotherapy.
- Do Not Exceed Recommended Dose: Do not take more than the prescribed dose, as higher doses may increase the risk of side effects, particularly QT prolongation.
Morning vs. Evening Dosing
Ondansetron is typically taken at scheduled times determined by your physician, especially for chemotherapy or surgery-related nausea. There is no specific clinical recommendation for morning versus evening dosing for general use. For chemotherapy, it is usually taken before the treatment session begins. Always follow the schedule recommended by your physician.
- Scheduled Dosing: For chemotherapy, take ondansetron before treatment as directed by your oncologist.
- Consistency: Take ondansetron at the same times each day if prescribed on a regular schedule.
- Missed Dose: If you miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and continue with your regular schedule. Do not take two doses at the same time.
- Professional Guidance: Your healthcare provider will determine the optimal timing based on your treatment schedule and condition.
Administration With or Without Food
Ondansetron can be taken with or without food. Food slightly increases the bioavailability of ondansetron, but this is not considered clinically significant. The orally disintegrating tablet (ODT) should be placed on the tongue and allowed to dissolve; it can be taken with or without food.
- Take ondansetron tablets with a full glass of water.
- ODT formulations should be placed on the tongue and allowed to dissolve. Do not chew or swallow whole.
- The oral solution should be measured carefully using the provided measuring device.
- Avoid taking ondansetron with antacids, as antacids do not significantly affect its absorption.
- If you have phenylketonuria (PKU), note that some ODT formulations contain aspartame, which is a source of phenylalanine.
Interaction Warnings
| Interaction | Advice |
|---|---|
| Apomorphine | Contraindicated. Severe hypotension and loss of consciousness have been reported with concomitant use. |
| Drugs that Affect Serotonin (e.g., SSRIs, SNRIs, tramadol, St. John's Wort, MDMA) | Increased risk of serotonin syndrome. Monitor for signs of serotonin toxicity such as agitation, hallucinations, rapid heart rate, fever, muscle twitching, and confusion. |
| Tramadol | Ondansetron may decrease the effectiveness of tramadol. Monitor pain control. |
| Carbamazepine, Phenytoin, Rifampicin | These medications may reduce the effectiveness of ondansetron by inducing its metabolism. Monitor clinical response. |
| Medications that Prolong the QT Interval (e.g., certain antiarrhythmics, antipsychotics, antibiotics) | Increased risk of QT prolongation and serious cardiac arrhythmias. Use with caution and monitor ECG if necessary. |
| Alcohol | No direct interaction with ondansetron. However, alcohol may worsen nausea and dehydration. Avoid excessive alcohol consumption. |
Indications for Ondansetron
| Condition | Status |
|---|---|
| Prevention of nausea and vomiting associated with emetogenic chemotherapy (including high-dose cisplatin) | Approved (Health Canada) |
| Prevention of nausea and vomiting associated with radiotherapy | Approved (Health Canada) |
| Prevention and treatment of postoperative nausea and vomiting | Approved (Health Canada) |
| Prevention of nausea and vomiting associated with opioid therapy | Off-label / Commonly used |
"Off-label" means use outside the official approved indication, usually based on current medical guidelines and scientific evidence.
Dosing According to Clinical Indication
| Indication | Adults | Children (4–11 years) | Duration |
|---|---|---|---|
| Chemotherapy-induced nausea and vomiting (highly emetogenic) | 8 mg orally 30 minutes before chemotherapy, then 8 mg 8 hours later, then 8 mg twice daily for 1–2 days | 4 mg orally 30 minutes before chemotherapy, then 4 mg every 4 hours for 2 doses, then 4 mg every 8 hours | 1–2 days after chemotherapy |
| Chemotherapy-induced nausea and vomiting (moderately emetogenic) | 8 mg orally 30 minutes before chemotherapy, then 8 mg 8 hours later, then 8 mg twice daily for 1–2 days | 4 mg orally 30 minutes before chemotherapy, then 4 mg every 8 hours | 1–2 days after chemotherapy |
| Radiotherapy-induced nausea and vomiting | 8 mg orally 1–2 hours before radiotherapy, then 8 mg 8 hours later, then 8 mg twice daily | 4 mg orally 1–2 hours before radiotherapy, then 4 mg every 8 hours | Duration of radiotherapy |
| Postoperative nausea and vomiting | 16 mg orally 1 hour before anesthesia, or 8 mg orally 1 hour before anesthesia followed by 8 mg 8 hours later | 4 mg orally 1 hour before anesthesia, or 4 mg orally 1 hour before anesthesia followed by 4 mg 8 hours later | Single or two-dose regimen |
| Maximum daily dose (adults) | 32 mg per day (oral), but single doses greater than 16 mg are not recommended due to QT prolongation risk | Not applicable | As directed by physician |
Doses should always be adjusted according to the advice of your physician and depending on your health condition. Do not exceed the recommended dose unless advised by a physician. Ondansetron is not recommended for use in children under 4 years of age for the oral formulations.
Side Effects and Safety Profile
| Common (>5%) | Occasional (1–5%) | Rare / Serious (<1%) | Warnings |
|---|---|---|---|
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Guidelines for Correct Use
- Take ondansetron exactly as prescribed by your physician. Do not change your dose without medical advice.
- Take the tablet with or without food, at the times directed by your physician.
- For ODT formulations, place the tablet on the tongue and allow it to dissolve. Do not chew or swallow whole.
- For the oral solution, measure the dose carefully using the provided measuring device.
- Do not take more than the recommended dose, as higher doses may increase the risk of QT prolongation.
- If you are receiving chemotherapy or radiation therapy, take ondansetron before the treatment session as directed.
- Inform every healthcare provider (including dentists, surgeons, and pharmacists) that you are taking ondansetron.
- If you are pregnant, planning to become pregnant, or breastfeeding, consult your physician before use.
- If you miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose. Do not double the dose.
- Store at room temperature in a dry place. Keep out of reach of children.
Alternative Treatment Options
- Granisetron (Kytril): Another 5-HT3 receptor antagonist available in oral and injectable forms. Used for prevention of chemotherapy-induced and postoperative nausea and vomiting.
- Palonosetron (Aloxi): A longer-acting 5-HT3 receptor antagonist with a half-life of approximately 40 hours. Available in injectable and oral forms. Used for chemotherapy-induced nausea and vomiting.
- Dolasetron (Anzemet): A 5-HT3 receptor antagonist available in oral and injectable forms. Note: oral dolasetron is no longer recommended due to QT prolongation risk.
- Metoclopramide (Maxeran): A dopamine receptor antagonist with prokinetic properties. Used for nausea and vomiting, particularly in diabetic gastroparesis and postoperative settings.
- Prochlorperazine (Stemetil): A phenothiazine antiemetic used for various causes of nausea and vomiting. Available in oral, rectal, and injectable forms.
- Aprepitant (Emend): A substance P/neurokinin 1 (NK1) receptor antagonist used in combination with other antiemetics for chemotherapy-induced nausea and vomiting.
- Dexamethasone: A corticosteroid commonly used in combination with 5-HT3 antagonists for chemotherapy-induced nausea and vomiting.
Comparison: Ondansetron is one of the most widely used 5-HT3 receptor antagonists for the prevention and treatment of nausea and vomiting. It is available in multiple formulations, including oral tablets, orally disintegrating tablets, oral solution, and injection, providing flexibility for different clinical situations. Compared with older antiemetics such as metoclopramide and prochlorperazine, ondansetron has a more favorable side effect profile, particularly with respect to extrapyramidal symptoms. However, ondansetron carries a risk of QT prolongation and serotonin syndrome, and higher doses should be avoided. Your physician will determine the best option for your specific condition.
Legal Status, Registration, and Coverage in Canada
- Registration: Ondansetron (Zofran) was initially authorized by Health Canada on March 30, 1998, and has undergone several label updates, most recently in November 2021. Generic formulations are widely available in Canada from multiple manufacturers.
- Prescription Status: Prescription only in Canada.
- Coverage: Coverage varies by province, territory, and private insurance plan. Ondansetron is generally covered by provincial drug plans for approved indications, including chemotherapy-induced and postoperative nausea and vomiting. Some jurisdictions may require special authorization or have formulary restrictions. Orally disintegrating tablets (ODT) may be formulary-restricted to patients unable to tolerate other dosage forms. Generic formulations are generally more affordable than the brand-name Zofran.
- Pharmacovigilance: Adverse reactions should be reported to Health Canada's MedEffect Canada program.
Recent Research and Clinical Guidelines (2022–2026)
- The Clinical Pharmacogenetics Implementation Consortium (CPIC) published an updated guideline in 2026 for CYP2D6 genotype and use of 5-HT3 receptor antagonists. The guideline provides therapeutic recommendations based on CYP2D6 genotype, particularly where genetic variation is associated with reduced drug efficacy. CYP2D6 genetic variation can influence the metabolism of ondansetron, potentially affecting its efficacy.
- The 2026 Norwegian drug handbook recommends that if the effect of ondansetron is not satisfactory, dose increase or shorter dosing intervals (e.g., ondansetron 8 mg three times daily) should be considered.
- International recommendations continue to support ondansetron as a first-line therapy for opioid-induced nausea and vomiting in patients with cancer. Metoclopramide can be used as an alternative in patients who are intolerant to ondansetron or have concurrent constipation.
- Research continues to explore the role of ondansetron in various clinical settings, including its use in the management of nausea and vomiting during pregnancy, where it has been associated with a small increased risk of cleft palate.
- Studies continue to investigate the optimal dosing of ondansetron in different patient populations, including pediatric and geriatric patients, with weight-based dosing being an effective way to normalize systemic exposure in children.
Availability and Supply in Canada
| Packaging Format | Typical Price (CAD, per unit) | Availability |
|---|---|---|
| Ondansetron 4 mg tablet (generic) | Approximately $0.10–$0.50 per tablet | Available at pharmacies across Canada; prescription required |
| Ondansetron 8 mg tablet (generic) | Approximately $0.15–$0.75 per tablet | Available at pharmacies; multiple generic manufacturers |
| Ondansetron ODT 4 mg (generic) | Approximately $0.20–$0.60 per tablet | Available at pharmacies; may be formulary-restricted |
| Ondansetron ODT 8 mg (generic) | Approximately $0.25–$0.80 per tablet | Available at pharmacies; may be formulary-restricted |
| Zofran 4 mg tablet (brand) | Approximately $1.00–$2.00 per tablet | Available at pharmacies; prescription required |
| Zofran 8 mg tablet (brand) | Approximately $1.50–$3.00 per tablet | Available at pharmacies; prescription required |
Prices and availability may vary by province, territory, and pharmacy. Generic ondansetron formulations are widely available in Canada and are generally more affordable than the brand-name Zofran. Oral disintegrating tablets may be subject to formulary restrictions. Check with your local pharmacy for current pricing and coverage options.
Frequently Asked Questions (FAQ)
- What is the difference between Zofran 4 mg and 8 mg?
The 4 mg and 8 mg doses are used for different indications and patient populations. For adults, the 8 mg dose is typically used for chemotherapy-induced and radiotherapy-induced nausea and vomiting. The 4 mg dose is commonly used for pediatric patients and for some postoperative settings. Your physician will determine the appropriate dose based on your condition, age, and treatment plan. - How long does ondansetron take to work?
Following oral administration, ondansetron begins to take effect within approximately 30 to 60 minutes. For intravenous use, the antiemetic effect begins within minutes. The medication is often taken before chemotherapy or surgery to prevent nausea and vomiting from occurring. - Can I take ondansetron with food?
Yes. Ondansetron can be taken with or without food. Food slightly increases the bioavailability of ondansetron, but this is not considered clinically significant. - What should I do if I miss a dose?
If you miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and continue with your regular schedule. Do not take two doses at the same time. - Can I stop taking ondansetron if I feel better?
Do not stop taking ondansetron without consulting your physician. Your physician will advise you on the appropriate duration of treatment based on your condition. For chemotherapy-induced nausea, ondansetron is typically taken for 1 to 2 days after treatment. - What are the serious side effects of ondansetron?
Serious side effects include QT prolongation (which can lead to irregular heartbeats), serotonin syndrome (which can cause agitation, hallucinations, rapid heart rate, fever, and muscle twitching), and severe allergic reactions. Seek immediate medical attention if you experience these symptoms. - Is ondansetron safe during pregnancy?
Ondansetron should be used during pregnancy only if clearly needed. Studies have suggested a small increased risk of cleft palate when used in the first trimester. Consult your physician if you are pregnant, planning to become pregnant, or breastfeeding. - Are there generic versions of ondansetron available in Canada?
Yes. Generic ondansetron is widely available in Canada from multiple manufacturers, including Teva Canada, Pharmascience, Mylan Pharmaceuticals, Jamp Pharma, Apotex, and Sandoz Canada. Generic versions are generally more affordable than the brand-name Zofran. - Can I take ondansetron with other medications?
Ondansetron can interact with several medications, including apomorphine (contraindicated), tramadol, carbamazepine, phenytoin, rifampicin, and drugs that affect serotonin. Always inform your physician and pharmacist about all medications and supplements you are taking. - What formulations of ondansetron are available in Canada?
Ondansetron is available in Canada as film-coated tablets (4 mg and 8 mg), orally disintegrating tablets (ODT, 4 mg and 8 mg), oral solution (4 mg/5 mL), and injection (2 mg/mL). The ODT formulation dissolves on the tongue and is convenient for patients who have difficulty swallowing tablets.
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