Generic Praziquantel

Praziquantel

Praziquantel is a broad-spectrum anthelmintic agent indicated for the treatment of infections caused by various species of parasitic flatworms, including schistosomiasis (all species of Schistosoma), clonorchiasis (Clonorchis sinensis), opisthorchiasis (Opisthorchis viverrini and Opisthorchis felineus), paragonimiasis (Paragonimus westermani and other species), fasciolopsiasis (Fasciolopsis buski), and intestinal tapeworm infections caused by Taenia saginata, Taenia solium, Diphyllobothrium latum, and Hymenolepis nana. It belongs to the pyrazinoisoquinoline class of anthelmintics and works through a dual mechanism of action. First, praziquantel causes a rapid and sustained influx of calcium ions across the parasite's tegumental membrane, leading to immediate tetanic contraction and spastic paralysis of the worm's musculature. Second, it disrupts the structural integrity of the parasite's outer tegument, exposing previously concealed surface antigens to the host immune system, which then facilitates immune-mediated phagocytosis, adherence, and elimination of the damaged parasites. This unique combined mechanism renders praziquantel highly effective against a wide range of trematodes (flukes) and cestodes (tapeworms).

Usual adult dose: The dosage of praziquantel is strictly dependent on the specific parasitic infection being treated and the patient's body weight. For Schistosoma haematobium, Schistosoma mansoni, and Schistosoma intercalatum infections, the recommended dose is 40 mg per kilogram of body weight administered as a single oral dose or divided into two doses given 4 to 6 hours apart on a single day. For Schistosoma japonicum and Schistosoma mekongi, a total dose of 60 mg per kilogram is recommended, divided into two or three doses over one day. For clonorchiasis and opisthorchiasis, the recommended dose is 75 mg per kilogram per day divided into three doses for 1 to 2 days. For paragonimiasis, 75 mg per kilogram per day divided into three doses for 2 to 3 days is recommended. For fasciolopsiasis, a single dose of 15 to 25 mg per kilogram is usually effective. For intestinal tapeworm infections, including Taenia saginata, Taenia solium, and Diphyllobothrium latum, a single oral dose of 5 to 10 mg per kilogram is sufficient. For Hymenolepis nana (dwarf tapeworm), a higher single dose of 15 to 25 mg per kilogram is recommended due to the potential for internal autoinfection. Tablets should be taken with food and swallowed whole with a full glass of water. They may be divided into segments along the scored markings to accommodate precise weight-based dosing. The tablets have a distinctly bitter taste and should not be chewed. For Taenia solium infections, it is crucial to exclude concurrent neurocysticercosis before treatment, as the death of cerebral cysticerci can precipitate severe neurological reactions.

Dosage form: Tablets: 600 mg (white to off-white, ovaloid, film-coated, scored into four segments). Each tablet features three deep score lines, allowing the tablet to be divided into four equal quarters of approximately 150 mg each. This quarter-scored design facilitates accurate weight-based dosing across a wide range of body weights, which is particularly important in pediatric patients, low-body-weight adults, and mass drug administration programs where precise milligram-per-kilogram calculations are essential.

Onset of action: Following oral administration, praziquantel is rapidly absorbed from the gastrointestinal tract, with peak plasma concentrations achieved within 1 to 3 hours. The onset of the paralytic effect on susceptible parasites occurs within minutes of drug exposure; tegumental damage and spastic paralysis begin within the first hour following peak plasma concentrations. In schistosomiasis, cessation of egg production and the initiation of worm elimination commence within the first 24 to 48 hours after treatment. Clinical improvement, including resolution of acute symptoms such as fever, abdominal pain, and hematuria, is typically observed within days to weeks, depending on the parasite burden, the species involved, and the chronicity of the infection.

Duration of action: The elimination half-life of praziquantel is approximately 0.8 to 1.5 hours in healthy individuals; however, the half-life of its active hydroxylated metabolites is approximately 4 to 6 hours. Despite the relatively short plasma half-life, the antiparasitic effect is sustained and generally curative with a single day of treatment for most indications, due to the irreversible nature of the tegumental and muscular damage inflicted on the parasites. Praziquantel is extensively metabolized in the liver via the cytochrome P450 system, primarily CYP3A4, and its metabolites are excreted predominantly in the urine (60% to 80%) within 24 hours of dosing, with the remainder eliminated in the feces.

Alcohol recommendation: Alcohol consumption should be avoided during treatment with praziquantel and for at least 24 hours after the last dose. Praziquantel undergoes extensive hepatic metabolism via the cytochrome P450 enzyme system, and alcohol may alter hepatic metabolic pathways, potentially affecting the drug's pharmacokinetics and therapeutic efficacy. Furthermore, alcohol can exacerbate the central nervous system side effects of praziquantel, including dizziness, drowsiness, headache, fatigue, and impaired coordination. Patients should not drive or operate machinery for at least 24 hours following treatment, and the concomitant use of alcohol significantly compounds the risk of sedation and accidents. Complete abstinence from alcohol for the duration of therapy is strongly recommended to ensure treatment safety and efficacy.

Most common side effects: In the treatment of schistosomiasis, the most frequently reported adverse effects are abdominal discomfort or pain, nausea, vomiting, diarrhea, anorexia, headache, dizziness, drowsiness, malaise, fatigue, fever, and urticaria. These effects are generally mild to moderate in severity, transient, and resolve spontaneously within 24 to 48 hours. It is important to note that many of these symptoms—particularly abdominal pain, nausea, headache, and fever—may be attributable to the host immune response to dying and disintegrating parasites and the release of parasitic antigens rather than to the drug itself. In patients with heavy parasitic loads, more pronounced systemic reactions may occur, including intense abdominal cramping, bloody diarrhea, and high fever. When used for neurocysticercosis, praziquantel must be administered under close medical supervision with concomitant corticosteroid cover, as the inflammatory response to dying cysticerci in the brain can precipitate seizures, elevated intracranial pressure, and meningoencephalitis. Praziquantel is contraindicated in patients with ocular cysticercosis, as parasite death within the eye may cause irreversible intraocular damage and vision loss. It is also contraindicated in patients with known hypersensitivity to praziquantel or any of its excipients. Concomitant administration with strong cytochrome P450 inducers such as rifampicin, phenytoin, carbamazepine, and dexamethasone may substantially reduce praziquantel plasma levels, potentially compromising therapeutic efficacy and leading to treatment failure. Conversely, CYP450 inhibitors such as cimetidine, ketoconazole, and grapefruit juice may increase plasma concentrations and the risk of toxicity. In patients with severe hepatic impairment or decompensated liver disease, dose reduction or alternative therapeutic strategies may be considered.

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Buy Generic Praziquantel () without prescription in Canada

At our pharmacy, you can buy Praziquantel without a prescription, with discreet and anonymous packaging delivered within 5-14 days across Canada.

What is Praziquantel?

Praziquantel is an anthelmintic medication used to treat parasitic worm infections. It's the drug of choice for schistosomiasis, a blood fluke infection that affects over 200 million people worldwide, and for liver fluke infections like clonorchiasis and opisthorchiasis. It's also highly effective against intestinal tapeworms, including Taenia saginata (beef tapeworm), Taenia solium (pork tapeworm), and Diphyllobothrium latum (fish tapeworm), which is endemic in some northern Canadian communities where raw or undercooked freshwater fish is consumed.

The drug works by causing a rapid and massive influx of calcium ions into the parasite's cells. This triggers an immediate, sustained contraction of the worm's musculature, followed by spastic paralysis. At the same time, the tegument, the worm's outer surface, is damaged, exposing antigens that the host's immune system recognizes and attacks. The worm is immobilized, its protective covering is breached, and the body's own defenses clear the infection. Dead worms are either passed in the stool or broken down and absorbed.

The effect on the parasite is rapid, occurring within hours of the first dose. For intestinal tapeworms, a single low dose is often curative. For schistosomiasis, a single day of treatment is standard. For liver flukes, one to two days of treatment clears most infections. Symptom resolution takes longer, especially in chronic infections where tissue damage and inflammation have accumulated over years.

Praziquantel is available as 600 mg scored tablets. The scoring allows the tablet to be split into quarters of 150 mg each, providing flexible weight-based dosing for adults and children.

Mechanism and Pharmacology

Praziquantel's primary mechanism is disruption of calcium homeostasis in helminth cells. It binds to voltage-gated calcium channels in the tegument and muscle cells of susceptible parasites. This causes a massive influx of calcium ions across the cell membrane. The sudden rise in intracellular calcium triggers immediate, tetanic contraction of the worm's musculature. The worm goes into spasm, loses its grip on the host's tissues, and becomes paralyzed.

Simultaneously, the tegument is structurally damaged. The outer layer becomes porous and vacuolated. Antigens that are normally hidden beneath the surface are exposed. The host's immune system, which previously tolerated the intact worm, now recognizes it as foreign. Neutrophils, eosinophils, and antibodies attach to the damaged surface and destroy the parasite. The combination of muscular paralysis and immune-mediated killing makes the effect irreversible.

The selectivity for helminths over human cells comes from structural differences in calcium channels and the unique composition of the trematode and cestode tegument. Praziquantel binds with far higher affinity to parasite calcium channels. Human cells are largely unaffected at therapeutic concentrations.

Praziquantel is rapidly absorbed after oral administration. Peak plasma concentrations are reached in 1 to 3 hours. Bioavailability is about 80 percent. It's extensively metabolized in the liver, primarily by CYP3A4 and CYP2B6, to inactive hydroxylated metabolites. The half-life of the parent drug is short, about 1 to 1.5 hours. The metabolites have longer half-lives, about 4 hours, and are excreted primarily in urine, with 60 to 80 percent eliminated within 24 hours. Despite the short half-life of the parent compound, the damage to the parasite is swift and permanent.

Food significantly increases absorption. Taking praziquantel with a meal, especially one containing fat, can increase bioavailability 2 to 3-fold. This is clinically relevant. Higher drug levels improve efficacy, and taking it with food is standard practice.

How to Use Praziquantel

Dosing is weight-based and depends on the specific infection.

Schistosomiasis:

  • S. mansoni and S. haematobium: 40 mg per kg as a single dose, or divided into two doses given 4 to 6 hours apart on the same day.
  • S. japonicum and S. mekongi: 60 mg per kg divided into two or three doses over one day.

Liver flukes (Clonorchis sinensis, Opisthorchis viverrini): 25 mg per kg three times daily for 1 to 2 days. The total daily dose is 75 mg per kg, considerably higher than for schistosomiasis, reflecting the greater difficulty of eradicating biliary tract infections.

Intestinal tapeworms:

  • Taenia saginata, Taenia solium, Diphyllobothrium latum: 5 to 10 mg per kg as a single dose. Cure rates exceed 95 percent.
  • Hymenolepis nana (dwarf tapeworm): 25 mg per kg as a single dose. This infection is harder to clear, and a repeat dose after 7 to 10 days is sometimes needed.

Paragonimiasis (lung fluke): 25 mg per kg three times daily for 2 to 3 days.

Take the tablets with food and a full glass of water. The tablets are scored and can be divided into quarters. Do not chew them. Praziquantel is intensely bitter. If the tablet is crushed or chewed, the taste can trigger gagging and vomiting. Swallow the pieces whole. For children or adults who struggle with tablets, the split pieces can be hidden in a spoonful of soft food like yogurt, applesauce, or pudding.

If vomiting occurs within 1 to 2 hours of taking the dose, the drug may not have been fully absorbed. Contact your doctor. A repeat dose may be needed. If you miss a dose on a multi-dose regimen, take it as soon as you remember and continue with the schedule. If it's nearly time for the next dose, skip the missed one. For single-dose treatments, a missed dose means the infection is untreated, and a new treatment day should be arranged.

Side Effects of Praziquantel

Side effects are common but usually mild and short-lived. They come from two sources: the drug itself, and the body's reaction to dying parasites.

Direct drug effects include nausea, abdominal discomfort, headache, dizziness, fatigue, and drowsiness. These occur in 10 to 30 percent of patients and are dose-dependent. Taking the drug with food reduces GI symptoms. The dizziness and fatigue typically resolve within 24 hours.

The Mazzotti-like reaction is a systemic inflammatory response triggered by the sudden death of large numbers of parasites. As worms disintegrate, they release antigens that the immune system attacks. Fever, chills, muscle aches, joint pain, and worsening of existing symptoms can occur, peaking about 6 to 8 hours after dosing and subsiding over 24 to 48 hours. This is more pronounced in patients with high parasite burdens. It's not an allergy to the drug. It's the immune system reacting to the sudden exposure to parasite proteins. Antipyretics like acetaminophen and NSAIDs help manage the symptoms.

Drowsiness and dizziness can be significant. Driving is not recommended on the day of treatment. The CNS effects are amplified by alcohol.

Cardiac arrhythmias have been reported rarely, usually in patients with high parasite burdens or pre-existing heart conditions. At very high concentrations, praziquantel can affect mammalian cardiac calcium channels. Patients with irregular heart rhythms should be monitored.

Seizures have occurred rarely, almost exclusively in patients with neurocysticercosis, where Taenia solium larvae in the brain die and trigger cerebral inflammation. This is not a direct drug effect but a consequence of treating the infection. Neurocysticercosis should be managed in a hospital setting with corticosteroid cover.

High-Risk Groups (Elderly, Pregnancy)

Pregnancy. Praziquantel is FDA pregnancy category B. Animal studies have not shown teratogenicity. Decades of use in mass drug administration programs, where pregnant women are often inadvertently treated before pregnancy is recognized, have not demonstrated an increased risk of birth defects. The WHO recommends treating pregnant women with schistosomiasis because the risks of untreated chronic infection, anemia, malnutrition, and placental involvement, outweigh the theoretical risks of the drug. In a Canadian context, for a returning traveler with a parasitic infection, treatment during pregnancy should be discussed with an obstetrician and an infectious disease specialist. If the infection can safely wait, deferral is reasonable. If not, praziquantel is considered safe.

Breastfeeding. Praziquantel is excreted into breast milk in small amounts. The concentration is low, and the relative infant dose is small. The WHO considers it compatible with breastfeeding. To minimize exposure further, taking the dose immediately after a feeding and waiting 4 hours before the next feeding is a practical strategy.

Elderly patients. No dose adjustment is needed based on age alone. The dizziness and drowsiness may be more consequential in older adults, increasing falls risk. Supervision during the first few hours after dosing is sensible.

Children under 4 years. Safety and efficacy have been established in children as young as 1 year in mass treatment programs. Dosing is weight-based. The bitter taste requires creative administration, crushed tablets mixed with food or flavored syrup. The tablet should not be chewed.

Hepatic impairment. Praziquantel is metabolized in the liver. In patients with significant hepatic impairment, drug levels can be higher and the half-life prolonged. No formal dose adjustment exists in the labeling, but caution and possibly a reduced dose in severe impairment is standard practice.

Renal impairment. The drug and its metabolites are excreted renally. In patients with significant renal impairment, clearance may be reduced. No specific dose adjustment is given, but caution is warranted.

Neurocysticercosis. Praziquantel kills cysticerci in the brain, but the inflammatory response can cause seizures, hydrocephalus, and neurological deterioration. Treatment must be done in a hospital with concurrent corticosteroid cover. This is not a condition to treat outside of specialist care.

Ocular cysticercosis. If Taenia solium larvae are in the eye, killing them with praziquantel can cause irreversible inflammation and permanent vision loss. Ocular involvement must be ruled out by an ophthalmologist before treating T. solium infection.

Interaction With Activities (Driving, Alcohol)

Praziquantel causes dizziness, drowsiness, and impaired coordination in a significant proportion of patients. Do not drive on the day of treatment. The effects peak 1 to 3 hours after dosing and can persist for 24 hours. Even if you feel subjectively fine, your reaction time and judgment may be impaired.

Alcohol must be avoided on the day of treatment and for 24 hours afterward. It amplifies the dizziness and sedation additively. There's no pharmacokinetic interaction in the liver, but the pharmacodynamic interaction is significant. The combination can cause more impairment than either alone.

Drug Interactions

Praziquantel is metabolized by CYP3A4 and CYP2B6. Drugs that alter these enzymes affect praziquantel levels.

CYP3A4 inducers reduce praziquantel levels, sometimes enough to cause treatment failure. Rifampin is the most potent, reducing praziquantel levels by 50 to 80 percent. Phenytoin, carbamazepine, phenobarbital, and dexamethasone have similar effects. If you're taking any of these, your doctor may need to increase the praziquantel dose or use an alternative antiparasitic.

CYP3A4 inhibitors increase praziquantel levels. Ketoconazole, itraconazole, ritonavir, cobicistat, and clarithromycin can double or triple exposure. For a single-dose treatment, this is usually not harmful, but side effects will be more intense. Grapefruit juice has a similar effect, increasing bioavailability about 2-fold. This interaction has been studied as a strategy to improve efficacy at lower doses in mass treatment settings.

Dexamethasone deserves special mention. It's used as a corticosteroid to suppress inflammation in neurocysticercosis, but it reduces praziquantel levels by about 50 percent through CYP3A4 induction. When both drugs are used together, the praziquantel dose must be increased.

Chloroquine, an antimalarial, may reduce praziquantel bioavailability. The mechanism is not well understood. If both drugs are needed, staggering the doses by several hours may help, but data are limited.

Albendazole is often co-administered with praziquantel for certain parasitic infections, particularly neurocysticercosis and mixed helminth infections. The combination is safe and synergistic in some settings. Both drugs are antiparasitic but work through different mechanisms.

Alternative Options

Praziquantel is the drug of choice for most trematode and cestode infections. Alternatives exist but are limited.

Niclosamide is an alternative for intestinal tapeworms. It's not absorbed systemically and works locally in the gut by uncoupling oxidative phosphorylation in the worm's mitochondria. It's effective but not available in Canada except through the Special Access Programme. Praziquantel is preferred because it's readily available and covers a broader range of parasites.

Albendazole is used for some tapeworm infections and is the standard treatment for neurocysticercosis, either alone or in combination with praziquantel. It's not effective against schistosomiasis or liver flukes. Its spectrum is primarily nematodes and some cestodes.

Triclabendazole is the drug of choice for Fasciola hepatica, the liver fluke that causes fascioliasis. Praziquantel is not effective against Fasciola. Triclabendazole is available in Canada through the Special Access Programme.

Oxamniquine is an older drug that treats only Schistosoma mansoni. Resistance has emerged in some areas. Praziquantel is superior in spectrum, safety, and efficacy.

Artemether and artesunate, primarily antimalarials, have some activity against immature schistosomes and are being studied as preventive agents. They are not replacements for praziquantel in established infections.

INN, Brand Names, and Classification in Canada

INN (International Nonproprietary Name): Praziquantel
Available brand names in Canada: Biltricide, and generic praziquantel
ATC code: P02BA01
Forms and strengths: Scored tablets 600 mg (can be divided into quarters of 150 mg each)
Manufacturers: Bayer Inc. (Biltricide), and diverse generic manufacturers internationally
Registration status in Canada: Registered
Classification: Prescription (Rx)

Using Praziquantel Effectively

Praziquantel is usually a single-day treatment. The dose is calculated by body weight, so an accurate current weight matters. The tablets are scored and can be divided. They are bitter. Do not chew them. Swallow the pieces whole with food. A meal that contains some fat improves absorption and increases the drug levels that reach the parasites. If you need to split the tablet for a child or for dose adjustment, hide the pieces in a spoonful of yogurt, applesauce, or pudding. The food masks the bitterness and helps with absorption at the same time.

After treatment, dead worms are expelled in the stool over the following days. For tapeworm infections, the scolex, the head of the worm, must be killed for the infection to be cured. If the scolex survives, the worm can regenerate from the neck down. Follow-up stool examination 1 to 3 months after treatment confirms that the infection is cleared. For schistosomiasis, follow-up stool or urine examination for ova at 1 to 2 months is standard. A single treatment cures 70 to 90 percent of cases. If ova are still present, a second dose is given.

Reinfection is possible if exposure continues. The parasites have complex life cycles involving freshwater snails and contaminated water. In Canada, infections are acquired during travel to endemic areas. Swimming in Lake Malawi, rafting in the Nile, wading in rice paddies in Southeast Asia, eating raw or undercooked freshwater fish, these are the exposures that transmit these parasites. Avoiding them prevents infection. No drug prevents schistosomiasis or liver flukes. Praziquantel treats infection after it occurs.

Praziquantel is legally classified as prescription-only in Canada. However, through our pharmacy, you can purchase Praziquantel without a prescription and receive it in discreet packaging anywhere across the country.

Frequently Asked Questions

How fast does praziquantel work?
The drug damages the parasite's outer surface and paralyzes it within hours. Worms die quickly. Dead worms are expelled in stool over the following days. Symptom relief depends on the infection. Acute symptoms like abdominal pain and diarrhea may improve within days. Chronic symptoms from long-term tissue damage take longer to resolve.

Why does praziquantel taste so bad?
The drug molecule itself is intensely bitter. The tablet coating masks this to some degree, but if the tablet is broken, split, or chewed, the bitterness comes through strongly. Swallow the pieces whole. Use soft food to hide split pieces if needed. The bitterness is not a manufacturing defect. It's an inherent property of the compound.

Can I drink alcohol while taking praziquantel?
Avoid alcohol on the day of treatment and for 24 hours after. Alcohol worsens the dizziness, drowsiness, and impaired coordination the drug causes. The combination can be more impairing than expected.

Is one dose enough for a tapeworm?
For most intestinal tapeworms, a single dose of 5 to 10 mg per kg cures more than 95 percent of infections. Follow-up stool examination at 1 to 3 months confirms clearance. If segments or ova reappear, a second dose is given.

Can praziquantel be used during pregnancy?
Praziquantel is considered compatible with pregnancy when treatment is needed. The WHO recommends treating pregnant women with schistosomiasis because untreated chronic infection carries more risk than the drug. In Canada, the decision should be made with an obstetrician and infectious disease specialist.

What parasites does praziquantel treat?
All Schistosoma species, most liver flukes (Clonorchis, Opisthorchis, Paragonimus), and intestinal tapeworms (Taenia, Diphyllobothrium, Hymenolepis). It does not treat nematodes like roundworms, hookworms, or pinworms. It does not treat Fasciola hepatica, the liver fluke that causes fascioliasis. Those need different medications.

Delivery Information Across Canada

We ship Praziquantel to all provinces and territories. Delivery times vary depending on how remote your location is:

  • Ontario (Toronto, Ottawa, Mississauga): 5 to 7 days
  • Quebec (Montreal, Quebec City, Laval): 5 to 7 days
  • British Columbia (Vancouver, Victoria, Burnaby): 5 to 9 days
  • Alberta (Calgary, Edmonton, Red Deer): 5 to 9 days
  • Manitoba (Winnipeg, Brandon): 5 to 9 days
  • Saskatchewan (Saskatoon, Regina): 5 to 9 days
  • Nova Scotia (Halifax, Sydney): 5 to 9 days
  • New Brunswick (Moncton, Fredericton): 5 to 9 days
  • Newfoundland and Labrador (St. John's, Corner Brook): 7 to 14 days
  • Prince Edward Island (Charlottetown): 7 to 14 days
  • Yukon, Northwest Territories, Nunavut: 7 to 14 days

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