Pyrimethamine (Daraprim) is a folate inhibitor and primarily used as an antiparasitic drug. It is used to treat patients with toxoplasmosis and other parasitic infections.
Pyrimethamine Uses:
- Toxoplasmosis:
- It is indicated in the treatment of toxoplasmosis (in combination with a sulfonamide).
- Off Label Use of Pyrimethamine in Adults:
- It is used in HIV infected persons in the following conditions
- Isospora belli infection (isosporiasis) in HIV-infected patients
- Pneumocystis pneumonia (PCP) in HIV infected patients
- Toxoplasma gondii encephalitis (For treatment/primary prophylaxis/chronic maintenance therapy) in HIV-infected patients
Pyrimethamine (Daraprim) Dose in Adults
Pyrimethamine (Daraprim) Dose in the treatment of Isosporiasis ( Isospora belli infection) in HIV-infected patients (alternative agent) (off-label): Oral:
- Treatment:
- 50 - 75 mg once a day with leucovorin calcium
- Chronic maintenance (secondary prophylaxis):
- 25 mg once a day with leucovorin calcium
Pyrimethamine (Daraprim) Dose in the treatment of Pneumocystis pneumonia (PCP) in HIV-infected patients (alternative agent): Oral:
- Primary prophylaxis:
- 50 - 75 mg once a week with dapsone and leucovorin calcium or
- 25 mg once a day with atovaquone and leucovorin calcium
- Chronic maintenance (secondary prophylaxis):
- 50 - 75 mg once a week with dapsone and leucovorin calcium or
- 25 mg once a day combined atovaquone and leucovorin calcium
Pyrimethamine (Daraprim) Dose in the treatment of Toxoplasmosis:
- Oral: 50 - 75 mg per day for 1 - 3 weeks then the dose can be reduced by 50% and continue for 4 - 5 weeks
- In combination with sulfonamide and leucovorin calcium.
Pyrimethamine (Daraprim) Dose in the treatment of Toxoplasmosis in HIV-infected patients (off-label): Oral:
- Primary prophylaxis (alternative agent):
- 50 or 75 mg once a week with dapsone and leucovorin calcium or
- 25 mg once a day with atovaquone and leucovorin calcium
- Chronic maintenance therapy (secondary prophylaxis):
- 25 - 50 mg once a day with sulfadiazine and leucovorin calcium or
- 25 - 50 mg once a day with clindamycin and leucovorin calcium or
- 25 mg once a day with atovaquone and leucovorin calcium (alternative regimen)
Pyrimethamine (Daraprim) Dose in the treatment of Toxoplasma gondii encephalitis:
- 200 mg as a single dose, followed by Weight based dose of 50 mg (<60 kg) or 75 mg (≥60 kg) daily, with sulfadiazine and leucovorin calcium for at least 6 weeks or
- 200 mg as a single dose, followed by a weight-based dose of 50 mg (<60 kg) or 75 mg (≥60 kg) daily, with leucovorin calcium plus clindamycin or atovaquone or azithromycin (alternative regimens).
Note:
- No longer available in retail pharmacies in the US and is only available through a special pharmacy program.
- According to the HHS Guidelines for the prevention and treatment of opportunistic infections in the HIV-infected adults, if pyrimethamine is not available readily and there is a delay in procuring for suspected or documented toxoplasmosis who have no history of sulfa allergy, trimethoprim-sulfamethoxazole should be used in place of pyrimethamine-containing regimens until pyrimethamine is available.
Pyrimethamine (Daraprim) Dose in Childrens
Pyrimethamine (Daraprim) Dose in the treatment of Isosporiasis (Isospora belli), HIV-exposed/-positive:
- Treatment:
- Infants and Children: Oral: 1 mg/kg once a day with leucovorin for 14 days; (maximum daily dose: 75 mg/day)
- Adolescents: Oral: 50 - 75 mg once a day with leucovorin
- Chronic maintenance:
- Infants and Children: Oral: 1 mg/kg once a day with leucovorin (maximum daily dose: 25 mg/day)
- Adolescents: Oral: 25 mg once a day with leucovorin
Pyrimethamine (Daraprim) Dose in the treatment of Toxoplasmosis:
- Treatment:
- Congenital toxoplasmosis (independent of HIV status): Oral:
- Infants:
- Initial: 2 mg/kg/dose once a day for 2 days followed by
- 1 mg/kg/day once a day with sulfadiazine for 2 - 6 months then
- 1 mg/kg/day 3 times/week (eg, MWF) with sulfadiazine
- To reduce chances of hematological toxicity oral leucovorin should be given throughout the course (total treatment duration: 12 months)
- Infants:
- Acquired infection:
- HIV-exposed/-positive:
- Infants and Children: Oral
- 2 mg/kg (maximum dose: 50 mg/dose) once a day for 3 days followed by 1 mg/kg (maximum dose: 25 mg) once a day
- combined with sulfadiazine or clindamycin and leucovorin
- continue for at least 6 weeks; if clinically or radiologically extensive disease or response is not adequate, longer duration should be given
- Adolescents: Oral
- Encephalitis: 200 mg once as a single dose followed by daily doses as follows
- Daily weight-based doses: For weight <60 kg: 50 mg or for weight ≥60 kg: 75 mg once a day
- Typically used in combination with sulfadiazine and leucovorin; other combination regimens include clindamycin, atovaquone, or azithromycin and leucovorin
- Continue for at least 6 weeks; If clinically or radiologically extensive disease or response is not adequate, longer duration should be given
- Infants and Children: Oral
- Non-HIV-exposed/-positive:
- HIV-exposed/-positive:
- Congenital toxoplasmosis (independent of HIV status): Oral:
Note: Use in combination with sulfadiazine or clindamycin and leucovorin. Leucovorin should be used to prevent hematologic toxicity. Continue until 1 - 2 weeks after the symptoms resolved.
- Children: Oral: 2 mg/kg (maximum dose: 50 mg/dose) once a day for 2 days , followed by 1 mg/kg/day (maximum dose: 25 mg/dose) once a day for 3 - 6 weeks
- Adolescents: Oral: 200 mg once as a single dose; then 50 - 75 mg once a day for 3 - 6 weeks
- Prophylaxis:
- The first episode of Toxoplasma gondii:
- HIV-exposed/-positive:
- Infants and Children: Oral:
- 1 mg/kg/day once a day with dapsone plus oral leucovorin (Maximum dose: 25mg/dose)
- Infants and Children 4 - 24 months: 1 mg/kg or 15 mg/m once a day with atovaquone plus oral leucovorin (Maximum dose: 25 mg/dose)
- Adolescents: Oral:
- 50 mg or 75 mg once a week with leucovorin and dapsone
- 25 mg once a day with leucovorin and atovaquone
- Infants and Children: Oral:
- HIV-exposed/-positive:
- Hematopoietic cell transplantation recipients:
- Infants and Children:
- Oral: 1 mg/kg/day of pyrimethamine once a day with clindamycin and leucovorin
- Start after engraftment and continue as long as the patient is on immunosuppressive therapy.
- Adolescents:
- Oral: 25 - 75 mg once a day with clindamycin and leucovorin
- Start after engraftment and continue as long as the patient is on immunosuppressive therapy.
- Infants and Children:
- Recurrence of Toxoplasma gondii (secondary prophylaxis; suppressive therapy):
- HIV exposed/-positive:
- Infants and Children:
- Oral: 1 mg/kg or 15 mg/m² once a day with oral leucovorin and sulfadiazine, clindamycin, or atovaquone
- Maximum dose: 25 mg
- Adolescents: Oral:
- 25 - 50 mg once a day with leucovorin, sulfadiazine, or clindamycin
- 25 mg once a day with leucovorin and atovaquone
- Infants and Children:
- HIV exposed/-positive:
- The first episode of Toxoplasma gondii:
Pyrimethamine (Daraprim) Dose in the treatment of Malaria:
Note: There is a prevalence of Pyrimethamine resistance worldwide. And CDC does not recommend malaria prophylaxis or treatment. However, the World Health Organization (WHO) guidelines still include pyrimethamine in prophylaxis and treatment of malaria.
- Chemoprophylaxis: Begin prophylaxis before entering the endemic area:
- Infants and Children <4 years: Oral: 6.25 mg once a week
- Children 4 to 10 years: Oral: 12.5 mg once a week
- Children >10 years and Adolescents: Oral: 25 mg once a week
- Treatment (non-falciparum malaria; use in conjunction with a sulfonamide [eg, sulfadoxine]):
- Children 4 to 10 years: Oral: 25 mg a day for 2 days
- Administer once a week chemoprophylaxis regimen (after clinical cure) for ≥10 weeks
- Children >10 years and Adolescents:
- Oral: 25 mg a day for 2 days
- Administer once a week chemoprophylaxis regimen (following clinical cure) for ≥10 weeks
- Note: Do not use Pyrimethamine monotherapy; If it needs to be given as monotherapy, give 50 mg a day for 2 days; then (following clinical cure) give once a week chemoprophylaxis regimen for ≥10 weeks.
- Children 4 to 10 years: Oral: 25 mg a day for 2 days
Pyrimethamine (Daraprim) Dose in the Pneumocystis jirovecii pneumonia (PCP) (HIV-exposed/-positive);
Primary prophylaxis or chronic maintenance (secondary prophylaxis):
- Adolescents: Oral:
- 50 - 75 mg once a week with dapsone and leucovorin
- 25 mg once a day with atovaquone and leucovorin
Pregnancy Risk Factor C
- Studies on animal reproduction have shown adverse effects.
- Folate supplementation is highly recommended if pyrimethamine is required to be administered during pregnancy.
- Avoid pregnancy while on therapy.
Use of pyrimetamine while breastfeeding
- Breast milk contains pyrimethamine, which can cause significant (or even greater) levels of pyrimethamine to be secreted by infants who are breastfed.
- It is worth considering the combination of sulfonamide (or dapsone) and pyrimethamine (a combination that is often used).
Dose in Kidney disease:
No dose adjustments listed in the manufacturer’s labeling. Use with caution.
Dose in Liver disease:
No dose adjustments listed in the manufacturer’s labeling. Use with caution.
Pyrimethamine (Daraprim) Side effects:
- Cardiovascular:
- Cardiac Arrhythmia (Large Doses)
- Dermatologic:
- Erythema Multiforme
- Skin Rash
- Stevens-Johnson Syndrome
- Toxic Epidermal Necrolysis
- Gastrointestinal:
- Anorexia
- Glossitis (Atrophic)
- Vomiting
- Hematologic & Oncologic:
- Leukopenia
- Megaloblastic Anemia
- Pancytopenia
- Thrombocytopenia
- Genitourinary:
- Hematuria
- Hypersensitivity:
- Anaphylaxis
- Respiratory:
- Eosinophilic Pneumonitis
Contraindications to Pyrimethamine (Daraprim):
- Hypersensitivity
- Megaloblastic anemia due to folate deficiency
Warnings and precautions
- Hematologic:
- Pancytopenia, anemia (megaloblastic), thrombocytopenia and leukopenia have all been reported. Usually, these were with high doses.
- Patients receiving high-dose therapy should be monitored twice weekly by the CBC
- Folate deficiency:
- Use caution if the patient has a folate deficiency such as malabsorption syndrome, pregnancy or alcoholism.
- G6PD deficiency:
- Patients with G6PD deficiency should be cautious when using this product.
- Hepatic impairment
- It is best to avoid it if you have a hepatic impairment.
- Renal impairment
- It is best to avoid it if you have renal impairment.
- Seizure disorders:
- Patients with seizure disorders history should be cautious.
Pyrimethamine: Drug Interaction
Note: Drug Interaction Categories:
- Risk Factor C: Monitor When Using Combination
- Risk Factor D: Consider Treatment Modification
- Risk Factor X: Avoid Concomitant Use
Risk Factor C (Monitor therapy) |
|
Antipsychotic Agents (Phenothiazines) |
Antipsychotic Agents' serum concentration may rise in response to antimalarial drugs (Phenothiazines). |
Could make pyrimethamine's hepatotoxic effects worse. |
|
Pyrimethamine may intensify Methotrexate's harmful or hazardous effects. |
|
May reduce Pyrimethamine's therapeutic impact. |
|
Pyrimethamine may intensify PEMEtrexed's harmful or hazardous effects. |
|
Pyrimethamine may intensify PRALAtrexate's negative/toxic effects. |
|
Proguanil |
Pyrimethamine may intensify Proguanil's negative or hazardous effects. |
Pyrimethamine may intensify Raltitrexed's harmful or hazardous effects. |
|
Sulfonamide Antibiotics |
The negative/toxic effects of sulfonamide antibiotics may be exacerbated by pyrimethamine. |
Pyrimethamine may intensify Trimethoprim's harmful or hazardous effects. |
|
Risk Factor D (Consider therapy modification) |
|
Dapsone (Systemic) |
Antimalarial drugs could intensify the harmful or hazardous effects of dapsone (Systemic). In particular, the use of antimalarial medications concurrently with dapsone may raise the risk of hemolytic responses. Dapsone (Systemic) may make antimalarial agents more harmful or poisonous. More specifically, using dapsone at the same time as an antimalarial drug may make hemolytic responses more likely. Treatment: Carefully observe patients for any indications or symptoms of hemolytic responses while administering dapsone and antimalarial medications, especially in those who have haemoglobin M, glucose-6-phosphate dehydrogenase (G6PD), or methemoglobin reductase deficiencies. |
Dapsone (Topical) |
Antimalarial drugs could intensify the harmful or hazardous effects of dapsone (Topical). Particularly, there may be a higher risk of hemolytic responses. Treatment: Apply topical dapsone and antimalarial medications while closely monitoring for hemolytic reactions' signs and symptoms. Patients who lack glucose-6-phosphate dehydrogenase may be especially vulnerable to negative hematologic consequences. |
Folic Acid |
May reduce Pyrimethamine's therapeutic impact. Management: Because there is a chance that sulfadoxine/pyrimethamine treatment will fail, folic acid doses larger than 2.5 mg per day should be avoided. For women of childbearing age, it may be wise to limit their folic acid intake to no more than 0.4 mg per day. |
Risk Factor X (Avoid combination) |
|
Artemether |
Could intensify the negative or hazardous effects of antimalarial drugs. Management: Unless there are no other treatment options available, artemether/lumefantrine (combination product) should not be used with other antimalarials. |
Lumefantrine |
Antimalarial drugs may intensify Lumefantrine's harmful or toxic effects. Management: Unless there are no other treatment options available, artemether/lumefantrine (combination product) should not be used with other antimalarials. |
Monitoring parameters:
- CBC, twice weekly with high-dose therapy
- Hepatic function
- Renal function
How to administer Pyrimethamine (Daraprim)?
Oral: Administer with meals (to minimize gastrointestinal discomfort)
Mechanism of action of Pyrimethamine (Daraprim):
- Pyrimethamine inhibits dihydrofolate reductase enzyme in parasites, resulting in inhibition of vital tetrahydrofolic acid synthesis.
- It inhibits the dihydrofolate reductase enzyme found in parasites.
- This results in inhibition of vital Tetrahydrofolic Acid synthesis.
Absorption:
- Well absorbed
Distribution:
- Distribution to organs like the kidneys, liver, lung, and spleen
Protein binding:
- 87%
Half-life elimination
- 80-95 hours
Time to reach peak
- Serum: 2-6 hours
Excretion:
- Urine (16%-32%)
International Brand Names of Pyrimethamine (Daraprim):
- Daraprim
- Daraprin
- Malocide
- Malomin
- Meta
- Primet
- Pyrison
- Tindurin
- Toxopirin
Pyrimethamine Brand Names in Pakistan:
Pyrimethamine Drops 10 mg/ml in Pakistan |
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Metakelfin |
Pfizer Laboratories Ltd. |
Pyrimethamine Tablets 25 mg in Pakistan |
|
Metakelfin |
Pfizer Laboratories Ltd. |