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Homepage / Eingetragen in Nigeria / Pyridox Tablets

Pyridox Tablets

NAFDAC Reg.-Nr. A11-100736 Medikament

Registriert bei NAFDAC. Registrierung aktivAs of 5 November 2026 · synced automatically from official sources.
Produkt-
Pyridox Tablets
NAFDAC-Nummer
A11-100736
Wirkstoff
Sulfadoxine; Pyrimethamine
Stärke
500 mg; 25 mg
Form
Tablet
VPE:
1 x 3's (in Alu-PVC blister)
Hersteller
Nicht aufgeführt
Applicant (holder)
Shalina Healthcare Nigeria Limited
Approved
31 Jul 2024
Status
Active View on NAFDAC ↗
Registration valid to
30 Jul 2029
WER WARNT
None found
Community reports
None
Times checked
0

About the medicine: Sulfadoxine: uses, dosage and brands worldwide

What we found

  • Pyridox Tablets is on the NAFDAC register with an active registration (A11-100736). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

How to use Pyridox Tablets

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

Treatment of Toxoplasmosis : Pyrimethamine tablets are indicated for the treatment of toxoplasmosis when used conjointly with a sulfonamide, since synergism exists with this combination.

How to take it and how often
  • For Treatment of Toxoplasmosis : The dosage of pyrimethamine tablets
  • For the treatment of toxoplasmosis must be carefully adjusted so as to provide maximum therapeutic effect and a minimum of side effects
  • At the dosage required, there is a marked variation in the tolerance to the drug
  • Young patients may tolerate higher doses than older individuals
  • Concurrent administration of folinic acid is strongly recommended in all patients
  • The adult starting dose is 50 to 75 mg of the drug daily, together with 1 to 4 g daily of a sulfonamide of the sulfapyrimidine type, e.g. sulfadoxine
  • This dosage is ordinarily continued for 1 to 3 weeks, depending on the response of the patient and tolerance to therapy
  • The dosage may then be reduced to about one half that previously given for each drug and continued for an additional 4 to 5 weeks
  • The pediatric dosage of pyrimethamine tablets is 1 mg/kg/day divided into 2 equal daily doses; after 2 to 4 days this dose may be reduced to one half and continued for approximately 1 month
  • The usual pediatric sulfonamide dosage is used in conjunction with pyrimethamine tablets
Children

See DOSAGE AND ADMINISTRATION section.

Talk to a doctor first if
  • Use of pyrimethamine tablets are contraindicated in patients with known hypersensitivity to pyrimethamine or to any component of the formulation
  • Use of the drug is also contraindicated in patients with documented megaloblastic anemia due to folate deficiency
Medicines it may not mix with

Pyrimethamine may be used with sulfonamides, quinine and other antimalarials, and with other antibiotics. However, the concomitant use of other antifolic drugs or agents associated with myelosuppression including sulfonamides or trimethoprim-sulfamethoxazole combinations, proguanil, zidovudine, or cytostatic agents (e.g., methotrexate), while the patient is receiving pyrimethamine, may increase the risk of bone marrow suppression. If signs of folate deficiency develop, pyrimethamine should be discontinued. Folinic acid (leucovorin) should be administered until normal hematopoiesis is restored (see WARNINGS ). …

Warnings

The dosage of pyrimethamine required for the treatment of toxoplasmosis has a narrow therapeutic window . If signs of folate deficiency develop (see ADVERSE REACTIONS ), reduce the dosage or discontinue the drug according to the response of the patient. Folinic acid (leucovorin) should be administered in a dosage of 5 to 15 mg daily (orally, intravenous, or intramuscular) until normal hematopoiesis is restored. …

Possible side effects

Hypersensitivity reactions, occasionally severe (such as Stevens-Johnson syndrome, toxic epidermal necrolysis, erythema multiforme, and anaphylaxis), and hyperphenylalaninemia, can occur particularly when pyrimethamine is administered concomitantly with a sulfonamide. Consult the complete prescribing information for the relevant sulfonamide for sulfonamide-associated adverse events. With doses of pyrimethamine used for the treatment of toxoplasmosis, anorexia and vomiting may occur. Vomiting may be minimized by giving the medication with meals; it usually disappears promptly upon reduction of dosage. …

Pregnancy and breastfeeding

Pregnancy Teratogenic Effects : Pyrimethamine has been shown to be teratogenic in rats when given in oral doses 2.5 times the human dose for treatment of toxoplasmosis. At these doses in rats, there was a significant increase in abnormalities such as cleft palate, brachygnathia, oligodactyly, and microphthalmia. …

If you take too much

Following the ingestion of 300 mg or more of pyrimethamine, gastrointestinal and/or central nervous system signs may be present, including convulsions. The initial symptoms are usually gastrointestinal and may include abdominal pain, nausea, severe and repeated vomiting, possibly including hematemesis. Central nervous system toxicity may be manifest by initial excitability, generalized and prolonged convulsions which may be followed by respiratory depression, circulatory collapse, and death within a few hours. …

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2021-08-19.

Label for sulfadoxine and pyrimethamine, the active ingredient registered with NAFDAC.

Check your pack of Pyridox Tablets

Add the expiry date on your pack for a full Trust Score.

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Pyridox Tablets

What is in Pyridox Tablets?

Pyridox Tablets contains Sulfadoxine; Pyrimethamine (500 mg; 25 mg), as tablet, according to its NAFDAC registration record.

Is Pyridox Tablets registered with NAFDAC?

Yes. Pyridox Tablets is listed on the NAFDAC register under registration number A11-100736, and its registration is active as of 5 November 2026.

Has Pyridox Tablets been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Pyridox Tablets in our automatically synced alert list.

How can I check that my pack of Pyridox Tablets is genuine?

Run a free authenticity scan with the NAFDAC number A11-100736, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

How do I take Pyridox Tablets?

Follow your prescription or the leaflet in your pack. The official label says: For Treatment of Toxoplasmosis : The dosage of pyrimethamine tablets for the treatment of toxoplasmosis must be carefully adjusted so as to provide maximum therapeutic effect and a minimum of side effects. At the dosage required, there is a marked variation in the tolerance to the drug. Young patients may tolerate higher doses than older individuals. Concurrent administration o…

What is Pyridox Tablets used for?

Treatment of Toxoplasmosis : Pyrimethamine tablets are indicated for the treatment of toxoplasmosis when used conjointly with a sulfonamide, since synergism exists with this combination. (Summarised from the official U.S. FDA label for sulfadoxine and pyrimethamine. Always follow your doctor or pharmacist.)

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