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Gomaxine Tablet

NAFDAC Reg. No. 04-4361 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 2 November 2026 · synced automatically from official sources.
Producto
Gomaxine Tablet
Número NAFDAC
04-4361
Principio activo
Sulfadoxine; Pyrimethamine
Dosis
500 mg; 25 mg
Forma
Tablet
Fabricante
No Constan
Solicitante (titular)
Richygold International Limited
Approved
3 Aug 2021
Estado
Inactive Ver en NAFDAC ↗
Registro válido hasta
2 Aug 2026
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

Pero sobre el medicamento, Sulfadoxine: uses, dosage and brands worldwide

Lo que encontramos

  • Gomaxine Tablet is on the NAFDAC register with an active registration (04-4361). 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.

Generado automáticamente a partir del registro NAFDAC, QUIÉN alerta y los datos de la comunidad a partir de hoy. Este no es un consejo médico. Siga siempre a su médico o farmacéutico.

How to use Gomaxine Tablet

Lo que dice el prospecto oficial. Si te lo recetó un médico, sigue la receta. Si el prospecto de tu caja es distinto, manda el de tu caja.

Para quién es

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

Cómo tomarlo y con qué frecuencia
  • 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
Infancia

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. …

Posibles efectos secundarios

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. …

Si olvidas una dosis

Tómala en cuanto te acuerdes, salvo que falte poco para la siguiente. En ese caso, sáltate la olvidada. Nunca tomes dos dosis a la vez para compensar. Revisa tu prospecto, porque algunos medicamentos son distintos.

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 Gomaxine Tablet

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

O haz fotos de la caja
Te quedan 3 verificaciones gratis hoy Fuentes oficiales: FDA de EE. UU. · EMA (UE) · NAFDAC · alertas de la OMS

About Gomaxine Tablet

What is in Gomaxine Tablet?

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

Is Gomaxine Tablet registered with NAFDAC?

Yes. Gomaxine Tablet is listed on the NAFDAC register under registration number 04-4361, and its registration is active as of 2 November 2026.

Has Gomaxine Tablet been flagged as fake or recalled?

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

How can I check that my pack of Gomaxine Tablet is genuine?

Run a free authenticity scan with the NAFDAC number 04-4361, 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 Gomaxine Tablet?

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 Gomaxine Tablet 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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