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Início / Registado na Nigéria / Kaosider Tablet## $

Kaosider Tablet## $

NAFDAC Reg. No. A4-6014 · Drug

Registered with NAFDAC. Registration activeAs of 30 October 2026 · synced automatically from official sources.
Product
Kaosider Tablet## $
Número NAFDAC
A4-6014
Princípio ativo
Sulfadoxine; Pyrimethamine
Dosagem
500 mg; 25 mg
Forma
Tablet
Tamanho da embalagem
1 x 3's
Manufacturer
Not listed
Applicant (holder)
Pauco Pharmaceutical Industry Nigeria Limited
Approved
27 Aug 2025
Situação
Active View on NAFDAC ↗
Registro válido até
26 Aug 2030
Alertas da OMS
None found
Community reports
None
Times checked
0

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

What we found

  • Kaosider Tablet## $ is on the NAFDAC register with an active registration (A4-6014). 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 Kaosider Tablet## $

O que diz a bula oficial. Se um médico receitou, siga a receita. Se a bula da sua caixa for diferente, vale a da sua caixa.

Para quem é

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

Como tomar e com que frequência
  • 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. …

Possíveis efeitos colaterais

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. …

Se esquecer uma dose

Tome assim que lembrar, a menos que esteja quase na hora da próxima dose. Nesse caso, pule a dose esquecida. Nunca tome duas doses de uma vez para compensar. Confira a bula, pois alguns medicamentos são diferentes.

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 Kaosider Tablet## $

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

Ou tire fotos da caixa
Restam 3 verificações grátis hoje Fontes oficiais: FDA dos EUA · EMA (UE) · NAFDAC · alertas da OMS

About Kaosider Tablet## $

What is in Kaosider Tablet## $?

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

Is Kaosider Tablet## $ registered with NAFDAC?

Yes. Kaosider Tablet## $ is listed on the NAFDAC register under registration number A4-6014, and its registration is active as of 30 October 2026.

Has Kaosider Tablet## $ been flagged as fake or recalled?

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

How can I check that my pack of Kaosider Tablet## $ is genuine?

Run a free authenticity scan with the NAFDAC number A4-6014, 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 Kaosider 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 Kaosider 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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