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Início / Registado na Nigéria / R Cotrim - 960 Tablets

R Cotrim - 960 Tablets

NAFDAC Reg. No. 04-4409 · Drug

Registered with NAFDAC. Registration activeAs of 2 November 2026 · synced automatically from official sources.
Product
R Cotrim - 960 Tablets
Número NAFDAC
04-4409
Princípio ativo
Sulfamethoxazole; Trimethoprim
Dosagem
800 mg; 160 mg
Forma
Tablet
Tamanho da embalagem
10 x 10's (in blisters)
Manufacturer
Not listed
Applicant (holder)
Sagar Vitaceuticals Nigeria Ltd
Approved
23 Feb 2023
Situação
Active View on NAFDAC ↗
Registro válido até
22 Feb 2028
Alertas da OMS
None found
Community reports
None
Times checked
0

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

What we found

  • R Cotrim - 960 Tablets is on the NAFDAC register with an active registration (04-4409). 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 R Cotrim - 960 Tablets

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

To reduce the development of drug-resistant bacteria and maintain the effectiveness of sulfamethoxazole and trimethoprim tablets and other antibacterial drugs, sulfamethoxazole and trimethoprim tablets should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to empiric selection of therapy. …

Como tomar e com que frequência
  • Sulfamethoxazole and trimethoprim tablets are contraindicated
  • In pediatric patients less than 2 months of age
  • Urinary Tract Infections and Shigellosis
  • In Adults and Pediatric Patients, and Acute Otitis Media in Children
  • Adults: The usual adult dosage in the treatment of urinary tract infections is 1 sulfamethoxazole and trimethoprim DS (double strength) tablet or 2 sulfamethoxazole and trimethoprim tablets every 12 hours for 10 to 14 days
  • An identical daily dosage is used for 5 days in the treatment of shigellosis
  • Children: The recommended dose for children with urinary tract infections or acute otitis media is 40 mg/kg sulfamethoxazole and 8 mg/kg trimethoprim per 24 hours, given in two divided doses every 12 hours for 10 days
  • An identical daily dosage is used for 5 days in the treatment of shigellosis
  • The following table is a guideline for the attainment of this dosage: Children 2 months of age or older: Weight Dose – every 12 hours lb kg Tablets 22 10 - 44 20 1 66 30 1½ 88 40 2 or 1 DS tablet For Patients with Impaired Renal Function When renal function is impaired, a reduced dosage should be employed using the following table: Creatinine Clearance (mL/min) Recommended Dosage Regimen Above 30 Usual standard regimen 15 to 30 ½ the usual regimen Below 15 Use not recommended Acute Exacerbations of Chronic Bronchitis
  • In Adults The usual adult dosage in the treatment of acute exacerbations of chronic bronchitis is 1 sulfamethoxazole and trimethoprim double strength tablet, or 2 sulfamethoxazole and trimethoprim single strength tablets, every 12 hours for 14 days. …
Talk to a doctor first if
  • Sulfamethoxazole and trimethoprim is contraindicated in patients with a known hypersensitivity to trimethoprim or sulfonamides, in patients with a history of drug-induced immune thrombocytopenia with use of trimethoprim and/or sulfonamides, and in patients with documented megaloblastic anemia due to folate deficiency
  • Sulfamethoxazole and trimethoprim is contraindicated
  • In pediatric patients less than 2 months of age. …
Warnings

Embryofetal Toxicity Some epidemiologic studies suggest that exposure to sulfamethoxazole/trimethoprim during pregnancy may be associated with an increased risk of congenital malformations, particularly neural tube defects, cardiovascular malformations, urinary tract defects, oral clefts, and club foot. If sulfamethoxazole/trimethoprim is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be advised of the potential hazards to the fetus. …

Possíveis efeitos colaterais

The most common adverse effects are gastrointestinal disturbances (nausea, vomiting, anorexia) and allergic skin reactions (such as rash and urticaria). FATALITIES ASSOCIATED WITH THE ADMINISTRATION OF SULFONAMIDES, ALTHOUGH RARE, HAVE OCCURRED DUE TO SEVERE REACTIONS, INCLUDING STEVENS-JOHNSON SYNDROME, TOXIC EPIDERMAL NECROLYSIS, FULMINANT HEPATIC NECROSIS, AGRANULOCYTOSIS, APLASTIC ANEMIA AND OTHER BLOOD DYSCRASIAS (SEE WARNINGS SECTION). Hematologic : Agranulocytosis, aplastic anemia, thrombocytopenia, leukopenia, neutropenia, hemolytic anemia, megaloblastic anemia, hypoprothrombinemia, methemoglobinemia, eosinophilia. …

If you take too much

Acute: The amount of a single dose of sulfamethoxazole and trimethoprim that is either associated with symptoms of overdosage or is likely to be life-threatening has not been reported. Signs and symptoms of overdosage reported with sulfonamides include anorexia, colic, nausea, vomiting, dizziness, headache, drowsiness and unconsciousness. Pyrexia, hematuria and crystalluria may be noted. Blood dyscrasias and jaundice are potential late manifestations of overdosage. …

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 2022-10-09.

Label for sulfamethoxazole and trimethoprim, the active ingredient registered with NAFDAC.

Check your pack of R Cotrim - 960 Tablets

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

Ou tire fotos da caixa
Restam 3 verificações grátis hoje Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About R Cotrim - 960 Tablets

What is in R Cotrim - 960 Tablets?

R Cotrim - 960 Tablets contains Sulfamethoxazole; Trimethoprim (800 mg; 160 mg), as tablet, according to its NAFDAC registration record.

Is R Cotrim - 960 Tablets registered with NAFDAC?

Yes. R Cotrim - 960 Tablets is listed on the NAFDAC register under registration number 04-4409, and its registration is active as of 2 November 2026.

Has R Cotrim - 960 Tablets been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches R Cotrim - 960 Tablets in our automatically synced alert list.

How can I check that my pack of R Cotrim - 960 Tablets is genuine?

Run a free authenticity scan with the NAFDAC number 04-4409, 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 R Cotrim - 960 Tablets?

Follow your prescription or the leaflet in your pack. The official label says: Sulfamethoxazole and trimethoprim tablets are contraindicated in pediatric patients less than 2 months of age. Urinary Tract Infections and Shigellosis in Adults and Pediatric Patients, and Acute Otitis Media in Children Adults: The usual adult dosage in the treatment of urinary tract infections is 1 sulfamethoxazole and trimethoprim DS (double strength) tablet or 2 sulfamethox…

What is R Cotrim - 960 Tablets used for?

To reduce the development of drug-resistant bacteria and maintain the effectiveness of sulfamethoxazole and trimethoprim tablets and other antibacterial drugs, sulfamethoxazole and trimethoprim tablets should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should (Summarised from the official U.S. FDA label for sulfamethoxazole and trimethoprim. Always follow your doctor or pharmacist.)

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