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Labcotrim Suspension_

NAFDAC Reg. No. 04-3108 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 30 October 2026 · synced automatically from official sources.
Producto
Labcotrim Suspension_
Número NAFDAC
04-3108
Principio activo
Sulfamethoxazole; Trimethoprim
Dosis
200 mg/5 mL; 40 mg/5 mL
Forma
Suspension
Tamaño del envase
1 x 50 mL (in amber PET bottle)
Fabricante
No Constan
Solicitante (titular)
Ugo Lab Productions (Nig). Ltd
Approved
29 Oct 2025
Estado
Activo Ver en NAFDAC ↗
Registro válido hasta
28 Oct 2030
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

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

Lo que encontramos

  • Labcotrim Suspension_ is on the NAFDAC register with an active registration (04-3108). 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 Labcotrim Suspension_

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

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. …

Cómo tomarlo y con qué frecuencia
  • 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. …

Posibles efectos secundarios

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. …

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 2022-10-09.

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

Check your pack of Labcotrim Suspension_

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 Labcotrim Suspension_

What is in Labcotrim Suspension_?

Labcotrim Suspension_ contains Sulfamethoxazole; Trimethoprim (200 mg/5 mL; 40 mg/5 mL), as suspension, according to its NAFDAC registration record.

Is Labcotrim Suspension_ registered with NAFDAC?

Yes. Labcotrim Suspension_ is listed on the NAFDAC register under registration number 04-3108, and its registration is active as of 30 October 2026.

Has Labcotrim Suspension_ been flagged as fake or recalled?

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

How can I check that my pack of Labcotrim Suspension_ is genuine?

Run a free authenticity scan with the NAFDAC number 04-3108, 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 Labcotrim Suspension_?

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 Labcotrim Suspension_ 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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Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.