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Avrotrim Tablet_

NAFDAC Reg. No. A4-4549 · Drug

Registered with NAFDAC. Registration activeAs of 1 November 2026 · synced automatically from official sources.
Product
Avrotrim Tablet_
رقم NAFDAC
A4-4549
المادة الفعالة
Sulfamethoxazole; Trimethoprim
التركيز
400 mg; 80 mg
الشكل
Tablet
حجم العبوة
10 x 10's, 10 x 100's (in PVC-Alu blisters)
Manufacturer
Not listed
Applicant (holder)
Avro Pharma Limited
Approved
29 Oct 2025
الحالة
Active View on NAFDAC ↗
التسجيل ساري حتى
28 Oct 2030
تنبيهات منظمة الصحة العالمية
None found
Community reports
None
Times checked
0

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

What we found

  • Avrotrim Tablet_ is on the NAFDAC register with an active registration (A4-4549). 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 Avrotrim Tablet_

ما تقوله النشرة الرسمية. إذا وصفه لك طبيب، فاتبع الوصفة. وإذا اختلفت نشرة عبوتك، فالأولوية لها.

لمن هو

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. …

كيف يُتناول وكم مرة
  • 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. …

الآثار الجانبية المحتملة

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. …

إذا نسيت جرعة

تناولها عندما تتذكر، إلا إذا اقترب موعد الجرعة التالية. عندها تخطَّ الجرعة المنسية. لا تتناول جرعتين معًا أبدًا للتعويض. راجع النشرة، فبعض الأدوية مختلفة.

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 Avrotrim Tablet_

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

أو التقط صورًا للعبوة
تبقّت 3 عمليات تحقق مجانية اليوم المصادر الرسمية: FDA الأمريكية · EMA (الاتحاد الأوروبي) · NAFDAC · تنبيهات منظمة الصحة العالمية

About Avrotrim Tablet_

What is in Avrotrim Tablet_?

Avrotrim Tablet_ contains Sulfamethoxazole; Trimethoprim (400 mg; 80 mg), as tablet, according to its NAFDAC registration record.

Is Avrotrim Tablet_ registered with NAFDAC?

Yes. Avrotrim Tablet_ is listed on the NAFDAC register under registration number A4-4549, and its registration is active as of 1 November 2026.

Has Avrotrim Tablet_ been flagged as fake or recalled?

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

How can I check that my pack of Avrotrim Tablet_ is genuine?

Run a free authenticity scan with the NAFDAC number A4-4549, 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 Avrotrim Tablet_?

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 Avrotrim Tablet_ 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.