Avlotrin DS
Generic Name
Co-trimoxazole (Sulfamethoxazole + Trimethoprim)
Manufacturer
Square Pharmaceuticals Ltd.
Country
Bangladesh
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Price Details
Current market pricing information
| Variant | Unit Price | Strip Price |
|---|---|---|
| avlotrin ds 800 mg tablet | ৳ 2.01 | ৳ 20.10 |
Description
Overview of the medicine
Avlotrin DS is a double strength antibacterial drug containing a combination of sulfamethoxazole and trimethoprim. It works by inhibiting two consecutive steps in the bacterial folic acid synthesis pathway, leading to synergistic antibacterial activity against a broad spectrum of bacteria.
Uses & Indications
Dosage
Adults
One Avlotrin DS tablet twice daily, typically for 10-14 days for UTIs, or as directed by physician.
Elderly
Similar to adult dose, but caution with renal impairment; dosage adjustment may be needed.
Renal_impairment
Dosage should be reduced in patients with impaired renal function (creatinine clearance <30 mL/min). Not recommended for severe renal impairment unless plasma levels can be monitored.
How to Take
Take orally with a full glass of water, with or without food. To minimize gastrointestinal upset, it can be taken with food. Ensure adequate fluid intake during treatment to prevent crystalluria.
Mechanism of Action
Sulfamethoxazole competitively inhibits the incorporation of para-aminobenzoic acid (PABA) into dihydrofolic acid, an essential precursor in the synthesis of folic acid. Trimethoprim reversibly inhibits dihydrofolate reductase, an enzyme that catalyzes the reduction of dihydrofolate to tetrahydrofolate. The combination blocks two successive steps in the biosynthesis of nucleic acids and proteins essential for many bacteria.
Pharmacokinetics
Onset
Antibacterial effects typically begin within 1-2 hours.
Excretion
Primarily excreted by the kidneys through glomerular filtration and tubular secretion. A small amount is excreted in feces.
Half life
Trimethoprim: 8-10 hours; Sulfamethoxazole: 10-12 hours.
Absorption
Well absorbed from the gastrointestinal tract following oral administration, with peak plasma concentrations reached within 1-4 hours for trimethoprim and 2-4 hours for sulfamethoxazole.
Metabolism
Both components are metabolized in the liver. Sulfamethoxazole undergoes N4-acetylation and glucuronidation. Trimethoprim undergoes oxidative metabolism.
Side Effects
Contraindications
- •Hypersensitivity to sulfamethoxazole, trimethoprim, or any excipients
- •Megaloblastic anemia due to folate deficiency
- •Severe renal impairment where plasma concentrations cannot be monitored
- •Severe hepatic impairment
- •Infants under 2 months of age
- •Pregnancy (especially near term)
Drug Interactions
Warfarin
May increase anticoagulant effect, requiring dose adjustment and INR monitoring.
Phenytoin
May increase phenytoin concentrations.
Cyclosporine
May decrease cyclosporine levels and increase risk of nephrotoxicity.
Methotrexate
Increased risk of methotrexate toxicity due to inhibition of renal excretion and displacement from plasma protein binding.
Pyrimethamine
Increased risk of megaloblastic anemia if pyrimethamine is used for malaria prophylaxis in doses exceeding 25 mg weekly.
Diuretics (especially thiazides)
Increased risk of thrombocytopenia in elderly patients.
Storage
Store in a cool, dry place, below 30°C. Protect from light and moisture. Keep out of reach of children.
Overdose
Symptoms of acute overdose include nausea, vomiting, dizziness, headache, and mental depression. Chronic overdose may lead to bone marrow depression (megaloblastic anemia, leukopenia, thrombocytopenia) due to folate deficiency. Treatment involves gastric lavage or emesis, forced diuresis, and acidification of the urine to increase trimethoprim excretion. Leucovorin may be administered to counteract folate deficiency.
Pregnancy & Lactation
Pregnancy Category D. Co-trimoxazole should be avoided during pregnancy, especially in the first trimester (due to potential for neural tube defects) and near term (due to risk of kernicterus in neonates). Excreted in breast milk; generally not recommended for breastfeeding mothers, especially if the infant is premature, jaundiced, or G6PD deficient.
Frequently Asked Questions
Common questions about this medicine
Pack Sizes
Shelf Life
Typically 3 years from the date of manufacture when stored correctly.
Availability
Available in pharmacies nationwide
Approval Status
Approved by DGDA
Patent Status
Generic available, original patent expired
WHO Essential Medicine
YesAlternative Medicines in Bangladesh
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Global Brand Names
International brand names for this medicine
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