Saltrim
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 |
---|---|---|
saltrim 200 mg suspension | ৳ 21.08 | N/A |
Description
Overview of the medicine
Saltrim-200 mg suspension is an antibiotic medication combining Sulfamethoxazole and Trimethoprim, used to treat various bacterial infections.
Uses & Indications
Dosage
Adults
For specific indications (e.g., PCP treatment), dosage is determined by physician; often higher strength tablets are preferred for adults.
Elderly
Dosage adjustment needed due to potential renal impairment and increased risk of adverse effects. Physician consultation required.
Renal_impairment
Dosage must be reduced and/or frequency altered based on creatinine clearance. Contraindicated in severe renal impairment.
How to Take
Administer orally with or without food. For best absorption and to minimize gastrointestinal upset, it can be taken with food. Ensure sufficient fluid intake to prevent crystalluria.
Mechanism of Action
Co-trimoxazole inhibits bacterial folic acid synthesis. Sulfamethoxazole competitively inhibits dihydropteroate synthase, an enzyme involved in converting para-aminobenzoic acid (PABA) to dihydrofolic acid. Trimethoprim inhibits bacterial dihydrofolate reductase, which converts dihydrofolic acid to tetrahydrofolic acid. This dual blockade provides synergistic antibacterial activity.
Pharmacokinetics
Onset
Antibacterial effects generally noticeable within a few hours of the first dose.
Excretion
Mainly renal excretion of both unchanged drug and metabolites.
Half life
Sulfamethoxazole: 9-11 hours; Trimethoprim: 8-10 hours.
Absorption
Well absorbed orally, peak plasma concentrations typically achieved within 1-4 hours.
Metabolism
Primarily hepatic metabolism (acetylation and glucuronidation) for sulfamethoxazole, and oxidation for trimethoprim.
Side Effects
Contraindications
- Hypersensitivity to sulfamethoxazole or trimethoprim or any component of the formulation
- Severe renal impairment where plasma concentrations cannot be monitored
- Severe hepatic impairment
- Megaloblastic anemia due to folate deficiency
- Porphyria
- Infants under 2 months of age
Drug Interactions
Digoxin
May increase digoxin levels in some patients.
Warfarin
May potentiate the anticoagulant effect of warfarin, requiring close monitoring of INR and dose adjustment.
Phenytoin
May increase phenytoin concentrations.
Methotrexate
May increase methotrexate levels, leading to increased risk of myelosuppression, especially in elderly patients or those with renal impairment.
Diuretics (Thiazide)
Increased risk of thrombocytopenia with purpura in elderly patients.
Storage
Store below 30°C, protected from light and moisture. Do not freeze. Keep out of reach of children. After reconstitution, store as directed on the label (e.g., refrigerated).
Overdose
Symptoms may include nausea, vomiting, diarrhea, anorexia, headache, dizziness, and mental depression. Acute massive overdose can lead to bone marrow depression and megaloblastic anemia. Treatment is supportive, including gastric lavage, forced diuresis, and administration of leucovorin for folate deficiency.
Pregnancy & Lactation
Pregnancy Category D (risk in late pregnancy due to displacement of bilirubin and risk of kernicterus in neonates). Should be avoided in the first trimester if possible, and definitely in the last few weeks of pregnancy. Excreted in breast milk; use with caution or avoid in breastfeeding mothers, especially if infant is jaundiced or G6PD deficient.
Frequently Asked Questions
Common questions about this medicine
Pack Sizes
Shelf Life
Typically 2-3 years for unopened bottles. Once reconstituted/opened, refer to package insert for specific expiry, often 7-14 days.
Availability
Pharmacies, hospitals
Approval Status
Approved by major regulatory bodies (e.g., FDA, DGDA)
Patent Status
Generic available, original patent expired
WHO Essential Medicine
YesClinical Trials
Extensively studied and widely used for decades; ongoing research focuses on resistance patterns and new applications.
Lab Monitoring
- Complete Blood Count (CBC) with differential, especially for long-term therapy or high doses
- Renal function tests (BUN, creatinine)
- Liver function tests (ALT, AST)
- Serum potassium (due to trimethoprim's effect)
Doctor Notes
- Consider G6PD deficiency screening before prescribing, especially in at-risk populations.
- Monitor CBC, renal, and liver function during prolonged therapy.
- Advise patients on adequate hydration to prevent crystalluria.
Patient Guidelines
- Complete the full course of medication even if symptoms improve.
- Drink plenty of fluids to prevent kidney stone formation.
- Avoid excessive sun exposure and use sunscreen.
- Report any severe rash, sore throat, fever, or unusual bleeding/bruising immediately to your doctor.
Missed Dose Advice
If a dose is missed, take it as soon as remembered. If it is almost time for the next dose, skip the missed dose and resume the regular dosing schedule. Do not double the dose.
Driving Precautions
May cause dizziness or fatigue in some individuals. Exercise caution when driving or operating machinery until you know how the medicine affects you.
Lifestyle Advice
- Maintain good hygiene to prevent recurrence of infections, especially UTIs.
- Ensure adequate rest during treatment.
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Global Brand Names
International brand names for this medicine. Click a brand to search for detailed information.