Cefim-3
Generic Name
Cefixime Trihydrate
Manufacturer
Square Pharmaceuticals Ltd.
Country
Bangladesh
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Price Details
Current market pricing information
| Variant | Unit Price | Strip Price |
|---|---|---|
| cefim 3 200 mg tablet | ৳ 34.00 | ৳ 238.00 |
Description
Overview of the medicine
Cefim-3 200 mg Tablet contains Cefixime Trihydrate, an oral third-generation cephalosporin antibiotic. It is used to treat a wide range of bacterial infections effectively targeting various Gram-positive and Gram-negative bacteria.
Uses & Indications
Dosage
Adults
The usual adult dose is 200 mg every 12 hours or 400 mg once daily, as directed by a physician. Treatment duration typically ranges from 7-14 days depending on the type and severity of infection.
Elderly
No specific dosage adjustment is generally required for elderly patients with normal renal function. However, renal function should be assessed before initiating therapy.
Renal_impairment
For patients with creatinine clearance between 21-60 mL/min, the dose should be reduced to 300 mg daily. For creatinine clearance less than 20 mL/min, the dose should be reduced to 200 mg daily. Patients on chronic ambulatory peritoneal dialysis (CAPD) or hemodialysis should also receive 200 mg daily.
How to Take
Cefim-3 200 mg Tablet should be taken orally, with or without food, as prescribed by your doctor. It is crucial to complete the entire course of treatment, even if your symptoms improve, to ensure complete eradication of the infection and prevent antibiotic resistance.
Mechanism of Action
Cefixime works by inhibiting bacterial cell wall synthesis. It binds to penicillin-binding proteins (PBPs) located in the bacterial cell wall, which prevents the cross-linking of peptidoglycan chains, leading to cell lysis and subsequent bacterial death.
Pharmacokinetics
Onset
Peak plasma concentrations are typically achieved within 2-6 hours after oral administration.
Excretion
The main route of excretion is renal, with approximately 50% of an absorbed dose being excreted unchanged in the urine over 24 hours. Some non-renal elimination also occurs.
Half life
The plasma elimination half-life averages 3-4 hours, though it can be longer in patients with renal impairment.
Absorption
Approximately 40-50% of an oral dose is absorbed. Food may delay the time to peak concentration (Tmax) but does not significantly affect the extent of absorption (AUC).
Metabolism
Cefixime undergoes very limited hepatic metabolism; it is primarily excreted as the unchanged drug.
Side Effects
Contraindications
- •Known hypersensitivity to cefixime or any other cephalosporin antibiotics.
- •History of serious hypersensitivity reactions (e.g., anaphylaxis, severe skin reactions) to penicillin or other beta-lactam antibiotics.
Drug Interactions
Nifedipine
Concomitant administration may increase the bioavailability of cefixime, potentially leading to higher plasma concentrations.
Carbamazepine
Elevated carbamazepine levels have been reported when administered concomitantly with cefixime. Therapeutic drug monitoring and dosage adjustment of carbamazepine may be appropriate.
Warfarin and other anticoagulants
Concurrent use may increase prothrombin time (PT) and INR, with or without clinical bleeding. Close monitoring of coagulation parameters is advised, and anticoagulant dose adjustment may be necessary.
Storage
Store in a cool, dry place, ideally below 30°C. Protect from light and moisture. Keep all medicines out of the reach and sight of children.
Overdose
In case of a significant overdose, gastric lavage may be indicated to remove unabsorbed drug. Cefixime is not removed in significant quantities by hemodialysis or peritoneal dialysis. Treatment should be symptomatic and supportive, addressing any specific symptoms.
Pregnancy & Lactation
Pregnancy Category B. Animal reproduction studies have not demonstrated a risk to the fetus, but there are no adequate and well-controlled studies in pregnant women. Cefixime should be used during pregnancy only if clearly needed. Cefixime is excreted in small amounts in human milk; use with caution during lactation, and monitor the infant for gastrointestinal disturbances or candidiasis.
Frequently Asked Questions
Common questions about this medicine
Pack Sizes
Shelf Life
Typically 24 to 36 months from the manufacturing date, provided proper storage conditions are maintained.
Availability
Available in pharmacies nationwide
Approval Status
Approved by regulatory authorities worldwide, including DGDA Bangladesh, for the treatment of various bacterial infections.
Patent Status
Off-patent (generic available)
WHO Essential Medicine
YesAlternative Medicines in Bangladesh
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Global Brand Names
International brand names for this medicine
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