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Other brands with the same active ingredient

These brands contain the same active ingredient (Cefditoren). Same strength and form. Confirm the switch with your doctor or pharmacist.

Available as: 400 mg

Indications & Uses

Pharmacology

Cefditoren is delivered as Cefditoren Pivoxil, a broad-spectrum third-generation cephalosporin antibiotic. It is a prodrug, hydrolyzed by esterases during absorption, so the active form, Cefditoren, is what circulates in the blood. Cefditoren acts against both gram-positive and gram-negative organisms. Its bactericidal effect comes from blocking cell wall synthesis, achieved by binding to penicillin-binding proteins (PBPs). Cefditoren also holds up well against several ß-lactamases, including penicillinases and certain cephalosporinases.

Dosage Reference

Reference Information Only

Dosages shown are general references from official sources. Always consult your doctor or pharmacist for personalized dosing.

Adults:

Cefditoren should be taken after meals. For Community-Acquired Pneumonia, the recommended dose is 400 mg twice daily for 14 days. For Acute Exacerbation of Chronic Bronchitis, it is 400 mg twice daily for 10 days. For Pharyngotonsillitis and Acute Sinusitis, the dose is 200 mg twice daily for 10 days. For Uncomplicated Skin and Soft Structure Infections, it is also 200 mg twice daily for 10 days.

Side Effects

Cefdiren commonly causes diarrhea, nausea, headache, abdominal pain, vaginal moniliasis, dyspepsia, vomiting, abnormal dreams, allergic reaction, anorexia, constipation, dizziness, dry mouth and fever.

Cautions & Contraindications

Warnings & Precautions

Cefdiren is not recommended for prolonged antibiotic treatment, since other pivalate-containing compounds have caused clinical signs of carnitine deficiency when used over a period of months. Prescribing Cefdiren without a proven or strongly suspected bacterial infection, or without a prophylactic indication, is unlikely to benefit the patient and raises the risk of developing drug-resistant bacteria.

Contraindications

Cefditoren should not be used in patients who are allergic to cephalosporin antibiotics or to any of its ingredients. It also contains sodium caseinate, a milk protein, so patients with a genuine milk protein allergy (as opposed to lactose intolerance) should avoid taking Cefditoren.

Pregnancy & Breastfeeding

Pregnancy category B. No adequate, well controlled studies have been conducted in pregnant women, so Cefditoren should be used during pregnancy only if clearly needed. Animal studies show that Cefditoren passes into breast milk, so caution should be exercised when giving it to nursing mothers.

⚠️ Talk to your doctor before taking any medicine during pregnancy or while breastfeeding.

Use in Special Populations

Children: Use of Cefditoren is not recommended for pediatric patients less than 12 years of age. The safety and efficacy of Cefditoren tablets in this population, including any effects of altered carnitine concentration, have not been established.

Geriatric: No dose adjustments are necessary in geriatric patients with normal (for their age) renal function. Patients with renal insufficiency: No dose adjustment is necessary for patients with mild renal impairment (ClCr: 50-80 mL/min/1.73 m2). It is recommended that not more than 200 mg BID be administered to patients with moderate renal impairment (ClCr: 30-49 mL/min/1.73 m2) and 200 mg QD be administered to patients with severe renal impairment (ClCr: <30 mL/min/1.73 m2 ). The appropriate dose in patients with end-stage renal disease has not been determined.Patients with hepatic disease: No dose adjustments are necessary for patients with mild or moderate hepatic impairment.

Overdose

There's no information on Cefditoren overdose in humans. With other ß-lactam antibiotics, though, overdose has caused nausea, vomiting, epigastric distress, diarrhea and convulsions. Hemodialysis may help remove Cefditoren from the body, particularly if kidney function is compromised.

⚠️ In an emergency call 999 or go to the nearest hospital emergency department.

Storage

Keep below 25°C temperature, away from light & moisture. Keep out of the reach of children.

Drug Interactions

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Moderate Famotidine
Moderate Estradiol

Common questions about CEFTOREN 400 FC TABLET 400 mg

What is CEFTOREN 400 FC TABLET 400 mg Tablet?

CEFTOREN 400 FC TABLET 400 mg Tablet is a medicine that contains Cefditoren. It is made by Advanced Chemical Industries PLC. It belongs to the Third generation cephalosporins group of medicines.

What is CEFTOREN 400 FC TABLET used for?

CEFTOREN 400 FC TABLET is used for: Chronic Obstructive Pulmonary Disease, Pneumonia, Bronchitis, Pharyngitis, Tonsillitis.

What are the side effects of CEFTOREN 400 FC TABLET?

Cefdiren commonly causes diarrhea, nausea, headache, abdominal pain, vaginal moniliasis, dyspepsia, vomiting, abnormal dreams, allergic reaction, anorexia, constipation, dizziness, dry mouth and fever.

Can I take CEFTOREN 400 FC TABLET during pregnancy or while breastfeeding?

Pregnancy category B. No adequate, well controlled studies have been conducted in pregnant women, so Cefditoren should be used during pregnancy only if clearly needed. Talk to your doctor before taking any medicine during pregnancy or while breastfeeding.

What happens if I take too much CEFTOREN 400 FC TABLET?

There's no information on Cefditoren overdose in humans. With other ß-lactam antibiotics, though, overdose has caused nausea, vomiting, epigastric distress, diarrhea and convulsions. In an emergency call 999 or go to the nearest hospital emergency department.

How should I store CEFTOREN 400 FC TABLET?

Keep below 25°C temperature, away from light & moisture. Keep out of the reach of children.

Can I take other medicines with CEFTOREN 400 FC TABLET?

Some medicines can interact with Cefditoren, for example: Famotidine, Estradiol. Tell your doctor or pharmacist about every medicine you take.

Do I need a prescription for CEFTOREN 400 FC TABLET?

CEFTOREN 400 FC TABLET is a prescription (Rx) medicine. Take it as your doctor advises.

Last updated: 15 Aug 2026