Cefpodoxime
سفپودوکسیم
🦠 Antiinfectives For Systemic UseThird-generation cephalosporin
Market / country: 🇺🇸 USA
Vantin (US)
🧮 Dose calculator
Acute otitis media · Regimen source: FDA Cefpodoxime susp. · Dosage and Administration
Enter age and weight.
🛡️ Safety & information
Contraindications
- ⛔ Allergy to cephalosporins. FDA Cefpodoxime susp. · Contraindications
Renal adjustment
- • eGFR < 30: CrCl <30: dose every 24 h. FDA Cefpodoxime susp. · Dosage and Administration
Formulations
- 50 mg / 5 mL — suspension 🇺🇸 USA FDA Cefpodoxime susp. · How Supplied
- 100 mg / 5 mL — suspension 🇺🇸 USA FDA Cefpodoxime susp. · How Supplied
👥 Special populations
- 🤰 PregnancyUse with caution
Label states no clear risk or has limited data; use only if needed, under medical advice. FDA Cefpodoxime susp. · Pregnancy - Teratogenic Effects:
“Pregnancy Category B Cefpodoxime proxetil was neither teratogenic nor embryocidal when administered to rats during organogenesis at doses up to 100 mg/kg/day (2 times the human dose based on mg/m 2 ) or to rabbits at doses up to 30 mg/kg/day (1 to 2 times the human dose based on mg/m 2 ).”
- 🤱 BreastfeedingDangerous / avoid
Label: breastfeeding not recommended, or choose between the drug and breastfeeding. FDA Cefpodoxime susp. · Nursing Mothers:
“Because of the potential for serious reactions in nursing infants, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.”
- 👶 ChildrenUse with caution
The label has conditions, age limits or notes for children; the label sentence is quoted below. FDA Cefpodoxime susp. · Pediatric Use:
“Safety and efficacy in infants less than 2 months of age have not been established.”
- 👴 Older adultsNo specific problem stated
Label: no specific difference or dose adjustment stated for older adults. FDA Cefpodoxime susp. · Geriatric Use:
“No overall differences in effectiveness or safety were observed between the elderly and younger patients.”
- ⚥ Females & males of reproductive potentialNo data
The source for this drug has no section for this group.
🔗 Reference links
- FDA (approval record)ANDA065409
- DailyMed (FDA label)FDA Cefpodoxime susp.
- MedlinePlus (NIH)Cefpodoxime
- WHO ATC/DDDJ01DD13
- Darooyab (Iran)Cefpodoxime-Proxetil
🇮🇷 Registered in Iran Darooyab · G-342/Cefpodoxime-Proxetil
Dosage forms with Iranian generic codes, per Darooyab.
- 08913 · CEFPODOXIM 100MG TAB · قرص سفپودوکسیم ۱۰۰ میلیگرم
📚 Reference status for this drug
Shows which sources have references recorded for this drug and which do not.
- FDA label (DailyMed)✅ PresentFDA Cefpodoxime susp. · How SuppliedFDA Cefpodoxime susp. · Dosage and AdministrationFDA Cefpodoxime susp. · ContraindicationsFDA Cefpodoxime susp. · Pregnancy - Teratogenic Effects:FDA Cefpodoxime susp. · Nursing Mothers:FDA Cefpodoxime susp. · Pediatric Use:FDA Cefpodoxime susp. · Geriatric Use:FDA Cefpodoxime susp. · SPL approval / marketing category
- UK SmPC (eMC / MHRA)❌ Not present
- Published guideline❌ Not present
- Licensed reference (medical school)❌ Not present
- Iranian leaflet (IFDA)❌ Not present
- Pharmacy website (secondary, unreliable)✅ PresentDarooyab · G-342/Cefpodoxime-Proxetil
- Clinical review⚠ Unverified