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Sevelamer carbonate
سولامر
🧪 VariousPhosphate binder
🤰 Pregnancy:No specific problem stated🤱 Breastfeeding:No specific problem stated👶 Children:Use with caution👴 Older adults:Use with caution 🇮🇷 Registered in Iran⛔ 1 contraindications 🇺🇸 FDA approved (NDA) NDA022318ATC V03AE02
Market / country: 🇺🇸 USA
Renvela (US)
🧮 Dose calculator
Hyperphosphataemia in dialysis · Regimen source: FDA Renvela · 2.1, Table 1
- • Phosphorus >5.5–<7.5: 0.8 g; ≥7.5: 1.6 g three times daily with meals. Titrate by 0.8 g per meal every 2 weeks to target. FDA Renvela · 2.1, Table 1
Enter age (weight is optional for this regimen).
🛡️ Safety & information
Contraindications
- ⛔ Bowel obstruction; hypersensitivity to sevelamer. FDA Renvela · 4
Formulations
- 800 mg tablet — tablet 🇺🇸 USA FDA Renvela · 3
👥 Special populations
- 🤰 PregnancyNo specific problem stated
Label: minimal systemic absorption; fetal exposure not expected. FDA Renvela · 8.1
“Risk Summary Sevelamer carbonate is not absorbed systemically following oral administration and maternal use is not expected to result in fetal exposure to the drug.”
- 🤱 BreastfeedingNo specific problem stated
Label: infant exposure not expected. FDA Renvela · 8.2
“Risk Summary Renvela is not absorbed systemically by the mother following oral administration, and breastfeeding is not expected to result in exposure of the child to Renvela.”
- 👶 ChildrenUse with caution
The label has conditions, age limits or notes for children; the label sentence is quoted below. FDA Renvela · 8.4
“The safety and efficacy of Renvela in lowering serum phosphorus levels was studied in patients 6 years of age and older with CKD.”
- 👴 Older adultsUse with caution
Label: use with caution in older adults, usually starting at the low end of the dose range. FDA Renvela · 8.5
“In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range.”
- ⚥ Females & males of reproductive potentialNo data
The source for this drug has no section for this group.
🔗 Reference links
- FDA (approval record)NDA022318
- DailyMed (FDA label)FDA Renvela
- MedlinePlus (NIH)Sevelamer
- WHO ATC/DDDV03AE02
- Darooyab (Iran)Sevelamer
🇮🇷 Registered in Iran Darooyab · G-1978/Sevelamer
Dosage forms with Iranian generic codes, per Darooyab.
- 04000 · SEVELAMER 800MG TAB · قرص سولامر ۸۰۰ میلیگرم
- 21183 · SEVELAMER CARBONATE 800MG TAB · قرص سولامر کربنات ۸۰۰ میلیگرم
- 50111 · SEVELAMER 2.5 gr Powder For Solution · پودر سولامر ۲٫۵ گرم
- 52717 · SEVELAMER CARBONATE POWDER, FOR SUSPENSION ORAL 800 mg · سوسپانسیون خوراکی سولامر کربنات ۸۰۰ میلیگرم
📚 Reference status for this drug
Shows which sources have references recorded for this drug and which do not.
- FDA label (DailyMed)✅ PresentFDA Renvela · 3FDA Renvela · 2.1, Table 1FDA Renvela · 4FDA Renvela · 8.1FDA Renvela · 8.2FDA Renvela · 8.4FDA Renvela · 8.5FDA Renvela · 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-1978/Sevelamer
- Clinical review⚠ Unverified