Trastuzumab
تراستوزوماب
🎗️ Antineoplastic And Immunomodulating AgentsAnti-HER2 antibody
Market / country: 🇺🇸 USA
Herceptin (US)
🧮 Dose calculator
Breast cancer (hormonal therapy) · Regimen source: FDA Herceptin · 2.3
- • Then 6 mg/kg every 3 weeks (adjuvant up to 52 weeks). LVEF before and regularly. Not interchangeable with ado-trastuzumab emtansine or fam-trastuzumab deruxtecan. IV infusion, never bolus. FDA Herceptin · 2.3FDA Herceptin · 2.1
- • Only under an oncologist; protocol, cycle interval and adjustment rest with the treating team. FDA Herceptin · 2
Enter age and weight.
🛡️ Safety & information
Warnings
- • Boxed warning: cardiomyopathy (higher with anthracyclines); infusion reactions and pulmonary toxicity; embryo-fetal toxicity (oligohydramnios). FDA Herceptin · Boxed Warning
Formulations
- 150 mg vial — powder for injection 🇺🇸 USA FDA Herceptin · 3
👥 Special populations
- 🤰 PregnancyDangerous / avoid
Label: can cause fetal harm. Dangerous in pregnancy. FDA Herceptin · Boxed Warning
“WARNING: CARDIOMYOPATHY, INFUSION REACTIONS, EMBRYO-FETAL TOXICITY, and PULMONARY TOXICITY See full prescribing information for complete boxed warning Cardiomyopathy: Herceptin can result in subclinical and clinical cardiac failure manifesting as CHF, and decreased LVEF, with greatest risk when administered …”
- 🤱 BreastfeedingUse with caution
Label: use with caution while breastfeeding; see the label text. FDA Herceptin · 8.2
“Risk Summary There is no information regarding the presence of trastuzumab in human milk, the effects on the breastfed infant, or the effects on milk production.”
- 👶 ChildrenSafety not established
Label: safety and effectiveness in children have not been established. FDA Herceptin · 8.4
“The safety and effectiveness of Herceptin in pediatric patients have not been established.”
- 👴 Older adultsNo specific problem stated
Label: no specific difference or dose adjustment stated for older adults. FDA Herceptin · 8.5
“No overall differences in safety or effectiveness were observed.”
- ⚥ Females & males of reproductive potentialUse with caution
Label has advice on pregnancy testing, contraception or fertility for females and males. FDA Herceptin · 8.3
“Contraception Females Herceptin can cause embryo-fetal harm when administered during pregnancy.”
🔗 Reference links
- FDA (approval record)BLA103792
- DailyMed (FDA label)FDA Herceptin
- MedlinePlus (NIH)Fam-trastuzumab deruxtecan-nxki InjectionTrastuzumab Injection
- WHO ATC/DDDL01FD01
- Darooyab (Iran)Trastuzumab
🇮🇷 Registered in Iran Darooyab · G-1083/Trastuzumab
Dosage forms with Iranian generic codes, per Darooyab.
- 05283 · TRASTUZUMAB 150MG VIAL · ویال تراستوزومب ۱۵۰ میلیگرم
- 02481 · TRASTUZUMAB 440MG VIAL · ویال تراستوزومب ۴۴۰ میلیگرم
- 50986 · TRASTUZUMAB 100MG VIAL · ویال تراستوزومب ۱۰۰ میلیگرم
- 50882 · TRASTUZUMAB 160MG VIAL · ویال تراستوزومب ۱۶۰ میلیگرم
- 52414 · TRASTUZUMAB INJECTION, SOLUTION PARENTERAL 600 mg/5mL · محلول تزریقی تراستوزومب ۶۰۰ میلیگرم / ۵ میلیلیتر
- 53090 · TRASTUZUMAB DERUXTECAN INJECTION, POWDER, FOR SOLUTION PARENTERAL 100 mg · پودر برای تهیه محلول تزریقی تراستوزومب دروکستکان ۱۰۰ میلیگرم
📚 Reference status for this drug
Shows which sources have references recorded for this drug and which do not.
- FDA label (DailyMed)✅ PresentFDA Herceptin · 3FDA Herceptin · 2.3FDA Herceptin · 2.1FDA Herceptin · 2FDA Herceptin · Boxed WarningFDA Herceptin · SPL approval / marketing categoryFDA Herceptin · 8.2FDA Herceptin · 8.4FDA Herceptin · 8.5FDA Herceptin · 8.3
- 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-1083/Trastuzumab
- Clinical review⚠ Unverified