Pemetrexed
پمترکسد
🎗️ Antineoplastic And Immunomodulating AgentsAntifolate antimetabolite
Market / country: 🇺🇸 USA
Alimta (US)
🧮 Dose calculator
Lung cancer (small-cell and non-small-cell) · Regimen source: FDA Alimta · 2.1
- • Only under an oncologist in an equipped centre. Calculator = label mg/m² × BSA (Mosteller); protocol, cycle interval and adjustment for CBC and renal/hepatic function rest with the oncology team. FDA Alimta · 2.1
- • Premedication: folic acid 400–1000 mcg daily from 7 days before, vitamin B12 IM every 9 weeks, dexamethasone 4 mg twice daily the day before, of and after. FDA Alimta · 2.4
Enter age and weight.
🛡️ Safety & information
Contraindications
- ⛔ History of severe hypersensitivity to pemetrexed. FDA Alimta · 4
Warnings
- • Myelosuppression (reduced with folate and B12); renal failure; bullous skin toxicity; interstitial pneumonitis; ibuprofen interaction; embryo-fetal toxicity. FDA Alimta · 5
Renal adjustment
- • eGFR < 45: CrCl below 45: no recommended dose — do not give. FDA Alimta · 2.3
Formulations
- 500 mg vial (also 100 mg) — powder for injection 🇺🇸 USA FDA Alimta · 3
👥 Special populations
- 🤰 PregnancyDangerous / avoid
Label: can cause fetal harm. Dangerous in pregnancy. FDA Alimta · 8.1
“Risk Summary Based on findings from animal studies and its mechanism of action, ALIMTA can cause fetal harm when administered to a pregnant woman [see Clinical Pharmacology ( 12.1 )] .”
- 🤱 BreastfeedingDangerous / avoid
Label: breastfeeding not recommended, or choose between the drug and breastfeeding. FDA Alimta · 8.2
“Because of the potential for serious adverse reactions in breastfed infants from ALIMTA, advise women not to breastfeed during treatment with ALIMTA and for one week after the last dose.”
- 👶 ChildrenSafety not established
Label: safety and effectiveness in children have not been established. FDA Alimta · 8.4
“The safety and effectiveness of ALIMTA in pediatric patients have not been established.”
- 👴 Older adultsNo specific problem stated
Label: no specific difference or dose adjustment stated for older adults. FDA Alimta · 8.5
“No overall differences in effectiveness were observed between these patients and younger patients.”
- ⚥ Females & males of reproductive potentialUse with caution
Label has advice on pregnancy testing, contraception or fertility for females and males. FDA Alimta · 8.3
“Contraception Females Because of the potential for genotoxicity, advise females of reproductive potential to use effective contraception during treatment with ALIMTA and for 6 months after the last dose.”
🔗 Reference links
- FDA (approval record)NDA021462
- DailyMed (FDA label)FDA Alimta
- MedlinePlus (NIH)Pemetrexed Injection
- WHO ATC/DDDL01BA04
- Darooyab (Iran)❌ None
🇮🇷 Not found in Iran list Darooyab · search
Darooyab lists no registered dosage form or brand for this drug. This does not prove it is unavailable.
📚 Reference status for this drug
Shows which sources have references recorded for this drug and which do not.
- FDA label (DailyMed)✅ PresentFDA Alimta · 3FDA Alimta · 2.1FDA Alimta · 2.4FDA Alimta · 2.2FDA Alimta · 4FDA Alimta · 5FDA Alimta · 2.3FDA Alimta · 8.1FDA Alimta · 8.2FDA Alimta · 8.4FDA Alimta · 8.5FDA Alimta · 8.3FDA Alimta · 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 · search
- Clinical review⚠ Unverified