Pegfilgrastim
Leukocyte Growth Factor — ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
Also known as: fulphila, g-lasta, neulasta, pegfilgrastim (genetical recombination), pegfilgrastim-jmdb, ristempa
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Pegfilgrastim is a drug in the Leukocyte Growth Factor class catalogued in DrugCentral. It was first approved by the FDA in 2002. DrugCentral lists 1 molecular target, including CSF3R. Recorded indications include Allogeneic peripheral blood stem cell transplant and Chemotherapy-induced neutropenia.
- Drug class: Leukocyte Growth Factor.
- Molecular targets: CSF3R (1 listed in DrugCentral).
- Indications: Allogeneic peripheral blood stem cell transplant and Chemotherapy-induced neutropenia.
- ATC code: L03AA13 (Colony stimulating factors).
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (2)
- Allogeneic peripheral blood stem cell transplant
- Chemotherapy-induced neutropenia
Mechanism & targets
| Established pharmacologic class | Leukocyte Growth Factor |
|---|
Molecular targets (1)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Granulocyte colony-stimulating factor receptor | CSF3R | activator | — |
Regulatory approvals (3)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2014-09-26 | PMDA | — | Kyowa Hakko Kirin Co., Ltd. | |
| 2002-08-22 | EMA | — | Amgen Europe B.V. | |
| 2002-01-31 | FDA | — | AMGEN |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
L03AA13 | ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS › IMMUNOSTIMULANTS › IMMUNOSTIMULANTS › Colony stimulating factors |
Reported adverse-event signals
Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.
| MedDRA term | LLR |
|---|---|
| Device adhesion issue | 63766.5 |
| Unintentional medical device removal | 48313.4 |
| Wrong technique in product usage process | 28194.9 |
| Device use error | 27756.5 |
| Device malfunction | 26906.7 |
| Device issue | 15157.6 |
| Accidental exposure to product | 14790.2 |
| Device occlusion | 12634.2 |
| Application site haemorrhage | 6535.0 |
| Drug dose omission by device | 6419.6 |
| Occupational exposure to product | 6360.0 |
| Intercepted product preparation error | 5825.4 |
Chemical structure
| Molecular formula | — |
|---|---|
| Molecular weight | — |
| CAS number | 208265-92-3 |
| InChIKey | — |
| PubChem CID | — |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Pegfilgrastim used for?
DrugCentral lists the following indications for Pegfilgrastim: Allogeneic peripheral blood stem cell transplant and Chemotherapy-induced neutropenia.
How does Pegfilgrastim work?
Its molecular targets in DrugCentral include CSF3R (activator).
When was Pegfilgrastim first approved?
Pegfilgrastim was first approved by the FDA in 2002.
What drug class does Pegfilgrastim belong to?
Pegfilgrastim is in the Leukocyte Growth Factor class.
Browse: all drugs starting with P · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 4986 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1201568 — compound record and bioactivity
- DrugBank DB00019 — drug record
- FDA UNII 3A58010674 — substance identity
- DailyMed: FDA labels for Pegfilgrastim — current prescribing information (label search)
- UniProt Q99062 (CSF3R) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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