Fenfluramine
ALIMENTARY TRACT AND METABOLISM
Also known as: DL-Fenfluramine, fenfluramine HCl, fenfluramine hydrochloride, fintepla, pondimin
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Fenfluramine is an onp drug catalogued in DrugCentral. It was first approved by the FDA in 2020. DrugCentral lists 21 molecular targets, including Slc6a4, ADRA1B and ADRA2C. Recorded indications include Dravet syndrome, Obesity and Seizures associated with Dravet syndrome.
- Approval status: onp (first approved 2020 by the FDA).
- Molecular targets: Slc6a4, ADRA1B, ADRA2C and ADRA2B (21 listed in DrugCentral).
- Indications: Dravet syndrome, Obesity and Seizures associated with Dravet syndrome.
- ATC code: A08AA02 (Centrally acting antiobesity products).
- Molecular formula: C12H16F3N; molecular weight 231.26 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (3)
- Dravet syndrome
- Obesity
- Seizures associated with Dravet syndrome
Contraindications (6)
- Alcoholism
- Diabetes mellitus type 1
- Diabetes mellitus type 2
- Glaucoma
- Hypertensive disorder
- Pulmonary hypertension
Mechanism & targets
Molecular targets (21)
Regulatory approvals (3)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2022-09-26 | PMDA | — | UCB JAPAN CO., LTD. | Yes |
| 2020-12-18 | EMA | — | UCB PHARMA S.A. | Yes |
| 2020-06-25 | FDA | — | UCB INC | Yes |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
A08AA02 | ALIMENTARY TRACT AND METABOLISM › ANTIOBESITY PREPARATIONS, EXCL. DIET PRODUCTS › ANTIOBESITY PREPARATIONS, EXCL. DIET PRODUCTS › Centrally acting antiobesity products |
N03AX26 | NERVOUS SYSTEM › ANTIEPILEPTICS › ANTIEPILEPTICS › Other antiepileptics |
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 |
|---|---|
| Tricuspid valve incompetence | 2007.7 |
| Seizure | 1409.6 |
| Mitral valve incompetence | 985.2 |
| Pulmonary valve incompetence | 836.1 |
| Mitral valve thickening | 579.9 |
| Aortic valve incompetence | 520.0 |
| Epilepsy | 445.9 |
| Off label use | 403.3 |
| Prescribed underdose | 361.9 |
| Aortic valve thickening | 314.2 |
| Petit mal epilepsy | 313.5 |
| Generalised tonic-clonic seizure | 307.5 |
Chemical structure
Full physicochemical, ADMET and 3D-structure analysis of Fenfluramine is on its molecule page.
| Molecular formula | C12H16F3N |
|---|---|
| Molecular weight | 231.26 g/mol |
| CAS number | 458-24-2 |
| InChIKey | DBGIVFWFUFKIQN-UHFFFAOYSA-N |
| PubChem CID | 3337 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Fenfluramine used for?
DrugCentral lists the following indications for Fenfluramine: Dravet syndrome, Obesity and Seizures associated with Dravet syndrome.
How does Fenfluramine work?
Its molecular targets in DrugCentral include Slc6a4, ADRA1B, ADRA2C and ADRA2B.
When was Fenfluramine first approved?
Fenfluramine was first approved by the FDA in 2020.
What is the chemical formula of Fenfluramine?
Fenfluramine has the molecular formula C12H16F3N and a molecular weight of 231.26 g/mol.
Browse: all drugs starting with F · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 1150 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL2106217 — compound record and bioactivity
- PubChem CID 3337 — chemical identifiers
- DrugBank DB00574 — drug record
- FDA UNII 2DS058H2CF — substance identity
- DailyMed: FDA labels for Fenfluramine — current prescribing information (label search)
- UniProt P35368 (ADRA1B) — target protein
- UniProt P18825 (ADRA2C) — target protein
- UniProt P18089 (ADRA2B) — target protein
- UniProt P35348 (ADRA1A) — target protein
- UniProt P08913 (ADRA2A) — target protein
- UniProt P41595 (HTR2B) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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