Fosamprenavir
Protease Inhibitor — ANTIINFECTIVES FOR SYSTEMIC USE
Also known as: amprenavir phosphate, fos-amprenavir, fosamprenavir calcium, GW-433908, GW433908, telzir
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Fosamprenavir is an ofp drug in the Protease Inhibitor class catalogued in DrugCentral. It was first approved by the FDA in 2003. Its mechanism of action is classified as Cytochrome P450 3A4 Inducers, Cytochrome P450 3A4 Inhibitors and HIV Protease Inhibitors. DrugCentral lists 2 molecular targets, including gag-pol and pol. Recorded indications include Human immunodeficiency virus infection.
- Approval status: ofp (first approved 2003 by the FDA).
- Drug class: Protease Inhibitor.
- Mechanism of action: Cytochrome P450 3A4 Inducers; Cytochrome P450 3A4 Inhibitors; HIV Protease Inhibitors.
- Molecular targets: gag-pol and pol (2 listed in DrugCentral).
- Indications: Human immunodeficiency virus infection.
- ATC code: J05AE07 (Protease inhibitors).
- Molecular formula: C25H36N3O9PS; molecular weight 585.61 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Human immunodeficiency virus infection
Off-label uses (1)
- Prevention of HIV Infection after Exposure
Contraindications (21)
- Breastfeeding (mother)
- Cardiovascular event risk
- Chronic hepatitis C
- Chronic type B viral hepatitis
- Diabetes mellitus
- Disease of liver
- Disorder of coronary artery
- Hemolytic anemia
- Hereditary factor IX deficiency disease
- Hereditary factor VIII deficiency disease
- Hypercholesterolemia
- Hyperglycemia
- Hypertensive disorder
- Hypertriglyceridemia
- Ketoacidosis in diabetes mellitus
- Kidney stone
- Lipodystrophy
- Liver function tests abnormal
- Myocardial infarction
- Obesity
- Smokes tobacco daily
Mechanism & targets
| Mechanism of action (MoA) | Cytochrome P450 3A4 Inducers; Cytochrome P450 3A4 Inhibitors; HIV Protease Inhibitors; P-Glycoprotein Inducers |
|---|---|
| Established pharmacologic class | Protease Inhibitor |
Molecular targets (2)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Gag-Pol polyprotein | gag-pol | unknown | — |
| Pol polyprotein | pol | inhibitor | — |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2003-10-20 | FDA | — | VIIV HLTHCARE |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
J05AE07 | ANTIINFECTIVES FOR SYSTEMIC USE › ANTIVIRALS FOR SYSTEMIC USE › DIRECT ACTING ANTIVIRALS › Protease inhibitors |
Pharmacogenomics
Drug-label and guideline annotations from PharmGKB and CPIC.
- EMA label: CYP3A4
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 |
|---|---|
| Viral mutation identified | 257.3 |
| Virologic failure | 250.1 |
| Cystitis noninfective | 145.2 |
| Pathogen resistance | 123.1 |
| Drug interaction | 122.9 |
| Lipodystrophy acquired | 112.3 |
| Drug resistance | 111.2 |
| Cerebral ischaemia | 99.8 |
| Blood HIV RNA increased | 99.1 |
| Blood bilirubin increased | 79.4 |
| Tumour lysis syndrome | 77.9 |
| Foetal exposure during pregnancy | 70.1 |
Chemical structure
| Molecular formula | C25H36N3O9PS |
|---|---|
| Molecular weight | 585.61 g/mol |
| CAS number | 226700-79-4 |
| InChIKey | MLBVMOWEQCZNCC-OEMFJLHTSA-N |
| PubChem CID | 131536 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Fosamprenavir used for?
DrugCentral lists the following indications for Fosamprenavir: Human immunodeficiency virus infection.
How does Fosamprenavir work?
Fosamprenavir is classified as Cytochrome P450 3A4 Inducers, Cytochrome P450 3A4 Inhibitors and HIV Protease Inhibitors; its molecular targets in DrugCentral include gag-pol and pol (inhibitor).
When was Fosamprenavir first approved?
Fosamprenavir was first approved by the FDA in 2003.
What drug class does Fosamprenavir belong to?
Fosamprenavir is in the Protease Inhibitor class.
What is the chemical formula of Fosamprenavir?
Fosamprenavir has the molecular formula C25H36N3O9PS and a molecular weight of 585.61 g/mol.
Browse: all drugs starting with F · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 1240 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1200734 — compound record and bioactivity
- PubChem CID 131536 — chemical identifiers
- DrugBank DB00701 — drug record
- FDA UNII WOU1621EEG — substance identity
- DailyMed: FDA labels for Fosamprenavir — current prescribing information (label search)
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
- PharmGKB / CPIC — pharmacogenomic label annotations
How this page is built: methodology · editorial policy & corrections.
For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.