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Duloxetine, sold under the brand name Cymbalta among others, is a medication used to treat major depressive disorder, generalized anxiety disorder, obsessive–compulsive disorder, fibromyalgia, neuropathic pain, and other types of chronic pain. It is taken by mouth.
History, Applications, Research & Standards
Explore the main themes, entities and connections around Duloxetine. Start with the topic map, then use the sections below for research and deeper semantic analysis.
Start with a few of the strongest sections from the source topic. These are research directions, not a list of keywords you must use.
High-confidence facts extracted from structured source data. Use them as anchors for further research.
Browse the full topic structure. Each item opens a new analysis centered on that subject.
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Use these terms to understand the vocabulary surrounding the topic, not as a checklist for keyword stuffing.
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| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Duloxetine | 3D model (JSmol) | Interactive image | 1.00 | infobox |
| Duloxetine | AHFS/Drugs.com | Monograph | 1.00 | infobox |
| Duloxetine | ATC code | N06AX21 (WHO) | 1.00 | infobox |
| Duloxetine | Bioavailability | ~50% (32–80%) | 1.00 | infobox |
| Duloxetine | CAS Number | 116539-59-4 Y | 1.00 | infobox |
| Duloxetine | CAS Number | as HCl: 136434-34-9 Y | 1.00 | infobox |
| Duloxetine | ChEBI | CHEBI:36795 Y | 1.00 | infobox |
| Duloxetine | ChEBI | as HCl: CHEBI:31526 Y | 1.00 | infobox |
| Duloxetine | ChEMBL | ChEMBL1175 Y | 1.00 | infobox |
| Duloxetine | ChEMBL | as HCl: ChEMBL1200328 Y | 1.00 | infobox |
| Duloxetine | ChemSpider | 54822 Y | 1.00 | infobox |
| Duloxetine | CompTox Dashboard (EPA) | DTXSID6048385 | 1.00 | infobox |
| Duloxetine | Drug class | Serotonin–norepinephrine reuptake inhibitor (SNRI) | 1.00 | infobox |
| Duloxetine | DrugBank | DB00476 Y | 1.00 | infobox |
| Duloxetine | ECHA InfoCard | 100.116.825 | 1.00 | infobox |
| Duloxetine | Elimination half-life | 10–12 hours | 1.00 | infobox |
| Duloxetine | Excretion | 70% in urine, 20% in feces | 1.00 | infobox |
| Duloxetine | Formula | C18H19NOS | 1.00 | infobox |
| Duloxetine | IUPHAR/BPS | 202 | 1.00 | infobox |
| Duloxetine | KEGG | D07880 Y | 1.00 | infobox |
| Duloxetine | KEGG | as HCl: D01179 Y | 1.00 | infobox |
| Duloxetine | Legal status | AU: S4 (Prescription only) | 1.00 | infobox |
| Duloxetine | Legal status | BR: Class C1 (Other controlled substances) | 1.00 | infobox |
| Duloxetine | Legal status | CA: ℞-only | 1.00 | infobox |
| Duloxetine | Legal status | UK: POM (Prescription only) | 1.00 | infobox |
| Duloxetine | Legal status | US: ℞-only | 1.00 | infobox |
| Duloxetine | Legal status | EU: Rx-only | 1.00 | infobox |
| Duloxetine | License data | US DailyMed: Duloxetine | 1.00 | infobox |
| Duloxetine | MedlinePlus | a604030 | 1.00 | infobox |
| Duloxetine | Metabolism | Liver, two P450 isozymes, CYP2D6 and CYP1A2 | 1.00 | infobox |
These clusters group vocabulary that occurs around closely connected concepts in the source material.
Bridges can reveal useful research angles that are easy to miss in a flat list of related terms.