| ADR Ontology |
| ADR Term |
Rhabdomyosarcoma |
| ADR ID |
BADD_A10865 |
| ADR Hierarchy |
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| Description |
A malignant solid tumor arising from mesenchymal tissues which normally differentiate to form striated muscle. It can occur in a wide variety of sites. It is divided into four distinct types: pleomorphic, predominantly in male adults; alveolar (RHABDOMYOSARCOMA, ALVEOLAR), mainly in adolescents and young adults; embryonal (RHABDOMYOSARCOMA, EMBRYONAL), predominantly in infants and children; and botryoidal, also in young children. It is one of the most frequently occurring soft tissue sarcomas and the most common in children under 15. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p2186; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1647-9) [MeSH] |
| MedDRA Code |
10039022 |
| MeSH ID |
D012208
|
|
ADR Severity Grade (FAERS)
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|
|
ADR Severity Grade (CTCAE)
|
Not Available
|
| Synonym |
| Rhabdomyosarcoma | Rhabdomyosarcoma NOS | Rhabdomyosarcoma previously treated | Rhabdomyosarcoma previously untreated | Rhabdosarcoma | Rhabdosarcoma previously treated | Rhabdomyosarcomas |
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| Drugs Leading to the ADR |
| Drug ID | Drug Name | ADR Frequency (FAERS) | ADR Severity Grade (FAERS) | | BADD_D01243 | Lamotrigine | 0.000110% | | | BADD_D01376 | Melphalan | 0.000224% | | | BADD_D01687 | Pazopanib | 0.000224% | |
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