Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4655341 | 5807764 | I | 4655341-X | 20050116 | 20050118 | 20050331 | PER | UK108101 | AMGEN | F | N | 20050224 |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
4655341 | 1005954368 | PS | NEULASTA | 1 | SUBCUTANEOUS | 6 MG, SC | N | D |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4655341 | 1005954368 | CHEMOTHERAPY |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
4655341 | COUGH |
4655341 | DYSPNOEA |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4655341 | FGN |
4655341 | HP |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
4655341 | 1005954368 | 20050113 | 20050113 |