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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5075125 | 6088434 | I | 5075125-0 | 20050901 | 20050921 | 20060809 | PER | US-AMGEN-KDL151448 | AMGEN | F | Y | 64.5 | KG | 20060809 | MD | UNITED STATES |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5075125 | 1007558798 | PS | PROCRIT | 1 | SUBCUTANEOUS | NOT PROVIDED | |||||
5075125 | 1007558799 | C | METHOTREXATE | 1 | |||||||
5075125 | 1007558800 | C | HUMIRA | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5075125 | 1007558798 | ANAEMIA |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
5075125 | ABDOMINAL DISCOMFORT |
5075125 | NAUSEA |
5075125 | VOMITING |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5075125 | 1007558798 | 20050828 |