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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5075638 | 6088383 | I | 5075638-1 | 20041101 | 20051121 | 20060809 | PER | US-AMGEN-KDL159293 | AMGEN | F | Y | 158.9 | KG | 20060809 | PH | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5075638 | 1007560426 | PS | PROCRIT | 1 | SUBCUTANEOUS | P041166 | |||||
5075638 | 1007560427 | C | ENBREL | 1 | SUBCUTANEOUS | ||||||
5075638 | 1007560428 | C | FUROSEMIDE | 1 | |||||||
5075638 | 1007560429 | C | IRON | 2 | INTRAVENOUS | ||||||
5075638 | 1007560430 | C | LANTUS | 1 | |||||||
5075638 | 1007560431 | C | GLYBURIDE | 1 | ORAL | ||||||
5075638 | 1007560432 | C | ALLOPURINOL | 1 | ORAL |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5075638 | 1007560426 | RENAL FAILURE CHRONIC |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
5075638 | ARTHRALGIA |
5075638 | BONE PAIN |
5075638 | DRUG INEFFECTIVE |
5075638 | FATIGUE |
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 |
---|---|---|---|---|---|
5075638 | 1007560426 | 20041101 | 20051118 |