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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6918936 | 7536739 | I | 6918936-6 | 20100722 | 20100804 | 20100811 | EXP | NL-AMGEN-KDL429144 | AMGENSAFETY | 58 | YR | F | Y | 20100811 | OT | NETHERLANDS |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6918936 | 1014391946 | PS | NEULASTA | 1 | 1020314 | ||||||
| 6918936 | 1014391947 | C | AMITRIPTYLINE HYDROCHLORIDE | 1 | |||||||
| 6918936 | 1014391948 | C | NEXIUM | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6918936 | 1014391946 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6918936 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6918936 | BACK PAIN |
| 6918936 | BONE PAIN |
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 |
|---|---|---|---|---|---|
| 6918936 | 1014391946 | 20100706 |