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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8248779 | 7721228 | F | 8248779-5 | 20060101 | 20120323 | 20120331 | EXP | US-AMGEN-TCS397884 | AMGENSAFETY | 66 | YR | M | Y | 20120331 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8248779 | 1019282850 | PS | ENBREL | 1 | SUBCUTANEOUS | 25 MG, Q2WK | 1015689 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8248779 | 1019282850 | ANKYLOSING SPONDYLITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8248779 | HO |
| 8248779 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8248779 | OSTEOPOROSIS |
| 8248779 | CHRONIC OBSTRUCTIVE PULMONARY DISEASE |
| 8248779 | BRONCHITIS |
| 8248779 | BACK PAIN |
| 8248779 | SPINAL COLUMN INJURY |
| 8248779 | RENAL STONE REMOVAL |
| 8248779 | HIP SURGERY |
| 8248779 | ARTHRALGIA |
| 8248779 | MOBILITY DECREASED |
| 8248779 | SPINAL FRACTURE |
| 8248779 | FALL |
| 8248779 | NEPHROLITHIASIS |
| 8248779 | LUNG DISORDER |
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 |
|---|---|---|---|---|---|
| 8248779 | 1019282850 | 20030101 |