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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7386000 | 7839922 | F | 7386000-0 | 20090901 | 20110323 | 20110331 | EXP | JP-AMGEN-JPNSP2011012311 | AMGENSAFETY | 67 | YR | M | Y | 20110331 | MD | JAPAN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7386000 | 1016135941 | SS | ENBREL | 1 | SUBCUTANEOUS | 50 MG, WEEKLY | |||||
| 7386000 | 1016135944 | C | ETODOLAC | 1 | ORAL | 200 MG, 2X/DAY | |||||
| 7386000 | 1016135950 | C | URSO /00465701/ | 2 | ORAL | 100 MG, 2X/DAY | |||||
| 7386000 | 1016135939 | PS | ENBREL | 1 | SUBCUTANEOUS | 25 MG, 2X/WEEK (0.5ML (TUESDAY AND FRIDAY)) | |||||
| 7386000 | 1016135940 | SS | ENBREL | 1 | SUBCUTANEOUS | 25 MG, 3X/2WEEKS | |||||
| 7386000 | 1016135946 | C | ADALAT | 1 | ORAL | 20 MG, 2X/DAY | |||||
| 7386000 | 1016135949 | C | MAINTATE | 2 | |||||||
| 7386000 | 1016135952 | C | GASTER /00661201/ | 2 | 20 MG, 2X/DAY | ||||||
| 7386000 | 1016135943 | SS | AZULFIDINE | 1 | ORAL | 500 MG, BID | |||||
| 7386000 | 1016135951 | C | OLMETEC | 2 | ORAL | 20 MG, 1X/DAY | |||||
| 7386000 | 1016135945 | C | PREDNISOLONE | 1 | ORAL | 2.5 MG, BID | |||||
| 7386000 | 1016135942 | SS | RHEUMATREX | 1 | ORAL | 6 MG, WEEKLY | |||||
| 7386000 | 1016135947 | C | FLUITRAN | 2 | ORAL | 2 MG, 1X/DAY | |||||
| 7386000 | 1016135948 | C | MAINTATE | 2 | ORAL | 5 MG, 1X/DAY |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7386000 | 1016135944 | RHEUMATOID ARTHRITIS |
| 7386000 | 1016135950 | CHOLELITHIASIS |
| 7386000 | 1016135939 | RHEUMATOID ARTHRITIS |
| 7386000 | 1016135946 | HYPERTENSION |
| 7386000 | 1016135949 | VENTRICULAR EXTRASYSTOLES |
| 7386000 | 1016135952 | GASTRITIS |
| 7386000 | 1016135943 | RHEUMATOID ARTHRITIS |
| 7386000 | 1016135951 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7386000 | 1016135945 | RHEUMATOID ARTHRITIS |
| 7386000 | 1016135942 | RHEUMATOID ARTHRITIS |
| 7386000 | 1016135947 | HYPERTENSION |
| 7386000 | 1016135948 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7386000 | HO |
| 7386000 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7386000 | HAEMOGLOBIN DECREASED |
| 7386000 | ENTEROCOLITIS HAEMORRHAGIC |
| 7386000 | RHEUMATOID ARTHRITIS |
| 7386000 | JOINT ARTHROPLASTY |
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 |
|---|---|---|---|---|---|
| 7386000 | 1016135941 | 20110121 | |||
| 7386000 | 1016135944 | 20060501 | |||
| 7386000 | 1016135950 | 20060601 | |||
| 7386000 | 1016135939 | 20100611 | 20101104 | 147 | DAY |
| 7386000 | 1016135940 | 20101105 | 20110120 | 77 | DAY |
| 7386000 | 1016135946 | 19980101 | |||
| 7386000 | 1016135952 | 20090501 | |||
| 7386000 | 1016135943 | 20060501 | |||
| 7386000 | 1016135945 | 20060501 | |||
| 7386000 | 1016135942 | 20090601 | 20110204 | ||
| 7386000 | 1016135947 | 19980101 | |||
| 7386000 | 1016135948 | 19980101 |