Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 818350811 | 8183508 | 11 | F | 201107 | 20160701 | 20111017 | 20160705 | EXP | BR-ROCHE-1001873 | ROCHE | 59.65 | YR | F | Y | 50.00000 | KG | 20160705 | OT | BR | BR |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 818350811 | 8183508 | 1 | PS | MABTHERA | RITUXIMAB | 1 | Intravenous (not otherwise specified) | U | 103705 | INFUSION | |||||||||
| 818350811 | 8183508 | 2 | SS | MABTHERA | RITUXIMAB | 1 | Intravenous (not otherwise specified) | U | 103705 | INFUSION | |||||||||
| 818350811 | 8183508 | 3 | SS | MABTHERA | RITUXIMAB | 1 | Intravenous (not otherwise specified) | U | 103705 | INFUSION | |||||||||
| 818350811 | 8183508 | 4 | SS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | MOST RECENT DOSE 22/OCT/014, 400 MG/20ML; LAST DOSE: 19/JAN/2016 | 125276 | INFUSION | /month | ||||||||
| 818350811 | 8183508 | 5 | SS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | 125276 | INFUSION | ||||||||||
| 818350811 | 8183508 | 6 | C | MELOXICAM. | MELOXICAM | 1 | 0 | ||||||||||||
| 818350811 | 8183508 | 7 | C | CYCLOBENZAPRINE | CYCLOBENZAPRINE | 1 | 0 | ||||||||||||
| 818350811 | 8183508 | 8 | C | MAGNOPYROL | 2 | 0 | |||||||||||||
| 818350811 | 8183508 | 9 | C | METHOTREXATE. | METHOTREXATE | 1 | Oral | 0 | 2.5 | MG | TABLET | BIW | |||||||
| 818350811 | 8183508 | 10 | C | MAGNOPYROL | 2 | Intravenous drip | 50 DROPS IN THE MORNING, FOR PAIN, SINCE 30 YEARS, (IF PERSISTENT, PATIENT TAKES IT DAILY) | 0 | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 818350811 | 8183508 | 1 | Rheumatoid arthritis |
| 818350811 | 8183508 | 4 | Rheumatoid arthritis |
| 818350811 | 8183508 | 9 | Rheumatoid arthritis |
| 818350811 | 8183508 | 10 | Pain |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 818350811 | 8183508 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 818350811 | 8183508 | Abasia | |
| 818350811 | 8183508 | Abdominal pain upper | |
| 818350811 | 8183508 | Arthralgia | |
| 818350811 | 8183508 | Disease progression | |
| 818350811 | 8183508 | Drug ineffective | |
| 818350811 | 8183508 | Fall | |
| 818350811 | 8183508 | Fatigue | |
| 818350811 | 8183508 | Hepatic enzyme increased | |
| 818350811 | 8183508 | Hypertension | |
| 818350811 | 8183508 | Mobility decreased | |
| 818350811 | 8183508 | Rash | |
| 818350811 | 8183508 | Rheumatoid arthritis | |
| 818350811 | 8183508 | Spinal osteoarthritis | |
| 818350811 | 8183508 | Therapeutic response decreased | |
| 818350811 | 8183508 | Tooth disorder |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 818350811 | 8183508 | 1 | 20100501 | 0 | ||
| 818350811 | 8183508 | 2 | 20101201 | 0 | ||
| 818350811 | 8183508 | 3 | 20111011 | 20111025 | 0 | |
| 818350811 | 8183508 | 4 | 20140722 | 0 | ||
| 818350811 | 8183508 | 5 | 20140624 | 0 | ||
| 818350811 | 8183508 | 9 | 20150204 | 0 | ||
| 818350811 | 8183508 | 10 | 1985 | 0 |