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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122871793 | 12287179 | 3 | F | 201505 | 20160805 | 20160420 | 20160822 | EXP | BR-JNJFOC-20151221089 | JANSSEN | 68.94 | YR | E | F | Y | 0.00000 | 20160822 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122871793 | 12287179 | 1 | SS | REMICADE | INFLIXIMAB | 1 | Intravenous (not otherwise specified) | N | UNKNOWN | 0 | LYOPHILIZED POWDER | ||||||||
122871793 | 12287179 | 2 | SS | REMICADE | INFLIXIMAB | 1 | Intravenous (not otherwise specified) | N | UNKNOWN | 0 | 200 | MG | LYOPHILIZED POWDER | ||||||
122871793 | 12287179 | 3 | SS | REMICADE | INFLIXIMAB | 1 | Intravenous (not otherwise specified) | N | UNKNOWN | 0 | 180 | MG | LYOPHILIZED POWDER | ||||||
122871793 | 12287179 | 4 | SS | REMICADE | INFLIXIMAB | 1 | Intravenous (not otherwise specified) | N | UNKNOWN | 0 | 200 | MG | LYOPHILIZED POWDER | ||||||
122871793 | 12287179 | 5 | PS | REMICADE | INFLIXIMAB | 1 | Intravenous (not otherwise specified) | N | UNKNOWN | 103772 | 180 | MG | LYOPHILIZED POWDER | ||||||
122871793 | 12287179 | 6 | C | MAREVAN | WARFARIN SODIUM | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
122871793 | 12287179 | 7 | C | METHOTREXATE. | METHOTREXATE | 1 | Unknown | 0 | UNSPECIFIED |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
122871793 | 12287179 | 1 | Rheumatoid arthritis |
122871793 | 12287179 | 2 | Rheumatoid arthritis |
122871793 | 12287179 | 3 | Rheumatoid arthritis |
122871793 | 12287179 | 4 | Rheumatoid arthritis |
122871793 | 12287179 | 5 | Rheumatoid arthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
122871793 | 12287179 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
122871793 | 12287179 | Aphthous ulcer | |
122871793 | 12287179 | Arthralgia | |
122871793 | 12287179 | Cardiac operation | |
122871793 | 12287179 | Colitis | |
122871793 | 12287179 | Drug ineffective | |
122871793 | 12287179 | Hand deformity | |
122871793 | 12287179 | Infusion related reaction | |
122871793 | 12287179 | Medication residue present | |
122871793 | 12287179 | Memory impairment | |
122871793 | 12287179 | Neck mass | |
122871793 | 12287179 | Off label use | |
122871793 | 12287179 | Pain | |
122871793 | 12287179 | Pain in extremity | |
122871793 | 12287179 | Product use issue | |
122871793 | 12287179 | Tongue discolouration | |
122871793 | 12287179 | Urinary tract infection | |
122871793 | 12287179 | Urticaria |
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 |
---|---|---|---|---|---|---|
122871793 | 12287179 | 3 | 20151120 | 0 | ||
122871793 | 12287179 | 4 | 20160715 | 0 | ||
122871793 | 12287179 | 5 | 201505 | 0 |