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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127438812 | 12743881 | 2 | F | 20160717 | 20160912 | 20160914 | 20160919 | EXP | JP-PFIZER INC-2016428242 | PFIZER | 80.00 | YR | F | Y | 31.40000 | KG | 20160919 | PH | JP | JP |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127438812 | 12743881 | 1 | PS | RHEUMATREX | METHOTREXATE SODIUM | 1 | Oral | 4 MG WEEKLY | Y | 11719 | 4 | MG | CAPSULE | /wk | |||||
127438812 | 12743881 | 2 | C | ULCERLMIN | SUCRALFATE | 1 | UNK | 0 | |||||||||||
127438812 | 12743881 | 3 | C | LOXONIN | LOXOPROFEN SODIUM | 1 | 0 | ||||||||||||
127438812 | 12743881 | 4 | C | PREDNISOLONE. | PREDNISOLONE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127438812 | 12743881 | 1 | Rheumatoid arthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127438812 | 12743881 | HO |
127438812 | 12743881 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127438812 | 12743881 | Hypokalaemia | |
127438812 | 12743881 | Hyponatraemia | |
127438812 | 12743881 | Pancytopenia |
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 |
---|---|---|---|---|---|---|
127438812 | 12743881 | 1 | 20160815 | 0 | ||
127438812 | 12743881 | 2 | 20160728 | 0 |