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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126973912 | 12697391 | 2 | F | 2016 | 20160907 | 20160830 | 20160916 | PER | US-PFIZER INC-2016408558 | PFIZER | 67.00 | YR | F | Y | 0.00000 | 20160916 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126973912 | 12697391 | 1 | SS | ENBREL | ETANERCEPT | 1 | 50MG WEEKLY ON SATURDAYS | U | 0 | 50 | MG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | /wk | ||||||
| 126973912 | 12697391 | 2 | SS | ENBREL | ETANERCEPT | 1 | U | 0 | SOLUTION FOR INJECTION IN PRE-FILLED PEN | ||||||||||
| 126973912 | 12697391 | 3 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | 2 TABLETS WEEKLY | U | 11719 | 2 | DF | TABLET | /wk | |||||
| 126973912 | 12697391 | 4 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | 3 TABLETS WEEKLY | U | 11719 | 3 | DF | TABLET | /wk | |||||
| 126973912 | 12697391 | 5 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | 6 TABLETS WEEKLY | U | 11719 | 6 | DF | TABLET | /wk | |||||
| 126973912 | 12697391 | 6 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | 8 TABLETS WEEKLY | U | 11719 | 8 | DF | TABLET | /wk | |||||
| 126973912 | 12697391 | 7 | SS | HYDROCORTISONE. | HYDROCORTISONE | 1 | UNK UNK, QD | U | 8697 | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126973912 | 12697391 | 1 | Rheumatoid arthritis |
| 126973912 | 12697391 | 2 | Osteoarthritis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126973912 | 12697391 | Arthritis | |
| 126973912 | 12697391 | Drug dose omission | |
| 126973912 | 12697391 | Injection site haemorrhage | |
| 126973912 | 12697391 | Macule | |
| 126973912 | 12697391 | Pain | |
| 126973912 | 12697391 | Product quality issue | |
| 126973912 | 12697391 | Pruritus | |
| 126973912 | 12697391 | Skin mass | |
| 126973912 | 12697391 | Wrong technique in product usage process |
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 |
|---|---|---|---|---|---|---|
| 126973912 | 12697391 | 1 | 2016 | 0 | ||
| 126973912 | 12697391 | 3 | 201510 | 0 | ||
| 126973912 | 12697391 | 4 | 201511 | 0 |