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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
93513312 | 9351331 | 2 | F | 20120920 | 20130620 | 20130617 | 20130630 | EXP | GB-TEVA-412548ISR | TEVA | 40.59 | YR | M | Y | 0.00000 | 20130630 | OT | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
93513312 | 9351331 | 1 | PS | COPAXONE | 1 | SUBCUTANEOUS | 20 MILLIGRAM DAILY; | U | 20622 | 20 | MG | INJECTION | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
93513312 | 9351331 | 1 | Relapsing-remitting multiple sclerosis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
93513312 | 9351331 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
93513312 | 9351331 | Multiple injuries | |
93513312 | 9351331 | Road traffic accident |
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 |
---|---|---|---|---|---|---|
93513312 | 9351331 | 1 | 20111101 | 0 |