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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126643431 | 12664343 | 1 | I | 1999 | 20160815 | 20160818 | 20160818 | EXP | US-JNJFOC-20160812965 | JANSSEN | 0.00 | M | Y | 0.00000 | 20160818 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126643431 | 12664343 | 1 | PS | DURAGESIC | FENTANYL | 1 | Unknown | U | U | 19813 | UNSPECIFIED |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126643431 | 12664343 | 1 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126643431 | 12664343 | DS |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126643431 | 12664343 | Arthralgia | |
126643431 | 12664343 | Back injury | |
126643431 | 12664343 | Hypoaesthesia | |
126643431 | 12664343 | Joint dislocation | |
126643431 | 12664343 | Pain | |
126643431 | 12664343 | Paraesthesia | |
126643431 | 12664343 | Sensory loss | |
126643431 | 12664343 | Surgery |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |