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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126773532 | 12677353 | 2 | F | 2016 | 20160927 | 20160823 | 20160928 | PER | US-JNJFOC-20160813110 | JANSSEN | 0.00 | A | M | Y | 90.72000 | KG | 20160928 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126773532 | 12677353 | 1 | PS | TRAMADOL HYDROCHLORIDE. | TRAMADOL HYDROCHLORIDE | 1 | Oral | N | UNKNOWN | 20281 | 300 | MG | TABLETS | QD | |||||
| 126773532 | 12677353 | 2 | SS | ULTRAM | TRAMADOL HYDROCHLORIDE | 1 | Oral | N | UNKNOWN | 20281 | 300 | MG | TABLETS | QD | |||||
| 126773532 | 12677353 | 3 | C | ULTRAM | TRAMADOL HYDROCHLORIDE | 1 | Oral | D | 0 | 50 | MG | UNSPECIFIED | |||||||
| 126773532 | 12677353 | 4 | C | ADVIL | IBUPROFEN | 1 | Oral | D | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126773532 | 12677353 | 1 | Pain |
| 126773532 | 12677353 | 2 | Pain |
| 126773532 | 12677353 | 3 | Breakthrough pain |
| 126773532 | 12677353 | 4 | Pain |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126773532 | 12677353 | Drug dose omission | |
| 126773532 | 12677353 | Drug ineffective | |
| 126773532 | 12677353 | Fatigue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |