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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127366101 | 12736610 | 1 | I | 201110 | 20160706 | 20160913 | 20160913 | PER | US-JNJFOC-20160705854 | JANSSEN | 47.97 | YR | A | F | Y | 68.04000 | KG | 20160913 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127366101 | 12736610 | 1 | PS | TRAMADOL ER | TRAMADOL HYDROCHLORIDE | 1 | Unknown | U | 21692 | 200 | MG | UNSPECIFIED | |||||||
| 127366101 | 12736610 | 2 | SS | ULTRAM ER | TRAMADOL HYDROCHLORIDE | 1 | Unknown | N | 21692 | 200 | MG | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127366101 | 12736610 | 1 | Product used for unknown indication |
| 127366101 | 12736610 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127366101 | 12736610 | Drug dose omission | |
| 127366101 | 12736610 | Reaction to drug excipients | |
| 127366101 | 12736610 | Throat tightness | |
| 127366101 | 12736610 | Urticaria |
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 |
|---|---|---|---|---|---|---|
| 127366101 | 12736610 | 1 | 201110 | 201110 | 0 | |
| 127366101 | 12736610 | 2 | 201110 | 2016 | 0 |