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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126800121 | 12680012 | 1 | I | 201608 | 20160817 | 20160824 | 20160824 | PER | US-JNJFOC-20160814803 | JANSSEN | 62.60 | YR | A | F | Y | 68.04000 | KG | 20160824 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126800121 | 12680012 | 1 | PS | ULTRAM ER | TRAMADOL HYDROCHLORIDE | 1 | Unknown | N | 21692 | 300 | MG | SUSTAINED RELEASE TABLETS | |||||||
126800121 | 12680012 | 2 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | U | 0 | UNSPECIFIED | |||||||||
126800121 | 12680012 | 3 | SS | ULTRAM ER | TRAMADOL HYDROCHLORIDE | 1 | Unknown | N | 21692 | 300 | MG | SUSTAINED RELEASE TABLETS |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126800121 | 12680012 | 1 | Arthralgia |
126800121 | 12680012 | 2 | Arthralgia |
126800121 | 12680012 | 3 | Arthralgia |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126800121 | 12680012 | Drug dose omission | |
126800121 | 12680012 | Pain | |
126800121 | 12680012 | Thinking abnormal | |
126800121 | 12680012 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |