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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125601731 | 12560173 | 1 | I | 20160122 | 0 | 20160714 | 20160714 | DIR | 63.00 | YR | M | N | 83.20000 | KG | 20160713 | N | PH | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125601731 | 12560173 | 1 | PS | LITHIUM. | LITHIUM | 1 | Oral | 600 MG PM PO | Y | D | 0 | 600 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125601731 | 12560173 | 1 | Bipolar disorder |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125601731 | 12560173 | RI |
125601731 | 12560173 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125601731 | 12560173 | Asthenia | |
125601731 | 12560173 | Blood creatinine increased | |
125601731 | 12560173 | Confusional state | |
125601731 | 12560173 | Disorientation | |
125601731 | 12560173 | Hypophagia | |
125601731 | 12560173 | Tremor |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | CASEID | RPSR COD |
---|---|---|
125601731 | 12560173 | HP |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
125601731 | 12560173 | 1 | 20110224 | 20160122 | 0 |