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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125844901 | 12584490 | 1 | I | 20160408 | 20160722 | 20160722 | EXP | GB-ABBVIE-16P-167-1683671-00 | ABBVIE | 0.00 | F | Y | 0.00000 | 20160722 | CN | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125844901 | 12584490 | 1 | PS | DEPAKOTE | DIVALPROEX SODIUM | 1 | Unknown | Y | UNKNOWN | 18723 | 500 | MG | TABLET | BID | |||||
125844901 | 12584490 | 2 | C | RAMIPRIL. | RAMIPRIL | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125844901 | 12584490 | 1 | Bipolar disorder |
125844901 | 12584490 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125844901 | 12584490 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125844901 | 12584490 | Abdominal pain upper | |
125844901 | 12584490 | Alopecia | |
125844901 | 12584490 | Balance disorder | |
125844901 | 12584490 | Gastric disorder | |
125844901 | 12584490 | Headache | |
125844901 | 12584490 | Loss of consciousness | |
125844901 | 12584490 | Peripheral swelling |
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 |
---|---|---|---|---|---|---|
125844901 | 12584490 | 1 | 20120629 | 20160311 | 0 |