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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125831011 | 12583101 | 1 | I | 201606 | 20160718 | 20160722 | 20160722 | PER | US-ELI_LILLY_AND_COMPANY-US201607006394 | ELI LILLY AND CO | 50.00 | YR | F | Y | 0.00000 | 20160722 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125831011 | 12583101 | 1 | PS | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | UNK UNK, UNKNOWN | U | U | 18936 | ||||||||
| 125831011 | 12583101 | 2 | SS | TRINTELLIX | VORTIOXETINE HYDROBROMIDE | 1 | Unknown | 5 MG, UNKNOWN | N | U | 0 | 5 | MG | TABLET | |||||
| 125831011 | 12583101 | 3 | SS | TRINTELLIX | VORTIOXETINE HYDROBROMIDE | 1 | Unknown | 10 MG, UNKNOWN | N | U | 0 | 10 | MG | TABLET | |||||
| 125831011 | 12583101 | 4 | SS | TRINTELLIX | VORTIOXETINE HYDROBROMIDE | 1 | Unknown | 20 MG, UNKNOWN | N | U | 0 | 20 | MG | TABLET | |||||
| 125831011 | 12583101 | 5 | C | SAPHRIS | ASENAPINE MALEATE | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
| 125831011 | 12583101 | 6 | C | XANAX | ALPRAZOLAM | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
| 125831011 | 12583101 | 7 | SS | PROPRANOLOL | PROPRANOLOLPROPRANOLOL HYDROCHLORIDE | 1 | Unknown | UNK, UNKNOWN | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125831011 | 12583101 | 1 | Product used for unknown indication |
| 125831011 | 12583101 | 2 | Depression |
| 125831011 | 12583101 | 5 | Product used for unknown indication |
| 125831011 | 12583101 | 6 | Product used for unknown indication |
| 125831011 | 12583101 | 7 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125831011 | 12583101 | Myalgia | |
| 125831011 | 12583101 | Oedema peripheral | |
| 125831011 | 12583101 | Pruritus generalised | |
| 125831011 | 12583101 | Weight increased |
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 |
|---|---|---|---|---|---|---|
| 125831011 | 12583101 | 1 | 20160616 | 0 | ||
| 125831011 | 12583101 | 2 | 201604 | 20160604 | 0 | |
| 125831011 | 12583101 | 3 | 20160604 | 20160616 | 0 | |
| 125831011 | 12583101 | 4 | 20160616 | 20160624 | 0 |