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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127225281 | 12722528 | 1 | I | 20160906 | 20160907 | 20160907 | PER | US-ELI_LILLY_AND_COMPANY-US201609001764 | ELI LILLY AND CO | 0.00 | F | Y | 57.00000 | KG | 20160907 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127225281 | 12722528 | 1 | PS | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | 20 MG, QD | N | U | C469654C | 18936 | 20 | MG | CAPSULE | QD | |||
| 127225281 | 12722528 | 2 | SS | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | N | U | 18936 | CAPSULE | |||||||||
| 127225281 | 12722528 | 3 | C | TIROSINT | LEVOTHYROXINE SODIUM | 1 | Unknown | UNK, UNKNOWN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127225281 | 12722528 | 1 | Depression |
| 127225281 | 12722528 | 2 | Anxiety |
| 127225281 | 12722528 | 3 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127225281 | 12722528 | Mental disorder | |
| 127225281 | 12722528 | 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 |
|---|---|---|---|---|---|---|
| 127225281 | 12722528 | 1 | 201512 | 201605 | 0 |