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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127392291 | 12739229 | 1 | I | 20160820 | 20160907 | 20160913 | 20160913 | EXP | GB-MHRA-EYC 00144666 | GB-ELI_LILLY_AND_COMPANY-GB201609002071 | ELI LILLY AND CO | 45.00 | YR | F | Y | 60.32000 | KG | 20160913 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127392291 | 12739229 | 1 | PS | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | Oral | 20 MG, UNK | 2654561 | 18936 | 20 | MG | |||||||
| 127392291 | 12739229 | 2 | C | CERAZETTE /00754001/ | DESOGESTREL | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127392291 | 12739229 | 1 | Depression |
| 127392291 | 12739229 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127392291 | 12739229 | DS |
| 127392291 | 12739229 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127392291 | 12739229 | Anorgasmia | |
| 127392291 | 12739229 | Dissociation | |
| 127392291 | 12739229 | Social avoidant behaviour |
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 |
|---|---|---|---|---|---|---|
| 127392291 | 12739229 | 1 | 20160818 | 0 |