Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6738845 | 7372045 | F | 1 | 6738845-5 | 20090701 | 20100514 | 20100520 | EXP | 2010SP011012 | SCHERING-PLOUGH CORPORATION | 22 | YR | F | N | 20100519 | MD | UNITED KINGDOM |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6738845 | 1013742320 | PS | IMPLANON | 1 | SUBDERMAL | 1 DF; SBDE | Y | D | 21529 | ||
| 6738845 | 1013752116 | C | DIHYDROCODEINE BITARTRATE INJ | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6738845 | 1013742320 | CONTRACEPTION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6738845 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6738845 | DEPRESSION SUICIDAL |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6738845 | FGN |
| 6738845 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6738845 | 1013742320 | 20090107 | 20100101 |