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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123536563 | 12353656 | 3 | F | 201602 | 20160630 | 20160511 | 20160701 | EXP | ZA-009507513-1604ZAF013250 | MERCK | 27.00 | YR | F | Y | 45.00000 | KG | 20160701 | CN | ZA | ZA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123536563 | 12353656 | 1 | PS | IMPLANON | ETONOGESTREL | 1 | Subdermal | UNK | 21529 | IMPLANT |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123536563 | 12353656 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123536563 | 12353656 | Alopecia | |
| 123536563 | 12353656 | Complication associated with device | |
| 123536563 | 12353656 | Complication of device removal | |
| 123536563 | 12353656 | Migration of implanted drug | |
| 123536563 | 12353656 | Musculoskeletal stiffness | |
| 123536563 | 12353656 | Pain in extremity | |
| 123536563 | 12353656 | Vaginal haemorrhage | |
| 123536563 | 12353656 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 123536563 | 12353656 | 1 | 201404 | 0 |