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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124542743 | 12454274 | 3 | F | 2016 | 20160804 | 20160610 | 20160829 | PER | US-009507513-1605USA010988 | MERCK | 35.18 | YR | F | Y | 0.00000 | 20160829 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124542743 | 12454274 | 1 | PS | ETONOGESTREL IMPLANT- UNKNOWN | ETONOGESTREL | 1 | Subdermal | AN IMPLANT | Y | 21529 | 1 | DF | IMPLANT | ||||||
| 124542743 | 12454274 | 2 | SS | IMPLANON | ETONOGESTREL | 1 | Subdermal | A ROD FOR 3 YEARS | 233808001 | 21529 | 1 | DF | IMPLANT |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124542743 | 12454274 | Complication associated with device | |
| 124542743 | 12454274 | Menstruation irregular | |
| 124542743 | 12454274 | Product use issue | |
| 124542743 | 12454274 | 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 |
|---|---|---|---|---|---|---|
| 124542743 | 12454274 | 1 | 20130426 | 0 | ||
| 124542743 | 12454274 | 2 | 20130426 | 0 |