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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126476371 | 12647637 | 1 | I | 2014 | 20160623 | 20160812 | 20160812 | EXP | DE-009507513-1606DEU011369 | MERCK | 29.00 | YR | F | Y | 0.00000 | 20160812 | MD | DE | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126476371 | 12647637 | 1 | PS | IMPLANON | ETONOGESTREL | 1 | Intramuscular | UNK | 21529 | IMPLANT | |||||||||
| 126476371 | 12647637 | 2 | SS | IMPLANON | ETONOGESTREL | 1 | Subdermal | UNK | 21529 | IMPLANT |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126476371 | 12647637 | 1 | Contraception |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126476371 | 12647637 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126476371 | 12647637 | Complication associated with device | |
| 126476371 | 12647637 | Device deployment issue | |
| 126476371 | 12647637 | Device difficult to use | |
| 126476371 | 12647637 | General anaesthesia | |
| 126476371 | 12647637 | Metrorrhagia |
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 |
|---|---|---|---|---|---|---|
| 126476371 | 12647637 | 1 | 2014 | 20160713 | 0 |