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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116457623 | 11645762 | 3 | F | 2012 | 20160822 | 20151020 | 20160829 | PER | US-009507513-1510USA008049 | MERCK | 0.00 | F | Y | 85.79000 | KG | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116457623 | 11645762 | 1 | PS | IMPLANON | ETONOGESTREL | 1 | Subdermal | UNK | 21529 | IMPLANT | |||||||||
| 116457623 | 11645762 | 2 | SS | NEXPLANON | ETONOGESTREL | 1 | Subdermal | UNK | Y | 0 | IMPLANT |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 116457623 | 11645762 | Complication associated with device | |
| 116457623 | 11645762 | Device deployment issue | |
| 116457623 | 11645762 | Device difficult to use | |
| 116457623 | 11645762 | Incorrect drug administration duration | |
| 116457623 | 11645762 | Infertility female | |
| 116457623 | 11645762 | Overdose |
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 |
|---|---|---|---|---|---|---|
| 116457623 | 11645762 | 1 | 2009 | 20160802 | 0 | |
| 116457623 | 11645762 | 2 | 2012 | 20151015 | 0 |