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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 105327137 | 10532713 | 7 | F | 20140822 | 20160713 | 20141021 | 20160725 | EXP | US-009507513-1409USA012359 | MERCK | 23.85 | YR | F | Y | 66.21000 | KG | 20160725 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 105327137 | 10532713 | 1 | PS | IMPLANON | ETONOGESTREL | 1 | A ROD (68 MG) | 802611 | 21529 | 68 | MG | IMPLANT |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 105327137 | 10532713 | 1 | Contraception |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 105327137 | 10532713 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 105327137 | 10532713 | Complication associated with device | |
| 105327137 | 10532713 | Complication of device removal | |
| 105327137 | 10532713 | Device difficult to use | |
| 105327137 | 10532713 | Implant site pain | |
| 105327137 | 10532713 | Incorrect drug administration duration | |
| 105327137 | 10532713 | Incorrect route of drug administration | |
| 105327137 | 10532713 | Migration of implanted drug |
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 |
|---|---|---|---|---|---|---|
| 105327137 | 10532713 | 1 | 20110822 | 0 |