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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120938645 | 12093864 | 5 | F | 201210 | 20160711 | 20160219 | 20160715 | EXP | US-009507513-1602USA008605 | MERCK | 32.50 | YR | F | Y | 90.70000 | KG | 20160715 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120938645 | 12093864 | 1 | PS | IMPLANON | ETONOGESTREL | 1 | Subdermal | 68 MG, ONCE (EVERY 3 YEARS) | Y | 21529 | 68 | MG | IMPLANT | 1X | |||||
| 120938645 | 12093864 | 2 | SS | IMPLANON | ETONOGESTREL | 1 | Y | 21529 | IMPLANT |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120938645 | 12093864 | 1 | Contraception |
| 120938645 | 12093864 | 2 | Menstrual cycle management |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 120938645 | 12093864 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120938645 | 12093864 | Chest pain | |
| 120938645 | 12093864 | Complication associated with device | |
| 120938645 | 12093864 | Device difficult to use | |
| 120938645 | 12093864 | Gastric infection | |
| 120938645 | 12093864 | Haemorrhage | |
| 120938645 | 12093864 | Implant site fibrosis | |
| 120938645 | 12093864 | Implant site scar | |
| 120938645 | 12093864 | Incorrect drug administration duration | |
| 120938645 | 12093864 | Paraesthesia | |
| 120938645 | 12093864 | Peripheral swelling | |
| 120938645 | 12093864 | Product use issue | |
| 120938645 | 12093864 | 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 |
|---|---|---|---|---|---|---|
| 120938645 | 12093864 | 1 | 201210 | 0 |