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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127272461 | 12727246 | 1 | I | 19990520 | 20160901 | 20160909 | 20160909 | EXP | BR-009507513-1609BRA002154 | MERCK | 23.00 | YR | F | Y | 63.00000 | KG | 20160909 | CN | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127272461 | 12727246 | 1 | PS | IMPLANON | ETONOGESTREL | 1 | Subdermal | LEFT ARM | 21529 | IMPLANT |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127272461 | 12727246 | 1 | Menstrual cycle management |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127272461 | 12727246 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127272461 | 12727246 | Caesarean section | |
| 127272461 | 12727246 | Maternal exposure before pregnancy | |
| 127272461 | 12727246 | Pre-eclampsia | |
| 127272461 | 12727246 | Product use issue |
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 |
|---|---|---|---|---|---|---|
| 127272461 | 12727246 | 1 | 19990520 | 20020520 | 0 |