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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126941091 | 12694109 | 1 | I | 20150911 | 20160819 | 20160829 | 20160829 | EXP | CL-009507513-1608CHL011189 | MERCK | 43.00 | YR | F | Y | 0.00000 | 20160829 | MD | CL | CL |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126941091 | 12694109 | 1 | PS | IMPLANON | ETONOGESTREL | 1 | 1 DF, UNK | Y | 636756/705648 | 21529 | 1 | DF | IMPLANT |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126941091 | 12694109 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126941091 | 12694109 | Coital bleeding | |
126941091 | 12694109 | Complication associated with device | |
126941091 | 12694109 | Device deployment issue | |
126941091 | 12694109 | Menstruation irregular | |
126941091 | 12694109 | Metrorrhagia | |
126941091 | 12694109 | Migration of implanted drug | |
126941091 | 12694109 | 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 |
---|---|---|---|---|---|---|
126941091 | 12694109 | 1 | 20150911 | 20160714 | 0 |