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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127070951 | 12707095 | 1 | I | 201604 | 20160823 | 20160901 | 20160901 | EXP | US-009507513-1608USA012084 | MERCK | 0.00 | F | Y | 0.00000 | 20160901 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127070951 | 12707095 | 1 | PS | IMPLANON | ETONOGESTREL | 1 | Subdermal | 1 DF, UNK | 21529 | 1 | DF | IMPLANT |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127070951 | 12707095 | 1 | Contraception |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127070951 | 12707095 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127070951 | 12707095 | Complication associated with device | |
127070951 | 12707095 | Incorrect drug administration duration | |
127070951 | 12707095 | Migration of implanted drug | |
127070951 | 12707095 | 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 |
---|---|---|---|---|---|---|
127070951 | 12707095 | 1 | 201304 | 0 |