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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126466432 | 12646643 | 2 | F | 20160831 | 20160812 | 20160909 | EXP | NL-009507513-1607NLD008814 | MERCK | 39.00 | YR | F | Y | 0.00000 | 20160909 | OT | NL | NL |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126466432 | 12646643 | 1 | PS | IMPLANON | ETONOGESTREL | 1 | Intramuscular | UNK | 21529 | IMPLANT |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126466432 | 12646643 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126466432 | 12646643 | Complication associated with device | |
126466432 | 12646643 | Device deployment issue | |
126466432 | 12646643 | Device difficult to use | |
126466432 | 12646643 | General anaesthesia | |
126466432 | 12646643 | Incorrect route of drug administration | |
126466432 | 12646643 | 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 |
---|---|---|---|---|---|---|
126466432 | 12646643 | 1 | 2013 | 0 |