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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
92006361 | 9200636 | 1 | I | 20130325 | 20130325 | 20130331 | 20130331 | PER | US-009507513-1303USA013148 | MERCK | 0.00 | F | Y | 0.00000 | 20130331 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
92006361 | 9200636 | 1 | PS | NEXPLANON | 1 | SUBDERMAL | UNK | D | 957621/129139 | 21529 | IMPLANT | ||||||||
92006361 | 9200636 | 2 | SS | NEXPLANON | 1 | SUBDERMAL | UNK | D | 21529 | IMPLANT |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
92006361 | 9200636 | 1 | Contraception |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
92006361 | 9200636 | Device difficult to use | |
92006361 | 9200636 | No adverse event |
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 |
---|---|---|---|---|---|---|
92006361 | 9200636 | 1 | 20130325 | 0 | ||
92006361 | 9200636 | 2 | 20130325 | 0 |