Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6703072 | 7384580 | I | 6703072-4 | 20100419 | 20100427 | EXP | 2010SP023039 | SCHERING-PLOUGH CORPORATION | YR | F | N | 20100426 | OT | FRANCE |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
6703072 | 1013597096 | PS | IMPLANON | 1 | 1 DF | D | D | 21529 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6703072 | 1013597096 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
6703072 | HO |
Reactions reported
Event ID | PT |
---|---|
6703072 | CHOLECYSTECTOMY |
6703072 | PREGNANCY WITH IMPLANT CONTRACEPTIVE |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6703072 | CR |
6703072 | FGN |
6703072 | HP |
6703072 | OTH |
Therapies reported
no results found |