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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6738073 | 7400191 | I | 6738073-3 | 20080401 | 20100512 | 20100520 | EXP | 2009SP028413 | SCHERING-PLOUGH CORPORATION | 23 | YR | F | N | 130 | LBS | 20100519 | UNITED STATES |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6738073 | 1013738491 | PS | NUVARING | 1 | D | D | 21187 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6738073 | 1013738491 | CONTRACEPTION |
Outcome of event
Event ID | OUTC COD |
---|---|
6738073 | HO |
6738073 | OT |
Reactions reported
Event ID | PT |
---|---|
6738073 | ABORTION SPONTANEOUS |
6738073 | DRUG EXPOSURE BEFORE PREGNANCY |
6738073 | THROMBOTIC STROKE |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6738073 | CSM |
6738073 | OTH |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
6738073 | 1013738491 | 20070101 | 20070901 |