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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6253704 | 7047486 | I | 6253704-2 | 20090616 | 20090630 | EXP | 2009-198956-NL | ORGANON USA INC. | 24 | YR | F | N | 69.4 | KG | 20090629 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6253704 | 1011826859 | PS | NUVARING | 1 | 1 NEW RING EVERY WEEK, 3 WEEKS LONG, WITH 1 RING-FREE WEEK | 21187 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6253704 | 1011826859 | CONTRACEPTION |
Outcome of event
Event ID | OUTC COD |
---|---|
6253704 | HO |
Reactions reported
Event ID | PT |
---|---|
6253704 | CONVULSION |
6253704 | DRUG PRESCRIBING ERROR |
6253704 | OVERDOSE |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6253704 | CSM |
Therapies reported
no results found |