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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5049307 | 6086848 | I | 5049307-8 | 20060623 | 20060706 | EXP | 2006-144358-NL | NV ORGANON | F | N | 20060703 | OT | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5049307 | 1007459735 | PS | NUVARING | 1 | DF | 21187 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 5049307 | CONTRACEPTIVE DEVICE COMPLICATION |
| 5049307 | IMPLANT SITE FIBROSIS |
| 5049307 | INJURY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5049307 | FGN |
| 5049307 | HP |
| 5049307 | OTH |
Therapies reported
| no results found |