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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5472344 | 6431112 | I | 5472344-6 | 20070101 | 20070921 | 20070930 | EXP | FR-SHR-FR-2007-035671 | BERLEX | 44 | YR | F | Y | 20070928 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5472344 | 1008989630 | PS | MIRENA | 1 | INTRA-UTERINE | 20 A?G/DAY, CONT | 021225 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5472344 | 1008989630 | CONTRACEPTION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5472344 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5472344 | DEEP VEIN THROMBOSIS POSTOPERATIVE |
| 5472344 | PREGNANCY WITH CONTRACEPTIVE DEVICE |
| 5472344 | PULMONARY EMBOLISM |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5472344 | 1008989630 | 20050317 | 20070101 |