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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5472356 | 6431119 | I | 5472356-2 | 20070501 | 20070920 | 20070930 | EXP | FR-SHR-FR-2007-035391 | BERLEX | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5472356 | 1008989658 | PS | MIRENA | 1 | INTRA-UTERINE | 20 A?G/DAY, CONT | 021225 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5472356 | OT |
Reactions reported
Event ID | PT |
---|---|
5472356 | CEREBROVASCULAR ACCIDENT |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |