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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5472345 | 6431113 | I | 5472345-8 | 20070910 | 20070921 | 20070930 | EXP | GB-SHR-GB-2007-035677 | BERLEX | 50 | YR | F | Y | 20070928 | OT | UNITED KINGDOM |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5472345 | 1008989631 | PS | MIRENA | 1 | INTRA-UTERINE | 20 A?G/DAY, CONT | 021225 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5472345 | 1008989631 | MENORRHAGIA |
Outcome of event
Event ID | OUTC COD |
---|---|
5472345 | OT |
Reactions reported
Event ID | PT |
---|---|
5472345 | RETINAL VEIN OCCLUSION |
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 |
---|---|---|---|---|---|
5472345 | 1008989631 | 20061101 |