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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5205818 | 6416432 | I | 5205818-3 | 20061227 | 20070105 | DIR | 51 | YR | F | N | 102.6 | KG | 20070104 | PH | N | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5205818 | 1008031813 | PS | MIRENA | 1 | INTRA-UTERINE | 1 INTRAUTERINE DEVICE Q 5 YEARS INTRA-UTERI | D | D | |||
5205818 | 1008060878 | SS | AVIANE-21 | 1 | ORAL | 1 TABLET DAILY PO | D | D |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5205818 | 1008031813 | DYSMENORRHOEA |
5205818 | 1008031813 | MENORRHAGIA |
5205818 | 1008060878 | DYSMENORRHOEA |
5205818 | 1008060878 | MENORRHAGIA |
Outcome of event
Event ID | OUTC COD |
---|---|
5205818 | HO |
5205818 | LT |
Reactions reported
Event ID | PT |
---|---|
5205818 | 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 |
---|---|---|---|---|---|
5205818 | 1008031813 | 20060801 | 20061227 | ||
5205818 | 1008060878 | 20061101 | 20061227 |