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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6737816 | 7400987 | I | 6737816-2 | 20100514 | 20100514 | 20100520 | EXP | 2010SP027449 | SCHERING-PLOUGH CORPORATION | YR | F | N | 20100518 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6737816 | 1013737425 | PS | MIRALAX | 1 | ORAL | PO | D | D | 22015 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6737816 | 1013737425 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
6737816 | OT |
Reactions reported
Event ID | PT |
---|---|
6737816 | PHARYNGEAL OEDEMA |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6737816 | CSM |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
6737816 | 1013737425 | 20100514 |