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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6523391 | 7234930 | I | 6523391-4 | 20091222 | 20091231 | EXP | US-ROCHE-676509 | ROCHE | M | Y | 20091231 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6523391 | 1012885613 | PS | MYCOPHENOLATE MOFETIL | 1 | UNKNOWN | 050722 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6523391 | 1012885613 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
6523391 | HO |
Reactions reported
Event ID | PT |
---|---|
6523391 | HOSPITALISATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |