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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6316030 | 7086200 | I | 6316030-9 | 20090501 | 20090813 | 20090820 | EXP | GB-JNJFOC-20090804320 | ORTHO-MCNEIL-JANSSEN PHARMACEUTICALS, INC. | 68 | YR | F | Y | 54 | KG | 20090820 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6316030 | 1012076350 | PS | RISPERIDONE | 1 | ORAL | 020272 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6316030 | 1012076350 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
6316030 | OT |
Reactions reported
Event ID | PT |
---|---|
6316030 | DEEP VEIN THROMBOSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |