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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523658 | 7212899 | I | 6523658-X | 20091101 | 20091222 | 20091231 | PER | JP-JNJFOC-20091203157 | ORTHO-MCNEIL-JANSSEN PHARMACEUTICALS, INC. | 33 | YR | F | Y | 20091231 | OT | JAPAN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523658 | 1012886671 | PS | CRAVIT | 2 | ORAL | 20634 | |||||
| 6523658 | 1012886672 | SS | SOLU-CORTEF | 1 | INTRAVENOUS | ||||||
| 6523658 | 1012886673 | SS | SOLU-CORTEF | 1 | INTRAVENOUS |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6523658 | 1012886671 | CYSTITIS |
| 6523658 | 1012886672 | OROPHARYNGEAL DISCOMFORT |
| 6523658 | 1012886673 | EYELID OEDEMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6523658 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6523658 | DYSPNOEA |
| 6523658 | ERYTHEMA |
| 6523658 | EYELID OEDEMA |
| 6523658 | LARYNGEAL OEDEMA |
| 6523658 | OROPHARYNGEAL DISCOMFORT |
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 |
|---|---|---|---|---|---|
| 6523658 | 1012886671 | 20091117 | 20091117 |