Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127598671 | 12759867 | 1 | I | 20160915 | 20160919 | 20160919 | EXP | BR-JNJFOC-20160914978 | JANSSEN | 0.00 | A | F | Y | 0.00000 | 20160919 | CN | BR | BR |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127598671 | 12759867 | 1 | PS | CONCERTA | METHYLPHENIDATE HYDROCHLORIDE | 1 | Unknown | U | 21121 | 54 | MG | SUSTAINED RELEASE TABLETS | QD | ||||||
| 127598671 | 12759867 | 2 | C | STILNOX | ZOLPIDEM TARTRATE | 1 | Unknown | D | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127598671 | 12759867 | 1 | Depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127598671 | 12759867 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127598671 | 12759867 | Exposure during pregnancy | |
| 127598671 | 12759867 | Off label use | |
| 127598671 | 12759867 | Product use issue | |
| 127598671 | 12759867 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |