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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125810381 | 12581038 | 1 | I | 20160628 | 20160721 | 20160721 | EXP | PHHY2016DE090166 | NOVARTIS | 0.00 | A | M | Y | 0.00000 | 20160721 | PH | DE | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125810381 | 12581038 | 1 | PS | RITALIN LA | METHYLPHENIDATE HYDROCHLORIDE | 1 | Unknown | 80 MG, QD (4DF) | 21284 | 80 | MG | EXTENDED RELEASE CAPSULES | QD | ||||||
| 125810381 | 12581038 | 2 | SS | RITALIN LA | METHYLPHENIDATE HYDROCHLORIDE | 1 | Unknown | 60 MG, QD (3DF) | 21284 | 60 | MG | EXTENDED RELEASE CAPSULES | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125810381 | 12581038 | 1 | Alcohol withdrawal syndrome |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125810381 | 12581038 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125810381 | 12581038 | Product use issue | |
| 125810381 | 12581038 | Unresponsive to stimuli |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |