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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121726193 | 12172619 | 3 | F | 20160714 | 20160311 | 20160718 | EXP | PHHY2016DE028971 | NOVARTIS | 0.00 | A | M | Y | 0.00000 | 20160718 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121726193 | 12172619 | 1 | PS | RITALIN LA | METHYLPHENIDATE HYDROCHLORIDE | 1 | Unknown | 100 MG, QD | S0001 | 21284 | 100 | MG | EXTENDED RELEASE CAPSULES | QD | |||||
121726193 | 12172619 | 2 | SS | RITALIN LA | METHYLPHENIDATE HYDROCHLORIDE | 1 | 21284 | EXTENDED RELEASE CAPSULES |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
121726193 | 12172619 | 1 | Fatigue |
121726193 | 12172619 | 2 | Narcolepsy |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
121726193 | 12172619 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
121726193 | 12172619 | Drug dependence | |
121726193 | 12172619 | Drug ineffective | |
121726193 | 12172619 | Overdose | |
121726193 | 12172619 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |