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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125574451 | 12557445 | 1 | I | 20160712 | 20160714 | 20160714 | EXP | PHHY2016CH096115 | NOVARTIS | 10.00 | YR | M | Y | 0.00000 | 20160714 | CN | CH | CH |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125574451 | 12557445 | 1 | PS | RITALIN | METHYLPHENIDATE HYDROCHLORIDE | 1 | Unknown | 10 MG, BID (1-0-0, SOMETIMES AT AN ADDITIONAL DOSE OF 1-0-1 (1 TABLET IN THE MORNING, 1 IN EVENING)) | 10187 | 10 | MG | TABLET | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125574451 | 12557445 | 1 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125574451 | 12557445 | LT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125574451 | 12557445 | Feeling abnormal | |
125574451 | 12557445 | Intentional self-injury | |
125574451 | 12557445 | Suicidal ideation |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |