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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126142091 | 12614209 | 1 | I | 20160726 | 20160802 | 20160802 | PER | US-SHIRE-US201609593 | SHIRE | 18.00 | YR | F | Y | 0.00000 | 20160802 | PH | US | US |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126142091 | 12614209 | 1 | PS | VYVANSE | LISDEXAMFETAMINE DIMESYLATE | 1 | Oral | 30 MG, AS REQ'D (ONLY TAKES BEFORE A TEST IN SCHOOL) | U | U | 21977 | 30 | MG | CAPSULE | |||||
126142091 | 12614209 | 2 | C | FOCALIN /01611102/ | 2 | Oral | 5 - 10 MG, 1X/DAY:QD (1/2 - 1 TABLET) | 0 | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126142091 | 12614209 | 1 | Product used for unknown indication |
126142091 | 12614209 | 2 | Attention deficit/hyperactivity disorder |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126142091 | 12614209 | Inappropriate schedule of drug administration | |
126142091 | 12614209 | No adverse event |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |