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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126687872 | 12668787 | 2 | F | 2012 | 20160817 | 20160819 | 20160825 | PER | US-SHIRE-US201610424 | SHIRE | 0.00 | M | Y | 68.27000 | KG | 20160825 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126687872 | 12668787 | 1 | PS | VYVANSE | LISDEXAMFETAMINE DIMESYLATE | 1 | Oral | 30 MG, 1X/DAY:QD | 3144414 | 21977 | 30 | MG | CAPSULE | QD | |||||
| 126687872 | 12668787 | 2 | SS | VYVANSE | LISDEXAMFETAMINE DIMESYLATE | 1 | Oral | 30 MG, 1X/DAY:QD IN MORNING | 21977 | 30 | MG | CAPSULE | QD | ||||||
| 126687872 | 12668787 | 3 | SS | VYVANSE | LISDEXAMFETAMINE DIMESYLATE | 1 | Oral | 20 MG, 1X/DAY:QD IN AFTERNOON | 3140593 | 21977 | 20 | MG | CAPSULE | QD | |||||
| 126687872 | 12668787 | 4 | SS | VYVANSE | LISDEXAMFETAMINE DIMESYLATE | 1 | Oral | 20 MG, 1X/DAY:QD | 21977 | 20 | MG | CAPSULE | QD | ||||||
| 126687872 | 12668787 | 5 | SS | VYVANSE | LISDEXAMFETAMINE DIMESYLATE | 1 | Oral | 20 MG, 2X/DAY:BID | 21977 | 20 | MG | CAPSULE | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126687872 | 12668787 | 1 | Attention deficit/hyperactivity disorder |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126687872 | 12668787 | Adverse event | |
| 126687872 | 12668787 | Decreased appetite | |
| 126687872 | 12668787 | Drug effect decreased | |
| 126687872 | 12668787 | Inappropriate schedule of drug administration | |
| 126687872 | 12668787 | Mood altered | |
| 126687872 | 12668787 | Personality change |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 126687872 | 12668787 | 1 | 2010 | 2012 | 0 | |
| 126687872 | 12668787 | 2 | 2012 | 2015 | 0 | |
| 126687872 | 12668787 | 3 | 2012 | 2015 | 0 | |
| 126687872 | 12668787 | 4 | 2015 | 201607 | 0 | |
| 126687872 | 12668787 | 5 | 201607 | 0 |