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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127365401 | 12736540 | 1 | I | 20160812 | 20160830 | 20160912 | 20160912 | EXP | US-SHIRE-US201611689 | SHIRE | 65.21 | YR | F | Y | 113.38000 | KG | 20160912 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127365401 | 12736540 | 1 | PS | VYVANSE | LISDEXAMFETAMINE DIMESYLATE | 1 | Oral | 20 MG, 1X/DAY:QD | Y | 3144404 | 21977 | 20 | MG | CAPSULE | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127365401 | 12736540 | 1 | Binge eating |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127365401 | 12736540 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127365401 | 12736540 | Blood pressure decreased | |
| 127365401 | 12736540 | Chest discomfort | |
| 127365401 | 12736540 | Chest pain | |
| 127365401 | 12736540 | Dyspnoea | |
| 127365401 | 12736540 | Feeling abnormal | |
| 127365401 | 12736540 | Heart rate irregular | |
| 127365401 | 12736540 | Unevaluable event |
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 |
|---|---|---|---|---|---|---|
| 127365401 | 12736540 | 1 | 20160812 | 20160813 | 0 |