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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127267281 | 12726728 | 1 | I | 2016 | 20160826 | 20160908 | 20160908 | PER | US-SHIRE-US201611814 | SHIRE | 15.00 | YR | M | Y | 0.00000 | 20160908 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127267281 | 12726728 | 1 | PS | VYVANSE | LISDEXAMFETAMINE DIMESYLATE | 1 | Oral | UNK, UNKNOWN | 21977 | CAPSULE | |||||||||
| 127267281 | 12726728 | 2 | SS | DAYTRANA | METHYLPHENIDATE | 1 | Transdermal | 60 MG (TWO 30 MG PATCHES)1X/DAY:QD | N | 0 | 60 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127267281 | 12726728 | 1 | Product used for unknown indication |
| 127267281 | 12726728 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127267281 | 12726728 | Anger | |
| 127267281 | 12726728 | Depressed mood | |
| 127267281 | 12726728 | Drug ineffective | |
| 127267281 | 12726728 | Feeling abnormal |
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 |
|---|---|---|---|---|---|---|
| 127267281 | 12726728 | 1 | 201605 | 0 | ||
| 127267281 | 12726728 | 2 | 201605 | 0 |