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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127208781 | 12720878 | 1 | I | 20160821 | 20160822 | 20160907 | 20160907 | PER | US-ELI_LILLY_AND_COMPANY-US201608010970 | ELI LILLY AND CO | 8.00 | YR | F | Y | 0.00000 | 20160907 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127208781 | 12720878 | 1 | PS | STRATTERA | ATOMOXETINE HYDROCHLORIDE | 1 | Unknown | 10 MG, QD | 21411 | 10 | MG | CAPSULE | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127208781 | 12720878 | 1 | Attention deficit/hyperactivity disorder |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127208781 | 12720878 | Abdominal discomfort | |
| 127208781 | 12720878 | Eye irritation | |
| 127208781 | 12720878 | Fatigue | |
| 127208781 | 12720878 | Lacrimation increased | |
| 127208781 | 12720878 | Nausea | |
| 127208781 | 12720878 | Ocular hyperaemia | |
| 127208781 | 12720878 | Sneezing | |
| 127208781 | 12720878 | Wrong technique in product usage process |
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 |
|---|---|---|---|---|---|---|
| 127208781 | 12720878 | 1 | 20160821 | 0 |