Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4330794 | 4117288 | F | 1 | 4330794-5 | 20040309 | 20040310 | 20040331 | EXP | USA040361710 | ELI LILLY AND COMPANY | 40 | YR | F | N | 20040324 |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4330794 | 1004757102 | PS | STRATTERA | 1 | 100 MG DAY | D | 7EE89B | 20050701 | 21411 | ||
| 4330794 | 1004765368 | C | LITHIUM | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4330794 | 1004757102 | ATTENTION DEFICIT/HYPERACTIVITY DISORDER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4330794 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4330794 | CHEST PAIN |
| 4330794 | GASTROOESOPHAGEAL REFLUX DISEASE |
| 4330794 | HYPERHIDROSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4330794 | CSM |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4330794 | 1004757102 | 20031201 |