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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4330793 | 4108447 | F | 1 | 4330793-3 | 20040211 | 20040316 | 20040331 | EXP | USA040260006 | ELI LILLY AND COMPANY | 39 | YR | F | N | 75 | KG | 20040324 | MD |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4330793 | 1004757101 | PS | STRATTERA | 1 | 80 MG DAY | Y | 21411 | ||||
| 4330793 | 1004765288 | C | ZOLOFT | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4330793 | 1004757101 | ATTENTION DEFICIT/HYPERACTIVITY DISORDER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4330793 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4330793 | BACK PAIN |
| 4330793 | BLOOD MAGNESIUM INCREASED |
| 4330793 | CHEST PAIN |
| 4330793 | CORONARY ARTERY DISEASE |
| 4330793 | DRUG INEFFECTIVE |
| 4330793 | ELECTROCARDIOGRAM QT PROLONGED |
| 4330793 | ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL |
| 4330793 | FLUSHING |
| 4330793 | MYOCARDIAL ISCHAEMIA |
| 4330793 | NIGHTMARE |
| 4330793 | SEROTONIN SYNDROME |
| 4330793 | TACHYCARDIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4330793 | CR |
| 4330793 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4330793 | 1004757101 | 20040115 | 2 | WK |