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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4832348 | 5847612 | F | 3 | 4832348-0 | 20050701 | 20051102 | 20051117 | EXP | USA0507101988 | ELI LILLY AND COMPANY | 49 | YR | F | N | 72 | KG | 20051109 | MD | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4832348 | 1006642223 | PS | CYMBALTA | 1 | 60 MG DAY | 8RG01M | 20060401 | 21427 | |||
| 4832348 | 1006665618 | C | VICODIN | 1 | |||||||
| 4832348 | 1006665619 | C | ULTRACET | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4832348 | 1006642223 | FIBROMYALGIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4832348 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4832348 | ABDOMINAL PAIN |
| 4832348 | CONVULSION |
| 4832348 | DIZZINESS |
| 4832348 | DRUG EFFECT INCREASED |
| 4832348 | FEELING HOT |
| 4832348 | GASTROINTESTINAL HAEMORRHAGE |
| 4832348 | HEADACHE |
| 4832348 | NAUSEA |
| 4832348 | VAGINAL HAEMORRHAGE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4832348 | CSM |
| 4832348 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4832348 | 1006642223 | 20050622 |