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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126509301 | 12650930 | 1 | I | 20160701 | 0 | 20160812 | 20160812 | DIR | 49.00 | YR | F | N | 106.00000 | LBS | 20160811 | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126509301 | 12650930 | 1 | PS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Oral | N | D | 0 | HS |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126509301 | 12650930 | 1 | Fibromyalgia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126509301 | 12650930 | LT |
| 126509301 | 12650930 | DS |
| 126509301 | 12650930 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126509301 | 12650930 | Aggression | |
| 126509301 | 12650930 | Anxiety | |
| 126509301 | 12650930 | Confusional state | |
| 126509301 | 12650930 | Depressed mood | |
| 126509301 | 12650930 | Dizziness | |
| 126509301 | 12650930 | Fatigue | |
| 126509301 | 12650930 | Hyperhidrosis | |
| 126509301 | 12650930 | Nervous system disorder | |
| 126509301 | 12650930 | Paraesthesia | |
| 126509301 | 12650930 | Suicidal ideation | |
| 126509301 | 12650930 | Tremor | |
| 126509301 | 12650930 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |