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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1095023510 | 10950235 | 10 | F | 200210 | 20160914 | 20150324 | 20160919 | EXP | US-ELI_LILLY_AND_COMPANY-US201503005337 | ELI LILLY AND CO | 1.16 | YR | Y | 0.00000 | 20160919 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1095023510 | 10950235 | 1 | PS | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | UNK UNK, UNKNOWN | U | 18936 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 1095023510 | 10950235 | 1 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 1095023510 | 10950235 | OT |
| 1095023510 | 10950235 | CA |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 1095023510 | 10950235 | Acute myocardial infarction | |
| 1095023510 | 10950235 | Atrial septal defect | |
| 1095023510 | 10950235 | Cardiac murmur | |
| 1095023510 | 10950235 | Chest pain | |
| 1095023510 | 10950235 | Dizziness | |
| 1095023510 | 10950235 | Dyspnoea | |
| 1095023510 | 10950235 | Foetal exposure during pregnancy | |
| 1095023510 | 10950235 | Headache | |
| 1095023510 | 10950235 | Palpitations | |
| 1095023510 | 10950235 | Tachycardia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |