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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127890382 | 12789038 | 2 | F | 2016 | 20160915 | 20160928 | 20160929 | EXP | FR-TEVA-690945ROM | TEVA | 16.00 | YR | M | Y | 0.00000 | 20160929 | MD | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127890382 | 12789038 | 1 | PS | PROPRANOLOL | PROPRANOLOLPROPRANOLOL HYDROCHLORIDE | 1 | HALF-TABLET PER DAY, IN THE MORNING | U | S13937 | 70233 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127890382 | 12789038 | 1 | Palpitations |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127890382 | 12789038 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127890382 | 12789038 | Asthma | |
| 127890382 | 12789038 | Drug ineffective | |
| 127890382 | 12789038 | Dyspnoea | |
| 127890382 | 12789038 | Palpitations | |
| 127890382 | 12789038 | Product substitution issue | |
| 127890382 | 12789038 | Wheezing |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |