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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126471621 | 12647162 | 1 | I | 20160809 | 0 | 20160811 | 20160811 | DIR | 49.00 | YR | F | N | 140.00000 | LBS | 20160810 | Y | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126471621 | 12647162 | 1 | PS | PROPRANOLOL, 80 MG | PROPRANOLOLPROPRANOLOL HYDROCHLORIDE | 1 | Oral | Y | Y | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126471621 | 12647162 | 1 | Hypertension |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126471621 | 12647162 | OT |
126471621 | 12647162 | LT |
126471621 | 12647162 | DS |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126471621 | 12647162 | Craniocerebral injury | |
126471621 | 12647162 | Dizziness | |
126471621 | 12647162 | Headache | |
126471621 | 12647162 | Hypoaesthesia | |
126471621 | 12647162 | Loss of consciousness | |
126471621 | 12647162 | Nausea | |
126471621 | 12647162 | Transient ischaemic attack |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |