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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124766933 | 12476693 | 3 | F | 20160706 | 20160617 | 20160907 | EXP | JP-PFIZER INC-2016300668 | PFIZER | 76.00 | YR | F | Y | 0.00000 | 20160907 | CN | JP | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124766933 | 12476693 | 1 | PS | TENORMIN | ATENOLOL | 1 | Oral | 25 MG, 2X/DAY | N | 73676 | 25 | MG | TABLET | BID | |||||
| 124766933 | 12476693 | 2 | SS | TENORMIN | ATENOLOL | 1 | Oral | UNK | N | 73676 | TABLET | ||||||||
| 124766933 | 12476693 | 3 | SS | TENORMIN | ATENOLOL | 1 | Oral | 5 MG, 2X/DAY | N | 73676 | 5 | MG | TABLET | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124766933 | 12476693 | 1 | Hypertension |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124766933 | 12476693 | Chest discomfort | |
| 124766933 | 12476693 | Drug dose omission | |
| 124766933 | 12476693 | Fall | |
| 124766933 | 12476693 | Limb discomfort | |
| 124766933 | 12476693 | Peripheral nerve palsy | |
| 124766933 | 12476693 | Prescribed underdose |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 124766933 | 12476693 | 1 | 2013 | 0 |