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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126615971 | 12661597 | 1 | I | 20160812 | 20160817 | 20160817 | PER | US-PFIZER INC-2016387074 | PFIZER | 57.00 | YR | F | Y | 99.79000 | KG | 20160817 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126615971 | 12661597 | 1 | PS | LIPITOR | ATORVASTATIN CALCIUM | 1 | N | 20702 | FILM-COATED TABLET | ||||||||||
| 126615971 | 12661597 | 2 | C | LOSARTAN. | LOSARTAN | 1 | 0 | ||||||||||||
| 126615971 | 12661597 | 3 | C | ATENOLOL. | ATENOLOL | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126615971 | 12661597 | 3 | Blood pressure measurement |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126615971 | 12661597 | Condition aggravated | |
| 126615971 | 12661597 | Feeling abnormal | |
| 126615971 | 12661597 | Gait disturbance | |
| 126615971 | 12661597 | Muscle spasms |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |