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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125998971 | 12599897 | 1 | I | 20160628 | 20160727 | 20160727 | EXP | ZA-PFIZER INC-2016362670 | PFIZER | 56.00 | YR | F | Y | 0.00000 | 20160727 | MD | ZA | ZA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125998971 | 12599897 | 1 | PS | ATENOLOL. | ATENOLOL | 1 | Unknown | U | U | 73676 | |||||||||
| 125998971 | 12599897 | 2 | SS | AMLODIPINE BESILATE | AMLODIPINE BESYLATE | 1 | Unknown | U | U | 19787 | |||||||||
| 125998971 | 12599897 | 3 | SS | ENALAPRIL MALEATE. | ENALAPRIL MALEATE | 1 | Unknown | U | U | 0 | |||||||||
| 125998971 | 12599897 | 4 | SS | METOPROLOL HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDEMETOPROLOL TARTRATE | 1 | Unknown | U | U | 0 | |||||||||
| 125998971 | 12599897 | 5 | SS | HYDRALAZINE | HYDRALAZINE HYDROCHLORIDE | 1 | Unknown | U | U | 0 | |||||||||
| 125998971 | 12599897 | 6 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | U | U | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125998971 | 12599897 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125998971 | 12599897 | Renal impairment |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |