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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126257431 | 12625743 | 1 | I | 20160721 | 20160728 | 20160805 | 20160805 | EXP | NL-LRB-223124 | NL-PFIZER INC-2016373292 | PFIZER | 64.00 | YR | F | Y | 0.00000 | 20160805 | MD | NL | NL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126257431 | 12625743 | 1 | PS | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Oral | 40 MG, QD | Y | 20987 | 40 | MG | TABLET | QD | |||||
| 126257431 | 12625743 | 2 | C | CALCI CHEW | 2 | Oral | 500 MG, QD | 0 | 500 | MG | CHEWABLE TABLET | QD | |||||||
| 126257431 | 12625743 | 3 | C | ATORVASTATINE | ATORVASTATIN | 1 | Oral | 40 MG, QD | 0 | 40 | MG | TABLET | QD | ||||||
| 126257431 | 12625743 | 4 | C | ALLOPURINOL. | ALLOPURINOL | 1 | Oral | 300 MG, QD | 0 | 300 | MG | TABLET | QD | ||||||
| 126257431 | 12625743 | 5 | C | ACETYLSALICYLZUUR | ASPIRIN | 1 | Oral | 80 MG, QD | 0 | 80 | MG | TABLET | QD | ||||||
| 126257431 | 12625743 | 6 | C | CARVEDILOL. | CARVEDILOL | 1 | Oral | 6.25 MG, QD | 0 | 6.25 | MG | TABLET | QD | ||||||
| 126257431 | 12625743 | 7 | C | SPIRONOLACTON | SPIRONOLACTONE | 1 | Oral | 25 MG, QD | 0 | 25 | MG | TABLET | QD | ||||||
| 126257431 | 12625743 | 8 | C | FOSINOPRIL | FOSINOPRIL | 1 | Oral | 10 MG, QD | 0 | 10 | MG | TABLET | QD | ||||||
| 126257431 | 12625743 | 9 | C | BUMETANIDE. | BUMETANIDE | 1 | Oral | 2 MG, QD | 0 | 2 | MG | TABLET | QD |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126257431 | 12625743 | HO |
| 126257431 | 12625743 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126257431 | 12625743 | Hypocalcaemia | |
| 126257431 | 12625743 | Hypomagnesaemia |
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 |
|---|---|---|---|---|---|---|
| 126257431 | 12625743 | 1 | 2006 | 20160721 | 0 |