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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125566402 | 12556640 | 2 | F | 20160721 | 20160714 | 20160801 | PER | US-PFIZER INC-2016329502 | PFIZER | 73.00 | YR | F | Y | 0.00000 | 20160801 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125566402 | 12556640 | 1 | PS | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | 40 MG, 1X/DAY | U | 20987 | 40 | MG | QD | |||||||
| 125566402 | 12556640 | 2 | C | LIPITOR | ATORVASTATIN CALCIUM | 1 | 10 MG, 1X/DAY | 0 | 10 | MG | QD | ||||||||
| 125566402 | 12556640 | 3 | C | MIRALAX | POLYETHYLENE GLYCOL 3350 | 1 | 2 GLASSES A DAY | 0 | |||||||||||
| 125566402 | 12556640 | 4 | C | PROCTOSOL HC | 2 | 1 DF, 1X/DAY (1 AT NIGHT, 2.5%) | 0 | 1 | DF | QD | |||||||||
| 125566402 | 12556640 | 5 | C | HYDROCORTISONE. | HYDROCORTISONE | 1 | UNKNOWN DOSE; 1X/DAY (AT BED) | 0 | CREAM | QD |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125566402 | 12556640 | Drug ineffective |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |