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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127251881 | 12725188 | 1 | I | 20160903 | 0 | 20160905 | 20160905 | DIR | US-FDA-349834 | FDA-CTU | 56.00 | YR | F | N | 125.10000 | KG | 20160905 | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127251881 | 12725188 | 1 | PS | LOVASTATIN. | LOVASTATIN | 1 | Oral | Y | D | K4886 | 20170930 | 0 | 1 | DF | COATED TABLET | HS | |||
| 127251881 | 12725188 | 3 | C | LISINOPRIL. | LISINOPRIL | 1 | 0 | ||||||||||||
| 127251881 | 12725188 | 5 | C | CITALOPRAM | CITALOPRAM HYDROBROMIDE | 1 | 0 | ||||||||||||
| 127251881 | 12725188 | 7 | C | AROMASIN | EXEMESTANE | 1 | 0 | ||||||||||||
| 127251881 | 12725188 | 9 | C | CPAP | DEVICE | 1 | 0 | ||||||||||||
| 127251881 | 12725188 | 11 | C | FLEXITOUCH | 2 | 0 | |||||||||||||
| 127251881 | 12725188 | 13 | C | B VITAMINS | CYANOCOBALAMINDEXPANTHENOLNIACINAMIDEPYRIDOXINE HYDROCHLORIDERIBOFLAVIN 5'-PHOSPHATE SODIUMTHIAMINE HYDROCHLORIDEVITAMIN B COMPLEX | 1 | 0 | ||||||||||||
| 127251881 | 12725188 | 15 | C | POTASSIUM | POTASSIUM | 1 | 0 | ||||||||||||
| 127251881 | 12725188 | 17 | C | TYLENOL | ACETAMINOPHEN | 1 | 0 | ||||||||||||
| 127251881 | 12725188 | 19 | C | BABY ASPIRIN | ASPIRIN | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127251881 | 12725188 | 1 | Blood cholesterol increased |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127251881 | 12725188 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127251881 | 12725188 | Diarrhoea | |
| 127251881 | 12725188 | Urine output decreased |
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 |
|---|---|---|---|---|---|---|
| 127251881 | 12725188 | 1 | 20160831 | 20160904 | 0 |