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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124687552 | 12468755 | 2 | F | 2011 | 20160902 | 20160615 | 20160910 | EXP | US-SANKYOGER-DSU-2012-05026 | DAIICHI | 0.00 | Y | 0.00000 | 20160910 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124687552 | 12468755 | 1 | PS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | UNK | N | 21532 | FILM-COATED TABLET | |||||||||
| 124687552 | 12468755 | 2 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | Oral | 40/12.5MG, QD | N | 21532 | 1 | DF | FILM-COATED TABLET | QD | |||||
| 124687552 | 12468755 | 3 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | Oral | 1/2 (40/12.5MG) TABLET QD | N | 21532 | FILM-COATED TABLET | QD | |||||||
| 124687552 | 12468755 | 4 | SS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | 20 MG, UNK | U | 0 | 20 | MG | TABLET | |||||||
| 124687552 | 12468755 | 5 | SS | WELCHOL | COLESEVELAM HYDROCHLORIDE | 1 | Oral | 1250 MG, TID | N | 0 | 1250 | MG | TABLET | TID | |||||
| 124687552 | 12468755 | 6 | SS | WELCHOL | COLESEVELAM HYDROCHLORIDE | 1 | N | 0 | TABLET | ||||||||||
| 124687552 | 12468755 | 7 | C | LIPITOR | ATORVASTATIN CALCIUM | 1 | UNKNOWN EVERY | 0 | |||||||||||
| 124687552 | 12468755 | 8 | C | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | UNKNOWN EVERY | 0 | |||||||||||
| 124687552 | 12468755 | 9 | C | XANAX | ALPRAZOLAM | 1 | UNKNOWN EVERY | 0 | |||||||||||
| 124687552 | 12468755 | 10 | C | AMBIEN | ZOLPIDEM TARTRATE | 1 | Oral | 10 MG, QD | 0 | 10 | MG | QD | |||||||
| 124687552 | 12468755 | 11 | C | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 124687552 | 12468755 | 12 | C | MULTIVITAMIN /00097801/ | VITAMINS | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124687552 | 12468755 | 1 | Hypertension |
| 124687552 | 12468755 | 4 | Hypertension |
| 124687552 | 12468755 | 5 | Blood cholesterol increased |
| 124687552 | 12468755 | 6 | Diarrhoea |
| 124687552 | 12468755 | 7 | Blood cholesterol increased |
| 124687552 | 12468755 | 8 | Product used for unknown indication |
| 124687552 | 12468755 | 9 | Product used for unknown indication |
| 124687552 | 12468755 | 10 | Product used for unknown indication |
| 124687552 | 12468755 | 11 | Product used for unknown indication |
| 124687552 | 12468755 | 12 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124687552 | 12468755 | HO |
| 124687552 | 12468755 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124687552 | 12468755 | Acute kidney injury | |
| 124687552 | 12468755 | Cholecystectomy | |
| 124687552 | 12468755 | Coeliac disease | |
| 124687552 | 12468755 | Depression | |
| 124687552 | 12468755 | Drug administration error | |
| 124687552 | 12468755 | Dyspnoea | |
| 124687552 | 12468755 | Malabsorption |
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 |
|---|---|---|---|---|---|---|
| 124687552 | 12468755 | 2 | 2005 | 2012 | 0 | |
| 124687552 | 12468755 | 3 | 20120620 | 0 | ||
| 124687552 | 12468755 | 4 | 2013 | 0 | ||
| 124687552 | 12468755 | 5 | 2012 | 0 | ||
| 124687552 | 12468755 | 7 | 2012 | 0 | ||
| 124687552 | 12468755 | 8 | 2012 | 0 | ||
| 124687552 | 12468755 | 9 | 2012 | 0 |