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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123158203 | 12315820 | 3 | F | 2008 | 20160823 | 20160428 | 20160830 | EXP | US-DSJP-DSU-2016-114687 | DAIICHI | 0.00 | Y | 0.00000 | 20160830 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123158203 | 12315820 | 1 | PS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | 25 MG, QD | U | 21286 | 25 | MG | TABLET | QD | ||||||
| 123158203 | 12315820 | 2 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | 40/25 MG, QD | U | 0 | 1 | DF | FILM-COATED TABLET | QD | ||||||
| 123158203 | 12315820 | 3 | C | PLAVIX | CLOPIDOGREL BISULFATE | 1 | UNK | 0 | |||||||||||
| 123158203 | 12315820 | 4 | C | CARTIA XT | DILTIAZEM HYDROCHLORIDE | 1 | 180 MG, QD | 0 | 180 | MG | QD | ||||||||
| 123158203 | 12315820 | 5 | C | CARVEDILOL. | CARVEDILOL | 1 | Oral | 25 MG, BID | 0 | 25 | MG | TABLET | BID | ||||||
| 123158203 | 12315820 | 6 | C | LOSARTAN/HCT | HYDROCHLOROTHIAZIDELOSARTAN POTASSIUM | 1 | 50-12.5 MG, UNK | 0 | 1 | DF |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123158203 | 12315820 | 1 | Hypertension |
| 123158203 | 12315820 | 2 | Hypertension |
| 123158203 | 12315820 | 3 | Anticoagulant therapy |
| 123158203 | 12315820 | 4 | Blood pressure measurement |
| 123158203 | 12315820 | 5 | Product used for unknown indication |
| 123158203 | 12315820 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123158203 | 12315820 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123158203 | 12315820 | Colon cancer | |
| 123158203 | 12315820 | Irritable bowel syndrome | |
| 123158203 | 12315820 | 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 |
|---|---|---|---|---|---|---|
| 123158203 | 12315820 | 1 | 2008 | 2014 | 0 | |
| 123158203 | 12315820 | 2 | 2008 | 2014 | 0 |