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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124535182 | 12453518 | 2 | F | 2014 | 20160413 | 20160609 | 20160720 | PER | US-DSJP-DSU-2015-133132 | DAIICHI | 41.77 | YR | M | Y | 140.00000 | KG | 20160718 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124535182 | 12453518 | 1 | PS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | UNK | U | 21532 | FILM-COATED TABLET | |||||||||
| 124535182 | 12453518 | 2 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | Oral | 20/12.5 MG, QD | U | 21532 | 1 | DF | FILM-COATED TABLET | QD | |||||
| 124535182 | 12453518 | 3 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | Oral | 40/12.5 MG, QD | U | 21532 | 1 | DF | FILM-COATED TABLET | QD | |||||
| 124535182 | 12453518 | 4 | SS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | 40 MG, UNK | Y | 0 | 40 | MG | TABLET | |||||||
| 124535182 | 12453518 | 5 | C | CRESTOR | ROSUVASTATIN CALCIUM | 1 | 20 MG, QD | 0 | 20 | MG | QD | ||||||||
| 124535182 | 12453518 | 6 | C | ALLOPURINOL. | ALLOPURINOL | 1 | 300 MG, QD | 0 | 300 | MG | QD | ||||||||
| 124535182 | 12453518 | 7 | C | VICODIN | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124535182 | 12453518 | 1 | Hypertension |
| 124535182 | 12453518 | 4 | Product used for unknown indication |
| 124535182 | 12453518 | 5 | Product used for unknown indication |
| 124535182 | 12453518 | 6 | Product used for unknown indication |
| 124535182 | 12453518 | 7 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124535182 | 12453518 | Diverticulum | |
| 124535182 | 12453518 | Gastroenteritis | |
| 124535182 | 12453518 | Haemorrhoids | |
| 124535182 | 12453518 | Hiatus hernia | |
| 124535182 | 12453518 | 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 |
|---|---|---|---|---|---|---|
| 124535182 | 12453518 | 1 | 200610 | 0 | ||
| 124535182 | 12453518 | 2 | 200611 | 201507 | 0 | |
| 124535182 | 12453518 | 3 | 200611 | 201507 | 0 |