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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125901882 | 12590188 | 2 | F | 20120315 | 20160502 | 20160725 | 20160725 | EXP | US-DSJP-DSU-2016-115256 | DAIICHI | 69.71 | YR | F | Y | 76.00000 | KG | 20160725 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125901882 | 12590188 | 1 | SS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | UNK | Y | 0 | TABLET | |||||||||
125901882 | 12590188 | 2 | SS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | Oral | 40 MG, QD | Y | 0 | 40 | MG | TABLET | QD | |||||
125901882 | 12590188 | 3 | PS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | 40MG/25MG, QD | U | 21532 | 1 | DF | FILM-COATED TABLET | QD | ||||||
125901882 | 12590188 | 4 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | 40MG/12.5MG, QD | U | 21532 | 1 | DF | FILM-COATED TABLET | QD | ||||||
125901882 | 12590188 | 5 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | 20MG/25MG, QD | U | 21532 | 1 | DF | FILM-COATED TABLET | QD | ||||||
125901882 | 12590188 | 6 | SS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | 20MG/12.5MG, QD | U | 21532 | 1 | DF | FILM-COATED TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125901882 | 12590188 | 1 | Product used for unknown indication |
125901882 | 12590188 | 3 | Hypertension |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125901882 | 12590188 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125901882 | 12590188 | Acute kidney injury | |
125901882 | 12590188 | Diverticulum | |
125901882 | 12590188 | Haemorrhoids | |
125901882 | 12590188 | Hiatus hernia | |
125901882 | 12590188 | 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 |
---|---|---|---|---|---|---|
125901882 | 12590188 | 1 | 2003 | 0 | ||
125901882 | 12590188 | 3 | 200702 | 201305 | 0 |