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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124536922 | 12453692 | 2 | F | 201305 | 20160517 | 20160609 | 20160720 | PER | US-DSJP-DSU-2016-112194 | DAIICHI | 46.44 | YR | F | Y | 122.00000 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124536922 | 12453692 | 1 | PS | BENICAR HCT | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | 40/25 MG, UNK | 21532 | 1 | DF | FILM-COATED TABLET | ||||||||
124536922 | 12453692 | 2 | SS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | UNK | Y | 0 | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124536922 | 12453692 | 1 | Hypertension |
124536922 | 12453692 | 2 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124536922 | 12453692 | Candida infection | |
124536922 | 12453692 | Gastrooesophageal reflux disease | |
124536922 | 12453692 | Hiatus hernia | |
124536922 | 12453692 | Malabsorption | |
124536922 | 12453692 | Perivascular dermatitis |
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 |
---|---|---|---|---|---|---|
124536922 | 12453692 | 1 | 201003 | 2014 | 0 | |
124536922 | 12453692 | 2 | 201011 | 20140401 | 0 |